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T-Med

Active in EUDAMED

Francefrom SRN EUDAMED SRN FR-MF-000017814

Devices
2
Registrations
EUDAMED

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor

Catalogue2

  • Wundo Ref APP-WUNDO

    Class I EUDAMED Active
  • Visio Ref VISIO-2022-01

    Class I EUDAMED Active

Company details

EUDAMED SRN
FR-MF-000017814
EU VAT number
FR80840095715
EUDAMED status
Active
EUDAMED registered name
T-MED
Registered address
12, RUE FOCH, 67450, MUNDOLSHEIM, France
Website
t-med.fr
PRRC contact
Sandra BILGER(public in EUDAMED)

What T-Med makes

T-MED manufactures the WUNDO, a wound care device designed for managing and treating chronic or acute wounds, and the VISIO, a diagnostic imaging system for visualizing soft tissue and wound conditions. These products are intended for clinical use in healthcare settings to support wound assessment and treatment planning.

The company’s portfolio is classified under Class I medical devices in the European Union, with both devices registered in the EUDAQD database (eudamed). T-MED operates from France, adhering to EU regulatory requirements for medical device compliance and traceability.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Frequently asked questions

How many devices does T-MED have in the registry?

The registry currently lists 2 devices for T-MED. Devices recorded under merged duplicate company entries are counted once.

Which registries list T-MED's devices?

Among its 2 most recently registered devices, T-MED has devices listed in EUDAMED (2 devices).

What risk classes do T-MED's devices fall under?

Among its 2 most recently registered devices, the classes recorded for T-MED's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from T-MED in the registry?

The most recently registered devices listed for T-MED include WUNDO and VISIO.

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