"JAGO-PRO" Spółka z ograniczoną odpowiedzialnością
PL-MF-000035503 · Poland · Jaworzno
"JAGO-PRO" Spółka z ograniczoną odpowiedzialnością is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 20 |
|---|
Most frequent device types declared: 100 ml, 30 ml, 50 ml, 85 ml.
Among these devices, 5 are declared active.
Devices declared under this manufacturer
- AQUATISO woda morska hipertoniczna
- AQUATISO woda morska izotoniczna
- BABYNEBUCAP
- Katarek woda morska izotoniczna
- NEBULINO woda morska izotoniczna
- NEBUMIST, Izotoniczny roztwór chlorku sodu w postaci mgiełki
- NEBUSPRAY woda morska hipertoniczna
- NEBUSPRAY woda morska izotoniczna
- Vidusol Marine
- Vidusol Marine baby
- Woda morska hipertoniczna
- Woda morska hipertoniczna Biocanto Pharma
Showing 12 of 20 declared devices.
Catalogue references include 425002, 425005, 425008, 425011, 425020, 425021.
European nomenclature codes declared: Q030103, Q030199, Q030303.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 20 |
| Country of registration | Poland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 20 |
|---|---|
| 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. "JAGO-PRO" Spółka z ograniczoną odpowiedzialnością was not found in either the U.S. or the Canadian register.