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Medtrace Pharma A/S

Active in EUDAMED

Denmarkfrom SRN EUDAMED SRN DK-MF-000034342

Devices
2
Registrations
EUDAMED

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor

What Medtrace Pharma A/S makes

Medtrace Pharma A/S manufactures the O15 H2O Patient Kit, a medical device designed for patient use in specific clinical procedures involving water-based solutions.

The O15 H2O Patient Kit is classified as a Class IIa device and is listed in the EU’s eudamed registry. The company is based in Denmark.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • O15 H2O Patient Kit Ref MT-PAT-002

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • O15 H2O Patient Kit Ref MT-PAT-001

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa

Company details

EUDAMED SRN
DK-MF-000034342
EU VAT number
36497661
EUDAMED status
Active
EUDAMED registered name
Medtrace Pharma A/S
Registered address
5A, Agern Allé, 2970, Hørsholm, Denmark
PRRC contact
Maja Damby Carøe(public in EUDAMED)

Frequently asked questions

How many devices does Medtrace Pharma A/S have in the registry?

The registry currently lists 2 devices for Medtrace Pharma A/S. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medtrace Pharma A/S's devices?

Among its 2 most recently registered devices, Medtrace Pharma A/S has devices listed in EUDAMED (2 devices).

What risk classes do Medtrace Pharma A/S's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Medtrace Pharma A/S's devices are Class IIa. Each device page shows its own class and authorisation.

What are the newest devices from Medtrace Pharma A/S in the registry?

The most recently registered devices listed for Medtrace Pharma A/S include O15 H2O Patient Kit.

Generated automatically from registry data and not verified by a human reviewer.