Dräger Babylog 8000 plus Instructions For Use Manual page 111

Electromagnetic immunity
The medical device is intended for use in an electromagnetic
environment as specified below. The user must ensure its use
in such an environment.
Immunity against
Electrostatic discharge
(ESD) (IEC 61000-4-2)
Electrical fast transients/
bursts (IEC 61000-4-4)
Surge on AC mains lines
(IEC 61000-4-5)
Power frequency mag-
netic field (50/60 Hz)
(IEC 61000-4-8)
Voltage dips and short
interruptions on AC
mains input lines
(IEC 61000-4-11)
Radiated RF
(IEC 61000-4-3)
Test level
(IEC 60601-1-2)
Contact discharge:
±6 kV
Air discharge: ±8 kV
Power supply lines:
±2 kV
Longer input / output
lines: ±1 kV
Common mode: ±2 kV
Differential mode: ±1 kV ±1 kV
3 A/m
Dip >95 %, 0.5 periods
Dip 60 %, 5 periods
Dip 30 %, 25 periods
Dip >95 %, 5 seconds
80 MHz to 2.5 GHz:
10 V/m
Compliance level Electromagnetic
(medical device) environment
±2, 4, 6 kV Floors should be wood,
concrete or ceramic tile.
If floors are covered with
±2, 4, 8 kV
synthetic material, the
relative humidity should
be at least 30 %.
±2 kV Mains power quality
should be that of a typi-
cal commercial or hospi-
±1 kV
tal environment.
±2 kV Mains power quality
should be that of a typi-
cal commercial or hospi-
tal environment.
3 A/m Power frequency mag-
netic fields should be at
levels characteristic of a
typical location in a typi-
cal commercial or hospi-
tal environment.
>95 %, 0.5 periods Mains power quality
should be that of a typi-
60 %, 5 periods
cal commercial or hospi-
30 %, 25 periods
tal environment. If the
user of the medical de-
>95 %, 5 seconds
vice requires continued
operation during mains
power supply interrup-
tions, it is recommended
that the medical device
be powered from an un-
interruptible power sup-
ply or a battery.
10 V/m Recommended mini-
mum distance to porta-
ble and mobile RF trans-
mitters with transmission
power P
ical device including its
lines: (1.84 m x √P
Technical Data
EMC Declaration
to the med-
EIRP
)*
EIRP
111