FDI FRANCE
FR-MF-000023166 · France · Les Abrets en Dauphiné
FDI FRANCE is registered in the European database on medical devices as a manufacturer, with 136 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 136 |
|---|
Most frequent device types declared: TRIPOD, Walking stick.
Devices declared under this manufacturer
- ACCESS COMFORT GREY
- ACCESS COMFORT RED
- ACCESS SAFE WALK GRIS V2
- ERGODYNAMIC
- ERGODYNAMIC M
- ERGOTECH
- ERGOTECH BEIGE
- ERGOTECH BLACK
- ERGOTECH BLUE
- ERGOTECH RED
- ERGOTECH VIOLET
- PREMIUM BEIGE
Showing 12 of 136 declared devices.
Catalogue references include ACO/07/08, AS2/07/02, EDS/05/02, ET/01/07, ET/02/08, ET/15/08.
European nomenclature codes declared: Y12030602, Y12030601, Y120380, Y120399, Y120315.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 136 |
| 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 | 136 |
|---|---|
| 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. FDI FRANCE was not found in either the U.S. or the Canadian register.