Citieffe s.r.l.
IT-MF-000007781 · Italy · Calderara di Reno (BO)
Citieffe s.r.l. is registered in the European database on medical devices as a manufacturer, with 56 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 56 |
|---|
Most frequent device types declared: GUIDE WIRES, MEASURERS.
Among these devices, 56 are declared reusable.
Devices declared under this manufacturer
- SURGICAL INSTRUMENTS (IR)
Showing 12 of 56 declared devices.
Catalogue references include 38259, 6614150, 66991, DT030001, DT070001, DT072003.
European nomenclature codes declared: L091001, L0923.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | CITIEFFE SRL (IT) · FDA 3003249380 |
| Devices in EUDAMED | 56 |
| 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 | 56 |
|---|---|
| Found in the U.S. device database | 25 |
| Share | 44.6 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.