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: Airline Stretcher NGS, Core Stretcher, Defibrillator Retainer, HEMS ON FLOOR RETAINER, Kartsana-HEMS Stretcher Fixation Unit.
Among these devices, 6 are declared active.
Authorised representative in the Union: Bucher Interiors GmbH.
Devices declared under this manufacturer
- ATS 16G Stretcher
- Defibrillator Retainer
- Footrest Frame Assy
- HEMS ON FLOOR H145 LH RETAINER 382.5
- Kartsana-HEMS Stretcher Fixation Unit
- Medical Device Interface
- Medical Device Interface ASSY
- NGS 16G Stretcher
- Quick Release Assy
- Rear Loading Device 382.5
- Retainer AY Propaq 104 LC
- Retainer Defi ASSY
Showing 12 of 190 declared devices.
Catalogue references include 1120030-320, 1352100, 1354920, 1361150, 1363900, 1374350.
European nomenclature codes declared: V0880, V08050101, V08050103, V0899.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 190 |
| 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 | 190 |
|---|---|
| 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. Bucher Leichtbau AG was not found in either the U.S. or the Canadian register.