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Beurer BY 40 Basic - Disposal; Technical Data

Beurer BY 40 Basic
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10. Disposal
Empty, completely flat batteries must be disposed of through specially designated
collection boxes, recycling points or electronics retailers. You are legally required to dispose
of the batteries.
The codes below are printed on batteries containing harmful substances: Pb = Battery
contains lead, Cd = Battery contains cadmium, Hg = Battery contains mercury.
For environmental reasons, do not dispose of the device in the household waste at the end
of its useful life. Dispose of the device at a suitable local collection or recycling point. Dis
-
pose of the device in accordance with EC Directive – WEEE (Waste Electrical and Electronic
Equipment). If you have any questions, please contact the local authorities responsible for
waste disposal.
11. Technical data
Model BY 40
Type BY 40
Power supply 4 x 1.5 V AA batteries (Alkaline batteries)
Voltage (input) 100-240 V (AC~) 50 / 60 Hz
Voltage (output) 6 V (DC
) 1.0 A
Dimensions 168 x 100 x 53 mm
Weight 310 g (without batteries)
Maximum suction pressure 0.35 bar
Permissible operating conditions
+5°C to +40°C, 30% to 85% relative humidity (non-con-
densing), 700 – 1060 hPa ambient pressure
Permissible storage conditions -20°C to +60°C, 10% to 95% relative humidity (non-con
-
densing), 700 – 1060 hPa ambient pressure
Expected life 500 hours
Equipment for intermittent use 30 min. ON/30 min. OFF.
Useful life of accessoires subject to the conditions the conditions of cleanliness and conservation
Safety requirements in accordance with EN 60601-1
Child use and care articles – Drinking equipment in accordance to EN 14350
Unit for suction of breast milk
Unit for medium vacuum alnd low flow
Class II equipment (safety insulation)
Unit suitable for use in the absence of atmosphere containing oxidising, exploding gases, nitrous oxide.
BF type equipment (unit with specific grade of protection against electrical hazards)
Unit suitable for use in the absence of atmospheres containing oxidising, explosive gases or ni
-
trous oxide.
The technical specifications are subject to change without notice!
Notes on electromagnetic compatibility
The device complies with the EU Medical Devices Directive 93/42/EEC, the German Medical Devices
Act (Medizinproduktgesetz) and the European standard EN 60601-1-2 (in accordance with CISPR 11,
IEC 61000-4-2, IEC 61000-4-3, IEC 61000-4- 4, IEC 61000-4- 5, IEC 61000-4- 6, IEC 61000-4- 11,
IEC 61000-4-8) and is subject to particular precautions with regard to electromagnetic compatibility.
The device is suitable for use in all environments listed in these instructions for use, including dome
-
stic environments.
The use of the device may be limited in the presence of electromagnetic disturbances. This could re
-
sult in issues such as error messages or the failure of the display/device.

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