CERICHEM BIOPHARM SRL
IT-MF-000031272 · Italy · CERIGNOLA
CERICHEM BIOPHARM SRL is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 7 |
|---|
Most frequent device types declared: GEL FAST, H-MATIC ACT, H-MATIC DET, H-MATIC SAD, H-Matic NP.
Devices declared under this manufacturer
- GEL FAST
- H-MATIC ACT
- H-MATIC AD
- H-MATIC DET
- H-MATIC NP
- H-MATIC NPC
- H-MATIC SAD
Catalogue references include GF100, HAD, HCT, HMD100/5, HMS, HNP.
European nomenclature codes declared: V0799, V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| 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 | 7 |
|---|---|
| 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. CERICHEM BIOPHARM SRL was not found in either the U.S. or the Canadian register.