Pivotal validationMaastricht cohort — high sensitivity and strong negative predictive value in the intended-use population.
Identify clinically significant CAD.
Automated assessment of CAD using routine clinical data.
ISO 13485
ISO 27001
How It Works
A New Way to Understand Coronary Artery Disease
Cardio Explorer® transforms routine clinical and biomarker data into a personalized estimate of obstructive CAD—placing each patient on the disease spectrum before imaging or catheterization.
Unlike conventional risk scores that rely on population-based correlations, Cardio Explorer® models the underlying biology of atherosclerosis to provide a more personalized and robust assessment of disease risk.
Risk class
Very Low
CAD-CL
4%Recommendation
Defer further cardiac testing; manage any modifiable risk factors in accordance with preventive care guidelines.
Learn more
05%15%50%85%100%
Very lowLowModerateHighVery high
For illustrative purposes only. Drag the marker to see how a clinical likelihood corresponds to the ESC guideline recommendation. Not a diagnostic tool.
Instructions for UseClinical evidence
Externally validated for its intended use
Independent validation studies demonstrate strong diagnostic performance in low- to intermediate-risk patients, supporting the intended clinical use of Cardio Explorer®.
Independent cohortsBasel I, LURIC, and Maastricht — validated externally, not using the development data.
5
Peer-reviewed publicationsSince 2014, including an abstract for the ESC 2026 AI Congress and a live prospective implementation trial.
Integration
Incorporate Cardio Explorer® into Your Workflow
Integrates seamlessly into your existing clinical workflow. Risk insights appear automatically where clinicians already work—with zero disruption and zero clicks. Now available in Dedalus ORBIS.
Are you using a different clinical information system?
+ Your EMR
Cardio Explorer®
Clinician
Automated Risk Report
Trust
A platform you can trust
Built to the standards that hospital teams expect.
Independently certified.
A CE-marked IVD under the EU IVDD, developed under an ISO 13485 quality management system.
Your data remains protected.
Patient data is protected through ISO 27001-certified information security processes.
Built to medical standards.
Every release follows the IEC 62304 medical device software development lifecycle.