Commission Implementing Regulation (EU) 2017/2185 of 23 November 2017 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
Proposed act with possible EEA relevance
Act under scrutiny by EEA EFTA
Draft Joint Committee Decision (JCD) under consideration
Entry into force of Joint Committee Decision (JCD) pending
Incorporated into the EEA Agreement and in force
Incorporated into the EEA Agreement but no longer in force
Legal status
EU legal act incorporated into the EEA Agreement by a Joint Committee Decision (JCD)
Area (EEA Agreement)
II Technical Regulations, Standards, Testing and Certification
II.XXX Medical Devices
Joint committee decision (JCD)
144/2021
In force in the EEA
Yes
Legal Documents
Commission Implementing Regulation (EU) 2017/2185 of 23 November 2017 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
Framkvæmdareglugerð framkvæmdastjórnarinnar (ESB) 2017/2185 frá 23. nóvember 2017 um skrána yfir kóða og samsvarandi gerðir tækja í þeim tilgangi að afmarka gildissvið tilnefningarinnar fyrir tilkynnta aðila samkvæmt reglugerð Evrópuþingsins og ráðsins (ESB) 2017/745 og lækningatæki til sjúkdómsgreiningar í glasi samkvæmt reglugerð Evrópuþingsins og ráðsins (ESB) 2017/746
Durchführungsverordnung (EU) 2017/2185 der Kommission vom 23. November 2017 über das Verzeichnis der Codes und der ihnen entsprechenden Produktarten zur Bestimmung des Geltungsbereichs der Benennung einer Benannten Stelle auf dem Gebiet der Medizinprodukte im Rahmen der Verordnung (EU) 2017/745 des Europäischen Parlaments und des Rates sowie auf dem Gebiet der In-vitro-Diagnostika im Rahmen der Verordnung (EU) 2017/746 des Europäischen Parlaments und des Rates
Kommisjonens gjennomføringsforordning (EU) 2017/2185 av 23. november 2017 om listen over koder og tilhørende typer utstyr for å presisere omfanget av utpekingen av meldte organer på området medisinsk utstyr i henhold til europaparlaments- og rådsforordning (EU) 2017/745 og medisinsk utstyr til in vitro-diagnostikk i henhold til europaparlaments- og rådsforordning (EU) 2017/746
History
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