Cutera GenesisPlus, Operator'S Manual, Page: 61 / 80

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GenesisPlus Operator Manual
D1151, R
EV
C, 10/16
Electromagnetic Compatibility
The GenesisPlus design complies with IEC 60601-1-2 (3rd edition) requirements for electro-
magnetic compatibility (EMC) with other devices. Like other electrical medical equipment, the
GenesisPlus requires special precautions to ensure EMC with other electrical medical devices
and must be installed and operated according to the EMC information provided in this manual.
CAUTION
Portable and mobile RF communications equipment may affect the
normal function of the GenesisPlus.
WARNING
Do not use cables or accessories other than those provided with the
GenesisPlus, as this may result in increased electromagnetic emis-
sions or decreased immunity to such emissions.
WARNING
If the GenesisPlus is used adjacent to or stacked with other equip-
ment, observe and verify normal operation of the GenesisPlus in the
configuration in which it will be used prior to using it in a surgical
procedure. Consult the tables below for guidance in placing the
GenesisPlus.
Guidance and Manufacturer’s Declaration: Electromagnetic Emissions
The GenesisPlus is intended for use in the electromagnetic environment specified below. The customer or the user of the
GenesisPlus should ensure that it is used in such an environment.
Emissions test Compliance Electromagnetic Environment: Guidance
RF emissions CISPR 11 Group 1 The GenesisPlus uses RF energy only for its internal function;
therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
RF emissions CISPR 11 Class B The GenesisPlus is suitable for use in all establishments,
including domestic establishments and those directly con-
nected to the public low voltage power supply network that
supplies buildings used for domestic purposes.
Harmonic emissions IEC61000-3-
2 Class A
Voltage Fluctuations/flicker emis-
sions IEC61000-3-3 Complies