LIDERMED S.A.
ES-MF-000004664 · Spain · MATARO
LIDERMED S.A. is registered in the European database on medical devices as a manufacturer, with 163 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 163 |
|---|
Most frequent device types declared: VENDAJE TUBULAR COMPRESIVO, VENDAJE TUBULAR DE MALLA, APÓSITOS PARA HERIDAS, LLAGAS Y ÚLCERAS, VENDAJE TUBULAR EXTENSIBLE, COLLARIN CERVICAL BLANDO.
Among these devices, 10 are declared sterile.
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 | 163 |
| 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.