Leisegang Feinmechanik-Optik GmbH
DE-MF-000006525 · Germany · Berlin
Leisegang Feinmechanik-Optik GmbH is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 14 |
|---|
Most frequent device types declared: 1D LED.
Among these devices, 14 are declared active.
Devices declared under this manufacturer
- Colposcope
Showing 12 of 14 declared devices.
Catalogue references include BG000280, BG002390, BG002688, BG005000, BG005100, BG005388.
European nomenclature codes declared: Z12020703.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | LEISEGANG FEINMECHANIK-OPTIK GMBH (DE) · FDA 9611604 |
| Devices in EUDAMED | 14 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 14 |
|---|---|
| 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: United States only. Leisegang Feinmechanik-Optik GmbH is registered in the United States but was not found in the Canadian register.