Gebrauchsanweisung Untersuchungseinheit cubeONE,
directions for use, refraction unit cubeONE
33
Wagner & Guder Medical GmbH
issue September 2020
Electromagnetic compatibility (EMC)
Medical electrical equipment is subject to special precautions with regard to EMC and must be
installed and commissioned in accordance with the following guidelines. Portable and mobile HF
equipment (e.g. cell phones) can affect medical electrical equipment. Third-party devices may only be
connected in compliance with the EN 60601-1 standard. The refraction unit fulfills the requirements on
electromagnetic compatibility according to EN 60601-1-2:2007 (IEC 3
rd
Edition) + EN 60601-1-2:2015
(IEC 4
th
Edition).
The following information is only valid in connection with the accessories supplied and included with the
device.
power cord (2,5m)
Guidance and manufacturer’s declaration – Electromagnetic emissions
This product is intended for use in the electromagnetic environment specified below. The customer
or the user of this product should assure that it is used in such an environment
Emission test
Compliance
Electromagnetic enviroment -
guidance
RF Emissions
according to
CISPR 11
Group 1
This product 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
according to
CISPR 11
Class B
This product 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.
Emission of harmonics
according to IEC 61000-3-2
Class B
Voltage fluctuations / flicker
emissions according to EN
61000-3-3
Matches
