MAGGI S.r.l.
IT-MF-000025772 · Italy · PIOVA' MASSAIA (AT)
MAGGI S.r.l. is registered in the European database on medical devices as a manufacturer, with 106 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 106 |
|---|
Among these devices, 106 are declared sterile, 106 implantable.
Devices declared under this manufacturer
- Bioplant
- Bioplant Elasta
- Bioplant Paste
- Exaflex
- Exaflex Polvere
- Osteogen
- Osteogen Gel
Showing 12 of 106 declared devices.
Catalogue references include EXF-55, OSD051S, OST-05B, OST-06B, OST-10P, OST-20.
European nomenclature codes declared: P900401, P900399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 106 |
| 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 | 106 |
|---|---|
| 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. MAGGI S.r.l. was not found in either the U.S. or the Canadian register.