I.T.A.-Intertact s.r.o.
CZ-MF-000003664 · Czechia · Praha
I.T.A.-Intertact s.r.o. is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- AFDF Kit - Alpha Defensin
- Fox-Flow 10L
- Fox-Flow 5L
- Fox-Flow Forte 0,5L
- Fox-Flow Forte 1L
- Fox-Lyz 10× (100ml)
- Fox-Lyz 10× (50 ml)
Catalogue references include 100-05000-01, 100-05000-02, 100-05000-03, 100-05000-04, 100-05000-05, 100-05000-06.
European nomenclature codes declared: W0103080699, W0103080599, W01021199,W0105900299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| Country of registration | Czechia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 7 |
|---|---|
| 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. I.T.A.-Intertact s.r.o. was not found in either the U.S. or the Canadian register.