Invacare France Operations SAS
FR-MF-000006807 · France · Fondettes
Invacare France Operations SAS is registered in the European database on medical devices as a manufacturer, with 332 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 332 |
|---|
Among these devices, 56 are declared active.
Devices declared under this manufacturer
- Action 1 R
- Action 2 NG
- Action 3 NG
- Action 4 NG
- Action Ampla
- Alu Lite
- Esprit Action
- Küschall Compact Attract
- Küschall Element
- Küschall K-Series
- Küschall The KSL
- Rea Azalea
Showing 12 of 332 declared devices.
Catalogue references include BW1533750 and suffix, BY1548472 and suffix, CS1567976 and suffix, DK1640969 and suffix, EG1672729 and suffix, EK1685690 and suffix.
European nomenclature codes declared: Y122106, Y122103, Y122103,Y122106, Y122127.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 332 |
| 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 | 332 |
|---|---|
| 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. Invacare France Operations SAS was not found in either the U.S. or the Canadian register.