1/21/2024

List of notified bodies under Regulation (EU) 2017/746 on in vitro diagnostic medical devices(23.11.02)

 


Body typeBody nameCountry
NB 0050National Standards Authority of Ireland (NSAI)Ireland
NB 0123TÜV SÜD Product Service GmbHGermany
NB 0124DEKRA Certification GmbHGermany
NB 0197TÜV Rheinland LGA Products GmbHGermany
NB 0344DEKRA Certification B.V.Netherlands
NB 0459GMED SASFrance
NB 0483MDC MEDICAL DEVICE CERTIFICATION GMBHGermany
NB 0537Eurofins Electric & Electronics Finland OyFinland
NB 22653EC International a.s.Slovakia
NB 2797BSI Group The Netherlands B.V.Netherlands
NB 2962QMD Services GmbHAustria
NB 3018Sertio OyFinland