Beurer BM 64 Manual De Instrucciones página 36

Notification of incidents
For users/patients in the European Union and identical regulation
systems (EU Medical Device Regulation (MDR) 2017/745), the fol-
lowing applies: If during or through use of the product a major in-
cident 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/patient is located.
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