Orientations réglementaires
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
Publié 1 sept. 2022
Référence
MDCG 2021-22
Source
MDCG
Thème
In Vitro Diagnostic medical devices (IVD)
Publié
1 sept. 2022
Révision
1
Langues
EN
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