# MDR — Certification marks and hazardous-area classifications: cross-market equivalences

For MDR, market / system is EU; meaning is Medical device regulation with strict clinical and documentation requirements; applies to is medical devices; governing standard / law is 2017/745, recorded from its source on 2026-08-11.

- **Designation:** MDR _(verified: appears in the quote below)_
- **Market / system:** EU
- **Meaning:** Medical device regulation with strict clinical and documentation requirements _(verified: appears in the quote below)_
- **Applies to:** medical devices
- **Governing standard / law:** 2017/745 _(verified: appears in the quote below)_

## What the source says

> MDR (2017/745): Medical device regulation with strict clinical and documentation requirements

## Source

- https://ecocomply.ai/blog/what-does-ce-marking-cost-for-your-product

Last verified: 2026-08-11. Review by: 2027-08-11.
Part of [Certification marks and hazardous-area classifications: cross-market equivalences](https://referencesource.org/certification-standards-equivalence/).