Cutera truSculpt, Operator'S Manual, Page: 51 / 66

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TRUSCULPT OPERATOR MANUAL
D1395, REV. K, 02/18
Electromagnetic Compatibility
The truSculpt system design complies with IEC 60601-1-2 (3rd edition) requirements for electromagnetic
compatibility (EMC) with other devices. Like other electrical medical equipment, the truSculpt system
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 truSculpt system.
WARNING
Do not use cables or accessories other than those provided with the
truSculpt system, as this may result in increased electromagnetic
emissions or decreased immunity to such emissions.
WARNING
If the truSculpt system is used adjacent to or stacked with other
equipment, observe and verify normal operation of the system 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
truSculpt system.
Guidance and Manufacturer’s Declaration: Electromagnetic Emissions
The truSculpt system is intended for use in the electromagnetic environment specified below. The customer or
the user of the truSculpt system should ensure that it is used in such an environment.
Emissions test Compliance Electromagnetic Environment: Guidance
RF emissions CISPR 11 Group 2 The truSculpt system must emit electromagnetic energy to
perform its intended function. Nearby electronic equipment
may be affected.
RF emissions CISPR 11 Class A The truSculpt system is suitable for use in all establishments
other than domestic and those directly connected 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
emissions IEC61000-3-3 Complies