MDR information

On May 26, 2021, the European Medical Device Regulation 2017/745 (MDR) came into force with a three-year transition period. Our medical devices have been continuously adapted to the increased requirements, so that finally Dreve Otoplastik has received the certificate in accordance with Regulation (EU) 2017/745 as proof since December 2023. This certificate covers all medical devices subject to mandatory monitoring and proves the high quality standard of Dreve products.

Unna, December 2023

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Certificate Dreve Otoplastik DIN EN ISO 9001

Certificate Dreve Otoplastik DIN EN ISO 13485

EG Certificate Dreve Otoplastik

MDSAP Certificate Dreve Otoplastik