DKMA
Danish Medicines Agency
About
The Danish Medicines Agency is the competent authority for medical devices in Denmark, responsible for market surveillance and device vigilance under EU MDR.
Regulatory Details
Regulatory FrameworkEU MDR 2017/745 (Danish implementation)
Device ClassificationClass I, Class IIa, Class IIb, Class III
Jurisdiction TypeNational
Country🇩🇰 Denmark
StatusActive