theseeus.eu Health

Medical Devices Regulation

← All instruments
in forceproduct
Type
regulation
Layer
product
Status
in force
In force
2017-05-26
CELEX
32017R0745
Last verified
2026-07-22
Official text
EUR-Lex / official source

Medical Devices Regulation (MDR)

Stub — deep dive in preparation.

Regulation (EU) 2017/745 is the core EU framework for placing medical devices on the market (classification, conformity assessment, post-market surveillance). Software and AI-enabled devices interact with the AI Act — see the AI area.

Sources