CE-mærket
Home
About DGM
Cooperators
What's new
Courses
Rules - MDD
Rules - IVDD
Routes to the CE
Links
Documents
Søg
Contact DGM

Rules - MDD

The Purpose of Classification

All medical devices must comply with all relevant requirements of the Directive. Therefore the classification only serves to determine which conformity assessment procedure to apply and whether or not a notified body must co-operate.



Back to index