EUROPODEX S.L.
ES-MF-000042401 · Spain · GIJON
EUROPODEX S.L. is registered in the European database on medical devices as a manufacturer, with 32 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 32 |
|---|
Most frequent device types declared: E4100,E4200,E4300,E4400,E4500,E4600,E4700,E4800, E2100,E2101,E2102,E2103,E2104,E2105, E2135,E2146,E2140S,EE2140M,E2140L,E2145, RODILLERA,,CODERA,MUÑEQUERA Y TOBILLERA ELASTICA CYMAM, E1070A,EE1072A,E1070,E1072,E1090.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 32 |
| Country of registration | Spain |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.