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Carl Zeiss Microscopy GmbH

Germany DE-MF-000024424 Last updated 30 May 2026

Devices
36
Registries
EUDAMEDGUDID
FDA recalls
0

Catalogue36

What Carl Zeiss Microscopy GmbH makes

Carl Zeiss Microscopy GmbH manufactures stereomicroscopes, compound microscopes, and associated imaging software, including models like the Stemi 508 trino, Axio Imager.M2p, and ZEISS Autoimmersion Module. Their portfolio also includes digital imaging solutions such as the ZEN 3.7 software and zoom microscopes like the Axio Zoom.V16. Additional offerings include standalone software platforms like Labscope 4.0 and 4.4 for laboratory use.

The company’s devices fall under EU Class A medical devices and are registered in the EUDAQ database (eudamed). The manufacturer is based in Germany.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Carl Zeiss Microscopy GmbH manufacture?

Carl Zeiss Microscopy GmbH specializes in optical microscopy solutions, including stereomicroscopes (such as the Stemi 508 trino and SteREO Discovery.V12), compound microscopes (like the Axio Imager.M2p), and zoom microscopes (e.g., Axio Zoom.V16). Their portfolio also includes imaging software and modules, such as the ZEN 3.7 software suite and the ZEISS Autoimmersion Module, as well as standalone laboratory software platforms like Labscope 4.0 and 4.4. These devices are designed for applications in research, education, and industrial inspection.

Where is Carl Zeiss Microscopy GmbH based?

The company is headquartered in Germany, specifically under Carl Zeiss Microscopy GmbH, which operates as part of the broader Carl Zeiss group. This location aligns with its role as a European manufacturer of microscopy equipment and software.

Which regulatory registries list Carl Zeiss Microscopy GmbH’s devices?

Carl Zeiss Microscopy GmbH’s devices are registered in the EUDAQ database (eudamed), which is the official European Union database for medical devices. This registry ensures transparency and compliance with EU medical device regulations, particularly for devices classified under the Medical Device Regulation (MDR).

How are Carl Zeiss Microscopy GmbH’s devices classified under EU regulations?

All devices manufactured by Carl Zeiss Microscopy GmbH fall under EU Class A classification. This classification applies to low-risk medical devices, such as certain microscopes and imaging software, which are deemed to pose minimal risk to patients and users. Classification is determined based on factors like intended use, duration of use, and potential risks, as outlined in EU medical device legislation.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Germany(from SRN)
Address
10, Carl-Zeiss-Promenade, Jena, Germany
Phone
+49 3641 64 0
PRRC contact
Matthias Müller
EUDAMED SRN
DE-MF-000024424
DUNS number
537598935