ResMed S8 - Manual (Page 35)

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G UIDANCE AND M ANUFACTURER ’ S D ECLARATION - E LECTROMAGNETIC
E MISSIONS AND I MMUNITY
Guidance and manufacturer’s declaration—electromagnetic emissions
The S8 series of devices is intended for use in the electromagnetic environment specified below. The
customer or the user of the S8 device should assure that the device is used in such an environment.
Emissions test Compliance
Electromagnetic environment—
guidance
RF emissions CISPR11 Group 1 The S8 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.
RF emissions CISPR 11 Class B* The S8 device is suitable for use in all
establishments, including domestic
establishments and those directly
connected to the public low-voltage
network that supplies buildings used for
domestic purposes.
Harmonic Emissions
IEC 61000-3-2
Class A
Voltage Fluctuations/Flicker
Emissions IEC 61000-3-3
Complies
* Class B for all system configurations except when a PC is attached to the S8 device via a serial adapter,
in which case the system is Class A compliant. Class A is suitable for use in all establishments other than
domestic and those directly connected to a low voltage power supply network which supplies buildings
used for domestic purposes.
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 S8 device should not be used adjacent to or stacked with other equipment.
If adjacent or stacked use is necessary, the S8 device 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 S8 device.
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