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Document 32022R2347
Reclassification of certain active devices without an intended medical purpose
Règlement d’exécution (UE) 2022/2347 de la Commission du 1er décembre 2022 portant modalités d’application du règlement (UE) 2017/745 du Parlement européen et du Conseil en ce qui concerne la reclassification de groupes de certains produits actifs n’ayant pas de destination médicale prévue (Texte présentant de l’intérêt pour l’EEE)
- Legal basis:
- 32017R0745 - A51P3PTB)
- EuroVoc thesaurus:
- politique de la santé; matériel médical; autorisation de vente; norme de commercialisation; législation sanitaire; appareil à radiations; norme de sécurité; sécurité des patients; application du droit de l'UE; marquage CE de conformité
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- Documents:
- Ares(2022)5696071 (Draft implementing regulation)Ares(2022)5696071 (Draft implementing regulation)
- Legal basis:
- 32017R0745 - A51P3PTB)
- Leading service:
- Directorate-General for Health and Food Safety
- Committee:
- Committee on Medical Devices
- Check the status of this initiative on the Better Regulation Portal
-
- Consultation type:
- Stakeholder feedback
- Consultation duration (weeks):
- 4
-
- Documents:
- C/2022/8638 final (Implementing regulation)
- Leading service:
- Directorate-General for Health and Food Safety
-
- Documents:
- 32022R2347 (Implementing regulation)
- Date of publication:
- 02/12/2022