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Beurer EM 39 Mode D'emploi page 19

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  • FRANÇAIS, page 20
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/patient is located.
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