Leica Biosystems Nussloch GmbH
DE-MF-000021943 · Germany · Nussloch
Leica Biosystems Nussloch GmbH is registered in the European database on medical devices as a manufacturer, with 29 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Devices declared under this manufacturer
- ASP6025 S
- HistoCore AUTOCUT
- HistoCore PEARL
- HistoCore PEGASUS
- HistoCore SPECTRA CV
- HistoCore Water Bath M
- Leica CM1520
- Leica CM1860
- Leica CV5030
- Leica DB80 HS
- Leica DB80 LS
- Leica RM2125 RTS
Showing 12 of 29 declared devices.
Catalogue references include 14035843488, 14035843490, 14042230535, 14047839700, 14049146881, 14049350667.
European nomenclature codes declared: W0202059010, V010302, W0202059003, W0202059005, W0202059002, W0202059008.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | LEICA BIOSYSTEMS NUSSLOCH GMBH (DE) · FDA 8010478 |
| Devices in EUDAMED | 29 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 29 |
|---|---|
| Found in the U.S. device database | 11 |
| Share | 37.9 % |
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. Leica Biosystems Nussloch GmbH is registered in the United States but was not found in the Canadian register.