VIDA SRL
IT-MF-000030547 · Italy · CRESPINA LORENZANA(PI)
VIDA SRL is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 14 |
|---|---|
| Class IIa | 1 |
Among these devices, 14 are declared sterile, 14 implantable.
Devices declared under this manufacturer
- OPÉRA I
- OPÉRA II
- OPÉRA III
- OPÉRA IV
- OPÉRA REV 10ML
- OPÉRA REV 1ML
- OPÉRA REV 3ML
- OPÉRA V
- TC PLUS STRONG
Showing 12 of 15 declared devices.
Catalogue references include IL710022, IL710039, IL710046, OPERAI, OPERAII, OPERAIII.
European nomenclature codes declared: P900402, M9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 15 |
| 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 | 9 |
|---|---|
| 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. VIDA SRL was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
CVD006126 | issued | 2031-04-09 |
CSQ003626 | issued | 2031-04-09 |