Spirit 3300 Series Dental Chair

Spirit 3300 Series Dental Chair
Model: 3301
Model: 3302
Spirit 3300
Series
Dental
Chair
Use and Care
Model: 3303
Model: 3304
Table of Contents
OVERVIEW................................................................................................................................................................................................................ 3
SAFETY...................................................................................................................................................................................................................... 5
Regulatory Information................................................................................................................................................................................. 6
operation............................................................................................................................................................................................................... 7
operation............................................................................................................................................................................................................... 8
operation............................................................................................................................................................................................................... 9
operation.............................................................................................................................................................................................................. 10
operation...............................................................................................................................................................................................................11
operation.............................................................................................................................................................................................................. 12
operation.............................................................................................................................................................................................................. 13
Cleaning, Disinfecting, & Sterilization..................................................................................................................................................... 14
Cleaning, Disinfecting, & Sterilization..................................................................................................................................................... 15
MEDICAL ELECTRICAL EQUIPMENT ELECTROMAGNETIC COMPATIBILITY..................................................................................................... 16
NOTES...................................................................................................................................................................................................................... 19
All registered trademarks are the property of their respective owners.
Technical Support
Technical assistance is available Monday through Friday,
8:00 am to 6:00 pm (Eastern Standard Time).
Phone: 800-659-5922
Fax: 800-659-7255
Customer Service: 800-659-6560
OVERVIEW
Quick Release
Articulating
Headrest
Chair Back
Articulating
Armrest
Chair Seat &
Toeboard with
Scuff Cover
Dual Integrated
Touch Pad
Pump
Cover
Optional
Foot Switch
062082 r01
3
General Information
Definition of Symbols
The following symbols and terms may be used
throughout this manual:
WARNING: Failure to carefully follow the
described procedure may result in damage to the
equipment and/or injury to the patient/operator.
Risk of electrical shock present.
Make sure power is disconnected before
attempting this procedure.
Product Disposal
Contact your local authorized dealer for proper disposal of the
device to ensure compliance with your local environmental
regulations.
Interference with Electromedical Devices
To guarantee the operational safety of electromedical
devices, it is recommended that the operation of mobile radio
telephones in the medical practice or hospital be prohibited.
Strong EMI sources such as electro surgery units or x-ray units
may affect performance. If performance problems occur, move
the unit to another electrical circuit or physical location.
Incompatible Units or Accessories
To guarantee the operational safety and function of this device,
the use of unapproved unit or accessories is not advised.
Doing so could result in potential hazard. Use authorized
accessories and devices only.
See operating instructions.
(AC) Alternating current.
Protective earth (Ground)
Product Identification
This product can be identified by its product label. This
label states the unit model and serial number, electrical
specifications, manufacture date and safety classification.
Note the SAMPLE labels shown below.
Manufacturing Date
Waste Electrical and Electronic Equipment.
046820 Rev. 3 02/11
Conforms with the Essential Requirements of the
European Medical Device Directive 93/42/EEC for
Class I Devices.
DENTAL CHAIR
(230 VAC, 50/60 Hz. 3.5 A)
MN
SP30
SN
MO
YR
IEC Type B, Class 1, IPX4
Operation Mode:Intermittent
Certified to EN 60601-1 UL 60601-1
Certifed to: CAN/CSA - C22.2 NO. 601.1
Conforms with the Essential Requirements of the
European Medical Device Directive 93/42/EEC for
Class IIa Devices.
C
Indicates conformity to General Requirements for
Safety is certified by Intertek Testing Services.
Off
On
EC
4
REP
SP18
SN
MO
YR
IEC Type B, Class 1, IPX4
Operation Mode:Intermittent
Certified to EN 60601-1 UL 60601-1
Certifed to: CAN/CSA - C22.2 NO. 601.1
C
34488
US C
052736 Rev 0, 10/06
11727 Fruehauf Dr.
Charlotte NC, 28273, U.S.A.
WARNING: This product is intended for use
by trained dental/medical professionals only.
Light Switch
European
Authorized
Medical
Device & Representative
QA Services Ltd.
76, Stockport Road,
Timperley.
WA15 7SN.
WARNING: Cheshire,
This
product
is intended for
United Kingdom.
byTel:
trained
dental
professionals
+44 (0) 845
527 5078
Fax: +44 (0) 161only.
903 9787
Email: [email protected] mdqas.com www.mdqas.com
(115 VAC, 50/60 Hz. 7A)
WARNING: Use only original replacement
parts. All repairs should be performed by an
authorized dealer and/or their representatives.
Warning, strong magnetic field.
REP
US C
052735 Rev 0, 10/06
DENTAL CHAIR
MN
WARNING: Only authorized service technicians
should attempt to service this equipment. Use
of other than authorized technicians will void the
warranty.
General mandatory action required, important to
follow instruction. Not a caution.
EC
34488
11727 Fruehauf Dr.
Charlotte NC, 28273, U.S.A.
046820 Rev. 3 02/11
Type B Applied part.
ELECTRICAL SPECIFICATIONS
Volts CyclesAmps
115 VAC 60 HZ 8 A ~
230 VAC 50 HZ 4 A ~
use
Medical Device & QA Services Ltd.
76, Stockport Road,
Timperley.
Cheshire, WA15 7SN.
United Kingdom.
Tel: +44 (0) 845 527 5078 Fax: +44 (0) 161 903 9787
Email: [email protected] mdqas.com www.mdqas.com
All fuses are labeled at point of use. Replace
fuses only with type and rating as indicated.
IEC Medical Device Classification
Classification:
1
Type:
B
Operation Mode:
Intermittent - 5% Duty Cycle
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SAFETY
Review the following safety precautions to avoid injury and prevent damage to this equipment. Use this product only as
specified.
WARNING: A dental chair may include
magnets in the construction of the device
which may temporarily affect the function/
programming of some implantable
pacemakers or defibrillators. If the implanted
device is programmed to respond to a
magnet, people who have these types of
devices should avoid dental chairs with
magnets.
WARNING: Failure to disinfect equipment
between patients could expose user/patient
to cross contamination and bio-burden/biocontamination.
WARNING: Maximum load rating for this chair
is 450 lbs. To avoid personal injury and/or
damage to the chair, do not exceed this limit.
WARNING: Use caution when using arm rests
for leverage when exiting the chair, as arms
may move and cause patient to fall or get
injured.
This product is designed for use in an indoor,
temperature-controlled, office environment.
WARNING: No modification of this
equipment is allowed.
WARNING: To avoid possible injury and/or
damage to the chair, do not apply full body
weight on the headrest, backrest, toeboard or
armrest(s). Doing so may cause the chair to tip.
WARNING: To avoid risk of electric shock, this
equipment must be connected only to supply
mains with protective earth.
To avoid instability, do not extend components
on poles (i.e. lights. monitors, units) to the
extreme extended position simultaneously on
the same side of the chair.
WARNING: Use a licensed electrician for all
wiring.
WARNING: Do not operate chair when any
cover is removed. Doing so may result in
injury to the operator.
WARNING: Power cords and their
associated parts cannot be substituted
without increased risk of electric shock
or fire. We recommend the use of original
equipment replacement parts only. Power
cords must be installed by qualified
personnel. Make sure all service loops,
strain reliefs, and cord guards are in place
and that line, neutral and ground wires are
secured.
WARNING: Do not place knees or legs
under chair arm support when chair is being
lowered.
WARNING: To avoid injury, discontinue use of
chair if oil is seen leaking from chair hydraulic
system and have serviced by an authorized
dealer.
WARNING: This product must be disinfected
before use.
WARNING: Use caution when filling the
hydraulic reservoir to avoid overflow and
spillage.
As manufacturers of electro-medical products we can assume responsibility for safety-related performance of the equipment
only if maintenance, repair and modifications are carried out only by us or agencies we have authorized for this purpose, and
if all components affecting safe operation of the chair that may be needed are replaced with original factory authorized parts.
We suggest that you request a certificate showing the nature and extent of the work performed, from those who carry out
such work, and specify that the certificate show any changes in rated parameters or working ranges, as well as the date, the
name of the firm and a signature.
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5
Regulatory Information
Technical Description
The dental chair is used to position the patient so that the oral cavity is in the desired position for the dentist to perform
various dental procedures and is hydraulically operated. There are two dynamic functions: the base (up/down) and the
back (incline/recline). These functions are activated by use of either a footswitch or a hand-operated touch pad.
The dental chair has the provision to mount additional dental equipment, including over-the-patient delivery systems. For
this purpose, the chair must provide a stable foundation for both the patient and the additional equipment.
Power to the chair is either 115 or 230 VAC. The power is delivered to a microprocessor controlled printed circuit board.
Software in the microprocessor controls the movement of the chair. The dentist can program some chair models to preset
positions.
The dental chair is classified as a Class I device per FDA CFR 21, Health Canada, and
under rule 1 of Annex IX of the MDD 93/42/EEC.
Product Identification
DENTAL CHAIR
(230 VAC, 50/60 Hz. 3.5 A)
MN
SP30
SN
MO
YR
IEC Type B, Class 1, IPX4
Operation Mode:Intermittent
Certified to EN 60601-1 UL 60601-1
Certifed to: CAN/CSA - C22.2 NO. 601.1
C
34488
US C
052735 Rev 0, 10/06
11727 Fruehauf Dr.
Charlotte NC, 28273, U.S.A.
6
062082 r01
046820 Rev. 3 02/11
046820 Rev. 3 02/11
This dental chair can be identified by its product label, located underneath the chair seat. This label states the chair model,
serial number, electrical specifications, manufacture date and safety classification. Note the SAMPLE labels shown below.
DENTAL CHAIR
(115 VAC, 50/60 Hz. 7A)
MN
SP18
SN
MO
YR
IEC Type B, Class 1, IPX4
Operation Mode:Intermittent
Certified to EN 60601-1 UL 60601-1
Certifed to: CAN/CSA - C22.2 NO. 601.1
C
34488
US C
052736 Rev 0, 10/06
11727 Fruehauf Dr.
Charlotte NC, 28273, U.S.A.
operation
Dual Intergrated Touch Pads
Dual touch pads are located on the arm supports and are
oriented so the practicioner can easily read the button
functions without moving out of position. The touch pad
can program up to 4 preset chair positions. Also, the user
can operate the dental light and the chair swivel lock by
depressing the corresponding buttons from the touch
pad.
Secure Touch Feature on Dual Touchpads
Each dual touchpad located on the arms is equipped
with a Secure Touch feature which prevents accidental
button activation or chair movement. The Secure Touch
button must first be pressed before any other buttons
are activated except for swivel break lock. To use the
dual touchpad, simply press Secure Touch first and
then immediately press the next desired key(s) for chair
movement.
NOTE: If chair has been left idle for 7 seconds, activate
the dual touchpads again by pressing the Secure Touch
button.
0
1
T
2
3
(Press once to activate Position 3)
3
Seat Base Up (Manual)
(Manual)
Chair back Recline (Manual)
Seat Base Down (Manual)
Chair Swivel Unlock Button
Chair Control and One Touch Programming
The chair can be controlled by the dual integrated touch
pads located on the arm supports or by the optional foot
control or other units. Chair positions are factory set with
preprogrammed positions which can be accessed by
using the Auto Buttons on either touch pad.
This chair also features a one-touch programming function
which allows the Auto buttons to be easily changed to a
new preprogrammed position. Programmed positions set
on one touchpad are available on the other touchpads.
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WARNING: When lowering chair, ensure
adequate distances between legs, chair and
equipment to prevent possible injury.
7
operation
To Operate Auto Buttons
After pressing Secure Touch Button once, press the desired auto button once. Chair should automatically move to the preprogrammed position.
Typical Preset Positions
POSITION 0: Entry/Exit
POSITION 1: Primary Operating
Position
POSITION 2: Secondary Operating Position
POSITION 3: X-Ray
or Rinse Position
Reprogramming Auto Buttons from Chair
30°
30°
1. Press and release Secure Touch button on the chair to activate the touchpad.
2. Adjust the chair to the desired position using the manual movement buttons as necessary.
3. While touchpad is still in active mode press and hold the desired Auto Button to be programmed (0, 1, 2 or 3) for a few seconds. Chair will beep to confirm the position has been set.
4. Repeat procedure to program the other Auto Buttons if desired.
Chair Swivel Lock Release
The chair rotates a total of +/- 30° at 10° detent intervals. To rotate the chair, press and hold the chair swivel unlock button
to release the brake mechanism. Once the chair is rotated to the new desired position, release the button and guide chair
into the new detent position.
8
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operation
Foot Control Operation
Chair Base Up (Manual)
0
1
Chair Back Incline
(Manual)
Chair Base Down (Manual)
Chair Back Declined
(Manual)
Reprogramming Auto Buttons 0 or 1
1. Using the manual buttons, adjust the chair to the desired
position.
2. Press and hold the LEARN button, the chair will beep once to confirm. While holding the LEARN button, press the desired auto button ("0" or "1") TWO TIMES and listen for one quick beep to confirm the position has been set.
3. To program the second auto button repeat the procedure.
NOTE: Chair control devices operate the same
programmed positions. Changing a position on one
device will change the position for all devices.
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9
operation
Articulating Headrest
The articulating headrest can be adjusted by pressing
and holding the Quick Release Button and positioning the
headrest into the desired position. Release the button to
lock headrest into place.
WARNING: Support the patient's head when
adjusting the headrest. Failure to do so may
result in injury to the patient.
10
062082 r01
operation
Armrest
The armrest is designed to slide out of the way for easier
patient entry and exit. To slide armrest back for entry of
exit, lift and slide the armrest release trigger and slide the
armrest until it reaches the back position. To return the
armrest to the normal position, slide the arm forward until
it locks into place.
WARNING: Use caution when using the
armrest for leverage while entering or
exiting the chair. Risk of injury to the patient
could occur.
Armrest
Release
Trigger
Lower Truss Cover Stop Feature
This is a dual switch stop feature located on lower truss
cover that will stop all downward movement of the chair
base if triggered.
Lower Truss
Cover
WARNING: Do not place anything under the
chair base cover while the chair is operating,
as it could result in injury.
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11
operation
ErgoSoothe™ Massage Option
ErgoSoothe™ Massage bladders are located in the backrest cushions. These bladders are air driven and will fluctuate as
the massage takes place.
To activate the full massage feature, flip both switches up to the“ON” position. Flip both switches down to the “OFF”
position to deactivate the entire massage.
If only the shoulder area is to be massaged, flip the shoulder switch to “ON” and keep the lumbar switch in the “OFF”
position (or vice versa to only activate the lumbar massage).
12
062082 r01
operation
Optional Air / Water Outlets and Electrical Outlet
The optional air / water outlets and electrical outlets are conveniently located underneath the seat and are attached to the
seat rail. These outlets can accommodate extra auxiliary equipment that is within the user's reach.
The outlet is rated at a maximum of 1.5 amp. per outlet. If the 4 amp. circuit breaker should open, reset by pressing reset
button.
The water outlet accepts 1/4 in. Quick Disconnect fitting and has an integral shut-off valve. Next to the water outlet is a
control valve to adjust flow from the water outlet.
The air outlet accepts a 3/8 in. Quick Disconnect fitting and has an integral shut-off valve.
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13
Cleaning, Disinfecting, & Sterilization
Equipment should be cleaned with a solution of mild detergent and warm water. Although many surface disinfectants
are available for use in dental treatment rooms, some of these can cause discoloration of painted, plated or anodized
surfaces with repeated use. This can be minimized by adhering to the disinfectant manufacturer's instructions
and by frequently washing the disinfected surface afterwords with mild detergent and water.
Important: Do not use powdered cleansers, scouring pads or abrasive scrubbers on any of the painted, plastic or metal
surfaces of this dental unit. To remove dried-on material, use a plastic soft-bristled brush and a solution of mild
detergent.
Disinfection & Sterilization
Infection control in the dental office continues to be a
high priority for our customers and end users. OSHA,
the ADA and the CDC are also involved in this complex
issue. The Manufacturer will not attempt to specify the
required intervals for disinfection nor can it recommend
the overall best surface disinfectant. The question is
often asked, "What should I use to disinfect my dental
unit, chair and light?" This question is more complex than
it seems because of the wide variety of products on the
market as well as formulations of the products changing
to meet the needs of increased asepsis. Please refer to
the Infection Control Recommendations published by the
American Dental Association for further information.
Barrier Technique
The Manufacturer strongly advocates that the barrier
technique be used whenever possible to preserve the
finish and appearance of the equipment.
Wherever possible disposable barriers should be used
and changed between patients. The barrier technique will
ensure maximum long term durability of the surfaces and
finishes of the equipment.
Chemical Disinfection
Regardless of the chemical disinfectant used, it is
imperative that the equipment be thoroughly washed with
mild soap and warm water at least once per day. This
wash down will minimize the harmful effects of chemical
disinfectant residues being allowed to accumulate on the
equipment. When using chemical disinfectants, always
pay strict attention to the disinfectant manufacturer's
directions. When using concentrated disinfectants,
measure the concentrate carefully and mix according
to package directions. Disinfectant solutions that are
relatively harmless to surfaces at their recommended
strengths can be corrosive at higher than recommended
dilution ratios.
Unacceptable Disinfectants
These disinfectants will harm the surface finishes of
dental equipment and are not recommended. Use of
any of these chemicals will void your warranty.
Conditionally Acceptable Disinfectants*
The following disinfectants have been found to be the
least harmful to the equipment surfaces by our test
methods.
Chemical Composition
Chemical Composition
Quaternary Ammonium
Strong Phenols/Phenol Alcohol combinations
Sodium Hypochlorite/Household Bleach
Sodium Bromide
Strong Alcohol
Household Cleaners (Dental EQuipment Only)
Citric Acids
Iodophors**
Ammonium Chloride
Accelerated Hydrogen Peroxide (0.5%)
Disinfect only by wiping, no spray disinfection.
Please be aware that Pelton & Crane expressly rejects any claims for warranty or damages when using any other
cleaning or disinfecting solutions.
WARNING *The Manufacturer makes no representation as to the disinfectant efficacy of these products. We
make no warranty expressed or implied that these disinfectants will not damage the surface finishes. Damage or
discoloration of the surface finishes are not covered under the warranty.
**lodophor-based disinfectants will cause yellow staining on many surfaces.
14
062082 r01
Cleaning, Disinfecting, & Sterilization
Cleaning Dental Chair Upholstery
NOTE: With all cleaning products, first clean a small, inconspicuous area to ensure the material will not discolor or fade.
It is recommended that each stain be cleaned in a step-by-step manner using the sequence below:
1. Regular Cleaning
Use a Solution of 10% household liquid dish soap with warm water applied with a soft damp cloth. Rinse area with
clean water and wipe dry. Cleaning frequency depends upon use. It is recommended that upholstery be cleaned
between patients.
2. Stubborn Stains
Use detergent cleaners such as Formula 409 ® or Fantastik ®. Wipe using a soft cloth or plastic soft bristle brush.
Rinse with clean water and wipe dry.
3. More Difficult Stains
Carefully clean the stained area with lighter fluid (naphtha) or rubbing alcohol. Apply using a soft, white cloth and
rub gently. Rinse with clean water and wipe dry.
4. Ultra Leather Upholstery
Clean spots with mild soap and water or an ordinary household cleaner such as Fantastik ® or Formula 409 ®.
Wipe off any residue using a clean, damp cloth. Air dry or dry quickly with the warm setting on a hair dryer.
Disinfect ultra leather upholstery with a 9:1 water:bleach solution.
Other Tips
Always apply cleaners with a soft white cloth. Avoid the use of paper towels.
When using strong cleaning solutions (such as alcohol), it is advisable to first test in an inconspicuous area.
Never use harsh solvents or cleaners that are intended for industrial use.
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15
MEDICAL ELECTRICAL EQUIPMENT ELECTROMAGNETIC COMPATIBILITY
INSTRUCTIONS FOR USE
ELECTROMAGNETIC COMPATIBILITY
Electrical medical devices are subject to special EMC safety measurements and as a result the equipment
must be properly installed according to the Pelton and Crane installation instruction manual.
PORTABLE ELECTRONIC DEVICES
Portable and mobile high frequency electronic communications equipment may interfere with electronic
medical devices.
STATIC SENSITIVE DEVICES
Where labeled this equipment contains static sensitive devices that require special
precautions when handling. At a minimum a grounded wrist strap that is connected
to ground stud should be worn to reduce the possibility of damage to the unit.
ATTENTION
OBSERVE PRECAUTIONS
FOR HANDLING
ELECTROSTATIC
SENSITIVE DEVICES
MEDICAL ELECTRICAL EQUIPMENT ELECTROMAGNETIC COMPATIBILITY
TECHNICAL DESCRIPTION
ELECTROMAGNETIC COMPATIBILITY
This equipment has been tested and found to comply with the requirements for medical devices of
IEC 60601-1-2 and is intended to be installed in a typical medical environment.
ACCESSORY USE
Using accessory devices not specified by Pelton and Crane for use with their equipment may results in an
increase of electromagnetic emissions and/or a decrease in electromagnetic immunity of the system.
INTERFERENCE FROM OTHER EQUIPMENT
If other equipment is used adjacent to or stacked with the Pelton and Crane equipment the system must be
observed to verify normal operation.
16
062082 r01
Guidance and manufacturer's declaration-electromagnetic emissions
The Model SP30 is intended for use in the electromagnetic environment specified below. The
customer or the user of the SP30 should assure that it is used in such an environment.
Emissions Test
Compliance
RF emissions
CISPR-11
Group 1
RF emissions
CISPR-11
Class A
Harmonic Emissions
IEC 61000-3-2
Class A
Voltage Fluctuations/ Flicker
Emissions
IEC 61000-3-3
Electromagnetic Environment Guidance
The SP30 chairs use RF energy only
for its internal function. Therefore, their
emissions are very low and are not likely
to cause any interference in nearby
electronic equipment.
The SP30 chairs are suitable for use
in all establishments, other than
domestic establishments and those
directly connected to the public low
voltage power supply network that
supplies buildings used for domestic
purposes.
Complies
Recommended separation distances between portable and
mobile RF communications equipment and the unit
The Model SP30 is intended for use in the electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the SP30 can help prevent electromagnetic
interference by maintaining a minimum distance between portable and mobile RF communications
equipment (transmitters) and the SP30 as recommended below, according to the maximum output of
the communications equipment.
Rated maximum output
power of transmitter
W
0.01
0.1
1
10
100
Separation distance according to frequency of transmitter
m
150 kHz to 80 MHz
d= 1.2√P
80 MHz to 800 MHz
d= 1.2√P
800 MHz to 2.5 GHz
d= 2.3√P
0.12
0.12
0.38
1.2
3.8
12
0.23
0.73
2.3
7.3
23
1.2
3.8
12
For transmitters rated at a maximum output power not listed above, the recommended separation
distance d in meters (m) can be estimated using the equation applicable to the frequency of the
transmitter where P is the maximum output power rating of the transmitter in watts (W) according to the
transmitter manufacturer.
NOTE 1: At 80 MHz to 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
062082 r01
17
Guidance and manufacturer's declaration-electromagnetic immunity
The Model SP30 Dental Chairs are intended for use in the electromagnetic environment specified
below. The customer or the user of the SP30 should assure that it is used in such an environment.
Immunity Test
Electrostatic Discharge
(ESD) IEC
61000-4-2
61000-4-2
Electrical Fast
Transient/Burst
IEC 61000-4-4
Surge IEC61000-4-5
Voltage Dips, Short
Interruptions and Voltage
Variations on Power
Supply Input Lines
IEC 61000-4-11
IEC60601
Test Level
+/-6 kV contact
+/-8 kV air
+/-6 kV contact
+/-8 kV air
+/-2 kV for power
supply lines
+/-2 kV for power
supply lines
+1-1 kV for input
output lines
Not applicable,
No I/O lines
+/-1 kV differential mode
+/-2 kV common mode
+/-1 kV
differential mode
+/-2 kV
common mode
Floors should be wood, concrete or
ceramic tile. If floors are covered
with synthetic material the relative
humidity should be at least 30%
Where labeled, a ground strap
(connected to ground lug) should be
worn to reduce the possibility of
damage to the unit when servicing.
Mains power quality should be that of
typical commercial or hospital
environment.
Mains power quality should be that of
typical commercial or hospital
environment.
Mains power quality should be that of
typical commercial or hospital
40% UT (60% dip in UT) 40% UT (60% dip in UT)
environment. If the user of the
for 5 cycles
for 5 cycles
SP30 requires continued operation
70% UT (30% dip in UT) 70% UT (30% dip in UT) during power mains interruptions, it is
recommended that the SP30 be
for 25 cycles
for 25 cycles
powered by an uninterrupted power
<5% UT (>95% dip in UT) <5% UT (>95% dip in supply or battery.
3 A/m
UT) for 5 seconds
3 A/m
UT is the AC. mains voltage prior to application of the test level.
18
Electromagnetic
Environment Guidance
<5% UT (>95% dip in UT) <5% UT (>95% dip in
UT) for 0.5 cycle
for 0.5 cycle
for 5 seconds
Power Frequency
(50/60 Hz) Magnetic
Field IEC 61000-4-8
Compliance
Level
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Power frequency magnetic fields
should be at levels characteristic
of a typical location in a typical
commercial or hospital environment.
NOTES
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19
©2014 Pelton & Crane
11727 Fruehauf Drive
Charlotte, NC, 28273 - USA
www.pelton.net
We reserve the right to make any alterations which may be due to any technical improvements.
P/N 062082 Rev. 01, 04/17/14
Printed in USA
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