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The 9002 complies with the EMC, electromagnetic compatibility, standard, IEC60601-1-2. Refer to the tables below for spe-
cific information regarding compliance to the standard.
The 9002, as a medical electrical equipment, needs special precautions regarding EMC and needs to be installed and put into
service according to
the EMC information provided below.
Portable and mobile RF communications equipments can affect the device.
The use of accessories other than those specified in this manual may result in increased emissions or decreased immunity of
the device.
The 9002 should not be used adjacent to or stacked with other equipment.
The 9002 is intended for use in the electromagnetic environment specified below.
The customer or the user of the 9002 should assure that it is used in such an environment.
Table 1 - Guidance and manufacturer’s declaration - electromagnetic emissions -
The 9002 is intended for use in the electromagnetic environment specified below.
The customer or the user of the 9002 should assure that it is used in such an environment.
Table 2 - Guidance and manufacturer’s declaration - electromagnetic immunity -
Technical Description
Emissions test
RF emissions CISPR 11
RF emissions CISPR 11
Harmonic emissions IEC 61000-3-2
Voltage fluctuations/flicker emissions
IEC 61000-3-3
Compliance
Group 1
Class B
Class A
N/A
Electromagnetic environment - guidance
The 9002 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 9002 is suitable for use in all establishments, including domestic establishments and di-
rectly connected to the public low-voltage power supply network that supplies buildings used for
domestic purposes.
Immunity test
Electrostatic discharge
(ESD) IEC
61000-4-2
Electrical fast
transient/burst IEC
61000-4-4
Surge IEC 61000-4-5
Voltage dips, short
interruptions and voltage
variations on power supply
lines IEC 61000-4-11
Power frequency
(50/60 Hz) magnetic
field IEC 61000-4-8
IEC 60601 test level
±6 kV contact
±8 kV air
±2 kV for power supply lines
±1 kV for input/ output lines
±1 kV differential mode
±2 kV common mode
<5% UT (>95% dip in UT) for 0,5 cycle
40% UT (60% dip in UT) for 5 cycles
70% UT (30% dip in UT) for 25 cycles
<5% UT (>95% dip in UT) for 5 sec
3 A/m
Compliance level
±6 kV contact
±8 kV air
±2 kV for power supply lines
±1 kV for input/ output lines
±1 kV differential mode
±2 kV common mode
<5% UT (>95% dip in UT) for 0,5 cycle
40% UT (60% dip in UT) for 5 cycles
v70% UT (30% dip in UT) for 25 cycles
<5% UT (>95% dip in UT) for 5 sec
3 A/m
Electromagnetic environment - guidance
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.
Mains power quality should be that of a typical
commercial or hospital environment. If the user
of the 9002 requires continued operation during
power mains interruptions, it is recommended
that the 9002 is to be powered from an
uninterruptable power supply or a battery.
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 a.c. mains voltage prior to application of the test level.
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