Ambu aView Instrukcja obsługi - Strona 8
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Video out is
No live image on the
not working.
external screen.
The colours, brightness
and contrast looks
different from the
aView screen.
Horizontal lines (noise)
on external monitor.
Appendix 1. Electromagnetic Compatibility
Like other electrical medical equipment the system requires special precautions to ensure
electromagnetic compatibility with other electrical medical devices. To ensure electromagnetic
compatibility (EMC) the system must be installed and operated according to the EMC
information provided in this manual.
The system has been designed and tested to comply with IEC 60601-1-2 requirements for EMC
with other devices.
Guidance and manufacturer's declaration – electromagnetic immunity
The system is intended for use in the electromagnetic environment specified below.
The customer or the user of the system should assure that it is used in such an environment.
Emissions Test
Compliance
RF emission CISPR 11
Group 1
RF emission CISPR 11
Class B
Harmonic emission
Not applicable
IEC/EN 61000-3-2
Voltage fluctuations
Complies
/ flicker emissions
IEC/EN 61000-3-3
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Make sure the external monitor is connect-
ed to aView using the composite cable and
that the external monitor is displaying the
correct input. The external monitor shall be
capable of receiving NTSC or PAL. Toggle
between NTSC and PAL in the video out
menu on aView for best result. The external
monitor is only displaying a live image
when aView is displaying a live image.
The image size on the external monitor is
determined by the settings in the external
monitor.
Adjust the colours, brightness and contrast
on the external monitor to achieve the
desired result.
If horizontal lines (noise) appear on the
external monitor, try to connect the aView
power supply.
Electromagnetic Environment Guidance
The system 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 system is suitable for use in all
establishments, including domestic
establishments and those directly
connected to the public low-voltage
power supply network that supplies
buildings used for domestic purposes.
Guidance and manufacturer's declaration – electromagnetic immunity
The system is intended for use in the electromagnetic environment specified below.
The customer or the user of the system should assure that it is used in such an environment.
Immunity Test
IEC 60601-1
test level
Electrostatic
+/- 8 kV contact
discharge (ESD)
+/- 2, 4, 8, 15 kV air
IEC 61000-4-2
Electrical fast
+/- 2 kV for power
transient / burst
supply lines
IEC 61000-4-4
+/- 1 kV for input /
output lines
Surge IEC 61000-4-5
+/- 1 kV line(s)
to line(s)
+/- 2 kV line(s)
to earth
Voltage Dips, short
<5% Ut (95% dip
interruptions and
in Ut) for 0.5 cycle
voltage variations
on power supply
40% Ut (60% dip
input lines
in Ut) for 5 cycles
IEC 61000-4-11
70% Ut (30% dip
in Ut) for 25 cycles
<5% Ut (95% dip
in Ut) for 5 sec.
Power frequency
30 A/m
(50/60 Hz)
magnetic field
IEC 61000-4-8
Compliance
Electromagnetic
Level
Environment Guidance
+/- 8 kV contact
If floors are covered with
+/- 2, 4, 8, 15 kV
synthetic material the
air
relative humidity shall
be least 30%.
+/- 2 kV power
Mains power quality
supply lines N/A
shall be that of a typical
commercial or hospital
environment.
Mains power quality
shall be that of a typical
commercial or hospital
environment.
100% reduction
Mains power quality
0.5 period
shall be that of a
typical commercial or
40% reduction
hospital environment.
for 5 periods
If the use of the system
requires continued
30% reduction
operation during power
for 25 periods
mains interruptions
the system can be
100% reduction
powered by the built in
for 5 sec.
rechargeable battery.
30 A/m
Power frequency
magnetic fields
should be at levels
characteristic of a
typical location in a
typical commercial or
hospital environment.
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