Titanox S.r.l.
IT-MF-000020325 · Italy · Torre de' Picenardi
Titanox S.r.l. is registered in the European database on medical devices as a manufacturer, with 356 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 345 |
|---|---|
| Class IIb | 11 |
Most frequent device types declared: Aluminum containers with filter, Aluminum containers with valve, Bowls and bowl stands, Delivery beds, Electric Pasteur hot air sterilizers.
Among these devices, 25 are declared active.
Devices declared under this manufacturer
- POSEIDONE
Showing 12 of 356 declared devices.
Catalogue references include A1-093-615, A1-096-319/G, A1-098-310/B, A2-129-30S, A3-214-535, M600694/2.
European nomenclature codes declared: S0199, V0899, V0402, V080602, S9080, V080603.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 356 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 356 |
|---|---|
| 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. Titanox S.r.l. was not found in either the U.S. or the Canadian register.