DEKRA’s Notified Body based in The Netherlands, DEKRA Certification B.V., has obtained designation to issue CE Mark certifications under the European Medical Devices Regulation (MDR).

DEKRA Certification’s designation now increases the number of Notified Bodies able to certify devices once the MDR takes effect in May 2020 to eight:

• BSI (UK)
• TÜV SÜD (Germany)      
• DEKRA (Germany)
• TÜV Rheinland (Germany)
• IMQ (Italy)
• BSI NL (The Netherlands)
• Dare!! (The Netherlands)
• DEKRA Certification B.V.

Related EU MDR and CE Marking resources from Emergo by UL:

• EU MDR preparation and compliance resource center
• On-site MDR training for medical device companies
• Whitepaper: How to select or change your Notified Body