Biopredictive
FR-MF-000003886 · France · PARIS
Biopredictive is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- AshTest
- FibroMax
- FibroTest
- FibroTest N
- FibroTest-ActiTest
- HCV-GenoFibroTest
- NASH-FibroTest
- NashTest
- NashTest2
- SteatoScreen
- SteatoTest
- SteatoTest2
Catalogue references include AshTest, FibroMax, FibroTest, FibroTest N, FibroTest-ActiTest, NashTest.
European nomenclature codes declared: W05030599.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 12 |
|---|---|
| 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. Biopredictive was not found in either the U.S. or the Canadian register.