HIDEMAR, S.A.
ES-MF-000004312 · Spain · COSLADA
HIDEMAR, S.A. is registered in the European database on medical devices as a manufacturer, with 43 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 43 |
|---|
Most frequent device types declared: H305 CAMILLA DE TRATAMIENTO CON ALTURA REGULABLE HIDRÁULICA, H601 CAMILLA GINECOLÓGICA Y DE PARTO, H07 CAMILLA DE RECONOCIMIENTO ALTURA FIJA PEDIÁTRICA INOX, H11TR CUNA PARA NEONATOS, H12 CUNA PARA NEONATOS EPOXI.
Among these devices, 43 are declared active.
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 | 43 |
| 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.