EU MDR — Regulation (EU) 2017/745 on medical devices
What is the applies to for EU MDR — Regulation (EU) 2017/745 on medical devices?
For EU MDR, meaning is Regulation (EU) 2017/745 on medical devices; applies to is medical devices; governing standard / law is Regulation (EU) 2017/745, verified against its source on 2026-09-22.
This page provides a range of documents to assist stakeholders in applying: Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 (IVDR) on in vitro diagnostic medical devices
— health.ec.europa.eu, retrieved 2026-09-22
- Designation
- MDR verified
- Market / system
- EU verified
- Meaning
- Regulation (EU) 2017/745 on medical devices verified
- Applies to
- medical devices verified
- Governing standard / law
- Regulation (EU) 2017/745 verified
Source
- health.ec.europa.euhttps://health.ec.europa.eu/medical-devices-sector/new-regulations/guidance-mdcg-endorsed-documents-and-other-guidance_en