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DATEXIM

France FR-MF-000000919 Last updated 21 Oct 2026

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Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

About

Discover Datexim, expert in digital cytology and artificial intelligence, creating innovative solutions to improve early cancer detection and save lives.

From the manufacturer's own website. Source

What DATEXIM makes

Datexim manufactures the CytoProcessor, an automated device designed for digital cytology analysis. This system processes cytological samples to facilitate microscopic examination and interpretation, supporting pathology workflows in diagnostic settings.

The CytoProcessor is classified under IVD General and is registered in the EUDAMED database. The company is headquartered in France.

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 Datexim manufacture?

Datexim specializes in automated devices for digital cytology. Specifically, it produces the CytoProcessor, which processes cytological samples to enable digital analysis and microscopic examination. This device supports pathology workflows by streamlining the preparation and review of samples, aiding in diagnostic processes.

Where is Datexim based, and what is its primary focus?

Datexim is headquartered in France. The company focuses on developing innovative solutions in digital cytology, leveraging artificial intelligence to enhance early cancer detection. Its primary product, the CytoProcessor, is designed to improve diagnostic accuracy and efficiency in pathology settings.

Which regulatory registries list Datexim’s devices?

Datexim’s devices, including the CytoProcessor, are registered in the EUDAMED database. This platform is the official European Union registry for medical devices, ensuring transparency and traceability of authorized products within the EU market.

How are Datexim’s devices classified under EU regulations?

The CytoProcessor, Datexim’s primary device, falls under the classification of IVD General. This classification applies to in vitro diagnostic medical devices that do not pose significant risks and are used for general diagnostic purposes, such as cytology analysis.

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

Information

Country
France
Address
24 - 26, Rue Saint Martin, Caen, France
Phone
+33 231436235
PRRC contact
Ouarda Beniken
EUDAMED SRN
FR-MF-000000919