Navi Mumbai Municipal Corporation - the e

Navi Mumbai Municipal Corporation - the e
Navi Mumbai Municipal Corporation
Health Dept, NMMC Bhavan,sec-15A,CBD, Belapur, Navi Mumbai
Retender no.2 for supply of Equipments (Group-I) for NMMC hospitals
Tender Notice No: NMMC/Health/ 57 /2017
Price of Blank Tender form
:- Rs 12,000/-(Non Refundable)
Sale of Tender
:- 6.7.2017 at11.00 a.m. to 25.7.2017 up to 14.00 p.m.
Online bid preparation
:- 6.7.2017 at11.00 a.m. to 25.7.2017 up to 14.00 p.m.
Pre-bid meeting
:- 13.7.2017 at 11.00 a.m.
Submission of tender (Bid Transfer) :- 25.7.2017 at 18.00 p.m. to 28.7.2017 up to 18.00 p.m.
Opening of tender
•
:- 29.7.2017 at 11.30 a.m.(If possible)
(This Tender Document contains 1 to 61 pages.)
Medical Officer of Health
Navi Mumbai Municipal Corporation.
Page 1 of 61
−Ö¾Öß ´ÖãÓ²Ö‡Ô
´ÖÆüÖ−֐ָü¯ÖÖ׻֍úÖ
Navi Mumbai
Municipal
Corporation
3 ¸üÖ ´Ö•Ö»ÖÖ,†Ö¸üÖê µÖ ×¾Ö³Ö֐Ö,
‹−Ö‹´Ö‹´ÖÃÖß ³Ö¾Ö−Ö, ÃÖê-15‹ê,
ÃÖß.²Öß.›üß.,−Ö¾Öß ´ÖãÓ²Ö‡Ô 400 614.
¤æü¸ü¬¾Ö−Öß Îú : 27567261,
27567382
3rd FLOOR,HEALTH DEPT., NMMC
BHAVAN, SEC-15A, CBD BELAPUR,
NAVI MUMBAI – 400 614.
TEL. No. : 27567261,
27567382
×−Ö×¾Ö¤üÖ ÃÖã“Ö−ÖÖ Îú´ÖÖӍú - −Ö´ÖãÓ´Ö¯ÖÖ/†Ö¸üÖꐵÖ/57 /2017.
−Ö¾Öß ´ÖãÓ²Ö‡Ô ´ÖÆüÖ−֐ָü¯ÖÖ׻֍úÖ †ÓŸÖÖÔŸÖ ¹ýÖÖ»ÖµÖß−Ö ˆ¯Öú¸üÖêü (ÖÏã¯Ö-1) ¯Öã¸ü¾ÖšüÖ ú¸üüµÖÖÃÖÖšüß, ˆŸ¯ÖÖ¤üú /
†×¬ÖéúŸÖ û‹•Ö−ÃÖß•Ö, µÖÖÓ“Öêú›æü−Ö ´ÖÖêÆüÖê¸ü²ÖÓÓ¤ü ï֬ÖÖÔŸ´Öú ±êú¸üü×−Ö×¾Ö¤üÖ Îú.2 ´Ö֐Ö׾֝µÖÖŸÖ µÖêŸÖ †ÖÆêü.
−Ö¾Öß ´ÖÓ²Ö‡Ô ´ÖÆüÖ−֐ָü¯ÖÖ׻֍úêŸÖ ÃÖ¾ÖÔ ×¾Ö³Ö֐ÖÖŸÖᯙ ×−Ö×¾Ö¤üÖ ¯ÖÏ׍ÎúµÖÖ Next Tendering Sify
Technologies ‡Ô-™ëü›üظüÖ ÃÖӐ֝֍ú ¯ÖϝÖÖ»Öß (E-tendering) ´Ö¬Öæ−Ö“Ö ú¸üÖê †ÃÖæ−Ö ×−Ö×¾Ö¤üÖ¬ÖÖ¸üúÖÓ−Öß
https://maharashtra.etenders.in µÖÖ ÃÖӍêúŸÖãÖôûÖ¾Ö¸ü −ÖÖë¤üÖß ú¸üÖê †Ö¾Ö¿µÖú †ÖÆêü. ¹ý.3.00 »ÖÖ ؍ú¾ÖÖ
ŸµÖÖ¯ÖêÖÖ †×¬Öú ¸üŒú´Öê“Öê úÖ´ÖÖӍú¸üߟÖÖ ÃÖ¾ÖÔ Óú¡ÖÖ™ü¤üÖ¸ü/¯Öã¸ü¾ÖšüÖ¤üÖ¸ü µÖÖÓ−ÖÖ ‡Ô-™ëü›üظüÖ ÃÖӐ֝֍ú ¯ÖϝÖÖ»Öß (Etendering) ´Ö¬Öæ−Ö“Ö ×−Ö×¾Ö¤üÖ Ö¸êü¤üß ú¸üÖ¾ÖµÖÖ“µÖÖ †ÖÆêüŸÖ.
úÖ´ÖÖ“ÖÖ ÃÖÓׁ֯ŸÖ ŸÖ¯Ö¿Öᯙ ÖÖ»Ö߻֯ÖÏ´Ö֝Öê †ÖÆêü.
†.
úÖ´ÖÖ“Öê −ÖÖ¾Ö
‡ÃÖÖ¸üÖ ¸üŒú´Ö ×−Ö×¾Ö¤üÖ ¯ÖãÛß֍êú“Öß
Îú.
(¹ý.)
؍ú´ÖŸÖ (¹ý.)
1 −Ö¾Öß ´ÖãÓ²Ö‡Ô ´ÖÆüÖ−֐ָü¯ÖÖ׻֍úÖ †ÓŸÖÖÔŸÖ ¹ýÖÖ»ÖµÖß−Ö ˆ¯Öú¸üÖê
1,50,000/12,000/(ÖÏã¯Ö-1) ¯Öã¸ü¾ÖšüÖ ú¸üÖê²ÖÖ²ÖŸÖ
×−Ö×¾Ö¤üÖ ×¤ü−ÖÖӍú 6/7/2017 ¸üÖê•Öß Ã֍úÖôûß 11.00 ¾ÖÖ•Öê¯ÖÖÃÖæ−Ö ŸÖê פü−ÖÓ֍ú 25/7/2017 ¸üÖê•Öß
¤ãü.2.00¾ÖÖ•Öê¯ÖµÖÔÓŸÖ ‡Ô-™ëü›üظüÖ(E-tendering)ÃÖӐ֝֍ú ¯ÖϝÖÖ»Öß“µÖÖ https://nmmc.maharashtra.etenders.in µÖÖ
ÃÖӍêúŸÖãÖôûÖ¾Ö¸ü ¾Ö −Ö´ÖãÓ´Ö¯ÖÖ“µÖÖ (www.nmmc.gov.in) µÖÖ ÃÖӍêúŸÖ ãÖôûÖ¾Ö¸ü ¯ÖÏÖ¯ŸÖ ÆüÖêŸÖß»Ö.×−Ö×¾Ö¤ü֍úÖ¸üÖÓ−Öß úÖê¸üß
×−Ö×¾Ö¤üÖ ±úÖò´ÖÔ ±úß ,‡ÃÖÖ¸üÖ †−ÖÖ´ÖŸÖ ¸üŒú´Ö ¾Ö ÃÖê¾ÖÖ ¿Ö㻍ú †Öò−Ö»ÖÖ‡−Ö ¯Öê´Öë™ü Öê™ü¾Öê«üÖ¸êü ³Ö¸üÖ¾ÖµÖÖ“Öê †ÖÆêü. ¾Ö¸üß»Ö
−Ö´Öã¤ü ÃÖ¾ÖÔ ¿Ö㻍ú úÖêÖŸµÖÖÆüß ²Öïêú“Öê ›êüײ֙ü úÖ›Ôü, Îêú›üß™ü úÖ›Ôü †£Ö¾ÖÖ −Öê™ü²ÖòúßÖ ´ÖÖ±ÔúŸÖ ³Ö¸üÖÖ ú¸üŸÖÖ
µÖê‡Ô»Ö.×−Ö×¾Ö¤üÖ ±úòÖ´ÖÔ ±úß ¿Ö㻍ú −Ö´ÖÓã´Ö¯ÖÖ“Öê »ÖêÖÖ ×¾Ö³Ö֐ÖÖŸÖ Ûþ֍úÖ¸ü»Öê •Ö֝ÖÖ¸ü −ÖÖÆüß,µÖÖ“Öß ×−Ö×¾Ö¤ü֍úÖ¸ÓüÖ−Öß −ÖÖë¤ü
‘µÖÖ¾Öß.
ÃÖ¤ü¸ü ×−Ö×¾Ö¤êüú¸üߟÖÖ ×−Ö×¾Ö¤üÖ¯Öã¾ÖÔ ²Öîšüúß“Öê פü. 13/7/2017 ¸üÖê•Öß Ã֍úÖôûß. 11.00 ¾ÖÖ. ¾ÖúßµÖ †Ö¸üÖꐵÖ
†×¬ÖúÖ¸üß µÖÖÓ“Öê ¤üÖ»Ö−ÖÖŸÖ †ÖµÖÖê•Ö−Ö ú¸üµÖÖŸÖ †Ö»Öê †ÖÆêü.
×−Ö×¾Ö¤ê“Öê ÃÖÖ¤ü¸üߍú¸üÖ ŸÖÃÖê“Ö Online Bid Preparation פü. 6/7/2017 ¸üÖê•Öß Ã֍úÖôûß 11.00
¾ÖÖ•Öê¯ÖÖÃÖæ−Ö ŸÖê פü. 25/7/2017 ¤ãü¯ÖÖ¸üß 2.00 ¾ÖÖ•Öê¯ÖµÖÕŸÖ ¾Ö ײ֛ü ™ÒüÖ−ÃÖ±ú¸ü פü. 25/7/2017 ¸üÖê•Öß ÃÖÖµÖÓ 06.00
¾ÖÖ•Öê¯ÖÖÃÖæ−Ö ŸÖê פü. 28/7/2017 ÃÖÖµÖÓ 06.00 ¾ÖÖ•Öê¯ÖµÖÕŸÖ. https://nmmc.maharashtra.etenders.in µÖÖ
ÃÖӍêúŸÖãÖôûÖ¾Ö¸ †Öò−Ö»ÖÖ‡Ô−Ö ú¸üÖ¾ÖµÖÖ“Öê †ÖÆêü.
https://nmmc.maharashtra.etenders.in µÖÖ ÃÖӍêúŸÖ ãÖôûÖ¾Ö¸ †Öò−Ö»ÖÖ‡Ô−Öü ¯ÖÏÖ¯ŸÖ —ÖÖ»Ö껵ÖÖ ×−Ö×¾Ö¤üÖ
פü. 29/7/2017 ¸üÖê•Öß Ã֍úÖôûß 11.30 ¾ÖÖ.¾ÖúßµÖ †Ö¸üÖêµÖ †×¬ÖúÖ¸üß µÖÖÓ“Öê ¤üÖ»Ö−ÖÖŸÖ Øú¾ÖÖ †−µÖ ÃÖÖêµÖß“µÖÖ
פü¾Ö¿Öß ×−ÖÛ¿“ÖŸÖ ÆüÖê‡Ô»Ö ŸµÖÖ ×šüú֝Öß ×−Ö×¾Ö¤ü֍úÖ¸ü ؍ú¾ÖÖ ŸµÖÖÓ“Öê †×¬ÖéúŸÖ ¯ÖÏןÖ×−Ö¬Öß ¾Ö ´ÖÆüÖ−֐ָü¯ÖÖ׻֍úÖ µÖÖÓ“Öê
¯ÖÏןÖ×−Ö¬Öß ÃÖ´ÖÖ ˆ‘Ö›üµÖÖŸÖ µÖêŸÖß»Ö. ‡ÃÖÖ¸Ö ¸üŒú´Ö −Ö ³Ö¸ü»Ö껵ÖÖ ×−Ö×¾Ö¤üÖÓ“ÖÖ ×¾Ö“ÖÖ¸ü êú»ÖÖ •Ö֝ÖÖ¸ü −ÖÖÆüß. úÖêÖŸÖßÆüß
×−Ö×¾Ö¤üÖ Ã¾ÖߍúÖ¸üÖê †£Ö¾ÖÖ −Ö֍úÖ¸üµÖÖ“ÖÖ †×¬ÖúÖ¸ü ´ÖÖ. †ÖµÖ㌟Ö, −Ö¾Öß ´ÖãÓ²Ö‡Ô ´ÖÆüÖ−֐ָü¯ÖÖ׻֍úÖ µÖÖÓ−Öß ¸ü֏Öã−Ö
šêü¾Ö»Öê»ÖÖ †ÖÆêü.
¾ÖúßµÖ †Ö¸üÖêµÖ †×¬ÖúÖ¸üß
−Ö¾Öß ´ÖãÓ²Ö‡Ô ´ÖÆüÖ−֐ָü¯ÖÖ׻֍úÖ
Page 2 of 61
−Ö¾Öß ´ÖãÓ²Ö‡Ô
´ÖÆüÖ−֐ָü¯ÖÖ׻֍úÖ
Navi Mumbai
Municipal
Corporation
3 ¸üÖ ´Ö•Ö»ÖÖ,†Ö¸üÖê µÖ ×¾Ö³Ö֐Ö,
‹−Ö‹´Ö‹´ÖÃÖß ³Ö¾Ö−Ö, ÃÖê-15‹ê,
ÃÖß.²Öß.›üß.,−Ö¾Öß ´ÖãÓ²Ö‡Ô 400 614.
¤æü¸ü¬¾Ö−Öß Îú : 27567261
3rd FLOOR,HEALTH DEPT., NMMC
BHAVAN, SEC-15A, CBD
BELAPUR,
NAVI MUMBAI – 400 614.
TEL. No. : 27567261
TENDER NOTICE NO. NMMC/HEALTH/ 57/2017
Navi Mumbai Municipal Corporation invites sealed retender no.2 for Supply of equipments
(Group-I) for NMMC hospitals from reputed manufacturer / authorized agency.
Navi Mumbai Municipal Corporation has adopted Next Tendering Sify Technologies Etendering system. Tenderers shall register their firm on https://maharashtra.etenders.in for
tender process. For works of Rs. 3.00 Lacs and above the Suppliers/Contractors shall buy the
tender form through E-tendering system only.
The detail of the work is as under:
Sr.
No.
1
Name of Work
EMD
Retender no.2 for Supply of equipments (Group-I)
for NMMC hospitals
1,50,000/-
Blank
tender cost
12,000/-
Blank tender form will be available from Dt.6/7/2017 at 11.00 a.m. to Dt. 25/7/2017 up to
2.00 p.m. on the E-tendering Website https://nmmc.maharashtra.etenders.in and NMMC’s
official website www.nmmc.gov.in to download,
Tenderers will be required to do payment for blank tender form, EMD, and service fee
through online payment gateway. All these payments can be made by debit/credit card of any bank
or net banking. Please note that fee for blank tender form will not be accepted at NMMC account
Dept.
Pre-bid meeting will be held on Dt. 13/7/2017 At 11.00 a.m. in the chamber of Medical
officer of Health.
Online preparation and submission of the tender from Dt.6/7/2017 at 11.00 a.m. to
Dt. 25/7/2017 up to 2.00 p.m. and Bid transfer from Dt. 25/7/2017 at 6.00 p.m. to Dt.28/7/2017 up
to 6.00p.m. Should be through E-tendering system only on the website
https://nmmc.maharashtra.etenders.in
Tender will be opened online on Dt.29/7/2017 at 11.30 a.m. or other decided date in office
of Medical Officer of Health or suitably decided place in the presence of tenderer or their
authorized representative in front of NMMC Officials. Tenderers who have not submitted EMD
will not be considered.
Hon. Commissioner of NMMC reserves the right to accept or reject any or all tenders
without assigning any reason thereof.
Medical Officer of Health
Navi Mumbai Municipal Corporation
Page 3 of 61
Detailed Tender Notice
1. Notice Inviting Tenders
1.1 Sealed Tenders are invited by and on behalf of Commissioner, Navi Mumbai Municipal Corporation
(NMMC) from eligible Tenderers for the proposed work specified in the Schedule ‘A’.
2. Issue of Tender
2.1 The tender book will be made available at E-tendering cell, NMMC
Bhavan,
Sector-15A,
Kille
Gavthan, C.B.D. from date of publication of tender notice on News paper to the contractors who have
enrolled at NMMC E-tendering cell for work of tender amount unto 3 lacs. or NMMC enrolled contractor may
buy tender from E-tendering website https://nmmc.maharashtra.etenders.in
2.2 For work of tender amount Rs 3 lacs above, tender book will be issued online through E-tendering
website https://nmmc.maharashtra.etenders.in to contractor, who is enrolled with NMMC
2.3 Price of blank tender form cost must be paid through online payment gateway. The payment can be
made by debit/credit card of any bank or net banking. Please note that fee for blank tender form will not be
accepted at NMMC account Dept.
2.4 The Tender Document is not transferable. Only the Tenderer who has purchased the tender form shall
be entitled to bid in the Tender.
3. Language of Tender / Contract
3.1 The language of the Tender shall be in English / Marathi and all correspondence, drawings etc. shall
conform to the English/Marathi
4. Clarification by tenderer and Pre-tender conference
4.1 A pre- tender conference of all intending tenders will be held at the scheduled date and time indicated in
tender-notice .Intending tenderers will be allowed to seek clarification and suggest suitable modifications in
specifications, conditions of contract, etc. The corporation will communicate such changes that are
accepted by it, to all they intending Tenderers who have purchased the Tender document from the
corporation. Only such changes that are so communicated shall be binding on the Corporation and all the
tenderers. Tenderer should submit in writing to Medical officer of Health clarification & modification
suggested one day prior to Pre-Bid meeting or before the Pre-Bid meeting held.
4.2 The tenderer should get its doubts cleared during pre-bid meeting only, if provided in the tender. In case
no pre-bid meeting is to be held, the Tenderer should seek clarification of any doubt in writing seven (7)
days before the last date for receipt of tenders.
5. Validity of Tenderers
5.1 The Tenders will be valid for a period of 180 days from the date of its opening.
6. Earnest Money
6.1 The Tenderer shall deposit the amounts indicated in the Tender Notice as Earnest Money Deposit
(EMD)., The Earnest Money deposit must be paid through online payment gateway. The payment can be
made by debit/credit card of any bank or net banking. Without Earnest Money deposit NMMC will be
disqualify the Tender and the Corporation shall exclude from its consideration such disqualified Tender(s).
No interest shall be payable by the Corporation in respect of such deposited Earnest Money.
The tenderer should refer user’s guide while depositing EMD through the E-tendering website
https://nmmc.maharashtra.etenders.in
6.2 If the Corporation accepts the Tender, the Earnest Money shall be appropriated towards Security
Deposit payable by the Tenderer in accordance with the Conditions of Contract. Alternatively on payment of
the required amount of the Security Deposit and the execution of the Contract Agreement, the Earnest
Money shall be returned to the Tenderer.
7. Forfeiture of EMD
7.1 The Tenderer shall not revoke his Tender or vary its terms and conditions without the consent of the
Corporation during the validity period of Tender, failing which the Earnest Money deposited by it shall stand
forfeited to the Corporation without prejudice to its other rights and remedies and the Tenderer shall be
disentitled to submit a Tender to the Corporation for execution of any work during the next thirty six (36)
months effective from the date of such revocation.
7.2 If the successful Tenderer does not pay the Security Deposit in the prescribed time limit or fails to sign
the agreement bond, The Earnest Money Deposit will be forfeited by the Corporation.
8. Refund of Earnest Money
The Earnest Money of unsuccessful Tenderers shall be refunded after the successful Tenderer furnishes
the required Initial Security Deposit to the Corporation and signs the Contract Agreement or within thirty
(30) days of the expiry of validity period of Tenders, whichever is earlier.
9. Cost of Tender
The Tenderer shall bear all costs associated with the preparation and submission of its Tender. The
Corporation shall in no case be responsible or liable for these costs, regardless of the conduct or the out
come of the Tendering Process.
Page 4 of 61
10. Eligible Tenderers
Only those Tenderers who fulfill the eligibility criteria as mentioned in Schedule A of the Tender Notice are
eligible to submit their Tenders for this work. The documents indicated against each of the eligibility criteria
shall be required to be submitted along with the technical bid to establish the eligibility of the Tenderer.
11. Relationship with Corporator(s)
The Tenderer shall not be associated presently or in the past with any of the office bearers of Corporators
of Navi Mumbai Municipal Corporation, either directly or indirectly as specified in the section 10(f), (g) of
MMC Act. 1949. The Tenderer shall furnish an affidavit (as per Annexure-3) on a Non-Judicial stamp paper
of Rs.100/-. If any information so furnished shall be found to be untrue or false, the Tenderer shall be liable
to be disqualified and the Earnest Money accompanying such Tender shall stand forfeited to the
Corporation. If the Information so furnished shall be found to be untrue or false during the currency of the
contract, the Tenderer shall be held to be in default and the Contract if any awarded to it shall be liable to
be terminated with its consequences.
12. Inspection of Site and Sufficiency of Tender :The Tenderer is expected to work out their own rates based on the detailed description of items, the
specifications, drawings and conditions and finally arrive at the cost of the Work/Service in the appropriate
place. The Tenderer shall be deemed to have satisfied itself before tendering as to correctness and
sufficiency of its Tender. The rates and prices quoted shall, except as otherwise provided, cover all its
obligations under the contract and all matters and things necessary for proper completion and maintenance
of the Works/Services.
Where necessary, before submitting its Commercial Bid the Tenderer should inspect and examine the site
and its surroundings and shall satisfy itself about form and nature of the Site, the quantities and nature of
the Work/Service and materials necessary for the completion of the Works/Services, means of access to
the site, the accommodation it may require, and in general, obtain all necessary information as to risk,
contingencies and other circumstances which may influence or affect its Tender. No extra charges
consequent on any misunderstanding or otherwise shall be allowed.
13. Manner of Submission of Tender
The tenders should be submitted online at https://nmmc.maharashtra.etenders.in
14. Last Date for Submission
14.1 Copies of uploaded documents (Excluding Financial Bid) should be submitted at the office of Medical
officer of Health before date of opening technical bid.
14.2 The Corporation may, as its discretion, extend this deadline for submission of Tenders online by
amending the Tender Documents, in which case all rights and obligations of the Corporation and Tenderer
will thereafter are subject to the deadline as extended.
14.3 Any Tender received by the Corporation after the deadline for submission of Tender as prescribed by
the Corporation, pursuant to the clause above, will be rejected and /or returned unopened to the Tenderer.
15. Instruction to tenderes
15.1 The Tender form will be available online only. No tender form will be sold/ issued manually from Navi
Mumbai Municipal Corporation.
15.2
The tender document will be uploaded / released on Govt. of Maharashtra e- tendering website
http://nmmc.maharashtra.etenders.in the tenderer is required to download the tender document from
this website as per the schedule of activities for online tender document download.
15.3
The tenderer is required to download the tender document within the schedule of activity for online
tender document download. After expiry of the date and time for tender document download, the
Navi Mumbai Municipal Corporation will not be responsible for any such failure
on account of tenderer for not downloading the document within the schedule even though he has
paid the cost of the tender to the Navi Mumbai Municipal Corporation office. In such case the cost of
the tender paid by the tenderer will not be refunded.
During the activity of bid preparation, the tenderer is required to upload all the documents mentioned
in the terms & conditions of the technical bid by scanning the documents and uploading it in the
PDF. This activity of uploading the documents as well as preparation of commercial bid and other
Annexure enclosed with the tender shall be completed within the schedule given for bid preparation.
After bid preparation, the tenderer is required to submit the bid again during the activity of
submission of bid without which the tender will not be submitted.
The tenders submitted online will be opened on the schedule date before the participant. At the time
of opening of technical bid the tenderer should bring all the original documents which have been
uploaded along with the technical bid so that same can be verified at the time of opening of technical
bid. If the tenderer fails to produce the original documents at the time of opening of technical bid
then the decision of the committee taken on the basis of document uploaded will be final and binding
on the tenderer
As the tenders are invited online, tenderers are required to upload tender as per the schedule given.
Navi Mumbai Municipal Corporation is not responsible for failure on the part of tenderer to upload
tender within the time schedule. In case of any help required for this purpose the tenderer shall
contact to help line of e- tendering agency M/s. Sify Nex Tenders on telephone nos. (020) 25315555 /(022)-2661-1117,2660-3142 Tenderers are requested to go carefully through the process of
15.4
15.5
15.6
15.7
Page 5 of 61
e- tendering given on the website of website http:// nmmc.maharashtra.etenders.in to avoid
disqualification of their tender on any ground.
15.8 The tenderer is required to pay tender processing fee of Rs1092/- per tender to e-tendering agency,
M/s Sify Nex Tenders at time of online submission stage through e-payment (Through credit card/
debit card/net banking) Non payment of fee will result in non- submission of the tender and Navi
Mumbai Municipal Corporation will not be responsible if the tenderer is not able to submit their offer
due to non payment of processing fees to the e-tendering agency.
16. Contents
Tenders are invited in two –envelops system
17. The two envelopes shall contain the following:
Envelope No.1
Technical Bid envelope should contain all the documents mentioned below
a.
b.
c.
d.
e.
f.
g.
h.
i.
j.
k.
l.
EMD (as per clause 6 )
Purchase of Tender Copy (as per clause 2.3)
Details of Tenderer (Annexure 1)
Audited financial statement of subsequent last 3 years
Undertaking (Annexure 2)
Affidavit (Annexure 3)
Manufacturer Authorization form (Annexure 5) in case of authorized Distributors
Detail of Hospital Equipments Supplied in last 2 years (Annexure-6)
Specification of Quoted Equipment as per (Annexure-7)
List of users of quoted Equipment (Annexure-8)
Undertaking of Manufacturer for Maintenance contract (Annexure -9)
Valid Firm/ company Registration certificate (Shop establishment certificate/S.S.I. Certificates /
Certificates In corporation etc)
m. Valid VAT /GST registration certificates
n. PAN card
All documents establishing the eligibility of tenderer as specified in schedule A
Documents submitted by the tenderer must be attested, clear and readable if not so. It will be
treated as non submission of document
Envelope No.2 (Financial Bid):
This envelope shall only contain the Financial Bid in schedule B only. The financial bid should be written
both in words and figures at appropriate places during uploading of Bid.
18. Rate
Rate should be quoted inclusive of all State/Central/Local Government taxes, duties and other expenses
like to carry out the scope of work as mentioned above, and otherwise the rates quoted shall be treated as
inclusive of all. Rates will be valid for one year after approval by NMMC.
19. Important Points to be noted by the Tenderer
1. At the time of opening of the tender, Agency has to submit original hard copies of Affidavit,
Undertaking & Original Manufacturer Authorization form.
2. Only Those tenderer who are eligible as per Schedule A , Should upload the tender
3. The tendrerer should ensure that no corrections or over writings or erasures are left for attestation.
4. The financial bid shall be inclusive of all taxes, Octroi, Local taxes, etc. to be paid by the tenderer
for the Work/Service and any claim for extra payment on any such account shall not be entertained.
5. No alterations or additions anywhere in the tenderer Document are permitted. If any of these are
found, the Tender may be summarily rejected.
6. In case of a firm, each partner or power of attorney holder shall sign the Tender and the signatures
shall be attested as witness by a reputed person in the space provided for the purpose. The
attested copies of power of attorney of person signing the Tender shall be enclosed with The
Tender. The power of attorney shall be signed by all partners. In case of Private limited /public
limited companies, the power of attorney shall be supported by Board Resolution and appropriate
and adequate evidence in support of the same shall be provided
7. Rate mentioned should be as per the specification & unit mentioned in the tender.
8. The Tenderer shall submit the Tender which satisfies each and every condition laid down in this
Tender Document, failing which the Tender will be liable to be rejected. Conditional Tenders will be
rejected.
9. The agency should carry hard copies of all documents submitted for E-tendering at the time of
opening of the tender.
10. Quantity mentioned in tender is indicative / approximate. NMMC reserves the right to purchase less
or more quantity at the sanctioned price as per the need. It is mandatory for the supplier to supply
the material at same rate during the entire contract period.
20. Corrupt of Fraudulent Practices
20.1 The Corporation requires that the Tenderer under this Tender observe the highest standards of ethics
during the procurement and execution of such Contracts. In pursuance of this policy, the Corporation
defines for the purposes of this provision, the terms set forth as follows:
a) “Corrupt Practice” means the offering, giving, receiving or soliciting of any thing of value to influence the
action of the public official In the procurement process or in contract execution; and
b) “fraudulent practice” means a misrepresentation of facts in order to influence a procurement process or a
execution of a contract to the detriment of the Corporation, and includes collusive practice among
Page 6 of 61
Tenderers (prior to or after Tender submission)designed to establish Contract Prices at artificial
noncompetitive levels and to deprive the Corporation of the benefits of the free and open competition.
20.2 The Corporation will reject a proposal for award if it determines that the Tenderer recommended for
award has engaged in corrupt or fraudulent practices in competing for the Contract in question; The
Corporation will deem a firm ineligible, either indefinitely or for a started period of time, to be awarded a
Contract if at any time it determines that the firm has engaged in corrupt and fraudulent practices in
competing for, or in executing, a Contract.
21. Manner of Opening of Tender
The Tender received before the time and date specified in the Tender Notice will be opened as per the
specified program in the office as mentioned in the Tender Notice (If Possible). The tenders will be opened
in the presence of Tenderers or their authorized representatives who choose to remain present.
22. Process to be Confidential
Information relating to the examination, clarification, evaluation and comparison of Tenders and the award
of a Contract shall not be disclosed to Tenderers or any other person not officially concerned with such
process until the award to the successful Tenderer has been announced.
23. Preliminary Scrutiny
23.1 The Corporation will scrutinize the Tender to determine whether they are complete, whether any errors
have been made, whether required technical documentation have been furnished, whether the documents
have been properly signed, and whether the Tenders are generally in order. The Corporation will also
determine the substantial responsiveness of the Tender. For purpose of these clauses, a substantially
responsive Tender is one that confirms to all the terms and conditions of the Tender Documents without
material deviations. The Corporation’s determination of a Tender’s responsiveness is to be based on the
contents of the Tender itself without recourse to extrinsic evidence.
23.2 A Tender determined as not substantially responsive will be rejected by the Corporation and may not
subsequently be made responsive by the Tenderer by correction of the non-conformity. The Corporation
may waive any minor infirmity or irregularity in a Tender which does not constitute a material deviation. This
shall be binding on all Tenderers and the Corporation reserves the right of such waivers.
24. Clarification of Offers
To assist in the scrutiny, evaluation and comparison of Tenders, the Corporation may, at its discretion, ask
some or all Tenderer for technical clarification of their Tender. The request for such clarifications and the
response shall be in writing. To speed up the Tender process, the Corporation, at its discretion, may ask for
any technical clarification to be submitted by means of facsimile by the Tenderer. In such cases, original
copy of the document describing the technical clarifications must be sent to the Corporation by means of
courier / in person.
25. Opening of Financial Bids
Agency will be technically qualified by Scrutinisation of documents & thereafter demonstration of
equipment. The financial bid of tenderers qualifying both above mentioned criteria will be opened.
26. Acceptance of Tender
Acceptance of Tender on behalf of the Corporation shall be done by an officer(s) to whom the powers are
delegated by the Municipal Commissioner. The Corporation is not bound to accept the lowest or any
Tender. The right to split up the Work/Service in two or more parts is reserved by the Corporation and also
the right to award the Work/Service to more than one agency is reserved. The Corporation reserves the
right to reject any or all Tenders received without assigning any reason whatsoever.
27. Intimation to Successful Tenderers
The acceptance of Tender may be communicated to the successful Tenderer in writing or otherwise either
by the Tender opening authority or any authority in the Corporation.
28. Security Deposit / Performance Security
28.1 Successful Tenderer shall pay a Security Deposit equal to the Amount indicated in the Schedule A of
the Detailed Tender Notice as security for due fulfillment of the contract, within seven (7) days after receipt
of intimation in writing of acceptance of Tender.
28.2 The mode of making this deposit is as under.
a) Initial Security Deposit:
It is optional to the Tenderer to make the initial Security Deposit in any one of the following ways:
i. wholly in cash; or
ii. wholly in form of National Saving Certificate pledged in favour of the Corporation or bank
guarantees/fixed deposit from Nationalized/Scheduled Banks in the enclosed format; Detailed Tender
Notice or
iii. Partly in cash and partly in form of National Saving Certificate pledged in favour of the Corporation or
Bank guarantees/fixed deposit from Nationalized/ Scheduled Banks in the enclosed format.
b) Retention Money:
The remaining amount of the Security Deposit (if applicable as per Schedule A )shall be recovered from
the tenderer’s running bills at rate of five (5) percent and such retention together with the Initial Security
Deposit made as aforesaid shall not exceed the total amount of security deposit maintained as per the
clause 28.1 after which such retention will cease.
Page 7 of 61
29. Execution of Contract Document
29.1 The successful Tenderer after furnishing the Initial Security Deposit, is required to execute an
Agreement in duplicate in the form attached with the Tender Documents on a stamp paper of proper value.
The Agreement should be signed within 7 days from the date of acceptance of the Tender. The Contract
will be governed by the Contract Agreement, the Conditions of the Contract (CoC) and other documents as
specified in the Conditions of the Contract (CoC).
29.2 It shall be incumbent on the successful Tenderer to pay stamp duty for the Contract Agreement, as
applicable on the date of the execution.
30. Licenses
Wherever relevant, before commencing the Work/Service the successful Tenderer shall be required to
produce to the satisfaction, of the Corporation a valid Contract Labour License issued in its favour under the
provision of the Contract Labour (Regulation and Abolition), Act 1970. On failure to do so, the acceptance
of the Tender is liable to be withdrawn and also the Earnest Money is liable to be forfeited.
31. Rights of the Corporation
31.1 The Corporation reserves the right to suitably increase/ reduce the scope of work put to this Tender. In
case of a Rate Contract, the Corporation does not in any way guarantee the quantity for which an order
may be placed and the Tender quantity may only be treated as indicative.
31.2 In case of any ambiguity in the interpretation of any of the clauses in Tender Document or the Contract
Document, interpretation of the Clauses by the Corporation shall be final and bindings on all Parties.
31.3 In case the tenderers quote prices higher than allowed as per DPCO, NPPA or higher than MRP or /
and fail to supply the goods consistently the tenderers will be declared as fraudulent and defaulters
a) The extra expenditure incurred because of risk purchase shall be recovered from the tenderer.
b) His Registration will be cancelled
c) The tenderer’s EMD/Security deposit amount, Bank Guarantee will be forfeited.
d) The tenderer will be debarred from participating in the tender for next three years.
31.4 In case if found that the tenderer has submitted forged documents the following actions will be taken
against the tenderers.
a) The extra expenditure incurred because of risk purchase shall be recovered from the tenderer.
b) The police case will be filed against the tenderer
c) His Registration will be cancelled
d) The tenderer’s EMD/Security deposit amount, Bank Guarantee will be forfeited.
e) The tenderer will be debarred from participating in the tender for next three years
32. Notice to form Part of Contract
Tender Notice and these instructions shall form part of the Contract.
33. Similar Work
Similar work means work experience for supply and installation of the equipments as mentioned in the
price bid.
Page 8 of 61
Scope of work
1. Delivery Place: Concerned hospital as per work order.
2. Delivery period: The delivery period of the Material will be maximum 45 days from the date of
issue of work order.
3. If the materials are not delivered with in prescribed period i.e. within 45 days from the date of issue
of work order, then the following action will be taken;
a. Delay Charges: Delay charges of 0.5 % per week will be charged on undelivered material
and maximum up to 5%. Thereof
b. Work order will be cancelled.
4. If the tenderer wants to extend the delivery period they should apply for extension with valid
reasons in writing within 7 days from the date of work order. NMMC reserves the right to accept or
reject such request.
5. The warranty of the equipment /Materials from manufacturer.
Warranty Clause: The good/stores/articles sold to NMMC under this contract shall be of the best
quality (and workmanship) and shall be strictly in accordance with the specifications and
particulars contained/mentioned in the schedule hereof and the Contractor hereby guarantees that
the said good/stores/articles continue to conform to the description and quality aforesaid for a
period of 24 months from the date of delivery of said good/stores/articles to the NMMC and that
not with standing the fact that the purchaser may have inspected and/or approved the said
good/stores/articles, if during the aforesaid period of 24 months the said good/stores/articles be
discover not to conform to the description and quality aforesaid or have deteriorated (and decision
of the purchaser in that behalf will be final and conclusive) the Purchaser will be entitled to reject
the said good/stores/articles or such portion thereof as may be discovered not to conform to the
said description and quality. On such rejection, the goods/articles/stores will be at the Seller's
risk.. The Contractor/Seller shall, if so called upon to do, replace the goods, etc. or such portion
thereof as is rejected by the purchaser within a period of 30 days otherwise a penalty as per delay
charges mentioned above will be levied. Nothing herein contained shall prejudice any other right
of the purchasers in that behalf under this contract or otherwise.
6. The supplier has to supply Materials with all accessories and spares for fully functioning of
Equipments.
7. Agency cannot mention different specification / standards other than asked by NMMC. The
corporation reserves the right to reject such offers without assigning any reasons thereof.
8. The supplier has to provide all original manufacturers spares during repair in warranty period.
9. Demonstration:
Demonstration should be arranged within 07 days from the date of intimation at the cost of bidder
either at NMMC hospital or at equipment supplied place as per the direction of Medical Officer Of
Health, NMMC
10. Packaging & transport of the Equipments /Materials will be in such a way that the Equipments
/Materials will not be damaged. NMMC will not be responsible for the damage to Equipments
/Materials in transport. Damage Equipments /Materials will be replaced immediately by tenderer at
their own expense.
11. The supplier will deliver the said Equipments /Materials at the specified location as per work order
and as instructed within jurisdiction of NMMC, at his own cost and labor.
12. Rates will be valid for one year from approval by NMMC.
13. Installation & maintenance:
1. The supplier has to install the said Equipments /Materials at the instructed sites, successfully within
07 days after the date of supply or as informed by NMMC.
2. The successful tenderer shall visit the scheduled institution and getting compliance of mandatory
prerequisite for successful installation will be responsibility of bidder.
3. Demonstration and hands- on training for the concerned Doctors, Nurses and technicians at the
site, by the company engineer.
14. Comprehensive Maintenance Contract (CMC):
As per annexure-9 the manufacturer will have to agree to enter into comprehensive maintenance
contract (CMC) @ 5% of the cost of the equipment for the period of 8 years after completion of
Warranty Period
15. Spare parts.
Agency will be required to provide any or all of the following materials, notifications and
information pertaining to spare parts manufactured or distributed.
a. Such spare parts as NMMC may elect to avail from the supplier providing that this election
shall not relive the supplier of any warranty obligations under the contract and
b. in the event of termination of production of the spare parts:
1. Advance notification to NMMC of the pending termination, in sufficient time to permit the
NMMC to procure needed requirements and.
2. Following such terminations, furnishing at no cost to the NMMC, the blue prints, drawings and
Specifications of the spare parts if requested.
3. Free maintenance service shall be provided by the supplier during the period of warranty.
a) Preventive maintenance & Servicing ,every three monthly
b) Breakdown maintenance-to be attended by the company engineer immediately for all
the life-saving equipment, and within 24hrs for the all other equipment.
c) History Sheet should be Maintain of the equipment with maintenance records date wise
and breakdown details along with spare parts repaired or replaced.
d) If any particular equipment is having repeated breakdown and downtime during the
warranty period, causing problem in patient care, then it would be considered aDefective piece and should be replaced with a new one.
4. Replacement of spares should be done within 07 days from the date of intimation.
5. If downtime of equipment is more than 07 days a penalty of Rs.1000/- per day will be levied.
Page 9 of 61
16. Payment: No advance payment will be given
The Payment will be released as follows
a. 80% payment will be released after successful delivery and successful installation of the
equipment at the specified location.
b. 20 % payment will be released after Certification by the user department after three
months.
.
17. Any loss or damages of NMMC property occurs at site while executing work will be sole
responsibility of tenderer and shall be rectified at their own cost or the same cost will be recovered
from their payable amount.
18. Increase in taxes
Tenderers must distinctly understand that they will not be allowed any increase over the rates
quoted by them during the contract period.
19. Procedure of Supply & Risk purchase:
If the Rate Contract holder fails to supply the Equipments /Materials within the stipulated period
according to terms & conditions of this tender or fails to replace rejected material as asked by
NMMC, within such time as may be stipulated NMMC, shall be entitled to purchase from any other
source, at such price which is decided by Medical officer of Health. The extra expenditure in such
cases shall be immediately recovered by the NMMC, from the outstanding bill of the rate contract
holder. If no bills of Rate Contract holder are outstanding with NMMC the same shall be recovered
from security deposit.
20. Selection Criteria.
1. Technical Qualification - Technical Qualification will be decided by technical committee after
scrutinizing documents.
2. Demonstration -. Physical verification & demonstration of the equipment, Only those rates of
technically qualified agencies will be considered for comparison
3. Commercial –
a) Initially category wise lowest rate will be considered for selection.
b) If any bidder gets selected for category wise lowest cost and if any item from the category
has higher rate/cost than the other bidder the lowest category wise bidder will have to
supply that particular item with the lowest rate of that particular item.
c) If the category wise lowest bidder is unable to supply that particular item with lowest rate of
that particular item, in such case those item/equipment will be selected from individual item
wise lowest bidder.
d) If NMMC does not receive any tender for all the items in any category then item wise lowest
cost will be considered.
21.INDEMNIFICATION: The Successful Bidder shall at his own expense, arrange for Insurance
policies, such as workmen compensation policy and Successful Bidder's All Risk policy effective
from the date of commencement of work until final completion against all of the following risks.
1. Injuries and damage of persons, property, animals or things, within or outside the site, arising out of
operations of the Successful Bidder or out of any actions of his employees, agents or
representatives
2. Injuries to any persons during supply & installation of equipment by Successful Bidder.
3. Damage to or loss of the property, Medical Equipment, and materials of the Successful Bidder, and
as a result of natural causes such as lightning, storm, flood, rain, fire, earthquake, explosion,
landslide, etc.
4. Damage and injuries to persons, property and materials arising out of riot and civil commotion,
theft, sabotage malicious acts, terrorist activities etc.
5. Any other unforeseen Risks
6. All the issues related to consumer protection act/medico legal aspects that shall arise will be
handled by the Bidder and in no way NMMC shall be held responsible and successful bidder shall
submit the indemnity bond for the same.
7. Demonstration of the quoted product must be demonstrated. All expenses to be undertaken by the
bidders/ tenderers.
Page 10 of 61
SCHEDULE ‘A’
Note : All the Contractors may note that Enrollment with NMMC is compulsory.
Re-tender no.2 for Supply of equipments (Group-I) for NMMC hospitals
1.
Name of tender
2
Persons
Responsible
3.
Eligibility Criteria and Documents Required to Establish Eligibility
Criteria
Medical Officer of Health, Navi Mumbai Municipal Corporation
Required eligibility
Documents Required to be attached with tender or
to be uploaded in case of e-submission to
Establish Eligibility
Valid Firm/ company Registration (Shop establishment
certificate/S.S.I. Certificates /Certificates In
corporation/ETC)
a
Registration
4
Pre qualification criteria.
a
Average
Turnover for last
three years
Bidder’s Average and annual Turnover
should be at least Rs. 2113 lakhs for
subsequent last three years.
Audited financial statements of subsequent last three
years / Turnover certificate certified by Charted
Accountant
b
Certification
ISO 9001 Certificate of Bidder
c
Experience
Bidder should have executed Project of
Rs.2113 lakhs for supply of medical
equipments Govt./Semi govt./ PSU
hospitals/ Private Hospitals in last 3
years
Manufacturer should have experience
of supplying quoted equipments
Positive net worth
Copy of ISO 9001 Or latest ISO Certificate of Bidder
to be uploaded
Copy of work order, completion certificate.(Annexure-6)
d
Positive net worth
5
Technical
Qualification
Copy of work order , completion certificate.
CA certificate showing positive net worth.
1.
2.
3.
4.
5.
6.
Document Required
7.
8.
9.
10.
11.
12.
13.
6
Demonstration
Agency will be qualified technically by
1. Tender committee by scrutinizing
documents
2. Technical committee by
demonstration of the equipment
EMD (as per clause 6 )
Purchase of Tender Copy (as per clause 2.3)
Details of Tenderer (Annexure 1)
Undertaking (Annexure 2)
Affidavit (Annexure 3)
Manufacturer Authorization form (Annexure 5) in
case of authorized Distributors
Experience in supplying medical equipments to
Govt./Semi govt./ PSU hospitals/ Private hospital
in last 3 years (financial year 2013-14, 2014-2015
and 2015-2016) (Annexure-6) work orders and
installation reports/ performance reports of Rs
2113 lakhs
Valid Firm/ company Registration (Shop
establishment certificate/S.S.I. Certificates
/Certificates In corporation etc)
Valid VAT / GST registration certificates
PAN card
Specification of Quoted Materials as per
(Annexure-7)
List of users of quoted equipments in last 2 years
along with work orders (Annexure-8 )
Undertaking of Manufacturer/ Bidder for
maintenance contract.(annexure-9)
Demonstration should be arranged within 07 days from
the date of intimation at the cost of bidder either at
NMMC hospital or at equipment supplied place as per
the direction of Medical Officer Of Health, NMMC
Rates of only technically qualified
agencies will be considered for
comparison.
7
Security Deposit
5% of the Contract Sum (validity 30 months from the
date of installation )
8
Type of Contract
Rate contract
9
Contract Period
One year
Special Conditions:
•
Hon. Commissioner, NMMC reserves the right to reject any or all offers.
Medical Officer of Health
Navi Mumbai Municipal Corporation.
Page 11 of 61
Annexure - 1
Details of Tenderer
1.
Name of Tenderer
2.
Address
3.
Telephone
4.
Fax
5.
E-Mail
6.
Details of Proprietor/partners/Directors
Name
7.
Address
Qualification & Experience
Financial Performance
Turnover
(Rs.)
Profit
Copy of Audited
Financial
statements
attached
(Yes/No.)
Previous Financial Year (Y-1)
Previous Financial Year (Y-2)
Previous Financial Year (Y-3)
8.
Registration Details
9.
Certification Details
10. Details of Black List /Arbitration/ Litigation
(If any)
11. Remarks
Details of Manufacturing Unit (Where Applicable)
1.
Exact Location of Manufacturing unit.
2.
Product Produced
3.
Manufacturing Capacity (Product-wise)
4.
Details of Certification obtained. (Copies to be attached.)
5.
Actual installation of Quoted items during last three years.
6.
Brief Description of Facilities for inspection, testing and quality assurance.
Note: The turnover amount should be certified and audited by CA of firm and separate sheet should
be enclosed.
Signature of Tenderer
Page 12 of 61
Signature of authorized Person
Annexure -2
Undertaking of Tenderer (Notarized)
(On a Rs.100/- Stamp paper)
Tender Ref.No. NMMC/HEALTH/
/2017
Having examined the tender document including all the annexures, the receipt of which is hereby
duly acknowledged, we, the undersigned, state that the specifications, conditions, etc. of this tender have
been carefully studied and understood by me / us before submitting this Tender . I / We hereby declare that
I / We have made myself / ourselves thoroughly conversant with the conditions of the tender and I / We
have based my / our commercial bid for the Tender and offer to undertake the work / supply / deliver/
maintain _____________ (Description of Work / Goods / Services) in conformity with the said tender
documents.
We agree to abide by this tender offer till the expiry of contract period and its extension.
I / We agree that the amount of Earnest Money shall not bear interest and shall be liable to be
forfeited to the Corporation, should I/we fail to (i) Abide by the stipulation to keep the offer open for the
period of 180 days from the date fixed for opening the same and thereafter until it is withdrawal by me / us
by the notice in writing duly addressed to the authority opening the Tender Notice. (ii) Security deposit as
specified in the time limit laid down in the Detailed Tender Notice. The amount of earnest money may be
adjusted towards the security deposit or refunded to me / us if so desired by me / us in writing, unless the
same or any part thereof has been forfeited as aforesaid.
Should this tender be accepted I / we hereby agree to abide by and fulfill all the terms and
provisions of the conditions of contract annexed hereto so far as applicable and in default thereof to
forfeited and pay to NMMC the sums of Money mentioned in the said conditions. If our tender offer is
accepted we will deposit the specified amount as security deposit for the due performance of the Contract
and during the warranty. I / we undertake to use only the best materials approved by the Municipal
Commissioner of N.M.MC. or his duly authorized representative, before starting the work and to abide by
his decision, Until a formal contract is prepared and executed, this tender offer, together with your written
acceptance thereof and your notification of award, shall constitute a binding contract between us. We
understand that you are not bond to accept the lowest or any offer you may receive.
The information / documents submitted by us are true to our knowledge and if the information /
documents so furnished shall be found to be untrue or false, the Tender shall be liable to be disqualified
and our Earnest Money accompanying the Tender will be forfeited.
Date the ........................................... day of .............................. 20
1) Signature of Witness
Name: .......................................................................................................................
Address .......................................................................................................................
2) Signature of Witness
Name: .......................................................................................................................
Address .......................................................................................................................
Authorized Person /Signature of Tenderer
Page 13 of 61
Annexure – 3
Affidavit (Notarized)
(On Rs.100/- Stamp Paper)
Tender Ref.No. NMMC/HEALTH/
/2017
I/We hereby state that we are aware of the provisions of section 10 (1) 10(f) and (g) of the
Maharashtra Municipal Corporation Act, which are reproduced below, and solemnly state that we
have no partnership with or any share with any Corporator of this Corporation in our company and
are not associated presently or in the past with any of the office bearers or Corporator of the Navi
Mumbai Municipal Corporation, either directly of indirectly.
Extract of Sec 10 of Maharashtra Municipal Corporation Act
10 (1) Subject to the Provisions of Section 13 and 404, a person shall be disqualified for being
elected and for being a councilor.
10 (f) “ Subject to the provisions of sub-section (2), has directly or indirectly, by himself or his
partner any share or interest in any Contract or employment with, by or on behalf of the
Corporation”.
10 (g) “Having been elected a councilor is retained or employed in any professional capacity
either personally or in the name of a firm in which he is a partner or with whom he is engaged in a
professional capacity in connection with any cause or proceeding in which the Corporation or the
Commissioner or the Transport Manager is interested or concerned”.
We are aware that the above information if found to be untrue or false, we shall be liable to be
disqualified and the Earnest Money accompanying the Tender shall stand forfeited to the
Corporation. We are also aware that if the information produced above is found to be untrue or
false during the currency of the Contract, we shall be held to be in default and the Contract, if any
awarded to us, shall be terminated with all its concurrence.
Tenderer ______________________________
Address _____________________________
______________________________
Date the _______________day of ___________20
Signature of Tenderer
Witness________________________________
Address _______________________________
________________________________
Date the _________________day of ___________20
Page 14 of 61
Signature of Witness
Annexure – 4
FORM OF BANK GUARANTEE BOND.
(FOR SECURITY DEPOSIT)
FOR THE PERIOD OF 30 MONTHS.
1. In consideration of the Navi Mumbai Municipal Corporation (hereinafter called 'NMMC') having agreed to
exempt ________________________________________ (hereinafter called "the said Operator /
Contractor / Tenderer / supplier (s)') form the demand under the terms and conditions of an Agreement
dated __________________________________________ for (hereinafter called "the said Agreement") of
security deposit for the due fulfillment by the said Tenderer as per the terms and conditions contained in the
said Agreement, and on production of a Bank Guarantee for Rs.____________________ (Rupees
____________________________________________________ Only), we, (indicate the name of
bank)______________________________ (hereinafter referred to as 'the bank') at the request of
______________________ the Operator / Contractor / Tenderer / Supplier (s) do hereby undertake to pay
the NMMC an amount not exceeding Rs. ______________________________________ against any loss
or demand caused to or suffered or would be caused to or suffered by the NMMC by reason of any breach
by the said Operator/ Contractor/ Tenderer/ Supplier (s) of any of the terms or conditions contained in the
said agreement.
2. The Bank do hereby undertakes to pay the amounts due and payable under this guarantee without any
demur, merely on a demand from the NMMC stating that the amount claimed is due by way of loss or
damage caused to or would be caused to or suffered by the NMMC by reason of breach by the said
Operator/ Contractor/ Tenderer/ Supplier (s) of any of the terms or conditions contained in the said
Agreement or by reasons of the Operator/ Contractor/ Tenderer/ Supplier (s) failure to perform the said
Agreement. Any such demand made on the bank shall be conclusive as regards the amount due and
payable by the Bank under this guarantee.
3. However, our liability under this guarantee shall be restricted to an amount not exceeding
Rs._________________
(Rs.___________________________________________________________in words). We, undertake to
pay to the NMMC any money so demanded not withstanding any dispute or disputes raised by the
Operator/ Contractor/ Tenderer/ Supplier (s) in any suit or proceeding pending before any Court or Tribunal
relating thereto our liability under this present being absolute and unequivocal. The payment so made by us
under this bond shall be a valid discharge of our liability for payment there under and the Operator/
Contractor/ Tenderer/ Supplier (s) shall have no claim against us for making such payment.
4. We, (indicate the name of Bank) __________________________________ further agree that the
Guarantee herein contained shall remain in full force and effect during the period that would be taken for
the performance of the said Agreement and that it shall continue to be enforceable till all the dues of the
NMMC under or by virtue of the said Agreement have been fully paid and its claims satisfied or discharged
or till the Municipal Commissioner of NMMC certifies that the terms and conditions of the said Agreement
have been fully and properly carried out by the said Operator/ Contractor/ Tenderer/ Supplier (s) and
accordingly of the said Agreement have been fully and properly carried out by the said Operator/ Contractor
/ Tenderer/ Supplier (s) and accordingly discharges this guarantee. Unless a demand or claim under this
guarantee is made on us in writing on or before the ..............................we shall be discharged from all
liability under this guarantee thereafter.
5. We, (indicate the name of Bank)_______________________________________ further agree with the
NMMC that NMMC shall have the fullest liberty without our consent and without affecting in any manner our
obligations hereunder to vary any of the terms and conditions of the said Agreement or to extend time to
performance by the said Operator/ Contractor / Tenderer/ Supplier (s) from time to time or to postpone for
any time or from time to time any of the powers exercisable by the NMMC against the said Operator/
Contractor / Tenderer/ Supplier (s) and to forbear or enforce any of the terms and conditions relating to the
said agreement and we shall not be relieved from our liability by reason of any such variation, or extension
being granted to the said Operator/ Contractor / Tenderer/ Supplier (s) or for any forbearance, act or
commission on the part of the NMMC or any indulgence by the NMMC to the said Operator/ Contractor /
Tenderer/ Supplier (s) or by any such matter or thing whatsoever which under the law relating to sureties
would but for this provision, have effect of so relieving us.
6. This guarantee will not be discharged due to the change in the constitution of the Bank or the Operator/
Contractor / Tenderer/ Supplier (s).
7. We, (indicate the name of Bank)_________________________________lastly undertake not to revoke
this guarantee during its currency except with the previous consent of the NMMC in writing.
Dated the ......................day of ............................20
For ..........................................................................
(Indicate the name of Bank)
Signature of Authorized Person
Page 15 of 61
Annexure - 5
Manufacturer’s Authorization Form (MAF)
Dated ...................................
To,
Municipal Commissioner,
Navi Mumbai Municipal Corporation.
NMMC Bhavan, C.B.D.Belapur.
Navi Mumbai - 400 614
Dear Sir,
Tender Reference No. _________
We _____________________ who are established and reputable manufacturers of
__________having factories at_____________and _______________ do hereby authorize M/s.
________________________ ( Name and address of Agent / Dealer ) to offer their negotiate and
conclude the contract with you against the above invitation for tender offer. for Whole contract
period including extension period of the said contract. l/we have not authorized any other
distributors/agents/dealers/importer etc. for this purpose
We hereby extend our full guarantee and warranty as per terms and conditions of the
tender and the contract for the goods and services offered against this invitation, for the goods
and services offered by the above Agent / Dealer. In case our above authorized Agent / Dealer is
unable to supply the goods and services during the period of the contract to the satisfaction of the
Municipal Corporation, we undertake to unilaterally fulfill the contractual obligations of the said
Dealer / Agent either directly or through another Dealer / Agent.
Yours faithfully,
(Name:
)
for and on behalf of
M/s. ________________
Authorized Signatory of the firm
with (Rubber Stamp)
Note : This letter of authority should be on the letterhead of the manufacturing concern and should
be signed with Date & Year by a competent person of the manufacturer along with sealed rubber stamp.
Page 16 of 61
Annexure - 6
Detail of Hospital Equipments Supplied in last 3 years
Sr. No.
Year
Name of
Equipments
Quantity of
supply
Amount of
Business Rs.
Name of the institute
to whom supply is
made
Note: It is mandatory to submit work order and Installation report/Performance report of above
mentioned equipment
1. Expected Amount –Rs. 42.16 lakhs
2. Amount of supplied equipments in last 2 years by the agency.-
Date : ---------------------------Place :-----------------------------
Signature of Tenderer
Page 17 of 61
Annexure - 7
Specification of quoted Equipment
Sr.
No.
Name of
Equipment
Tender
Specification.
Specification
of quoted
Equipment
1
2
3
4
Mfg. Model
no.
5
Manufacturer
authorization
Yes/no.
6
Brochure
attached
Yes/No
7
A. The agency should mention their specification in column no 4 in comparison with tender specification
mention in column 3.
B. If specification of quoted equipments as per tender specification (Column3) then agency should write
“AS PER NMMC SPECIFICATION” in column 4.
C. Deviations/ Range can be mentioned in column 4. The corporation reserves the right to accept or reject
such offers without assigning any reasons thereof.
D. Agency cannot mention different specification /standards other than asked by NMMC. The corporation
reserves the right to accept or reject such offers without assigning any reasons thereof.
Date : ---------------------------Place :-----------------------------
Signature of Tenderer
Page 18 of 61
Annexure - 8
List of users of the quoted
Equipment/ Materials of the manufacturer
Sr.
No.
Name of Equipment
1
Dialysis Machine
2
R.O.Plant
3
Multipara Monitor
4
Defibrillator
1.
Name of Institution,
Phone no.& Address.
Work order with
Installation report/
Performance report
attached Yes /No
If work orders, Installation report/ Performance report are not attached, the agency shall be
disqualified for that product.
Date : ---------------------------Place :-----------------------------
Signature of Tenderer
Page 19 of 61
Annexure – 9
Undertaking of Manufacturer/ Bidder for Maintenance contract
(For Indian Manufacturer Notarized on Rs.100/- Stamp paper)
* We _____________________ who are established and reputable manufacturers of __________having
factories at_____________and _______________ do hereby authorize M/s. ________________________
( Name and address of Agent / Dealer ) to offer their negotiate and conclude the contract with you against
the above invitation for tender offer. for Whole contract period including extension period of the said
contract. l/we have not authorized any other distributors/agents/dealers/importer etc. for this purpose and
further I/We undertake that I/We will enter into agreement with NMMC after completion of warranty period
for comprehensive maintenance contract (CMC).
OR
(Manufacturer firm not having a register office within India the Distributor / Dealer
should submit Undertaking of Maintenance contract on Rs.100/- Stamp paper duly
Notarized)
*
We_____________________
are
authorized
distributors
of
manufacturers
of
____________________having factories at_____________ conclude the contract with you against the
above invitation for tender offer for Whole contract period including extension period of the said contract.
and further I/We undertake that I/We will enter into agreement with NMMC after completion of warranty
period for comprehensive maintenance contract (CMC).
I/We provide any or all of the following materials, notifications and information pertaining to spare
parts manufactured or distributed through above mentioned authorized distributors/agents/dealers/importer
etc
• Such spare parts as NMMC may elect to avail from the supplier providing that this election
shall not relive the supplier of any warranty obligations under the contract and
• in the event of termination of production of the spare parts: Advance notification to NMMC of
the pending termination, in sufficient time to permit the NMMC to procure needed
requirements and.
• Following such terminations, furnishing at no cost to the NMMC, the blue prints, drawings
and specifications of the spare parts if requested.
• Free maintenance service shall be provided during the period of warranty.
1. Preventive maintenance & Servicing ,every three monthly
2. Breakdown maintenance-to be attended by the company engineer immediately for all
the life-saving equipment, and within 24hrs for the all other equipment.
3. History Sheet should be Maintain of the equipment with maintenance records date wise
and breakdown details along with spare parts repaired or replaced.
4. If any particular equipment is having repeated breakdown and downtime during the
warranty period, causing problem in patient care, then it would be considered aDefective piece and should be replaced with a new one.
• Replacement of spares will be done within 07 days from the date of intimation.
• NMMC can levy a penalty of Rs.1000/- per day if downtime of equipment is more than 07
days.
We hereby extend our full guarantee and warranty for comprehensive maintenance contract (CMC)
@5% of the cost of the equipment for the period of 8 years after completion of warranty period as per terms
and conditions of the tender and the contract. In case our above authorized Agent / Dealer is unable to
supply the goods and services during the period of the contract to the satisfaction of the Municipal
Corporation, we undertake to unilaterally fulfill the contractual obligations of the said Dealer / Agent either
directly or through another Dealer / Agent.
Place—
Date--
(Name:
)
For and on behalf of
M/s. ________________
Authorized Signatory of the firm
with (Rubber Stamp)
* Strikeout whichever is not applicable
Page 20 of 61
TECHNICAL SPECIFICATION
Item
code
1
Name of Equipment
Technical Specification
Anesthesia
machine ( basic
Boyles) without
compressor
1 set includes :
1. Boyle’s Apparatus should have rigid steel structure with four antistatic
castors wheels having front with brakes.
2. It should have Approx. (10”) long rotating bobbin flow meters, (rotameters)
with color coded control knobs, calibrated in multiple scales for accurate
reading.
3. It should have Oxygen (1st tube)-10 cc/mm to 3.5 liter/min.
4. It should have Oxygen (2nd tube)- 3.5 liter/min to 10 liter/min.
5. It should have Nitrous oxide (1st tube)- 200 cc/ min to 5 liter/min.
6. It should have Nitrous oxide (2nd tube)- 5 liter / min to 12 liter/min.
7. It should have Air-100 cc/min to 12 liter/min.
8. It should be Gas specific, gas blocks pin indexed yokes, two each for oxygen
& nitrous oxide & one for air suitable for pin- indexed cylinder.
The equipment shall also have attachment for connection of compressed air.
9. It should be Fitted with pressure gauges 100 mm diameter mounted on O2
and N2O cylinder (2 each) for clear visibility.
10. There should be Temperature compensated vaporizer for halothane/
isoflourine.
11. It should be Fitted with regulators and non return cum pressure release
valves for gases.
12. It should have Two Numbers oxygen pneumatic power outlets operating at
50 psi to operate ventilator.
13. It should have Extended rear platform for mounting two no. additional 10
liter water capacity cylinders.
14. It should have Patient circuit to include elephantine tubing reservoirs bag,
connections for change over from open to closed circuit and vice versa.
15. It should have Top tray for monitoring equipment
16. It should have Drawer for keeping instruments.
17. In other respects the equipment shall comply with IS-11378-1985.
18. It should have adjustable pressure limiting valve, breathing circuit pressure
measuring device.
19. It should have a bag/ventilator selecting valve integrated onto the absorber.
20. It should be suitable to use low flow techniques - Facility to attach oxygen
sensor.
21. It should have C02 absorbent dual chamber canister with provision to
change soda lime without disconnecting the circuit & during the operation..
22. It should have Automatic cutoff of nitrous oxide in case of oxygen supply
{nitro lock system} falls.
23. It should have Pneumatic device with audible alarm mechanical (not
electrical) when oxygen supply falls to 10-15 psi.
24. It should have Hypoxic safety device to ensure that the patient is never
subjected to pure N2O in flow out doses (shall ensure protection against
singular flow of N2O) until a minimum flow of 1 liter-1.5 liter oxygen released.
25. Unit shall incorporate oxygen analyzer (oxygen concentration level
indicator).
26. The Regulator and Yoke should force with S.S fittings.
27. The machine should have 3 inlets for O2 and N2O.
28. It should have 2 oxygen outlets
29. There should be at least one operating pressure gauge for O2 and N2O
separately.
30. The operating pressure should be 4.22 kgf/ sq.cm (+/-0.5% )
31. There shall be provision of adequate supply of oxygen to the patient even if
the flow meter knobs are fully turned off.
32. Unit shall conform to relevant safety standards and general safety
standards as per IS-8607.OR CE MARKED
33. It should have battery backup of 90 min.
Page 21 of 61
Item
code
2
Name of Equipment
Technical Specification
Anesthesia
Machine with
ventilator (without
compressor)
1. Technical Specifications:
1. Should be completely integrated system, with all components like Anesthesia
machine, Ventilator, Circle absorber, Vaporiser and Monitor should be from a
single manufacturer.
2. Should have provision for delivery of oxygen, nitrous oxide and medical air
with pressure gauges.
3. Should have independent attachments for connecting central gas supply and
pin indexed cylinders.
4. Should have analog display of cylinder and pipeline gas pressures
5. Should have provision to attach one cylinder for Oxygen and one for Nitrous
Oxide.
6. Digital/ electronic depiction of O2, N2O and Air Flow
7. Oxygen and Nitrous oxide should be linked to ensure a minimum of 25%
oxygen delivery at all times to avoid delivery of hypoxic mixture. Lever based
anti hypoxic device is not acceptable.
8. Should have back bar with ISO pin type to attach vaporiser easily.
9. Should have top shelf and a table top to keep drugs and equipments.
10. The machine should possess battery back up for ventilator.
11. Castor wheel should be durable and moisture resistant.
12. Unlockable oxygen flush to deliver oxygen flow of approximately 40 l/min.
13. Should have two deep drawers.
14. Should have Anesthetic Gas Scavenging System (AGSS)
2. Standard Circle Absorber System
1. Should have adjustable pressure limiting valve, breathing circuit pressure
measuring device.
2. Should have bag / vent selecting valve integrated onto the absorber and
should automatically turn on the ventilator when positioned to vent mode.
3. Should be suitable to use low flow techniques.
4. Should have facility to attach oxygen sensor.
5. Should have complete breathing system to be Autoclavable including
canister & bellows.
3. Vaporiser
1. Temperature, pressure and flow compensated.
2. Should provide keyed filler based Isoflurane and Sevoflurane vaporisers.
3. Should be easy to mount and dismount from the back bar.
4. Should have ISO pin type (Selectatec) back bar mount.
5. Vaporiser should be maintenance free for ten years.
6. Should have extended delivery range from 0 to 6 for iso and 0-8%vol for
sevo
4. Ventilator
1.Should be integrated with the anesthesia system, with bag in bottle
ascending type bellows or equivalent Technology Piston Technoloqv .
2. Should have tidal volume range from 5ml to 1500 rnl.
3. Should be able to set TV, RR and I:E ratio.
4. Should have 12" TFT colour display with touch screen and wheel based
adjustments.
5. Shall have the following modes: Ventilation modalities APCV ,APCV-TV ,
PSV ,APNEA BACK-UP ,SIMV ( Volumetric +PS,SPONT) ,VCNAC ,VCN AC
BABY ( integrated NEONATAL ventilation mode) , MANUAL
6. Ventilator should monitor and display integrated Oxygen monitoring, Inspired
and expired volumes ,PAW, Pressure waveform, Flow waveform and
spirometry loops
7. Ventilator should have Inspiratory pause, Sigh function, Patient trigger 5 –
15lpm.
8. Ventilator should have a max flow of 120 litres per minute in PCV mode..
9. Ventilator should provide all user alarms.
10.Ventilator should provide Fresh gas compensation and Compliance
compensation& Fresh gas decouplinq Fresh gas decouplinq
11. Ventilator shall have an active proportional exhalation valve to prevent the
potential of over delivery during pressure modes of ventilation.
12. On switching on, the ventilator system check can be bypassed in the case
of an emergency.
Page 22 of 61
Item
code
Name of Equipment
Technical Specification
13. Flow sensors measurement at the patient end of the circuit is preferred.
14. Should be supplied with necessary reusable and disposable breathing
circuits.
15. Resp. frequency from 4 to 120 bpm
16. I:E Ratio 1:1, 1:1.5, 1:2, 1:3, 2:1,3:1
17. Pressure from 10-100 cmH2O
18. Insp pause setting off 0 to 60% if insp time
19. PEEP from off, 3-30 cms H20 electronically adjustable
20. It should have battery backup of 120 min.
21. Should be CE OR ISO OR USFDA approved.
3
Ventilator (Adult,
Paed.)
It should be fully microprocessor controlled ventilator for Adult, Pediatric
and neonatal patients, facility to monitor respiratory parameter Should
be upgradable to Neonatal package in Future
It should be compressor based / Turbine; for compressor based system
compressor should be European CE Certified
It should be upgradeable design for software and hardware for new functions
and advance technology
It should be based on reliable flow measuring technology, preferably proximal
flow sensor which ensures the most precise flow and pressure measurements
for better patient assessment
Models of Ventilations :
It should have Assist - control Mandatory ventilator, SIMV, CPAP, Pressure
Support ventilation with APRV, DuoPAP/ Biphasic / BiPAP modes of ventilation
It should have combination modes : PRCV, PAV+/ auto mode, Apnea Backup
for safe ventilation offering both volume guarantee and lung protective
strategies like volume limit
It should have enhanced invasive as well as non invasive modes (NIV) with
mask - should be available as independent mode.
Parameter Settings :
Tidal Volume : 20 ml to 2000 ml
Respiratory : 4 to 120 BPM or better
Peak Flow: 0 to 120 lpm or better.
Trigger sensitivity : Flow 0.2 to 15 LPM, Pressure 0-20cmH20
PEEP : 0 to 35 cm H2O or better
FiO2 : 21 to 100%
I :E Ratio 1:10 to 4:1
Inspiratory time (TI) : 0.1 to 10 s
Pressure control: 1-100 em H20, added to PEEP/CPAP
Pressure support : 1 to 100 cm H2O, added to PEEP/CPAP
Pressure ramp : 0 to 2000 ms or 1-20 setting
Expiratory trigger sensitivity (ETS) 10 to 70% of inspiratory peak flow
It should have additional advance features like Manual breath, 02
enrichment, standby, screen-lock, apnea backup ventilation, inspiratory
Hold, , suctioning tool, Adjustable Brightness configurable quick start- settings
start-up over body height and IBW
It should have facility to permanently deactivate the O2 alarm, if the O2 cell is
depleted or defective
It should be integrated nebuliser synchronized with inspiratory cycle
It should have following alarms :
Low & high minute volume
Low & high pressure
Low & high tidal volume
Low & high Rate
Low & high Time
Low & high oxygen
Oxygen concentration, disconnection
PEEP
Exhalation obstruction
Flow Sensor & Power Supply
Display:
Page 23 of 61
Item
code
Name of Equipment
Technical Specification
It should have more than 7" inbuilt colour touch screen display with adjustable
scale and sweep speed
It should have real time waveforms for Paw, Flow and Volume
It should display trends for minimum of 1hr, 6 hr, 12 hr, 24 hr
Source input pressure of oxygen: 40 to 60 psi. Facility to also input low
pressure O2.
It should have battery backup of minimum 6 hrs. for complete system including
the compressor
Ventilator should be upgradeable to inbuilt EtCo2
Should be European CE & US FDA
Scope of Supply :
Basic Unit 220 V, 50 Hz
Modular Corrosion Free Trolley
Compress – European CE Certified
Thermostatically servo controlled Humidifier with reusable chamber and Heated
wire
Support arm for Breathing Circuit
Nebulizer
Oxygen Connecting Hose
Air Connecting hose
Reusable Flow sensor Qty 2 / Disposable Flow sensor - Qty 100
Reusable Breathing circuit for Adult pediatric Qty 2 / Disposable Breathing
circuit - Qty 100
Test Lung
4
Ventilator Portable
(Neonatal)
Suitable for Patients from 500gms to 10kgs
Compact ideal for transport or low cost NICU
Standard modes IMV(Pressure), CPAP
Fio2 monitoring is standard in all versions
Heated hose set and compact humidifier
Integrated air compressor
Apnea backup, NIV NIV YAPS YAPS
Tidal volume : 5 to 600 ml Our suggestion to add Tidal volume : 5 to 600 ml
Should have battery backup of 2 hours or more Our suggestion to add battery
backup of 2 hrs or more Trigger Flow: 1Ljmin to 15 Ljmin Pressure: 0.5 to 20
cmH20 Our suggestion to add Flow and pressure trigger.
The unit should have European CE & USFDA approved For quality assurance
both certifications necessary. Our suggestion to allow
European CE and USFDA certified product.
Certification: CE 0482
5
Ventilator Neonatal
Should be an upgradeable design with software/hardware upgradeability for
new/ future functions with inbuilt or integrated touch screen of more than 10"
Should have both invasive and non invasive ventilation mode available in the
same machine for use on neonatal and premature patients with suitable
accessories.
The ventilator should be supplied with heated servo controlled humidifier with
suitable hoses and chambers for neonatal patients.
Compact ideal for transport or low cost NICU
Standard modes IMV (Pressure), CPAP, TCPL
Fio2 monitoring is standard in all versions
Heated hose set and compact humidifier
Integrated air compressor
Should have standard Air compressor
Should have integrated filters to provide better air quality
Flow sensor:
The flow sensor should be of higher accuracy, Reusable
It should calibrate quickly within 5 seconds and data should be measured at
proximal end.
It should be easily replaceable without disassembling the machine or
disassembling the expiratory valve.
Page 24 of 61
Item
code
Name of Equipment
Technical Specification
At least 5 no.of reusable & autoclavable flow sensor should be supplied with the
equipments.
The ventilator should have ventilation modes as below: Pressure controlled
assist control, CPAP with continuous flow, TCPL, SIMV(TCPL)+PSV,
SIMV(VCV)+PSV,SIMV(PCV)+PSV, APRV ,CPAP+ PSV should have volume
limit/Volume guarantee function.
should have volume limit function
Should be slope control: 0 - 2 sec or equivalent.
should have setting for:
Tidal volume:25-300ml
Peak Inspiratory pressure : 3 to 50mbar
Flow independent PEEP : 0-25cm H2O
Inspiratory Time : 0.1-2 sec
Expiratory Time : 0.2- 30 sec
Maximum Rate (Based on Insp. Time and exp. Time): 150 BPM
Inspiratory flow : 1-30 BPM/ IPM
Expiratory flow (VIVE)(based flow) : 1- 30 BPM
slope control : 0 - 2 sec or 1-20 setting
FiO2 (Integrated blender without bleed flow):21-100%
Trigger : 1 to 5 IPM
i:e Ratio (dependant on insp. Time and exp. time) :3:1 to 1:3
Should have Trigger: Flow - 0.2 to 15 LPM Pressure - 0.5 to 20 mH20
Automatic altitude compensation : 780 -1060 hPa/mbar/cmH2O
The real time data should be monitored for:
Pressure- peak, plateau, mean, CPAP/PEEP
Expired Tidal volume (Monitored), Expired minute volume, leakage in %
Frequency / rate - set (Inspiratory), Spontaneous MV in % total, I:E ratio
FiO2
Integrated graphical trend
Integrated alarm log
Should have automatic alarm settings for all alarms with clear text messages /
corrective action for
Lung Mechanics - Resistance (insp & expi), Compliance (stat & dyn), Trapped
Volume, Time constant Te, RVR,
Disconnection
Tube blocked
Ventilation hose kinked
High / low pressure
High/ Low Minute Volume
High Rate
High Tidal Volume
Annoea / apnoea alarm time
FiO2 (high & low ) (user selectable)
Oxygen line failure
Compressed air failure
Total electronic failure (with error code)
Scope of supply should include
Basic Unit (220-240V)
Modular corrosion free Trolley- of same make as the quoted brand and no local
substitute will be accepted / should be offered
Silicon heated Hose set for use for neonatal patients.
Standard Servo controlled humidifier with reusable chamber.
Air Compressor European USFDA certified
Heated Flow sensor
O2 cell should be supplied till warranty
Nebulising facility
Oxygen connecting Hose of significant length
Air connection Hose of significant length
Hinged arm Support for patient circuit - should be of same make as the quoted
brand and no local substitute will be accepted / should be offered
Page 25 of 61
Item
code
Name of Equipment
Technical Specification
Nasal Prongs with headgear in three different sizes .(0,1 & 2 ) Qty-10 each of
different sizes.
Respiratory mechanics: Compliance (stat & dyne) Resistance (insp. & exp.)
Trapped Volume Slow Vital Capacity
Instruction Manual
Quality Standards and Support requirementsShould be European CE & US FDA
the unit should comply with relevant IEC Certification
A Complete system include air source should have two hour battery backup. &
without compromising on delivered Fi02.
Should have more than 10" inbuilt color touch screen display with adjustable
scale and sweep speed or automatic scale adjustment and sweep speed.
It should have real time waveforms for Paw Flow and Volume
It should display trends for minimum of 1hr, 6hr,12hr, 24hr.
It should have battery backup of minimum 6hrs. For complete system including
the compressor, air source mounted on same trolley / stand.
It should have international safety standards and requirements with European
CE 0482 or US FDA approved.
Scope of Supply
Basic Unit 220 V, 50 Hz
Modular Corrosion free Trolley
Compressor- In compressor based system; compressor should be of the same
manufacturer of OEM with CE marking.
Thermostatically servo controlled Humidifier with reusable chamber and Heated
wire.
Support arm for Breathing Circuit
Nebulizer : Volume compensated , sterlisable Nebuliser should be supplied.
Oxygen Connecting Hose
In case of compressor based system Air connecting hose should be supplied.
Reusable and autoclavable Flow sensor for adult and pediatric - Qty 2 each &
Disposable Flow sensor -Qty 100
Scope of Supply Reusable and autocleavable Breathing circuit for
neonatal patient Qty. - 03/ Disposable Breathing circuit -Qty 100,
Should provide mask With separate harness for neonatal patient with each
breathing circuit.
6
Ventilator Portable
(adult, ped.)
1. Should be suitable for emergency and critical care use by professionals in
pre-hospital and hospital settings.
2.Suitable for adults, children and infants operations
3.Should have Emergency preset mode for adults, children and infants, which
can be used in case of emergency and when doctors/professionals are not
available.
4. Should have provisions for wall mounting.
5. Should be light weight, robust and user friendly
6. Should have ability to show waveforms & loops PV, FV, FP
7. Should have large colour TFT display of min. 6" size, with option to change
into night mode
8. Modes of Ventilation: IPPV,SIMV & PRVC, BiPAP, CPAP with ASB & PCV,
Apnea, NIV
9. Should have adjustable FiO2 21% to 100%.
10. Should have option to give Oxygenation in case of emergency.
11. Should have optional EtCO2 Monitoring and can be upgraded later
12. NIV should be able to operate in all modes.
13. Should have leak compensation facility.
14. Should have the measurements of p-Peak, p-Plat, p-Mean.
15. High inflation pressure alarm.
16. Should have visible bright red alarm light and volumes should be regulated
separately for adjusting limits as per requirement.
17. Should have battery back up of 4 hours and one additional battery should
be provided.
18. Charging time of battery should not exceed 4 hours.
Tidal Volume : 20ml to 2000ml
Rate : 0 to 80/min
Page 26 of 61
Item
code
Name of Equipment
Technical Specification
Pinsp. : 5mbar to 60 mbar
Pressure support (ASB) : 0 to 30 mbar
PEEP : 0 to 30mbar
I:E ratio : 4:1 to 1:4
Maximum flow : 150 L/min
Trigger Flow : 1L/min to 15 L/min
Should be European CE & US FDA
7
Central Monitor
1.Central Station .
It should have large screen (min21”), medical grade resolution TFT/LCD
monitor (1600X1200) with a real time and review screen
Alarms should also be configurable from/at the central station
It should be possible to delete/change/stop an event recognition that is an
artifact or erroneous/ not needed. A high end black and white laser printer
should be provided.
2. Server should have state of the art processor, > 4 GB RAM, 1TB memory
inbuilt / external CD/DVD writer, USB ports and necessary software (including
updateable /up gradation antivirus if needed.
3. A complete UPS system with 15 mins backup will also have provided in the
quoted price.
4. Compatible at least for 10 beds, upgradeable to 32 beds
Installation and cabling should be done by manufacturer
Central monitor should be treated as part of other monitors.
Should be of same make
Laser printer should be provided.
Should be CE or ISO or USFDA approved
8
Defibrillator
Defibrillator should be Bi- Phasic, light weight and latest model
Should monitor vital parameters and display them
Should print the ECG on thermal recorders.
Should work on Manual and Automated external defibrillation (AED) mode.
Manual selection up to min. 200 J.
Should be capable of doing synchronized & asynchronized cardioversion.
Can be operated from mains as well as battery
Should have defibrillator testing facility
Should be a Low Energy Biphasic defibrillator monitor with Recorder, having
capability to arrest all arrhythmia within a maximum energy of 200 (min) Joules
Should monitor ECG through paddles, pads and monitoring electrodes and
Defibrillate through pads and paddles.
Should have Automatic Lead switching to see patient ECG through paddles or
leads
Should measure and compensate for chest impedance for a range of 25 to 150
ohms
Should have a built in 50mm strip printer/ thermal recorder
Should have charging time of less than 5 seconds for maximum energy.
Charging indicator should be there.
Should have bright electroluminescent display for viewing messages
ECG waveform of 4 seconds
and
Should have external & internal paddles with paddles contact indicator – for
good paddle contact.
Single Adult and pediatric paddles should be available.
Should have event summary facility for recording and printing at least 250
events and 50 waveforms.
Should have a battery capable of usage for at least 90 minutes or 30
Page 27 of 61
Item
code
Name of Equipment
Technical Specification
discharges.
Should be capable of printing Reports on Event summary, configuration, self
test, battery capacity etc
Should have facility for self test/check before usage and set up function
Should be capable of delivering energy in increments of 1-2 joules up to 30J
and increments of maximum 50J thereafter.
Should have user friendly 1,2,3 color coded operation.
It should have Automatic internal discharge of charge on paddles when unit is
turned off
The equipment should have US FDA or C.E. approval and documentary
evidence to that effect shall be submitted the equipment must be having
Operating temp. : upto 40degC
Storage room temp : upto 55degC
Relative humidity : upto 90% non condensing
9
ECG machine(with
trolley)
1. LCD Display with 320X240 pixels resolution. Data to be display Heart rate,
patient name, ID, ECG curves, electrode control, ADS, clock, leads, speed,
filter settings.
2. ECG Acquisition AUTO (12 leads), RHYTHM (3 and 6 pre-set lead
selections)
3. Signal Processing/Acquisition Sampling Rate more than 1000 samples per
second per electrode/lead.
4. 24-bit A/D conversion provides 5µV resolution.
5. Auto Frequency Response 0.05-150 Hz, 0.15-150 Hz, 0.5-150 Hz, 0.05-100
Hz,0.15-100 Hz, 0.5-100 Hz, 0.05-40 Hz, 0.15-40 Hz, 0.5-40 Hz.
6. Rhythm Frequency Response 0.05-150 Hz, 0.15-150 Hz, 0.05-100 Hz, 0.15100 Hz, 0.05-40 Hz, 0.15-40 Hz, 0.15-100 Hz, 0.5-100 Hz, 0.05-40 Hz, 0.15-40
Hz, 0.5-40 Hz.
7. Filters: AC, Artifact, High and low pass
8. Printer: High-resolution, digital-array printer using thermal-sensitive A4 size
paper
9. Report Formats: 3x4, 1R & Rhythm (3 and 6 pre-set lead selections)
10. Power supply: AC with built-in Replaceable and rechargeable battery.
Voltage rating: 220-240 V/110-120 V.
11. Battery Capacity: 30 minutes of continuous rhythm recording.
12. Battery Recharge Eight hours to full capacity.
13. Should be able to store at least 100 ECG tests in test directory and internal
memory to store up to 50 patients information and USB connectivity to store
and transfer patient data
14. Gain settings for Auto ECGs : 2.5,5,10,20mm/mV ; for rhythm ECGs :
2.5,5,10,20 mm/mV
15. Unit should include battery, lead wire, and electrode pack and paper pack
16. Must be CE or US FDA certified.
10
Infusion pump
1) Should have delivery rate settings in both the mode i.e. Drops/Min. and
Ml/Hr. setting can be done by the Nurse/Para Medical Staff by using up & down
button
2) Air Bubble detection helps to detect air bubbles having size of 50 ul or larger
size.
3) LCD/ LED Display with 5 inches and above pixels resolution. Data to be
display
heart rate, Patient Name ,ID,ECG Curves, Electrode Control, ADS
Clock,Leads,Speed,Filter,Settings.
4) Both Audio & Visual alarm.
5) Small Size to economise on Space in I.C.U. & O.T. (Not bigger than
9cmx20cmx20cm)
6) Standard I.V. Sets of all brands can be used.
Page 28 of 61
Item
code
Name of Equipment
Technical Specification
7) Fuse in Power Cable, for protection of equipment in case of power
fluctuation.
8) Flow rate range : 1-1500 ml/h in normal mode (1ml/h increment). 0.1-99.9
ml/h in micro mode(0.1 ml/h increment)
9) Flow rate accuracy : +/- 5% and even better in most clinical situations
10) Should have Dose time mode
11) Should have OCS (occlusivity check system)
12) Battery : Li-Ion , battery life at least 8 hours at 100ml/h
13) Should provide display of battery charge level available and remaining
battery life.
14) Should be certified with CE or ISO 13485
15) Bolus 1500ml/h adjustable from 50 to 1500ml/h in 50ml/h increments.
(manual or Programmable)
11
Multipara Monitor 5
para with NIBP
Specification for Multipara monitor 5 para with NIBP, preferably with Masimo /
Oximax technology
Multi parameter monitor suitable for adult, pediatric and neonatal, for
monitoring
It should have following parameters :
ECG
Non-Invasive Blood pressure
Oxygen Saturation (Pulse Oximeter)
Respiration
Temperatures
It should have minimum 12" TFT Display
It should have Modular upgradeable design with 24 hours trends and user
defined alarm setting for all parameters
It should display 3/5 lead ECG selectable
It should be able to display at least 6 waveforms with facility of overlapping
pressure wave form. Apart from the capability of accepting the above parameter
modules monitor shall be capable of accepting two more invasive blood
pressure modules i.e. total three IBP modules.
Should have a Wall mount stand with skirting borders and rotating base for
easy adjustability can be considered for ICU bedside monitors.
All modules in the monitor should be replacable externally in the console by
Doctors / Paramedical Staff without need for turning off and without opening the
console.
All monitors to have modules for all parameters.
E.C.G.
Numeric display of Heart Rate in range : 20 - 300 BPM with resolution 1
Accuracy : +/- 1 beat per minute
ECG with arrhythmia capability (adult and pediatric) and ST details
Electro cautery and defibrillator pacer rejection capability
Accessories: a) 5 Lead ECG cable - 2 Nos.
NIBP
i) Should measure and display systolic, diastolic and mean pressure
ii) Mode of operation : Automatic, Manual and Stat
iii) Cuff inflation / deflation automatic.
iv) Inflation pressure shall be automatically released if error.
v) Measurement Range 20- 250 mm Hg. Resolution 1 mm Hg, Maximum error
+/- 5 mm Hg
vi) Measurement interval : 2,3,5,10,15,30 minutes, upto 4 hours
vii) Reusable NIBP cuff size for neonates should be 2, 3 and 4 cms
viii) Accessories : Disposable NIBP cuff : 3 Adults, 2 pediatric, 2 neonates each
size should be provided per monitor
Pulse Oximeter
i) O2 saturation : 0 to 99%
ii) Accuracy : +/- 2% between ranges 70 to 100%
iii) Motion artifacts should not affect the readings
iv) Display of pulse strength, plethysmography and Spo2 values
v) Accessories: Reusable finger - adult and pediatric probes 1 each per monitor
should be provided. Also neonatal probe should be provided.
Respiration (Part of ECG)
i) Range o to 150 breaths per minutes
Page 29 of 61
Item
code
Name of Equipment
Technical Specification
ii) Resolution : 1 breath / minute
iii) Accuracy : +/- 2 breaths / min or +/- 2% which is greater
iv) Apnea Alarm : selectable 10, 15, 20, 25, 30, 35, 40 s
Invasive Blood Pressure :
i) Display of systolic, diastolic and mean pressure
ii) Min. scale range : 30 to 300 mm Hg (user selectable)
iii) Measurement range : 15 to 300 mm Hg
iv) Resolution : 1 mm of Hg
v) Accuracy : +/- 1 mmHg or +/- 2% whichever is greater
vi) Accessories : 50 nos. disposable transducers with two reusable cables per
monitor should be provided
Temperature
i) Simultaneous monitoring of two channels
ii) Range 15 to 44 degree C (59 degree F to 113 degree F)
iii) Resolution : 0.1 degree C
iv) Accuracy : 0.1 degree C or 0.2 degree C
v) Accessories : Skin probes and rectal probes 1 each per monitor to be
provided
General Requirements
1. All the modules should be defibrillator and surgical diathermy proof.
2. All software upgrades should be provided free of cost during the period of
warranty and AMC
3. Accessories should be indicated at Standard
4. Power supply : 230 V +/- 15%, 50 Hz +/- 3% the monitors shall have to be
operated on mains with built-in-re-chargeable battery. Back up of min 2 hrs.
The battery and charger shall be in the monitor itself.
( Please include all other requirements same as basic monitor)
General Requirements
All the equipments shall be new and manufactured from virgin materials. All the
requirements of this supply shall be sourced from the original equipment
manufacturer of the model quoted. In case this machine is imported one no
import substitution is permitted neither before the award nor after the award for
any part or accessory. Third party inspection certificate should be applied from
the port of origin of shipping of equipment (from the parent companies country
of origin)
Equipment shall operate on 230 V, 50 Hz and single-phase electric supply. The
necessary protective relaying / circuitry shall be there with the machines. The
main supply voltage variation may be max 15% and frequency variation max
3%.
The equipment shall be US FDA or C.E. approval and documentary evidence to
that effect shall be submitted
The equipments shall be having warranty of 2 years as described in the tender
document elsewhere. The warranty and CMC shall cover the X-Ray tube
irrespective of whether those are treated as consumables or otherwise.
The equipments should be provided with one hard copy in Original of the
detailed service manual and operation manual. Further, a soft copy is also
required.
Repairs and maintenance training should be given
The equipment must be tropicalized as below Operating room temperature : upto 40 degree C
Storage room temperature : upto 55 degree C
Relative Humidity : Upto 90% non condensing
12
Multipara monitor
with IBP and EtCO2
Minimum 12 inches or more multi colored Medical grade TFT display screen.
preferably with Masimo technology.
Separate CPU/Module rack.
Eight digital and waveforms/traces display
Combination of single, dual and multi parameter modules.
Parameter modules freely exchangeable between all the monitors.
Multi channel (up to 12 leads) ST segment analysis.
Facility to monitor and display - ECG, Respiration, NIBP, SPO2, IBP – 4 Nos.,
CO2 with capnography, Temp, Cardiac output, NMT, BIS/Entropy ,
Gastrictonometry (optional) & IBP – 2 nos.
Automatic arrhythmia detection & alarm for standard and lethal arrhythmia.
Page 30 of 61
Item
code
Name of Equipment
Technical Specification
EtCO2 -Main stream/ side stream. Display both inspired and expired values,
showing capnography.
NMT Module/monitor: For measurement and display of TOF count, TOF %, ST,
DBS, Tetanic and Trend for continuous usage. Automatic measurement facility
in selected time interval. Automatic selection of supramaximal current. Include
standard accessories.
ECG Module with all accessories.
Should provide hemodynamic, oxygenation Ventilation calculation package.
Should have drug calculation package.
Trend of at least 24 hours.
200 nos. event recall/snapshot facility both manually and automatically
triggered by alarm. Automatic zoom in facility in the monitor display.
The monitors should have monitor-to-monitor overview facility and data transfer
over the network.
Web browsing facility to review each networked monitors data through hospital
LAN via office PC in Hospital LAN Network and/or through dial up facility from
remote location Communications with Information Management Systems:
Should be compatible with hospital’s network.
To provide HL-7 compatible server for sending and receiving information to and
from the monitoring network to and from Hospital Information System,
Laboratory information etc for integration of various information (OPTIONAL)
Integrated or external printer for report output.
System Configuration Accessories, spares and consumables
ECG/Resp.: 5 Lead ECG Cable with clip- 2 sets per monitor and 10 Lead ECG
Cable with clip- 1 set per monitor.
NIBP: Adult cuff- 2nos. per monitor and two sizes of pediatric cuffs- one per
monitor (complete sets)
SPO2: Adult SPO2 sensor with cable- two nos. per monitor and Pediatric SPO2
sensors- one no. per monitor.
IBP: Include four nos. per monitor of reusable pressure transducer with bracket,
holder and 100 nos. disposable domes per monitor.
Temperature: Rectal temperature probe- two per monitor and skin temperature
probe- two per monitor.
EtCO2 module with all accessories. In case of side stream EtCO2-10 sets of
sampling tubes for each module to be included.
Built in rechargeable battery
Should have apnea alarm
Low battery audio and visual alarm
Waveform Freeze option with scrolling upto 60sec.
Should have stand for monitor and cables.
General Requirements
All the equipments shall be new and manufactured from virgin materials.
All the requirements of this supply shall be sourced from the original equipment
manufacturer of the substitution is permitted neither before the award nor after
the award for any part or accessory.
Third party inspection certificate should be applied from the port of origin of
shipping of equipment (from the parent companies country of origin)
Equipment shall operate on 230 V, 50 Hz and single-phase electric supply. The
necessary protective relaying / circuitry shall be there with the machines.
The main supply voltage variation may be max 15% and frequency variation
max 3%.
The equipment shall be US FDA or C.E. approval and documentary evidence
to that effect shall be submitted
The equipments shall be having warrant of 3 years as described in the tender
document elsewhere.
The warranty and CMC shall cover the X-Ray tube irrespective of whether
those are treated as consumables or otherwise.
The equipments should be provided with one hard copy in Original of the
detailed service manual and
Operation manual. Further, a soft copy is also required.
Repairs and maintenance training should be given.
The equipment must be tropicalized as below -
Page 31 of 61
Item
code
Name of Equipment
Technical Specification
Operating room temperature : upto 40 degree C
Storage room temperature : upto 55 degree C
Relative Humidity : Upto 90% non condensing
13
Pulse Oximeter
Pulse-oximeter (Table-top model)
• Table top design
• Low perfusion, Motion artifact rejection
• Light, compact, portable masimo/ oximax technology
To include: 2 Adult probes & pediatric size finger tip probes, Rechargeable
batteries
Display- LCD, Backlight illuminated
Parameters and waveform displayed- SpO2, pulse rate, system status,
plethysmogram, menus for user settings
SPO2 range- 70-100 %
Accuracy SpO2 for Adult, Pediatric & Neonate- 70% to 100% (+ - 2 digits) & 6
Pulse rate range should be 30-240 bpm
Audiovisual Alarms- High/low SpO2 and pulse rate, sensor off, sensor failure,
low battery
Should includes neonatal probes also
Alarm override facility / battery backup of minimum 3 to 4 hrs
Cable length
Should be CE or ISO or USFDA approved
14
Syringe pump
1. Should hold Syringe of 5, 10, 20, 30/35, 50/60 CC capacity.
2. Auto Syringe detection.
3. Large Delivery rate 0.1 - 99.9 ml/hr.
4. LCD Display, color screen.
5. Audio Visual alarm.
6. Bolus rate (manual)
1200ml/h(50ml syringe), 600 ml/h(30ml syringe), 400ml/h(20ml syringe).
7. Display Total volume delivered(Σml)
8. KVO(Keep-Vein-Open) Rate (0.5±0.2)ml/h
9. Occlusion Pressure (KPa)
High level: 100KPa; Medium level: 60KPa; Low level: 40KPa
10. Alarms: Near Empty alarm; Infusion complete alarm; Occlusion alarm; Low
Battery alarm, Mains Power off alarm
11. Power: AC 100V~240V, 50Hz/60HZ; DC12V, Rechargeable batteries can
work more than 2 hours after 15 hours fully charged.
12. Flow rate Accuracy : +/- 1% on mechanism ; +/- 2% on syringes
13. Infusion modes : a. mL/h (0.1 ml/h increments)
14. Anti-Bolus System: reduces significantly bolus after occlusion release (0.2
ml approx.)
15. Drug Library: Initial drug list of 50 agents adjustable with Vigilant R, the IV
medication safety solution.
Adjustment of the dilution , authorized infusion modes, default infusion modes,
flow rates and bolus limits in ml/h
16. DPS (dynamic pressure system) should incorporated to avoid risk of
obstruction or possible leak.
17. Should be certified with CE or ISO 13485
18 Auto/ manual keypad locking system should not be locked.
15
Semi Automated
Elisa Reader &
washer
Microplates :- 96 well plates
Optical System:- quartztungster halogen lamp {8v/50w} chopper wheel,
aperture condenser lens, semitransparent mirror, interference filter, fiber bundle
focusing lenses, upper lenses and detectors,
Wavelength range :- 400-750nm
Filter:- 8 positions filter wheel standard filters 405nm, 450nm and 620nm
Page 32 of 61
Item
code
Name of Equipment
Technical Specification
Hall bandwidth of filters:- 3-9nm
Wavelength accuracy:- + _ 2nm
Detector:- Eight silicon photo detectors.
Measuring range :- 0-4.0 Abs
Resolution 0.001 Abs
Integrated printer should be provided.
Linearity :- 0-2 Abs, + _ 2.0% at 405
Accuracy:- 2.0%or + _ 0.007 Abs whichever is greater, typical value+ _ 1% (02.0Abs} at 405nm
Precision: - cv < 0. 5%{0.3/1.5.Abs}at 405nm Cv < 1.0% { 1.5-2Abs} at 405nm
Start- up time :- one {1} minute
20s/96-well plate { stepping mode}
Auto blanking procedure should be available.
Shaker: - linear shaking, 3 speed
alphanumeric LCD display
Onboard software:- primary EIA, cutoff and cubic spline calculation programs.
and provision for LG chart for quality control purpose.
UPS back up for elisa reader
Programs:- 50 to 60 user- friendly programs
Interface: - RS 232c serial interface.
Centronics type parallel printer interface.
ELISA WASHER:
Washer should have 8 and 12 channel wash head.
User friendly programs for different elisa kits.
16
Bedside ABG
Analyser
1) The instrument should have accurate bedside results in about 30 seconds
2) It should have barcode test cards for quality and inventory management
3) The analyser should have data capture and transmission
4) There should be HCT parameter NOT HCL as per parameter.
5) The analyser should include calculated parameters like CTCO2,
CHCO3,BE,SO2,CHgb
6) It should have input characters for patient temperature, Hb type.
17
3 Part Heamatology
Cell counter
1) Heamatology analyser with 18 parameters, 3 parts diffential count
2) Large screen to display all parameters along with histograms.
3) 50µl sample in whole blood mode and 20µl in predilute mode.
4) Cyanide free Hb method
5) Throughput: Approx 60 sample/hr
6) Highly Accurate Detection Technology including Highly precise sample rotor
valve ( SRV) Pressure Syringe
7) Data storage : 240 patient result
8) Precision: (Whole blood mode)
WBC: 3.5% OR less, RBC:2%, Hb:1.5%, HCT:2%, PLT:6%
9) Linearity (Whole blood mode) : 2 to 5%
10) Power consumption : 230VA OR less
11) Long calibration stability
12) Simple touch key for sample analysis
13) Patented aperture technology
14) It should have integrated micro- processing technology
15) Excellent after sale service reputed use's list
18
Semi Automated
Biochemistry
Analyser
1) It should be microprocessor controlled, programmable, semi autoanalyser to
perform routine biochemistry tests (including endpoint, fixed time & kinetic
assays), enzyme immunoassays (with multistandard curve calibration &
memorisation) etc.
2) It should offer a minimum of 150 user definable chemistry parameters with
result memory of atleast 1000 results.
Page 33 of 61
Item
code
Name of Equipment
Technical Specification
3) It should have optional battery back up system.
4) It should have a peltier controlled reading block and flowcell volume less
than 20 µl with temperature programmable for 25, 30 & 37° C.
5) It should require minimum reagent per test typically not more than 500 µl /
test.
6) Key pad to Access the chemistry programs directly and alphanumeric Patient ID.
7) Flowcell with peristaltic pump should be part of the main unit.
8) It should have facility to use both 6mm glass cuvettes and 10mm plastic
cuvettes additionally.
9) It should have minimum 7 narrow band static interference filter with
wavelength selectable from 340 - 650 nm.
10) lt should have a minimum 6 lines LCD display alphanumeric display and
built-in full graphic printer for printing reaction curves and test results.
11) lt should have the facility to display the actual temperature on screen
especially for fixed time and kinetic tests.
12) lt should have facility to store reagent blank O.D., standard blank O.D., QC
data, minimum 500 tests 'results and capable to recall store results patient 10
or date-wise.
13) The software should be user friendly and guide the programmer step by
step. It should have the facility to connect to Key board and Printer directly .
14) The instrument should also be capable of doing coagulation assays
15) The manufacturer / supplier should have a full-fledged service force and
installation base for the quoted equipment.
16) The manufacturer/supplier should be able to provide their own reagents
required for functioning of the instruments.
17) It should follow international standard/safety requirement, CE or USFDA
approval.
18) Demonstration compulsory and training to MEC Engineers and laboratory
staff.
19) Operating and detailed service manual should be provided.
20) Power supply :230V +/15%,50hz+/3%
21) Tropicalisation : operating temperature upto 40'C,storage upto 60' C,
relative humidity upto 90% non condensing.
19
Electrolyte
Analyser
1. It should be an easy operation instrument for Electrolytes Na + ,K +, CLbased on the principal of Ion Slective Electrodes.
2. It should perform the test using whole blood, serum plasma and Urine.
3. The required sample volume should. not be more than 150 micro liters for
whole blood, serum and plasma and 400 to 450 micro liters for Urine.
4. It must have automatic probe wiping facility to avoid manual contaminations.
5. After every sample analysis, While cleaning the electrode path All Analyzers
does one point calibration
6. Apart from automatic calibration the user should be able to calibration the
machine as, and when required.
7. The sample processing time should not be more than 60 seconds (for whole
blood, serum and plasma) and 100 seconds for urine samples.
8. The instrument should be to store minimum 12 patients result in its memory
and minimum 15 normal and 15 abnormal Q.C. result for quality reports.
9. The Electrodes should be preferable maintenance free or easily maintainable
with minimum possible keys of the instrument.
10. The reproducibility of the result should not very more than CV < - 2% ( for
whole blood, serum and plasma) and CV<- 5% (for Urine)
11. Operators manual and detailed service manual to be supplied along with
machine.
Page 34 of 61
Item
code
20
Name of Equipment
Technical Specification
ESR Analyser
1) The analyser should have an inbuilt miner for automatic mining of samples
with anticoagulant
2) Throughput should be 100 tests/hour
3) Sample volume should not exceed 1.2ml
4) Built in quality programme for precise and accurate evaluation
5) It should permit bidirectional data transfer
6) It should permit external barcode reader interface
7) Comprehensive service backup by the established company
8) It should be USFDA or CE approved.
21
Heamatology 5 part
Cell counter
Automated heamatology analayser with precise CBC results, including 5-part
differential
Flow cytometry method using a semiconductor laser
Hydrodynamic focusing DC detection method (RBC, RFT)
Throughput : Upto 60 to 100 samples /hr
Sample volume : 20-80ul manual mode, 20-40ul capillary mode
Data storage: 1500 Sample & upgrade to USB drive also
Power consumption : 150 VA or less
Semi conductor laser
External Barcode reader
Manual cap piercing unit
CBC mode, CBC + Diff. mode
Linearity +5 -10%
22
Fully Automated
Biochemistry
Analyesr
1) It should be discrete, Patient Prioritized, Automated, Random Access, Walk
away Clinical Chemistry Analyzer for Routine chemistries, Immunochemistry.
2) It should have throughput of not less than 300 Tests I hour
3) The reagent tray should have at least 48 positions for reagents with a
capability to run up to 2 reagents per test.
4) The Minimum Reagent requirement should be 280 IJL I test or less.
5) It should have a facility of on board cooling for all reagent bottles
6) The Photometric range should be from 340-750 nm using diffraction grating
and the system should offer minimum of 12 wave lengths
7) The absorbance range should be between 0 - 3.0 Abs.
8) The instrument should have two separate reagent arms along with two
separate mixers for performing double reagent test.
9) It should be capable of storing 95 Test Programs,9 profiles ,9calculated
items and 250 doctors name in its memory.
10) It should have sample tray to accommodate at least 50.samples
11) !t should be able to load primary tubes( 5,7 or 10ml) and also sample cups
12) It should have separate dedicated Standard tray with minimum 20 position
for standards/calibrators, 2 blanks and 7 controls on the same tray. The
analyzer should allow loading 20 stat/emergency samples on this standard tray.
13) It should have permanent/Semi permanent glass/Plastic reaction curettes.
14) It should have on board laundry with low deionised water requirement of not
more than 9 liters/hr.
15) It should have vertical obstruction detection for detection of any obstruction
and protection of needles from any possible damage.
16) It should have Q.C option with daily & monthly L-J graph and twin plot
facility, with facility to get analytical flags on proper inputs.
Page 35 of 61
Item
code
Name of Equipment
Technical Specification
17) It should have reagent monitoring facility with the real time display of the
reagent level and the message for refilling or replacing the reagent.
18) Incubation bath should be of dry bath/Water bath.
19) It should have level detection method for reagents and samples to provide
accurate level detection
20) The unit should have facility of recalculation of results for last 700 reactions.
21) It should have the facility to store at least 700 reaction curves
22) The unit should be able to collect Bio-hazard waste in a separate container
23) The unit should be supplied with weight based level sensing platform with
facility to give alarm for keeping the D.I.Water tank, cleaning solution tank ,biohazard waste tank and normal waste tank.
24) The unit should be supplied with the appropriate configuration of CPU,
monitor, keyboard, mouse and printer.
25) The unit should be able to' provide the calibration trace data, test statistics
and it should allow to do the offline entry of the results also.
26) The manufacturer should have CE or ISO certification.
23
ABG Machine
Sample size : As minimum 1ml sample is collected for ABG sample volume up
to syringe 150 ul should allowed.
Sample Type: Whole blood & Dialysate fluid
Analysis time : 60 seconds
Calibration: Automatic on demand
Input Parameters
Temperature: 10.0°C–43.9°C
Hemoglobin:2.0–25.0 g/dL
FIO2 : 15.0%-100%
Patient/Operator IDs: Up to 20 characters (alphanumeric)
Sample location: Radial, brachial, femoral, cord, arterial & Veins
Display Interface :color touch screen icon based
Storage Capacity/ Memory : Up to 250 patient test records. Up to 90 results for
each level of QC
Environmental
Temperature :15ºC–32ºC
Humidity: max. 85% at 32ºC non-condensing
Barometric Pressure :400-825 mmHg
Power Requirements
Rating : 80VA
Voltage: 100-240V
Frequency: 50/60 hz
Should be USFDA approved
24
Refrigerated
Centrifuge
1) For separation of blood component like pack cell, fresh frozen plasma,
platelet rich plasma, platelet concentrate, Cryoprecipitate & buffy coat.
2) Wind Shield swinging bucket rotor with oval metal buckets having middle
partition, Total Capacity upto 6 X 1900 to 2000ml, for 12 Quadruple blood
bag systems of 350ml/450 ml with SGAM bag and I
3) Easy to clean, corrosion resistant with provision of both drain and condensed
water collection container.
4) Temperature control Range :- 20c to +40c, Minimum Temperature at
maximum speed <or = 4c
5) Quite Operation Noise Level:- < or =58 Db
6) Provision for to stored data ( tamper proof)
7) Removable Plastic inserts to spin double blood bag system, supplied with
four variable balancing weights ( set of pairs)
8) Plastic inserts with hook adapters to spin buffy coat or small volume of blood,
supplied with four variable balancing weights ( set of 6 pairs) hangers
9) Digital display of temperature, speed/rct, time, accel/decal, program Number.
Page 36 of 61
Item
code
Name of Equipment
Technical Specification
10) Micro processor controlled rotor speed adjustable in steps of 10 RPM/RCF
11) Safety Features: Lid -lock, interlock, imbalance detection with automatic
shut down of centrifuge, steel - armored chamber, over temperature protection
for rotor.
12) Power Requirement: 230V, Single Phase, 50Hz, 32 Amps, Supplied with
voltage stabilizer of 10KVA capacity
13) Energy Efficient Performance, Power Consumption:. 4.2 K W
14) Should be CE or UL Certified or ISO or IEC / EN 61010/61326/60529
approved.
25
DEEP FREEZER
80°C)
(1) Temperature- -80Dc ± 2c
2) Controlling resolution: O. l c
3) Mounting i- castor wheels
4) Voltage stabilliser : External stabilizer
5) Display resolution:- 10c
6) Recording is made on a weekly chart paper
7) Battery backup: battery for 12 hour
8) Cabinet material: - corrosion resistant.
9) Capacity:- ( 320 to 320 units of plasma bags)
10) No. of Trays: 3 to 4 trays
11) Doors: PUF insulated door with rubber gasket sealing and level type lock
12) Audio - visual alarm :- indication for 1 stage compressor, 2 stage
compressor, high temp, low temp, door open, power failure, battery low system
ok, chart range condenser clogged etc.
13) Temperature Controller:- microprocessor based digital temp controller
14) Temperature Hold Time during Power Failure: Minimum 4.2 Hours
15) Standard & approval:- ISO or CE Marks
26
Deep Freezer- (40°c)
Tempt - -400c± 2°
Temperature:-Temperature is maintain minus 40 ° c
Controlling resolution:-O.5C
Bag capacity:-300 to 320 plasma bags
No. of Tray:-3 to4 no.
Display resolution :- 0.5 c
a. Recording:- / weekly /
b. Cabinet material :- External- MS sheet, power coated after 7 tank process,
Internal- stainless steel sheet.
Mounting:- The unit is mounted on castor wheels
Condensate evaporator: - Automatic evaporation of the condensate.
Internal Lighting: - Flicker free CFL.
Trays:- sliding trays ( stainless steel)
Doors:- Double door, MS exterior, Locking Facility.
Standard & Approval:- ISO or CE Marks Available.
27
Blood Bank
refrigerator for
Blood storage for
2°c to 8°c
1. Temperature- 2°c to 8°c
2. Cntro/ling resolution: O. 5°c
3. Bag Capacity :-300 to 350 bags
4. Number of trays:-4 to 6
5. Mounting:- castor wheels
6. Voltage stabilizer: External stabilizer
7. Display resolution:- 10c
8. Recording is made on a weekly chart paper
9. Battery backup: battery for 12 hour
a. Cabinet material :- External- MS sheet, power coated after 7 tank process
Page 37 of 61
Item
code
Name of Equipment
Technical Specification
i. Internal - stainless steel sheet Capacity :- ( 300 to 320 units of plasma bags)
10. No. of Trays: 3 to 4 trays
11. Doors: PUF insulated door with rubber gasket sealing and level type lock
12. Audio - visual alarm :- indication for 1 stage compressor, 2 stage
compressor, high temp, low temp, door open, power failure, battery low system
ok, chart range condenser clogged etc.
13.Temperature Controller:- microprocessor based digital temp controller
14. Temperature holding time during power failure is 145 Minutes or better.
15. Standard & approval:- ISO or CE Marks
28
Refrigerator General 300 ltr
1.Minimum Gross storage Capacity : 310 to 330 ltrs
2. Model Type : Double door
3. Voltage range at 40 deg. Centigrade : Capable of working on 220 volts + 12
% A.C 50 Hz
4. Power source : AC , 220 Volts to , 50 Hz
5. Method of Defrosting : Frost Free
6. Insulation : Puff / Maxi 2 / Polyurethane
7. Refrigerant gas : CFC free
8. Compressor : Power saver compressor
9. Accessories required : Adjustable shelves , chiller Tray , Temperature
controller Auto lamp On/off feature , should be supplied with all standard
accessories as per manufacturer catalog for the model supplied
10. Stabilizer Should be supplied with required capacities – CVT (Continuous
Variable Transmission) type without any extra cost.
The CVT will also carry 2 years warranty.
11. Colors Steel grey with metallic finish ( Metallic Color)
Should be CE OR ISO certified
29
Refrigerator General 800 ltr
Capacity: 800 liters
Microprocessor controller with display, Static cooling, Forced Air cooling, Air
circulating fan
No. of Shelves: 5,Adjustable shelves
Alarm: Adjustable High/Low Temperature alarm, Door open alarm
Temperature range: 1°C to 8°C
Temperature Display: Digital
No. of Doors: 2 Big Glass doors Locking system: YES
4 Castor Wheels
Buit-in Batery Backup for control Pannel during power failure
Temperature holding time during power failure is 145 Minutes or better.
Inbuilt Surge suppressors-Designed to prevent issues related to voltage surges.
Should be CE OR ISO certified
30
Quadriceps Table
One pair chromated torque unit with different weight options - two sets of ½ kg,
1 kg, 2 kg, 3 kg weights. Well cushioned back support and seat
31
Exercise
Table/Therapy
Couch
Made by teak wooden frame and leg size L x W x H – 200 cm x 70 cm x 80 cm,
Top 19 mm thickness ply, 4 inch cushioned with rexin cover legs cross section
8 x 10 cm.
32
Medicine Ball Set
1 set of 2,3,4, kg
33
Peg boards and
games
Wooden made, colour full pieces of square rectangular, hexagon, cylindrical
etc.
34
Hydrocollatrol for
hot packs
Complete stainless steel
Set of four packs, silica gel filled packs
Automated Thermostat
Net weight: 20kg, water temp.-110° c
Gross weight: 26.60kg
Page 38 of 61
Item
code
Name of Equipment
Technical Specification
Voltage:220v, power-1500watt
Frequency-50Hz, Dimension: 47cm, 55cm, 82cm
35
INFRA-RED LAMP:
Automatic Thermostat
Floor stand model lamp for IR radiation treatments. .
IR bulb of 150w is fitted in metal casing with wire guard, automatic cut off timer
of 30 min. and an intensity control switch
Adjustable arm permits wide range of adjustments
Mounted on wide base with ball bearing casters.
36
ULTRAVIOLET
LAMP:
Floor stand model UV Lamp (Luminious) for Ultra-violet treatments. .
The UV bulb of 300w is fitted in metal casing with wire guard and automatic cut
off Timer of 30 min.
Adjustable arm permits wide range of adjustment
Mounted on heavy duty base fitted with ball bearing casters
Comes with suitable power cord.
37
Parallel Bars
1) Epoxy covered tubular steel frame
2) Floor platform of wood or plastic material.
3) Floor-mounted type, with bolts for stability, bolts to be supplied with.
4) Heavy-duty bracing and plates to secure uprights.
5) Continuous non-slip lower walking surface with inclined ends for easy
wheelchair access.
6) Weight capacity at least 110 kg.
Approximate Dimensions
7) Length approx. 300 cm.
8) Adjustable height adult bars at least in the range 70 to 90 cm.
9) Adjustable height children bars at least in the range 55 to 80 cm.
10) Grab bars width adjustment at least in the range 40 to 60 cm.
11) Hand Rail Diameter no less than 3 cm.
38
Theraband
There are total 5 bands yellow, Red, Green, Blue, Black uses for resistance
exercises.
It is made up of natural rubber latex which use for strenthing exercises.
1.5 mtr, length and 5 inch width
39
Paraffin wax bath
40
Shoulder ladder
It Should be of:
● Stainless Steel
● Double chamber
● Adjustable thermostat
● Thermostat indicator
● Pilot lamp and on/off key
● Capacity of 8 kg paraffin
● Cart with wheels included
● Power supply: 110 or 220 volts 50/60 Hz
● Potency consumption: 1500watts
These ladders feature 36 finger steps for patients to perform finger climbing
activities increasing movements in shoulder
Wall mountable
Available in gray laminate or wood
Laminate
Dimension: 6 inch(W) x 47 inch(L)
36 smooth round corner step
Color: loded every sixth step
Easy to clean laminate purpose
Pre drilled wall mounting holes
Wood
Dimension: 2.5 inch(W) x 58 inch(L)
36 vertical finger steps
Page 39 of 61
Item
code
Name of Equipment
Technical Specification
Solid wood with heavy topcoats for durability and easy cleaning
Pre drilled wall mounting holes
41
Shoulder Wheel
Chrome plated for long life
Tension / resistance control
Can be used for Shoulder as well as Wrist
Adjustable bar length
Easy mounting on wall
42
Cervical and
lumbar traction
Solid state Technology, Static, intermittent modes
Specially designed Gear box to give long life to the unit
Noiseless , Reliable and durable heavy duty Motor
Digital Timer, Patient safety switch
Weight: 5-45kgs,
Hold time: 20, 40, 60 sec, Rest time: 1, 5, 10 sec
Traction Table
Powder coated Mild steel frame, Two section table
Foam mattress for patient comfort
Facility to attached lumber belt, chest belt
Platform to place traction unit
43
CPM (Continuous
passive Motion
Knee )
Range of Motion
From 0° to 120° of flexion
Allows treating all pathologies of the knee.
The anatomically correct system increases the comfort of the patient and
decreases the points of pressure
Light
12kg (26 pounds) Provided with two handles transport board easy to transport
for a use in the hospital (IPD / OPD).
The remote control is easy to use and intuitive, that allows a precise and quick
adjustment of the movement
The large LCD screen shows the immediate and the programmed range of
motion allowing a patient stimulation.
Warm up : The patient should reach gradually the pre-set full ROM
Modulation: Allow manual setting of the range of motion end-point based on
patient tolerance. This mode is generally use at the beginning of the session.
ROM by Pass : use during the session this mode allow a manual setting base
on new patient tolerance, Offering real progressive work of the Range of
motion.
Treatment time : 5 minute to 1 hour
Timer : Control of the session time.
Programme : Allows set-up of 16 customized programmes.
Technical Specification
Broad bearing surface improving stability
Detachable remote control which facilitates maintenance.
Site dedicated for storage of the remote control when the machine is not used
or during transport.
Possibility to block the adjustment of the parameters
Exclusive Load Reserve ensures patient protection when excessive force is
exerted on the joint.
Large LCD screen.
Range of motion : 0° to 120°
Speed : from 45° / minute to 155°/ minute
Weight : 12 kg (26 pounds )
Size : Length : 95cm (37 inch), Width :33cm ( 13 inch)
Height : 33 cm (13 inch)
Patient sizing : from 1,45m to 1,95 m (57 to 77 Inch)
Full leg : 71 to 99 cm (30 to 39 Inch)
Tibia : 38 to 53 cm ( 15 to 21 Inch)
Femur : 33 to 46 cm (13 to 18 Inch)
Page 40 of 61
Item
code
Name of Equipment
Technical Specification
With paediatric foot plate ( in option )
Full leg : 53 to 109 cm (21 to 43 Inch)
Tibia: 20 to 56 cm ( 8 to 43 Inch )
Dimmsion 320 mm x 335 mm x 150 mm
Operational Voltage 220 v, 50 Hz
Hold time 0 to 10 sec
Rest time 0 to 10 sec.
44
CPM Elbow
Anatomically correct passive motion of the elbow joint with or without
sychronised pronation / supination of the forearm. It is convenient and easy to
use in a bed or chair.
Antomical movements
Extension / Flexion 0° to 135°
Extension / Flexion with sychronized pronation - supination
Patient height : 1.40m (4'7") to 1.90m (6' 3")
Patient arm length : from 50cm (19.7") to 72 cm (28.3")
Machine weight : 21 kg (46.2 lb)
Dimensions : 72cm (25.3") x 65 cm (25.6") x 130m (51.2")
Exclusive Load Reserve ensures patient protection when excessive force is
exerted on the joint.
Electric power:50VA, Voltage:100 to 240volts,50/60Hz
Simple hand control : Start / Stop / Reverse
The patient can stop and reverse the movement at any time
45
CPM Shoulder
In this movement perform
Abduction - Adduction 20° to 160°
Abduction -Adduction with synchronized rotation 20° to 160° with -30° to 90°
Flexion Extension 20° to 180°
Horizontal Abduction -30° to 110°
Extension Flexion of the elbow -10° to 135°
Technical Specification
Anatomical Shoulder CPM Specifications:
Dimensions (set-up position): 27” L x 27” W x 35” H (70 x 70 x 90 cm)
Patient Height Range: 4’2” – 6’6” (1-2m)
Speed:5 speeds, from 30° to 120°/minute
Weight : 50 lbs. (23kg)
Passive Range of Motion:
Flexion 180°
: Extension 20°
Abduction 160° : Adduction 20°
External Rotation 90° : Internal Rotation 60°
Horizontal Abduction : −30° to 110°
Synchronized Abduction and Rotation:
Abduction 160° : Adduction 20°
External Rotation 90° : Internal Rotation 30°
Quality and number of movements
Synchronisation system
Flexible and evolutionary machine
Soft chair for patient comfort.
Automatic movement or Manual
resetting of the parameters when changing of the movement to allow and
incompatible range of motion with the patient condition
Possibility to block the adjustment of the parameters
Load reverse enusres patient protection when excessive force is exerted on the
joint.
Adjustment of the session time form 1 minute to 24 hours
Pause in movement limit form 1 second to 15 minutes
Adjustment of the speed from 50 to 140° per minute (5 levels)
Possibility of customisation and storage of 16 rehabilitation programme
Voltage : from 100 to 240 Volts 50/ 60 Hz
Electrical Power : 50 VA
Programmable hand control allow pre-programming 16 different protocols
Page 41 of 61
Item
code
Name of Equipment
Technical Specification
Break down for convenient transportation also include a carrying case for
detachable part.
46
IFT machine with
Russian current
LCD
Micro-controller based, Hospital Model
Feather touch keys, ABS Plastic shockproof cabinet
4 Pole, 2 Pole , 4 Pole Vector, Russian current , 4 pole classic
Aesthetic look, Light weight, Easy to use
Built in Clinical 16 Programs, Treatment timer
Separate Display of Timer, Output Display, Frequnecy
The unit must have a provision to control the output beat frequency with the
help of an external knob.
The output frequency range from 1Hz to 150Hz or more.
It should have the provision for the following electrodes:
Plate electrodes- plates made of conducting rubber which are comfortable and
long lasting.
Vacuum electrodes- they’re really plate electrodes kept in position by a vacuum
instead of bandaging.
Combined electrodes- all four contacts are embedded in some insulating
material and can be applied as one pad.
It must also have indicator and display for frequency used for treatment, output
peak current and the time of the treatment remaining.
Unit should be operational on 230VAC, 50Hz
47
Micro control 4
channel TENS
1. No. Of outputs should be 4 (four)
2. No. Of channels 4 (four)
3. Stimulation types tens (continues / pulse)
4. Output wave form symmetrical biphasic spare wave.
5. Tens made should be burst, conventional, modulation type.
6. Power should be operable with both battery and alk maliry current
7. It should be approved – ISO certified
8. Treatment time - 1 to 60 minutes
9. Output voltage 40 volts peak to peak on 500 ohms load.
10. Output current 80ma maximum
11. Display system LCD
12. Burst mode Fventilatorpulse width 50 ms to 250 ms in steps of 10 ms Pulse
rate 1 hz & 120hz in step of 1 hz upto 20 hzs and hz from 20 - l2hz
13. Modulation mode pulse width - 50 ms to 250 ms in steps of 10 ms. Pulse
rate – same
14. Convectional : -- continuous output,
Pulse width same as above
Pulse rate .:- same
It should be FDA approved or ISO certified.
48
Micro control
Ultrasound therapy
unit
· Ultrasound frequencies: 1 and 3 Mhz
·Ultrasound outputs modes: continuous and pulsed (pulse duration 0.5 or 2 ms
pulse repetition 100 Hz)
· Intensity: continuous US: 0.05 –3w /cm2 pulsed US: 0.05 –5w/cm2
Page 42 of 61
Item
code
Name of Equipment
Technical Specification
· Timer – 0-15 minutes
·Mains supply - 240V±10% 50Hz
· Treatment heads
· Treatment head large 1MHz – with standard length cable
· Treatment head small 1MHz – with standard length cable
· Treatment head large 3MHz – with standard length cable
· Treatment head large 3MHz – with standard length cable
Head specification:
- water resistant
Treatment head small 3 MHZ cable
Head specification:
- water resistant
- Low weight
49
Short wave
diathermy
High frequency electromagnetic energy to generate heat in body tissues.
1. Used in physical therapy treatment to heat body tissues 1 to 3mm below the
skin to promote healing and pain relief
2. Short-wave diathermy shall essentially consist of an oscillator of typically
27.12 MHz crystal, Power amplifier and applicators (electrodes).
3. The oscillator shall generate high-frequency current and shall have an
electronic timer that controls the application time
4. It shall have all the necessary certification, FDA or CE marks etc.
Electrodes
The diathermy shall have the provision for following electrodes:
Pad applicator
Induction cable
Drum applicator
Power supply
The unit should be mobile and be operative at 500V, 15A, 50Hz power supply.
50
Static cycle with
magnetic
resistance
Computerized cycle Ergo meter
Has both aerobic and anaerobic testing protocols
Cycle height and paddle length adjustable.
· A very stable, light weight exercise cycle which is easy to move around the
department.
· Easy to read electronic meter.
· Adjustable seat height and handle bars.
· Non wearing magnetic brake(preferable)
· Weight resistance settings.
· Step through frame easy to mount / dismount
51
Dental Chair Unit
with RVG
DENTAL CHAIR /UNIT WITH ATTACHMENT 1 EACH
A. Dental chair \unit
B. Compressor
C. Piezo electric scaler
D. Motorized Suction
E.. Dental X-ray unit
F. Intra oral Camera
G. RVG
H. Hand piece cleaning system
Specifications for Dental chair/unit and attachments:
A. With Over Head Continental delivery system consisting of:
1. 3-way syringe (sterilisable)
2. 3-way assistant syringe
Page 43 of 61
Item
code
Name of Equipment
Technical Specification
3. 2 high speed terminals with 1 being air, Switzerland fiber optic air
rotor(titanium based air rotor) H/P with quick disconnect coupling and 1more
mini head air rotor H/P(400000RPM) with straight and contra angle hand piece.
4. 1 Air micro motor terminal with H/P
5. LED light cure unit
6. Infection control system with Non retraction valves (Bio-system) & removable
and autoclavable holders protecting hand pieces.
7. Latest foot operated light of 20000 and 2500 lux
8. Medium vacuum suction and canula only for high vacuum
9. water system rotable
10. Dental chair with independent up and down movement.
11. The synchronized movement between the seat and backrest with
TRENDELNBURG position.
12. Headrest with SEESAW movement suitable for Paediatric patients.
13. Auto return to zero position
14. Two programmable working positions
15. Spitting and last position
16. Lock the movements
17. Emergency stop control
18. X-ray viewer with light generated by LED
19. Arm rest option of fixed, lateral 90 degree swivel available
20. Multi functional foot control (base fixed or mobile)
21. Doctors stool with adjustable backrest tilt includes an adjustable rim (2
doctors stool)
22. Operating voltage 105V to 250 volts (specially designed for Indian
condition)
23.Maximum height 90 cm-minimum height 45 cm.
24. With Gear Motor.
B. Compressor (one No)
Oil free medical grade (Noise free) suitable for driving the dental unit.
C. Piezoelectric Scalar (Fiber Optic) (One No.)
1. Based on piezoelectric technology.
2. High power turbo mode and low power perio mode.
3. Having torque, tool for tightening of the tip.
4. Having titanium tip adapter.
5. Automatic smart power feedback control3.
6.Basic vibration frequency of 50 KHZ
7. Four tips and one endodontic kit.
D. Motorized suction (One No) Having direct drainage system.
E. Dental X-ray unit (one No.)
1. Mobile x-ray mounted on a very stable base with rounded lines, reinforced
casters with a transversal brake stability and mobility with wall mounting
2. Intra oral x-ray Unit 70KW/7 ma tube
3. Having more current and better quality
4. Intra oral dental Radiography (Compatible with RVG)
5. Unit has electrical cord of four meters.
6. Manufactured with International Safety standards.
7. Fully imported soft positioning arms for accurate tube positions
8. Great lightness and flexibility in the movements.
9. Free swivel head allows easy positioning of the Head.
10. Head tube and cone are internally lead coated to avoid scattered radiation.
11. High voltage generator with high efficiency in the emission of the x-rays.
12. Digital control equipped with an easy ready display indicating with precision
the selected time.
13. Exclusive angular indicating system for precise head positioning in various
radiography techniques.
14. High efficiency and greater sharpness of the Radiography.
Page 44 of 61
Item
code
Name of Equipment
Technical Specification
15. Dental x-ray with Pantographic arm with vertical and horizontal smooth
movements.
16. Shorter exposure time and greater safety.
F. Intra oral Camera
1. Direct USB connectivity
2. Single cord operated
3. Light weight (just 45 gms)
4. Four cool white LED light
5. Taken intra/extra oral images.
6. Taken power from USB cable
7. Detachable coupling with softly lock system.
8. Auto focus with intra/extra oral image
9. Supplied with a PC with core Duo processor, 1 GB RAM, 80 GB Hard disc
and video
10. Processing hardware and software with an ink jet color printer.
11. RVG software capacity.
12. Split image.
13. Having latest microprocessor technology; means image capture should be
function of the camera every image can be freezed directly on
Laptop/computer.
14. Having single lens (8.0x5.9mm) focusing adjust intra/extra oral image.
15. Having automatic magnetic on/off and clear all buttons to save time, energy
and money
16. Having lightweight chassis (45gm) for easy to use.
G. RVG
1. Sensor thickness app. 3 mm.
2. Outer dimension not more than app. 35-40 mmX25-30mm.
3. 100% active area.
4. Approx. 2500000 pixels.
5. 22 Lines pairs/mm resolution.
6. CCD Technology protected optical fiber.
7. Reduction in Radiation as compared to X-ray films is up to 90%.
8. USB connectivity with computer.
9. Compatible with PC as specified in the intraoral camera.
10. User friendly software.
11. Protective sheaths are provided.
H. Hand piece cleaning system:
To automatically and correctly clean and lubricate all high speed hand pieces,
low speed hand pieces, and air motors before autoclaving .
The system with automatic cycle cleans and lubricates high speed and/or low
speed hand pieces, plus air motors.
The system should have pneumatic operation and should have 3-ports to
maintain all hand pieces brands. Easy oil filling with oil indicator.
Documentation:
Certificate of calibration and inspection from the manufacturer.(copy of the
certificate issue by CE etc.)
List of Equipments available for providing calibration and routine maintenance
support as per manufacturer documentation in service/technical manual.
52
Blood Bag Tube
Sealer
1)
2)
3)
4)
5)
6)
7)
53
Page 45 of 61
Incubator
Power supply: 100 - 240 vac
Input Frequency: 50/ 60 HZ
Tube Detection: Automatic
Maximum dia. Of tube that can be sealed: 6 mm
Sealing time: 1-3 sec
Indication: Cover open ,Power ,Seal, ready etc..
Standard & Approval: ISO or CE Marks if available
Item
code
Name of Equipment
Technical Specification
Capacity : 30to 40 bags
Temperature: 22 c +2c
Recording: Recording is made on a weekly, circular chart paper
Cabinet Material: External- MS sheet, powder coated after 7 tank process
Internal - Stainless steel sheet
Door: Transparent door which enable inspection of content without opening the door
Air circulation : Air circulate to.
Condensate evaporator: Provided built-in
Voltage stabilizer: of suitable capacity
Standard approval: ISO or CE Mark
54
Blood bag stripper
with cutter
1)
2)
3)
4)
55
Stainless steel body
Light weight
Spring powered handle
Sturdy
Blood collection
monitor
Sturdy, light weight
For blood bag (350ml and 450ml) blood bags
Battery backup
56
Plasma Thawing
bath
1) Capacity: 10-12 Plasma bags (Approx 16 bags)
2) Microcontroller based.
3) Temperature Range: 37° C /4° C
4) Smooth Acrylice tray for
Accommodating Plasma bags.
5) Integrated pump for temperature uniformity
57
Laboratory
Centrifuge
1) Microprocessor controlled laboratory centrifuge with brushless induction
motor with frequency drive, suitable for routine sample analysis in hospital &
pathology lab for minimum 16 tubes of 15ml each with various adaptor
2) Should be able to achieve 6000RPM & 5070 G force fixed angle.
3) Should have safety lid interlock to prevent lid opening during centrifugation.
4) Should have imbalance detection & centrifuge stop with display of error
5) Should have gas hinges to prevent door filling with emergency lid lock
release
6) Should able to give stable speed output even under unstable voltage
conditions. supply should with suitable voltage stabilizer
7) Should have feather touch setting leys for various parameter setting.
8) Should have alphnumeric LCD display for speed & RCF
9) Should have choice of 3 acceleration & deceleration profiles
58
Binocular
Microscope
1) Study for routine laboratory purpose
2) Halogen bulb
3) 4xL, 10x L, 40xL & 100 x L Lens
59
VDRL Shaker
1) RPM - up to 180
2) For VDRL Test by RPR method
60
Oven
1)
2)
3)
4)
5)
Page 46 of 61
Medium size
Double walled, Stainless steel body
Bottom heaters made of nichrome wire
Inner cabinet with heat resistant silver
Tempt. Regulator and display
Item
code
Name of Equipment
Technical Specification
6) Shelves (2 or 3 )
61
Plasma Expresser
1) Manual.
2) Spring Loaded Acrylic Plate.
3) Uniform Pressure.
62
Gel cards.
( semi automated
method)
1) All cards must have V bottom shaped microbe tubes containing gel particles
premixed with reagents.
2) Gel particles: Sephadex ( Dextran Acrlylamide )
3) Sensitivity of Anti- Ig G gel card must be minimum of 0.1IU/ml
4) Gel must contains particles of different sizes to exhibit different gradation of
reaction.( 4+, 3+, 2+, 1+, and negative.
5) No washing steps for tests.
6)The card for ICT/DCT MUST CONTAIN POLYSPECIFIC AHG.
7) The storage temperature of the gel cards must be easy(18 to 25)RT.
8)Cards have must also for- l) compatibility testing and Ab testing with saline,
enzyme,and coombs..
9) Monospecific DCT cards, dilution cards, Ig G sub class.
10) Weak D confirmation cards.
11) Easy disposable.
12) Quality control coombs cells.
13) Quality control system for gel cards.
14) Ready to use elution kit.
63
Weighing Scale for
blood bag
1. Digital
2. 3 digit display
3. Max. capacity : 1 kg
64
Instrument dryer
1. Hot air blower should be of adequate flow.
2.Electric connected load should be around 3 to 4 KW
3. It should be single phase operated.
4.Overall size of the cabinet-Door closed-660 mm X 545 mm X 1800 mm
approx.
5.Overall size of the cabinet-Door open-740mm X 11555 mm X 1800mm
approx
6. Digital Timer and Digital Controller should be provided.
7. There should be provision to hang the tubes along with shelves.
The storage cabinet permit the drying of surgical instruments, anesthesia
circuits and hospital blankets
The cabinets are made in SS 304, sound damped by fireproof material inside
and front panel with tempered double glass
Touch screen control panel with colors graphic LCD display which permit the
setting of drying parameters as temperature and time depending by articles to
process with acoustic signal in case of alarms and process end
The temperature and times are set every start-up of program from min 70 to
90degC with a time of1-999 min or continuously
One sensor, placed on floor, permit to open the cabinet and reset the
automatically in every moment
Equipped of air aspiration through Hepa FilterH14 with automatic alarm of
pressure leakage in the circuit and changing of filter
65
Floor Mounted
Perforated Storage
Rack
comprising the following
·
S.S. frame and body.
·
S.S. shelf – 5 Nos.
Size: 900mm (L) X 450mm (W) X 1800mm (H)
Page 47 of 61
Item
code
Name of Equipment
Technical Specification
i.e. 3 Ft. (L) X 1.5 Ft. (W) X 6 Ft. (H)
Mounting will be on heavy duty rubber / nylon / bush.
66
Work Table
Size : 2.5’ X 4’
Comprising the following:
·Frame in 18mm diameter 16 gauge hollow SS pipe with rigid configuration,
argon arc welded, and ground smooth and polished.
·Machine pressed top in 18 gauge 304 grade SS bent twice at edges to form
25mm thick edges with 12mm projection inside, fully reinforced against bending
and treated for sound deadening.
·One no. SS under shelf with round edges also in 18 gauge SS with 25mm thick
edges
·Rubberized, adjustable SS feet.
67
Closed Transfer
Trolley
Closed Transfer Trolley, Fully S.S. with Robust Handles & Side Railing with 6’
Dia. Castors, with 3 compartments
Size: 3’ (Length) X 1.5’ (Width) X 3’ (Height)
Each will be provided with 3 selves – 1st at 10” above Ground, 2nd at 22”
above ground & 3rd at 32” Above Ground
68
Pass Box for
C.S.S.D
SIZE: 600X 600 X 600 {2’ X 2’ X 2’}
.MATERIAL OF CONSTRUCTION:
The Pass Box will be fabricated from S.S. 304 sheets with double wall
construction. Pass box with two doors. The two doors should be interlock such
a way that two doors can not be opened at the same time. All welding will be
full argon welding for superior hygiene.
69
Single Sink with
Platform
with total length of 5feet
Sink Size: 20” X 28” S.S. Tubular Stand
715mm X 600mm
16 gauge S.S. 304
70
Ultrasonic cleaner
Ultrasonic Cleaner with Rinsing Tank (Two tanks-30+L each for approx).
The compact cabinet type automatic ultrasonic cleaning system console with
two chambers for cleaning & rinsing /Drying for effective cleaning of surgical
instruments and rigid lumens of the surgical scopes prior to sterilization.
Automatically controlled St. Steel cabinet type ULTRASONIC cleaner with four
lockable castors.
Should be able to hold min. 10kg weight of the instruments
To achieve high degree of fast and efficient cleaning, the ultrasonic waves
generators in the wash tank should provide min. 750 Watts of sonic power and
transducers
Provide four trays with tray hooks to hold instruments
Should be CE or ISO or USFDA approved
71
Scrub station two
port Elbow
operated as well as
foot operated
Made of 18 gauge S.S. of 304 quality sheet
(L)(52”) X (W) 18" X ( H) 52’’ X 21” (D).
SPECIFICATION:
Two elbow operated cock will be provided which when required operate
manually.
One soap dish and One betadine dispenser will be provided.
Page 48 of 61
Item
code
72
Name of Equipment
Technical Specification
Washer disinfector
1. Should be a fully automatic PLC micro processor based High pressure,
Disinfector for washing hospital materials.
2. Should have Rectangular, horizontal chamber with single hinged door and
well insulated jacket.
3. Should have option for double door to have a pass through system.
4. Should have Chamber Volume approx. 320 Liters. Internal Dimension:
605x620x860mm (WXHXD).
External Dimension: 750x870X1700 mm approx
5. Should be high grade Stainless steel construction inside and outside
including all internal piping and external panels.
Chamber, Jacket & Door Material: Stainless steel 304 Grade, All Piping
components and connections Stainless Steel AISI 304 grade, External Panel &
Frame: S.S. 304 grade.
6. Should have a built in multi colored Touch screen User’s interface cum
Display with 5" display.
7. It Should have a single dosing pump.
8. It should be possible to control & display of Washing cycles, parameters
values, Time etc.
9. Should have programmable Operators access level.
10. It should have powerful water pump
11. The unit should be equipped with multiple safety mechanisms for
Emergency Stop, door safety with inter lock incase of double door system and
electrical safety.
12. Should have audio visual alarms in case of undesired situation. All Alarms
should be color coded.
13. The unit should include Built-in Recorder for printing the step by step
progress values during the cycle with time and date and alarm condition if any.
14. All Valve Operation should be Electric Solenoid type
15. Should be certified as per latest product specific quality recommendations
like: - ISO 9001:2008,ISO 13485,CE Certified . As per ASME guidelines
16. Should be offered with in built water heating arrangement, Water Saving
System.
17. High quality stainless steel trays will be provided.(Minimum 4 qty)
73
Baby warmer
Material used : conductive antistatic material
Neonatal open care system
Warmer Servo controlled ( Air probe required -8 qty)
Microprocessor based electronic system
Attached slow suction
Collapsible railings
Stand alone LED phototherapy unit
Bed can be tilted along its horizontal axis.
Swivel heater unit to facilitate X-ray procedure.
Height adjustable pole for hanging intravenous fluid bottles.
Alarm (Audio and visual ) for high and low temperature, power failure and
system failure and sensor failure
One monitor tray should be provided.
Trolley of the warmer should have a shelf down to keep undersurface
phototherapy unit
ICMED 13485Certificates.
74
Phototherapy Unit
Each Phototherapy unit should be double surface ( undersurface should be
detachable)
· Phototherapy with LED lamps having dominant wavelength range from 450 to
465 nm. light weight (approx. 10-15 kilograms) with effective surface area of 50
X 30 centimeters at 35 centimeters from light source
· 20 W maximum at 100-240 V.
· Irradiance level should be adjustable 3 steps (Low, Medium & High)
· Should have programmable timer with reset option.
· Display should show the treatment time.
Page 49 of 61
Item
code
Name of Equipment
Technical Specification
· Should have a sturdy base with wheels
· Should have time tantalizer to show the total hours of treatment given by the Unit.
LED lamp change alarm
Height should be adjustable
Cooling fan should be provided
Life- 40000 hrs
ICMED 13485Certificates.
75
Resuscitation
Warmer
The unit should have CE 1023 certification.
The manufacturing activity should be carried out in an ISO 13485:2003 certified
industry.
THE RESUSCITATOR SHOULD COMPRISE FOLLOWING:1. T SHOULD INCORPORATES a Pressure regulator in the system to reduce
the pressure of compressed Air and oxygen from 60 PSI to 1.5 PSI to ensure
utmost safety of the infant to avoid wastage of gases.
2. Inbuilt air oxygen blender with marking should be provided to indicate and
set FIO2 from 21 to 100% with an accuracy of +/- 3#
3. Flow meter with flow control valve should be provided to indicate and control
the flow of blended gas delivered to patient.
4. Inbuilt water manometer should be provided to indicate CPAP and PIP
levels.
5. Unit should be provided with “TEE” piece with the facility to set the CPAP
level from 2 to 10 cm of H2o. The “TEE” piece is placed on the infant face
mask.
6. A fixed internal safety valve is provided.
7. It should incorporate gas driven slow suction which can be operated on
either compressor air or on oxygen & Venturi Suction
8. A dial to indicate suction pressure should be provided.
9. Unbreakable suction collection bottle should be provided with the unit.
10. A separate suction level controller should be provided for selecting the
suction values.
11. Maximum suction pressure should ne exceed 150mm hg
12. It should comprise large baby bed with foam mattress. The baby bed should
have a tilt facility.
13.Three [3] rotatable molded Instrument shelves should be provided to keep
essential kit / monitors.
14. It should be Micro processor based proportional Controller with Three level
safety system.
15.It should comprise following modes of warming
A] Servo Skin mode B] Servo Air Mode C] Manual Mode
16. It should have incorporated with 3 level safety systems.
17. It should facility of temp display in ° Centigrade & ° Fahrenheit.
18. It should have separate feather touch keys for above setting.
19. Feather touch keys should be provided
20. It should have Display of 3 Digit Green LED for indicating baby's actual
Temp
21. Bar graph should be provided with the unit to indicate heater output
Following Alarms should be incorporated:Over temp.
2nd Safety active,
Sensor fail
3rd Safety active,
Apgar Time.
Flat skin SENSOR with one side sensing should be provided with the unit.
Baby sensing material should be plated in “SILVER”. Sensor top side should
be molded in ABS material It should have a soft silicone cable
Air Sensor : Extra Air sensor should be provided with the unit to control
surrounding temp. of the baby.
Page 50 of 61
Item
code
Name of Equipment
Technical Specification
22. It should incorporate a bank of CE Marked infrared ceramic heater along
with stainless steel reflector to ensure uniform warming of baby bed
23. Drop down acrylic side supports should be provided for easy access to
baby.
24. Should be provided with resuscitation kit
25. Euopean CE & USFDA
76
Transport Baby
Incubator
Physical Attributes (without options/accessories) with 147 stand
Height 32 in (81.3 cm) max- 44in (111.8 cm)
Width 22.3 in (56.5 cm)
Length 40.3 in (102 cm)
Weight159 lbs (72 kg)
Distance from vertical hood to mattress High Hood (54.8 cm)
Standard Features
Double wall
Skin temperature probe
O2 inlet
Examination lamp
2 access doors
2 disposable infant restraint straps
1 Iris port
2 Quiet Touch™ port doors
6 tubing ports
Locking power control receptacles
DC cable
2D or 2E size tank mounts The tank mount permits mounting gas cylinders with
a diameter of up to 4.5 in (11.6 cm) and up to 34 in (85 cm) in length
Humidity Pad(2)General Specifications
O2 concentration range 21% to 58% minimum
Humidity capacity 50% to 70%
Noise level <60 dBA(3)
Performance Characteristics
Temperature set range 22.0° C - 38° C (71° F - 100° F)
Temperature rise time 30 minutes
Temperature variability ≤1.0° C
Temperature overshoot ≤2.0° C
Temperature uniformity ≤1.0° C
Correlation of display temperature to set point at temperature equilibrium ≤ 2.0°
C in l0-20° C ambient ≤1.5° C in 20-30° C ambient
Humidity pad Holds 400 ml.(14 oz) sterile distilled water with no significant
spillage for up to 45 deg. In either direction.
Air filter Removes >99% of airborne particles greater than 0.5 micron diameter
Relative humidity 50 to 70% for 10-12 hours using humidity pad
Check calibration key 36.0° ± 0.l° C
Controller Displays
On/standby Illuminates when “On”
Battery condition status 4 LED indication of battery charge condition 25-100%
Power mode Illuminates AC, DC, or external DC
Heater power 4 LED indication of heater power; 25-100%
Baby temperature ° C Displays infant temperature
Air temperature ° C Displays incubator air temperature
Page 51 of 61
Item
code
Name of Equipment
Technical Specification
Set temperature Illuminates when changing set temperature
Alarm indicators High temp, Power fail, Sensor fault, Heater temp, Air flow, Low
DC
Battery Specifications(4)
Incubator 1 battery standard
Type Vented rechargeable, 12 Vdc, 24 AH gel-type battery (lead acid)
Battery rating Incubator maintains a differential of 25° C (77°F) between
ambient and set point for 90 minutes on 1 battery or 180 min. on 2 batteries at
full heater power
Life expectancy 200 complete charge/discharge cycles minimum
Charge time 10 hours per battery from full discharge
Safety Alarms
High temperature. Actuates if incubator air temp. >39 ± 0.5° C
Sensor (temperature) Actuates if sensor fails
Heater temperature Actuates if heater temp >77° C (l70° F)
Power fail Actuates if AC fails and no DC power present, and activates if unit
switches from AC to DC current
Air flow Actuates for fan failure
Low DC Actuates if DC<10.5 Vdc, or external 28 Vdc falls below 25.5 Vdc
nominal
Silence/reset Silences the audible portion of alarms for 5 minutes, except
Power fail.
Resets Sensor & High Temp alarms after 100% conditions corrected.
Resets intermittent power alert if unit switches from AC to DC current
Environmental
Storage temperature -40° C to 70° C ambient
Operating range Sea level to 3 km (10,000 ft.) non--pressurized environment.
Sea level to 12 km (40,000 ft.)-pressurized environment
Relative Humidity
Operating range 0% to 95% RH, non-condensing
Electrical
AC power requirements 110/120 V, 50/60/400 Hz - 220/240 V, 50/60/400 Hz
DC power requirements 11-13 V, 200 W (max) - 26-30 V, 200 W (max)
Observation lamp 35 foot candles - 4 inches above mattress 376 lux - 10 cm
above mattress
Should be European CE &USFDA Approved
77
Fetal Doppler
Technical Specification
· Display LCD
· Heart Rate Display
· Low Battery Display
· Signal Quality Display
· Heart Rate Range 50-240 bpm
· Accuracy ± 2%
· Ultrasound Frequency 2MHz
· Ultrasound Intensity 10mW/cm2
· Speaker Output Power 1.2W
· Built-in Loudspeaker
· Audio output for Earphone
· Auto Shut Off 5 minutes
· Auto Shut Off on signal 1 minute
· Power 1.5V Battery x 2 (Type: AA)
· Sensitivity From 10 - 12 weeks
with battery adapter and rechargeable cell and in built printer
Should be CE or ISO or USFDA Approved
78
Fetal Monitor
Fetal monitoring system which provides accurate & reliable monitoring
information using non-invasive FHR and Toco facilities.
Page 52 of 61
Item
code
Name of Equipment
Technical Specification
Graphical Display of FHR & UA waveforms, enabling continuous & cost
effective monitoring.
In built Keyboard for easy patient data entry for documentation along with CTG
& UA waveforms on paper.(printer)
Directional pulsed Doppler FHR detection with auto correlation.
Elapsed time counter for automatic reminder facility
Analysis Report automatically printed highlighting abnormalities
Fully flexible software based System
Multi patient Recording
Compact, light weight, modular
Color Coded Transducer
FHR Storage up to 6 Hrs of FHR, Toco and Fetal movement
Large LCD display of FHR & UA as a trace
High/low Heart rate alarms
True Twins tracing facility with separate and distinct FHR traces.
Analysis of the CTG & UA pattern.
Selectable chart speed 1,2,3cm/min
Up gradable system to SpO2 and NIBP monitoring enabling to assist user in
high risk pregnancy management(Optional)
PC Connectivity for remote monitoring of the patient from consulting room or
residence for Maternity clinic(Optional)
Specifications:
Ultrasound
1. Frequency :>1.5 MHz
2. H.R. Range : 60 to 220 BPM
Uterine Contraction
1. Range : 0 to 100 units
2. Resolution : 1bpm
3. Speed : 1,2,3 cm/min.
4. Display : LCD & Alphanumeric(LED)
5. Alphanumeric Mode : FHR & UA
6. Graphical Mode : LCD FHR & UA
7. Alarms : Low / High FHR, Signal Loss, Elapsed time, clinical events
Should be CE or ISO or USFDA Approved
79
Nebulizer
1. Compact, light weight, low noise
2. Durable long life compressor. Suitable for heavy duty/ institutional (hospital)
use,
should be able to run uninterruptedly for one hour, Max Press 2.0-2.5 bars
3. Should produce particle of size 1-5 micron
4. Aluminium cabinet painted with epoxy powder.
5. Piston-type electric aspirator that offers high performance and great
durability.
6. Protective thermal cut out relay
7. Air delivery rate app.15 L/min.
8. 24 hours continuous work for hospital use.
Should be CE or ISO or USFDA approved
80
Patient Warmer
Reusable patient warming system
·Constant, evenly distributed warming directed towards patient, without air
circulation.
· Flexible system suitable for all type of surgeries.
·Maximum possible coverage of the patient.
·Gently warming directed toward patient ,no upward radiation of heat
·Precise & selectable temp. Control between patient and blanket (from 30deg to
42 deg c)
·Should have display showing temp. & have alarm system
·No threat of nosocomial infection.
·Non latex, anti-bacterial coated, blood and fluid resistant, cover material.
·Reusable, washable and replaceable covers.
·Small and light weight, control unit, easily attachable to iv pole /side rail of ot
table.
Page 53 of 61
Item
code
Name of Equipment
Technical Specification
·Available in pediatric and adult sizes.
Should be CE OR ISO OR USFDA approved
Note: Equipments which are Interfaceable must be Interfaceable with
NMMC HIMS ( NIC e-hospital software)
Page 54 of 61
Schedule - B
FINANCIAL BID
Name of Bidder/Tenderer
Address of Firm
Category
No.
Sr.
No.
1
-
M/s. ............................................................
......................................................................
.......................................................................
Name of Equipment
Name of
Manufacturer
Total
Req.
Qty
Rate /Equipments (Rs)
Rate per Equipments (Rs) In words
Anesthesia & Ventilators
1
Anesthesia machine ( basic Boyles)
without compressor
10
2
Anesthesia Machine with ventilator (without
compressor)
22
3
Ventilator – Adult and Pediatric
14
4
Ventilator - portable neonatal
4
5
Ventilator Neonatal
9
6
Ventilator – portable Adult & pediatric
4
Category total amount
2
Page 55 of 61
Monitors
1
Central Monitor
6
2
Defibrillator
18
3
ECG Machine
33
Total Cost
(Rs)
Category
No.
Sr.
No.
Name of Equipment
Name of
Manufacturer
Total
Req.
Qty
4
Infusion Pump
80
5
Multipara monitor 5 para with NIBP
50
6
Multipara monitor with NIBP & ETCO2
1
7
Pulse oximeter
70
Syringe pump
55
Rate /Equipments (Rs)
Rate per Equipments (Rs) In words
8
Category total amount
3
Page 56 of 61
Analysers
1
Semi automated Elisa reader & washer
1
2
Bedside ABG analyser
4
3
3 Part Heamatology Cell counter
1
4
Semi Automated Biochemistry Analyser
7
5
Electrolyte Analyser
4
6
ESR Analyser
4
7
Heamatology 5 part Cell counter
5
Total Cost
(Rs)
Category
No.
Sr.
No.
Name of Equipment
Name of
Manufacturer
Total
Req.
Qty
8
Fully Automated Biochemistry Analyesr
1
9
ABG machine
2
Rate /Equipments (Rs)
Rate per Equipments (Rs) In words
Category total amount
4
Fridge & Refrigerators
1
Refrigerated Blood bank Centrifuge
1
2
Deep Freezer (-80°c)
1
3
Deep Freezer (-40)
1
4
Blood Bank Refrigerator
6
5
Refrigerator - General 300 ltr
60
6
Refrigerator - General 800 ltr
20
Category total amount
5
Page 57 of 61
Physiotherapy Equipments
1
Quadriceps Table
3
2
Exercise Table/Therapy Couch
3
3
Medicine Ball Set
2
4
Peg boards and games
3
Total Cost
(Rs)
Category
No.
Sr.
No.
Name of Equipment
Name of
Manufacturer
Total
Req.
Qty
5
Hydrocollatrol for hot packs
3
6
Infrared Lamp
3
7
Ultraviolet Lamp
3
8
Parallel Bars
3
9
Theraband
3
10
Paraffin wax bath
3
11
Shoulder ladder
3
12
Shoulder Wheel
3
13
Cervical & Lumber Traction
3
14
CPM Knee
3
15
CPM Elbow
3
16
CPM Shoulder
3
17
IFT Machine with Russian Current LCD
3
18
Micro Control 4 Channel TENS Stimulator
3
19
Micro control Ultrasound Therapy Unit
3
20
Shortwave Diathermy
3
21
Static Cycle Magnetic Resistance
3
Rate /Equipments (Rs)
Rate per Equipments (Rs) In words
Category total amount
Page 58 of 61
Total Cost
(Rs)
Category
No.
Sr.
No.
6
Name of Equipment
Name of
Manufacturer
Total
Req.
Qty
Rate /Equipments (Rs)
Rate per Equipments (Rs) In words
Dental Equipments
1
Dental Chair unit with RVG
3
Category total amount
7
Laboratory Equipments
1
Tube sealer
4
2
Incubator
3
3
Blood bag stripper cum cutter
2
4
Blood collection monitor
1
5
Plasma Thawing bath
3
6
Laboratory Centrifuge machine
13
7
Binocular microscope
12
8
VDRL shaker
12
9
Hot air Oven
8
10
Plasma Expresser (Manual)
1
11
Gel Card
1
12
Weighing Scale for blood bag
6
Category total amount
Page 59 of 61
Total Cost
(Rs)
Category
No.
Sr.
No.
8
Name of Equipment
Name of
Manufacturer
Total
Req.
Qty
Rate /Equipments (Rs)
Rate per Equipments (Rs) In words
C.S.S.D. Equipments
1
Instrument Dryer
4
2
Floor Mounted Perforated Storage Rack
105
3
Work Table for CS.S.D Department
35
4
Closed Transfer Trolley
35
5
Pass Box for CS.S.D Department
4
6
Single Sink with Platform
14
7
Scrub station two port Elbow operated as
well as foot operated
12
8
Ultrasonic Cleaner
3
9
Washer Disinfector
3
Category total amount
9
Page 60 of 61
N.I.C.U. Equipments
1
Baby Warmer
25
2
Phototherapy Unit
23
Total Cost
(Rs)
Category
No.
Sr.
No.
Name of Equipment
Name of
Manufacturer
Total
Req.
Qty
3
Resuscitation Warmer
12
4
Transport baby incubator
4
5
Fetal Doppler
40
6
Fetal monitor
8
7
Nebuliser
8
Patient Warmer
Rate /Equipments (Rs)
Rate per Equipments (Rs) In words
Total Cost
(Rs)
105
8
Category total amount
Note : Rate should be quoted Only in Indian rupees for all items which should be inclusive of all State/Central / Local Government VAT/Taxes, Custom Duties, CVD, SVD, Custom Clearance, Excise, Octroi or
any state levies.
I/We agree to keep the offer valid for one year from the date of opening of financial bid.
I/We declare that we shall treat these documents and other documents connected with the work confidential and shall not communicate the information delivered there from to any person other than a
person to whom we have authorized to communicate.
Signed for and on behalf of the firm
(Authorized signatory of the firm)
Dated:
1.
2.
3.
4.
Put this paper in a separate envelope marked as a “Financial Bid”
Above rates include all taxes.
Submit the technical details of tender in the Technical Bid Envelope. Don’t put any other document, other than the financial bid in the financial bid envelope.
Financial bid will be opened of only those tenderers who are technically qualified.
Page 61 of 61
Was this manual useful for you? yes no
Thank you for your participation!

* Your assessment is very important for improving the work of artificial intelligence, which forms the content of this project

Download PDF

advertising