TEKNIMED successfully passed its QMS audit under the EU MDR! -- MEDICA - World Forum for Medicine

01/05/2021

Teknimed S.A.S

TEKNIMED successfully passed its QMS audit under the EU MDR!

As medical device manufacturer, Teknimed is proud to have passed the Quality Management System audit with BSI NL Notified Body and obtained a positive recommendation on the European Medical Device Regulation 2017/745 (MDR).
We also have finished our first class III CE technical documentation review under the MDR.

Exhibitor Data Sheet