BIOXAL SAS
FR-MF-000000481 · France · Chalon sur Saône
BIOXAL SAS is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 6 |
|---|---|
| Class IIa | 5 |
Devices declared under this manufacturer
- Thermosept PAA additive
- Thermosept PAA additive (adapter)
- Thermosept PAA additive BHT-PIN
- dialox
- dialox active
- exeol PA
- gigasept PAA
- terralin PAA
- thermosept PAA additive
Catalogue references include 125802, 70000167, 70004047, 70004048, 70004084, 70004085.
European nomenclature codes declared: D050103, V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 11 |
|---|---|
| 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. BIOXAL SAS was not found in either the U.S. or the Canadian register.