EKOM DK50 Benutzerhandbuch Seite 11

DK50
7.2. Electromagnetic compatibility declaration
Medical equipment needs special precautions regarding electromagnetic compatibility (EMC) and
needs to be installed and put into service according to the EMC information provided below.
Guidance and manufacturer's declaration - electromagnetic emissions
Pursuant to IEC 60601-1-2:2014 - Medical electrical equipment - Part 1-2: General requirements for
basic safety and essential performance - Collateral Standard: Electromagnetic disturbances
The equipment is intended for use in the electromagnetic environment specified below. The customer or the
user of the equipment 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
06/2020
Compliance
Group 1
Class B
Class A
The equipment is not likely
to cause any flicker, as the
current flow is approx.
constant after the start up.
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Electromagnetic environment - guidance
The equipment uses RF energy only for its
internal functions. Therefore, the RF emissions
are very low and are not likely to cause any
interference in nearby electronic equipment.
The equipment 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.
NP-DK50 simple s DE-4_06-2020