Professional Derma SA
CH-MF-000052108 · Switzerland · Lugano
Professional Derma SA is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 10 |
|---|
Among these devices, 10 are declared sterile.
Authorised representative in the Union: Quaser S.r.l..
Devices declared under this manufacturer
- JALUPRO
- JALUPRO BIOFILLER LIGHT
- JALUPRO BIOFILLER MEDIUM
- JALUPRO HMW
Catalogue references include CONDRAMIN, HYALUAMIN STRONG, JALUPRO, JALUPRO BIOFILLER LIGHT, JALUPRO BIOFILLER MEDIUM, JALUPRO HMW.
European nomenclature codes declared: P900402.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| Country of registration | Switzerland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 10 |
|---|---|
| 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. Professional Derma SA was not found in either the U.S. or the Canadian register.