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EU MDR Regulation

Regulation (EU) 2017/745 (consolidated)

Medical Device Regulation — consolidated 19 July 2026
European UnionEuropean CommissionRegistration
What this code is

Regulation (EU) 2017/745 (consolidated) is the official EC identifier for “Medical Device Regulation — consolidated 19 July 2026”. Regulation (EU) 2017/745 (consolidated) is the official identifier EC uses for this instrument.

Instrument
Regulation
Full name
Regulation (EU) 2017/745 (consolidated)
Category
Registration
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English
Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
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123 articles · 1 language version
Direct citations can link to a specific article or section by appending its fragment identifier.
Dates
Published
—
Effective
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Consolidated through
2026-07-19
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About this regulation

Medical Device Regulation — consolidated 19 July 2026

EUR-Lex consolidated expression 02017R0745-20260719 (007.001), current through 19 July 2026 — the newest official consolidation, confirmed by enumerating every 02017R0745 expression in the Publications Office Cellar (SPARQL). Bytes fetched from the Cellar master repository (publications.europa.eu) because eur-lex.europa.eu redirects script egress to a Today-OJ interstitial. 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.