9
D-Light
®
Pro
Guidance and manufacturer’s declaration – Electromagnetic immunity
EN 60601 – 1-2 / Table 202
Immunity test Test level Compliance Electromagnetic environment guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
±6 kV contact
±8 kV air
The device continues
to work regularly and
in safety.
Floors should be wood, concrete or ceramic
tile. If fl oors are covered with synthetic material,
the relative humidity should be at least 30%.
Radiated RF
IEC 61000-4-3
3 V/m 80 Mhz to 2.5 GHz The device continues
to work regularly and
in safety
Field strengths from fi xed transmitters cannot
be predicted theoretically with accuracy. To
assess the electromagnetic environment due
to fi xed RF transmitters, an electromagnetic
site survey should be considered.
Electrical fast
transient / burst
IEC 61000-4-4
±2 kV for power supply
lines
±1 kV for input / output
lines
The device continues
to work regularly and
in safety
Mains power quality should be that of a typical
commercial or hospital environment.
Surge
IEC 610004-5
±1 kV diff erential mode
±2 kV common mode
The device continues
to work regularly and
in safety.
Conducted RF
IEC 61000-4-6
3 Veff 150 kHz to 80 MHz The device continues
to work regularly and
in safety.
Portable and mobile RF communications
equipment should be used no closer to any
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
Power frequency
(50/60 Hz) magnetic
fi eld IEC 61000
3-100 A/m The device continues
to work regularly and
in safety.
Power frequency magnetic fi elds should be at
levels characteristic of a typical location in a
typical commercial or hospital environment.
Voltage dips, short
interruptions and
voltage variations on
power supply input
lines
IEC 61000-4-11
<5% U/10ms
70% U/ 0.5s
40% U/0.1s
The device can vary
from the required
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.
Mains power quality should be that of a typical
commercial or hospital environment.
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