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Regolament (UE) 2024/1860 tal-Parlament Ewropew u tal-Kunsill tat-13 ta’ Ġunju 2024 li jemenda r-Regolamenti (UE) 2017/745 u (UE) 2017/746 fir-rigward tal-introduzzjoni gradwali tal-Eudamed, tal-obbligu ta’ informazzjoni f’każ ta’ interruzzjoni jew waqfien tal-provvista, u ta’ dispożizzjonijiet tranżitorji għal ċerti apparati mediċi dijanjostiċi in vitro (Test b'rilevanza għaż-ŻEE)
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 1977-074X | ISBN | DOI | Catalogue number FXL2401860MT |
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