DKMA

Danish Medicines Agency

DKMA 🇩🇰 Denmark National Active
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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

Contact Information

Country🇩🇰 Denmark
AddressAxel Heides Gade 1, 2300 Copenhagen S, Denmark
Phone+45-44-88-95-95

Official Website

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