3 M.C. Società per azioni
IT-MF-000022649 · Italy · Bari
3 M.C. Società per azioni is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 14 |
|---|
Most frequent device types declared: BROCCA, PAPPAGALLO.
Devices declared under this manufacturer
- BROCCA MONOUSO GRADUATA LT.1
- PAPPAGALLO MONOUSO 800 ML
- PROTEX
- PROTEX cappellino chirurgico monouso in TNT non sterile
- Protex cappellino chirurgico in TNT con elastico nucale
- Protex cappellino monouso in TNT a scafandro
- Protex federa monouso non sterile in tnt
Showing 12 of 14 declared devices.
Catalogue references include 2201, 2207, 2221, 2238, 2240, D/1006.
European nomenclature codes declared: T0207, T0208, T0306, Y091299, T030502, T0205.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| 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 | 14 |
|---|---|
| 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. 3 M.C. Società per azioni was not found in either the U.S. or the Canadian register.