Use Instructions

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11. ELECTROMAGNETIC COMPATIBILITY
11.1 GENERAL PRECAUTIONS AND WARNINGS
 Electrical medical devices and systems are subject to special measures concerning
electromagnetic compatibility (EMC) and must be installed in accordance with the EMC
instructions contained in this enclosed document.
 Portable and mobile radiofrequency communication systems may interfere with electrical
medical devices.
 The use of accessories and cables other than those supplied with the devices, with the
exception of the cable sold by the equipment manufacturer as spare parts, may result in
increased emissions and reduced device or system immunity.
 The device must not be used when it is in contact with other electro-medical devices.
11.2 ELECTROMAGNETIC EMISSIONS
The device is intended for use in the following electromagnetic environment. You must ensure
compliance with this guideline.
GUIDANCE AND MANUFACTURER’S DECLARATION
–
ELECTROMAGNETIC EMISSIONS
The EMBODY is intended for use in the electromagnetic environment specified below.
The operator of the EMBODY should ensure that it is used in such an environment.
Emission test
Compliance
Electromagnetic environment
-
Guidance
Radiated RF emission
acc. to CISPR 11
Group 1
Class B
EMBODY uses RF energy only for its internal
functions. Therefore, its RF emissions are very
low and are not likely to impair nearby
electronic equipment.
Conducted RF
emissions acc. to
CISPR 11
Group 1
Class A
EMBODY is suitable in all establishments other
than those in residential areas and those
directly connected to the public low voltage
power supply network that also supplies
buildings used for residential purposes.
Harmonic emissions
acc. to IEC 61000-3-2
compliant
Voltage fluctuations /
Flicker emissions acc.
To
IEC 61000
-
3
-
3
compliant
Table 20 - Electromagnetic emissions