Regulatory guidance
Application of transitional provisions for certification of class D in vitro diagnostic medical devices according to Regulation (EU) 2017/746
Published Sep 1, 2024
Reference
MDCG 2021-4
Source
MDCG
Topic
In Vitro Diagnostic medical devices (IVD)
Published
Sep 1, 2024
Revision
1
Languages
EN
© European Union — European Commission, DG SANTE. Reuse under CC BY 4.0.
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