Junquera y Diz S.L.
ES-MF-000002269 · Spain · Gijón
Junquera y Diz S.L. is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 10 |
|---|
Most frequent device types declared: INMOVILIZADOR DE RODILLA, ORTESIS PECTUS CARINATUM, SOPORTE CERVICAL SOMI.
Devices declared under this manufacturer
- INMOVILIZADOR DE RODILLA
- ORTESIS DE RODILLA TELESCOPICA CON BLOQUEO
- ORTESIS PECTUS CARINATUM
Catalogue references include PEC-001, PEC-002-L, PEC-002-M, PEC-002-S, RII-001-4000, RII-001-5000.
European nomenclature codes declared: Y061209, Y060307, Y060306, Y060315.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| 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 | 10 |
|---|---|
| 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. Junquera y Diz S.L. was not found in either the U.S. or the Canadian register.