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: H07 CAMILLA DE RECONOCIMIENTO ALTURA FIJA PEDIÁTRICA INOX, H101 SILLÓN GINECOLÓGICO HIDRÁULICO FIJO, H11TR CUNA PARA NEONATOS, H12 CUNA PARA NEONATOS EPOXI, H12 CUNA PARA NEONATOS INOX.
Among these devices, 43 are declared active.
Devices declared under this manufacturer
- H03 CAMILLA DE RECONOCIMIENTO ALTURA FIJA 190 X 60 X 80 cm
- H07 CAMILLA DE RECONOCIMIENTO ALTURA FIJA PEDIÁTRICA INOX
- H101 SILLÓN GINECOLÓGICO HIDRÁULICO FIJO
- H11TR CUNA PARA NEONATOS
- H12 CUNA PARA NEONATOS EPOXI
- H12 CUNA PARA NEONATOS INOX
- H13 CUNA PARA NIÑOS
- H168 PORTASUEROS
- H169 PORTASUEROS
- H305 CAMILLA DE TRATAMIENTO DE ALTURA REGULABLE HIDRÁULICA
- H321 LUPA CON LUZ
- H514 SILLA DE TRASLADO
Showing 12 of 43 declared devices.
Catalogue references include H07 CAMILLA DE RECONOCIMIENTO ALTURA FIJA PEDIÁTRICA INOX, H11TR CUNA PARA NEONATOS, H12 CUNA PARA NEONATOS EPOXI, H12 CUNA PARA NEONATOS INOX, H13 CUNA PARA NIÑOS, H305 CAMILLA DE TRATAMIENTO CON ALTURA REGULABLE HIDRÁULICA.
European nomenclature codes declared: V9099, V080603, V0809, V080299, V080202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 43 |
| Country of registration | Spain |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 43 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. HIDEMAR, S.A. was not found in either the U.S. or the Canadian register.