Pure Global AI
EU MDR Regulation

Regulation (EU) 2017/746

In Vitro Diagnostic Medical Devices Regulation
European UnionEuropean CommissionGeneralEffective May 26, 2022
Official source linked
What this code is

Regulation (EU) 2017/746 is the official EC identifier for “In Vitro Diagnostic Medical Devices Regulation”. Regulation (EU) 2017/746 is the official identifier EC uses for this instrument.

Instrument
Regulation
Full name
Regulation (EU) 2017/746
Category
General
Source links
Authority source
English
Open the issuing-authority text
Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
Readable HTML
113 articles · 1 language version
Read the full text →
Direct citations can link to a specific article or section by appending its fragment identifier.
Dates
Published
May 5, 2017
Effective
May 26, 2022
Readable full text

Open a language version

Each version has stable article anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.

English full text113 articles · English — official textRead HTML →
About this regulation

In Vitro Diagnostic Medical Devices Regulation

Authentic Official Journal expression of the IVDR. Ingested from EUR-Lex CONVEX HTML for CELEX 32017R0746. Date of the act is 5 April 2017; OJ L 117/176 publication is 5 May 2017.

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

Verified