JOSE MESTRE S.A.
ES-MF-000008198 · Spain · BARCELONA
JOSE MESTRE S.A. is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 14 |
|---|
Devices declared under this manufacturer
- ASIENTO ANTILLAGAS JM 40 cm
- ASIENTO ANTILLAGAS JM 45 cm
- COJIN DE GEL ANTIESCARA CERRADO
- COJÍN DE GEL ANTIESCARAS ABIERTO
- CUBRE ESCAYOLA ADULTO JOYA BRAZO CORTO
- CUBRE ESCAYOLA ADULTO JOYA BRAZO LARGO
- CUBRE ESCAYOLA ADULTO JOYA PIERNA CORTO
- CUBRE ESCAYOLA ADULTO JOYA PIERNA LARGO
- CUBRE ESCAYOLA INFANTIL JOYA BRAZO CORTO
- CUBRE ESCAYOLA INFANTIL JOYA BRAZO LARGO
- CUBRE ESCAYOLA INFANTIL JOYA PIERNA CORTO
- CUBRE ESCAYOLA INFANTIL JOYA PIERNA LARGO
Showing 12 of 14 declared devices.
Catalogue references include 0000003306, 0000134017, 0009053601, 0009503201, 0009505201, 0009505601.
European nomenclature codes declared: Y090612, Y090618, V080302, Y093399, R060203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| 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 | 14 |
|---|---|
| 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. JOSE MESTRE S.A. was not found in either the U.S. or the Canadian register.