SA.VE.PA. SRL
IT-MF-000031471 · Italy · arese
SA.VE.PA. SRL is registered in the European database on medical devices as a manufacturer, with 45 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 45 |
|---|
Devices declared under this manufacturer
- BENDE DI GARZA CAMBRIC MT. 10 X 10 CM.
- BENDE DI GARZA CM.12 X 5 MT.
- BENDE DI GARZA CM.12 X 8 MT.
- BENDE DI GARZA CM.15 X 5 MT.
- BENDE DI GARZA CM.20 X 10 MT.
- BENDE DI GARZA CM.20 X 5 MT.
- BENDE DI GARZA CM.5 X 5 MT.
- BENDE DI GARZA CM.6 X 10 MT.
- BENDE DI GARZA ORLATA MT. 10 X 15 CM.
- BENDE DI GARZA ORLATA MT. 10 X 20 CM.
- BENDE DI GARZA ORLATA MT. 10 X 7 CM.
- BENDE DI GARZA ORLATA MT. 5 X 10 CM.
Showing 12 of 45 declared devices.
Catalogue references include BG12, BG2, BG22, BG3, BG7, BGO12.
European nomenclature codes declared: M030101, M020107, M0201050102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 45 |
| 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 | 45 |
|---|---|
| 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. SA.VE.PA. SRL was not found in either the U.S. or the Canadian register.