Alfakjn S.r.l.
IT-MF-000009936 · Italy · Garlasco
Alfakjn S.r.l. is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 7 |
|---|---|
| Class IIb | 1 |
Most frequent device types declared: 32 mg / 2 mL, 32 mg / 2 mL (sample), 32 mg+100 mg / 2 ml (sample), 40 mg / 2 ml, 40 mg / 2 ml (sample).
Among these devices, 7 are declared sterile, 7 implantable.
Devices declared under this manufacturer
- Artrosulfur HA
- Artrosulfur MSM+HA
- Collaflexin
- Condronil IAL
- Condronil IALDUE
- Corakjn C Gel
Catalogue references include MD00027SA, PFS00001SG, PFS00002SG, PFS00002VD, PFS00010VD, PFS00015SG.
European nomenclature codes declared: P900402, M9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| 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. Alfakjn S.r.l. was not found in either the U.S. or the Canadian register.