Commission Implementing Regulation (EU) 2023/2713 of 5 December 2023 designating European Union reference laboratories in the field of in vitro diagnostic medical devices
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Incorporated into the EEA Agreement but no longer in force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)
122/2024
In force in the EEA
Yes
Legal Documents
Commission Implementing Regulation (EU) 2023/2713 of 5 December 2023 designating European Union reference laboratories in the field of in vitro diagnostic medical devices
Framkvæmdarreglugerð framkvæmdastjórnarinnar (ESB) 2023/2713 frá 5. desember 2023 um tilnefningu tilvísunarrannsóknarstofa Evrópusambandsins á sviði lækningatækja til sjúkdómsgreiningar í glasi
Durchführungsverordnung (EU) 2023/2713 der Kommission vom 5. Dezember 2023 zur Benennung von Referenzlaboratorien der Europäischen Union im Bereich der In-vitro-Diagnostika
History
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