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EU MDR Regulation

Regulation (EU) 2017/745 (consolidated)

Medical Device Regulation — consolidated 10 January 2025
European UnionEuropean CommissionRegistration
What this code is

Regulation (EU) 2017/745 (consolidated) is the official EC identifier for “Medical Device Regulation — consolidated 10 January 2025”. Regulation (EU) 2017/745 (consolidated) is the official identifier EC uses for this instrument.

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Regulation
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Regulation (EU) 2017/745 (consolidated)
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Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
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123 articles · 1 language version
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About this regulation

Medical Device Regulation — consolidated 10 January 2025

EUR-Lex consolidated expression 02017R0745-20250110 (005.001). Official disclaimer: the consolidation is a documentation tool and has no legal effect; authentic recitals remain in the Official Journal expression. Kept distinct from CELEX 32017R0745.

Regulation (EU) 2017/745 (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.