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
Certificate Dreve Otoplastik DIN EN ISO 9001
Certificate Dreve Otoplastik DIN EN ISO 13485
EG Certificate Dreve Otoplastik
MDSAP Certificate Dreve Otoplastik