Flowstim Technology
FR-MF-000018490 · France · La Teste-de-Buch
Flowstim Technology 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: ANKLE BRACE, FLOWTENS FULL SYSTEM, STIMULATEUR FLOWTENS.
Among these devices, 2 are declared active.
Devices declared under this manufacturer
- FLOWTENS FULL SYSTEM CHEVILLERE DROITE
- FLOWTENS LEFT ANKLE BRACE
- FLOWTENS PATCH
- FLOWTENS RIGHT ANKLE BRACE
- STIMULATEUR FLOWTENS
Catalogue references include FLO-02-108-L, FLO-02-108-R, FLO-02-109, FLO-02-201, FT01-R.
European nomenclature codes declared: Z12062785, Z12062780.
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. Flowstim Technology was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
Z-22-160-S-IX-E | issued | 2027-07-31 |