Gima ECG90A Manuel D'utilisation page 71

Appendix II EMC Guidance and Manufacturer Declaration
Warning
The use of ACCESSORIES other than those specified by the MANUFACTURER of

the device or system, may result in increased EMISSIONS or decreased IMMUNITY
of the ME EQUIPMENT or ME SYSTEM.
① Active medical devices are subject to special EMC precautions and they must be
installed and used in accordance with these guidelines.
② Portable and mobile communication radiation equipment may affect the normal
use the medical device.
③ The device should not be used when they are close to or stacked with other
equipment, if necessary, please observe and verify that they can operate normally in
the configurations.
Basic performance: Stability of working state: Waveform noise and measurement

error appeared during measuring are automatically eliminated 10s after removing
the interference, the working state of device are not changed, it could collect and
record data continuously, and the waveform does not show obvious changes before
and after the test.
Electromagnetic emission
Guidance and manufacture's declaration-electromagnetic emission
The device is tended for use in the electromagnetic environment specified below. The
purchaser or the user of the device should assure that it is used in such an environment.
Emission test
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/
flicker emission
IEC 61000-3-3
Compliance Electromagnetic environment-guidance
Group 1 The device 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.
Class B
The
establishments, including domestic establishments
Class A
and those directly connected to the public low
voltage power supply network that supplies
buildings used for domestic purposes.
Applicable
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device is suitable for use in all