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9. TECHNICAL SPECIFICATIONS
Model LifePad
®
Type RH 112
Dimensions 210 x 160 x 20 mm
Weight Approx. 130 g
Volume 66 dB
Permissible operating conditions 5°C to 40°C,
15 to 93% relative humidity
700 –1060 hPa ambient pressure
Permissible storage and transport
conditions
5°C to 35°C,
45 – 85% relative humidity
700 –1060 hPa ambient pressure
Protection class IP44
Power supply 1x CR2032 (3 V)
Battery life Approx. 1 hour in continuous operation
Frequency of the acoustic signal 100 bpm
Use-by date See type plate
(5 years after production)
Expected useful life Single-use product
Classification Internal supply, continuous operation, application part defibrilla
-
tion-proof type CF (back side of device is considered as defibrilla-
tion-proof type CF applied part)
The technical data is subject to change without notice, as updates are possible.
The serial number is located on the device or in the battery compartment.
• The device complies with the Regulation (EU) 2017/745 of the European Parliament and of the Coun
-
cil on medical devices, as well as the respective national provisions.
• This device complies with European standards EN 60601-1 and EN 60601-1-2 (in compliance with
CISPR 11, IEC 61000-4-2, IEC 61000-4-3, IEC 61000-4-8) and is subject to special precautionary
measures with regard to electromagnetic compatibility. Please note that portable and mobile HF
communication systems may interfere with this device. Further information can be obtained from the
Customer Services address provided.
10. WARRANTY/SERVICE
Further information on the warranty and warranty conditions can be found in the warranty leaflet supplied.
For users/patients in the European Union and identical regulation systems (EU Medical Device Regu
-
lation (MDR) 2017/745), the following applies: If during or through use of the product a major incident
occurs, notify the manufacturer and/or their representative of this as well as the respective national au
-
thority of the member state in which the user/patient is located.
Subject to errors and changes
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