Dyno Rechi
ES-MF-000035525 · Spain · Castelló
Dyno Rechi is registered in the European database on medical devices as a manufacturer, with 117 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 117 |
|---|
Most frequent device types declared: CODERA TUBULAR NEOPRENO, CORRECTOR CHEPPING UP, FAJA ABDOMINAL 3MM NEOPRENO, FAJA DORSOLUMBAR ANCHA, FAJA PREVENTIVA.
Among these devices, 10 are declared with a measuring function.
Devices declared under this manufacturer
- BANDA ABDOMINAL XXL
- BANDA BOVEDA METATARSAL
- CODERA LARGA NEOPRENO
- CODERA TUBULAR NEOPRENO
- DYNO RECHI
- ESPALDILLERA
- FAJA 2 BANDAS L BEIGE
- FAJA 2 BANDAS S BLANCA
- FAJA LUMBAR ANCHA
- FAJA PREVENTIVA
- FAJA REFUERZOS NEOPRENOT/M
- HOMBRERA NEOPRENO IZQUIERDA NEGRO T/S
Showing 12 of 117 declared devices.
Catalogue references include 0115001S06, 0115002M06, 011505XL06, 011654XL00, 0511500U07, 0512001S07.
European nomenclature codes declared: Y060499, Y060307, Y060308, Y060615, Y060621, Y060606.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 117 |
| 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 | 117 |
|---|---|
| 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. Dyno Rechi was not found in either the U.S. or the Canadian register.