Version in force
Made by Regulation (EU) 2024/1860 32024R1860 on EUR-Lex (external, EUR-Lex)
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)
2 changes in this version
02017R0745-20240709 → 02017R0745-20250110
Changes this amending act made: Art. 106