Reviewed 21 Jul 2026
Completeness Strong (64%)
Mindpeak Breast ER/PR is intended for in vitro diagnostic use as an aid to the pathologist in the assessment of samples from human breast cancer patients.
Image analysis consists of the detection and classification of IHC stained tumor cells on the whole slide. Tumor cells are classified as not-stained (tumor negative) or stained (tumor positive).
A corresponding ER or PR score is provided as the proportion of the number of tumor positive cells divided by the sum of tumor positive and tumor negative cells.
Supported by 1 paper




General Information
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Regulatory Information
Pathway:
In Vitro Diagnostic Directive (IVDD)
Class:
General IVD Devices
Verified by Health AI Register
Scanner Brands Certified for Use (CE-IVD)
Scanner Models Certified for Use (CE-IVD)
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Technical Specifications
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Based on
First published: Jul 30, 2025 | Last updated: Jul 21, 2026