CENTERVUE S.P.A.
IT-MF-000017082 · Italy · Padova
CENTERVUE S.P.A. is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 17 |
|---|
Most frequent device types declared: iCare RETCAD.
Among these devices, 16 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 register | Similar name found — unverified |
|---|---|
| Matched entry | CENTERVUE (IT) · FDA 3008422902 |
| Devices in EUDAMED | 17 |
| Country of registration | Italy |
⚠️ A similar name exists in the FDA register. We do not assert that it is the same company — the two registers share no common identifier, and a name alone is not proof. This entry needs a human check.