MARTÍN BALART TARRIDA
ES-MF-000044818 · Spain · PIERA
MARTÍN BALART TARRIDA is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 17 |
|---|
Devices declared under this manufacturer
- COJÍN DE FLOTACIÓN CUADRADO
- COJÍN DE GEL CUADRADO
- COJÍN DE GEL HERRADURA
- COJÍN DE GEL SILICONA CUADRADO
- COJÍN DE GEL SILICONA HERRADURA
- COJÍN VISCOELÁSTICA CUADRADO
- COJÍN VISCOGEL CUADRADO
- CUBRE ESCAYOLA BRAZO CORTO INFANTIL
- CUBRE ESCAYOLA BRAZO LARGO ADULTO
- CUBRE ESCAYOLA BRAZO LARGO INFANTIL
- CUBRE ESCAYOLA PIERNA CORTA ADULTO
- CUBRE ESCAYOLA PIERNA CORTA INFANTIL
Showing 12 of 17 declared devices.
Catalogue references include MB0003, MB0004, MB0005, MB0008, MB0011, MB0012.
European nomenclature codes declared: M0499, V080302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| 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 | 17 |
|---|---|
| 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. MARTÍN BALART TARRIDA was not found in either the U.S. or the Canadian register.