Physidia S.A.S.
FR-MF-000011761 · France · Saint-Barthélemy-d'Anjou
Physidia S.A.S. is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 1 |
|---|---|
| Class IIa | 5 |
Most frequent device types declared: CC39.
Among these devices, 1 are declared active.
Devices declared under this manufacturer
- Interlayers for S³.PHYSI.LACT.SUPPORT
- S³ Haemodialysis Machine
- S³ PHYSIFLOW ERGO
- S³.PHYSI.FLOW-150
- S³.PHYSI.LACT.SUPPORT
- S³.PHYSI.POD
Catalogue references include 850004, 850007, 850013, 850015, 850016, CC39.
European nomenclature codes declared: Z12099080, Z12090285, Z12090201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 6 |
|---|---|
| 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. Physidia S.A.S. was not found in either the U.S. or the Canadian register.