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All interface cables used to connect
peripherals must be shielded in order to
comply with the limits for a digital device
pursuant to Subpart B of part 15 of FCC
Rules.
For the customers in the U.S.A.
This device complies with part 15 of the FCC
Rules.
Operation is subject to the following two
conditions:
(1) This device may not cause harmful
interference, and
(2) this device must accept any interference
received, including interference that may
cause undesired operation.
For the customers in Canada
CAN ICES-3 (A)/NMB-3(A)
For the customers in Canada
This unit has been certified according to
Standard CAN/CSA-C22.2 No.60601-1.
WARNING on power connection
Use a proper power cord for your local power
supply.
1. Use the approved Power Cord (3-core
mains lead) / Appliance Connector / Plug
with earthing-contacts that conforms to
the safety regulations of each country if
applicable.
2. Use the Power Cord (3-core mains
lead) / Appliance Connector / Plug
conforming to the proper ratings
(Voltage, Ampere). If you have
questions on the use of the above Power
Cord / Appliance Connector / Plug,
please consult a qualified service
personnel.
Warning on power connection for medical use
Please use the following power supply cord.
With connectors (plug or female) and cord
types other than those indicated in this table,
use the power supply cord that is approved
for use in your area.
Plug Type
Cord Type
Minimum Rating for
Plug and Appliance
Couplers
Safety Approval
*Note: Grounding reliability can only be
achieved when the equipment is connected
to an equivalent receptacle marked 'Hospital
Only' or 'Hospital Grade'.
For the customers in the U.S.A and Canada
When you use this product connected to
240 V single phase, be sure to connect this
product to a center tapped circuit.
Important safeguards/notices for use in the
medical environments
1. All the equipments connected to this unit
shall be certified according to Standard
IEC60601-1, IEC60950-1, IEC60065 or
other IEC/ISO Standards applicable to
the equipments.
2. Furthermore all configurations shall
comply with the system standard
IEC60601-1-1. Everybody who connects
additional equipment to the signal input
part or signal output part configures a
medical system, and is therefore,
responsible that the system complies
with the requirements of the system
standard IEC60601-1-1.
If in doubt, consult the qualified service
personnel.
3. The leakage current could increase
when connected to other equipment.
4. For this particular equipment, all
accessory equipment connected as
noted above, must be connected to
mains via an additional isolation
transformer conforming with the
construction requirements of IEC60601-
1 and providing at least Basic Insulation.
5. This equipment generates, uses, and
can radiate radio frequency energy. If it
is not installed and used in accordance
with the instruction manual, it may cause
interference to other equipment. If this
United States and
Canada
HOSPITAL GRADE*
Min.Type SJT
Min.18 AWG
10A/125V
UL Listed and CSA
3
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