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Document 32022R2347
Reclassification of certain active devices without an intended medical purpose
Commission Implementing Regulation (EU) 2022/2347 of 1 December 2022 laying down rules for the application of Regulation (EU) 2017/745 of the European Parliament and of the Council as regards reclassification of groups of certain active products without an intended medical purpose (Text with EEA relevance)
- Legal basis:
- 32017R0745 - A51P3PTB)
- EuroVoc thesaurus:
- health policy; medical device; market approval; marketing standard; health legislation; apparatus based on the use of rays; safety standard; patient safety; application of EU law; EC conformity marking
-
- 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