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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.

Instrument
Regulation
Full name
Regulation (EU) 2017/746 (consolidated)
Category
General
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English
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113 articles · 1 language version
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Dates
Published
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Effective
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Consolidated through
2025-01-10
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English full text113 articles · English — official textRead HTML →
About this regulation

In Vitro Diagnostic Regulation — consolidated 10 January 2025

EUR-Lex consolidated expression 02017R0746-20250110 — still the newest official IVDR consolidation: every 02017R0746 expression in the Publications Office Cellar was enumerated via SPARQL on 29 August 2026 and none is dated later than 10 January 2025. 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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