LABORATOIRES QUINTON INTERNATIONAL S.L.
ES-MF-000004083 · Spain · COX
LABORATOIRES QUINTON INTERNATIONAL S.L. is registered in the European database on medical devices as a manufacturer, with 29 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 29 |
|---|
Most frequent device types declared: QUINTON NASAL SPRAY, Quinton Skin Spray.
Among these devices, 29 are declared active.
Devices declared under this manufacturer
- Kruidvat Neusspoeling Spray met zeewater
- Quinton Action Plus Nasal Hygiene
- Quinton Action Plus Nasal Hygiene spray
- Quinton Daily Nasal Hygiene spray
- Quinton Medical Nasal Health Baby Spray
- Quinton Medical Nasal Health Plus Spray
- Quinton Medical Nasal Health Spray
- Quinton Medical Nasal Health plus Spray
- Quinton Medical Skin Health
- Quinton Medical Skin Health Spray
- Quinton Ocular Care spray Spray
- Quinton Pediatric Nasal Hygiene Spray
Showing 12 of 29 declared devices.
Catalogue references include PT431, PT802, PT804, PT813, PT819, PT820.
European nomenclature codes declared: M9002, Q030103.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | LABORATORIES QUINTON INTERNATIONAL S. L. (ES) · FDA 3025604927 |
| Devices in EUDAMED | 29 |
| Country of registration | Spain |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 29 |
|---|---|
| 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.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
2024 PR 0032 | issued | 2029-07-21 |