Brusaferri & C. srl
IT-MF-000039891 · Italy · Milano
Brusaferri & C. srl is registered in the European database on medical devices as a manufacturer, with 43 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 43 |
|---|
Devices declared under this manufacturer
- 1126 - SOSUL
- 1127 - SOSUL 2000
- 1139 LEMI 4 BI-ZAK
- 1155 - SOSUL TOP 3M
- 1167 - SOSUL TOP 2M
- 1168 PODO MIX 2M
- 1218 DENTAMED MOVE
- 1286 PODO 5
- 1340 - LEMI X
- 1470 - GEMINI
- 1473 - VERONA EVO
- 1502 - GEMINI CLASSIC
Showing 12 of 43 declared devices.
Catalogue references include ABOUT LEMI 2024, ABOUT LEMI MD, ABOUT LEMI MD 2026, LEMI MD - 2025, LEMI MD 2025, https://tyromotion.com/wp-content/uploads/2018/09/OmegoPlus.pdf.
European nomenclature codes declared: V08020101, V08020101,V080603, V080603, V08060101, V080202.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | BRUSAFERRI & C. SRL (IT) · FDA 3012240979 |
| Devices in EUDAMED | 43 |
| Country of registration | Italy |
Device-level evidence
| Devices with a numeric GTIN | 43 |
|---|---|
| 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: United States only. Brusaferri & C. srl is registered in the United States but was not found in the Canadian register.