Intended Use; Target Group - Beurer LIFE PAD RH 112 Mode D'emploi

Protection class
Protected against solid foreign
objects ≥ 1 mm in diameter and
against splashing water.
Temperature limit
The temperature limit values to
which the medical device can safely
be exposed are indicated
Humidity, limit
Indicates the humidity range to
which the medical device can safely
be exposed
Disposal
Disposal in accordance with the
Waste Electrical and Electronic
Equipment EC Directive – WEEE
Direct current
The device is suitable for use with
direct current only
Dispose of packaging in an envi-
ronmentally friendly manner

3. INTENDED USE

Use the LifePad for the purpose it was developed for only and in the manner specified in these instruc-
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tions for use.
Intended use
The LifePad motivates and supports first-aiders in cardiopulmonary resuscitation (CPR) of individuals
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over 12 years of age after a sudden cardiac arrest (SCA) through an acoustic and visual feedback system
to evaluate the compressions performed. The LifePad
used multiple times under any circumstances.

Target group

The LifePad is intended for use by adults and adolescents over the age of 12 and has been specially
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designed for use by lay persons. Therefore, no specific knowledge or professional ability is required to
use the LifePad .
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Indication/clinical benefits
The LifePad should be used once the first-aider has identified that the patient is experiencing a cardiac
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arrest. For this reason, the first-aider must check whether the person who has collapsed is conscious and
breathing, as described in the section "What to do in an emergency?" before using the LifePad
patient is not responsive and is not breathing, it should be assumed they are experiencing a cardiac ar-
rest. In this case, the first-aider should make an emergency call and start using the product immediately.
The LifePad consists of a flexible and non-slip mat that adapts to every body shape. It is placed on the
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patient's bare upper body and aligned using reference lines and pictograms.
Once the product has been automatically activated by pulling the battery strip, the feedback system
starts. It consists of an acoustic signal that tells the user the correct rhythm for 100 compressions per
minute, as well as the colour-coded LEDs that, in combination with the built-in pressure sensor, indicate
whether the compressions are being performed correctly. In doing so, the sensor checks whether suf-
Defibrillation-proof type CF applied part
CE labelling
This product satisfies the requirements
of the applicable European and national
directives
Atmospheric pressure, limit
Indicates the range of atmospheric pres-
sures to which the medical device can be
safely exposed
Battery disposal
Do not dispose of batteries containing harm-
ful substances with household waste
Marking to identify the packaging material.
A = Material code, B = Material number:
1-6 = Plastics, 20-22 = Paper and cardboard
B
A
is intended for single use only and must not be
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15
. If the
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