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EU MDR Regulation

Regulation (EU) 2017/746 (consolidated)

In Vitro Diagnostic Regulation — consolidated 10 January 2025
European UnionEuropean CommissionGeneral
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Regulation (EU) 2017/746 (consolidated) is the official EC identifier for “In Vitro Diagnostic Regulation — consolidated 10 January 2025”. Regulation (EU) 2017/746 (consolidated) is the official identifier EC uses for this instrument.

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Regulation
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Regulation (EU) 2017/746 (consolidated)
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113 articles · 1 language version
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About this regulation

In Vitro Diagnostic Regulation — consolidated 10 January 2025

EUR-Lex consolidated expression 02017R0746-20250110. Kept distinct from the authentic OJ text. Recitals are omitted from this consolidation, as EUR-Lex states.

Regulation (EU) 2017/746 (consolidated) is the official identifier EC uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.

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