Regulation (EU) 2024/1860 of the European Parliament and of the Council of 13 June 2024 amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards a gradual roll-out of Eudamed, the obligation to inform in case of interruption or discontinuation of supply, and transitional provisions for certain 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Incorporated into the EEA Agreement but no longer in force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 included in a Joint Committee Decision (JCD); entry into force of the Decision is pending fulfilment of constitutional requirements by Iceland, Liechtenstein and/or Norway pursuant to Article 103 EEA
Area (EEA Agreement)
II Technical Regulations, Standards, Testing and Certification
II.XXX Medical Devices
Joint committee decision (JCD)
172/2025
Legal Documents
Regulation (EU) 2024/1860 of the European Parliament and of the Council of 13 June 2024 amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards a gradual roll-out of Eudamed, the obligation to inform in case of interruption or discontinuation of supply, and transitional provisions for certain in vitro diagnostic medical devices
Reglugerð Evrópuþingsins og ráðsins (ESB) 2024/1860 frá 13. júní 2024 um breytingu á reglugerðum (ESB) 2017/745 og (ESB) 2017/746 að því er varðar að innleiða Evrópska gagnabankann um lækningatæki (Eudamed) smám saman, skylduna til að tilkynna um það ef truflanir verða á afhendingu eða ef afhendingu er hætt og um umbreytingarákvæði vegna tiltekinna lækningatækja til sjúkdómsgreiningar í glasi
Verordnung (EU) 2024/1860 des Europäischen Parlaments und des Rates vom 13. Juni 2024 zur Änderung der Verordnungen (EU) 2017/745 und (EU) 2017/746 hinsichtlich der schrittweisen Einführung von Eudamed, der Informationspflicht im Falle einer Unterbrechung oder Beendigung der Versorgung und der Übergangsbestimmungen für bestimmte In-vitro-Diagnostika
History
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