Fiterman Pharma SRL
RO-MF-000001410 · Romania · Iasi
Fiterman Pharma SRL is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|---|
| Class IIb | 1 |
Devices declared under this manufacturer
- ALINAN COLIC AND BLOATING (emulsion)
- BALONIX MED chewable tablets
- ECCO Spray
- GASTIMAX MED (chewable tablets)
- GASTIMAX MED (oral suspension)
- LAXIT MED (powder for oral solution - sachets 10g)
- LAXIT MED (powder for oral solution - sachets 5g)
- STOPTRANS MED (powder for oral suspension - sachets)
Catalogue references include BXMED, BXMEDEM, ECCO se250, ECCO se50, GXMED, GXMEDSSP.
European nomenclature codes declared: G0401, M9002.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| Country of registration | Romania |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 3 |
|---|---|
| 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. Fiterman Pharma SRL was not found in either the U.S. or the Canadian register.