Glossary › EU MDR › MDR Annex XI (Product Conformity Verification)

GLOSSARYEU

MDR Annex XI (Product Conformity Verification)

Conformity assessment that ensures devices conform to the type certified under Annex X and meet the Regulation's provisions that apply to them. Part A covers production quality assurance and Part B covers product verification.

Parts

Part A
Production quality assurance
Part B
Product verification
Where it is written
Regulation (EU) 2017/745, Annex XI (consolidated text of 10 January 2025)
Also called
Annex XI, product conformity verification

Related terms