Carl Zeiss Microscopy GmbH
DE-MF-000024424 · Germany · Jena
Carl Zeiss Microscopy GmbH is registered in the European database on medical devices as a manufacturer, with 37 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Most frequent device types declared: Stereo Microscope.
Devices declared under this manufacturer
- Axio Observer 5 clinical
- Labscope 4.2 Software
- Labscope 4.3
- Labscope 4.5
- Labscope 4.6
- SteREO Discovery.V12
- Stemi 508
- Stemi 508 doc
- Stemi 508 trino
- ZEISS Axio Imager.M2
- ZEISS Axio Imager.Z2
- ZEISS Axioscan 7
Showing 12 of 37 declared devices.
Catalogue references include 410135-0002-370, 410135-0052-000, 410135-0052-450, 410135-0052-460, 424533-8245-000, 430000-9902-000.
European nomenclature codes declared: W0202050303, W0202050382, W0202050380, W0202050304.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Carl Zeiss Microscopy, GmbH (DE) · FDA 8010666 |
| Devices in EUDAMED | 37 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 37 |
|---|---|
| Found in the U.S. device database | 9 |
| Share | 24.3 % |
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. Carl Zeiss Microscopy GmbH is registered in the United States but was not found in the Canadian register.