Saeg srl
IT-MF-000022747 · Italy · Vigevano
Saeg srl is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 17 |
|---|
Among these devices, 17 are declared reusable.
Devices declared under this manufacturer
- Avvitatore da manipolo
- Avvitatore manuale
- Bussola per Pin
- Fresa Intermedia finale
- Fresa Pilota
- Fresa Rivestita TIN
- Fresa carotatrice
- Fresa-Preparatore di spalla
- Maschiatore da manipolo
- Mucotomo da manipolo
- Pin crestale
- Prolunga per fresa
Showing 12 of 17 declared devices.
Catalogue references include AME-1, BPL-1, CMU-300, FCR-300, FIL-235, FIP-120.
European nomenclature codes declared: L149009, L159099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| 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 | 17 |
|---|---|
| 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. Saeg srl was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
0425-MDR-030024-01 | issued | 2028-05-07 |
0425-MDR-030024-00 | issued | 2028-05-07 |