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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 (Text with EEA relevance)
Publication metadata
- Published:
- Corporate author(s): Council of the European Union , European Parliament
- Subject: EC conformity marking , exchange of information , information system , market approval , medical device , medical diagnosis , public health , security of supply , single market
- IMMC : PE 54 2024 REV 1
- OJ : L_202401860
- CELEX : 32024R1860
- ELI : reg/2024/1860/oj
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| ISSN 1977-0677 | ISBN | DOI | Catalogue number FXL2401860EN |
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