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

Download certificates

Certificate Dreve Otoplastik DIN EN ISO 9001

Certificate Dreve Otoplastik DIN EN ISO 13485

EG Certificate Dreve Otoplastik

MDSAP Certificate Dreve Otoplastik

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