3
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)
This unit has been certified according to Standard
CAN/CSA-C22.2 No.60601-1.
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 IEC 60601-1-1. 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 unit causes
interference (which can be determined by
unplugging the power cord from the unit), try these
measures: Relocate the unit with respect to the
susceptible equipment. Plug this unit and the
susceptible equipment into different branch circuit.
Consult your dealer. (According to standard IEC60601-
1-2 and CISPR11, Class B, Group 1)
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