Electromagnetic immunity, Electromagnetic compatibility guidance – Physio-Control TrueCPR User Manual

Page 24

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TrueCPR Device Instructions for Use

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

IEC 60601

Test Level

Compliance

Level

Electromagnetic Environment -

Guidance

Electrostatic
discharge (ESD)
IEC 61000-4-2

±6 kV contact
±8 kV air

±6 kV contact
±8 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%.

Electrical fast
transient/burst
IEC 61000-4-4

±2 kV for power
supply lines
±1 kV for input/
output lines

Not applicable

The TrueCPR device is battery-
powered.

Surge
IEC 61000-4-5

±1 kV line(s) to
line(s)
±2 kV line(s) to
earth

Not applicable

The TrueCPR device is battery-
powered.

Voltage dips,
short
interruptions
and voltage
variations on
power supply
input lines
IEC 61000-4-11

<5% U

T

(>95% dip in U

T

)

for 0.5 cycle
40% U

T

(60% dip in U

T

)

for 5 cycles
70% U

T

(30% dip in U

T

)

for 25 cycles
<5% U

T

(>95% dip in U

T

)

for 5 sec

Not applicable

The TrueCPR device is battery-
powered.

Power
frequency (50/
60 Hz) magnetic
field
IEC 61000-4-8

3 A/m

3 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 AC Mains voltage prior to application of the test level.

3312954-901.book Page 20 Tuesday, March 26, 2013 9:45 AM

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