Guidance And Manufacturer's Declaration - Electromagnetic Immunity - Medtronic LIFEPAK 500 Bedienungsanleitung

Konformitätserklärung / Elektromagnetische Verträglichkeit
Elektromagnetische Störfestigkeit – Grundsätzliches und Herstellererklärung
Tabelle D-2

Guidance and Manufacturer's Declaration - Electromagnetic Immunity

The LIFEPAK 500 AED is intended for use in the electromagnetic environment specified below. The customer
or the user of the LIFEPAK 500 AED should ensure that the defibrillator 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 supply
transient/burst lines
IEC 61000-4-4 ±1 kV for input/output
lines
Surge ±1 kV differential mode
IEC 61000-4-5 ±2 kV common mode
Voltage dips, <5 % U
short
(>95% dip in U
interruptions and
for 0.5 cycle
voltage variations
on power supply
40% U
input lines
(60% dip in U
IEC 61000-4-11
for 5 cycles
70% U
(30% dip in U
for 25 cycles
<5 % U
(>95% dip in U
for 5 s
Power frequency 3 A/m
(50/60 Hz)
magnetic field
IEC 61000-4-8
Note: U is the a.c. mains voltage prior to application of the test level.
T
D-4
IEC 60601
Compliance Level
Test Level
±8 kV contact
±15 kV air
Not Applicable
Not Applicable
Not Applicable
T
)
T
T
)
T
T
)
T
T
)
T
3 A/m
Electromagnetic Environment - Guidance
The LIFEPAK 500 AED is suitable for use
in a dry environment.
Not Applicable
Not Applicable
Not Applicable
Power frequency magnetic fields
should be at levels characteristic of a
typical location in a typical commercial
or hospital environment.
Automatisierter Externer Defibrillator LIFEPAK 500 – Bedienungsanleitung