Sensopro AG
CH-MF-000010122 · Switzerland · Münsingen
Sensopro AG is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|
Authorised representative in the Union: Medical Technology Promedt Consulting GmbH.
Devices declared under this manufacturer
- Sensopro Luna Physio
- Sensopro Seat Physio
- Sensopro Tube Aquamarin/Aquamarine
- Sensopro Tube Azurblau/Azure blue
- Sensopro Tube Korall-Rot/coral-red
Catalogue references include A-10008, A-10009, A-10015-05, A-10015-06, A-10015-07, A-10042.
European nomenclature codes declared: Z12069099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 6 |
|---|---|
| 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. Sensopro AG was not found in either the U.S. or the Canadian register.