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Document 52023PC0010
Extension of the transition period for medical devices
Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards the transitional provisions for certain medical devices and in vitro diagnostic medical devices
- EuroVoc thesaurus:
- medical diagnosis; security of supply; EC conformity marking; quality standard; marketing standard; medical device; market approval; safety standard; single market; public health
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- Documents:
- COM/2023/10 final (Proposal for a regulation)
- Leading service:
- Directorate-General for Health and Food Safety
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- Consultation type:
- Stakeholder feedback
- Consultation duration (weeks):
- 8