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Document Ares(2017)4704363
Codes for the designation of Notified Bodies in the field of medical devices and in vitro diagnostic medical devices
COMMISSION IMPLEMENTING REGULATION (EU) …/... on the list of codes and corresponding types of devices for the purpose of specifying the scope of the designation as notified bodies in the field of medical devices under Regulation (EU) 2017/745 of the European Parliament and of the Council and in vitro diagnostic medical devices under Regulation (EU) 2017/746 of the European Parliament and of the Council
- Legal basis:
- 32017R0745 - A42P13 ; 32017R0745 - A39P10 ; 32017R0746 - A35P10 ; 32017R0746 - A38P13
- EuroVoc thesaurus:
- single market; research body; harmonisation of standards; marketing standard; market supervision; market approval; medical device; EC conformity marking; testing; cataloguing
-
- Documents:
- Ares(2017)4704363 (Draft implementing regulation)Ares(2017)4704363 (Draft implementing regulation)
- Legal basis:
- 32017R0745 - A42P13 ; 32017R0745 - A39P10 ; 32017R0746 - A35P10 ; 32017R0746 - A38P13
- Leading service:
- Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
- Committee:
- Committee on Medical Devices
- Consultation type:
- Stakeholder feedback
- Consultation duration (weeks):
- 4
- Check the status of this initiative on the Better Regulation Portal
-
- Documents:
- C/2017/7779 final (Implementing regulation)
- Leading service:
- Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
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- Documents:
- 32017R2185 (Implementing regulation)
- Date of publication:
- 24/11/2017