Beurer BM 54 Manual De Instrucciones página 43

Notification of incidents
For users/patients in the European Union and identical
regulation systems (EU Medical Device Regulation (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 authority of the member state in which the user/pa-
tient is located.
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