Anel AG
CH-MF-000033240 · Switzerland · Bern
Anel 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 |
|---|
Most frequent device types declared: resi1.
Authorised representative in the Union: Basmed GmbH.
Devices declared under this manufacturer
- Helmet for resi PRONE
- Spiegelplatte zu resi PRONE
- resi IMT Inspiratory muscle trainer
- resi OPEP Atemtherapiegerät
- resi PRONE Face Cushion, large
- resi PRONE Kopfkissen, klein
Catalogue references include IMT1, PFCL, PFCS, PFHT, PFMR, resi1.
European nomenclature codes declared: Z12011280, Z12011285, R900902.
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. Anel AG was not found in either the U.S. or the Canadian register.