Commission Implementing Regulation (EU) 2022/944 of 17 June 2022 laying down rules for the application of Regulation (EU) 2017/746 of the European Parliament and of the Council as regards the tasks of and criteria for 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Incorporated into the EEA Agreement but no longer in force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)
049/2023 In force in the EEA
Yes Legal documents
Commission Implementing Regulation (EU) 2022/944 of 17 June 2022 laying down rules for the application of Regulation (EU) 2017/746 of the European Parliament and of the Council as regards the tasks of and criteria for European Union reference laboratories in the field of in vitro diagnostic medical devices
Durchführungsverordnung (EU) 2022/944 der Kommission vom 17. Juni 2022 mit Durchführungsbestimmungen zur Verordnung (EU) 2017/746 des Europäischen Parlaments und des Rates hinsichtlich der Aufgaben von und der Kriterien für Referenzlaboratorien der Europäischen Union im Bereich der In-vitro-Diagnostika
History
18.03.2023
Adopted JCD confirmed entry into force date
18.03.2023
Compliance date in the EEA
17.03.2023
Adoption of Joint Commitee Decision (JCD) incorporating the act into the EEA Agreement
04.01.2023
Draft Joint Commitee Decision (JCD) incorporating the act into the EEA Agreement sent to Commission
17.06.2022
Adoption date in the EU
10.07.2022
Compliance date in the EU
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