We are happy to announce that the European Commission updated the NANDO website with a new name: DEKRA Certification GmbH.
DEKRA, the German Notified Body, was designated under the Regulation (EU) 2017/745 on medical devices to assess these categories of devices.
This is the third Notified Body accredited under the MDR, following the TÜV SÜD Product Service GmbH Zertifizierstellen and BSI Assurance UK Ltd designated earlier this year.
Follow our MDlaw News to remain updated with all the recent MDR/IVDR developments!
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