Electromagnetic Immunity - Dräger 8413417 Instrucciones De Uso

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Emissions
Radio frequency emissions
(CISPR 11)
Harmonic emissions
(IEC 61000-3-2)
Voltage fluctuations/flicker
emissions (IEC 61000-3-3)

Electromagnetic immunity

The medical device is intended for use in an
electromagnetic environment as specified below.
The user must ensure its use in such an
environment.
Immunity against
Electrostatic discharge
(ESD) (IEC 61000-4-2)
Electrical fast transients/
bursts (IEC 61000-4-4)
Surge on AC mains
lines (IEC 61000-4-5)
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Compliance according to Electromagnetic environment
Group 1
Class A
Not applicable
Not applicable
Test level
IEC 60601-1-2
Contact discharge:
±6 kV
Air discharge: ±8 kV
Power supply lines:
±2 kV
Longer input/ output
lines: ±1 kV
Common mode: ±2 kV
Differential mode: ±1 kV ±1 kV
The medical device uses RF energy only
for its internal function. Therefore, its RF
emissions are very low and are not likely
to cause any interference in nearby
electronic equipment.
The medical device is suitable for use in
all establishments other than domestic
establishments and those directly
connected to the public low-voltage
power supply network that supplies
buildings used for domestic purposes.
Compliance level
(medical device)
±2, 4, 6 kV
±2, 4, 8 kV
±2 kV
Not applicable
±2 kV
Instructions for Use Air Compressor
Electromagnetic
environment
Floors should be wood,
concrete or ceramic tile.
If floors are covered with
synthetic material, the
relative humidity should
be at least 30 %.
Mains power quality
should be that of a
typical commercial or
hospital environment.
Mains power quality
should be that of a
typical commercial or
hospital environment.