STERIFY S.R.L.
IT-MF-000032120 · Italy · TORINO
STERIFY S.R.L. is registered in the European database on medical devices as a manufacturer, with 36 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 36 |
|---|
Among these devices, 36 are declared sterile, 36 implantable.
Devices declared under this manufacturer
- PDF-Gel
- PerioWall
- STERIFY GEL
Showing 12 of 36 declared devices.
Catalogue references include PDF-GEL1001, PDF-GEL1003HM, POW-GEL0303, POW-GEL0303HM, POW-GEL0501HM, POW-GEL0503.
European nomenclature codes declared: P900402.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 36 |
| 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 | 36 |
|---|---|
| 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. STERIFY S.R.L. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
032-00-01-MDR | supplemented | 2028-10-05 |
031-00-02-MDR | supplemented | 2028-10-05 |