EKOM ASPINA DO M Benutzerhandbuch Seite 14

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
NP-DO M-39_12-2021
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.
14
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.
TECHNICAL DATA
12/2021