Bucher Leichtbau AG
CH-MF-000017716 · Switzerland · Fällanden
Bucher Leichtbau AG is registered in the European database on medical devices as a manufacturer, with 190 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 190 |
|---|
Most frequent device types declared: SIT2, Core Stretcher, Retainer for Corpuls C3, Side and Rear-Loading, Retainer for Ferno Stretcher.
Among these devices, 6 are declared active.
Authorised representative in the Union: DE-AR-000006455.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 190 |
| Country of registration | Switzerland |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.