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EN
INFORMATION ABOUT ELECTROMAGNETIC COMPATIBILITY (EMC)
The stimulator is designed to be used in typical domestic environments approved in accordance with the safety standard EMC
EN 60601-1-2.
This device emits very low levels in the radio frequency (RF) interval and is therefore not likely to cause interference with
nearby electronic equipment (radios, computers, telephones, etc.).
The stimulator is designed to withstand foreseeable disturbances originating from electrostatic discharge, magnetic elds
from the power supply or radio frequency emitters.
However, it is not possible to guarantee that the stimulator will not be aected by powerful RF (radio frequency) elds
originating, for example, from mobile phones.
For more detailed information about electromagnetic emissions and immunity, please contact Compex.
STANDARDS
To ensure your safety, the stimulator has been designed, manufactured and distributed in accordance with the requirements
of the amended European Directive 93/42/CEE covering medical devices.
The stimulator also complies with the CEI 60601-1 standard covering general safety requirements for electromedical devices,
with the CEI 60601-1-2 standard covering electromagnetic compatibility and the CEI 60601-2-10 standard covering special
safety requirements for nerve and muscle stimulators.
In accordance with current international standards in force, a warning must be given about applying electrodes to the thorax
(increased risk of cardiac brillation).
The stimulator also complies with Directive 2002/96/CEE covering waste electrical and electronic equipment (WEEE).
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