Physio Control TrueCPR Gebrauchsanweisung Seite 24

Electromagnetic Compatibility Guidance
Electromagnetic Immunity
Table 2 Guidance and Manufacturer's Declaration - Electromagnetic Immunity
The TrueCPR device, model 80596-000003, is intended for use in the electromagnetic
environment specified below. The customer or user should ensure that the TrueCPR
device is used in such an environment.
Immunity Test
Electrostatic ±6 kV contact
discharge (ESD)
±8 kV air
IEC 61000-4-2
Electrical fast ±2 kV for power
transient/burst supply lines
IEC 61000-4-4 ±1 kV for input/
output lines
Surge ±1 kV line(s) to
line(s)
IEC 61000-4-5
±2 kV line(s) to
earth
Voltage dips, <5% U
short (>95% dip in U
interruptions for 0.5 cycle
and voltage
40% U
variations on
(60% dip in U
power supply
for 5 cycles
input lines
70% U
IEC 61000-4-11
(30% dip in U
for 25 cycles
<5% U
(>95% dip in U
for 5 sec
Power 3 A/m
frequency (50/
60 Hz) magnetic
field
IEC 61000-4-8
Note: U is the AC Mains voltage prior to application of the test level.
T
20
IEC 60601 Compliance
Test Level
±6 kV contact
±8 kV air
Not applicable
Not applicable
Not applicable
T
)
T
T
)
T
T
)
T
T
)
T
3 A/m
Electromagnetic Environment -
Level
Floors should be wood,
concrete, or ceramic tile. If floors
are covered with synthetic
material, the relative humidity
should be at least 30%.
The TrueCPR device is battery-
powered.
The TrueCPR device is battery-
powered.
The TrueCPR device is battery-
powered.
Power frequency magnetic fields
should be at levels characteristic
of a typical location in a typical
commercial or hospital
environment.
TrueCPR Device Instructions for Use
Guidance