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TRUSCULPT OPERATOR MANUAL
D1395, REV. K, 02/18
The Cutera truSculpt system has been tested and found to comply with the limits for medical devices to
IEC/EN 60601-1-2:2001. These limits are designed to provide reasonable protection against harmful
interference in a typical medical installation. The truSculpt system generates, uses, and can radiate radio
frequency energy and, if not installed and used in accordance with the instructions, may cause harmful
interference to other devices in the vicinity. If the truSculpt system does cause harmful interference to
other devices, which can be verified by turning the console off and on, the user is encouraged to try to
correct the interference by one or more of the following measures:
• Reorient or relocate the receiving device.
• Increase the separation between the affected equipment and the truSculpt system.
• Connect the affected equipment to an outlet or circuit different from that to which the
truSculpt system is connected.
• Consult the manufacturer or field service technician for help.
The truSculpt system is a high frequency medical device with respect to electrical shock, fire, and
mechanical hazards only in accordance with: IEC/EN 60601-1, IEC/EN 60601-1-2, IEC/EN 60601-1-4,
and IEC/EN 60601-2-2.
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