ResMed III Guidance and Manufacturer’s Declaration, Electromagnetic Emissions and Immunity

Guidance and Manufacturer’s Declaration -

Electromagnetic Emissions and Immunity

Guidance and manufacturer’s declaration – electromagnetic emissions

The VPAP is intended for use in the electromagnetic environment specified below. The customer or the user of the VPAP should assure that it is used in such an environment.

Emissions test	Compliance	Electromagnetic environment -
		guidance
RF emissions CISPR11	Group 1	The VPAP 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.
RF emissions CISPR 11	Class B	The VPAP is suitable for use in all
		establishments, including domestic
Harmonic Emissions	Class A	establishments and those directly
IEC 61000-3-2		connected to the public low-voltage
		network that supplies buildings used
Voltage Fluctuations/Flicker	Complies	for domestic purposes.
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 should not be used adjacent to or stacked with other equipment.

If adjacent or stacked use is necessary, the VPAP 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.

System Specifications 39