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Pathomation BV

Belgium BE-MF-000035661 Last updated 21 Oct 2026

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Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

  • PMA.core Ref PMA.core 3.0

    IVD General EUDAMED Active

About

Discover Pathomation's scalable digital pathology software solutions for diagnostics, research, education, and pharma. Empower your pathology workflows today.

From the manufacturer's own website. Source

What Pathomation BV makes

Pathomation BV develops digital pathology software designed for image management, analysis, and collaboration in pathology workflows. The PMA.core platform supports diagnostic imaging, research applications, educational training, and pharmaceutical development by enabling digital slide viewing, annotation, and data integration.

The company’s products fall under the EU’s In Vitro Diagnostic Medical Device (IVD) General category and are registered in the EU’s eudamed database. Pathomation BV is based in Belgium.

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 Pathomation BV manufacture?

Pathomation BV specializes in digital pathology software solutions. Their primary offering, PMA.core, is a platform designed for managing, analyzing, and collaborating on pathology images. This includes diagnostic imaging, research applications, educational training, and pharmaceutical development. The software enables functionalities like digital slide viewing, annotation, and data integration, all within pathology workflows.

Where is Pathomation BV based?

Pathomation BV is headquartered in Belgium. The company’s location in Belgium aligns with its focus on developing and distributing medical software within the European market, particularly for digital pathology applications.

Which regulatory registries list Pathomation BV’s devices?

Pathomation BV’s devices are listed in the eudamed database, which is the official EU registry for in vitro diagnostic medical devices. This registration ensures transparency and compliance with EU regulatory requirements for IVD devices.

How are Pathomation BV’s devices classified under EU regulations?

Pathomation BV’s devices fall under the EU In Vitro Diagnostic Medical Device (IVD) General classification. This classification applies to software and systems that assist in the examination of samples (e.g., pathology slides) to detect or monitor conditions, aligning with their core functionality in digital pathology workflows.

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

Information

Country
Belgium
Address
78-80, Sint-Bavostraat, Antwerp, Belgium
Phone
+32 3 304 76 75
PRRC contact
Veerle Persy
EUDAMED SRN
BE-MF-000035661