QUIROSA, S.A.
ES-MF-000014841 · Spain · Artés
QUIROSA, S.A. is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 27 |
|---|
Devices declared under this manufacturer
- Conexión T multimedida
- Conexión en T Mediana transparente
- Conexión en T Mini blanca
- Conexión en T mediana blanca
- Conexión en Y grande blanca
- Conexión en Y mediana transparente
- Conexión en Y pequeña blanca
- Conexión recta grande-grande transparente
- Conexión recta grande-pequeña blanca
- Conexión recta grande-pequeña transparente
- Conexión recta mediana-grande blanca
- Conexión recta pequeña-mediana transparente
Showing 12 of 27 declared devices.
Catalogue references include 00100004, 00100006, 00100008, 00100012, 00100019, 00100105.
European nomenclature codes declared: A070101, V030206.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 27 |
| 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 | 27 |
|---|---|
| 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. QUIROSA, S.A. was not found in either the U.S. or the Canadian register.