Atesos medical AG
CH-MF-000010304 · Switzerland · Aarau
Atesos medical AG is registered in the European database on medical devices as a manufacturer, with 244 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 135 |
|---|---|
| Class I | 109 |
Most frequent device types declared: Inlay Extractor, Pyramid Hip Shell, Pyramid Hip Shell Revision, Pyramid Hip Stem, Pyramid Hip Stem cemented.
Among these devices, 110 are declared sterile, 109 implantable, 83 reusable.
Authorised representative in the Union: hestomed GmbH.
Devices declared under this manufacturer
- Aiming Device
- Guided Stem Impactor
- Punch
- Pyramid Hip Insert
- Pyramid Hip Shell
- Pyramid Hip Stem
- Pyramid Rasp
- Pyramid Stem
- Retractor blade 40
- SORT-P sterile, reflective sphere
- Sphere carrier
- Trial Head ø28 M
Showing 12 of 244 declared devices.
Catalogue references include 321065, 332008, 350001, 350003, 500.B005.1, 800098.
European nomenclature codes declared: L091199, P090804010201, L091201, P090804010101, L091104, P0908030302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 244 |
| 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 | 244 |
|---|---|
| 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. Atesos medical AG was not found in either the U.S. or the Canadian register.