Unolab manufacturing, S.L.
ES-MF-000000272 · Spain · Getafe (Madrid)
Unolab manufacturing, S.L. is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 8 |
|---|
Among these devices, 8 are declared sterile.
Devices declared under this manufacturer
- Deliplus Lágrimas Hidratantes 30 x 0,4 mL
- Fisiocare Fiale Eurospital 20 x 2 mL
- IEA Medical Augentropfen 0.1% HA 20 x 0.4 mL
- Saline Steridose 30 x 10 mL
- Sanavita Collirio +day Monodose 10 x 0.4 mL
- Spectrum Saline Isotonic Buffered Saline Solution 100 x 5 mL
- Vidi Pharma Baby Saltvannsdråper 20 x 5 mL
- Vidi Pharma Saltvannsdråper 20 x 2 mL
Catalogue references include 0200400414, PSU-0004, PSU-0011, PSU-0012, PSU-0013, PSU-0015.
European nomenclature codes declared: Q02030299, Q02030301, Q02030206, Q02030399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 6 |
|---|---|
| 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. Unolab manufacturing, S.L. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
2024 CR 0040 | issued | 2029-11-19 |