Specifications
44
PhysioMem
®
PM 100 2G
77811011
10.9.2
Guidance and manufacturer’s declaration –
electromagnetic immunity (line-bound disturbances)
The device is intended for use in the electromagnetic environment specified below. The
customer or the user should ensure that the device is used in such an environment.
Immunity test
IEC 60601 test level* Compliance level*
Electromagnetic envi-
ronment – guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
8 kV contact
15 kV air
8 kV contact
15 kV air
Floors should be wood,
concrete, or ceramic tile.
If floors are covered with
synthetic material, the
relative humidity should
be at least 30%.
Electric fast
transient / burst
IEC 61000-4-4
2 kV for power sup-
ply lines
1 kV for input / out-
put lines
2 kV for power
supply lines
1 kV for input /
output lines
Mains power quality
should be that of a typi-
cal commercial or hospi-
tal environment.
Surges
IEC 61000-4-5
1 kV
differential mode
1 kV
differential mode
Mains power quality
should be that of a typi-
cal commercial or hospi-
tal environment.
Voltage dips,
short interrup-
tions and volt-
age variations
on power supply
input lines
IEC 61000-4-11
< 5% U
T
(>95% dip in
U
T
) for 1/2 period
70% U
T
(30% dip in
U
T
) for 25 periods
<5% U
T
(>95% dip in
U
T
) for 5 s
< 5% U
T
(>95% dip in
U
T
) for 1/2 period
70% U
T
(30% dip in
U
T
) for 25 periods
<5% U
T
(>95% dip in
U
T
) for 5 s
Mains power quality
should be that of a typi-
cal commercial or hospi-
tal environment.
If the user of the device
requires continued oper-
ation during power
mains interruptions, it is
recommended that the
device be powered from
an uninterruptible power
supply or a battery.
