Guidance And Manufacturer's Declaration - Electromagnetic Emissions And Immunity - ResMed VPAP III ST-A Manuel Utilisateur

Guidance and Manufacturer's Declaration - Electromagnetic
Emissions and Immunity
Guidance and manufacturer's declaration – electromagnetic emissions
The VPAP III ST-A is intended for use in the electromagnetic environment specified below. The
customer or the user of the VPAP III ST-A should assure that it is used in such an environment.
Emissions test
RF emissions CISPR11
RF emissions CISPR 11
Harmonic Emissions
IEC 61000-3-2
Voltage Fluctuations/Flicker
Emissions IEC 61000-3-3
Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed
and put into service according to EMC information provided in this document.
Warnings: The VPAP III ST-A should not be used adjacent to or stacked with other equipment.
If adjacent or stacked use is necessary, the VPAP III ST-A should be observed to verify normal
operation in the configuration in which it will be used.
The use of accessories (eg, humidifiers) other than those specified in this manual is not
recommended. They may result in increased emissions or decreased immunity of the
VPAP III ST-A.
Electromagnetic environment -
Compliance
guidance
Group 1 The VPAP III ST-A 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 VPAP III ST-A is suitable for use in
all establishments, including domestic
Class A establishments and those directly
connected to the public low-voltage
network that supplies buildings used
Complies for domestic purposes.
System Specifications 45