Technical Specifications - AUDIOLINE Babysense 5 Operating Instructions Manual

Audioline Babysense 5_V1_0-DE_4 250711 991074_20 Seiten_250713_XP9_A5_Layout 1 26.07.13 10:03 Seite 16
Appendix
Perform a test which will detect the source of the movement that the device detects. For
example, sources of wind such as: air conditioner, an open window or a fan; movements
of a baby mobile (which can vibrate even if it's not turned on) walking around the bed
area or an intercom placed near the bed with intense transmission levels. Solutions: Eli-
minate sources of wind, remove the mobile etc. After neutralizing all environmental influ-
ences, perform the test again. If even after neutralizing all of the environmental influen-
ces, the alarm does not go off within 20 seconds, perform the following:
1. In the back of the sensor pads (see illustration 2) reduce the sensitivity level to position
2 (on both sensor pads) and perform again the Performance Test. If the alarm sounds
within 20 seconds, than keep this sensitivity level.
2. If the alarm does not go off in time, than reduce the sensitivity level to position 1 and
perform again the Performance Test. If the alarm sounds within 20 seconds, than keep
this sensitivity level.
3. If the alarm does not go off in time at this level, than it is suggested using only one
sensor pad with the sensitivity level adjusted on position 1.
4. PAY ATTENTION: Should false alarms sound as a result of reduced sensitivity, than
increase the level of sensitivity and perform the Performance Test.

Technical Specifications

Powered by 4 size AA, 1.5 volt batteries.
Power consumption approx. 1 mA.
Battery life approx. 6 months using alkaline batteries.
Alarm volume typically 85dB SPL at distance of one meter.
Size of sensor pad is ø 216 mm.
Declaration of Conformity
This device fulfils the requirements stipulated in the EU directives.
BABYSENSE Infant Movement Respiratory Monitor (Model CU-100/2 revD.) is in conformity with
the essential requirements and provisions of Annex VI and Annex III of the Medical Devices Directi-
ve 93/42/EEC as amended by 98/79/EC, 2000/70/EC, 2001/104/EC and 2007/47/EC.
The product is classified as Class IIb medical device, in accordance with Rule 10, Annex IX of the
Directive.
Notified Body:
LNE No. 0459
1 rue Gaston Boissier
75724 PARIS Cedex 15, France
Authorised Representative:
Obelis S.A.
Boulevard Général Wahis 53
1030 Brussels, BELGIUM
Conformity with the above mentioned directives is confirmed by the CE symbol on the device.
To view the complete Declaration of Conformity, please refer to the free download available on our
web site www.audioline.de.
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