Guidelines And Manufacturer's Statement - Electromagnetic Emissions - Arthrex Synergy Insufflation FM134 Instructions D'utilisation

Insufflateur pour la laparoscopie
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Electromagnetic Compatibility
EN
56
12.5
Guidelines and Manufacturer's Statement – Electromagnetic
Emissions
The insufflator is intended for use in an environment as described below. The
user/operator of the insufflator should make sure the device is operated within
such an environment.
Emitted interference
Compliance
measurements
HF emission according
Group 1
to CISPR 11
HF emission according
Class B
to CISPR 11
Emission of harmonic
Class A
oscillations according
to IEC 61000-3-2
Emission of voltage
In compliance
fluctuations / flickers
according to IEC 61000-
3-3
Electromagnetic environment guide-
lines
The insufflator uses HF energy solely
for its internal functions. Therefore,
the camera's HF emission is very low
and it is unlikely that devices in close
proximity will experience interfer-
ence.
The insufflator is suitable for use in
all facilities including those in resi-
dential areas and those directly con-
nected to a public utility network
also supplying buildings used for res-
idential purposes.

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