gc D-Light Pro Bedienungsanleitung Seite 9

Guidance and manufacturer's declaration – Electromagnetic immunity
EN 60601 – 1-2 / Table 202
Immunity test Test level
Electrostatic ±6 kV contact
discharge (ESD) ±8 kV air
IEC 61000-4-2
Radiated RF 3 V/m 80 Mhz to 2.5 GHz
IEC 61000-4-3
Electrical fast ±2 kV for power supply
transient / burst lines
IEC 61000-4-4 ±1 kV for input / output
lines
Surge ±1 kV diff erential mode
IEC 610004-5 ±2 kV common mode
Conducted RF 3 Veff 150 kHz to 80 MHz
IEC 61000-4-6
Power frequency 3-100 A/m
(50/60 Hz) magnetic
fi eld IEC 61000
Voltage dips, short <5% U/10ms
interruptions and
voltage variations on 70% U/ 0.5s
power supply input
lines 40% U/0.1s
IEC 61000-4-11
Compliance Electromagnetic environment guidance
The device continues Floors should be wood, concrete or ceramic
to work regularly and tile. If fl oors are covered with synthetic material,
in safety. the relative humidity should be at least 30%.
The device continues Field strengths from fi xed transmitters cannot
to work regularly and be predicted theoretically with accuracy. To
in safety assess the electromagnetic environment due
to fi xed RF transmitters, an electromagnetic
site survey should be considered.
The device continues Mains power quality should be that of a typical
to work regularly and commercial or hospital environment.
in safety
The device continues
to work regularly and
in safety.
The device continues Portable and mobile RF communications
to work regularly and equipment should be used no closer to any
in safety. part of the disposal, including cables, than the
recommended separation distance calculated
from the equation applicable to the frequency
of the transmitter.
Recommended separation distance1):
d = 1.2 √P
d = 1.2 √P 80 MHz to 800 Mhz
d = 2.3 √P 800 MHz to 2.5 GHz
The device continues Power frequency magnetic fi elds should be at
to work regularly and levels characteristic of a typical location in a
in safety. typical commercial or hospital environment.
The device can vary Mains power quality should be that of a typical
from the required commercial or hospital environment.
levels of immunity
with a duration for as
long as the device
remains in safety; no
malfunctions have
been detected and
can be restored to
pre-test status with
the intervention of
the operator.
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