Mobiclinic TX-01 Manual De Instrucciones página 28

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Guidance and manufacturing declaration - electromagnetic immunity - for all EQUIPMENT
& SYSTEMS
The blood pressure monitor is intended for use in the electromagnetic environment
specified below. The customer or user must ensure that it is used in these environments.
Immunity test
Electrostatic
discharge (ESD)
IEC61000-4-2
Electric frequency
magnetic field (50
Hz) IEC 61000-4-8
Guidance and Declaration of Manufacture - electromagnetic immunity - for EQUIPMENT
AND SYSTEMS other than LIFE ASSISTANCE
The blood pressure monitor is intended for use in the electromagnetic environment
specified below. The customer or user must ensure that it is used in these environments.
Immunity IEC
test 60601
test
level
IEC 3 V/m
61000- 80
4-3 RF MHz
radiated to 2.5
GHz
DE PT NL
SWE
IEC 60601 Compliance
test level level
±6 kV ±6 kV
contact contact
±8 kV air ±8 kV air
3 A/m 3 A/m
Com- Guidance on the electromagnetic environment
pliance
Portable and mobile RF communication equipment
should be used no closer to any part of the foetal bag
detector, including cables, than the recommended
separation distance, calculated from the equation
applicable to the frequency of the transmitter.
Recommended separation distance
3 V/m
Where P is the maximum output power of the transmitter
in watts (W) according to the transmitter manufacturer
and, d is the recommended separation distance in
metres (m).
The field extent of fixed RF transmitters, as determined
by an electromagnetic site survey (a), should be less than
the compliance level in each frequency range (b).
Interference may occur in the vicinity of equipment
marked with the following symbol:
PL DK
Blood Pressure Monitor
Electromagnetic environment
Floors should be wood, concrete or
ceramic tiles. If the floor is covered with
synthetic material, the relative humidity
should be at least 30%.
Magnetic power
should be at levels characteristic of a
typical hospital or commercial environ-
ment.
800 MHz at 2,5 GHz
frequency fields
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