TENDER DOCUMENT - Coach Outlet online

TENDER DOCUMENT - Coach Outlet online
TENDER DOCUMENT
TENDER NO. 004 (SECOND CALL) :
Due Date : 02/01/2013
GMC/Equipment/12-13/---------------
FOR SUPPLY OF EQUIPMENT
:
(MACHINERY, INSTRUMENTS
& OTHER ITEMS)
CONTRACT DOCUMENT CONSISTING OF TENDER NOTICE. TENDER
FORM, RATE SHEET, TENDER CONDITIONS, SPECIFICATIONS AND
TECHNICAL PARTICULARS., FORM OF AGREEMENT ETC.
1
DEAN
GANDHI MEDICAL COLLEGE
BHOPAL
NATIONAL COMPETITIVE BIDDING FOR THE SUPPLY OF EQUIPMENTS
(MACHINERY, INSTRUMENTS & OTHER ITEMS)
BID DOCUMENT PURCHASE START DATE
: 07/12/2012
LAST DATE AND TIME FOR
SUBMISSION OF BIDS. 02/01/2013
Time up to 1.00 P.M.
: DATE AND TIME OF OPENING OF BIDS
Starting New Post Graduate Disciplines and Incresing PG
Seats & other Equipments for Various Department
(ENVELOP "A")
02/01/2013
Time at 3.00 P.M.
-
PLACE OF OPENING OF BIDS
: CONFERENCE HALL
DEAN, GANDHI MEDICAL COLLEGE
BHOPAL
ADDRESS FOR CORRESPONDENCE
: DEAN, GANDHI MEDICAL COLLEGE,
SULTANIA ROAD, BHOPAL (M.P.)
PIN-462001
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3
.SECTIONII:INSTRUCTIONTOBIDDER TABLEOFCLASSES
S.No.
Topic.
Page No.
Page No
S.No.
Topic
.
A. Introduction
1.
2.
3.
4.
Scope of work
Eligible Bidders
Eligible and services
Cost of Bidding
5
5
5
5
20.
21.
22.
23
24
25
26
B. Bidding Documents
5. Contents of Bidding Documents
6. Clarification of Bidding Documents
7. Amendments of Bidding Documents
C. Preparation of Bids
8. Language of Bid
9. Documents Comprising the Bid
10. Bid Form
11. Bid Prices
12. Bid Currencies
13. Documents Establishing Bidder’s
Eligibility and Qualifications
14. Documents Establishing Goods
Eligibility and Conformity to
Bidding Documents
Late bids
13
Modification and withdrawl of bids 13
Bid Opening and Evaluation of bids 14
Clarification of bids
15
Preliminary Examination
15
Evaluation & Comparison of bids 15
Contacting of the purchaser
16
Award of contract
6
6
6
27 Post Qualification
28. Award criteria
29. Purchaser's right to vary quantities
7
30.
7
7
7
8
8
31.
32.
33.
34
35
16
16
17
The purchaser's right to
17
accept any bid and to reject any or all bids
Notification of Rate Contract
17
Signing of Rate Contract
17
Performance Security &
18
Inspection Charges
Placement of supply order
18
Corrupt or Fraudulent Practices
18
9
15. Bid Security
16. Period of validity of Bids
10
10
D. Submission of Bids
17. Bid stages
18. Price Bid
19. Deadline for submission of bids
11
13
13
4
-4-
5
A. Introduction
1.
Scope of Work
1.1
The Dean Gandhi Medical College Bhopal M.P. require Equipments ( Machinery Instruments and other
items) for various Departments of Gandhi Medical College, Bhopal & associated Hospitals Bid is issued for
procurement of equipment (list of equipments enclosed) at competitive rates. After finalization of the bid the
contract will be awarded to successful bidders for supply of the items, during one year or till further order on rate
contract basis on approved rates The Machines / Equipments have to be Supplied and installed to the various
department of Gandhi Medical College Bhopal & associated Hospitals.
2.
Eligible Bidders
2.1
The invitation for Bids is open to all eligible bidders.
2.2
Bidders should not be associated, or have been associated in the past, directly or indirectly with a firm or
any of in affiliates which have been engaged by the Purchaser to provide consulting service for the
preparation of the design, specification and other to be used for the procurement of the goods to the
purchaser under this invitation of Bids.
2.3
Government owned enterprise in the Purchaser’s country may participate only if they are legally and
financially autonomous, if they operates under commercial law, and if they are not a dependent agency of
the Purchaser.
2.4
The tenders shall clarify/state whether he/they are manufacturer, accredited agent or sole representative
indenting principals name & address. The offers of firms who are not manufacturer or direct authorized
agent will be summarily rejected. Sub-distributors will not be accepted.
3.
3.1
3.2
3.3
Eligible Goods and Services
All goods and ancillary services to be supplied under the Contract shall be from their country of origin
For purposes of this clause, “origin “ means the place where the goods are mined, grown, or produced or
from which the ancillary services are supplied. Goods are produced when, through manufacturing,
processing or substantial and major assembling of components, a commercially recognized product results
that is substantially different in basic characteristics or in purpose or utility from its components.
The origin of goods and services is distinct from the nationality of Bidder.
4.
Cost of Bidding
4.1
The Bidder shall bear all costs associated with the preparation and submission of its bid, and Dean Gandhi
Medical College Bhopal (hereinafter referred to as “the Purchaser”) will in no case be responsible or liable
for these costs, regardless of the conduct or outcome of the bidding process.
-5-
6
B. The Bidding Documents
5.
Contents of Bidding Documents
5.1
The goods required, bidding procedures and contract terms are prescribed in the Bidding Documents. In
addition to the Invitation for Bids, the Bidding Documents include:
(a)
(b)
(c)
(d)
(e)
(f)
(g)
(h)
(i)
(j)
(k)
(l)
(m)
(n)
(o)
(p)
(q)
5.2
Instruction to Bidders (ITB);
General Conditions of Contract (GCC);
Special Conditions of Contract (SCC);
Bid Form;
Annexure-I ( Commercial Tax Clearance Certificate);
Annexure-II (Manufacture Authorization Form);
Annexure-III (Declaration / Undertaking Form);
Annexure-IV (Proforma for Performance statement);
Annexure-V (Annual Turnover Statement);
Annexure-VI (Specification of required. Various equipments
Annexure-VII (Performance Security form);
Annexure-VIII ( Contract Agreement form);
Annexure-IX (Details of Manufacturing Unit);
Annexure-X (Price Schedule); and
Annexure-XI (Price Schedule for CMC (include free labour repair, other service and spare parts);
Annexure-XII (Details of Service Centre in Bhopal / M.P.);
Annexure-XIII (Check list A,B,C);
5.3
The Bidder is expected to examine all instructions, forms, terms, specifications and annexure in the Bidding
Documents. Failure to furnish all information required by the Bidding Documents or submissions of a bid
not substantially responsive to the Bidding Documents in every respect will be at the Bidders risk and may
result in rejection of its bid.
The Bidding document is not transferable
6.
Clarification of Bidding Documents-
6.1
A Prospective Bidder requiring any clarification of the Bidding Documents may notify the Purchaser in
writing or by Fax at the Purchaser’s mailing address indicated in the invitation for Bids. The Purchaser will
respond in writing to any request for clarification of the Bidding Documents, which it receives not later than
10 days prior to the dead line for submission of bids prescribed by the purchaser.
7.
Amendment of Bidding Documents
7.1
At any time prior to the deadline for submission of bids, the purchaser may , for any reason, whether at it on
initiative or in response to a clarification requested by the prospective bidders, modify the bidding
documents by amendment.
The Prospective bidders will be notified of the amendment through mail, and will be binding on them.
7.2
6
7.3
In order to allow prospective bidders reasonable time in which to take the amendment in to account in
preparing their bids , the Purchaser, at its discretion , may extend the deadline for the submission of bids.
C.
Preparation of Bids
8.
Language of Bid
8.1
The Bid prepare by the bidder, as well as all correspondence and documents printed literature and leaflets
relating to the bid exchanged by the Bidder and the the purchaser shall be written and in English/Hindi
language. Numeric numbers should always be in english only.
9.Documents
9.1
Comprising the Bid
The bid prepared by the bidder shall comprise the following components :
(a)
A bid Form and price schedule completed in accordance with ITB Clause 10,11 and 12;
(b)
Documentary evidence established in accordance with ITB clause 13 that the bidder is eligible and is
qualify to perform the contract if its bid is accepted;
(c)
Documentary evidence established in accordance with ITB clause 14 that the good sand
ancillary services to be supplied by the bidder are eligible goods and services and conform to the
bidding documents ; and
(d)
Bid Security furnished in accordance with ITB clause 15
10. Bid Form
10.1
The Bidders shall complete the Bid form and the appropriate Price Schedule Furnished in the Bidding
Documents indicating for the goods to be supplied, a brief description of the goods, their country of origin
and prices.
11.
Bid prices
11.1
Bid has been called for the various equipments / machines given in the specification in technical annexure
VI The bidder should quote the price for the equipments/machines offered for. The specification of the
equipments/machines should be as per details given in annexure VI Any variation on lower side may result
in the rejection of the tender.
11.2
Prices (inclusive of excise duty/ custom duty transportation packing, insurance, installation, training,
loading.- Unloading warranty service charge , inspection and any incidental charges, but exclusive of
CST/VAT) should be quoted for each of the required equipments/ machine separately on door delivery basis
according to the unit ordered. Tender for the supply of equipments etc. with cross condition like “AT
CURENT MARKET RATES “ shall not be accepted. Handling, clearing, transport charges etc. shall not be
paid . The delivery should be made as stipulated in the supply order placed with successful bidders
conditional tenders will not be accepted.
11.3
Each bid must contain the unit price of each equipment in digits as well as alphabets. Any discrepancy
between the figures and words, the amount written in words will prevail. Alterations/over-writings, unless
legibly attested by the tenderer, shall disqualify the tenders. The tenders should be signed by the tenderer
himself/themselves or his/their authorized agent on his/their behalf (Authorization may be enclosed, if
applicable) under his stamp. The tenderers should take care that the rates and amounts are written in such a
way that interpolation is not possible, no blanks should be left which would otherwise, make the tender
redundant.
11.4 The price quoted by the bidders shall not, in any case exceed the controlled price, if any, fixed by the
7
Central/State Government and the Maximum Retail DGS & D Price (MRP) Rate Constricting Authority at
its discretion, will exercise, the right to revise the price at any stage, on lower side so as to confirm to the
controlled price or MRP as the case may be. This discretion will be exercised without prejudice to any other
action that may be taken against the bidder.
11.5
11.6
To ensure sustained supply without any interruption the The purchaser, reserves the right to split
orders for supplying the requirements among more than one bidders, provided the prices and other
conditions of supply are equal.
The prices quoted and accepted will be binding on the bidder for the stipulated period and any increases
in the
price will not be entertained till the completion of this tender period. Cross Conditions
such as “SUBJECT TO AVAILABILITY” “ SUPPLIES WILL BE MADE US AND WHEN
SUPPLIES ARE RECEIVED” etc., will not be considered under any circumstances and the tenders of
those who have given such conditions shall be treated as incomplete and Tender will be summarily rejected.
12.
Bid Currencies
12.1
Prices shall be quoted in Indian Rupees.
13.
Documents establishing Bidder's eligibility and qualification
13.1
Pursuant to ITB Clause 9, the Bidder shall furnish, as part of its bid, documents establishing the bidder's
eligibility to bid and its qualification to perform the Contract if its bid is accepted.
13.2
The documentary evidence of the Bidder's qualifications to perform the Contract if its bid is accepted, shall
establish by “the Purchaser” satisfactions.
(a)
Bids may be submitted by the primary manufacture or importer or their authorized distributor
provided the bid is accompanied by a duly notarized letter of authority from the primary
manufacturer/importer. In case of authorized distributor the bidder should have minimum three
years association with manufacturer / importer (as per authorization form given in Annexure II)
(b)
Documentary evidence for the Registration of the company with details of the Name, Address,
Telephone Number, Fax Number, E-mail Address of the Managing Director / Partners / Proprietor
and Name, Address, Telephone number, fax, email of primary manufacturer/ The instruments such
as power of attorney, resolution of board etc., authorizing an officer/person of
the bidder should be submitted with the tender and such Authorized officer/person of the bidder
should sign the tender documents. Authorization letter nominating a responsible person of the
bidder to transact the business with the purchaser.
(c)
The bidder shall submit printed original catalogues of primary manufacturer and any other technical
documents like data sheet or operational manual of equipment with highlighting the features in
portal along with the other documents. In catalogue, the quoted product number and name should be
highlighted and item code should also be written with catalogue, against which that product is
quoted. These documents are also to be submitted in physical form before due date along with Bid
security. Specification of equipments supplied should match the specification in catalogue. Leaflets,
literatures, should invariably be attached for ready reference clearly marking the item code no.
(d)
The Bidder/manufacturer should have at least three years manufacturing / distributorship experience.
The Bidder should submit a list of user of quoted equipments manufactured by the Principal
Manufacturer for last three years. These list should also contain the supplies related to the Govt.
hospital/ Medical Colleges / Public Sector undertaking / Undertaking hospital and other institutions
of repute. Bidder should submit details of installation in Annexure IV.
(e).
The bidder should have at least one service centre in Madhya Pradesh, with a team of trained service
engineer/technical staff the details in this regard as per Annexure-XII shall be submitted. In case at
the time of tender service centre is not available in M.P., then he shall submit undertaking to
establish the service centre before the award of contract.
(f).
The bidder shall submit the specification's compliance / deviation report duly filled and signed
which clearly bring out the deviation from the specification if any 'given in Annexure-VI.
(g).
Sales Tax / VAT Clearance certificate, as on 31.03.2011/12 (as per form attached in
Annexure-I).
(h).
Details of Manufacturing Unit I Annexure - IX. The details containing the name and address of the
premises where the items quoted are actually manufactured.
(i).
Documents, if any, to show that the manufacturing unit/importer has been recog11ized, by WHO,
UNICEF, ISO/ or any other Certificate The bidder should also submit national and
international quality certificates like ISI/CE/C" mark/IEC standard or equivalent certificate of
quoted product, if available.
j.
The bidder shall furnish a notarized affidavit in the format given in Annexure-III declaring that the
bidder accepts all terms and conditions of the tender.
k. .
Annual turnover (i.e. turnover for each year separately) in the last three financial years shall not be
less than Rs.100.00 Lacs .for Manufacturer and Rs. 50.00 Lacs for the authorized distributor.
Annual turnover statement for 3 years submitted in the format given in Annexure- V certified by the
Auditor/CA.
In case of imported equipment IEC certificate of importer / bidder shall be submitted.
l.
m.
Concern / Company have not been debarred / blacklisted either by The purchaser or by any State
Government or Central Government Organization for the quoted product or as a whole. Affidavit to
this effect shall be submitted by the concern / company.
n.
All documents should be seal and stamped.
14. Documents establishing Goods Eligibility and Conformity to Bidding Documents
14.1 Pursuant to Clause 9, the Bidder shall furnish, as part of its bid, documents establishing the eligibility
and conformity to the Bidding Documents of all goods and services, which the Bidder proposes to
supply under the Contract.
15. Bid Security
15.1 Pursuant to ITB Clause 9, the Bidder shall furnish, as part of its bid, the bid security which shall be
equal to 3% of the total aggregate value of Item's of Equipments tendered for, subject to a maximum
of Rs 3.00 Lacs . ( Rs. three Lacs Only) No concession / exemption shall be allowed F.D.R. should
be attached. The aggregate values of items tendered for and 3% amount of it should be shown
separately in Envelop "A.
15.2
The bid security is required to protect the Purchaser Contracting Authority against risk of Bidder's
business conduct which would warrant the security's forfeiture, pursuant to ITB Clause 15.7.
15.3
The bid security shall be in Indian Rupees and shall be in form of Fixed Deposit for 18 months in
favour of Dean, Gandhi. Medical College, Bhopal: of any Nationalised Bank.
15.4
Any bid not secured in accordance with ITB Clause 15.1 and 15.3 above will be rejected by the "The
Purchaser" as non-responsive, pursuant to ITB Clause 23.
15.5
Unsuccessful Bidder's bid security will be discharged / returned as promptly as possible upon the
successful Bidders signing the Contract, pursuant to ITB Clause 31 or after the expiration of the
period of bid validity prescribed by the "The Purchaser" pursuant to ITB clause 16. No interest is
payable on bid security.
15.6
The successful Bidder's bid security will be discharged upon the Bidders signing the Contract,
pursuant to ITB Clause 30, and furnishing the performance security, pursuant to ITB Clause 31. No
interest is payable on bid security.
15.7
The bid security may be forfeited:
a.
If a bidder
(i) withdraws its bid during the period of bid validity specified by the Bidder on the Bid
Form;
b.
In case of a successful Bidder, if the Bidder fails:
(i) to sign the Contract in accordance with ITB Clause 30; or
(ii) to furnish performance security and Inspection Charges in accordance with ITB Clause
31.
Period of Validity of Bids
Quoted Prices of Bids shall be valid for 180 (One hundred eighty) days after the date of bid opening
prescribed by The purchaser pursuant to ITB clause 21. A bid valid for a shorter period shall be
rejected by The purchaser as non-responsive. This price or negotiated price on acceptance shall
remain fixed till contract period or till further order.
16.
16.1
16.2
In exceptional circumstances, the purchaser may solicit the Bidder's consent to an extension of the
period of validity. The request and the responses thereto shall be made in writing. A Bidder may
refuse the request without forfeiting its bid security. A bidder granting the request will not be
required nor permitted to modify its bid.
16.3
No bid may be modified subsequent to the deadline for submission of Bids.
10
16.4
No Bid may be withdrawn in the interval between the deadline for the submission of Bids and
expiration of the period of bid validity specified by the Bidder on the Bid Form. Withdrawal of a bid
during this interval may result in the Bidders forfeiture of its bid security pursuant to ITB Sub-clause
15.7.
D. Submission of Bids
17.
Bid Stages
17.1
Bid should be submitted in following system and should furnish the following documents failing
which their bid shall not be accepted:Envelops - D: Main Tender Envelop
(E.M.D. in the form of F.D.R./DD only)
(1) Fixed Deposit for 18 Months 3% of total aggregate value of item or equipments tendered for as
E.M.D. (issued by Nationalized bank in the name of Dean, Gandhi Medical College Bhopal.
(Refundable). (Any other instrument for example like Cheque will not be accepted).
A statement of Aggregate value of total items tendered for and value of 3% (E.M.D. maximum of
Rs. one Lack.)
· Without submission of E.M.D. the. tender will be summarily rejected as per rules.
(2) Tender document fee if uploaded from website Rs 5000.) Those bidders who have already
submittted their tender document & tender fees in response to our tender dated 12/10/2012 of
Rs. 5000/- in previous tender need not submit this fees again however they are required to
enclose the photocopy of the reciept of the Tender document fees.
· In no case the tender cost fee should be mixed with E.M.D. amount. Fee cost is not
refundable.
Essential Documents as mentioned below.
.
3.
The bidders have to submit name of the items, its code no. for which they are quoting in the price
bid. Such names and items code of the items should be submitted along with the technical bid falling which
the tendere4' price bid will not be opened. The bidder has to submit name of item and the code number in
the format given below.
Sr. No.
Item Code
Name of Equipment
4
Registration Certificate of the company with details of the Name, Address, Telephone Number, Fax
Number, e-mail address of the firm and of the Managing Director / Partners / Proprietor.
Authorization letter from manufacturer authorizing a person to transact a business with the purchaser.
The instruments such as power of attorney, resolution of board etc., authorizing an officer/person of the
bidder should be submitted with the tender and such Authorized officer/person of the bidder should sign the
tender documents.
5.
Bidders should have the registration under Commercial Tax Authority should be attached.
6.
Sales Tax VAT Clearance certificate, as on 31.03.2012 (as per form attached in Annexure-I).
(Note: Sales Clearance from sales tax department up to 31.03.2012 must be attached with this
annexure)
Annexure-II (Manufacture Authorization Form)
Annexure-III (Undertaking Form / Declaration Form)
Annexure-IV (Proforma for installation in last Three years of the manufacturers.
11
7.
8.
9
10.
11.
12
Annexure-V (Annual Turnover Statement)
Annexure - IX (Details of Manufacturing Unit)
Annexure - XII (Details of Service Centre at Bhopal/M.P.)
13.
The bidder should also submit national & international quality certificates like ISI/CE/C ISO-9002, IP/BP
etc" mark / lEC standard or equivalent certificate of quoted product, if available.
Concern / Company have not been debarred / blacklisted either by the purchaser or by any State
Government or Central Government Organization. this effect shall be submitted by the concern /
company. Affidavit that the firm has no vigilance case / CBI case pending against him / s. Affidavit that
the firm has not supplied the same item at the lower rate than quo-~" tender to any Govt. / Semi Govt. or
any other organization.
14.
15.
Original Bid Form duly signed by authorized signatory as per Section V, duly sealed and
signed by the bidder on each page for acceptance of Terms and Conditions.Please submit Only Annexure V (as whole
tender documents from page No. 1 to 57)as acceptance of all terms and conditions of tender from page No. 1 to 57,
(This Section V page will be considered as acceptance of all tender terms and condition from the bidder)
(Save Paper Save Environment).
16.
17.
18..
Statement of good financial standing from bankers.
In case of imported equipment IEC certificate of importer / bidder shall be submitted.
Any other document if required.
Technical/Financial bid documents must not be submitted with this envelope.
Envelop - B: (Technical Bid)This envelop must be submitted department wise.
(i)
Technical bid for the quoted equipments etc. should be signed and stamped on each page.
The bidder shall submit the specification's compliance / deviation report duly filled and signed which clearly
bring out the deviation from the specification if any given in Annexure-VI.
(ii)
A list of user of quoted equipments by the Principal Manufacturer for last three years. These
list should also contain the supplies related to the Govt. hospital/Medical Colleges / Public
Sector undertaking / Undertaking hospital and other institutions of repute. Bidder should
submit details of installation in Annexure IV
(iii) Literature of original catalogue of the product attached for reference in two copies.
(iv) Quality certificates such as CE/ US FDA product wise.
Envelop - C: (Financial Bid) This envelop must be submitted department wise.
i.
Financial bid for the quoted equipments etc. should be signed and stamped on each page (ANNEXURE-X)
ii.
CMC charges as per Annexure Xl.
iii.
Bidder should show recurring expenditure of each equipment separately.
All the three envelops sealed in main envelop i.e. marked ENVELOP-D"TENDERFOR
EQUIPMENTSETC."All the envelopes A, B. C. must be Wax sealed using sealing Wax and official seal,
sealed cello taped, moisture free and strong.
All the enclosures and photocopies should be self certified and stamped. i.
Reference No. of the tender
ii.
Tender regarding
iii.
Due date of submission of tender form
iv.
Due date for opening of the tender
v.
Name of the firm
12
NOTE:TENDERSUBMITTEDWITHOUTFOLLOWINGTHEABOVE'PROCEDURESWIL BE
SUMMARILYREJECTED.
13
17.2
PRICE BID-
The Bidder should furnish the following:
i)
The rate quoted per unit (landed price) in Annexure-X (Suggested sample proforma of price
schedule) shall be inclusive of Excise Duty / Custom Duty, freight, packing, insurance, inspection &
testing charges etc. exclusive of VAT and should be F.O.R. destination.
ii)
The rate quoted in column 8 of annexure (suggested sample proforma of price schedule) should be
for a unit and given specification. The bidder is not permitted to change / alter specification or unit
size given in the Annexure - X.
iii)
Bidder has to quote rates strictly for the items which are mentioned in the tender.
iv)
Rates quoted for items other than mentioned in the tender form then that particular item will not be
entertained.
v)
If a bidder has quoted same rates for an equipment manufactured by two different manufacturers
then the choice to make the contract from any of them or both will be the discretion of The
purchaser.
vi)
The rates of each item should be quoted in figures as well as in words also otherwise the tender is
liable to be rejected.
vii)
The bidder/parent company will have to inter into comprehensive Maintenance Contract (include
free labour, repair, other services & spare parts) for the next seven years after the expiry of three
years warranty period in Annexure - XI.
(viii) The bidder should quote equipments which will have guarantee / warranty of atleast 3 years,
equipments which have less than 3 years warranty will not be entertainment and so should not be
quoted.
ix)
Bidder should show recurring expenditure of each equipment separately.
18. Deadline for Submission of Bids
18.1 Bids will not be accepted after the time and date specified in the invitation for Bids (Section I).
18.2 The The purchaser may, as its discretion, extend the deadline for submission of the bids by
amending the Bid Documents in accordance with ITB Clause - 7 in which case all right and
obligations of the The purchaser and Bidders previously subject to the deadline shall thereafter be
subject to the deadline as extended.
18.3 The The purchaser will not be responsible for any delay or non-receipt of tender documents.
19. Late Bids
19.1 No Bid shall be considered after the last date and time of submission of bid
20.
Modification and Withdrawal of Bids
20.2 No bid may be modified subsequent to the deadline for submission of bids.
20.3 No bid may be withdrawn in the interval between the deadline for submission of bids and the
expiration of the period of bid validity specified by the Bidder on the Bid Form. Withdrawal of a
bid during this interval may result in the Bidder's forfeiture of its bid security, pursuant to ITB
Clause 15.7
13
E. Bid Opening and Evaluation of Bids
21.
Opening of Bids by the purchaser
Opening of Bid process:
21.1 Bid will be opened on the day, date & place specified by the The purchaser.
21.2 All bidders are entitled to be present at the date and time & place for opening of Bids.
21.3 Only one representative of each Bidder is entitled to remain present at the time of bid opening.
Bidder's representative who is present shall sign a register evidencing his/her attendance. In the
event of the specified date of Bid opening being declared a holiday for the The purchaser, the Bids
shall be opened at the appointed time and location on the next working day.
21.4 Opening of bid will be sequential process.
21.5 Bids will be opened in the presence of Bidder's representatives who choose to attend on the
specified date and time fixed for opening the bid. Envelop D containing envelop A, B and C,
E nvelop " A", will be immediately opened. Documents together with contents of envelop A will
be subject to scrutiny, those bidders whose documents and contents are as per tender conditions
will only be deemed qualified for opening of technical bid. The date and time of opening of
technical bid (envelop B) will be made available on website at the earliest of opening of bid and
will be communicated simultaneously to those who qualify for opening of bid. Technical and
Price bid will be submitted separately. Technical Bid will be evaluated as per specification and
NCB terms and conditions by the Technical Committee. Those bidders who qualify for the
technical bid will be invited for· demonstration of equipment on the day, date & place specified
by the purchaser. The bidders will have to demonstrate the equipments on the date, day and place
specified, failing which their bid will be rejected. Thereafter, Price Bid (envelop C) will be opened
only for those bidders whose bid will be found technically responsive after demonstration.
Opening of date of price bid will be communicated separately only to those who qualify and will
be displayed on the specified website.
21.6 The Bidders' names, presence or absence of the requisite bid security will be announced at the
opening of Technical Bid.
21.7 Bidders who were found eligible on satisfying the criteria for technical evaluation and inspection by
the technical committee can only be invited to be present at the date and time for opening of Price
Bid of the tender.
14
22. Clarification of Bids
22.1 During evaluation of bids, the The purchaser may, at its discretion, ask the Bidder for clarification
of its Bid. Any clarification submitted by a bidder in respect to its bid and that is not in response to
a request by the The purchaser shall not be considered. The request for clarification and the
response shall be in writing and no change in prices or substance of the bid shall be sought, offered
or permitted except to confirm the correction of arithmetic errors discovered by the The purchaser
in the evaluation of the bids.
23.
Preliminary Examination
23.1 The the purchaser will examine the bids to determine whether they are complete, whether any
computational errors have been made, whether required sureties have been furnished, whether all
documents are there, whether the documents have been properly signed, and whether the bids are
generally in order.
23.2 The purchaser may waive any minor informality or non-conformity or irregularity or omissions in a
bid which does not constitute a material deviation, provided such a waiver does not prejudice or
affect the relative ranking of any Bidder.
23.3 Prior to the detailed evaluation, pursuant to ITB Clause 24, the The purchaser will determine the
substantial responsiveness of each bid to the bidding documents. For purposes of these Clauses, a
substantially responsive bid is one which conforms to all the documents terms, conditions and
specifications of the bidding documents without material deviations. The Rate Contracting
Authorities determination of a bid's responsiveness is to be based on the contents of the bid itself
without recourse to extrinsic evidence.
23.4 If a bid is substantially responsive, the The purchaser may request that the bidder submit the
necessary information or documentation, within a reasonable period of time to rectify nonmaterial
nonconformities or omissions in the bid related to documentation requirements.
Such omissions shall not be related to any aspect of the price of the bid. Failure of the bidder to
comply with the request within the stipulated time may result in the rejection of its bid.
23.5 If a bid determined as not substantially responsive, it will be rejected by the The purchaser and may
not subsequently be made responsive by the bidder by correction of the nonconformity.
24. Evaluation and Comparison of Bids
24.1 The purchaser will evaluate and compare the bids previously determined to be substantially
responsive, pursuant to Clause 23. Bids will be evaluated with reference to various criteria as
15
Specified in bid document and one of such criteria is that the rate per unit of (landed price) i.e. rate
per equipment for determining the Lt rate (Lowest rate).
24.2 Purchase will also be made from SC / ST firms as per State Government rules.
25. Contacting the The purchaser
25.1 Subject to ITB Clause 22, no Bidder shall contact the The purchaser on any matter relating to its
bid, from the time of the bid opening to the time Rate Contract is awarded.
25.2 Any effort by a Bidder to influence the The purchaser in its decisions on bid evaluation, bid
comparison or contract award may result in rejection of the Bidder's bid. If the bidder wishes to
bring additional information to the notice of the The purchaser, it should do so in writing.
F. Award of Contract
26. Post Qualification
26.1 Based on the qualification criteria listed in ITB Clause 13, the The purchaser will determine to its
satisfaction whether the Bidder selected as having submitted the lowest evaluated responsive bid is
qualified to satisfactorily perform the Contract.
26.2 The determination will take into account the Bidder's financial, technical, and production
capabilities. It will be based upon an examination of the documentary evidence of the Bidder's
qualifications submitted by the Bidder. Pursuant to ITB Clause 13, as well as such other
information as the The purchaser deems necessary and appropriate.
26.3 The The purchaser shall ask for demonstration of the quoted equipment. The cost of demonstration
shall be born by the bidder. Day, date & place of demonstration shall be decided by R.C.A.
26.4 An affirmative determination will be prerequisite for award of the Rate Contract to the Bidder. A
negative determination will result in rejection of the Bidder's bid in which event the The purchaser
will proceed to the next bid to make a similar determination of that Bidder's capabilities to perform
the contract satisfactorily.
26.5 The tenderness shall demonstrate the quoted model of the equipments during the technical
evaluation on the day, date & place specified, failing which their bids/offer shall be rejected.
27.
Award Criteria (Negotiation)
27.1 Subject to ITB Clause 29 - The the purchaser will award rate contract to the successful bidders on
lowest evaluated prices or the price approved by the Purchase Committee after negotiation from L,
bidder, whichever is lower, based on the performance, quality, capacity, quality control facilities,
delivery period, and geographical coverage of the supply etc.
16
If successful bidder shall not be capable, then in this respect the decision of the committee will be
final which may go up to L-3 bidder.
28.
Purchaser's Right to vary Quantities
28.1 The details of the required equipments etc. are shown in Annexure-VI. The quantity mentioned is
only the tentative requirement and may increase or decrease as per the decision of the Purchaser.
The rates quoted should not vary with the quantum of the order or the destination.
29.
The purchaser's Right to Accept any Bid and to Reject any or all bids
29.1 The purchaser reserves the right to accept or reject the tender for the supply of all items of
equipments or for anyone or more of the items of equipments tendered for in a tender without
assigning any reason, without thereby incurring any liability to the affected Bidder or Bidders or
any obligation to inform the affected Bidder or Bidders of the grounds for the. The purchaser's
action.
30.
Notification of Rate Contract
30.1 Prior to the expiration of the period of bid validity, the The purchaser will notify the successful
Bidder in writing by registered letter or fax or e-mail, that its bid has been accepted.
30.2 The notification of Rate Contract will constitute the formation of the Contract.
30.3 Upon the successful Bidder's signed Rate Contract pursuant to ITB Clause 31, the The purchaser
will promptly notify each unsuccessful Bidder and will discharges its bid security, pursuant to ITB
Clause 15.
30.4 If, after notification of rate contract, a Bidder wishes to ascertain the grounds on which its bid was
not selected, it should address it's request to the The purchaser. The The purchaser will respond in
writing to the unsuccessful Bidder.
31.
Signing of Rate Contract
31.1 At the same time the The purchaser will inform to the successful Bidder that its bid has been
accepted the purchaser will send the Bidder the Rate Contract Form provided in the bidding
document incorporating all agreements between the parties.
31.2
Within 10 days of receipt of the Notification of Rate Contract, the successful Bidder shall sign and
date the Contract on a non-judicial stamp paper of value of Rs. l00/- (stamp duty to be paid by the
Bidder) and return it to the purchaser.
17
31.3 The validity of Rate Contract will be one year and may be extended for further period as agreed
mutually unless revoked.
32.
Performance Security & Inspection Charges
32.1 Within 15 days of the receipt of firm order from the purchaser or the date specified by the
purchaser, the successful Bidder shall furnish the performance security and inspection charges in
accordance with the Clause 7 of General Conditions of Contract.
32.2 Failure of successful bidder to comply with the requirement of ITB Clause 31 or ITB Clause 32.1
shall constitute sufficient grounds for the annulment of the award and forfeiture of the bid
security/previously deposited performance security and disqualify the firm to participate in the
tender for the next five years.
33. Placement of Supply Order
33.1 After finalization of the contract, the successful bidders may be asked to submit the delivery
schedule. as per requirement of the Purchaser. While placement of orders, the schedule given to the
bidders, along with the other conditions stated at 27.1 will be considered.
33.2 To ensure sustained supply without any interruption the Purchaser, reserves the right to split orders
for supplying the requirements among more than one L-l bidder.
34.
Corrupt or Fraudulent Practices
34.1 For the purpose of this provision, the terms set forth as follows:
(i)
"Corrupt practice" means the offering, giving, receiving or soliciting of any thing of value to
influence the action of a public official in the procurement process or in contract execution, and (ii)
"Fraudulent practice" means a mis-presentation , hiding of facts in order to influence a procurement
process or the execution of a contract to the detriment of the other bidders, and includes collusive
practice among Bidders (prior to or after bid submission) designed to establish bid prices at
artificial noncompetitive levels and to deprive the other bidders of the benefits of free and open
competition;
(iii) Will reject a proposal for award if it determines that the Bidder recommended for award has
engaged in corrupt or fraudulent practice in competing for the contract in question.
(iv)
Will declare a firm ineligible, either indefinitely or for a stated period of time, to be allowed to
participate, awarded a contract if at any time determines that the firm has engaged in corrupt or
fraudulent practice in competing for, or in executing, a contract.
34.2 Furthermore, Bidders shall be aware of the provision stated in sub clause 21.4 of the General
Conditions of contract.
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SECTIONIII:GENERALCONDITIONSOFCONTRACT
TABLEOFCLAUSES
Clause
Number
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
14.
15.
16.
17.
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
Topic
Page Number
Definitions
Applications
Country of Origin
Standards
Use of contract documents and information
Patent Rights
Performance Security
Inspection and Tests
Packing
Delivery and Documents
Insurance
Transportation
Warranty
Payment
Prices
Change orders
Contract Amendments
Assignment
Delays in the Supplier's Performance
Liquidated Damages
Termination for default
Force majeure
Termination of insolvency
Termination for convenience
Resolution of disputes
Limitation of liability
Governing
Applicable law
Notices
Taxes and duties
Fall clause
Jurisdiction
19
20
20
20
21
22
22
22
22
23
24
24
24
24
27
27
27
28
28
28
28
28
30
30
30
31
31
31
31
32
32
32
32
General Conditions of Contract
1.
Definitions
1.1
In this Contract, the following terms shall be interpreted as indicated:
(a)
"Rate Contract" means the agreement entered into between the The purchaser and the Supplier, as
recorded in the Contract Forms signed by the parties, including all the attachments and appendices
thereto and all documents incorporated by reference therein for supply of material in agreed time
period.
(b)
"Price" means the price payable to the Supplier for the full and proper performance of its
contractual obligations.
(c)
"Goods" means all the equipments (Machines, instruments & Other Items) etc., which the supplier
is required to supply to the purchaser under the Contract.
(d)
"Services" means services ancillary to the supply of the Goods, such as. transportation and
insurance and any other incidental services, and other obligations of the Supplier covered under the
Contract.
(e)
"GCC" means the General Conditions of Contract contained in this section.
(f)
"scc" means the Special Conditions of Contract.
(g)
"The Purchaser" means the Organization purchasing the goods, as named in SCe.
(h)
"The Purchaser's Country" is the country named in SCC.
(i)
"The Supplier" means the individual or firm supplying the Goods and Services under this Contract.
(j)
"The purchaser" means the Dean Gandhi Medical College, Bhopal Chairman, Purchase Committee.
(k)
"The Project Site" where applicable, means the place or places named in SCC.
(l)
"Day" means calendar day.
2.
Applications
2.1
These General Conditions shall apply to the extent that they are not superseded by provisions in
other parts of the Contract.
3.
Country of Origin
3.1
All goods and services supplied under the Contract shall be specified their country of origin.
20
3.2
For purpose of this Clause "origin" means the place where the Goods are mined, grown or product,
or from which the Services are supplied. Goods are produced when, through manufacturing,
processing, or substantial and major assembling of components, a commercially recognized new
product results that is substantially different in basic characteristics or in purpose or utility from its
components.
3.3
The origin of Goods and Services is distinct from the nationality of the Supplier.
4.
Standards
4.1
The Goods supplied under this Contract shall confirm to the standards mentioned in the Technical
Specifications and when no applicable standard is mentioned, latest standards agreeable to the
purchaser. should be supplied.
4.2
Genuine EQUIPMENTS (Machinery, Instruments & Other Items) must be supplied. tenderers
should indicate the source of supply i.e. name & address of the manufacturers from whom the items
are to be imported.
4.3
While quoting the rates of MACHINERY, INSTRUMENTS & OTHER ITEMS etc. as enclosed
list, the name of the manufacturer, must be mentioned otherwise the tender is liable to be rejected.
4.4
The rates of every item should be quoted from standard and well reputed firms / companies and
they should be minimum possible.
4.5
For MACHINERY, INSTRUMENTS & OTHER ITEMS etc. means should bear quality assurance
certification like ISO 9002 of CE Mark of ISI standardization.products passing USFDA criteria
shall be preferred.
4.6
Software and Hardware Upgradation - Free Digital Up-gradation of software (all update &
upgrades) up to 5 years.
4.7
Voltage stabilizer or UPS & digital technology should be supplied with the equipments required it.
4.8
Technical specification of equipments / work mentioned is basic, however, equipments of higher
specifications may be quoted at no extra cost.
4.9
No change in make/manufacturer will be allowed at the time of supply. Changes resulting out of
technology upgradation of the same manufacturer can be permitted at no extra cost.
4.10 Circuit diagram with operator's and service manual must be enclosed along with the equipment.
4.11 Names of the institution in India, where quoted equipment / work has been supplied / installed and
working
satisfactory
done
during
last
three
years
must
be
attached.
21
4.12 The Bidders are not allowed to quote for equipments / components with less than desire
specification. Deviation from specification on lower / negative side shall not be considered if at any
time during evaluation / after supply of equipments / components are found below specification
EMD / performance guarantee shall be forfeited and action will be taken for black listing.
5.
Use of Contract documents and information
5.1
The supplier shall not, without the The purchaser's prior written consent, disclose the Contract, or
any provision thereof, or any specification, plan, drawing, pattern, sample or information furnished
by or on behalf of the The purchaser in connection therewith, to any person other then a person
employed by the supplier in performance of the contract.
Disclosure to any such employed person shall be made in confidence and shall extent only so far as
may be necessary, for purposes of such performance.
5.2
The Supplier shall not, without the The purchaser's prior written consent, make use of any
document or information enumerated in GCC Clause 5.1 except for the purposes of performing the
Contract.
5.3
Any document, other than the Contract itself, enumerated in GCC Clause 5.1 shall remain the
property of the The purchaser and shall be returned (in all copies) to the The purchaser on
completion of the Supplier's performance under the contract if so required by the The purchaser.
6.
Patent Rights
6.1
The Supplier shall indemnify the The purchaser against all third-party claims of infringement of
patent, trademark or industrial design rights arising from use of the Goods or any part thereof in
India.
7.
7.1
7.2
7.3
7.4
8.
Performance Security
The supplier shall furnish performance security in the amount specified in SCC to the purchaser as
specified in GCC 1.1 (g).
The proceeds of the performance security shall be payable to the purchaser as compensation for any
loss resulting from the Supplier's failure to complete its obligations under the Contract.
The Performance Security shall be denominated in Indian Rupees and shall be in the form of
Demand Draft/FDR/Bank Guarantee of Nationalized Bank located· in India in the prescribed form
provided in bidding document or another acceptable to the purchaser in favour of Purchaser till
completion of warranty period.
The performance security will be discharged by the purchaser and returned to the Supplier not later
than 90 days following the date of completion of the Supplier's satisfactory performance
obligations, including warranty obligations, unless specified otherwise in sec.
Inspection and Tests
22
If purchaser wishes:
8.1
The purchaser or its representative shall have the right to inspect and/or test the Goods to confirm
their conformity to the contract. The Special Conditions of Contract and/or the Technical
Specification shall specify what inspections and tests the purchaser requires and where they are to
be conducted. The purchaser shall notify the Supplier in writing of the identity of any
representatives retained for these purposes.
(i)
The Supplier shall notify the purchaser or its representative at least 10 days prior to the date when
Goods are available for inspection.
(ii)
The Supplier will provide to the purchaser or its representative all reasonable facilities for the
conduct of such inspections and tests at no additional cost to the purchaser. The Supplier may seek
an independent quality test report for batch ready for shipment. The cost of such tests will be borne
by the Supplier.
(iii)
Where the Supplier contests the validity of the rejection by the purchaser or his representative,
whether based on product or packing grounds, a sample drawn by the Inspection Authority will be
forwarded for analysis to an independent technical inspection. The Finding, which will be promptly
obtained, will be final and biding on both the parties. The cost of umpire analysis will be borne by
the losing party.
(iv)
The Purchaser's right to inspect, test and where necessary, reject the Goods after the Goods arrival
in at Site shall in no way be limited or waived by reason of the Goods having previously been
inspected, tested and passed by the purchaser or its representative prior to the Goods shipment from
the country of origin.
(v)
Nothing in Clause 8 shall in any way release the supplier from any warranty or other obligations
under this Contract.
9.
Packing
9.1
The Supplier shall provide such packing of the Goods as is required to prevent their damage or
deterioration during transit to their final destination as indicated in the' contract. The packing shall
be sufficient to withstand, without limitation, rough handling during transit and exposure to extreme
temperatures, salt and precipitation during transit and open storage. Packing case size and weights
shall take into consideration, where appropriate the remoteness of the Goods final destination and
the absence of heavy handling facilities at all points in transit.
The packing marking and documentation within and outside the packages shall comply strictly with
such special requirements as shall be provided for in the contract including additional requirements,
if any,
23
9.2
specified in SCC, Technical specification and in any subsequent instruction ordered by the Purchaser. .
10. Delivery and Documents
10.1 The supply should be completed within 21 days from the date of supply order unless otherwise
specified in the supply order. Purchaser will place order by fax &/or e-mail &/or speed post.
10.2 It shall be the responsibility of the Supplier to make good for any shortage/damage at the time of
receipt at designated place.
10.3 The details of shipping and/or other documents to be furnished by the Supplier are specified in
SCC.
10.4 The delivery of EQUIPMENTS should be made at the point / place specified by the Purchaser in
Purchase Order.
10.5 the successful bidders should strictly adhere to the following delivery schedule Supply, Installation
& Commissioning should be effected within a fortnight from the date of supply and this clause
should be strictly adhered to failing which necessary administrative action as deemed fit under rules
will be taken against the defaulter.
10.6 Supply must be toto i.e. not in fraction.
11.
Insurance
11.1 The Goods supplied under the contract shall be fully insured in Indian Rupees against the loss or
damage incidental to manufacture, acquisition, transportation, storage, delivery, installation and test
running in the manner specified in SCC.
12. Transportation
12.1 Where the Supplier is required under the Contract to transport the Goods to Gandhi Medical
College/Sultania Zanana Hospital/Hamidia Hospital Bhopal defined as Project site, transport to
Bhopal including insurance as shall be specified in the Contract shall be arranged by the Supplier,
and the related cost shall be included in the Contract Price.
12.2 The loss or damage of material whatsoever, whether insured or not, during transit shall be made
good by bidder free of charge, failing which the losses will be deducted from their bill /
performance security.
12.3 Wharf age, demurrages etc. on account of incorrect or delayed dispatch of material or documents
shall be the responsibility of the supplier and shall be recovered from his bill / performance
security.
13. Warranty
13.1 The Bidder shall provide on site warranty of the' equipment for the period of three years from the
date of satisfactory installation. Warranty will cover services, repairs, maintenance, replacement of
24
spare parts, broken / damaged / worn out spare parts and other services free of cost during the
whole warranty period of three years. Warranty shall clearly indicate that what items covered by it
and item not covered in warranty. The warranty shall also include "on call service" which should
not exceed three days from the date of lodging of complaint. The purchaser shall have the right to
get the work done at the cost of bidder's responsibility, if machine is not repaired within three days.
13.2 The Purchaser shall promptly notify the Supplier in writing of any claims arising under the
warranty.
13.3 Upon receipt of such notice, the Supplier shall, with all reasonable speed, replace the sub standard
equipments, without cost and to the satisfaction of Purchaser.
13.4 If the Supplier, having been notified, fails to remedy the defect(s) within seven days, the Purchaser
may proceed to take such remedial actions as may be necessary, at the Supplier's risk and expense
and will have right to impose penalty without prejudice to any other rights which the Purchaser may
have against the Supplier under the Contract.
13.5 The stores supplies shall be strictly in accordance with the Specifications / Standards and shall be of
the best quality. The stores are demanded to carry the Supplier's own guarantee of the items by the
consignee.
13.6 If at any time during/after the supply if equipment is not found as per specification, sub standard or
refurbished the bidder shall replace defective equipment at his own cost, immediately, failing which
the total amount is recoverable from him and he will be black listed.
13.7 UPTIME GUARANTEE: The firm should provide uptime guarantee of95%.
13.8 Downtime penalty Clause:
During the Guarantee / Warranty period, desired uptime of 95% of 365 days (24 hours), if
downtime exceeds 5%, penalty in the form of extended warranty, double the number of days for
which the equipment goes out of service will be applied. The vendor must undertake to supply all
spares for optimal upkeep of the equipments for at least THREE YEARS after handing over the
unit to the Institute. If accessories /other attachment of the system are procured from the third paIty
, then the vendor must produce cost of accessory/other attachment and the CMC from the third
party separately along with the main offer and the third party will have to sign the CMC with
the Purchaser if required. In no case instrument should remain in non working condition for more
than 7 days, beyond which a penalty of 2 % of machine cost will be charged per day. The
Principals or their agents are required to submit a certificate that they have satisfactory service
arrangements and fully trained staff available to support the uptime guarantee.
13.9 Guarantee I Warranty period: The tenderers must quote for 3 years warranty from the date of
completion of the satisfactory installation.
25
Also the Bidders should submit their quote for subsequent 7 years) / CMC (include free labour,
repair, other services & spare parts). Failure to comply this condition will entail the rejection of
the Bids. The price comparison shall be made taking into account on basic price and post
warranty / CMC.
.
So the price of CMC should be quoted according to the cost of equipment.
13.10 SPARE PARTS: The spare parts should be of standard quality. The bidder must take guarantee of
availability of supply of spare parts upto 10 years.
13.11 TRAINING: Training of equipments within the stipulated time should be done by the supplier at his
cost. The time & place of training shall be stipulated by purchaser. Training should be of 2 doctors
and 2 technicians of user department.
13.12 The Tenderers should clearly indicate the name of the Manufacturers / Beneficiary of the Letter of
Credit, country of origin, place of shipment / air freightrnent etc.
13.13 Local agents quoting on behalf of their foreign suppliers must attach authority letter in their favour.
13.14 Successful tenderers will have to furnish performance Bank Guarantee for 10% contract value from
any Nationalized Bank valid for the warranty period.SUBJECT TO MAXIMUM OF 2 LAKCS PER
DERARTMENT
13.15 The rates quoted for the Stores Equipments, under the reference, by the supplier shall in no event
exceed the lowest price at which the suppliers of the Stores / Equipments of identical description
are made to any other person / organization / institution during the period and should attach an
undertaking.
13.16 Equipment should be brand new & of latest technology along with digital technique wherever
applicable.
13.17 The the purchaser reserves the right to increase the accessories and their numbers, payment will be
made only for ordered accessories. Bidder shall enclose undertaking from the company providing
the equipments that it will undertake to provided warranty/ /CMC for the required period of
time.
26
14. Payment
14.1 The method and conditions of payment to be made to the Supplier under the contract shall be
specified in the SCC.
14.2 The Supplier's request(s) for payment shall be made to the Purchaser in writing accompanied by an
invoice describing, as appropriate, the Goods delivered and the service performed, and by
documents, submitted pursuant to GCC Clause 10, and upon fulfillment of other obligations
.stipulated in the contract.
14.3 Payments shall be made by the Purchaser after submission of the claim by the Supplier. All sincere
efforts will be made for payment of due amount which has been submitted to the purchaser within
30 days unless the situation being out of control of the purchaser. Performa invoice should also be
submitted.
14.4 Payment shall be made in Indian Rupees.
14.5 The payment of the claim / bill will be made after deduction of VAT as per rules of M.P.
Commercial Tax Act Section 34 and other taxes from the bill.
14.6 No payment shall be made for rejected Stores. Rejected items must be removed by the supplier
within two weeks of the date of rejection at their own cost and replace immediately. In case these
are not removed these will be auctioned at the risk and responsibility of the suppliers without any
notice.
14.7 Supply of equipments means - installation and commissioning and also test running at site. No
separate charges will be paid separately on this account.
14.8 Payment will be made after installation, commissioning and successful test running at the site, due
verification and subsequent satisfactory report of the user department.
15. Prices
15.1 Prices charged by the Supplier for Goods delivered and Services performed under the Contract shall
not vary from the prices quoted by the Supplier in its bid.
15.2 Recurring expenditure of the machine / equipment should be mentioned.
16. Change orders
16.1 The The purchaser may at any time, by written order given to the Supplier pursuant to GCC Clause
29 make changes within the general scope of the Contract in anyone or more of the following:
16. 1.
the method of shipping or packing, installation;
2.
Any other terms & conditions in public interest.
16.2 If any such change causes an increase or decrease in the cost of, or the time required, for the
Supplier's performance of any provision under the Contract, and equitable adjustment shall be made
in the Contract Price or delivery schedule or both and the Contract shall accordingly be amended.
Any claims by the Supplier for adjustment under this clause must be asserted within fifteen (15)
days from the date of the Supplier's receipt of the Purchaser's change order.
16.3 The Purchase Orders on approved rates will be placed by the Purchaser.
27
17. Contract Amendments.
17.1 Subject to GCC Clause 16, no variation in or modification of the terms of the Contract shall be
made except by written amendment signed by both the parties.
18.
Assignment
18.1 The Supplier shall not assign, in whole or in part, its obligations to perform under the Contract,
except with the Purchaser's prior written consent.
19.
Delays in the Supplier's Performance
19.1 Delivery of the Goods and performance of the Services shall be made by the Supplier III
accordance with the time schedule specified by the Purchaser in the Supply order.
19.2 If at any time during performance of the Contract, the Supplier should encounter conditions
impeding timely delivery of the Goods and performance of the Service, the Supplier shall promptly
notify the Purchaser in writing of the fact of the delay, its likely duration and its cause(s). As soon
as practicable after receipt of the Supplier's notice the Purchaser shall evaluate the situation and
may at its discretion extend the supplier's time for performance.
19.3 Except as provided under GCC Clause 22, a delay by the Supplier in the performance of its delivery
obligations shall render the Supplier liable to the imposition of liquidated damages pursuant to
GCC Clause 20, unless an extension of time is agreed upon pursuant to GCC Clause 19.2 without
the application of liquidated damages.
20.
Liquidated Damages
20.1 Subject to GCC Clause 22, if the Supplier fails to deliver any or all the Goods or to perform the
services within the period(s) specified in the supply order, the Purchaser shall, without prejudice to
its other remedies under the Contract, deduct from the Contract Price, as liquidated damages, a sum
equivalent to the percentage specified in SCC of the delivered price of the delayed goods or
unperformed services for each week or part thereof of delay until actual delivery or performance, up
to a maximum deduction of percentage specified in SCe. Once the maximum is reached, the
Purchaser may consider termination of the Contract pursuant to GCC Clause 21.
21.
Termination for Default
Contract may be terminated by the Rate Contract Authority if:
21.1 If the supplier fails to execute the supply within the stipulated time, the Purchaser is at liberty to
make alternative purchase, in the event of making ALTERNATIVE PURCHASE, the supplier will
be imposed penalty apart from the forfeiture of Performance Guarantee. The excess expenditure
over and above contracted prices incurred by the Purchaser in making such purchases from any
28
other sources or in the open market or from any other supplier who has quoted higher rates and
other losses sustained in the process, shall be recovered from the Performance Security or from any
other money due and become due to the Supplier and in the event of such amount being
insufficient, the balance will be recovered personally from the Supplier. The penalty would be as
under:
1.
First extension 22nd day thereof from the date of issue of supply order - 3% of supplied
ordered item.
2.
Second & maximum extension for an additional 21 days from the date of issue of supply
order - 5% of supplied ordered item. .
21.2 The order may be cancelled after expiry of delivery period as mentioned in the supply order and the
supplier shall also suffer forfeiture of the Performance Security and shall invite other penal action
like blacklisting / disqualification from participating in present and future tenders.
21.3 The purchaser will be at liberty to terminate by assigning justifiable reason thereof the contract
either wholly or in part on one month notice. The Supplier will not be entitled for any compensation
whatsoever in respect of such termination.
21.4 If the Supplier, in the judgment of the The purchaser has engaged in corrupt or fraudulent practices
in competing for or in executing the contract.
F or the purpose of this Clause.
"Corrupt practice" means offering, giving, receiving or soliciting of anything of value to
influence the action of a public official in the procurement process or in contract execution.
"Fraudulent practice" means a mis-presentation / hiding of facts in order to influence a
procurement process or the execution of a contract to the detriment of the other bidders, and
includes collusive practice among Bidders (prior to or after bid submission) designed to establish
bid prices at artificial noncompetitive levels and to deprive the other bidders of the benefits of free
and open competition.
21.5 For infringement of the stipulations of the contract or for other justifiable reasons, the contract may
be terminated by the The purchaser, and the supplier shall be liable for all losses sustained by the
The purchaser, in consequence of the termination which may be recovered personally from the
supplier or from his properties, as per rules.
21.6 Non performance of any of the contract provisions will disqualify a firm to participate in the tender
for the next five years.
21.7 In all the above conditions, the decision of the. The purchaser shall be final and binding.
29
22.
Force Majeure
22.1 . Not with standing the provision of GCC Clause 19, 20, 21, the Supplier shall not be liable for
forfeiture of its performance security, liquidated damages, penalty or termination for default, if and
to the extent that, its delay in performance or other failure to perform its obligations under the
Contract is the result of an event of Force Majeure.
22.2 For purpose of this Clause, "Force Majeure" means an event beyond the control of the Supplier and
not involving the Supplier's fault or negligence and not foreseeable. Such events may include, but
are not limited to, acts of the The purchaser either in its sovereign or contractual capacity, wars or
revolution, fires, floods, epidemics, quarantine restrictions and freight embargoes.
22.3 If a Force Majeure situation arises, the Supplier shall promptly notify the The purchaser in writing
with adequate proof of such conditions and the cause thereof. Unless otherwise directed by the The
purchaser in writing the Supplier continue to perform its obligations under the Contract as far as it
is reasonably practical, and shall seek all reasonable alternative means for performance not
prevented by Force Majeure event.
23.
Termination for insolvency
23.1 The The purchaser may at any time terminate the contract by giving written notice to the Supplier,
if the, Supplier becomes bankrupt or otherwise insolvent. In this event, termination will be without
compensation to the Supplier, provided that such termination will not prejudice or affect any right
of action or remedy which has accrued or will accrue thereafter to the The purchaser.
24.
Termination for Convenience
24.1 The The purchaser, by written notice sent to the Supplier, may terminate the Contract, in whole or
in part, at any time for its convenience. The notice of termination shall specify that termination is
for the The purchaser's convenience, the extent to which performance of the Supplier under the
contract is terminated, and the date upon which such termination become effective. .
24.2 The Goods that are complete and ready for shipment within 21 days after the Supplier's receipt of
notice of termination shall be accepted by the The purchaser at the Contract terms and prices. For
the remaining Goods, the The purchaser may elect:
i)
ii)
to have any portion completed and delivered at the Contract terms and prices; and / or
to cancel the remainder and pay to the Supplier an agreed amount for partially completed
Goods and for materials and parts previously procured by the Supplier.
30
25.
Resolution of Disputes
25.1 The purchaser and the Supplier for the rate contracts & purchaser and supplier for supply order,
supply, delivery and payment and other issues shall make every effort to resolve amicably by direct
informal negotiations any disagreement or dispute arising between them under or in connection
with the Contract.
25.2 If, after thirty (30) days from the commencement of such informal negotiations, the The purchaser
and the Supplier & purchaser and the supplier have been unable to resolve, amicably a Contract
dispute, either party may require that the dispute be referred for resolution to the formal
mechanisms specified in the SCC. These mechanisms may include, but are not limited to,
conciliation mediated by a third party, adjudication in an agreed national or international forum,
and/or international arbitration.
i.
Any dispute or difference in respect of which a notice of intention to commence arbitration
has been given in accordance with this clause shall be finally settled by arbitration.
Arbitration may be commenced prior to or after delivery of the goods under the contract.
ii.
Arbitration proceedings shall be conducted in accordance with the rules of procedure
specified in SCC.
25.3 Notwithstanding any reference to arbitration herein the parties shall continue to perform their
respective obligations under the contract unless they otherwise agree.
26.
Limitation of Liability
26.1 Except in cases of criminal negligence or willful misconduct, and in the case of infringement
pursuant to Clause 6.
I.
the supplier shall not be liable to the The purchaser, whether in contract, tort, or otherwise,
for any indirect or consequential clause or damage, loss of use, loss of production or loss of
profits or interest costs, provided that this exclusion shall not apply to any obligation of the
suppliers to pay liquidated damages to the The purchaser, and
ii
the aggregate liability of the supplier to the The purchaser, whether under the contract, in tort
or otherwise, shall not exceed the total ordered price, provided that this limitations shall not
apply to the cost of replacing sub-standard/defective goods.
27. Governing Language
27.1 The contract shall be Written in English language. Subject to GCC Clause 28, English language
version of the Contract shall govern its interpretation. All correspondence and other documents
pertaining to the Contract which are exchanged by the parties shall be written in the same language.
28. Applicable Law
28.1 The Contract shall be interpreted in accordance with the laws of the Union of India.
31
29.
29.1
Notices
Any notices given by one party to the other, pursuant to this Contract, shall be sent to other party in writing,
confirmed in writing to the other Party's address specified in SCe.
29.2 A notice shall be effective when delivered or on the notice's effective date, whichever is later.
30.
Taxes and Duties
30.1 In case of any enhancement in Excise Duty due to notification of the Government after the date of
submission of tenders and during the tender period, the quantum of additional excise duty so levied will be
paid extra, if the rates of excise duty prevailing at the time of tender, has been shown extra and actually paid
by the supplier. For claiming the additional cost on account of the increase in Excise Duty, the supplier
should produce a letter from the concerned Excise authorities for having paid additional Excise Duty on the
goods supplied to Purchaser and also must claim the same in the invoice separately.
30.2 Suppliers shall be entirely responsible for all taxes, duties license fees, octroi, road permits, etc.
incurred until delivery of the contracted Goods to the Purchaser. However, Sales tax VAT (not surcharge in
lieu of Sales Tax/V AT) in respect of the transaction between the Purchaser and the Supplier shall be
payable extra, if so stipulated in the supply order.
31.
Fall Clause
31.1 . Prices charged for supplies under Rate Contract by the supplier should in no event exceed the lowest prices
at which he offers to sell or sells the stores of identical description to any other State Government / DGS &
D/ Public Undertaking during the period of the contract.
31.2 If at any time during the period of contract, the price of tendered items is reduced or brought down by any
law or Act of the Central of State government, the supplier shall be bound to inform The purchaser
immediately about such reduction in the contracted prices, in case the supplier fails to notify or fails to
agree for such reduction of rates, The purchaser will revise the rates on lower side. If there is a price
increase for any product after quoting the rates, the bidder will have to supply the item as per quoted rates.
This office will not accept any higher rates after wards.
31.3 If at any time during the period of contract, the supplier quotes the sale price of such Equipments or sells
such Equipments to any other State Govt. / DGS&D and Public Undertakings at a price lower than the price
chargeable under the rate contract he shall forthwith notify such reduction to The purchaser and the prices
payable under the rate contract for the Equipments supplied from the date of coming into force of such price
stands correspondingly reduced as per above stipulation however reduction shall not apply to :(a)
Export by the supplier
(b)
For all contracts entered into prior to the date of the tender or for any backlog of pending orders.
31.4 Within six months of the commencement of the rate contract and at the rate contract period a certificate in
the following forms will have to be submitted by the supplier :I/We certify that the stores of description identical to the store supplied to the Govt. of M.P. under the
contract herein have not been sold by me/us to any other State Govt. / Central Govt. / DGS & D / Public
Undertaking during the period of the rate contract of Madhya Pradesh under the contract! except for the
quantity of under sub-clause (a) & (b) of the clause 31.3.
32.
Jurisdiction
32.1 In respect of all disputes or claims related with Rate Contracts out of or under this contract, Bhopal Court
alone shall have jurisdiction to entertain the same.
32.2 In respect of all disputes or claims related with Supply, Payments and any other out of or under this
contract, the concerned Court of Purchaser's place shall have jurisdiction to entertain the same.
32
SECTIONIV:GENERALCONDITIONSOFCONTRACT
TABLEOFCLAUSES
Item No.
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
13.
14.
15.
16.
17.
Topic b
Definition (GCC Clause I)
Performance security (GCC Clause 7)
Inspection and tests (GCC Clause 8)
Annual / Comprehensive Maintenance Contract) & training
Packing (GCC Clause 9)
Delivery and documents (GCC Clause 10)
Insurance (GCC Clause 11)
Payments (GCC Clause 14)
Prices (GCC Clause 15)
Liquidated damages & deduction in payments (GCC Clause 20)
Resolution of disputes (GCC Clause 25)
Supplier Integrity
Supplier's Obligations
Patent right (GCC Clause 6)
Progress of supply
Bid Form
33
Page
Number
34
34
34
35
36
36
36
37
37
37
38
38
38
38
39
40
SpecialConditionsofContract
The following special conditions of contract shall supplements the general conditions of contract
whenever there is a conflict, the provisions herein shall prevail, over those in the general conditions of
contract the corresponding clause numbers of the general conditions is indicated in parentheses.
1.
Definitions (GCC Clause 1)
GCC 1.1 (g) (a)
2.
The Purchaser is concerned Dean & Superintends of Associated Hospitals of
Gandhi Medical College, Bhopal which is also Good's Receiving Authority.
GCC 1.1 (i) (b)
The Supplier is the individual or firm supplying the Goods and Services under
this Contract.
GCC 1.1 (h) (c)
The Purchaser Country is India.
GCC 1.1 (1) (d)
The project site is as per supply order.
Performance security (GCC Clause 7)
2.1
The supplier shall be required to pay 10% performance security of the order value or maximum Rs.
15 lac which ever is less. The performance security should be paid upfront in respect of each supply
order or before the due date fixed by the Purchaser, valid up to the end of guarantee / warranty
period for performance obligations including warranty obligations.
2.2
Substitute clause 7.4 of the GCC by the following.
The performance security will be discharged by the Purchaser and returned to the supplier not later
than 90 days following the date of completion of the supplier's satisfactory performance obligations
including the warranty obligations under the contract.
2.3
Add as clause 7.5 to the GCC the following:In the event of any contract amendment, the supplier shall, within 07 days of receipt of such
amendment furnish the amendment to the performance security, rendering the same valid for the
duration of the contract as amended for further period of 60 days thereafter.
3.
Inspection and tests (GCC Clause 8)
If purchaser wishes:
A.
The inspections shall be carried out by the appointed Technical Committee or Inspection Agency at
the premises of the suppliers / go down or stores of the supplier / at point of delivery / installation.
Inspection and testing charges for the above purpose shall be borne by the supplier.
B.
Inspection note will be issued by the inspection committee verifying the specification, performance,
details of accessories supplied with the machine, test certificate issued by the respective authority
etc. as decided by the purchasing committee.
34
C.
The machine will be dispatched only after the inspection procedure has been followed and
inspection note issued to accept the consignment.
D.
The consignee may also draw the sample, at random, from the consignment within 45 days of their
receipts, and get them re-tested to satisfy whether the lots conform to the laid down specification. In
the event of the sample failing to conform to specification, the consignee shall reject the batch of
supply and inform the supplier for arranging replacement of the rejected batches at his own cost.
E.
When the inspection conducted on the premises of the supplier, all reasonable facilities and
assistance including access to drawing and production data shall be furnished to the inspectors at no
charge to the Purchaser.
In the event of the sample of EQUIPMENTS failing quality test and found to be not as per
specification the Purchaser is at liberty to make alternative purchase of the items, of
EQUIPMENTS for which the supply orders have been placed, from any other sources or in the
open market or from any other suppliers who might have quoted higher rate at Bid and the cost of
the supplier and in such cases the Purchaser has every right to recover the excess cost from
supplier's performance security.
F.
G.
H.
4.
4.1
If any items of equipments supplied by the supplier have been partially or wholly used or consumed
after supply and are subsequently found to be in bad order, unsound, inferior in quality or
description or otherwise faulty or unfit for consumption and if payment had already been made to
him then the contract price or prices of such articles or things will be recovered from the supplier,.
The supplier will not be entitled to any payment, whatsoever, for items of equipments found to be
NOT OF STANDARD QUALITY whether consumed or not and the purchaser is entitled to deduct
the cost of such equipments from any amount payable to the supplier. On the basis of nature of
failure, the product / supplier will be moved for black listing.
For equipments labelled as NOT OF STANDARD QUALITY, the concerned administration will be
informed for initiating necessary action against the supplier and that product shall be banned / black
listed and no further supplies will be accepted from him till he is legally discharged. The supplier
shall also not be eligible to participate in tenders for supply of such equipments for a period of five
subsequent years.
/ Comprehensive (include free labour, repair, other services & spare parts) Maintenance
Contract (CMC) & Training
Comprehensive (include free
lab our, repair, other services & spare parts) Maintenance Contract for the next seven years after the
expiry of three years warranty period in Annexure-XII.
4.2
The bidder shall provide operational training to Technician staff / operator for minimum of 3 days
by the expert or as instructed at the time of agreement.
4.3
The bidder should take guarantee of the availability of all spare parts for a minimum period of 10
years from the date of installation.
4.4
Genuine equipments and instruments etc. should be supplied. Tenderers should indicate the source
of supply i.e. name and address of the manufacturers from whom the items are to be imported.
35
5.
Packing (GCC Clause 9)
Add as clause 9.3 of the GCC of the following:Packing Instructions: The Supplier will be required to make separate packages for each Consignee.
Each package will be marked on three sides with proper paint/indelible ink, the following:
(i) Project (ii) Contract No. (iii) Country of Origin of Goods (iv) Supplier's Name; and (v) Packing
list reference number.
5.1
Packing should be able to prevent damage or deterioration during transit.
5.2
In the event of items of equipments supplied found to be not as per specifications in respect of their
packing, the Purchaser is at liberty to make alternative purchase of the items of equipments for
which the supply orders have been placed from any other sources or in the open market or from any
other bidder who might have quoted higher rates at the risk and the cost of the supplier and in such
cases the Purchaser has every right to recover the cost and imposes penalty as mentioned in GCC
clause 21.1.
Delivery and documents (GCC Clause 10)
6.
Upon delivery of the goods, the supplier shall submit the following documents to the Purchaser.
(i)
Three copies of the supplier invoice showing Goods description, quantity, unit price, and total
amount.
(ii)
Acknowledgement of receipt of goods from the consignee(s).
(iii)
Installation certificate signed by respective consignee.
(iv)
Manufacturer's / supplier's warranty certificate.
(v)
Inspection certificate issued by the nominated inspection agency, and the Supplier's factory
inspection report; and
(vi)
(vii)
Certificate of origin.
Photocopy of all test report of all equipments etc. should be submitted with every delivery challan.
7.
Insurance (GCC Clause 11)
For delivery of goods at site, the insurance shall be obtained by the supplier in an amount equal to
the value of the goods from final destinations as specified in the supply order of "All Risks" basis
including war Risks and strike.
Should any loss or damage occurs, the supplier shall:
(a)
Initiate and pursue claim till settlement, and
36
(b)
8.
Promptly make arrangement for replacement of any damaged items irrespective of
settlement of claim by the underwriters.
Payments (GCC Clause 14)
Payment for goods and services shall be made in Indian Rupees as follows:-
8.1
No advance payments towards cost of equipments etc. will be made to the supplier.
8.2
All payments shall be made by way of crossed cheques drawn in favour of the supplier.
8.3
All bills / invoices should be raised in triplicate in the name of Concerning Purchaser.
8.4
Payment will be made after completion of supply of goods / service as per supply order,
installation, commissioning and successful test running at the site, due verification and subsequent
satisfactory report of the user department. Payments shall be made by the Purchaser after
submission of the claim by the Supplier. All sincere efforts will be made for payment of due
amount which has been submitted to the purchaser within 30 days unless the situation being out of
control of / unforeseen for the purchaser. Proforma invoice should also be submitted.
8.5
FALL CLAUSE: if , at any time, during the said period, the supplier reduce the said prices of such
Stores/ Equipment or sales such stores to any other person/organization at a price lower than the
chargeable, he shall forthwith notify such reduction or sale to the PURCHASER and the price
payable for the Stores supplied after the date of coming into force of such reduction or sale shall
stand correspondingly reduced.
9.
Prices (GCC Clause 15)
Substitute clause 15.1 of the GCC with the following:
Prices payable to the supplier as stated in the contract shall not be subject to adjustment during
performance of the contract
10. Liquidated damages & deduction in payment (GCC Clause 20)
10.1 For delay:
Substitute GCC clause 20.1 by the following:
Subject to GCC clause 20, if the supplier fails to deliver any or all the goods or perform the
,services within the time period(s) specified in the contract. The Purchaser shall, without prejudice
to its other remedies under the contract, deduct from the contract price as liquidated damages, as
shown below of the delivered price of the delayed goods or unperformed services for each week of
delay or part thereof until actual delivery or performance up to maximum deduction of 5% of the
delayed goods or services contract price. Once the maximum is reached, the purchaser may
consider termination of the contract.
A
First penalty: 22nd day from the date of issue of supply order - 3% of supply ordered item.
B.
Second penalty: After additional 21 days from the date of issue of supply order - 5% of
supply ordered item.
37
10.2 Purchaser has every right to receive supply even after expiry of delivery period as mentioned in the
supply order and in such case, liquidated damages will be levied @ 3% of the delivery price of the
delayed goods or unperformed services for each week of delay or part thereof until actual delivery
or performance.
10.3 Supply in damaged condition shall not be accepted. In case of damage in the packing, the supply
will be accepted only after levying penalty or replacement of damaged supply on the total value of
supply to that particular / other designated place.
10.4 Supply must be in toto i.e. not in fraction.
11.
Resolution of disputes (GCC Clause 25)
Add as GCC clauses 25A and 25.5 the following:
25.4 The dispute resolution mechanism to be applied pursuant to GCC clause 25 shall be as follows:
(a)
In case of dispute or difference arising between the The purchaser / Purchaser and supplier
relating to any matter arising out of or connected with this agreement, such disputes or
difference shall be settled in accordance with the Arbitration and Conciliation Act, 1996.
The Next Higher Authority shall be the Arbitrator.
25.5 The Venue of Arbitration shall be at concerned place of next higher authority of R.C.A / Purchaser.
13. Supplier Integrity
The supplier is responsible for and obliged to conduct all contracted activities in accordance with
the contract using state-of-the-art methods and economic principles and exercise all means available
to achieve the performance as specified in the contract.
14.
Supplier's obligations
The supplier is obliged to work closely with the R.C.A. & Purchasers staff, act within its own
authority and abide by directives issued by the Purchaser and implementation activities.
The supplier will abide by the job safety measures prevalent in India and will free the purchase
from all demands or responsibilities arising from accidents or loss of life the cause of which is the
supplier's negligence. The supplier will pay all indemnities arising from such incidents and· will not
hold the Purchaser responsible or obligated.
The supplier is fully responsible for managing the activities of its personnel or sub contracted
personnel and will hold itself responsible for any misdemeanors.
The Supplier will treat all data and information about the The purchaser / Purchaser, obtained in the
execution of his responsibilities, in strict confidence and will not reveal such information to any
other party without the prior written approval of the The purchaser / Purchaser.
15.
Patent right (GCC Clause 6)
In the event of any claim asserted by a third party of infringement of copyright , patent, trademark
or industrial design rights arising from the use of goods or any part thereof in the Purchaser's
country, the supplier shall act expeditiously to extinguish such claim. If the supplier fails to comply
and the Purchaser is required to pay compensation to a third party resulting from such infringement,
the supplier shall be responsible for the compensation including all expenses court cost and lawyers
fees. The Purchaser will give notice to the supplier of such claim, if it is made, without delay.
38
16.
Progress of Supply
Supplier
:
(To be filled at the time of Contract Signature)
Supplier shall regularly intimate item wise progress of supply in writing, to the Purchaser as under:
·
·
·
·
·
Quantity offered for inspection and date:
Quantity accepted / rejected by inspecting agency and date:
Quantity dispatched / delivered to consignee and date:
Quantity where incidental services have been satisfactorily completed with date:
Quantity where rectification / replacement effected / completed on receipt of any
communication from consignee / Purchaser with date:
(In case of state-wise inspection, details required may also be specified).
39
SECTION V
Ref. Clause No. 17.1(p) of ITB
BIDFORM
This Bid Form is to be submitted against acceptance of
all terms and conditions of tender from page No. 1 to 57
(Save Paper Save Environment)
To,
The Dean,
Gandhi . Medical College
Bhopal, (M.P.)
i.
ii..
iii.
iv.
v.
vi.
vii.
viii.
ix.
x.
xi.
xii.
xiii.
I/We, the undersigned, declare that:
I/We have examined the bidding documents the receipt which is hereby acknowledged.
I/We have gone through all terms and conditions of the tender document before submitting the same. I/We hereby
agree to all terms and conditions as stipulated in the tender document and offer to supply and deliver ........ _.. . . . ... . .
. ... (Brief description of equipments) in conformity with the bidding documents in accordance with the schedule of
prices attached herewith and made part of this bid.
I/We undertake, if our bid is accepted, to deliver the goods in accordance with delivery period specified in the supply
order.
I/We agree to abide by this bid for a period of 180 (One Hundred Eighty) days after the date fixed for bid opening and
shall remain binding upon us and may be accepted at any time before the expiration of that date.
If our bid is accepted, we commit to obtain a performance security in accordance with GCC clause 7 & SCC clause 2
for the due performance of the contract.
Until a formal contract is prepared and executed, this bid together with your written acceptance thereof and your
notification of rate contract shall constitute a binding contract between us.
I/We undertake if at any time, it is found that any information furnished by us to the The purchaser, either in our bid
or otherwise, is false, the The purchaser servers the right to terminate the contract without assigning any reasons,
forfeiting the bid security or performance security and blacklisting us for a period of 5 years.
I/We understand that you are not bound to accept the lowest or any bid you may receive.
I/We hereby submit our tender for the
dated
I/We now enclosing herewith the E.M.D. No.
I/We have noted that overwritten entries shall be deleted unless duly cut & re-written and initialed.
Tenders are duly signed (No thumb impression should be affixed).
I/We undertake to sign the contract / agreement, if required, within 15 (fifteen) days from the date of issue of the
letter of acceptance, failing which our/my security money deposited may be forfeited and our/my name may be
removed from the list of suppliers.
Dated this ....................... day of .................... 2011.
(Signature) .................
(in the capacity of:............................)
Duly authorized to sign for and on behalf of....................
Witness
Witness
40
TABLEOFANNEXURES
Item
Topic
Page No.
No.
1.
Annexure - I (Sales Tax Clearance Certificate)
42
2.
Annexure - II (Manufacture Authorization Form)
44
3.
Annexure - III (Declaration / Undertaking Form)
45
4.
Annexure - IV (Proforma for Performance Statement)
46
5.
Annexure - V (Annual Turnover Statement)
47
6.
Annexure - VI (Specification of require equipments)
48
7.
Annexure - VII (Performance of Security Form)
49
8.
Annexure - VIII (Contract Agreement)
50
9.
Annexure - IX (Details of Manufacturing Unit)
52
10.
Annexure - X (The Price Schedule)
53
11.
Annexure - XI (Price Schedule for CMC)
54
12.
Annexure - XII (Details of Service Centre in M.P.)
55
13.
Check List
56
.
41
ANNEXURE-I
Ref. Clause No. 17.1 (g) of ITB
FORM OF CERTIFICATE OF SALES TAX / V A T VERIFICATION TO BE PRODUCE}) BY
AN APPLICANT FROM THE CONTRACT OR OTHER PATRONAGE AT THE DISPOSAL OF
THE GOVERNMENT OF MADHYA PRADESH
(Tobefilledupbytheapplicant)
01.
02.
03.
04.
Name of style in which the applicant is addressed or assessable to sales tax / VAT addresses or
assessment
a.
Name and address of all companies, firms or associations or persons in which the applicant
is
interested in his individual or fiduciary capacity
b.
Places of business of the applicant (all places of business should be mentioned)
The Districts, blocks and division in which the applicant is assessed to sales tax / VAT (all places of
business should be furnished)
a.
Total contract amount or value of patronage received in the preceding three years
2009-10
2010-11
2011-12
b.
Particular of sales - Tax / VAT for the preceding three years
Year
.
Total Turnover
be assessed
(Rs.)
Total Tax
Assessed
(Rs.)
Total tax
paid (Rs.)
Balance
due (Rs.)
Reasons for
Balance (Rs.)
2009-10
2010-11
2011-12
c.
If there has been no assessment in any year, whether any returns were submitted? if yes, the
division in which the returns were sent?
d.
Whether any penal action or proceeding for the recovery of Sales tax / VAT is pending?
e.
The name and address of Branches, if any:
f.
sales tax clearance up to 31.03.2012 issued by Sales Tax Department must be compalsory
attached with this annexure.
I declare that that the above information is correct and complete to the best of my knowledge and
belief
Signature of Applicant:
Address:
Date:
42
ANNEXURE - II
Ref. Clause No. 17.1 (q) ITB
MANUFACTURER'S AUTHORIZATION LETTER
No...................................... Dated. ..................
To,
Dear Sir,
Tender No.:
We
factories at
an established and reputable Manufacturers of having
_ and
do hereby agree to supply confirming to the required specification and
required quantity to M/s
(Bidder) as offered by them to supply against the above stated Tender.
We hereby extend our full guarantee and warranty as per Clause 15 of the General Conditions of
Contract for the supply against this invitation for Bid by the above firm.
Yours faithfully,
(name) for and on behalf of M./s
(Name of manufacturers)
Note: This letter should be signed by a person competent and having authority to sign on behalf of
manufacturer, and should be duly Notarized.
43
ANNEXURE - III
Ref. Clause No. 17.1 (T) of ITB
DECLARATION/UNDERTAKlNG
I/We/ M/s.
represented by its Proprietor / Managing Partner / Managing Director
and its Factory Premises at
do declare that I/We have
having its Registered Office at
carefully read all the conditions of tender in Ref. No. for supply of equipment, floated by the Purchase
Committee, and accept all conditions of Tender.
I/We agree that the Purchaser has rights of forfeiting the Bid Security and or Performance Security
Deposit and blacklisting me/us for a period of 7 years if any information furnished by us proved to be false
at the time of inspection and not complying to the tender conditions.
Signature of the Bidder
Name & Address in capital letters with Designation
TobeAttestedbyNotary.
45
ANNEXURE - IV
Ref. Clause No. 17.1(e) of ITB
PROFORMA FOR LIST OF INSTALLATIONS IN LAST THREE
YEARS OFTHE MANUFACTURER'S
Name of the Manufacturer
Sl.
No.
Name of the Purchaser &
Address with phone number
1
Name of installed
machines and model
2
Date of
installation
3
Quantity
4
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
Signature and seal of the Bidder
46
Annexure-V
Ref. Clause No. 13.3(I) of ITB
ANNUAL TURNOVER STATEMENT
The annual Turnover of M/s ........................................................... for the past three years are given
below and certified that the statement is true and correct.
Turnover in Crore (Rs)
Sr. No.
Year
1.
2009-10
2.
2010-11
3.
2011-12
Turnover in Crores (Rs.)
Date :
Seal :
Signature of Auditor /
Chartered Accountant
(Name in Capital)
47
Annexure-VI
Ref. Clause No. 11.1 of ITB
SPECIFICATIONS OF EQUIPMENTS
Tender No.
Sr.
No.
1.
2.
Item
Code
Name of Item /
Equipment
48
Specification Compliance /
Deviations
ANNEXURE-VII
Ref. Clause No. 7.3 of GCC
PERFORMANCE SECURITY FORM
(to be filled after award of contract )
To: ...................................................... ...................... (Name of Purchase)
Whereas................................................................ .... (Name of Supplier)
hereinafter called "the supplier" has undertaken, in pursuance of Contract No. ......... dated...... 2012 to
.supply. ............................................ [description of goods and related services] hereinafter called "the
Contract" .
AND WHEREAS it has been stipulated by you in the said Contract that the Supplier shall furnish you with
a Bank Guarantee by a recognized bank for the sum specified therein as security for compliance with the
Suppliers performance obligations in accordance with the Contract.
AND WHEREAS we have agreed to give the Supplier a Guarantee:
THEREFORE, WE hereby affirm that we are Guarantors and responsible to you, on behalf of the Supplier,
up to a total of . (Amount of the Guarantee in Words and Figures) and we undertake to pay you, upon your
first written demand declaring the Supplier to be in default under the Contract and without cavil or
argument, any sum or sums within the limit of
(amount of Guarantee) as aforesaid, without
needing to prove or to show grounds or reasons for your demand or the sum specified therein.
This guarantee is valid until the.................................... day of....................... 2012
Signature and Seal of Guarantors
.......................................................................
.......................................................................
Date ...........................2012
Full Address of the Bank:
.................................................
.................................................
49
ANNEXURE-VIII
Ref. Clause No.3l of ITB
CONTRACTAGREEMENTFORM
)
(Tender No.
(to be filled after award of contract )
THIS CONTRACT AGREEMENT made the ...........................day of ........2012 between The purchaser
(Dean,Gandhi Medical College, Bhopal M.P.) (Name of The purchaser) of India (country of The
purchaser) (hereinafter called "the purchaser") of one part and
M/s ..................................... (name of supplier) of ........................................ (city and country of supplier)
(hereinafter called "the supplier") of the other part :
WHEREAS the The purchaser invited bids for certain goods and ancillary services viz.
EQUIPMENTS (Brief description of goods" and services) and has accepted a bid by the supplier for the
supply of those goods and services.
NOW THIS AGREEMENT WITNESSETH AS FOLLOWS:
1.
In this agreement words and expression shall have the same meaning as are respectively assigned to
them in the conditions of contract referred to :
2.
The following documents shall constitute the contract between the The purchaser and the supplier,
and each shall be read and construed as an integral part of the contract:
a.
This contract agreement:
b.
Instructions of contract:
c.
General conditions of contract:
d.
Special conditions of contract:
e.
Technical Specifications:
f.
The supplier's bid and original price schedules
g.
The The purchaser's notification of rate contract.
3.
This contract shall prevail all other contract documents. In the event of any discrepancy or
inconsistency with the contract documents, then documents shall prevail in the order listed above.
4.
In consideration of the payments to be made by the Purchaser to the supplier as hereinafter
mentioned, the supplier hereby covenants with the Purchaser to provide the goods and services and
to remedy defects therein in conformity in all respects with the provisions of the contract.
5.
The Purchaser hereby covenants to pay the supplier in consideration of the provision of the goods
and services and the remedying of defects therein, the contract price or such as may become
payable under the provisions of the contract at the times and in the manner prescribed by the
contract.
Brief particulars of the goods and services which shall be supplied / provided by the supplier are as
under:Item
Item Description
Unit
Sr.
F.O.R. Rate per
No.
unit (Rs.)*
Code
* The above rates are inclusive of excise duty, transportation, insurance, inspection & testing
charges and any incidental charges, but exclusive of CST/VAT.
50
6.
7.
8.
9.
10.
11.
12.
13.
The prices shall be valid for one year from the date of agreement, unless revoked and thereafter for
a further period as agreed upon mutually.
The supplier shall agree to deposit inspection and testing charges and service tax as per tender
conditions, in advance by cash /demand draft, against the value of supply order.
The supplier shall agree to deposit 10% performance security, along with as mentioned at point no.
7 (above), in advance by cash / demand draft / FDR / Bank Guarantee, against the value of
particular supply order for a period of 18 months.subject to maximum of 2 lacks department wise
The suppliers are not authorized to supply material directly to any state Govt. / Semi Govt. / any
other organization on the rate lower than the rate contract.
The supplier shall supply the goods directly to the indentor / purchaser at the address given in the
supply order.
The supplier shall raise bills directly in the name of indenting officer /purchaser against the supplies
made directly by them to the indentor's satisfaction in compliance with the conditions contained in
the supply order.
The supplier shall receive payment against its bill directly from the indenting department /
purchasing department. In case of Non-payment for the supplies made by supplier, they will
demand payment directly from the department / indentor concerned and in no case Purchase
Committee shall be responsible for the consequence for delayed payment or non-payment.
The supplier shall carefully read all the conditions of tender for supply of equipment, floated by the
Purchase Committee, and accept all terms and conditions in the tender document. Signing this
contract means that the supplier has read all the terms and conditions and abide by it.
IN WITNESS whereof the parties here to have caused this agreement to be executed III
accordance with their respective laws the day and year first above written.
That, in token of this agreement, both parties have today affixed their signature at Bhopal.
Signed, Sealed and delivered by the
Said..................................................... (For THE PURCHASER)
In the presence of:..................................................................
Signed, Sealed and Delivered by the
Said............................................................... (For the supplier)
In the presence of: ............................................................
51
ANNEXURE-IX
Ref. Clause No. 13.3 (D of ITB
DETAILS OF MANUFACTURING UNIT/AUTHORIZED
DISTRIBUTORS
Name of the Tenderer & Full Address
(Whether manufacturer / authorized distributor)
PAN number
Phone Nos.
Fax No.
E-mail Address
Date of Inception
Equipments Manufacturing / Distribution License No & Date
Issued by
Valid upto
CST / VAT Registration No.
If bidder is authorized distributor then
name, address, telephone, fax of
authorized manufacturer.
Name & Designation of Authorized Signatory
Signature of the Authorized Signatory
The details of manufacturing unit I authorized distributor shall be for the premises where items
QuotedareactuallymanufacturedIstoked.
52
ANNEXURE- X
Ref. Clause No. 17.2 of ITB
PRICES CHEDULE
Sr. Code
No.
(1)
(2)
Name of
Name of
Make
&
the
Manufacturer
Model
Equipment
No.
/ Item
(3)
(4)
(5)
Rate per unit
Rate of
Rate of
(Landed
Excise /
CST /
Price)
Custom VAT as
(Inclusive of
Duty
applicabl
excise /
(included
e
custom duty, in quoted
transportation, rate per
unit)
insurance, and
any incidental
charges etc.)
(6)
(7)
(8)
Place :
Date :
Signature
Name in Capital Letters
Designation
Note : This format of price schedule is a sample for the Bidder's Price schedule should not be
submitted in Technical Bid, otherwise tender shall be rejected.
53
ANNEXURE- XI
Ref. Clause No. 17.2 (VII) of ITB
PRICE SCHEDULE FOR COMPREHENSIVE(INCLUDEFREE
LABOUR,REPAIR,OTHERSERVICES&SPAE PARTS)
MAINTENNACE CONTRACT(. /C.M.C.)AFTER EXPIRY OF
WARRANTY
(RATESSHOULDBEQUOTEDINPERCENTAGEOFTHEVALUEOFTHEMACHINE)
Sr.
No.
Code
No.
(1)
(2)
Name of For first
the
year
Equipment
with
spare
parts
and
labour
(3)
(4)
For
second
year
with
spare
parts
and
labour
(5)
For
third
year
with
spare
parts
and
labour
(6)
For
For fifth
fourthyear
year
with spare
with
parts and
spare
labour
parts
and
labour
(7)
(8)
For
sixth
year
with
spare
parts
and
labour
(9)
For
seventh
year with
spare
parts and
labour
(10)
Place :
Date :
Signature
Name in Capital Letters
Designation
Note : This format of price schedule is a sample for the Bidder's Price schedule should not be
submitted in Technical Bid, otherwise tender shall be rejected.
Prefer of CMC Separate perform Guarantee Three Years
54
ANNEXURE- XII
Ref. Clause No. 13.3 (g) of ITB
DETAIL OF SERVICE CENTER AT BHOPAL / M.P.
S.No.
Name & Place of
Service Center
Address, Telephone, Fax
& Email
No. of Service Engineer
with Name / Mobile No.
Remark
Name & designation of the authorized signatory signature of the
authorised signatory
55
CHECK LIST FOR ENVELOPE A (Must Be Submitted as Page-1)
Check list for Terms and Conditions (To be filled by the bidder and submitted along with E n v e l o p - A ) Page No. must be mentioned
against each serial.
S.No. Particulars
Yes
1.
2.
Check List Page One.
Covering Letter of company/ bidder
3.
4.
5.
6.
7.
8.
9.
10
11
12
13
14
15.
16
17.
18
EMD and Tender document fee.
The Bidder Should submit list of quoted item as per format given
Registration Certificate of Bidder (Such As Proprietor Ship, Partner, Article of Memo. etc )
Bidders registration under Commercial Tax Authority.
Annexure - I (Sales Tax Clearance Certificate)
Annexure-II (Manufacture Authorization Form)
Annexure - III (Declaration / Undertaking Form)
Annexure-IV Proforma for installation in last three years of the manufacturer.
Annexure - V (Annual Turnover Statement)
Annexure - IX (Details of Manufacturing Unit)
Annexure - XII (Details of Service Centre at Bhopal/M.P.)
The bidder should also submit national & international quality certificates like ISI/CE/C
ISO-9002,/ Company
.X, IP/BP have
etc" mark
/ IECdebarred
standard/ or
equivalenteither
certificate
of purchaser
quoted product,
Concern
not been
blacklisted
by The
or by
any StateBid
Government
Central
Organization.
to duly
this effect
Original
Form dulyorsigned
byGovernment
authorized signatory
as perAffidavit
Section V,
sealedshall
and
signed
by
the
bidder
on
each
page
for
acceptance
of
Terms
and
Conditions.Please
submit
Statement of good financial standing from bankers
In case of imported equipment IEC certificate of importer / bidder shall be submitted.
56
No
Enclosure
No.
CHECK LIST FOR ENVELOPE B (TECHNICAL BID) (Must Be Submitted as Page-1)
Check list for Terms and Conditions (To be filled by the bidder and submitted along with E n v e l o p - B ) Page No. must be mentioned
against each serial. This envelop must be submitted department wise.
S.No. Particulars
Yes
1.
Check List Submitted as page No.1
2.
Technical bid for the quoted equipments etc. should be signed and stamped on each
page. The bidder shall submit the specification's compliance / deviation report duly
filled and signed which clearly bring out the deviation from the specification if any
given in Annexure-VI.
A list of user of quoted equipments by the Principal Manufacturer for last three years. Th
contain the supplies related to the Govt. hospital/Medical Colleges / Public Sector und
hospital and other institutions of repute. Bidder should submit details of installation i
3.
4.
5.
No
Enclosure
No.
Literature of original catalogue of the product attached for reference in two copies
Quality certificates such as CE/ US FDA product wise
CHECK LIST FOR ENVELOPE C (FINANCIAL BID) (Must Be Submitted as Page-1)
Check list for Terms and Conditions (To be filled by the bidder and submitted along with E n v e l o p - c ) Page No. must be mentioned
against each serial. This envelop must be submitted department wise.
S.No. Particulars
1.
Yes
Check List Submitted as page No.1
No
Enclosure
No.
1
57
2.
Financial bid for the quoted equipments etc. should be signed and stamped on each
page (ANNEXURE-X)
3.
CMC charges as per Annexure XI.
4.
Bidder should show recurring expenditure of each equipment separately.
DEAN,
GANDHI MEDICAL COLLEGE BHOPAL
58
INDEX
S.no.
01
02
03
04
05
06
07
08
09
10
11
12
13
14.
15
Name of Department
F. Medicine
Biochemistry
Surgery
Paedi. Medicine
Radiodignosis
Medicine
Radiotherapy
Anaesthesia
Physiology
Dermatology
Orthopaedics
ENT
Anatomy
P.S.M.
Microbiology
Page No.
02-09
10-23
24-39
40
41-83
84-88
89-110
111-149
140-161
162-163
164-167
168-170
59
S.No.
1
2
3
4
5
6
7
8
9
10
Name of Department
Burn & Plastic Surgery
Pathology
Pharmacology
Cardiology
Paediatric Surgery
CTVS
OPhthalmology
Psychitary
Dentistry
Obst & Gyane
Page No.
60
DEPARTMENT OF FORENSIC MEDICINE
S.No.
Item Code No.
Name of Equipment
Cold storage
Research Bnocular
microscopes
Specification
The chamber for four Dead bodies.
Temperature between (4 to 6c)
Insulation poly urethane foam.
Roof top refrigeration unit with air cool
condenser.
Electric supply 230+10 V-50 Hz
A vapour proof incadescent lamp.
Digital type temperature indicator cum
controller.
Rust Proof Body.
Door stainless steel.
Stainless steel tray in single pieces two and four
respectively for both unit edge and handles.
The assembly should have three pieces carriage
assembly which includes frame and lower and
upper carriage and should ride on wheels.
Minimum 20 installations in India and 3 in
Bhopal and should have 20 in this field.
Company should have service centre in Bhopal.
Three years warranty and after warranty two
years free service contract.
• Colour corrected Infinity Optical System,
Anti-fungus.
• Microscope Stand with coaxial fine and
coarse focussing mechanism.
• Coarse motion Torque adjustable, Upper
stage drive stop incorporated.
• Trinocular Eyepiece Tube, Siedintorp
61
Comp./Divt.
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
62
design, 300 inclined with
Built in 3 megapixal microscopic Digital
Camera.
USB 2.0 PC connection.
Live Image resolution : 3.0 mega pixels
(2048x1536 pixels)
Calibration slide.
Eyepiece High Eye point 10x20 mm with
dioptre adjustment.
On both eyepieces & rubber eyecups
(pair)
Reversed quintuple nosepiece.
EF-N Plan Achromat Objective 4x0.10
EF-N Plan Achromat Objective 10x0.25
EF-N Plan Achromat Objective 40x0.65,
Spring loaded
EF-N Plan Achromat Objective
100x1.25, spring loaded, oil
Rectangular Mechanical Stage - 175x140
mm
Cross travel range of 76x50 mm in x & y
direction.
With vernier scale, hard coated, right
hand control.
Abbe condender, N.A 1.25 with iris
diaphragm.
Built in Koehler illumination with
6V/30W Halogen Lamp and intense.
Vinyl Dust Cover, Immersion oil (5 ml)
Images plus software
Instant image capturing, real time full
screen image
Autopsy table
• Programmed interval captures, Video
capture by time settings
• Easy measurement calibration,
Measurement in microns, inches mill
• Length measurements, Ellipse rectangle,
Irregular shape measurement
• Perimeter, radius, Circumference
Measurements, Angle measurement
• Magnifier (zoom) function, Online files
sending / receiving, Sound
• Automatic image amalgamation, Image
adjustment effects counting.
• Data export, Report generating and print
out, interactive file format.
• Compatible computer, Photo quality
printer and UPS for use Microscope.
1. Table Top
- Stainless steel, Type 304, Satin Finish /
Stainless steel
- Should have dissecting area and sink.
2. Dissecting Area
- should have grid plates.
3. Sink
- Plumbing should be factory finished.
- should have hydro aspirator with reverse flow
features, control valve and vacuum breaker.
- should have hot / cold water fixtures with wrist
blade handles and goosneck faucets
- Should have sink rinse with hose fittings and
hose hanger.
4. Table Pedestal
- Stainless steel, Type 304, Satin finish
63
LED TV
- Pedestal type
5. Ventilation
- down draft ventilation system
6. Electrical Receptacles
- GFCl type 220-240 volts AC 50 Hz
7. Disposer unit
- should have soulnoid valve, vacuum breaker
with off/on switch control and internal overload
protector.
8. Dimensions
- length 250-260 cm
- width 75-80 cm
- height - 90-100 cm
9. Polyurethane head rest - must be able to support neck while dissection
10 Stainless steel centimeter scale - Must be
engraved type
11. Scale support socket - must be able to hold
the scale support bar steadily.
12. Scale support bar - must be able to hold the
dial type weighing scale.
13. Weighing scale - dial type - must measure
upto 5 kg.
14. Polyurethane dissecting board - 2 feet x
11/2 feet x 1/4 inch.
grained trace, white
LED TV
• Remote system
• Flat panel
• Wall mountable
• Screen size 46 inch
• Dolby digital sound
64
•
•
•
•
•
Digital Camera
Internet TV option
Ethernet connection
USB Tv option
Wifi adaptor support optional
DVl & HDMl input
Digital SLR Cameras
Type - Single lens reflex digital camera with
interchangeable lenses.
Effective pixels - 6 million (app)
CCD-25x16 mm (App)
Picture Angle equivalent in 35 MM format (App
1.5 times
Lens focal length)
View finder - Fixed eye-level mirror type
Diopter adjustment - 1.6 - +0.5 m
Eye point - 18-20 mm
Frame coverage - >90% of lens (horizontal to
vertical)
Magnification -0.75
Lens aperture - instant return with preview.
Lens Servo - Auto and manual focus
Exposure metring - Three mode through the lens
exposure metering.
Matrix - 3D color matrix metering
Range - 0.2EV (3D color matrix)
Center weighed - 75% in center of frame
Shutter - Mechanical and CCD electronic.
Sensitivity - 200-1600 (ISO equivalent)
Self timer - Electronically controlled timer with
2-20s duration
Card - 1 GB
65
Video output - Selective
Weight - App -500-600 GMS
Power sources - Rechargeable battery with
charger 7.4 VDC
with separate adapter
Dimension - 6"x4.5"x3" (App)
Tripod socket - 0.25" (ISO)
Monitor - 2.0" Polysilicon TFT LCD with
brightness
Adjustment
Flash - SB800DX
Zoom lens - 17-80
OPETATING ENVIORNMENT - ROOM
TEMPERATURE IN ALL SEASONS
CD/DVD Player
5.1 Ch. Digital out DIVX, progressive scan,
multi format playability, remote with battery
5.1 Surround speakers
Weighing machine for human Made up of premium quality materials
dead bodies
- Provide accurate weight information.
- Complete SS platform for easy cleaning and
anti staining.
- Platform size 2100 mm x 600 mm approx.
- To weigh a maximum of 200 kg. accuracy 20
gms.
- TARE function provided.
- Imported load cells for enduring performance.
- Digital display
- Imported load cells for enduring performance.
- Provide hygienic and efficient weighing.
- Stainless steel 304 grade construction.
- Available in varied specifications.
- Rechargeable battery back up pack provided
for usage in power failure.
66
Anthropological instrument
seat
Anthrop meter type
measurement of
length. Range 0.2.100 mm
sliding caliper with
250/0-140 mm
vernier (1/10 mm)
aluminium
Condyle caliper
Co-ordinate calliper
made of
Spreading calliper
with
Spreading caliper
with rounded ends
Harpenden skin fold
Caliper
Orbitometer
Goniometer
Mandibulometer
67
Anthropometer made
of aluminium, GPM
for location of all
height measure whole
body.
sliding caliper with
vernier range 0minimum calibration
1/10 mm made of
Condyle caliper
Range - 0-140 mm
nickel plated.
Co-ordinate calliper
range 20-200 mm
aluminium
Sliding calliper with
pointed ends
Range 0-600 mm,
made of brass
Sliding caliper with
rounded ends range 0600 mm made of
brass.
Harpendens skin fold
calliper.
Range of upto 80 mm.
Orbitometer
Made - aluminium
Goniometer (molisons
type)
Range 0 - 180 degree
Mandibulometer
made of metal
Interactive teaching board
with LCD Projector
Range - 0
Baby weighing
Baby weighing scale
digital
Range upto 150 kg
Minimum calibration
100 grams
Digital professional
Digital professional
scale 150 kg
scale range upto
Minimum calibration
100 gms.
Stadio meter
Stadiometeric
telescopic
telescope
Range 10-70"
Minimum 1/8"
Infant head measuring Infant head measuring
type
Range 6-22"
minimum 1mm.
baby infantometer
upto 3'
Made upto P.V.C.
Interactive teaching board - 64 inches screen,
Electromagnetic technology
Wireless electromagnetic sensitive pen touch
system
Aspect ratio 4:3
Resolution - 13850*9760 pixels
Cursor speed - 120 dots / sec
Operation system - windows 2000/XP/Vista/7
Accessories - wireless pen, wall mounting parts,
USB extended cables, stand eraser
LCD Projector - LUN no SME1123366
68
69
DEPARTMENT OF BIOCHEMISTRY
S.No.
1
2
Item Code No.
Name of Equipment
Automated High Speed
electrophoresis apparatus
Fully automated ELISA with
Specification
With power pack
• Integrated Robotic sample processor built
in incubator elisa reader and automatic
washer with complete modular system.
• Should have an open system for different
make kits and manual over ride.
• Predilution facility should be present.
• Upto 256 samples can be assayed more
than one type of ELISA at same time.
• Parallel samples pipetting should be
present.
• Bar code reading facility for tubes should
be preferable.
• 6 litres with a range of 340-750 mm are
required.
• 12 measurement and 1 ref. channel.
• 16 way manifold washing with 4 wash
channels should be provided.
• Volume of wash liquid dispensed variable
and adjustable.
• Residual volume / well should be <2ul.
• User friendly software with option for
manual intervention.
• Tem. range room to 45 C+1 C.
• 4 plate incubator.
• Liquid detection should be present.
• Clot dettection should be present.
• Color monitoring check should be
70
Comp./Divt.
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
71
provided.
There should be no carry over of sample.
Password protection to prevent
unauthoried person access to software.
CVT 0.5 KVA
Printer to provide printed reports of
testes.
Teflon coated stainless steel tip.
Inbuilt quality control.
Patient name, ID keyboard entry &
individual report printouts in present
format.
File search by name ID no date Reg. no
etc.
Training of laboratory staff for the
purchased equipment.
Three years warranty 5 year
comprehensed AMC should be available
with service centres in close proximity.
Availability of spares/ disposables for at
least 10 years.
All consumables required for installation
and standardization of system to be given
free cost.
List of users and satisfactory report of
quoted model from reputed institute
Government institute / Hospital.
Should have all the accessories required
for the functioning of the equipment.
ISI mark or other equivalent quality
certification.
All electrical peripherals required for
3.
Poly Acrylamide Gel Electro
phoresis Equipment
smooth functioning e.g. voltage stabilizer
and UPS should be provided with the
equipment.
• There should be provision for
demonstration before final approval of
equipment.
(Page electrophoresis system)
Vertical and horizontal with universal power
pack)
Horizontal unit :
Dimension Gel plate size : 10.1x7.3 cm
Gel size
8.3x7.3 cm
Number of gels 1-4
Buffer tank
Main unit with single
molding casted with safety
lid
Tank volume
Upper volume : 160 ml for 2
gels set
Lower volume : 550 ml for 2
gels set
Casting units
Casting stand casting frames
Combs
Combs of variable size
Spacers
Spacer of varaible thickness
Electrodes
It must have fixed &
adjustable platinum
electrodes
Power cables
Should provide suitable
power cables
Typical run
45-50 min (at 200 V
time
constant)
Vertical unit
Dimension Gel plate size : 20x22.3 cm
Spacer plate : 10.1x8.2 cm
72
-18.3 x 20 cm
Gel size
18.3x20 cm
Get plate size- Inner plate width : 20 cm
Inner plate width : 20 cm
Outer plate width : 20 cm
Outer plate width : 23 cm
Number of gels 1-4
Buffer tank
Main unit with single
molding casted with safety
lid
Tank volume
Upper volume : 350 ml for
2 gels set
Lower volume : 1200 ml
for 2 gels set
Casting units
Leak proof casting stand
casting frames.
Combs
Combs of variable size
Spacers
Spacer of varaible
thickness
Electrodes
It must have fixed &
adjustable platinum
electrodes
Power cables
Should provide suitable
power cables
Typical run
5h
time
Cooling
Syst should include central
cooling core that can
reduce running time to 3.5
h
Accessories
Flexing hubble, clamps,
alignment card system
should be useful to run in
73
Power
Supply
Output range
Volts
Output
terminals
Input
protection
Volt hour
control
Current
Power
Timer
Programmable
Methods
Safety feature
74
2D electrophoresis setup
Should be compatible for
both submarine agarose
and vertical
acrylamide gel
electrophoresis
10-500 V easily
programmable and
adjustable
with 1 V steps
There should be
uninterrupted constant
voltage or current output
with automatic crossover
Atleast 4 pair recessed
banana jacks floating in
parallel
Fuse on both hot and
neutral
99.000 V-h
0.01-2.5 A adjustable with
1 A steps
1.500 W
1.999 min fully adjustable
There must recovery after
power failure
It should be atleast 10
methods with real time
Clock upto 10 steps each
There should be no load
detection system.
Sudden load change
4.
High performance liquid
chromatography (HPLC)
detection
Over load/short circuit
detection
Over voltage protection
Ground lead dection
Arc detection
System should be provided long with a
suitable (prefereably) APC make UPS with a
minimum capacity of 1 hour back up with a 3
years onsite warranty.
Warranty : Minimum five year free warranty
(or two years warranty and three years
comprehensive AMC) including free
placement and free repairs, without any
charges whatsoever within warranty period to
be pledged by the dealers suppliers Agents
etc.
I. Quarternary pump for semiprep work
• Operating pressure - upto 6000 psi
• Flow accuracy - <2%
• Flow precision - +0.1% RSD
• Flow rate - 0.01-40.00 ml / min
• No of eluents - 4
• Auto stat programming - Capability for
auto stat & multi method programming
storage of upto 1 complet method
parameter tables with external events.
• Composition range - 0-100%
• Composition accuracy - +0.5%
(independent of back pressure)
• Flow extendable to 45.00 ml/min
II Sample injection system with dual injector
75
option for analytica and semi prep analysis - For
analytical injector
III Degasser (optional) - In line
Flow rate analytical - 0.2-5.0 ml / min
Semi prep. analysis - 20-40 ml/min
IV. Detectors
a) UV - VIS Detector
• Wavelength range Complete UV-VIS
range
Demerin and / or
• Light source
tungsten
+0.35x10-5 all dry
• Noise
cell 254
2x10-4 AU hr.
• Drifit
<5% at 2.5 AU
• Linearity
5 nm
• Band width
10ul
• Flow cell
+1nm
• Accuracy
-0.1 nm
• Reproducibility
The detector should be have lamp optimization
software
b) Fluorescence detector.
200-900 nm
• Wavelength
range
Xenon lamp
• Light source
ul
• Cell volume
• Sean function
20 mm
• Band with
• Sensitivity S/N 800 nm
Raman pack of
water
c) Refractive index detector
76
5.
Chromatography (exchange)
instrument
1-1.75 R/U
• Refractive
index range
0.2-0-3 ml / min
• Flow rate
1.5x10-9 RIU
• Drift
Internal oven 300C to
• Temperature
550C
control
V. Column oven model - temperature range
ambient +4C to 600C
VI. Columns
250 x 4.6 mm
• C-18
250 x 4.6 mm
• C-9
250 x 20 mm
• C-18
250 x 20 mm
• Pre column
derivation
4.6 x250 mm
• Bio suit
7.8mm x 300 mm
• Protein pak
VII. Fraction collector
upto 150 ml/min
• Flow rate
• And
accessories
VIII. Software computer system
• Single point control of the entire HPLC
• Customizable data reports online help
wizards
• Report publisher.
IX. Coloured laser printer.
X. Water purification system (from tap water to
ultra water for HPLC)
XI. Laboratory establishment.
Technical specifications
Ion exchange type
Capta Q Impes
Quaterney a
77
Fluid
Average particle
size (d50)
Matrix
Total ionic capacity
Capto Q hrpRes
Cap Sp
Binding capacity
Capto Q Impsres
Capto Sp Res
pH Stability
Capto Q ImpRes
Capto SP ImpRes
Chemical stability
78
minimum strong
anion
Sulfonate group,
strong cation
Approx 400 cm/h( <4
bar or 04 mpa) or
approx 800 cm/l (<3
bar or .03 Mpa) in a
packed bed in a 1 m
diameter column
with 20 cm bed
height at 20C using
process buffer with
same viscosity as
water.
36-44 um
High flow agarose
.015-0.18mnol (Ci)
ml medium
0.13-0.16 mmol ml
medium
-2-14 (short term) 212 (long term)
-3-14 (short term) 412 (long term)
all commonly used
aqueous buffers 1 M
Working temperature
Storage
Capto Q ImpRes
Capto SP ImpRes
sodium hydroxide
8M urea 6 M guanide
hydrochloride. 30%
insopropanol and
70% ethanol.
40C to 300C
20% ethanol
20% ethanol 0.2 M
sodium acetate
HiTrap prepacked columns
Column volume
ml and 5 ml
Column
0.7x25 cm (1ml)
1.65x25 cm (5ml)
Dimensions
Column hardware
5 bar (0.5 Mpa,
73psi)
Pressure limit
Recommended fluid 1 ml/min (1ml) 5
ml/mi (5ml)
1. d50V is the average particle size of the
cumulative volume distribution.
2. Dynamic binding capacity at 10% break
through measured at a residence time of 4
minutes.
(150 cm/h) in a Tricom 5/100 column with 10
cm bed height in 50 mM tris pH 80 (BSA on
capta Q hmpres) 20 mM medium phosphate pH
7.2 (hysozyme) 50 mM pH (BSA on cap SP
ImpRes)
3. Short term pH interval where the medium can
be subjected to cleaning or place with significant
change in function long pH interval where be
79
6
Water Deionizer
operated without significant change in function.
4. No significant change in capacity and carbon
content after 1 week storage in 1 M naOh at
400C.
Conductivity matter with linear scale and alarm
system to indicate the regeneration cycle operate
on AC/DC, mixed ion exchange resin column air
mixing system FRP/PVC chemical proof
regeneration tank PVC value arrangements all
houses in trolley mounted and chemical proof
metal stand rugged construction to with stand
any external accident and chemical corrosion
easily portable deionised water with have the
conductivity of less than 1 ms/cm and pH of 6.8
to 7 output / hrs in liter - 100 liter.
7
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DEPARTMENT SURGERY
S.No.
1
Item Code No.
Name of Equipment
Specification
Upper and lower urinary tract
TECHNICAL SPECIFICATIONS OF CYSTOendoscopy set with visual
URETHROSCOPE, OPTICAL URETHROTOME,
optical urotome with camera
RESECTOSCOPE, COLD LIGHT FOUNTAIN, CAMERA,
and endovision with flexible
LIGHT SOURCE, MONITOR ETC.
endoscope, lithoclast & laser.
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Digital Signal Processing, resolution
1920 x 1080 pixel, Digital Zoom on Screen display with
BNC, S- Video , RBG cale with
remote. Power supply 240 V , 50 Hz
3 Chip Autoclavable Camera Head integrated Lens
focal length 18 mm, programmable
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Portable ultrasound machine
3
Impedance based bipolar
RFA for endoluminal
ablation. With accessories
and disposables.
General
• Should be based on the principle of Radio
frequency induced Thermotherapy for
endovenous
treatment
of
venous
insufficiency.
• Current should be induced through bipolar
applicators. Should not need any neutral
electrodes.
• Should be intersitial form of therapy which
can be performed under local anaesthesia.
• Tissue should be heated between 60 degree C
to 100 degree C using Catheter like
monitored and indicated by an acoustic
signal.
• The power output of the RF generator should
automatically correspond to the tissue
resistance and ensure that the radio
frequency is emitted as the proper rate so that
thermal injuries or burns are avoided.
• Should have footswitch control.
Should be a compact unit and should be supplied
with 25 units of single use applicators.
Power Unit
Output power : 1-25 Watts
98
Frequency - 470kHz
Channels : 1 Bipolar
Applicator - 2 boxes of 5 pcs
• Should be flexible and ultrathin (1.8mm
diameter)
• The tip should be hemispherical to avoid
intravenous injuries.
• The length should be 1200 mm.
• The electrode length should be 15 mm.
Should have 3 m long cable in each applicator.
99
DEPARTMENT OF PEAD. MEDICINE
S.No.
1
2
Item Code No.
Name of Equipment
Resuscitation Trolley
Portable ECG Machine
3
Flux meter
4
Double surface phototherapy
unit & single surface
phototherapy units
5
Resuscitation kit
6
7
8
Suction machine portable
Nebulizers
Electronic weighing scale
Specification
To hold all resuscitation equipment & medicine
12 lead ECG machine with neonatal & pediatric
probes
Required for cardiac patients
Flex meter with a well designed filter which
should have a transmission area of 425-475 nm
spectrum range To timely mentioned the
irradiance output of phototherapy unit
Combination of special blue & white fluorescent
light delivering irradiance of 12-16 UW/cm2/nm
For neonates with hyperbilirubinemia to reduce
serum conc. of bilirubin & the risk of bilirubin
toxicity
Ambu bags (250 & 500 ml capacity) with mask
of different sizes and laryngoscopes with blades
00, 0, 1
For proper sanctioning i
Multiport For Nebulization
For Anthropometric measurements
100
Comp./Divt.
NAME OF DEPARTMENT:- Radio diagnosis
S.No. Item
Name of
Code
Equipment
No.
1
Portable
colour doppler
Specification
System Specification for Portable colour doppler
1. The system should be a state of the art, high end digital system
with whole body applications including obstetric, gynecology
pediatric, urology, pediatric and small pan and vascular application.
The system should have both adult and pediatric cardiac facilities
with continuous wave doppler imaging.
2. State the total No. of installations in India
3. mention the no of model quoted installed globally
4. Pls mention the year of introduction
5. specify the no of probe connectors
6. The system should have a high resolution monitor
7. The system should have 8000 digital processing channels. Higher
channels is desirable Pls mention the no of processing channels
8. The system should have windows operating system. Pls specify the
operating system used in the machine
9. The system should have advanced calculation package for all
mentioned application obs, gy tv, tr, small parts, doppler and
cardiac (adult and pediatric)
10. The system should have the below mentioned modes- B mode, CF
mode, PW mode, Power angio, M mode,
11. Transducers should have tissue harmonics imaging as standard.
12. The system should have Real time triplex imaging on all
transducers.
13. The system should have trapezoidal imaging for all linear probes.
14. The system should have 3D imaging.
101
Comp./Divt.
15. System should have real time compounding with all probes. It
should have facility for Real time compounding with color doppler
mode too.
16. The system should have one touch optimization function for
adjusting doppler function while doing doppler scans.
17. System should have post processing facility on Frozon mode for
pulse and continuous wave doppler imaging.
18. System should have post processing facility for multiple frequency
selection for fat patients at one touch of a button
19. System should have a maximum depth of 30 cm.
20. Dynamic range of 120 Db or more
21. System should have real time zoom and zoom facility on frozen
image too.
22. System should have a facility for real time calculation for spectral
doppler.
23. The system should have extended loop capability of upto 3 minutes
or 2000 frames at acquisition rates
24. The system should have minimum 20 GB harddisk facilty for
image storage.
25. System should have an integrated image management system for
printing and storing image for the offline analysis
26. System should have Dicom facility to connect it to the hospital
server/ Printer system should be DICOM ready.
27. The system should store real time loops in B mode and color mode.
28. The system should have direct printing facility on both thermal and
color inkjet printer
29. System should have broad band high frequency transducers with
multiple frequency selection option.
30. Multifrequency convex transducer of approx 2-5 Mhz for abdomen
obst and gyn application
102
31. Multifrequency linear transducer of approx 5-12 Mhz for small
parts and vascular imaging
32. Multifrequency transducer from approx 5-9 Mhz for transvaginal
and transrectal imaging
33. Convex multifrequency probe for general purpose cardiac
scanning.
General description: Large field of view digital mammography system
Digital
mammography for general screening, diagnostics and interventional applications.
The system should consist of:
system
1. large field digital flat panel detector
2. Ergonomic examination gantry designed for mammography
applications with motorized movements
3. integrated digital acquisition system with user console and flat panel
monitor
4. dual track mammography X-ray tube with additional beam filters
and automatic collimator
5. High frequency generator
6. Exposure control system and selectable dose modes
7. Radiation shield and a mammography image receptor grid
8. motorized compression device and compression paddles
9. FFDM based stereotaxy availability
10. Upgradable to advanced applications
11. Magnification device
TECHNICAL SPECIFICATIONS
X-Ray Generator
High frequency generator type
3.0 kw or more generator power
103
kV range: 20 to 35 or more in 1 kV steps
mAs range: 0 to 500
mA range: up to 100 or more
Exposure monitoring generator and tube load pre- exposure display of
the exposure parameters
Displayed parameters kV, mAs, target filter, density selection Auto
record of the exposure parameters for each mammogram
2. X-Ray tube
Dual focus x-ray tube preferably Mo/Rh spot sice small focal spot: 0,1
mm
Spot sice large focal spot: 0,3 mm
Rotating Anode
Anodo heat storange capacity >300 kHU
Anode heat dissipation: 40 kHU/min
Beam filters: Mo and Rh
Target/ filter combinations Mo/Mo and Mo/Rh
Target/filter combination Rh/Rh
Tube heat monitoring system / device/ program
Tube current large focal spot (25-30kV): -100 mA
Tube current small focal spot (25-30 kV): 40mA
3. Gentry assembly
Isocentric system
Motorized rotation and vertical movement
Dual speed movements
Rotation angle: -+180 to -165 degree
Distance floor to image receptor:-65 to 150 cm
Source to image receptor distance (SID) : 66 cm
Wheelchaire access
Face shield
Compression force display
104
Pair of dual foot- pedals
Automatic decompression after exposure
magnification stand with dedicated paddles
Magnification: 1,5
Magnification: 1,8
Motorized compression force: 0 to 200 newtons
Manual compression force: up to 270 newtons
Large paddle
Regular 19 x23 sliding paddle
Square spot sliding compression paddle
Round spot sliding compression paddle
4 Exposure control
Both manual and Auto mode (Automatic Technique selection) Should
be available
Parameters controlled: kV mAs, filter
5. Automatic technique selection
Parameters: Anode track, filter, kV mAs, Virtual cell and dose should
be chosen automatically
Different modes should be available for selection
6. Collimator
Beam filter: Mo and Rh
Light beam intensity (Lux)> 300
FOV can be modified manually and can also be selected automatically
based on the paddle and magnification platform
7. Flat panel detector
Detector size:- 24 x30 cm
Pixel size: 100 um
DQE at OLP/mm: 60%
DQE at 5LP/mm : 29%
105
Image depth>=14 bit
Operating temperature: - 15 to 35 degrees Celsius
8. Digital acquisition system
Local storage capacity:8000 images & more
Preview image: <16 seconds
LCD image monitor
High luminance LCD: up to 500 cd/m2
Image annotation
Measurement functions
Automatic dose (Skin dose and average Glandular Dose) annotation
Automatic windowing
Multi format display
Zoom and roam
Image invert
Print layout for multi format printing
Integrated CD R/W
Thickness equalization (image harmonization)
Fine view (improved conspicuity)
Integrated quality Assurance program
Repeat reject analysis
9. Connectivity
Autosend (Autopush)
Autoprint
Autodelete based on storage commitment
DICOM SEND (storage provide)
DICOM storage commitment (storage commitment user)
DICOM Worklist (Modality worklist user)
DICOM Query/ Retrieve user
DICOM Print (basic grayscale print user)
Verification service (verification provider)
106
DICOM CD
10. Printer interface
Basic Grayscale print user
Validated printer list for hardcopy diagnostic
11. Grid/ Breast support assembly
Grid ratio:5:1
Removal and installation of the grid/ breast support motorize
Low attenuation carbon fiber support
12. Accessories included
Pair of dual foot pedals
Radiation shield with 0,3 mm Pb equivalent at 49 kV
Face shield
Large paddle- 24x31cm
19x23 cm sliding paddle
Square spot sliding compression paddle
Round spot sliding compression paddle
Remote service modem
Quality control toolkit
User manual and technical documentation
UPS for power supply
13. Display workstation
Mammography diagnostic workstation
Two high contrast and resolution 5 MP LCD B & W monitors
Multi-modality viewer to display U/S, DX,MR,MG,NM,PET & CT
Customizable having protocols
Dedicated mammography keypad
Customizable functions buttons
Patient list management tool
User selectable auto contrast modes
On line storage capacity for > 15000 images
107
Is the hard disk capacity expandable
Image retrieval time to display (4 Views) : <4 seconds
RAM: minimum 2 GB
Quadrant glass
Flip, Rotate, Invert
Annotations and graphics
Measurements
Zoom and roam
Brightness and contrast
Print screen
Contrast enhancement processing
Internal DVD-ROM drive
DICOM storage SCU/SCP
DICOM Query/ Retrieve SCU/SCP
DICOM Print Storage commitment SCU
DICOM Print (Color and B&W)
DICOM Media interchange
TCP/IP network layer
14. FFD based stereotaxy Unit
Digital stereo tactic breast biopsy
System should be patient comfort, efficient, accurate in upright/
Recumbent position with good image quality Stereotaxy angle should
be-150 and +150 automatic stop at stereotaxy angles
Tube parking position should be available up to-330 and + 330 for easy
access to the breast biopsy procedure Biopsy window should be 50x40
mm or more
Positioning at any angle +/-90 deg should be available
Decubitus Biopsy table for patient positioning during srereotaxy
procedure
15. CAD Solutions-CAD solution should be FDA approved.
108
4D
colour
doppler
16. Optional
System should be upgradable to tomosynthesis
System should be available / upgradable to contrast enhanced
mammography
System Specification for 4D colour doppler
1. The system should be a state of the art, high end digital system
with whole body applications including obstetric, gynecology
pediatric, urology, pediatric and small pan and vascular application.
The system should have both adult and pediatric cardiac facilities
with continuous wave doppler imaging.
2. State the total No. of installations in India
3. mention the no of model quoted installed globally
4. Pls mention the year of introduction
5. specify the no of probe connectors
6. The system should have a floating / adjustable key board with
Backlit alphanumeric display
7. The system should have a non interlaced high resolution monitor
with tilt and swivel facility.
8. The system should have integrated recording keys for remote control
storage and printing options.
9. The system should have 8000 digital processing channels. Higher
channels is desirable Pls mention the no of processing channels
10. The system should have windows operating system. Pls specify the
operating system used in the machine.
11. The system should have minimum 80 user defined preset per
transducer, More presets is desirable
12. The system should have advanced calculation package for all
mentioned application obs, gy tv, tr, small parts, doppler and
cardiac (adult and pediatric)
13. The system should have the below mentioned modes- B mode, CF
109
mode, PW mode, Power angio, M mode,
14. Transducers should have tissue harmonics imaging as standard.
15. The system should have Real time triplex imaging on all
transducers.
16. The system should have panoramic View imaging.
17. The system should have trapezoidal imaging for all linear probes.
18. The system should have volume 3D and 4D imaging.
19. System should have real time compounding with all probes. It
should have facility for Real time compounding with color doppler
mode too.
20. The system should have one touch optimization function for
adjusting doppler function while doing doppler scans.
21. System should have post processing facility on Frozon mode for
pulse and continuous wave doppler imaging.
22. System should have post processing facility for multiple frequency
selection for fat patients at one touch of a button
23. System should have a maximum depth of 30 cm.
24. Dynamic range of 120 Db or more
25. 4D Frame rates should be more than 20 frames/ sec
26. System should have real time zoom and zoom facility on frozen
image too.
27. System should have a facility for real time calculation for spectral
doppler.
28. The system should have extended loop capability of upto 3 minutes
or 2000 frames at acquisition rates
29. The system should have minimum 40 GB harddisk facility for
image storage.
30. System should have an integrated image management system for
printing and storing image for the offline analysis
31. System should have Dicom facility to connect it to the hospital
110
server/ Printer system should be DICOM ready.
32. System should have inbuilt CD/DVD drive for copying images
directly on CD
33. The system should store real time loops in B mode and color mode.
34. The system should have direct printing facility on both thermal and
color inkjet printer
35. System should have broad band high frequency transducers with
multiple frequency selection option.
36. Multifrequency convex transducer of approx 2-5 Mhz for abdomen
obst and gyn application
37. Multifrequency linear transducer of approx 5-12 Mhz for small
parts and vascular imaging
38. Biopsy Needle guides with kit
39. Multifrequency volume transducer from approx 2- Mhz for
obstretic and abdominal 4D imaging
40. Multifrequency volume transducer from approx 5-9 Mhz for
transvaginal and transrectal 4D imaging
41. Convex multifrequency probe for general purpose cardiac scanning
42. System should have real time coronal imaging facility possible
43. system should have advanced 4d fetal echo facility both with color
and power doppler imaging
44. system should have the facility for the parallel slicing of the
volume in real time mode.
111
NAME OF DEPARTMENT:- MEDICINE
S.No.
Item Code No.
Name of Equipment
Specification
BODY
PLETHYSMOGRAPH
SYSTEM
WITH
DIFFUSION STUDY
1. Fully automatic computerized unit for
the measurement of following parameters:
o Spirometry
&
Flow
Volume
Parameters.
o Maximum Voluntary Ventilation
(MVV),
o Lung Volumes & capacities including
RV & TLC.
o Airway Resistance & conductance Raw (Insp. Exp. tot), SRaw, Gaw,
SGaw,
o Single Breath Diffusion Capacity of
Lungs (DLCO-He) & Intra Breath.
o Lung
compliance
(Static
&
Dynamic),
o MIP/MEP for Reapiratory Muscle
Strength,
o Pre & Post Bronchodilator tests,
Should Meet Criteria for ATS Standards.
Automatic DTPS correction.
Should meet all International Safety
Standards.
Should have predicted equations.
2. Body Plethysmograph System with
Box (size > 900L or more) to provide
sufficient space to patient, With
Visibility from all directions.
112
Comp./Divt.
Fiber optic
Bronchoscope
source
and
light
3. Intercom System to be provided for
Communication with patient while sitting
inside the Box.
4. Should be supplied with PFT Software
Window XP based.
5.
Manufacturer should have a local
office with complete technical backup
capability (preferably)
1. field of View should be 120 degree or
more
2. Depth of field should be 3-50 mm or
better
3. Distal end diameter should be 5.8 mm or
less
4. Insertion tube diameter should be 5.8
mm or less
5. Channel diameter should be 2.2 mm or
more
6. should be light weight and easy to use
7. Working length should be 550 mm or
more
8. Total length should be 800mm or better
9. UP and DOWN angulations should be
180 degree and 120 degree or better
10. Can be fully immersed in disinfectant
solution and water
11. Should have autoclavable suction valve
12. Should be compatible with laser and
electro-cautry.
Light Source should be compatible with 150
113
Polysomnography System
For Sleep Disorders Study
watt halogen bulb with sharp output.
13. Manufacturer should have a local office
with complete technical backup
capability (preferably)
Polysomnography system that records and
displays physiological parameters. Should
have following Channels:o EEG
o ECG
o Sp02
o Snoring detection
o Chin and leg EMG
o Pulse Rate.
o Respiratory Effort,
o CPAP Pressure
- Should have adjustable gain and filters.
- Should have facility of on line scoring of
events during the recording
- Should have LAN interface for Data
communication to PC.
-Should have automatic Sleep staging with
Manual Over-ride, Respiratory
Analysis /PLM's Analysis, Neurological
events.
- Should be supplied with fully
synchronized Digital Video.
- System should have option of scoring
sleep and other events as per AASM
guidelines
- Manufacturer should have a local office
114
with complete technical backup
capability (preferably)
Vido Bronchoscope
Suction Machine
1. It should have good crisp, clear image
quality.
2. Outer diameter should be 6.0mm or less.
3. Channel diameter should be 2.8mm.
4. Insertion tube length should be approx.
600mm.
5. field of view should be 120 degree or
more.
6. Angulation - UP- 180 degree, down - 130
degree.
7. Minimum visible distance should be 3mm
or less.
8. Should be compatible with laser and
electricity
9. Manufacturer should have a local office
with complete technical backup
capability (preferably)
• Should be based on diaphragm technology.
• Vacuum should be more than – 60 mmHg
with flow rate of at least 8 Ltr. per minute
or more.
• Should be made for continuous purpose.
• Should be operated from mains or battery
mode (over 100 minutes).
• Should have optical and acoustic warming
signal for battery charge.
• Jar capacity should have minimum 2 Ltrs.
115
Steel Cot
(Non breakable).
• Should have provision for trolley
Steel cot drawing code NO. 2K9-E-30
Size : 1910 x 1880 x 950 x 450
116
NAME OF DEPARTMENT : RADIOTHERAPY
S.No. Item
Code
No.
Name of
Equipment
Linear
accelerator
high energy
Specification
1.
Description of function
1.1 Dual energy medical linacs utilize photons of 6 MV and less than 15 MV
and electron beams up to 20 MeV to treat both benign and malignant
disease.
2.
Operational requirements
2.1 High energy linear accelerator complete with treatment planning system
and working console is required.
3.
Technical specifications
3.1 A. STANDARD EQUIPMENT
1. Photon energy : 6 MV for low energy and less then 15 MV for high
energy
2. Electron energy : 6 Beam energies between 4-20 MeV.
3. RF source :Magnetron / Klystron
4. Waveguide type : Standing / Traveling wave
5. Electron gun : Sealed /unsealed
6. Treatment modes Normal - TSD/TAD
Rotation - CW/CCW
ARC-CW/CCW
Dose rate - MU/degree
7. Dose rate for photon energy : 200 MU/min and above in steps or higher
dose rates for both photon beams.
8. Dose Rate for electron energy : 100-1000 MU/min in steps or higher
117
Comp./Divt.
dose rates.
9. Field size (Unclipped)
10. Field size (Unclipped)
For electrons : Max - 25 x 25 cm2 or more , Min - 4x 4 cm2
A method to obtain irregular field shapes shall be provided.
11. Beam Flatness (PHOTON) :
Variation of x-ray intensity relative to the central axis sizes 10x10 cm2 to
40x40 cm2 at 10 cm depth.
12. Beam flatness (electrons):
Variation of electron intensity relative to the central axis sizes 10x10 cm2
to 10x10 cm2 at 10 cm depth.
13. Focal spot size :
14. Photon Arc Therapy : Bi-directional arc therapy should be included
with automatic calculation of dose per degree based on the dose rate
selected and the arc angle set.
15. Beam symmetry :
The maximum percent difference of average doses shall not exceed 2%
for electrons and 3% for photons.
16. Gantry rotation :
a) Read out - Digital and Mechanical
b) Accuracy dig readout 0.5.
c) Control - Hand pendent and control console.
d) Target - Axis distance - 100 + 0.2 cm
e) ODI Range - 75 cm to 150 cm
f) ODI Accuracy + 0.1 cm
118
g) Gantry rotation iso centre 2 min diameter. sphere
h) No beam stopper.
17. Collimator :
Rotation +95 about mid position
Control hand pendent and control console
Readout accuracy + 0.5
Collimator rotation iso centre 2 mm diameter sphere
Dynamic wedge / motorize wedge.
18. Asymmetric collimators x Y both asymmetrical
specify travel ranges and over travel range.
19. Multi leaf collimator (MLC)No. of physical leaves 80 and above.
a) Independent drives
b) Leaf width as iso centre = 10 mm
c) Capable of performing dynamic conformal therapy procedure interface
between MLC & existing network system should be provided.
d) Facility to treat patients conventionally using blocks without MLC
e) Work station HW/SW- specify details
f) Integration (full networking) with planning system, simulator, CT, CT
simulator, MRI & RFA should be done
g) IMRT delivery should be possible
h) Max. leaf retracting position
i) High over center travel of MLC leaves for IM"RT treatments
119
j) Max field length
k) Leaf height and material
l) Coincidence of light and x-ray field
m) Penumbra
n) Transmission
o) Interleaf leakage
p) Leaf position accuracy
q) Max. carriage speed
r) Max. leaf speed
s) Positional accuracy of the leaves during treatment
t) Inter digitations of leaves if available
u) Two Numbers of treatment parameter monitor 21" TFT to be provided
20. Treatment couch :
1. Versatile extended range couch with indexed immobilization
movements.
2. Longitudinal lateral vertical and rotation
3. Electrical / mechanical control
4. Control local and /or remote
5. Opening window - Tennis racket / mylar
6. Fully carbon fiber table top for better quality portal images.
7. Minimum height from floor - app 60-65.
2.1 Treatment planning system
120
1. The TPS software shall run on a very powerful graphics intensive
computer system with adequate latest backup technology. The system shall
have high capacity hard disk and a DVD writer.
2. Capable of performing conventional 3D-CRT, SRT,.intensity modulated
radiotherapy treatment planning for coplanar and non coplanar beams and
IGRT Planning in the same system.
3. Supports, multiple dose calculation algorithms such as anisotropic
analytical algorithm convolutioal and pencil beam algorithm monte carlo
etc.
4. At least two calculation algorithm for photons and two for electron beam
shall be quoted.
5. Virtual simulation using the software and licenses for virtual simulation
feature and for controlling moving laser shall be provided.
6. DICOM ready image networking.
7. Two workstations enabling simultaneous contouring with license and
additional two treatment planning work station with calculation license
should be provider.
A.
Beam data
1. Dosimetric data for IMRT fields must be transferred from RFA.
2. Conventional standard beam data for electrons and photons must be
stored and modification of it for IMRT and conformal treatment must be
done.
B.
Patient anatomical data transfer :
121
1. The patient data must be transferred from CT/MRI, simulator in the form
of fluoroscopic image and CT/MRI via Dicom, CD and DVD's.
. Data from CT/MRI slices must be transferred via film scanner, digitizer
and direct from CT/MRI scanners, simulator and RFA.
3. The system must select more than or equal to 100 images per patient and
to do real time multi planer reconstructions from original CT/MRI image
data sets.
4. The system must have auto contouring of external and internal organs
from CT/MRI images either taken form CT/MRI film or via other mode of
data transfer as mentioned above.
C.
Planning :
1. Geometric planning :
System must have auto contouring of organs. After dose prescription and
fractional scheme system must create geometric treatment plan with 3-D
visualization and virtual simulation.
2. Dose optimization :
System should have provision to generate the treatment plans from
templates that satisfy the organ dose constraints. Following steps should be
taken :
1) Define dose volume constraints
2) Set optimization parameters.
3) Evaluate optimization
3. Dose calculation :
System should be able to provide dynamic / step and shoot IMRT treatment
122
planning and license for Florence map to be exported on DICOMRT
format. The necessary interface for transfer of treatment plans to any linear
accelerator should be provided. The final dose distribution is calculated as
per selected dose delivery technique.
4. Plan, Review and evaluation :
It must provide 3-D dose visualization and differential and cumulative DVH
analysis tools to review the plan.
5. Plan export :
The IMRT plans can be exported directly after approval to linear
accelerated for dose delivery.
D.
The inverse planning system :
Should be complete in all respects and be able to perform static / dynamic
MLC plans. The system should be able to generate multiple plans for
selection. The accuracy of forward dose calculation using intensity
modulated beams should be less than 2%. The IMRT planning and
treatment should be based on step and shoot and or sliding window MLC
technique as per the user choice.
The total time for inverse planning should be less than 20 minutes.
A complete QA kit for the system must be supplied. Necessary software for
linking RFA to the planning system must be supplied.
22. Oncology information system complete with networking
Record and verify system
Transfer of all parameters from simulator and treatment planning system,
Cad plan to the accelerator for automatic treatment set up and delivery
should be provided.
123
Transfer fluoroscopy images from simulator to portal imaging system for
comparison should be provided.
23. Accessories :
1. Wedges - Stationery 150,30,450 and 60 wedge angle.
2. Front pointer - Mechanical
3.Accessory mount - shadow block tray
4. Blocks - divergent / non divergent
5. universal clamps
6. Side rails on both sides of couch for mounting accessories
7. CCTV/Camera two Nos. one wide angle and one remote control with
remote zoom and focus facility.
8. In room color monitor 20" or higher.
9. Laser alignment system 4 cross laser system
10. Interface mount to be provided for the simulator to stimulate accessories
like shadow block tray etc of the quoted accelerator model.
24. Dosimetry system (Photons)
Built in chambers. Two separate sealed chambers
Precision + 1% or 1 MU
Linearity+ 1% or 1 MU
Reproductively + 2% or 1 MU
Dose Rate Dependence
B.
Portal imaging and dosimeters accessories
1. Portal imaging :
Should fully integrate with accelerator
124
Should be able to images at any gantry angles with variable X-Y-Z
movements,
Robotics arm with remote control.
Should have digital technology with high resolution 1024 x 1024 pixels or
more imaging (Amorphous silicon flat panel based technology).
2. Auto field sequencing
3. Dosimetry accessories :
1. 3D Servo controlled radiation field analyzer having compact water
phantom of minimum dimension 60x60x60 cms or more with reservoir
build up caps. TNC connector and latest PC control system with IPS
interface program.
2. Dual channel electrometer
3. Ionization chambers (Signal, Reference and Pinpoint)
4. Diode detectors (Photons, electrons and sterotactic)
5. Parallel plate chambers
6. 2D arrays of either semi conductor / ionization based dosimetry system
for measurement of fluence along with computer hardware and software.
7. Solid water phantom universal tissue equivalent along with necessary
and for the chamber of size 30 x 30 30 cm should be provided.
4.
System configuration accessories, spares and consumables.
4.1
System as specified
4.2
All consumables required for installation
standardization of system to be given free of cost.
4.3
The chiller system shall be provided along with the
125
and
machine by the principals.
8.
4.4
A closed circuit color TV system with TV monitors and
two cameras in the linac treatment room shall be supplied.
A patient calling system with 6 channels shall be
supplied. Internet broad band connectivity for remote
control shall be provided. A LCD projector should be
supplied.
4.5
Patient immobilization accessories
4.5.1
Standard supine base plate
4.5.2
Lateral base plate
4.5.3
Head and neck prone baste plate
4.5.4
Head and neck supports A, B, C, D, E
4.5.5
Knee crutch and arm position with hand grip
4.5.6
Overhead arm postioner
4.5.7
Shoulder retractor
4.5.8
Universal tissue equivalent bolus 30x30x0.5 cms
Documentation
8.1
User /Technical / Maintenance manuals to be supplied in
English.
8.2
Certificate of calibration and inspection
8.3
List of equipments available for providing calibration and
routine preventive maintenance supports as per
manufacturer documentation in service / technical
manual.
126
8.4
List of important spare parts and accessories with their
part number and costing.
8.5
Log book with instruction for daily, weekly, monthly
quarterly maintenance checklist the job description of the
hospital technician and company service engineer should
be clearly spelt out.
8.6
Additional documents to be enclosed with quotation :
a. No of similar models : India / World (enclose list of
institutions)
b. No. of certified engineers in India (enclose list of
names)
c. Remote diagnosis facility (India / Abroad) availability
details
CT
Simulator
A-1
Dedicated CT Simulator is required for Radiotherapy Department for conventional
3D CRT and IMRT planning. The CT simulator is required for most accurate
simulation placement of treatment fields and marking of radiation field portals on
patient skin for radiation therapy of cancer patients. It should be latest, state of the
art model. The CT scanner should be a spiral, multi slice incorporating, latest
technology available in the market. The simulation software should be user
friendly and should ensure easy, error free and total compatibility between scanner
and simulation workstation. If third party software is supplied, it will be sole
responsibility of the vendor supplying the CT simulator to run the software. The
system should be able to integrate the virtual simulation software, workstation to 3D TPS and linear accelerator of the department and this will be entirely and direct
responsibility of the vendor. The equipment supplied should be typed approved by
AERB Mumbai.
127
A-2
CT-Scanner Specification
A-3
Whole body spiral, multi slice (minimum 16 slices per rotation) CT with flat table
and other accessories for radiotherapy treatment planning and simulation. The
system should have following essential features :
A-4
Gantry :
1. Gantry aperture should be minimum 80 cm or more.
2. Gantry tilt should be at least 30 degree.
3. Scan field of view should be 50 cm or more.
4. Metal free scan able range should be at least 150 cm.
A-5
X-Ray Generator
High frequency x-ray generator with an output of at least 50 KW or more. Please
give details.
A-6
X-Ray tube
i) The x-ray tube should have anode heat storage capacity of 5 MHU or more.
ii) The anode peak heat dissipation rate should be 700 KHU / min or more.
iii) The x-ray tube should have dual focal spot (please specify the size of each focal
spot).
128
A-7
Detector system
1. The detectors should be solid state, preferably rare earth material.
2. It should be free from repeated calibrations.
3. The detector system should be able to acquire at least 16 slices per rotation.
A-8
Patient Couch :
a) The scanning table should be universally flat with flat table top and should be
compatible with the tables of linear accelerator installed. The table should have
patient positioning index system on carbon fibre table top. It should have following
features :
i) The table should be able to bear weight up to 180 kg or more.
ii) Horizontal accuracy should be 0.50 mm or less.
iii) It should be possible to move the table top from the table side and control
console and hand pendent.
iv) The table should have auto home facility.
v) All patients positioning accessories including tilt should have control both from
gantry and control console.
A-9
Control Console
i) It should have 18 or more color monitor for display of 1024x1024 matrix or
more.
ii) All the function viz scanning, image, reconstruction, film documentation, MPR,
CT, maximum intensity projection, 3D with SSD etc should be possible from main
console and workstation.
iii)Image storage of 120 GB or more for at least 100000 images in 512x512 matrix
129
uncompressed or better.
iv) DVD facility for archiving must be available.
A-10
CT Scanning Parameters
i) The slice thickness should be users selectable from 1.0 mm to 10 mm.
ii) KV range 90 to 140 KV
iii) mA : 400 mA or more in increment of 10 mA.
iv) Scan time for full 360 degree rotation should be 0.5 sec. or less.
v) Display field of view should be 50 cm or more.
vi) Intra-plan delay of 5 sec or less should be possible.
vii) Retrospective reconstruction should be possible raw data files change in
parameter such as FOV.
viii) The following scanning mode should be possible scan gram : Axial and spiral.
It should be possible to mix spiral and axial mode. Specify how may modes can be
mixed.
ix) Pilot scan : The pilot scan field size should be more than 1000 mm long. The
reconstruction time for pilot scan should be 3 seconds for a 512 matrix and 5
second for a matrix of large size.
x) Reference scan should be possible on an arbitrary slice within the proposed
treatment volume.
A-11
Image Quality :
i) Highest contrast spatial resolution :
It should be 15 lines pair per cm or better (for 50 cm FOV) maximum at 0% MTF
for a slice of 1 cm thickness. Clearly specify the photon used, scan time, mA filter
for image construction, scan field, dose and MTF. Phantom should be supplied.
130
ii) Low contrast detectably :
The low contrast resolution for CATHPHAN should be at least 5 mm or less at
0.35% with 10 mm slice on 20 cathphan phantom.
iii) Spiral parameters : Different selection of pitch should be possible from 0.5 to 3
in 0.1 increment inter scan delay in different group of spiral should not be more
than 5 seconds.
A-13
Standard Software's :
Should provide standard software including following features :
i) Complete scanning and evaluation software.
ii) 3-D surface shaded and 3D volume rendering.
iii) Quantitative CT measurement tools should be provided.
iv) 3D small volume analysis software for solitary nodules is desirable.
A-14
Hard copy system
A dry chemistry laser camera 500 dpi or more with digital interface and control
integrated with main console. the camera should print a 14"x17" film size and it
should be DICOM compatible.
the price should be quoted separately.
A-15
Essential Accessories :
1. Head holding position kit
2. Standard supine base plate (head and neck)
3. Lateral base plate.
4. Carbon fiber titling base plate (head and neck)
131
5. Head and neck prone base plate
6. Belly board for hip and pelvis positioning and fixation
7. Hip fix
8. Breast and thorax positioning system CT compatible.
9. Overhead arm positioned
10. Breast board (carbon fiber) CT compatible.
ii) Lead Glass :
200 cm x 150 cm or more with lead equivalent to meet the radiation.
MOVING LASER SYSTEM
The CT simulator should have at least three lasers. Out of which one should be
mounted on the ceiling and two lasers should be mounted on side walls. The lasers
should be computer control moving lasers. The simulation work station should
control the moving lasers for marking the field reference points other than couch
movement. Since the computerized moving laser for making the field reference
point other than couch movement. Since the computerized moving laser marking
system is of paramount importance the vendor has to support the claim in this
regard by authenticated broachers and documents. In addition to the moving laser
the CT-scanner should have conventional in built lasers for positioning the patient.
A-17
CT SIMLUATION WORK STATION
A-18
GENERAL
The work station should have advanced CT simulation tools for radiation therapy
treatment planning include work station that can control the laser marking system.
Any CT simulation work station that can not control the laser marking system is
not acceptable and liable to be rejected. The vendor should give a completed
132
description about the laser marking system offered and how the CT simulation
software integrates with it and TPS. All necessary calibration / quality assurance
phantom / check device should also be provided, please specify. The work station
should be able to provide complete volume definition and geometric beam
placement for radiotherapy. It should have complete compatibility and error free
networking with the CT scanner computer and TPS. The CT simulation should
generate digitally reconstructed radiographs a true volumetric environment. It
should be possible to overlay the beams on any DRRs or on any slice (obtained and
reconstructed). It should be possible to load over 250 CT images per patient for
reconstruction and simulation.
a) Hardware
i) Hardware specification should be mentioned clearly the system should be
running on a high end work station platform of reputed bran dlsike sun micro
system / H.P. workstation / Del / Silicon Graphics with at least 2 GB RAM or
more. Minimum 128 bits processor with minimum of 120 GB hard disk or more.
ii) The user interface should be windows based and menu driven. Display should
be on a 18" or more LCD flat panel display monitor of high resolution of
1024x1024 pixel or more should be provided.
iii) Mention the number of full512x512 slices real time processor can hold online.
iv) A compatible 56 kb internal / external modem should be provided for remote
diagnostic upgrades.
v) The archiving media should be a DVD.
vi) Networking with TPS-all the software with license required should be included.
vii) Laser printer should be provided.
viii) It should be possible to take print out on this printer from any of the TCT
simulation workstation.
133
b) Software
i) Software should be unix /window / silicon graphics based system.
ii) The software should have a volume accelerator for high speed 3D rendering at
full spatial resolution.
iii) On the monitor screen it should be possible to view at least 36 images or more.
iv) The standard screen layout should consist of one main view port and three sub
view ports for frequent usage of other images, quick manipulation of images, or for
displaying reference views, while the main view port is used for high resolution
display.
v) Image manipulation such as changing window width and window level, hot keys
activated automated study archive, deletion, screen layout changes, disk space
display archiving and graphic overlays such as annotation.
vii) It should possible to visualize interactive reference views in axial, coronal,
sagitals, iso center image planes and in any oblique directions with overlay of
beams in DRRs.
viii) DRR must provide fully divergent beam's eye view of 512x512 matrix.
ix) The DRR/BEV and Room eye view image should display the machine diagram
to allow real time checking of machine and patient geometry.
x) Facility for multi modality fusion to accept the data from other DICOM
compatible and DICOM supporting modalities such as MRI / CT / SPECT / PET
should be able to fuse them.
A-19
CONTOURING
i) Volume definition should be possible using volume segmentation using
threshold free hand contour tracing, contour editing 3D an isotropic margin etc and
any other advanced tools.
134
ii) System must be able to contour in axial sagital, coronal and oblique projections.
iii) It should be possible to do manual semi automated, fully automated contouring
/ segmentation in the images by defining volume of interest.
iv) Mention the time taken for automated contour with a single mouse operation for
250 slices.
v) The software should have facility for automated uniform or non-uniform
margins. For example it should be possible to expand the clinical target volume
CTV on all three dimensions by same magnitude or by different magnitude to
define the planning target volume. Any software without this automated uniform /
non uniform feature will be considered as inadequate.
vi) It should be possible to copy one organ to another with margin and margins on
a single slice a range of slices or all slices.
viii) Interpolate algorithm should be available to provide shape based interpolation
i.e. after contouring only in selected slices. The algorithm should automatically
interpolate the closely fitting contour in other slices.
ix) Interpolated contour may be edited accepted or rejected.
x) Tracking of source to skin distance should be possible.
xi) Contouring and editing and extraction of wall should be possible.
A-20
ISOCENTER MANAGEMENT
i) The advance should support separate iso center for multiple target volume or
general regions.
ii) Marked and final iso centers should be reported and displayed in the localization
package for easy confirmation of a physical simulation session.
iii) Hardcopy of the isocenter coordinates should be possible for record of the
135
simulation session.
iv) Isocenter positioning should be automate.
v) No limit on number of isocenter per target.
A-21
VIEW AND VOLUME RENDERING CAPABILITES
1) Post processing features like volume rendering real time multi axial volume
reconstruction, 3-D surface rendinger color 3D should be available.
ii) It should allow completed 3D volume to be defined including complex 2D
volume user selectable multi image views, became eye view room eye and DRR.
iii) DICOM radiotherapy plans and data structure with import / export of data
should be possible. The DICOM compliance statement should be provided.
iv) Accuracy of locating any point in 3-D should be 0.1 mm or less.
A-22
BEAM PLACEMENT & DEFINITION
i) If should support extensive beam shapers (shielding blocks etc) and beam
definition methods.
ii) Manual or automatic beam placement tool.
iii) Tools for real time checking of machine geometry.
iv) Beam shaping should be possible in multiple ways like automatic shielding
block definition confirmation to selected volume definitions aperture or shielding
manual free hand definitions automatic collimator jaw or multiyear position
definition.
v) It should be possible to define this asymmetric collimator feature where both the
X and y axis of jaws are asymmetric in the CT simulation software, similarly the
software should allow multi leaf collimator placement up to 40 pairs or more. Any
software that can not handle 40 pairs of MLC leaves is not acceptable.
136
A-23
DRR FEATURES
1) Interactive DRR calculation mode must be available
ii) Automatic window width /. level selection for DRR.
iii) DRR should be interactively updated when the isocenter position is modified.
iv) Should be possible to highlight or suppress different density region in the DRR.
vi) Macro function to save a used steps
vii) Specify DRR image enhancement tools to improve DRR quality.
viii) Reconstruction of DRR should be real time or in sub seconds.
ix) Direct printing of DRR on laser film should be possible.
x) Real time display of DRR as beam parameter changes.
A-24
DEPTH CONTROL :
i. System should support depth control mode creating a DRR from slab of 3-D
mode, perpendicular to beam axis.
ii) DRR must be calculated over a user defined thickness.
iii) Depth control in oblique projection must be possible.
iv) Should be possible to merge two DRR image on the same beam.
v) Cross hair display on DRR to provide scale information.
A-25
DATA IMPORT / EXPORT
i) System should be able to export image, volume and plan data in DICOM 3.0
standard long with all Radiotherapy specific data and private objects, DICOM RT
plans and data sets.
137
ii) System should be able to import DICOM RT data to the linear accelerator of
any vendor.
iii) CT simulation system should be fully integrated with the existing TPS. The
vendor should inspect and will be responsible for complete integration.
iv) All import and export license should be provided.
A-26
DOCUMENTATION AND ARCHIVING
i) Should be on a color dye sublimation or alternative suitable and economic printer
to be supplied along with the system and DICOM print should be possible. Abode
post script print should be available.
ii) Archiving should be on DVD in DICOM format.
A-27
MEASUREMENT PACKAGE :
i) The software should provide the density value (in House field unit) of a
particular point on image. It should compute distance along straight lines and
curved lines angle between the lines and radius of curvature for curves.
ii) For a specified region of interest, ROI, the area, minimum and maximum voxel
values mean and standard distribution and a density histogram should be available.
iii) The software should be able to calculate the volume of a displayed 3-D object.
A-28
IMAGE MANIPULATION
i) Different kinds of image manipulation features should be available like multi
planer reconstruction curved formatting.
ii) 3D reconstruction with no waiting for reprocessing.
iii) The vendor should provide comprehensive training by application specialist for
the CT simulator at the site on installation and to the full satisfaction of the head
138
department of radiotherapy. The training period should be at least for four weeks or
more.
2.1 Complete installation should include :
1. Room Planning and designing and construction. Space requirements to
be spelt out in advance.
5. Air conditioning and monitoring of temperature and relative humidity
and air changes (To specify no. per hour) to be installed.
2.2 The unit shall be capable of being stored continuously in ambient
temperature of 0-50 deg C and relative humidity of 15-90%.
2.3 The unit shall be capable of operating in ambient temperature of 20-30 deg.
C and relative humidity of less than 70%.
2.4 Shall meet IEC-60601-1-2:2001 (or equivalent BIS) General requirements
of safety for electromagnetic compatibility or should comply with
89/366/EEC; EMC-directive.
3. Power supply
3.1 Should work on three phase 400-440 V/50 Hz power
3.2 Online UPS of suitable rating should be supplied for the complete system
including Gantry, computer system, anesthesia delivery system, monitor
and defibrillators with at least 30 minutes back up.
3.3 Reset-table over current breaker shall be fitted for protection.
4.
Standards, Safety and Training
4.1 Warranty : 60 months from the date of satisfactory installation & handing
over to the department. The warranty shall cover all the accessories
including CT tube. Comprehensive maintenance contract for five years
shall cover all the accessories including CT tube.
139
4.2 Shall comply with AERB guidelines and type approved.
4.3 Should be FDA, CE, UL or BIS approved product.
5.
Documentation
5.1 User / Technical / Maintenance manuals to be supplied in English.
5.2 Certificate of calibration and inspection.
5.3 List of equipments available for providing calibration and routine.
Preventive maintenance support as per manufacture documentation in
service / technical manual.
5.4 List of important spare parts and accessories with their part number and
costing.
5.5 Log book with instruction for daily, weekly, monthly and quarterly
maintenance.
140
DEPARTMENT OF ANAESTHESIOLOGY
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GENERAL:
AC input
Power consumption
Battery type
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100 to 230 V AC; +/- 15 %; 50/60 Hz.
100VA
Rechargeable SMF Lead Acid
Battery Capacity
12 V, 4.5 AH 7 hrs only
monitoring; 100 discharges of 360 joules.
Environment Operating temperature:0 degree
Celsius to 40 degree Celsius.
DEFIBRILLATOR:
Waveform
Energy select
5 msec Monophasic pulse
- External
0 to 360 joules in steps
2,3,5,7,10,20,30,50,70,100,150,200,300,360.
- Internal
0 to 50 joules in steps 2,3,5,7,10,20,30,50
Charge Time
< 5 secs to 360 joules with battery
< 15 secs to 360 joules without battery (AC mains only).
Charge indicator
Charge ready lamp and audible tone
Charge ready lamp on apex paddle.
Available and delivered energy to be displayed on screen.
Synchronization Defibrillation synchronized to the R
wave with marker indication on the ECG
waveform.
Sync message display message to be displayed on
the monitor screen and lamp on front panel.
Energy/ Heart Rate display on the screen.
Paddles Standard adult anterior electrodes Slide off
to expose paediatric electrodes.
Retractable Cable with stretched length of atleast 3mts
142
Monitor section of defibrillator:
Display
Monochrome LCD 5” diagonal with CCFL
backlight.
Display resolution
320x240 pixels.
ECG modes
Paddle ECG and Patient Cable ECG (I, II and III
standard leads)
Leads off message
Onscreen message with alert tone.
CMRR
> 90 dB @ 50 Hz; input impendence > 2.5 mOhm.
Frequency response
0.5 to 35 Hz with filter.
Sweep speed
25 mm/sec.
Display time
4 sec.
HR display
30 to 250 BPM; +/-2 BPM
HR alarm
Audiovisual user selectable alarm limits;
30 to 300 BPM.
1mV cal Signal
Vertical line (variable amplitude w.r.t. Gain)
Patient cable length
3 meters
Electrical isolation & shielding Input protected
against high voltage, DF pulses and radio
frequency interference.
Built-in Cautery filter
Printer section:
Recording type
Paper size
Paper speed
Print delay
Event Recording
!
•
•
•
•
•
Thermal Array recording
60mm x 30 mts; print width: 50 mm.
25mm/sec.
6 secs.
Stores and prints 3 sec. Pre and 8 secs.
Post critical event data upto 28 events.
Print annotations
Time, Date, heart Rate, HR
limit, Event marker, ECG parameters, Defibrillator
mode, selected and delivered energy, patient
impedance, peak current and hospital name.
Defib design should be with biphasic technology
Energy selection should be adjustable between 2 – 200 joules
Charge and discharge button should be available both on monitor and paddles
Charging time for maximum energy level ( 200 J) should be less than 5 sec
Charge indicator: audio and visual
143
•
•
•
•
•
•
•
•
•
•
Internal discharge when unit is turned OFF or automatically after time limit
Built in test charging facility, shall be available at any energy level (2- 200 J) against
50 ohms impedance
Built in automatic external defibrillator ( AED) with voice prompt
Manual and AED operation
Display of selected energy
Built in thermal recorder
It should offer synchronized cardio version
Summary storage facility ( INTERNAL MEMORY)
Sync and async modes shall be indicated on monitor and recorder
Defibrillator should have option for pacing
Monitor
•
•
•
•
•
•
•
•
•
Sweep speed ; 25 MM/sec
Heart rate indicator 15 – 300 bpm
Alarm setting ; upper limit 100-250,lower limit 30-100 bpm
Hi and Lo adjustable alarm setting
Adjustable ECG size 5 levels
Monitor should have bright LCD display
Display resolution ( 320∗240 Pixels)
ECG should also be available thru paddles
Audio visual indication should be available for R wave detection
External pacing :
• Pacing rate 30- 180 pulse /min +/- 1.5%
• Output current 10 – 200 mA ( +/- 5mA) monophasic
• Pacing mode : Demand or fixed rate
• Status indicator : ECG lead fault , pace lead fault
• Pulse width : 20 msec
Defibrillator shock should be delivered thru paddles as well as thru multifunction disposable
electrode pads
GENERAL:
AC input- 100 to 230 V AC; +/- 15 %; 50/60 Hz.
Power consumption – 100VA
144
Battery type - Rechargeable SMF Lead Acid
Battery Capacity – 12 V, 4.5 AH 7 hrs only monitoring; 100 discharges of 360
joules.
multi-parameter monitor
Monitor should have high-resolution active matrix SVGA TFT display.
Display should be integrated and not less than 8.4” in size.
Display resolution should be 800 x 600.
Monitor should have adult, paediatric and neonatal modes.
Monitor should have options for integrated dual channel thermal recorder.
The monitor should have the following parameters:
1) ECG:
- 3 leads facility.
- HR ranges 15-300 bpm.
- HR accuracy +/- 1 bpm.
- Pacemaker detection and lead off failure alarms.
- ECG should meet AAMIU standards and should comply with IEC
2) NON INVASIVE BLOOD PRESSURE:
- Auto, manual and stat mode of operation
- Measurement ranges 30-255 mm of Hg.
- Accuracy +/- 5 mm of Hg.
3) PULSE OXIMETRY :
- Measurement range 0 – 100%
- Pulse range 30 –300bpm
- Accuracy +/- 3 %
4) GENERAL
- Monitor should have more than 90 hr trends for all parameters
- Trends should be available in graphical and tabular format
- Monitor should have 2 level of alarm monitoring
- Display should have intensity control for adjusting brightness
- Monitor should have in-built facility for battery back up
- BATTERY TYPE: Li-Ion and battery charge time: 4 Hrs to charge
- BATTERY RUN-TIME: More than 3.5 Hrs with 15 min NBP operation
- Monitor should have built in central station connectivity with Ethernet output
145
- Monitor should be truly portable weighting less than 3.2 Kg
- Monitor should be portable with carrying handle
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Stainless Steel sheet wall panels
Stainless Steel Ceilings Panels inside OT
Antibacterial Paint inside OT
Double Dome LED OT Light inside OT
Air Ceiling Management System inside OT
Homogenous Low Turbulence Unidirectional Laminar Air Flow
Ceiling
X-Ray View Screen, Writing Board, PRD
Surgeon Control Panel
Electrical wiring and fixtures inside OT
Hermetically Sealed Sliding Automatic Door
Antistatic Conductive Tile Flooring inside OT
Extension of Medical Gas Pipe Line System
AGSS system
Suction and Oxygen Therapy System
Scrub Sink to be fitted outside OT
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It should have an accuracy is +/- 1% of full range. Keep the elegant
REG/OFF/FULL mode set up design
Compact Light weight and durable construction design. Easy pressure adjusting
knob, simple operation
Large digital number display with Low/Med/High level Display Design. Eye
catching LED indicate color lights corresponding to
color code
ranges(Green/Yellow/Red). It will not waste battery power when the status is on
OFF mode to allow extending battery life. Digital battery power bar alarm
display. Allows easy understanding of battery Power condition.
3 mode selection digital
REG/OFF/FULL
Vacuum regulator:
Pressure indicator light:
U
Green Light: 0-80 mmHg
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ELECTRICALLY
OPERATED
<
!
1. It should be a Closed, easy-to-clean and corrosion-free powdercoated resp. anodized, resistant to chemicals.
2. It should have Ground clearance over the whole width and length at
least 18,5 cm. Customary patient lifters comply with the bed.
3. It should have Ground clearance under the lift columns amounts 4
cm.
4. It should have Triple-telescope-columns maintenance-free and
capsuled integrated.
5. It should have 2 synchronized motors (24 V low voltage) for parallel
height positioning with electrical control (synchronization control) in
max. 26 seconds.
6. It should have Trendelenburg 12°/reverse-Trendelenburg 14°
electrically adjustable by the nurse control.
7. It should have Load capacity 100 kg/caster.
8. It should have 4-caster central brake directional stability/wheel
alignment by means of footboard pedal. The lying surface should
be removed in 4 parts. It should have Optimized mattress fixtures
on both sides. It should have Ergonomic arrangement of back, seat,
thigh and lower leg section with 90 cm (35.46 in.) long back section.
9. Pressure in the stomach section should be avoided and breathing
improved.
10. Back section (0-70°) and thigh section (0-45°) should be
individually positioned with safety freewheel.
11. It should have Preselection of the leg section positioning (bent-knee
or stepped bed positioning).
12. It should have additionally manual positioning of the lower leg
section for stretched raised leg positioning (0-16°) by means of a
step less hydro-lift positioning unit.
13. It should have quick lowering of the back section for reanimation
(CPR).
14. It should have Headboard acceptance on both sides for trapeze
bar, IV pole and further Accessories.
15. It should have Bed sides with integrated accessory rails over the
whole length for flexible acceptance of accessories.
175
16. It should have quickly removable head and foot sections.
17. It should have Frame with heavy collision edge.
18. It should have four horizontal wall protection wheels at the four
edges, two vertical walls
19. Protection wheels Headboard.
20. It should have Pressure reduction system (The patients are
motivated to further mobility by the micro-Stimulating effect of the
pressure reduction due to their proper motion).
21. This innervations leads to pressure ulcer prevention due to an
improved circulation up to a therapy support and treatment of
chronicle wounds.
22. The insert elements of the lying surface should be removed
completely and are expandable to an active System.
23. It should have hand control unit (can be fixed on both sides) in
execution incl. lock switch.
24. It should have following Versions for hand control unit:
25. Horizontal with clip for assist rails
26. With additional auto-contour-function
27. With thigh-section adjustment
28. Nurse control with complete locking in the bedding deposit:
29. Positioning of the lying surface as "Hold-to-run" function.
30. The functions of the height positioning, Trendelenburg and reverseTrendelenburg "Hold-to-Run" and automatic function.
31. It should have 4 electric motors of the electrical protection class II
(double protective insulated).
32. It should have Thermal fuse and electronical control against
overheating.
33. It should have Emergency lowering possible by means of batteries.
34. It should have battery backups 7,2Ah for operation without power
supply, sufficient for at least 10 positioning cycles under maximum
allowable load.
35. The bed should be electromotive operated continuously max. 4
minutes within 10 minutes.
36. It should have Data communication by means of standardized LIN
bus.
37. It should have Absolute placement by means of potentiometer that
176
means no limit switches.
38. It should have reset possible by means of pushing a button without
reference run.
39. It should have 2-parts, variable assist rails made of aluminum
profiles.
40. It should have unhindered access to fixed accessories and patients
in all positions of the assist rail–Also in unused status.
41. It should also elevate no modification of outside dimensions of the
bed.
42. It should have Therapy and side bedding function.
43. Assist rails should be positioned in two-stages. (First stage as
visualization of the bed sides and Mobility grip. Second stage as
protection against unintentional falling down. Safe hold between the
two-part assist rails during getting in and off)
44. It should have Simple operation and safety lock.
45. It should not be unlocked on-load for safety reasons.
46. It should have Lateral ram protection made of special plastics.
47. In case of overload plastically deformation. No sudden break of the
guide or the assist rails.
48. Assist rails should be permanently with good sliding quality without
greasing.
49. Color and design of the head and foot boards should be acc. to
choice of the customer based on the design and color chart of the
offerer.
50. It should have Diagnosable bed system of an automotive standard.
51. It should have Software and gateway for data transfer, diagnostics
and error detection, repair instructions, spare part orders, guided
technical inspections including all necessary documentation locally
or on a web server made available including all software updates.
52. It should have closed components with smooth surfaces make the
bed extremely easy-to-clean.
53. It should have following Dimensions:
54. Width lying surface:
55. Length lying surface:
177
90 cm (35.46 in.)
200 cm (78.80 in.)
56. Width outside dimensions:
99 cm (38.61 in.)
57. Length outside dimensions: 216 cm (85, 10 in.)
BED SORE
PREVENTIVE
MATTRESS FOR
ICU BED
ELECTRICALLY
OPERATED
58. Height positioning range:
40 – 80 cm (15.76 – 31.52 in.)
59. Steel single caster:
150 mm diameter
60. Weight:
150 Kg
1. It should be a basic hygienic mattress with excellent price
performance suitable for short term patients or when a firmer
mattress is required
2. The mattress should be cleaned by using alcohol based
detergents.
3. Mattress cover must have a vapor permeability that is lower
than 300gr/m2/24h,to avoid transmission into the materials.
4. It should provide good medical comfort for the patients without
reducing quality or hygiene.
5. The mattress must have a pressure distribution test from an
independent test institute.
(Please enclose test report)
6. It should be a homogenous mattress made from coldfoam with
a density of 35 kg/m3
7. The mattress should operate without any electrical supply
8. The mattress must fulfil EN 597-1/2 (Cigarette and match fire
178
resistance test) (Please enclose test report)
9. The mattress should be a sealed system without any zipper or
seams
10. It should have medical device standards
11. The mattress should provide the hospitals the best possible
total cost performance
12. Minimum warranty of the mattress cover should be 5 yrs.
MULTIPURPOSE
ELECTROMECHAN
ICAL OPERATION
TABLE
ORTHOPADEIC
ATTACHMENTS
1. Five section x-ray translucent top with inbuilt kidney bridge
2. Provides all surgical positions
3. Minimum height 28” & maximum height 42”
4. 304 grade S.S fully electro-polished
5. Die presses S.S cover on base without any edges and wielding.
6. Head, leg & pelvic sections are interchangeable
7. Electric floor locking mechanism
8. Very heavy duty base for total stability
9. Addition fixed control provided on the table top in case main Hand set fails
10. Approx. weight 250 kg.
11. Mattress size:-(50mm thick & 60 density)
12. Base size: 18”W x 36”L x 5”H
13. Side Railing 30 x 10 mm
Should be provided with following attachments
1.
2.
3.
4.
5.
6.
7.
Traction Device Arm
Extension Arms
Traction Device
Traction Shoe
Movable Pelvic Support (Adult)
Inner Thigh Column with Pad.
L-Shape Knee rest with Pad.
179
8. Lower Leg Support.
9. Inner thigh support with pad for traction in lateral
NEURO ATTACHMENTS
1.
2.
3.
4.
Sujita head clamp (prone for adult & ped.)
Mayfield head clamp
Horse Shoe
M-type face head rest
UROLOGY
ATTACHMENTS
1.
2.
3.
4.
5.
6.
7.
8.
9.
A Set of mattresses
A pair of shoulder support
A pair of Side Support
A pair of knee crunches with ball & socket joints
Anesthetic screen
Arm Rest – 2Nos.
Urological drainage tray
with sive attachement
Instrument Tray
AIR STERILISER
1. Rated voltage should be 230V 50 Hz
2. Consumption should be 70 W
3. Should have Level of air purification 92%
4. Range should be 56 m3/h
5. Noise level should be 29dB
6. Installation should be vertical wall mounting
7. Operation should be continuous
8. External UV-C emission should be none
9. Danger level should be none
180
10. Equipment should have pre-filter in the air intake
11. Life of UV-C tubes should be 3000 hours
12. Air nozzles should be fixed
13. Casing should be in aluminium
14. Lamp switch should have anti UVC glass
15. Lamps should have 2x 6w- T5 UVC tubes
16. Wavelength should be 254 nm
17. Colour should be Ral 9010
18. Weight should be 3.5kg
19. Dimensions should be 45x18x8cm
20. Dimensions of packaging should be 50x19x9cm
21. Volume should be 0.008 cu.m.
181
Department of Physiology
S.No.
1
Item Code No.
Name of Equipment
Specification
Manneqin for clinical exm.&
artificial respiration
This manikin provides maximum student/instructor
feedback in four practice mode: compression rate,
compression depth, and Ventilation duration and
ventilation volume. Red light indicates improper hand
placement. The performance of each skill is displayed
separately while averages are stored in the memory. With
the flip of a switch, memory unit evaluates performance
based on chilled or adult CPR standards.
The disposable tracheal airway and lower airway with
lung bag eliminate time consuming disinfection
procedures. Includes ten disposable airways, ten
disposable tracheal airways, and five sanitary face
masks.
2
Projection Microscope
NAC. Code BDI
With 200mm diam. Graduated screen 360 degree rota
table quadruple revolving nose piece total magnification
ranging 100X to 800X or 125X to 1000X.
Work able on 220 V AC main with variable light control
arrangement to eye piece with stage micrometer slide for
measuring optical combination built eye piece (10X, 15X)
objective 5X, 10X,20X,40X.
Advanced research model incorporated with binocular
head and pointer arrangement.
3
Anthropometric set
(complete with all type of calipars
Height, Weight recorder, Calipers for measuring skin fold
thickness’.
Calipers for measuring head circumference waist
circumference hip
Circumference and all accessories.
Accessories: Anthropometer Rod, Complete with
scale and carrying bag for height measurement, Sliding
Calliper (POECH type), Cubic Craniophore, With built in
bone holder, Skin fold Calliper herpendent type, Skin
182
Comp./Divt.
Folder, Skin guide, Finger & palm printing pad, complete
set,
4
Portable Spirometer
Data transmission : Rs 232 interface to Pc through SeMA
software.LCD display for graphical and numerical values.
5
Aesthesiometer
For Tactile Sensation(Von Freyes)
6
Dynamometer
-Hand spring (grip) dynamometer
7
Wright peak Flow Meter
Wrights peak floe meter:• Type of device: variable orifice peak flow meter
• Range: 50-800L/min
• Accuracy: better than 10%
• Scale interval: 10 L/min below 700, 20L/min above
• Measuring principle: piston/ spring and moveable
pointer
• Frequency response: profile A/B difference less than 15
L/min
• Cleaning: alcohol wipe
• Life in clinic use: annually
• Net weight: 74 grams
Dimension: 150X60X34 mm( including internal
mouthpiece)
8
Stethoscope Demonstration with
multiple ear pices
Stethoscope with a single chest piece and multiple ear
pieces for demonstration purposes
183
DEPARTMENT OF DARMATOLOGY
S.No.
1
Item Code No.
Name of Equipment
RADIOFREQUENCY UNIT
Specification
Frequency 3.8 Mhz Power output 140 walts
Tungsten wire electodes Autoclavable hand piece and
neutral Plate Finger switch and foot switch activated
2
3
PUVA Chamber
Cryo Surgery Unit
4
Long Pulse Nd : YAG Lager
5
Fractional CO2 Lager
6
IPL
7
Hyfrequator
8
Woods Lamp
32 Lams 120/240 VAC 311 UVB NB LT 100W
Wave Length 1064 mm/532 nm
Spot Size 2 mm, 4 mm, 6 mm
Fluence upto 12.5 J/Cm2
Pulse width 3+/– 1 NS
Freq. 532, 1064 nm
Energy 200-2000 mj
Spot Size 3 mm, 6 mm, 9 mm
Fractional HP 9 mm
Wavelength - 10600
Power to Tissu 25 W
Operation Mode CW,
Single Pulse
Ultra Pulse
Repeat Pulse
Ultra Peak Power 800 W
Ultra Peak Freq. 10-990
Ultra Pulse Duration 100 s- 1700 s
Source Flash Lamp
Wavelength 550 nm
600 nm - Fluence
2-25 J/cm2
Power - 230 V AC
Frequency 3.5 Mhz
Power s140 W
184
Comp./Divt.
9
10
11
12
13
Dermascope
OT Table, OT Light, Surgical
Instruments, Resuscitation kit
Electric Derma Brader
Output - 40 VA, Speed foot control
Iontophoresis Unit
Hand and Foot Plate
Q Switch Nd : YAG Lager
Wavelength - 1064 / 532 nm
Energy - 12.5 J
Pulse Duration - 8 ns
Spot Size 1-7 mm
Electrical Power 220 V
185
DEPARTMENT - ORTHOPAEDITRS
S.No.
1
2
Item Code No.
Name of Equipment
Specification
Battery operated hand drill
with charging station with drill and saw attachment,
fully cannulated with reverse and forward operation
with lock, autoclavable with maximum speed of
800-1000 rpm with a set of three batteries, 15 saw
blades of various sizes
Foot operated with drill and saw attachment/flexible
reamer attachment with flexible reamer set and
flexible shaft autoclavable with quick coupling, And
reamer heads of all sizes from 8-16 mm at increment
of 0.5
Autoclavable with stainless steel body with key
Infrared Remote control, Variable colour
Temperature, Digital confrol panel with light
rotation of 360 degree with a sterilizaable hndle to
focus and position with illumination intensity of
approx 2.5 lux
With 5 cuff sizes with extra one set of 5 cuffs and
alarm. Electronic Digital Display with 3 hrs Battery
Backup
With oscillating saw with variable speed and all
sizes of blades
With foot and knee attachmentswith height
adjustables
To suit OT size of 625 sq. feet with mini HEPA
filters with noise requctrion with ss body PU coated
with air conditioning
As per dgsnd rates and with staking facility
Universal jig for tibia and femur, with nail extraction
device, drill sleeves, trocar hammer.
With 50 memory
With 50 memory
Electric drill system
3
4
Manual Drills
LED OT lights
mounted
5
Electronic pneumatic tourniquet
6
Electric plaster cutter
7
Watson-jones type traction table
8
Ceiling suspended laminar air
flow
ceilling
Colour photo copier
Interlocking nail instrument set
universal for tibia and femur
Glucometre
Digital B.P.instrument set
186
Comp./Divt.
LED View Box
Large, wall mounted
Flexible reamers set with fixed Stainless steel with silicon exchange tube box
reamm heads from 8-16 mm
Bipolar Cautery
Operated on 230V+/-15V, 50 Hz+/-3%
Should have 4 output features
Monopolar Cutting 1 and Monopolar Coagulation 1
Monopolar Cutting 2 and Monopolar Coagulation 2
Bipolar Cutting 1 and Bipolar Coagulation 1
Bipolar Cutting 2 and Bipolar Coagulation 2
Should have digital display and colour coding and
acoustic signal and can be operable by both hand
and foot switches.
It should have following Rated Frequency
Monopolar Generatior:> 300 KHz
Bipolar Generator : Upto 1000 KHz
Bipolar Cutting should offer following Modes
Pure Blend Cut: Cut with low degree of eschar form
Blend Cut : Cut with considerble eschar current
Forfex: Mechanical cutting with strong hemostasis
Bipolar Coagulation should offer following
Modes
Macro Coagulation: Large forceps
Macro Stop Large forceps with auto stop
Auto macro: Large forceps with auto start and suto
stop
Micro Coagulation: Small forceps
Micro Stop : small forceps with auto stop
Auto Micro: Small forceps with auto start and auto
stop
SEAL SAFE: For vessel sealing
Endo Seal Safe: Endoscopic vessel sealing
It should have
LED Display for monopolar and bipolar cut and
187
coagulation
Acoustic signal for monopolar and bipolar cut and
coagulation
Colour code for cut and coagulation
The Unit should be quoted along with the following
Accessories
1)Monopolar set of Accessories (1 set)
Consisting of :
Hand control pencil
1 No
Double pedal Footswitch
1 No
Patient plate
1 No
Electrode set of 5
1 set
2) Bipolar Footswitches
1 No
3) Bipolar Forceps
1 No
4) Bipolar Cable
1 No
C-Arm Image intensifer
1/A mobile C-Arm with 9 tube inches High
Frequency generator with rotating anode tube with
17 inches Dual TFT Monitor B/W Display along
with the trolley
2/It should have vertical and horizontal hold with
180 rotation on monitor with all standard
displacements of control unit with foot lock with
built-in 5 KV Auto stabilizer with printing facility
with printer.
3/ Fluor mA from 0.5 - 1 mA contious variable
4/ Unit should have control panel with KV selection
from 40 to 120 KV with LCD Display and Digital
display of KV & FLR time with feather touch
control. Should have 5 minute timer with Buzzer
5/ Unit should be operable on 230 V with 2 monitor
system for LIH, Live and storage image. It should
have permanent image storage capacity of aprrox.
10,000 image and 50 temporary image storage for
quick review.
188
6/ Monitor should be operable on windows and have
CD writer facility.
7/Unit should have CE, AERB and/ISO certification,
Short Wave Diathermy Unit
Intermittent cervical and lumber
Traction Unit
Ultrasound therapy Unit (Dual
band)
Output 500 watts, floor model, LED display timer
with audible alarms with one pair of Both disc and
rubber electrode, neon tester lamb.
LED Display. timer with alarm, & patient switch
Traction table - MS made frame, 2 section bed well
cushioned, 1 section free rolling.
Microprocessor based, output 1 mhz & 3 Mhz.
Mode pulse & continuous, LCD Display,
189
Name of Department - E.N.T.
S.No.
1
Item Code No.
Name of Equipment
Specification
Bipolar Radio-Frequency
Ablation
system for
ENT Treatment with auto
stop function
- Should be based on the principle of Radiofrequency induced
Thermotherapy for minimal invasive surgeries.
- Should be interstitial form of terapy which can be performed
under local anaeshtesia. Surface of the organ should remain intact.
- Current should be induced through bipolar applicatiors. Should
not need any neutral elecctrodes.
-Tissue should be heated over 60 deg.C
-Should provide a rapid procedure.
-Should have constant real-time monitoring of the coagulation
process.
-Should provide end-of-procedure singal.
-Should have automated power contral to exclude overdosing.
-Should have footswitch control.
-Should be supplied with bipolar cutting system for the
consevative removal of tissue and with special surgical forceps, a
cutting electrode grip, the necessary connection cables and special
cutting electrodes for combined treatment of sleeprelated breathing
disordes.
-Should be compact unit and should be supplied with different
applicators and probes.
-Should be certified acc.to CE and IEC601.10 safety standards.
Consumables
--Probes for treatment of Habitual snoring &Hyperplastic palatine
tonsils in adults and children with conical tip & 1.3mm dia
-Probes for treatment of Hyperplasia of the nasal concha, Habitual
snoring (combined treatment) and Mild obstructive sleep apnea
(combined treatment)with conical tip & 1.1mm dia.
-Brobes for treatment of Nasal polyps, especially recurrent polyps
with conical tip; and 1.3mm dia.
190
Comp./Divt.
- Angled and bayonet Forceps with cables for tissue and vessel
coagulation to stop bleeding in ENT and surgery.
-
Department - Anatomy
S.No.
01
Item Code No.
ANT-01
Name of Equipment
Specification
Mortuary
The Chamber for two and four dead bodied, temperature less than 5, insulation
Cooler
pillycurethine foam , rooftop refrigeration unit with air cooler condenser,
electric supply 230+ 10 volts-50 hz. A vapour proff incandescent lamp, digital
type temperature indicator cum controller, rust proof body, door stainless
steel, stainless still tray in single pieces two and four respectably for both units
with tubular edge and handles, the assembly should have three pieces carriage
assembly which includes stationary frame and lower and upper carriage and
should ride on wheels. Minimum 20 installations in india and three in bhopal
service center in bhopal, three years warranty and service contract.
Accessories- Automatic voltage stabilizer 3KBA
02
ANT-02
CADAVERIC
INJECTION
MACHINE
(EMBALING
MACHINE)
For injecting formaldehyde solutions in cadavers and much higher speed
than normal gravity process. Unit to be covered and mounted on a portable
trollery having four castor wheel for easy movement. Unit consisting of
one air compressor filled with half HP motor which is
connected with stainless steel tank of 10 liters capacity ment for storage and
injecting the solution. Tank to be fitted with safety valve, pressure gauge and
rubber tubing having provision for injection. Supplied with complete electric
cord plug suitable to work 220 volts 50 hz AC supply.
03
ANT-03
DIGITAL VIDEO
Color corrected with din plan optics.
IMAGING
Resolution more than 400000 pixels high resolution chip, RCA, S-Video,
USG 2.0 output, high resolution built kin digital camera to produce brilliant
191
Comp./Divt.
SYSTEM
image. Video and digital signals can be obtained at the microscope base and
displayed on TV set and PC monitor at same time
by high resolution CCP chip. Built in Mock / digit converter. 40x to 1000x
standard magnification range optionally up to 2000x with additional eye piece.
A versatile software for image depturing, processing and editing.
04
ANT-04
05
ANT-05
Distllation Plant 01 gallon
menerty per hours
Embrylology models
Medium skeleton with
nerves and blood vessels
Life size skeleton 170 cm
tall
Life size skeleton with
stand
Adult male pelvis with
stand
Adult female pelvis with
stand
Female pelvic muscles
and organs
Magnified human larynx
model
Jumbo heart model
New style giant ear model
Enlarged skin model
Giant eye model
Magnified human
pulmonary Alveoli model
Model of transparent lung
Developing Heart
Dev. of Heart in 30 days embryo
Dev. of atria and Ventricles- At 4 weeks
Dev. Of atria and Ventricles- At 5 weeks
Dev. Of atria and Ventricles- At 8 weeks
Undifferentiated Genital System
Male UG system in 12 week embryo
Female UG System in 12 week embryo
This model depicts the position. Course and distribution of main arteries and
peripheral nerves of the human body.
Features nerve branches,Vertebral arteries and herniated lumber disc. Skull includes
movable jaw, cut calvarium.
Durable parts Stand with wheels
Comparison between two sexes
Comparison between two sexes
To get an integral knowledge of various important structures
Demonstrate movements of epiglattis and cartilages in the voice box
To understand external and internal features of heart and its relation with the large
blood vessels
Shows the three main structural parts of the hearing organ and the posistion of
equilibrium organ of the body
Showing structure and appendages of skin
The different part of the eye ball model are detachable to show its structures
This model shows relation and branches of principal bronchus
Shows bronco pulmonary segments and their arrangements
192
segment
Larynx Heart and Lung
model
Model of the anatomical
nasal cavity
Liver model
Male urogenital system
Liver pancreas and
duodenum mode
Female urogenital system
Appendix and caecum
Disco torso 15 slices
Brain 8 part
Brain Ventricles
Spinal cord with nerve
ending
Separating into seven parts. The two lung have removable lobes to show internal
structures of heart
Removable parts to show external and internal features of human nose
The complex vessels nwtwork in the open liver are displayed in different color
To show external and internal futures.
Relation an opening of the ducts can be seen
To show external features
The model shows wall of the caecum and appendix Various positions are described
Horizontally sectioned in to 15 slices showing topographical relations
DEtailed model divided medially showing external and internal features
Shows both side ventricles, the third and fourth ventricle
Showing composition of spinal cord
193
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S.No.
01
Item Code
No.
MB-001
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Name of Equipment
Real Time PCR
Specification
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Fully automated blood
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Fully automated technology with ability to take patient I.D. by barcode.
Should process blood samples, other sterile body fluids both aerobic and
anaerobic systems.
Sample capacity more than 200 samples.
Besides phylogenic, system should have facility of detection for yeasts and
194
fastidious organisms
Should include pediatric and adult samples.
Media in bottles should have agents for neutralization of antibiotics.
Continuous agitation system.
Analyze each sample separately as per ID, time of entry, incubation period,
growth etc.
Should have built in calibration check and alarms/reminder for the same.
Decontamination facility.
High sensitivity and specificity with continuous monitoring of all samples.
Minimum 3 days stand alone data storage capabiligy.
All media and consumables for setting up and standardization should be
provided free of cost
Additional identifiction and sensitivity (with wide range of antibiotics) to be
provided with the equipment.
The unit shall be capable of being stored continuously in ambient temperature
of 0-50 deg C and relative humidity of 15-90%
The unit shall be capable of operating continuously in ambient temperature of
10-40 deb C and relative humidity of 15-90%
Power input to be 220-240VAC, 50Hz fitted with Indian plug,
Reset tabke iver cyrrebt breaker
Suitable voltage corrector/stabilizer
Suitable UPS with maintenance free batteries for minimum one-hour back-up
should be supplied with the system
Attach original manufactures produc catalogue and specification sheet
photocopy/Computer print and accepted. All techni al data to be supported
195
with original product data sheet . Please quote page number on compliance
sheet as well on technical bid corresponding to technical specifications.
Should be FDA or CE approved or ISI marked product.
Should be compliant to ISO 13485 : Quality systems-Medical devices
particular requirements for the application of ISO 9001 applicable to
manufactures and service providers that perform their own design activities.
Comprehensive training for lab staff and supppport services till familiarity
with the system.
03
MB-003
Fluorescent Microscope
04
MB-004
Trinocular Microscope
Three years warranty, 5 yrs comprehensive AMC should be abailable with
service centers in close proximity.
Trinocular head
6 positions nose piece.
Objectives- 5x, 10x, 40x, 100x(A Plan achromatic)
Halogen filament lamp 12 V, 35 W for fluorescence 50 W
Binocular Phototube
Conversion filters-blue & green, CB-12 d32x2.
Condenser 0.9/1.25H
Phase stop pH 1,2, 3
Pin hole diaphragm
Eye piece 2 pairs WF 10x & WF 15x
Eye piece eye cup
Dust over
Ergonomic design to provide user comfort and avoid eye fatigue. Comfortable
knee rest position.
Power slot G2
With computers compatible accessories.
Mega fixed CCD, 3x zoom,Digital zoom
LCD & optical view finder
USB interface for Windows
Remote control via USB or control unit
Line image via USB or video out. 4
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Dean
Gandhi Medical College
Bhopal
198
NAME OF DEPARTMENT : PATHOLOGY
S.No.
1.
Item Code
PAT-01
Name of Equipment / Instrument
Laboratory Centrifuge
Specification
1. Table top model with swing out rotor head 16
tubes of 15 ml glass tubes.
2. Digital speed indicator with 60 min. count
down timer.
3. Speed 4000 rpm & RCF 2750 with rotor head.
4. Dynamic breaks, imbalance detector, cut off in
case of uneven load.
5. Step less speed regulator & safety lid interlock
to prevent lid opening during operation.
6. 220-240 volts 50 Hz.
2.
PAT-02
Laboratory Centrifuge (Research)
1. Table top model with swing out rotor head 16
tubes of 15 ml. glass tubes.
2. Digital speed indicator with 60 min. Count
down timer.
3. Speed 4500 rpm & RCF 3485 with rotor head.
4. Dynamic breaks, imbalance detector, cut off in
case of uneven load.
5. Brushless induction motor with frequency
drive.
6. Step less speed regulator & safety lid interlock
to prevent lid opening during operation.
7. 7 segment LED display of speed
8. 220-240 volts 50 Hz
3.
PAT-03
Centrifuge for Micro Hematocrit
1. Centrifuge for micro hemtaocrit.
2. Table top model with rotor head to accomdate
24 capillaries with reading device.
3. Digital speed indicator with 15 min count
down timer.
4. Speed 12000 rpm & RCF 15300 with rotor
head.
5. Switch to quick accelerate to full speed.
6. Dynamic brakes, imbalance detector, cut off in
case of uneven load.
7. Brushless induction motor with frequency
drive.
8. Step less speed regulator & safety lid interlock
to prevent lid opening during operation
9. 7 segment LED display of speed
10. Automatic door opening through gas hinges
11. 220-240 volts 50 Hz
4.
PAT-04
Deep Freezer (-200C) Horizontal
1. Capacity 170 litres & required temperature
lowest 200C
2. Outer body made of powder coated steel.
3. Inner chamber non corrosive, non magnetic
stainless steel 304 AISI grade.
4. PUF insulation between inner and outer
chamber.
5. High tech solid state digital temperature
indictor cum.
6. Unit to be supplied with voltage stabilizer.
7. Dimensions outer : mm
1150(W)x500(D)x910(H) inner.
600(W)x400(D)x700(H)
5.
PAT -05
Blood bank Centrifuge for component
1. Unit suitable for high load blood processing
separation
centre.
2. Required swing out rotor head to accomodate
4 double bags or 6 single bags
3. Should have advance microprocessor control.
4. Inbuilt pre cooling programme self diagnosis
of error option to set and indicate RCF
5. Should have features of acceleration and
declaration profile.
6. Imbalance detector & cut off in case of uneven
load.
7. Brushless induction motor with frequency
motor.
8. Temper proof password protection safely lid.
9. Simultaneous display of set and run
parameters.
10. Max speed 4500 rpm & max RCF 60000.0
6.
PAT-06
Rotary Microtome (Spencer type)
1. Manual rotary microtome with knife holder
and specimen holder and all accessories.
2. With imported heavy duty knives 200 & 240
mm.
3. Range of thickness 0.5 um to 60 um increment
1 um to 10 um.
4. Horizontal advance of specimen 30 mm and
vertical stroke 60 mm
5. Universal knife holder base for different
knives along with disposable knife ho0lder with
safety finger projection guard.
6. Maximum specimen size 50x60x40 mm.
7.
PAT-07
Cytospin for Cytology
1. Suitable for cytology preparations.
2. Swing out rotors with adaptor all tube sizes
down to 1.5 to 2 mm.
3. Maximum speed 6000 RPM with RCF 4186 g.
4. Capacity 12x15 mm.
8.
PAT-08
Automatic Tissue processor
1. Fully automatic tissue processor with capacity
of 200 cassettes per run.
2. LCD display with 4 lines, digital
programming upto 9 programmes. All controls
should be operated by feather touch keys.
3. Should have 12 heated stations with (3 wax
baths) with cover.
4. 2 litre glass jars with fume hood with
continuous agitation.
5. Programmable 12 stage timing sequence for
each stage for duration 1 min to 9 hrs in steps of
one minute with delay time upto 99 hrs.
6. Automatic wax bath (PID temperature
controller and PT 1000 sensors). With facility of
Vacuum operation and protection hood.
9.
PAT-09
Bone Decalcifier digital
1. Suitable for use in histology for
decalcification of bone tissue by electrolytic
action.
2. Through the combination of heat and fluid
agitation.
3. Basket movement provided by an electric
motor to raise and lower the basket as well as
rotate it.
4. Digital temperature control and display along
with timer.
10.
PAT-10
Fully Motorized programmable
1. Fully automatic microtome for variable
Rotary Microtome
specimen retraction and sectioning.
2. Two separate programmes for timing and
sectioning.
3. Speed control through cutting window.
4. Section thickness setting from 1 um to 99um
in 1 um increments.
5. Section thickness from 0.5um to 99um.
6. Three sectioning modes one manual and two
motorized (continuous and separate)
7. Section thickness from 0.5um to 99um.
8. Three sectioning modes one manual and two
manual motorized (continuous and separate)
11.
PAT-11
Slide warming table
1. Rectangular histology slide warming table.
2. With jet black top surface minimum 300x200
mm
3. Programmed and set temperature digital
display.
4. Set values memory.
12.
PAT-12
Knife sharpener Automatic
1. Automatic knife sharpener A.O. spencer type
for manual knives.
2. To permit perfect cutting edge at an equal
bevel angle on both sides.
3. Constant rotation of ground glass plate.
4. Can hold knife up to 300 mm and should have
metal scale 0-25 with 10 divisions.
5. Unit should be powder coated.
13.
PAT-13
Paraffin dispensers digital
1. Specially designed equipment to dispense wax
for embedding.
2. Capacity 3 litres /5 litres.
3. Thermostatically controlled tem. with Tap
control at 560.
14.
PAT-14
Tissue flotation bath
1. Tissue flotation bath for histopathology.
2. Micro processor based digital temperature
control range ambient to 70+1.
3. Inner chamber rectangular, seamless (die
pressed) stainless steel with high grade
insulation.
4. Size minimum 240 (L) x 150(W) x 50(D) mm.
15
PAT-15
Table top Blood cell counter
1. 5 keys for simple manual different count with
(Clay adam type)
computation including percentage.
2. Each unit counts 999 and last unit totalize
different cells with bell at 100.
16
PAT-16
Micro slide cabinet
1. Closed pack manner with vertical storage of
75x25 mm glass slides.
2. Steel cabinet with powder coating, paint,
finish.
3. Movable drawer in slots with lockable door.
4. Capacity 10000 slides /30 drawers or 25000
slides / 80 drawers.
17
PAT-17
Autoamated immunoassay analyzer
1. Bench top analyzer with built in thermal
printer with facility for external printer.
2. Based on enzyme linked fluoroscent assay.
3. System must have at least 12 sample testing
positions.
4. System should not have carry over between
samples and reagents.
5. The test device for one test should contain all
the reagents required for that particular test.
6. System should be able to run if required a
single test at a time.
7. Calibration stability should be minimum 14
days.
8. Controls and calibrators should be included in
the test kit.
9. All the kit components should be stable upto
expiry date of the kit.
10. The test menu should be more than 80
parameters.
11. No co9nsumables required for daily start up
shut downs and periodic maintenance.
12. The test device should be bar coded.
18
PAT-18
Automated ELISA SYSTEM
1. Should be CE Approved Fully Automated
continuous access, walk away micro plate
system.
2. Sample capacity at least 180/Batch
3. Individual racks for sample loading (at least
12) should be provided.
4. Multi tasking system with simultaneous
functioning of different processing steps.
5. System should have at least 4 micro plate at a
time & 3 micro plates in archiving.
6. Upto 12 parameters per batch.
7. System should have Clot detector.
8. Original kit vial loading facility (direct
loading of reagent vials irrespective of the
manufacturer)
9. Singe probe system.
10. Should have carbonized disposable tips for
reagent dispensing & sample dispensing.
11. System should have at least 280 positions for
primary tubes.
12. Should have automatic sample sensing & bar
coding.
13. Sample dilutions should be upto 10000.
14. 31 positions for reagents & 22 positions for
calibrations required.
15. Signature / simultaneous multi reagent
pipetting to ensure fast processing.
16. 8 channel washer manifold.
17. Should have independent micro plate
transporter.
18. System should be 96 well plate reader with
both bicrhomaticad monochromatic reading
options.
19. At least 8 independent incubators with temp
options from RT to 470C.
20. Should have a Bi directional interface.
21. Start up time should be less than 2 minutes.
22. Option for performing individual modular
functions e.g. washing, reading, incubation and
sample addition.
23. Windows based operating system.
24. 24 Hrs. service support.
25 Should enclose list of installations in India.
26. 1 year warranty and 5 years spare parts
availability.
27. The company quoted should be direct
importer of the system.
19.
PAT-19
Thalassemia and Hemoglobinopathy
1. The system should be an automated integrated
testing / screening equipment
system, dedicated to HbA1c, Thalasseaemia and
Hemoglobinopathy testing and screening based
on HPLC technology.
2. The system should be able to screen and
quantitative hemoglobins, Hb, A2, HbA, Hb, F
and Hb, Al, Hb, S, Hb, C, Hb, Q India and other
rare abnormal hemoglobin.
3. Complete ready to use kit should be provided
with buffers, columns, primers, calibrators and
sample vials.
4. It should at least have a through out of <7
minutes per sample.
5. The system should have in kit external
standards for instrument calibration ensuring
accurate quantitation of results.
6. The system should contain low pulsation dual
piston pump with programmable solvent deliver
system.
7. The system should have integrated 1/4 LCD
touch screen.
8. The system should have built in Graphic
thermal paper printer, 112 mm, 4.4' wide.
9. The system should have a bi directional LIS.
10. The system should have an audible alarm
system for low buffer in the mobile phase
reservoirs, low level value for cartridge injection
and overflow for the waste tank, as well as built
in alarm for calibration failure.
11. The system should be capable of positive
sample identification using a Barcode reader.
12. The system should have the facility of
primary tube sampling and direct dilution of the
samples without manual intervention.
13. It should have an inbuilt system check
facility which checks all the system parameters
(e.g. cartridge, buffer, reagent, waste etc.) are
ready before the sample analysis.
14. The system should have a dual program
mode to perform either Hba1c or Hba2/Hb
F/Hba 1 c without changing any reagents or
columns.
15. Assay time should be maximum 3 minutes
for HbA1c testing and maximum 7 minutes for
A2/F/A1c testing.
16. It should be able to print a hard copy report
filing identification and information on the
subtype and quantity for haemoglobin detected.
It should the facility to view current and stored
chromatograms & should enable storage of
chromatograms.
17. It should have a remote data access feature
when connected to LAN or internet.
18. Manual and explanatory supplementary
reference reading material on abnormal
haemoglobin variants should be provided with
reference to the system.
19. Normal and Abnormal controls and quality
control should be provided.
20. The system should have a hardware upgrade
available for an increase in the sample workload.
21. Product related technical support, instrument
service and maintenance support should be
provided.
22. Installations list in India to be enclosed.
23. The instrument should be supplied complete
with a starter pack consisting of all reagents and
consumable for 400 HbA1c tests or 200
HbA2/F/A1c tests.
20.
PAT-20
5-Part Haematology Analyser
1. Fully Automatic and compact haematology
analyzer 5 part differentiation of WBC.
2. Open vial sampling mode requiring maximum
2 oul blood.
3. 23+4 parameters including RDW/SD.
4. Through put : at least 60 samples / hour.
5. At least 4 quality control programs and 60
files storage.
6. Storage capacity : 400,000 samples with data
and graph.
7. Technology : Laser scatter, flow cytometry,
impedance.
8. Should have facility to analyse CBC, CBC +
Diff mode.
9. Fully customized report formats including
microscopic exam results.
10. Automatic diluent dispensing for capillary
samples.
11. Should have syringe based measurement
technology.
12. Linearity range performance
WBC : 0-99.99 x 109/L
RBC : 0-8.00 x 1012/L
HGB : 0-250 g/L
HCT : 0-67%
PLT : 0-1000
13. Reproducibility performance
WBC :  2.0%
RBC :  1.5%
HGB :  1.55%
MCV :  1.0%
PLT : 4.0.%
14. There must be PC operation of the
instrument.
21.
PAT-21
Binocular LED Microscope
1. Optical system : Universal infinity corrected
optical system anti fungus.
2. Nosepiece : Revolving nosepiece.
3. Coarse / fine focusing knob.
4. Stage: Mechanical fixed stage (120x132mm)
with specimen holder.
5. Eyepiece tube : Binocular tube (30 degree
inclination and 48-75 mm IPD)
6. Condenser : Abbe condenser with objective
guide marking position factory fitted
7. Eyepiece lens : 10 x(anti fungus) , factory
fitted.
8. Objectives :
a) Plan Achromat 4 x
b) Plan Achromat 10 x
c) Plan Achromat 40 x
d) Plan Achromat 100 x
9. Illumination : LED illumination source
voltage : 100-240 volts AC
22
PAT-22
Imported Binocular Research
1. Optical system universal infinity corrected
Microscope
optical system anti fungus.
2. Nosepiece : Revolving nosepiece.
3. Coarse / fine focusing knob.
4. Stage : Mechanical fixed stage (120x132mm)
with specimen holder.
5. Eyepiece tube : Binocular tube (30 degree
inclination and 48-75mm IPD) Rotable 360
6. Condenser : Abbe condenser with objective
guide marking position. Factory fitted.
Numerical aperture : 1.25
7. Eyepiece lens : 10 x (anti fungus), factory
fitted.
8. Objectives :
a) Plan Achromat 4x
b) Plan Achromat 10x
c) Plan Achromat 40x
d) Plan Achromat 100x
9. Illumination : Halogen 12/20W illumination
source.
10. Voltage : 100-240 volts AC
23.
PAT-23
Research Microscope with
Epifluorescnce attachment with
 Colour corrected infinite optical system,
Anti fungus.
microscopic digital camera
 Microscope stand with coaxial focusing
control knobs upper stage drive stop.
 Siedentopf type binocular / trinocular
eyepiece tube 300 rotatable 360.
 Wide field eye piece 10x18 mm with
rubber shield (pair)
 Quintuple revolving nose piece with click
stop.
 Objectives :
o CCIS plan achromatic PL 4/NA0.13
o CCIS plan achromatic phase Ph
10/NA0.25
o CCIS plan achromatic phase Ph
40/NA0.65 spring loaded.
o CCIS plan achromatic Phase Ph
100/NA0.125 spring loaded.
 Phase contrast 5 position Turret
Condensor for phase 10x40x100xBF&DF
 Centering telescope.
 Sub stage illuminator 6v/30w helogen
lamp power supply 100-240 CE
 Epi fluorscent attachment with filter
cassette.
 Mercury lamp socket for HBO 100W,
starter unit HBO 100W.
 Lamp centering tool.
 Mercury lamp HG 100W
 High resolution Digital camera with 1/2"
CMOP chip.
 +USB 2.0 PC connection.
 Real time live image resolution 5.0 mega
pixel, 2580x1944 pixel.
 16 mm lens, Macro viewing tube,
calibration slide.
 Microscope eyepieces adaptors (28mm,
30mm, 34 mm, 35mm)
 Image software: instant image capturing
real time full screen image, programmed
interval capturing video capturing. All
measurements in micro, inch, mm, length,
angle, etc.
 Facility for on line file sending.
 Image assembly at high magnification.
 Image capturing at multi focal depths.
 Branded PC computer : Pentium 1 Core
Chipset with 4 GB rams 300 GB HDD,
DVD Writer with Graphic card and High
Resolution 19" TFT Monitor with Key
Board and Mouse.
24.
PAT-24
RESEARCH MICROSCOPE
Optical system: Infinity corrected system
PENTAHEAD
Focus : Vertical stage movement 25 mm per
coarse.
Stroke, Vertical stage movement 1 micron per
fine stroke, stage rotation of 27 degrees.
Illuminator : Built in Koehler illumination for
transmitted.
Light 12V100W Halogen bulb (Pre centered).
Light intensity adjustment centrally located.
so both hand can be used to increase and
decrease light preset switch for photography
built in filters (LBD-IF, ND6, ND25)
Revolving Nosepiece : Interchangable reversed
coded
Quintuple / Sextuple Nose Piece with click stop.
Objectives : Plan 4X, Plan Achromat Phase
10x/0.25WD 10.6 Plan Achromat 20X/0.4 WD
1.2 (spring) Plan flourite phase objective
40x0.75 (spring loaded) WD 0.51 & Plain semi
apopchromat 100x0.
Observation Tube : Wide field Trinocular head
with field no. 22 mm. Stage : Ceramic coated
coaxial stage with right hand low drive.
Control condenser : Phase contrast / Dark field
condenser (N.A. 1.1)
Teaching attachment : For 1+4 persons
Head with eyepiece of field no. 22
LED arrow pointer (Green and Red)
Fluorescence Attachment :
 Eight position Coded Filter unit with Fly
eye lens for even fluorescence
illumination.
 100W Mercury Apochromatic Light
illuminator.
 Filters should be Narrow band UV, Blue
& Green.
Digital Camera : Cooled Colour C-Mount CCD
Camera having large CCD size of 1/1.8" with 12
bit A/D converter having 3.0 Mpix or more
resolutions. Camera should have pixel size of
3.45 um2. It should have frame rate of 17 frames
/second at 2080x1542 resolutions. Exposure
time should be 30us 180s. Digital camera should
be suitable for bright field & fluoroscene
applications.
Imaging system : Image analysis software for
measurements time. Lapse and the software
should be capable to drive. The camera and the
microscope parts with latest. Branded Pentium 1
Core Chipset 4 GB Rams 300 GB DVD writer
with Graphic card and High. Resolution 19"
TFT monitor with keyd board and mouse.
 LCD Display for live presentation.
 Appropriate table for microscope.
25.
PAT-25
Vacuum Infiltration tissue Processor
At least 9 Processing Programme with cleaning
programme and warm water flush programme.
 Solution vol. upto 4 litres.
 Control panel with easy monitoring &
functionality.
 Pressure / Selectable.
 Vaccum agitation.
 Should be supplied complete with all
accessories,
reagent
bottle
with
attachments.
 Water reservoir & carbon filter.
 Cassette Basket.
 Paraffin container.
 Scraper
 Aspirated carbon carbidge
26
PAT-25
ELEVATED GROSS STATION
With Gross Tool system grossing board and
WITH INFRARED CONTROLS
instrument for grossing and trimming.
Constructed from high quality stainless steel,
elevated grossing station, floor model.
o Camera mount
o Cassette holder
o Disposal, 3/4 HP (Factory Mount) and 1
HP (Factory mount)
o Dissecting Board
o Eyewash Assembly
o Filter Activated carbon and potassium
permanganate.
o Flammable Storage Cabinet.
o Foot Pedal control voice activation.
o Formalin Dispense / Collection system
o Forms holder
o Full perimeter rinse
o Glove Box Holder
o Magnifier Light, Deck mount
o Microphone on flex arm
o Monitor and keyboard stand
o Rule
o Scale Digital
o Seismic Anchoring kit
o Shelving / Cabinets - Stainless steel
o Side Splashes, Splash Shield and Plexiglas
o Trash Container (Ventilated)
o Utility Drawer
o Valve air and gas
o Self contained Ventilation assembly
o Video camera arm
o Video or Dictation mount
o Voice activated dictation
o Writing platform (preferably pull out)
viewing device.
o X-ray illuminator
THE BID SHOULD INCLUDE QOUTATION
FOR:
(A) IMPORTED GROSSING TOOLS :
Standardized
Grossing
tools
eg
Trimming
Semi
disposable
Knives,
Grossing
Forks,
autopsy
knives,
dissecting,
scalpel
and
replaceable blade scissors. Should be easy to
clean and decontaminate.
(B) IMPORTED GROSSING BOARD :
- Not less then 50x40x2.5 cm size along with
grossing forks 1.5x 2x 2.5mm
- Cleaning Brush
- Easily adjustable wells, calibration of wells
position of tissue and desirable thickness.
27
PAT-27
CRYOSTAT
Cryo 220V, 50/60 Hz with disinfection system
and motorized.
- Instrument used to freeze and section tissue
specimen.
- With all necessary accessories.
- Chamber Temperature range - 350C to 00C
- Cryobar temperature - 500C minimum (Cryo +
Section)
Sectioning speed Range
o Maximum : 28 Sections per minute.
o Minimum : 2 sections per minute.
o Specimen Size Round 25, 38 and 55 mm.
o Specimen orientation 80 to 100 (X and Y
axis 3600) (z Axis)
o Sectioning range 1 to 99 u in 1 u
increments.
- Travel Range :
o Vertical 63mm
o Horizontal 31.75mm
28
PAT-28
CONTINUOUS RAPID TISSUE
Upto 120 specimens per hour
PROCESSOR (Microwave Based)
Should be complete in respect of :
o Load station
o Microwave station
o Vacuum station
o Unload station
o Continuous loading and unloading should
be possible.
o Maximum : 28 Sections per minute.
o Minimum : 2 sections per minute.
o Specimen size round 25, 38 and 55 cm
o Specimen orientation 80 to 100 (x and Y
axis) 3600 (z Axis)
o Sectioning range 1 to 99 u in 1 u
increments.
o Processing time ranging from 60 to 120
min.
o Maximum : 28 sections per minute.
o Minimum : 2 section per minute.
o Specimen size round 25, 38 and 55 mm
o Specimen orientation 80 to 100 (x and Y
axis) 3600 (z Axis)
o Sectioning range 1 to 99 u in 1 u
increments.
Temperature ranges :
o Microwave stations 610C + 20C
o Vacuum stations 650C + 20C
o LCD display with tough screen.
- Complete software for manual and auto stats
should be able to do standard or extended
programs.
- Reagents management system with counter for
cassette.
29.
PAT-29
Automatic Micropipettes
1. With high accuracy & Precision Calibration at
200C - 220C
II. Fixed volume :
a) 10 ml
b) 100 ml
- 4 Set
c) 1000 ml
2. Delivery volume display in clear digits in read
out window.
3. Light weight eugenic design.
4. Insulating jacket with tip ejector.
5. Autoclavable
6. Mechanically durable & chemically resistant.
30.
PAT-30
Coagulometer
1. Semi automated haemostasis analyser
a) 4 channel optics.
b) Low reagent volume 25 ul to 50 ul assay
range 50 -8.000ngm/ml
c) Can be used for clotting based chromogenic
method.
d) PC interface option
e) Should be provided with electronic pipette of
25-200ul.
f) Open system facility for reagents and
automatic INR calculations.
g) Machine to be installed by the company
personnel, operational with all tests running.
h) Starter kits to be provided.
i) Training of operators.
31
PAT-31
Turbidometer
1. Semi automated analyser with end point,
kinetic fix time MSD and absorbance modes.
2. 90 open location for open MSD
3. At least has 6 programmes in MSD
4. Should have automated flagging of outline
results.
5. Measuring system with cuvette mode.
6. Filter range Biomatic filter, 340, 405, 505,
546, 578, 630
7. Temp - 370C with temperature lock.
8. Measuring range : 200 to +2000 O.D.
NAME OF DEPARTMENT : BLOOD BANK
S.No.
1.
Item Code
BB-01
Name of Equipment / Instrument
Refrigerator Blood Bank
Specification
1. System required with weekly chart recorder and
digital displays.
2. Temp range should have adjustable temperature
control range from 1 degree to +8 C, factory present
at 4 degree C.
3. Capacity should accommodate 350 or more units
blood and storage internal volume should be 700
liters.
4. Refrigerator system.
a) The system should have high density CFC - free
urethane foam insulation to protect cabinet from
ambient temperature fluctuation.
b) The system should have positive, forced, air
circulation to maintain tempereature uniformity at all
shelf level, with quick recovery +/- 1 degree C.
c) The system should have sensors for activating
automatic defrost cycle to minimize the frost build
up.
d) The system should have automatic condensate
removal with no requirement for separate drainage
lines.
5. Internal construction should be made up of high
grade stainless steel (min 22 (i) External construction
Corrosion resistant sheet at least 1 mm thickness).
6. 5 Internal Temp Control :
a) System should have temperature control range
from +1 degree C to +8 degree C.
b) Temperature should resolution should be better
than 0.1 degree C.
c) Cooling down time of max of 150 min on half load.
7. External ambient temp should perform in ambient
temp up to +43 degree C.
8. Door system should lockable double glass for
better safety.
9. Safety system :
a) System should have large and clear digital displays
for the set / run parameters.
b) The system should have weekly chart recorder
temperature changes.
c) The system should have key operated set point for
the added security.
10. Alarms :
a) System should have audible / visual warnings for
over temperature under temperature and power failure
with visual status reports on critical functions.
b) System should have battery backup and
connections for remote alarm contacts.
11. Should have adjustment for uneven bases. The
adjustment should be easy to use like rotating a screw
at the legs in the base.
12. Scratch resistant internal lining of the cabinet
(stainless steel or aluminum).
2.
BB-02
Equipment Specifications for
Sterile Connecting Device
 The Sterile Connecting Device should be
compatible with all standard tubing for blood
bags.
 Compatible with all standard tubing for blood
bags.
 Compatible with all standard tubing for blood
bags.
 Should be possible to weld external diameter
3.9 to 4.5 mm and internal diameter of 2.9 to
3.1 mms.
 Sensor controlled temperature welding.
 To be operational on 220 to 240 V at 50 Hz.
 Sterile connecting Device - Qty 1
 The cost of Wafers may be ascertained during
tendering since it would be a proprietory item
and not possible to quantify requirement
initially.
 The unit shall be capable of operating
continuously in ambient temperature of 10-40
deg C and relative humidity of 15-90.
 The unit shall be capable of being store
continuously in ambient temperature of 0-50
deg C and relative humidity of 15-90.
 Shall
meet
IEC
-60601-1-2:
2001
(or
Equivalent BIS) General Requirements of
Safety for Electromagnetic Compatibility.
 Power Input - 270-MOV/50 Hz AC Single
phase or 380-400V AC 50 Hz three phases,
fitted with appropriate Indian plugs and
sockets.
 Resettable ovcrcurrent breaker shall be fitted
for protection.
 Voltage corrector / stabiliser of appropriate
ratings meeting ISI Specifications. (Input
160.260 V and output 220-240V at 50 Hz).
 Should be FDA, CE, LJL or BIS approved
product.
 Electrical safety conforms to standards for
electrical safety IEC-60601/IS-13450.
 Manufacturer should have ISO certification for
quality standards.
 User manual in English.
 Service manual in English.
 List of important spare parts and accessories
with their part numbers and cost.
 Certificate of calibration and inspection from
factory.
 Log book with instruction or daily, weekly,
monthly and quarterly maintenance checklist.
 The job description of the hospital technician
and company service engineer should be
clearly specified.
 List of equipment available for providing
calibration
and
routine
maintenance
documentation in service / technical manual.
3.
BB-03
ID-GEL MICRO TYPING
SYSTEM
 System should be based on US-FDA approved
gel particles.
 System should be based on 'no washing
antiglobulin test principle'.
 Company should have quality control reagent
like cross matching, grouping and antibody
screening.
 There should be provision to perform following
procedures:
o Grouping
o Cross Matching
o Do test using IC method
o Blood grouping including partial D detection.
o Rh confirmation
o Syphilis Antibody test.
o Single Antigen test cards and antisera like Rh
system
(C.e.F.e.e.C)
Kell,
Duffy,
Levis,
Lutheran MNS etc.
o Special Antigen test cards for DCT positive
patients that can detect IgG, IgM, IGa, C3d,
C3e etc.
o Special reagent for acid caution method.
 Add pack insert of all the products mentioned
in 3.4.
 There shall be special blood grouping card for
donors and patients to detect partial RhD i.e.
DVI
variant
to
reduce
risk
of
Allo
immunization.
 There shall be commercial red cell panel i.e. 2
and 3 cell panel for antibody screening and 11
cell panel for antibody identification. Further,
should have pooled 'O' cell with phenotype for
donor screening as per NACO guideline.
 Body should be non metallic and non corrosive
plastic to avoid corrosion and electrical shock.
 Should have computer based automated data
recording system with her code security.
 Centrifuge and incubator should have a
Plexiglas top for transparent viewing of
centrifugation
cycle
in
centrifugal
and
incubation cards inculcator.
 Centnfuge should provide 85g centrifugel force
during centrifugation.
4.
BB-04
ELISA READER WITH
Technical Specifications
PRINTER
1.1 ELISA reader complete with Printer is reacquired.
1.2 Should have 8-12 measuring channel & reference
channel.
1.3 Should have wave length range of 340-750 nm 6
filler 340, 405, 450, 492, 540, 620nm with provision
for filling any additional fillers.
1.4 Should have in absorption range of 0-4.000 A
1.5 Should have 4 resolution of 0.001 A
1.6 Should read with in 0-8 seconds.
1.7 The control panel should have soft colored touch
screen display, capable of showing graph etc.
1.8 Should have external & Internal programmable
time & speed shaking.
1.9 Should be able to read all types of platese.
1.10. Should have a single halogen lamp with save
features as light source.
1.11 Should have user defined programmes 30 or
more.
1.12 RS 232/USB output for printer, P'C connectivity
and Data acquisition should be there.
1.13 Should have data memory of 300 plates.
1.14 Should have external printer, capable of printing
complete results & graphs etc. from Elisa system.
1.15 Accessories , Spare and consumables :
1. Halogen 1 amps : 2
2. Thermal print paper : 10 Rolls / Fold
3. Dust Cover - 01
4. Set of pipettes consisting of single channel variable
volume color prpetter 0.5-10 ul, 40-200 ul, 200-1000
ul.
5. 8 channel variable volume color multi channel
pipettes 5-50 ul and 50-300 ul.
2. Environmental factors :
2.1 The unit shall be capable of being stored
continuously in ambient temperature of 0-50 deg C
and relative humidity of 15-90%.
2.2 The unit shall be capable of operating
continuously in ambient temperature or 10-40 deg C
and relative humidity of 15-90%.
3. Power Supply.
3.1 Power input to be 220-240VAC, 50 Hz fitted with
Indian plug.
3.2 Resettable over current breaker shall be fitted for
protection.
3.3 Voltage corrector / stabilizer of appropriate
ratings meeting ISI Specifications (Input 160-260 V
and output 220-240V and 50 Hz)
3.4 Suitable UPS with maintenance free batteries for
minimum one hour back up should be supplied with
the system.
4. Standards and Safety:
4.1 Comprehensive training for lab staff and support
services till familarity with the system.
4.2 Comprehensive warranty for 3 years.
4.3 Should he complaint to ISO 13485: Quality
systems - Medical devices - Particular requirements
for the application of ISO 9001.
Applicable to manufactures and service providers
their perform their own design activities.
4.4 Should be FDA/VCE/UL approved product.
5. Documentation :
5.1 User/ Technical /Maintenance manuals to be
supplied in English.
5.2 Certificate of calibration and inspection from
factory.
5.3 List of equipment available for providing
calibration and routine Preventive Maintenance
Support as per manufacturer documentation in service
/ technical manual.
5.4 List of important spare parts and accessories with
their part number and costing.
5.5 Log hook with instruction for daily, weekly,
monthly and quarterly maintenance checklist.
The job description of the hospital technician and
company service engineer should he clearly spelt out.
5.
BB-05
AUTOMATIC MICRO PLATE
2.1 Fully automate programmable micro plate
WASHE
washers with 8/12 manifold.
2.2 Then micro plate washer should offer the
possibility of flexible programming of the desired
washing procedures. It should have 1-4 liquid
channels.
2.3 It should be capable of storing up to 75 user
definer washing procedures.
2.4 The dispensing volume / well should be 50-3000
ul.
2.5 Plate soaking be programmable at any point of the
washing procedure.
2.6 Should have soak time of 1-999 sec.
2.7 Performance sequence should be either on whole
plate "Plated Mode" or strip by strip "Strip mode".
2.8 It should offer the possibility to present physical
parameters & well shape (round or Hal bottom) of the
user micro plate (upto 10) & store this information
under freely definable names.
2.9 Application aspiration should be performed at the
edge of the well altering from one side to the other or
in the centre when using round bottom plates.
2.10 Residual volume /well should be less than 2 ul.
2.11 The desired number of cycle as well as the
interval lime between the steps should be freely
definable.
2.12 Necessary sequence should be defined as a
combination of single steps, which are freely
adjustable be selling the corresponding parameter.
2.13 The result of the washing procedure may be
intensified by an optional wash cycle limited to the
bottom area (bottom wash)
2.14 Aspiration should prevent an overflow of the
well contents.
2.15 A variety of pre programing procedures should
over majority of standards application.
2.16. This should be able to be used as -COOMBS
WASHER with vertical and horizontal movements
performed with 0.1 mm steps.
3. System Configuration Accessories, Spares and
Consumables:
3.1 System as specified :
4. Environment factors :
4.1 The unit shall be capable of being stored
continuously in ambient temperature of 0-50 deg C
and relative humidity of 15-90%.
4.2 The unit shall be capable of operating
continuously in ambient temperature of 10-40 deg C
and relative humidity of 15-90%.
5. Power Supply :
5.1 Power input to be 220-240 VAC 5()1 Hz fitted
with Indian plug.
5.2 Resettable over current breaker shall be fitted for
protection.
5.3 Voltage corrector / stabilizer of appropriate
ratings meeting ISI Specifications (Input 160-260 V
and output 220-240 V and 50 Hz)
5.4 Suitable UPS with maintenance free batteries for
minimum one hour back up should be supplied with
the system.
6. Standard and Safety :
6.1 Should be FDA/CE/UL approved product.
6.2 Comprehensive warranty for 2 years.
6.3 Comprehensive training for lab staff support
services till familiarity with the system.
6.4 Electrical safety conforms to standards for
electrical safely IEC-60601 / IS-13450.
Documentation :
7.1 Certificate of calibration and inspection from
factory.
7.2 List of equipments available for providing
calibration and routine.
Preventive maintenance support as per manufacturer
documentation in service / technical manual.
7.3 User / Technical / Maintenance manual to be
supplied in English.
7.4 List of important spare parts and accessories with
their part number and costing.
6.
BB-06
Blood Cell Washing System
1. Technical Specifications
1.1 It should be made of stable Roburt. All Steel
Cabinet
1.1 Max. rpm: 3.000 or more.
1.3 Max. KCT: K gm or more
1.4 Max. Volume : 12 place stainless steel rotor for
12 mm X 75 min or 10 mm x 75 nun
1.5 Drive unit should be Three speed brushless
induction motor with sealed, Lubricated bearings.
1.6 Should have sensor touch control billions with
digital LED display.
1.7 Should have safety indication of disorders by self
diagnosis program.
1.8 Should display the number of wash cycles and
time selected Saline level Ltd latch and have alarm at
end of run.
1.9 Indication of digital selectable from 1 to 4 wash
cycles.
1.10 All consumables required for installation and
standardization of system to be given free of cost.
2. Environmental factors :
2.1 The unit shall be capable of being stored
continuously in ambient temperature of 0-50 deg C
and relative humidity of 15-90%.
2.2 The unit shall be capable of operating
continuously in ambient temperature of 10-40 deg C
and relative humidity of 15-90%.
3. Power supply :
3.1 Power input to be 220-240 VAC, 50 Hz fitted
with Indian plug.
3.2 Resettable over current breaker shall be fitted for
protection.
3.3 Voltage corrector / stabilizer of appropriate
ratings meeting ISI specifications (Input 160-240 V
and Output 220-240V and 50 Hz).
3.4 Suitable UPS with maintenance free batteries for
minimum one hour back up should he supplied with
the system.
4. Standard and Safety :
4.1 The automated cell cashing system should ensure
precise cell washing in compliance with AABB
guidelines.
4.2 Should be FDA/VCE/UL approved product.
4.3 Electrical safety conforms to standards for
electrical safely IEC-60601/IS-13450.
4.4 Comprehensive warranty for 3 years.
4.5 Manufacture / Supplier should have ISO
certification for quality standards.
4.6 Comprehensive training for lab staff and support
services till familiarity with the system.
5 Documentation :
5.1 Certificate of calibration and inspection from
factory.
5.2 List of equipment available for providing
calibration and routine preventive maintenance
support as per manutaeliror documentation in service
/ Technical manual.
5.3 User / Technical / Maintenance manual to be
supplied in English.
5.4 List of important spare parts and accessories with
their part number and costing.
5.5 Log hook with instruction for daily, weekly,
monthly and quarterly maintenance checklist.
The job description of the hospital technician and
company service engineer should he clearly spelt out.
7.
BB-07
Sealer, Stripper and Cutter for
 For sealing and cutting the blood bag tubings.
Blood bag tubing
 Each sealer, stripper and cutter should be
supplied with 50000.
8.
9.
BB-08
BB-09
VDRL Shaker
Platform size 300x300 mm spring holder which can
(Rotator)
accommodate concave slider etc.
Coagulometer,
1. 16 incubation positions for sample (4 cells x 4
Semi Automated
columns).
2. 2 measurement channels
3. 2-4 positions for reagents (one with magnetic
stirrer) and 2 pipette.
4. Four independent built in timers for incubation
5. Measurement possible in plasma.
6. Automatic pipette (Electronically connected or
manual start up)
7. Backlight LCD display, 4 lines of 40 characters
with built in printer
8. Results in seconds and in various units (INR, Ratio,
Gm/L mg/ds, IC/ml)
9. Rs 232 interface.
10. Incubation and measurement wells at 370C +/0.50C
11. Tests : PT, PTT, TT, FIB (Claus and PT derived),
Factor II, V, VII, VIII, IX, X, XI, XII Flctcher, VT
(Venom time), APCR, AT III (clot)
Protein C (clot), Protein S (clot), Heparin, STAT
(PT/PTT).
10
BB-10
Water Bath
1. Small (app dimensions 40-45 x 35-10 x 20-25 cms)
light stainless steel body.
2. Micro processor controlled programmable digital
display for temperature etc.
3. Temp. Range 370C to 560C + 0.50C
4. Should have a stirrer for circulation.
5. Bath capacity 8-10 liters.
11
BB-11
Digital Analytical Balance
 Capacity : 200 grams.
(Single Pan)
 Readability : 0.01 grams.
 Linearly : Plus Mnus 0.002 grams
 Reproducibility : Plus Minus 0.001 grams
 Dimension : To be declared
 Stainless steel path
 Percentage weighing counting tar (0-200
grams) auto calibration with built in masses.
 220/240 volts, 59 cycles, single phase.
 The balance should be supplied with graft
shield. The equipment should be suitable for 0
to 400C at 95% ambient condition.
 Complete technical specification, illustrative
technical literature / leaflet shall be enclosed
along with the offer indicating the model
quoted.
 Complete and satisfactory type test certificate
as per T/E specification shall be submitted at
the time of final inspection.
12.
BB-12
Refrigerated Water Bath
(Cryobath)
 Features : Should include timer of 2 hours
fixed and variable temperature control, over
temperature safety limit with audio visual
alarm, power switch and digital temperature
display, number of digit and resolution shall be
included in the offer.
 Capacity : 65 liters.
 Storage capacity : Holds upto minimum 5
stainless steel racks.
 Overall interior dimensions : Should be
indicated by the bidder.
 Operating
temperature
:
+40C
control
sensitivity plus minus 0.20C.
 Uniformity
plus
minus
0.20C
ambient
temperature may be as high as 4500C.
 The equipment should be able to thaw 15
plasma units in about 90 minutes. The
equipments hold have:
(a) Stainless steel filter screen for protecting pump in
the take from debris such as levels etc.
(b) Stainless steel tank of 22 gauge designed with
curved corners for easy cleaning.
c) Stainless steel lid at least 20 gauge.
d) Out side mild steel sheet of 18 gauge.
 The following accessories should be pat of
configuration.
(i) Compression rack holder.
(ii) Frozen plasma rack holder.
(iii) Thermometer for visual verification of water
temperature.
 A suitable battery charger shall also be
supplied so that charging batteries continue
when the equipment on main.
 Equipment shall be supplied in suitable case.
13.
Di-Electric tube sealer
 It should be less than 3 kgs with carry bag.
 The sealing should be 750 per hour / 1500
sealing per charged battery.
 Rechargeable batteries with a back
up of
minimum 6 hours.
 Automatic detection of the tube by pressing of
a lever which activates sensor.
 Minimum sealing time ( <2sec).
 Detection of wet tube, leakage and sealing
detect. Alarm in case of sealed not safe and
completed.
 Compatible
with
the
tubes
of
various
manufactures of blood bag.
 Should seals 3.0 to 5 mm tubes with wall
thickness of 0.75 mm.
 Protection against electric shock.
NAME OF DEPARTMENT : PSM
S.No.
1.
Item Code
PSM-01
Name of Equipment
Extraction apparatus fat complete
Specification
Fat extractor operates on 115 volts. 50/60 Hz
(Max) at 5.2 amps. It is shipped complete with
power cord and grounded 3 wire plug. Standard
features are as follows:
1. Main power on -off non spark mercury switch.
2. Full range variable heat control switch. Each
switch controls two heats.
3. All stainless steel type 301 condenser
assembly.
4. Pressure relief values for each condenser.
2.
PSM-02
Filter paste chamber land complete set -
3.
PSM-03
Filter burke felt
SS-4 stainless produces 24 galloons per day.
4.
PSM-04
Hydro meter spirit
5 Let swing top seal.
5.
PSM-05
Hydrometer milks
6.
PSM-06
Hydrometers wet & dry Bulb 1
Hyudro
Range g/
meters 1
ml
designation
No. 1
1.025 to
1.035
No. 2
.035
No. 1A
1.015 to
1.025
-
Sub
division
Length
(mm)
0.002
240
0.0005
0.002
215
240
7.
PSM-07
Balance analytical 200 gm
200 gm
8.
PSM-08
Balance for weighing food
Capacity 2 kg
9.
PSM-09
Baby weighing
-
10.
PSM-10
Herpenders calipers with for skin fold
-
thickness
11.
PSM-11
Height measuring stand
-
12.
PSM-12
Refrigerator 9 cu ft.
9 cu ft
1
13.
PSM-13
Ice lined refrigerator (ILR)
140 ltr.
14.
PSM-14
Dissecting microscope
-
15
PSM-15
Microscope 0-1 immersion
HB Laboratory Microscope
Magnification - 100 x 1000
NAME OF DEPARTMENT : PEDIATRIC SURGERY
S.No.
Item Code
1.
PS-01
Name of Equipment
Pediatric Fibreoptic Sigmoid scope
Specification
Paediatric
sigmoidoscope
(colonoscope)
is
with working snare biopsy forceps etc. needed as per MCl norm. This equipment is
needed for diagnostic and therapeutic use for
lower gastrointestinal bleeding in children.
2.
PS-02
Ceiling Operation Theatre Light
Shadow less ceiling OT lights are needed for up
gradation of operation theatre in Paed Surgery.
This shadow less OT light include, Double,
Dome 50-55 cm diameter with four reflectors,
halogen bulb etc.
3.
PS-03
SPO2 Monitors
This is needed for monitoring of vital during
surgery and in post operative periods in children.
4.
PS-04
Pediatric CO2 insufflators with
Pediatric CO2 insufflators is needed for use
accessories for laparoscopy
during laparoscopic procedures in children. This
equipment must include automatic pressure &
flow control high degree of safety control
functional and user friendly gas worming,
multiple display etc.
5.
PS-05
Operation Tables
Must be made from acid proof, stainless steel
easy to clean and immune to disinfection agents.
Needed for pediatric surgery operation theatre.
6.
7.
PS-06
PS-07
Anesthesia work station (Anesthesia
Needed for up gradation of the pediatric surgery
machine)
operation theatre.
Syringe infusion pumps
This is needed for I/V fluids and drugs
administration for neonates.
8.
PS-08
Standard infusion pumps
This is needed for I/V fluids and drugs
administration for children.
9.
PS-09
Miscellaneous Operating Instruments
Needed for routing use in pediatric surgery OT.
(forceps, scissors etc.)
All operating instruments must be of standard
company.
10.
PS-10
Radiant warmers
Needed for pediatric surgery NICU and for use
din infants.
11.
PS-11
CO2 cylinders for laparoscopy
CO2 is needed during laparoscopic procedures.
NAME OF DEPARTMENT : PSYCHIATRY
S.No.
Item Code
1.
PSY-01
Name of Equipment
Alcohol Breath Analyser
Specification
Alcohol breath analyser should be a digital
detector which is accurate and easy to use.
Space for Operation :
Available
Necessary Technical staff:
Test will be done by Psychiatrist
Breathlayer specifications :
Should display the breadth alcohol concentration
as a 3 digit read out in mg/l and easy to use.
Indication of BrA/c 0.00 to 2.00 mg/litre %
BrAC
Warm up time below 20 seconds.
Response time within 3 seconds.
Auto adjust / rest with rest button
Automatic switch off after 30 sec.
Recycle time 10 seconds.
Mouth piece 5 x washable mouth piece
Sensor semi conductor oxide sensor
Continuous using time
Without battery
Over 200 test
Replacement
Power supply - DC
Dimensions (mm) should be compact.
2.
PSY-02
Biofeedback machine
Space for operation
Cabin beside the HOD chambers.
Necessary technical staff
Machine will be operated by psychologist and
psychiatrists
Specifications:
Biofeedback apparatus should be able to record
following parameters:
Pulse
GSR
Temperature
EEG
EMG
Parameters relax - 1 relax II
Biofeedback instruments should be compact i
size and through its ergonomically designed
front panel facilitates ease of operation. Each
biofeedback
instrument
physiological
changes
converts
(GSR,
Oulse
patient
rate,
temperature, EEG & EMG) into audio as well as
visual signals which helps the patient performs
self control or autogenic training leading to
relaxation.
Relax-1
GSR
Input : Through two silver - chloride electrodes,
one connected to the sweat glands and the other
to any inactivate point forming the reference.
GSR balance range : 0 to 1999 K Ohms
Display : Visual LED bar in 21 steps (Green 10
steps, yellow 1 step, Red 10 steps) each steps
changed by deviation of 10%, 5% or 1% (switch
selectable) from the mean GSR value.
Actual change in GSR value in K ohms is also
displayed on a digital panel meter.
TEMPERATURE
Input : Through a surface temperature probe.
Temperature balance range : 200C to 400C.
3.
PSY-03
EEG Machine
Space for Operation
Cabin beside the HOD chambers.
Necessary technical staff:
The post of EEG technician to be created and
technician to be appointed. However, machine
can be installed in the department and the
technician services can be outsourced.
Specification :
 Windows based 32 channel digital EEG
with Pentium PC and inkjet Printer
features are:
o Featuring with Brain Mapping
User definable montages
Scrolling facility, test review, filter selection,
network enabled.
 32 channel acquisition comprising at 24
EEG and at least 5 bipolar channels also
unable as EEG and 03 DC/Transducer
channels.
 Raw data storage for reformatting of
sweep, speed, filters and montages during
analysis.
 Choice of multiple reference to brain
mapping i.e. Car A1, A2 unked ear, C2.
 Facility to view analysis and acquisition of
same time.
 High performance machine is capable of
taking record in ICU condition.
 Unlimited continuous storage depends
upon hard disk capacity.
 Facility to archieve data on CD
 Facility to measure amplitude and time
duration.
 Unlimited montage formation can be
possible.
 Facility for auto searching of events and
comments.
 Facility to mark and delete events in
analysis.
 User definable events with user definable
hot keys.
 Facility of reporting in MS word (MS
office software optional).
 Facility to store pre define comments with
user definable hot keys.
 Different modes of going to any part of
EEG i.e.
a) Page forward and backward
b) Auto FWD & BWD
c) Event to event jump
d) Search bar
 User editable photic sets with frequencies
ranging from 1 to 30 Hz.
 Optical
isolation
of
head
box
to
electrically isolate patient from data
system can be provide.
 Compatible with windows 98 and window
millennium.
 Fully compatible with celero pentium P-
III, Pentium IV and Hardware.
 CSA/DSA facility should be provided.
 User has facility to make its own LF & HF
filter.
 A/D conversion 14 bit in hardware.
 Sampling rate 1024 Hz/Channel with
resolution enhancement to 16 digital
signal processing.
 Storage rate 256 Hz. Channel with
resolution enhancement to 16 bits by
signal processing.
 Noise level < 1 u Mohm (0.1 to 1000 Hz)
 Input independence > 10 M Ohm (0) to
100 Hz
 Acquisition method raw data with full
sensitivity and full bandwidth.
 Sensitivity / LF/HF/Notch / Muscle Rej /.
Montage implemented in a only for
display / printouts.
 Sensitivity 1 to 1000 uv / mm
 Lf (Hz) 0.1, 0.3, 0.5, 1.0, 3.0, 5.0 Hz and
other user definable (0 to 7 Hz) pole.
 Muscle Rej. ON/00, 30 Hz double pole.
 Hardware : Head box, photic stimulator
with adjustable stand.
 Accessories : Re-usable patients leads,
EEG, Jelly, PC cable etc.
4.
PSY-04
ECT Machine
Space for operation
1. Room beside the medicine seminar hall with
allotted by superintendent Hamidia Hospital.
However it has not been handed over to
department of psychiatry because in this room
tea canteen is running.
Necessary technical staff:
ECT Machine will be operated by psychiatrists.
Specifications:
Constant current brief ECT machine with EEG
and ECG recorder full microcomputer based.
Other ECT specification:
Three modes of operation provides wide choice:
- Mode 1:
Brief pulse PLS (frequency, pulse width duration
current selectable energy J calculated by micro
computers).
Mode 2 :
Brief PLS 2 (Current, energy, selectable
frequency pulse width.
Duration calculated by the micro computer)
Mode 3 :
Sine wave gives a controlled current sine wave.
Current :
Constant current ECT. The current is continuous
adjustable from 500 mA to 800 mA in steps mA.
Frequency range:
30 to 90 Hz in 7 steps of 10 Hz each.
Pulse width :
Selectable from 0.8 mS to 2 mS in 7 steps of mS
each.
Duration :
Selectable from 0.5 mS to 2 mS in 7 steps of mS
each.
 The energy that would be delivered to a
standard impedance of 200 ohm by the
selected
parameter
set
is
calculated
dynamically.
 The actual energy delivered is displayed
on screen according to the actual have
impedance.
 The patient head impedance continuously
measured dynamically during treatment of
the on set of every pulse.
 At any time if the head impedance is
outside the permissible limit the shock
prematurely terminated and display show
ERR.
 Provision for automatic stop of the
operation in case of any deviation from the
present limit or malfunctioning of any
part.
 Isolation provided to separates both the
operator and the patient from the mal
supply. Any accidental mishandling of the
electrodes can not result in unwarranted
mains supply sock under any condition.
 All the function keys are sequentially
locked with the Reset key. the key needs
to be depressed prior to depressing a
function key.
Recorder selection:
 Chat speed - 10 mm and 25 mm /sec.
 Paper width : 105 mm.
 Recording system : ink writer
 Recording pen - Metallic light weight
recording pen with 120 length.
Marker - Gives continuous mark as 1 Sec.
intervals.
EEG Section :
 Sensitivity - Selectable from 20, 100, 200,
500 uv per chan.
 Frequency response : 2-60 Hz with 50 line
filter.
 CMRR : > 80 db.
 Calibration voltage : 50 uv.
ECG section :
 Sensitivity - Selectable from 0.5, 1 & 2
mv/cm.
 Calibration voltage 1 mv.
 Frequency response : 2-60 Hz with 50 Hz
line filter.
CMRR : > 80 db
5.
PSY-05
Lithium analyser
Lithium analyser can be use to measure serum
lithium.
Cabin beside the HOD chambers.
Necessary technical staff:
Machine will be operate by psychiatrists.
Specification :
01. Compact design
02. High performance and accuracy
03. Easy operation
04. Direct printer connectivity.
6.
PSY-06
Psychometric tools
Space for operation :
Available
Necessary technical staff:
The post of clical psychologist will be created
and to be filled. At present psychometric tests are
done by Rahul Sharma (Clinical Psychologist)
who is appointed under District Mental Health
program, Sehore.
Following psychological tests are required:
A. Personality Test:
01. Rorschach test with manual (Exiner's system)
02. 16PF Test : Farm A, B, C and D with
manual.
B. Intelligence Tests:
01. Wechsler Adult intelligence scale - R (Indian
Adaptation) with manual.
02. Wechsler children intelligence scale-R
(Indian adaptation) with manual.
03. Raven's progressive color matrices with
manual.
04. Segulin from board with manual.
C. Cognitive Test:
01.
AIIMS
Battery
assessment with manual.
of
Neuro
cognitive
NAME OF DEPARTMENT : BURN AND PLASTIC SURGERY
S.No.
1.
Item Code
Name of Equipment / Instrument
Specification
Electic Dermatome (S/S Stainlesst
1. The Dermatome should be able to out grafts or
steel, Tunguston Coated Rust
various widths. Should be provided with
Resistant)
variable Gparts to adjust the width of the graft to
2". 2" or 4" should not need any earner to lift the
graft from the donor (slite. The cut graft should
automatically fold into the pock jet of the
dermatome. The graft should be served by
simplify lifting of the dematome up & away
from the donor site without a carrier. The
thickness of the graft should be adjusted with a
pointer on the scale. The thickness of the graft
should be adjustable to thousands of an inph.
The Dermatome unit should be supplied
complete with motor unit i the handle set of
guard, calibration guide, power plug cord, screw
driver and should be supplied complete with a
carrying case for proper maintenance J and 20
blades.
2.
Skin Graft Mesher (S/S-Stainlesst
Mesher should have a full range of meshing
steel, Tunguston Coated Rust
ratios with adjustable meshing drum allowing
Resistant)
meshing ratios from 1:1 to 4:1.
Should be able to use any sterile smooth plastic
plate of 0.5 mm thickness as skin graft corner.
Variable mesher should be able to operate both
as powered or manual mesher.
Should be simple & ergonomic design should be
provided with
1. Sterilizing container
2. Skin graft carrier
3. Power pack including motor gear, batteries
4. Ratchet
5. Skin graft mesher
6. Mesher sheet
3.
Skin Grafting Handle (S/S Stainlesst
1. Skin graft handle humbys
Steel, Tunguston Coated Rust
2. Silver knife handle (Razor blade handle)
resistant)
3. Skin graft handle box autoclavable
4. Skin graft board (graft spreader)
4.
Pneumatic Tourniquet
The tourniquet should be automatic one wit
instant increase in pressure auto regulator to
control pressure in the cuff, automatic time
setting with auto alarm.
Should have battery back up system
automatically engaged in AC current is
interrupted should have computerized memory.
Should have micro processor monitors and gives
alarm both by audible and visual indicators.
Should have alarm for low pressure low battery,
leaks, kinks elapse time and start up checks.
Should be able to operate either as single or
double cuff functions.
Should be provided with autoclavable tourniquet
cuffs with silicone bladder single and double for
baby child and audit for ami and thigh.
Singled cuff set of 5 set of 3
Singled cuff set of 5 set of 2
5.
Microprocessor controlled power
Microprocessor controlled power driver system
driver systems
should provide complete functions of bone
(S/S stainlesst steel, Tunguston coated
harvesting drilling & fixation of small bone and
Rust resistant)
helps in osteosynthesis.
Should have computerised control with touch
screen facility having options of digital display
of spjeed & to preselect acceleration and
beraking of handpiece speed.
Should be provided with cable & footswitch &
should be provided with complete set of
following accessories.
Universal drill multiple handpiece 1:5 speed upto
30000 rpm.
Micro Saggital saw with blades with speed of
20000 cycles/min.
Micro Oscillating saw with blades with speed of
15000 rpm.
Micro reciprocating saw with blades with speed
of 20000.
Basic plastic surgery instrument set
The instruments should be of improved steel
(S/S Stainlesst steel, tungustom coated
with high precision quality with CE, TUV or
rust resistant)
ISO 9002 certification.
1. The fine cutting instruments should be of
Tungsten carbide - Supercut variety.
The needle holders should be with Tungsten
Carbide inserts for extra durability.
1. Converse skin hook small.
1. Converse skin hook large.
1. Mathieu retractor (Cat's Paw)
1. Hajek's retractor
1. Langenbeck's retractor signal 1.
1. Langenbeck's retractor large.
1. Weislander retractor (self retaining)
1. Dental Syringe
1. Stainless steel scale 6"
1. Stainless steel scale 12"
1. Castroviejo calipers
1.Bristovv Bone Laver
1. Smith Peterson Osteotome 1 Omm
1 Smith Peterson Osteotome 20 Omm
1. Smith Peterson Osteotome 25 Omm
1. Tessier Osteotome set of 8.
1. Gouge 7"2mm
1. Gouge 7"4mm
1 French Chisel 11mm
1 Halsted Mosquito artery forceps 5 3/4" Cvd
1 Halsted Mosquito artery forceps 5 3/4" St.
1 Kocher Forceps
1 Kely Artery forceps st.
1 Kelly Artery forceps cvd
1 Dandy Tissue forceps
1 Mcindoe dissecting forceps 6" non toothed
serrated jaws.
1 Potts Smith Dressing forceps 7"
1 Adson Tissue forceps 4 3/4" toothed delicate
1 Adson Tissue forceps serrated jaws 43/4"
1 Gillis Dissecting forceps 6" toothed.
1 Allies Tissue forceps 6" 4x5" teeth.
1 Elevator double ended, spoon shaped, Molt
Dissector
1 Howarth Elevator
1 Scissor angle short blades 18 mm width
serrated bleades
1 Kliner scissors straight with fine points.
1 Kliner scissors curved on flat 12 cm
1 Mcindoe scissors cvd. On flat with round
points 7"
1 Iris Scissors straight sharp Tc supercut.
1 Surgical scissors 5" st. sharp points TC
1 Mayo Hegar needle holder 614"
1 Derf needle holder 4 3/4"
1 Maltz Rasp Tc
1 Mcindoe rasp TC
1 Mallet 8 Oz
1 Asch forceps
1 Ruskin Bone cutting forceps
1 Luc's forceps
1 Padgett St bone cutting forceps
1 Padgett angled bone cutting forceps
1 Bunnel Bone drill small
1 Knuckle Bender Large
1 Knuckle bender Medium
1 Knuckle bender Small
1 Mcindoes Raspatory
1 Bard Parker Knife Handle No. 3
1 Bard Parker Knife Handle No. 4
1 Bard Parker long knife handle No. 3
Barron Knief Handle Octagonal
Backhaus Towel clips 3 /2
Sponge holding tube 9 A"
Frazier suction tube 8 French
Frazier suction tube 10 French
Magilli's suction tube size 2
Meade wire cutter pilers
Dressing Trolley
Cleft Palate Instruments
Dingman Mouth GAG - Adult
(S/S - Stainlesst Steel, Tunguston
Dingman Mouth GAG - Paediatric
Coated Rust Resistant)
Dingman Mouth GAG - Advanced Millart
Model
Dingman Mouth GAG - With Fibre optic
connection for the blades
Cleft Palat Elevators Short Straight
Cleft Palat Elevators Short Left
Cleft Palat Elevators Short Right
1 Cleft Palate Elevators CD Left
1 Cleft Palate Elevators CD Right
1 Downs Cleft Palate Elevators Left
1 Downs Cleft Palate Elevators Right
1 Downs Cleft Palate Elevators Straight
1 Howarth Dissector / Elevator 5mm
1 Howarth Dissector / Elevator 3mm
1 Septal Elevator
1 Kilner skin hook
1 Flat Skin Hook
1 Cleft Palate Hook Single
1 Cleft Palate Hook Double
1 Long Tonsil Artery Forceps Straight
1 Long Tonsil Artery Forceps Curved
1 Long toothed Waugh forceps
1 Long non toothed Waugh Forceps
1 Adsons Forceps 4 3/4"
1 Adsons Toothed forceps 4 3/4"
1 Senn Double End retractor plain
1 Senn Double End retractor claw type
1 Hajek Cheek Retractor
1 Disposable Cheek Retractor Paediatric
1 Disposable Cheek Retractor Adult
1 Cats Paw Pair
1 IRIS scissor straight sharp 4'/2"
1 IRIS Scissor curved sharp 4'/4"
1 Tenetomy Scissor curved
1 Cleft Palate Scissors
1 Dental Sealers Set
1 Dental Sealer Double Ended : Types
Dental Curette 6"
1 Mithchells Trimmer
Ruler
Calipers
Long Needle Holder
1 Knot Tier / Pusher - Negus 1
1 Mouth Prop.
Boxes, Containers
Stainless steel Box for Max kit with two trays.
(S/S-Stainlesst Steel, Tunguston
Stainless steel box for Bone plates & screw.
Coated Rust resistant)
Stainless steel box for Bone Plate & Screw Small
for 1.5 or 2 or 2.5 mm Stailess Steel Box for
General Instruments small medium big. Box
with 12 containers for screw & plates.
Drill Bits container
K write container
Mini screw container
Mini plate container
General instrument box with Sijicone Mate
1. Round skin hook gillies & medium
2. Flat Skin hook
3. Flat skin hook long
4 Double skin hook sharp small
5 Double skin hook sharp wide
6. Double hook blunt
7. Killans septal elevator
8. Freer elevator
9. Joseph Skin elevator
10. Cottle elevator
11. Pierce elevator
12. Masing - graduate elevator
13. Farabeuf elevator straight
14. Farabeuf elevator curved
15. Killians septal elevator with suction
16. Aufricht retractor wide /narrow
17. Aufricht waiter retractor
18. Kliner ala retractor
19. Senn double and retractor - claw type
20. Senn double end retractor
21. Senn Miller retractor
22. Cottle columella clamp
23 MM chisel
24. 3/4 MM Chisel
25. 7MM Chisel
26. Single guarded chisel
27. Silver chisel left
28. Silver chisel right
29. Double guarded chisel 7/8/14/16MM
30. Me Indoes nasal chisel 13/15 MM
31. Silver cartilage chisel cd lt/rt
32. Converse osteotome 1 mm / 2mm
33. Nasal saw straight
34. Nasal saw left
35. Nasal saw right
36. Ballengers swivel knife
37. Ballengers swivel knife dbayonet shaped
38. Joseph button end knife
39. V cut Gouge
40. Blunt gouge
41. Bayonet gouge
42. Cross Serrated Rasp
43. Forward cutting rasp
44. Backward cutting rasp
45. Double action rasp
46. Glabellar Rasp
47. Maltz Rasp double ended
48. Diamond Rasp Small
49. Diamond Rasp medium
50. Mallet Nylon head
51. Mallet Ordinary
52. Cartilage crusher
53. Septal lower Lateral Morselizer
54. Suction Tio No. 7/9/12
55. Ruler
56. Calipers
57. Killains Nasal Sdpeculam
58. Thudichums Nasal Spectulam
59. Trocar & Cannula
60. Flat Knife Handle No. 3
61. Nasal Splint Pack of 10
62. Nasal Splint with forehead extension Pack of
100
63. Webster Needle holder
64. 5" Needle holder
65. Gilldies Needle Holder
66. TC Needle holder
67. Adsons Forceps non Toothed
68. Adsoons forceps Toothed
69. Adsons Forcept Cross Serrated
70. Bayonet forceps
71. Tilleys Dressing forceps
72. Lues forceps set of 3
73. Septum Punch forceps
74. Asch forceps
75. Walsharm forceps
76. Baby Waishram forceps
77. Nasal Septal Forceps Straight & Angled
78. Baby Mosquito forceps straight
79. Baby Mosquito forceps curved
80. Tenetomy Scissors Straight
81. Tenetomy Scissors curved
82. Kliner scissors straight
83. Kliner scissors curved
84. Iris Scissor curved
85. Foraon Angular Scissors
86. Aufricht Scissors
87. Cartilage Scissors
Infusion Pump
Infusion Pump
(S/S- Stainlesst Steel, Tunguston
Medical pump (4169) Dispenser DP 20 For
Coated Rust resistant)
Tumescense Local Anesthesia
For Lipio Suction Surgery of 0-20
LT/H with On-OFF Pdeal OT suitable with
forward mode, tubing set.
Nouvag Swiss Make
Radio frequency machine
With Monopolar and bipolar resurfacig and other
(S/S Stainlesst steel, Tunguston coated
accessory probes and models.
Rust resistant)
Dermabrasion instrument
1 Korean Micro motor with detachable NSK
(S/S-Stainlesst Steel, Tunguston
hand piece.
Coated Rust resistant)
2. Keren micro Motor with detachable NSK hand
piece.
Diamond Burrs (Round Wheels)
3. 15x1 Omm
4. 14x1 Omm
5. 11xSmm
Cylindrical
6. 6x11mm
7. 7x11mm
8. 12x14mm
Horizontal Laminar flow
Size : 4' x 2' x 2' size of Hepa filter 4 x 2' x 6'
- Stainless steel top, transparent front door (5mm
size)
- Unit fitted with prefilter & one 2 x 40 W HEPA
filter (0.03 Micron size)
- Fluorscent illumination
- Built in germicidal UV light.
- Cock for gas
- Height of working table should be comfortable
in sit down.
- Working position for the operator.
- Recessed knee space.
Electrophoresis complete set
Mini plus horizontal gel unit with removable
casting tray and 2 x 1 mm thick, 16-sample
combs and coloured loading strips.
Technical specification
Unit dimensions (WxLxH) - 16.5 x 23 x 6.5 cm
Gel Dimension (W X L) 10 x 11.5 cm
Buffer volume - 450 ml
Maximum sample capacity - 80
Combs -2
Comb thickness - 1, 1.5, or 2 mm
Comb throughput - 4 to 20 samples
Comb slots - 4
Migration Distance between comb slots - 2.5
Recommended Running voltage - 75 to 125v
Power output connectors (diameter) - Shrouded,
4 mm.
Dean
Gandhi Medical College
Bhopal
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