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Document 32022R2346
Amendments to Common Specifications on products without an intended medical purpose listed in Annex XVI MDR
Regolament ta’ Implimentazzjoni tal-Kummissjoni (UE) 2022/2346 tal-1 ta’ Diċembru 2022 li jistabbilixxi speċifikazzjonijiet komuni għall-gruppi ta’ prodotti li l-għan maħsub tagħhom mhuwiex mediku elenkati fl-Anness XVI tar-Regolament (UE) 2017/745 tal-Parlament Ewropew u tal-Kunsill dwar apparati mediċi (Test b’rilevanza għaż-ŻEE)
- EuroVoc thesaurus:
- leġiżlazzjoni tas-saħħa; standard tal-kummerċjalizzazzjoni; prova klinika; armonizzazzjoni tal-istandards; sikurezza tal-prodotti; speċifikazzjoni teknika; immarkar ta' konformità CE; approvazzjoni ta' bejgħ; ġestjoni tar-riskju; apparat mediku
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- Documents:
- C/2022/8626 final (Implementing regulation)
- Leading service:
- Directorate-General for Health and Food Safety
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- Documents:
- 32022R2346 (Implementing regulation)
- Date of publication:
- 02/12/2022