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Document 32017R2185
Codes for the designation of Notified Bodies in the field of medical devices and in vitro diagnostic medical devices
Regolament ta' Implimentazzjoni tal-Kummissjoni (UE) 2017/2185 tat-23 ta' Novembru 2017 dwar il-lista ta' kodiċijiet u t-tipi ta' apparati korrispondenti bil-għan li jiġi speċifikat il-kamp ta' applikazzjoni tad-deżinjazzjoni bħala korpi notifikati fil-qasam tal-apparati mediċi skont ir-Regolament (UE) 2017/745 tal-Parlament Ewropew u tal-Kunsill u l-apparat mediku dijanjostiku in vitro skont ir-Regolament (UE) 2017/746 tal-Parlament Ewropew u tal-Kunsill (Test b'rilevanza għaż-ŻEE. )
- Legal basis:
- 32017R0745 - A42P13 ; 32017R0745 - A39P10 ; 32017R0746 - A35P10 ; 32017R0746 - A38P13
- EuroVoc thesaurus:
- suq uniku; korp tar-riċerka; armonizzazzjoni tal-istandards; standard tal-kummerċjalizzazzjoni; superviżjoni tas-suq; approvazzjoni ta' bejgħ; apparat mediku; immarkar ta' konformità CE; ittestjar; katalogar
-
- 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
-
- Documents:
- 32017R2185 (Implementing regulation)
- Date of publication:
- 24/11/2017