DK50-10
NP-DK50-10-16_01-2022-MD - 14 - 01/2022
Guidance and manufacturer's declaration - electromagnetic immunity
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.
Electromagnetic environment -
guidance
discharge (ESD)
IEC 61000-4-2
Floors should be wood, concrete
or ceramic tile. If floors are covered
with synthetic material, the relative
humidity should be at least 30%.
transient/burst
IEC 61000-4-4
lines
±1 kV for
input/output lines
100 kHz repetition
frequency
Applied to mains
connection
Mains power quality should be
that of a typical commercial or hospital
environment.
±2 kV L-PE; N-PE
Applied to mains
connection
Mains power quality should be that of
a typical commercial or hospital
environment.
short interruption,
and voltage
variations on
power
supply
input lines IEC
60601-4-11
(at 0, 45, 90, 135,
180, 225, 270
and 315°)
U
T
=0%, 1 cycle
U
T
=70% 25/30
cycles (at 0°)
U
T
=0%, 250/300
cycles
(at 0, 45, 90, 135, 180,
225, 270 and 315°)
U
T
=>95%, 1 cycle
U
T
=70% (30% dipp
U
T
),
25(50Hz)/30(60Hz)
cycles (at 0°)
U
T
=>95%,
250(50Hz)/300(60Hz)
cycle
Mains power quality should be
that of a typical commercial or hospital
environment.
The device stops and restarts
automatically at each dip. In this case
does not occur unacceptable pressure
drop.
The equipment does not contain
magnetically sensitive components or
circuits.
NOTE: U
T
is the A.C. mains voltage prior to application of the test level.