THUASNE
FR-MF-000001201 · France · Levallois-Perret
THUASNE is registered in the European database on medical devices as a manufacturer, with 3 530 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 3 530 |
|---|
Devices declared under this manufacturer
- Biflex Self Adjust
- CICATREX
- GenuPro Comfort
- GenuStart Ice
- Knee Osteoarthritis brace
- Ligaflex Classic
- Lombastart
- Lymphatrex Revolution
- Venoflex City Confort Coton
- Venoflex Elegance
- Venoflex Elegance 3 chaussettes
- Venoflex Kokoon Absolu
Showing 12 of 3 530 declared devices.
Catalogue references include 23460420109899, 23890129900399, 50200220106213, 51390120402512, 52250320300412, 52250320400333.
European nomenclature codes declared: M030405, M030499, Y061209, Y060308, Y060609, Y06120601.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Thuasne, LLC (MX) · FDA 3025770454 |
| Devices in EUDAMED | 3 530 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 3 530 |
|---|---|
| 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: United States only. THUASNE is registered in the United States but was not found in the Canadian register.