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.
Devices declared under this manufacturer
- COMPASS
- EIDON
- EIDON AF
- EIDON FA
- iCare MAIA
Showing 12 of 17 declared devices.
Catalogue references include ACMASME002, ADDRSME002, AIFLAME001, AIFLUME001, AMFUNME001, AMGSDME001.
European nomenclature codes declared: Z12120199, Z1212012003, Z12129092, Z12120180.
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; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 17 |
|---|---|
| Found in the U.S. device database | 14 |
| Share | 82.4 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | CENTERVUE S.P.A. |
What it holds in Canada
| Licences on record | 10 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 10 |
| First licensed | 2011-02-03 |
Licence types: Single Device (8), System (2).
Licensed under: DIGITAL RETINOGRAPHY SYSTEM - DRS, MAIA, EIDON, COMPASS, EIDON AF, EIDON FA.