The MDR, navigable.
10 chapters · 123 articles · 17 annexes. Search by keyword or article number; click any item to jump straight to that article, chapter or annex in the official EUR-Lex text.
The practical path to market
Six moves from "is it a device?" to ongoing post-market duties.
Chapters & articles
Click any article or annex to jump straight to it in the English text on EUR-Lex; use the EUR-Lex ↗ link on a chapter to open the whole chapter. Hover or focus an underlined term for a plain-language explanation.
Annexes
The operational detail you work from day to day — classification rules, conformity routes, technical documentation and clinical requirements.
Transition timeline
Key dates in the MDR's application and transitional provisions. The extended deadlines reflect later amending regulations — verify against the current Official Journal text.
Transitional rules carry conditions and class-specific exceptions. Always confirm against the current Official Journal text and the latest MDCG guidance for your specific device.
Understand what you're reading.
The navigator shows you where everything lives. The courses explain what it means.