Dima Italia S.r.l.
IT-MF-000020327 · Italy · Bologna
Dima Italia S.r.l. is registered in the European database on medical devices as a manufacturer, with 41 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIb | 25 |
|---|---|
| Class IIa | 16 |
Most frequent device types declared: COR0000070, COR0000090, COR0000110, COR0000140, Luna Belt.
Among these devices, 25 are declared active.
Devices declared under this manufacturer
- BB RESPIRATOR
- COR0000070
- COR0000090
- COR0000100
- COR0000110
- COR0000140
- LUNA 150
- MiniPegaso A-Cough
- MiniPegaso A-Cough Perc
- Multilevel Night & Day ST30
- NEGAVENT T 230
- PEGASO A-COUGH PERC
Showing 12 of 41 declared devices.
Catalogue references include COR0000070, COR0000090, COR0000110, MPP-00050, NV11, NV21.
European nomenclature codes declared: R020199, Z1203010504, R9099, Z1203019099, Z12159009, Z1203010585.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | DIMA ITALIA SRL (IT) · FDA 3007123976 |
| Devices in EUDAMED | 41 |
| Country of registration | Italy |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 40 |
|---|---|
| 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.