EUR-Lex Access to European Union law
This document is an excerpt from the EUR-Lex website
Use quotation marks to search for an "exact phrase". Append an asterisk (*) to a search term to find variations of it (transp*, 32019R*). Use a question mark (?) instead of a single character in your search term to find variations of it (ca?e finds case, cane, care).
Need more search options? Use the
Advanced search
You are here
Document 32020R1207
Common Specifications for the reprocessing of single-use medical devices
Kommissionens genomförandeförordning (EU) 2020/1207 av den 19 augusti 2020 om tillämpningsföreskrifter för Europaparlamentets och rådets förordning (EU) 2017/745 vad gäller gemensamma specifikationer för reprocessing av engångsprodukter (Text av betydelse för EES)
- Legal basis:
- 32017R0745 - A17P5
- EuroVoc thesaurus:
- inre marknad; medlemsstat i EU; hälsolagstiftning; säkerhetsstandard; handelsnorm; produktsäkerhet; icke-varaktig konsumtionsvara; begagnad vara; riskhantering; teknisk specifikation; medicinsk-kirurgisk utrustning
-
- Documents:
- Ares(2019)4763425 (Draft implementing regulation)
- Legal basis:
- 32017R0745 - A17P5
- Leading service:
- Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
- 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/2020/5607 final (Implementing regulation)
- Leading service:
- Directorate-General for Health and Food Safety
-
- Documents:
- 32020R1207 (Implementing regulation)
- Date of publication:
- 20/08/2020