Aleva Neurotherapeutics SA
CH-MF-000015804 · Switzerland · Lausanne
Aleva Neurotherapeutics SA is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: 11500, 12000, 12050, 12200, 12310.
Among these devices, 6 are declared sterile, 13 implantable, 13 active, 2 with a measuring function.
Authorised representative in the Union: Veranex Germany GmbH.
Devices declared under this manufacturer
- directSTIM 12-connector extension
- directSTIM 12-electrode lead
- directSTIM 24-channel Implantable Pulse Generator
- directSTIM Adjustable Harness
- directSTIM Charging Paddle
- directSTIM Clinician Programmer
- directSTIM External Pulse Generator
- directSTIM Magnet
- directSTIM Patient Programmer Charger kit
- directSTIM Port Plug
- directSTIM Power Cord
- directSTIM Trial Cable
Showing 12 of 13 declared devices.
Catalogue references include 12000, 12200, 12310, 12320, 12340, 12400.
European nomenclature codes declared: J020780, J020701, J020102, J02010101, J020199, J020180.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 13 |
| 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 | 13 |
|---|---|
| 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. Aleva Neurotherapeutics SA was not found in either the U.S. or the Canadian register.