Physio Control Lifepak 1000 - Page 96

Electromagnetic Compatibility Guidance
G-2 LIFEPAK 1000 Defibrillator Operating Instructions
ELECTROMAGNETIC IMMUNITY
Essential Performance
The LIFEPAK 1000 defibrillator maintains safe and effective performance of the defibrillation
therapy and patient monitoring functions when operated in the electromagnetic environment
specified in Tables 2 through 4.
The LIFEPAK 1000 defibrillator is intended for use in the electromagnetic environment specified
below. The customer or the user of the LIFEPAK 1000 defibrillator should ensure that the device
is used in such an environment.
Table 2 Guidance and Manufacturer’s Declaration - Electromagnetic Immunity
* Uninstalled battery pack is ±6 kV contact, ±8 kV air.
Immunity Test
IEC 60601
Tes t L e vel
Compliance Level
Electromagnetic Environment -
Guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
±8 kV contact
±2 kV, ±4 kV, ±8 kV,
±15 kV air
±8 kV contact*
±2 kV, ±4 kV, ±8 kV,
±15 kV air*
The LIFEPAK 1000 defibrillator is
suitable for use in a dry
environment.
Electrical fast
transient/burst
IEC 61000-4-4
±2 kV for power
supply lines
±1 kV for input/
output lines
Not Applicable Not Applicable
Surge
IEC 61000-4-5
±1 kV differential
mode
±2 kV common
mode
Not Applicable Not Applicable
Voltage dips,
short
interruptions
and voltage
variations on
power supply
input lines
IEC 61000-4-11
0% U
T
during 1/2
cycles at 0°, 45°,
90°, 135°, 180°,
225°, 270°, and 315°
70% U
T
during 25/30
cycles
Single phase at 0°
Not Applicable Not Applicable
Power
frequency (50/
60 Hz) magnetic
field
IEC 61000-4-8
30 A/m 30 A/m Power frequency magnetic fields
should be at levels characteristic
of a typical location in a typical
commercial or hospital
environment.
Note: U
T
is the a.c. mains voltage prior to application of the test level.