nubeca BA2110, Инструкция по эксплуатации

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Guidance and manufacture’s declaration
24
Warranty Information
Caution: This unit has been thoroughly tested and inspected to assure
proper performance and operation!
WARNING:
The use of ACCESSORIES, transducers and cables other than those
specified, with the exception of transducers and cables sold by the
MANUFACTURER of the COMPRESSOR NEBULIZER as replacement
parts for internal components, may result in increased EMISSIONS or
decreased IMMUNITY of the ME EQUIPMENT or ME SYSTEM.
Guidance and manufacture’s declaration – electromagnetic emission
Emission test
RF emission
Harmonic
Voltage
Group 1
Class B
Not applicable
Not applicable
The Digital Blood Pressure Monitor use 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 Digital Blood Pressure Monitor is suitable for use in all
establishments other than domestic and those directly
connected to the public low-voltage power supply network
that supplies buildings used for domestic purposes.
CISPR 11
RF emissions
emissions
fluctuations/
flicker emissions
IEC 61000-3-3
IEC 61000-3-2
CISPR 11
Compliance Electromagnetic environment – guidance
The Digital Blood Pressure Monitor is intended for use in the electromagnetic environment
specified below. The customer of the user of the Digital Blood Pressure Monitor should
assure that it is used in such an environment.
25
Warranty Information
Guidance and manufacture’s declaration – electromagnetic immunity
Immunity test
Power frequency
magnetic field IEC
61000-4-8
±6 kV contact
±8 kV air
±6 kV contact
±8 kV air
3A/m 3A/m
Floors should be wood, concrete or
ceramic tile. If floor are covered with
synthetic material, the relative humidity
should be at least 30%.
Power frequency magnetic fields should
be at levels characteristic of a typical
location in a typical commercial or
hospital environment.
(50Hz/60Hz)
Electrostatic
IEC 61000-4-2
discharge (ESD)
IEC 60601 test Compliance
level level
Electromagnetic environment - guidance
The Digital Blood Pressure Monitor is intended for use in the electromagnetic environment
specified below. The customer or the user of Digital Blood Pressure Monitor should assure
that it is used in such an environment.
NOTE UT is the a.c. mains voltage prior to application of the test level.
Guidance and manufacture’s declaration – electromagnetic immunity
Immunity test
80 MHz to 2.5
GHz
3A/m
3A/m
80 MHz to 800 MHz
800 MHz to 2.5 GHz
Portable and mobile RF communications
equipment should be used no closer to any
part of the Digital Blood Pressure Monitor,
including cables, than the recommended
separation distance calculated from the
equation applicable to the frequency of the
transmitter.
Where P is the maximum output power
rating of the transmitter in watts (W)
according to the transmitter manufacturer
and d is the recommended separation
distance in metres (m).
Field strengths from fixed RF transmitters,
as determined by an electromagnetic site
Radiated RF
IEC 61000-4-3
IEC 60601 test Compliance
level level
Electromagnetic environment - guidance
Recommended separation distance
The Digital Blood Pressure Monitor is intended for use in the electromagnetic environment
specified below. The customer or the user of Digital Blood Pressure Monitor should assure
that it is used in such an environment.