PLASMABIOTICS
FR-MF-000003777 · France · ARGENTEUIL Cedex
PLASMABIOTICS is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|
Most frequent device types declared: CONNECTION SET, CONNECTION SET (autoclavable), Typhoon V2TD.
Among these devices, 1 are declared active.
Devices declared under this manufacturer
- AUTOCLAVABLE CONNECTION SET
- CONNECTION SET
- CONNECTION SET (autoclavable)
- Connection set
- PlasmaTYPHOON
Catalogue references include Fg5W B-Bp, Fg5W B-Bp/A, Fg5W EB, Fg5W EB/A, Typhoon V2TD.
European nomenclature codes declared: V9099, Z12011314.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 5 |
|---|---|
| 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. PLASMABIOTICS was not found in either the U.S. or the Canadian register.