Adria S.r.l.
IT-MF-000027852 · Italy · San Giovanni in Persiceto
Adria S.r.l. is registered in the European database on medical devices as a manufacturer, with 205 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 205 |
|---|
Among these devices, 205 are declared sterile.
Devices declared under this manufacturer
- Herniatome
- Spinertome
- Spinertome kit
- X-Pander - Direct access kit
Showing 12 of 205 declared devices.
Catalogue references include 5050815, 5051310, 5051310 D, 5060812 DC, 5060910 C, 5060910 DC.
European nomenclature codes declared: A019011, A01020102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 205 |
| 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 | 205 |
|---|---|
| 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. Adria S.r.l. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
0425-MDR-030171-00 | issued | 2031-01-15 |