DIN EN ISO 13485 certification according to KRINKO/BfArM
We conduct certification according to DIN EN ISO 13485 in compliance with KRINKO/BfArM recommendations, ensuring the highest standards of quality and safety in the reprocessing of medical devices.
The EN ISO 13485 certification ensures that manufacturers and suppliers of medical devices meet the highest requirements for their quality management system. Learn how TÜV NORD CERT can support you on your path to successful ISO 13485 certification.