Well Walking S.r.l.
IT-MF-000037941 · Italy · ASOLO
Well Walking S.r.l. is registered in the European database on medical devices as a manufacturer, with 193 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 193 |
|---|
Most frequent device types declared: FINISHED INSOLES, FOREFOOT - MESOFOOT - ALUX, MODEL 1 - MODEL W - MODEL H.
Devices declared under this manufacturer
- ALUX LIGHT GREY 33/34
- FOREFOOT DARK GREY 43/44
- MESOFOOT BLACK 47/48
- MODEL 1 LIGHT GREY 38
- MODEL 1 LILAC 35
- MODEL 1 LILAC 41
- MODEL 1 LILAC 42
- MODEL 1XL BLACK 41
- MODEL 1XL BLACK 45
- MODEL H BLACK 37
- MODEL H BLACK 46
- MODEL W ANTHRACITE 47
Showing 12 of 193 declared devices.
Catalogue references include FD0105, FD0107, FD0201, FD0202, FH0101, PS0101.
European nomenclature codes declared: Y063303, Y061203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 193 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 193 |
|---|---|
| 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. Well Walking S.r.l. was not found in either the U.S. or the Canadian register.