Regulatory guidance
Clarification on “first certification for that type of device” and corresponding procedures to be followed by notified bodies, in context of the consultation of the expert panel referred to in Article 48(6) of Regulation (EU) 2017/746
Published Sep 1, 2022
Reference
MDCG 2021-22
Source
MDCG
Topic
In Vitro Diagnostic medical devices (IVD)
Published
Sep 1, 2022
Revision
1
Languages
EN
© European Union — European Commission, DG SANTE. Reuse under CC BY 4.0.
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