89
GB/IE
This device complies with EU Medical Devices
Directive 93/42/EEC, the Medical Devices Act
and standard DIN EN ISO 80601-2-61 (Medical
electrical equipment–Particular requirements for
basic safety and essential performance of pulse
oximeter equipment).
We hereby confirm that this product complies
with the European RED Directive 2014/53/EU.
The CE declaration of conformity for this product
is available at: www.beurer.com/web/we-land-
ingpages/de/cedeclarationofconformity.php.
Information on
electromagnetic
compatibility
The device is suitable for use in all environments
that are listed in these instructions for use, includ-
ing in the home.
In the presence of electromagnetic disturbances,
the device may under some circumstances only
be useable to a limited extent. This can result in
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