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Manufacturer's EMC declaration
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Medical electrical devices such as Soleo SonoStim / Soleo Stim are subject to special precautions
regarding electromagnetic compatibility (EMC) and must be installed and put into service according to
the EMC information provided in these operating instructions for use and any accompanying
documents.
Portable and mobile RF communications devices (such as mobile telephones) may interfere with
medical electrical devices.
Soleo SonoStim / Soleo Stim should only be operated with the original mains cable specified in the list
of contents delivered. The use of accessories other than those specified may result in increased
emissions or decreased immunity of the device.
Guidance and manufacturer's declaration – electromagnetic emissions
The Soleo SonoStim / Soleo Stim is intended for use in one of the electromagnetic environments specified below.
The customer or the user of the Soleo SonoStim / Soleo Stim device should ensure that the device is used in such
an environment.
Emissions tests
Compliance
Electromagnetic environment – guidance
RF emissions CISPR 11
Group 2
The Soleo SonoStim / Soleo Stim device must
emit electromagnetic energy in order to
perform its intended function. Nearby
electronic equipment may be affected.
RF emissions CISPR 11
Class B
The Soleo SonoStim / Soleo Stim device is
suitable for use in all establishments, including
domestic establishments and those directly
connected to the public low-voltage power
supply network that supplies buildings used for
domestic purposes.
Harmonic emissions IEC 61000-3-2
Class A
Voltage fluctuation emissions and flicker
IEC 61000-3-3
Complies
Table 201 as per EN 60601-1-2:2006-10
The device should not be used adjacent to or stacked with other equipment. If adjacent or stacked use
is necessary, the device should be monitored to verify normal operation in the configuration in which it
will be used.
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