ELECTROMAGNETIC COMPATIBILITY
Technical Description
The device satisfies the EMC requirements of the international standard IEC 60601-1-2. The
requirements are satisfied under the conditions described in the table below. The device is an
electrical medical product and is subject to special precautionary measures with regard to EMC
which must be published in the instructions for use. Portable and mobile HF communications
equipment can affect the device. Use of the unit in conjunction with non-approved accessories
can affect the device negatively and alter the electromagnetic compatibility. The device should
not be used directly adjacent to or between other electrical equipment.
Table 1
Guidance and declaration of manufacturer-electromagnetic emissions
The device is intended for use in the electromagnetic environment
specified below. The customer or the user of the device should assure that it
is used in such an environment.
Emissions test
RF emissions CISPR 11
RF emissions CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Electromagnetic environment
Compliance
-guidance
The device uses RF energy only for
Group 1
its internal function. Therefore, its
emissions are very low and are not
likely to cause any interference in
nearby electronic equipment.
Class B
The device is suitable for use in all
establishments, including domestic
establishments and those directly
Class A
connected to the public low-voltage
power supply network that
Compliance
supplies buildings used for domestic
purposes.
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