FAR Srl
IT-MF-000041136 · Italy · SETTIMO DI PESCANTINA (VR)
FAR Srl is registered in the European database on medical devices as a manufacturer, with 54 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- ACE
- ACE liquid
- ALBUMIN
- ALKALINE PHOSPHATASE
- AMMONIA
- AST / GOT
- CREATININE
- GPT /ALT
- METANEPHRINES
- PHOSPHOLIPIDS
- PORPHYRINS T
- PROTO PORPHYRINS
Showing 12 of 54 declared devices.
Catalogue references include CL01-100, CL04-200S, CL36-275, CL37-200, CY02-36, CY04-55.
European nomenclature codes declared: W01010207, W01010110, W01010109, W01010201, W01010301, W01010103.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 54 |
| 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 | 54 |
|---|---|
| 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. FAR Srl was not found in either the U.S. or the Canadian register.