MedArt ApS
Active in EUDAMEDDenmarkfrom SRN EUDAMED FDA SRN DK-MF-000018610 FEI 3005616124
- Devices
- 1
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
What MedArt ApS makes
MedArt ApS makes medical devices such as the MedArt 620 FRx Intenz.
The company's portfolio, including devices classified as Class IIb, is listed in the Eudamed registry, and MedArt ApS is based in Denmark.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
MedArt 620 FRx Intenz Ref 620.000
Regimes: CE MDD Registry: EUDAMED
Company details
- EUDAMED SRN
- DK-MF-000018610
- FDA FEI number
- 3005616124
- EU VAT number
- DK41925736
- EUDAMED status
- Active
- EUDAMED registered name
- MedArt ApS
- Registered address
- 15a, Industriholmen, 2650, Hvidovre, Denmark
- Website
- www.medart.dk
- [email protected]
- Phone
- +4536342300
- PRRC contact
- Olav Balle-Petersen
Frequently asked questions
How many devices does MedArt ApS have in the registry?
The registry currently lists 1 device for MedArt ApS. Devices recorded under merged duplicate company entries are counted once.
Which registries list MedArt ApS's devices?
Among its 1 most recently registered device, MedArt ApS has devices listed in EUDAMED (1 device).
What risk classes do MedArt ApS's devices fall under?
Among its 1 most recently registered device, the classes recorded for MedArt ApS's devices are Class IIb. Each device page shows its own class and authorisation.
What are the newest devices from MedArt ApS in the registry?
The most recently registered devices listed for MedArt ApS include MedArt 620 FRx Intenz.