Extension of our MDR certification

This year, we have also made progress in the extensive process of the latest MDR guidelines.
According to Annex IX, Chapters I and II of Regulation (EU) 2017/745 – Conformity Assessment, we were able to certify many products according to MDR, including non-active, non-implantable instruments for surgery such as our Suture Passer, the Airflow Gas Insufflator, the Stunner Shaver System, the P-Line of our suction and irrigation pumps, and instruments such as endoscopes, sheaths and retractors.
RZ stays on the ball in the MDR certification process!

Visit our download section to download the latest certificates.