Pathomation BV
Belgium BE-MF-000035661 Last updated 21 Oct 2026
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- Devices
- 1
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
PMA.core Ref PMA.core 3.0
About
Discover Pathomation's scalable digital pathology software solutions for diagnostics, research, education, and pharma. Empower your pathology workflows today.
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.
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.
Information
- Country
- Belgium
- Address
- 78-80, Sint-Bavostraat, Antwerp, Belgium
- Website
- www.pathomation.com/
- linkedin.com/company/pathomation
- [email protected]
- Phone
- +32 3 304 76 75
- PRRC contact
- Veerle Persy
- EUDAMED SRN
- BE-MF-000035661