Electromagnetic Immunity - Dräger Fabius GS premium Instructions For Use Manual

Electromagnetic immunity

The medical device is intended for use in an
electromagnetic environment as specified below.
The user must ensure that the medical device is
used in such an environment.
Immunity against
Electrostatic discharge
(ESD)
(IEC 61000-4-2)
Electrical fast tran-
sients/bursts
(IEC 61000-4-4)
Surges
(IEC 61000-4-5)
Magnetic field with sup-
ply frequency
(50/60 Hz)
(IEC 61000-4-8)
Voltage dips and short
interruptions of supply
voltage
(IEC 61000-4-11)
Instructions for use Fabius GS premium SW 3.n
IEC 60601-1-2 test
level
Contact discharge:
±6 kV
Air discharge: ±8 kV
Power supply lines:
±2 kV
Longer input lines/out-
put lines: ±1 kV
Common mode: ±2 kV
Differential mode: ±1 kV ±1 kV
3 A/m
Voltage dip >95 %,
0.5 periods
Voltage dip 60 %,
5 periods
Voltage dip 30 %,
25 periods
Voltage dip >95 %,
5 seconds
Compliance level
(medical device)
±6 kV
±8 kV
±2 kV
±1 kV
±2 kV
3 A/m
>95 %,
0.5 periods
60 %,
5 periods
30 %,
25 periods
>95 %,
5 seconds
Technical data
Electromagnetic environ-
ment
Floors should be wood, con-
crete, or ceramic tiles. If
floors are covered with syn-
thetic material, the relative
humidity should be at least
30 %.
Mains voltage quality should
be that of a typical commer-
cial or hospital environment.
Mains voltage quality should
be that of a typical commer-
cial or hospital environment.
Power frequency magnetic
fields should be at levels
characteristic of a typical
commercial or hospital envi-
ronment.
Mains voltage quality should
be that of a typical commer-
cial or hospital environment.
If the user of the medical
device requires continued
operation during mains
power supply interruptions,
it is recommended that the
medical device is powered
from an uninterruptible
power supply or a battery.
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