RECFRANCE
FR-MF-000000820 · France · BEDARIEUX
RECFRANCE is registered in the European database on medical devices as a manufacturer, with 108 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 108 |
|---|
Most frequent device types declared: AIR CUSHIONS, Accessories for Custom Orthotic Systems, Air Cushions Inserts, Modular Standing System, Modular mobility system for walking and standing support.
Devices declared under this manufacturer
- AB-BOUT2
- AB-BOUT3
- BOOMER
- COUSY T4 20
- KANGOU ANT T2
- KIWI 3R
- MODUL'AIR MODR70002
- PROFIL'AIR RECCPA007
- PROFIL'AIR RECCPA020
- TET INOX B
- TET.CRA.003
- TYGRYS T2 GR
Showing 12 of 108 declared devices.
Catalogue references include AB-BOUT3, COUSY T4 20, KIWI 3R, RECCPA007, RECCPA020, TET INOX B.
European nomenclature codes declared: Y0699, V080399, Y1299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 108 |
| 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 | 108 |
|---|---|
| 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. RECFRANCE was not found in either the U.S. or the Canadian register.