EU → US Device Access

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 IIa345
Class IIb11

Most frequent device types declared: Aluminum containers with filter, Round drums, Aluminum containers with valve, IV stands, Stainless steel boxes.

Among these devices, 25 are declared active.

No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED356
Country of registrationItaly
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.

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