EC DG GROW
European Commission — DG GROW
About
The European Commission Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs (DG GROW) coordinates EU medical device regulation. EUDAMED is the EU database for medical devices.
Regulatory Details
Regulatory FrameworkEU MDR 2017/745 & EU IVDR 2017/746
Device ClassificationClass I, Class IIa, Class IIb, Class III (MDR); Class A, B, C, D (IVDR)
Jurisdiction TypeSupranational
Country🇧🇪 Belgium
StatusActive