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Emergency Lung AI Suite for COVID-19

Fast access to lung quantification results and tissue characterization

Emergency Lung AI Suite 

Our rapid response platform allows physicians to upload cases and receive fast quantification results, regardless of where they sit - the emergency department, radiology, pulmonology, or at home. The Eureka Clinical AI Emergency Lung AI Suite delivers newly enhanced segmentation data science and automated measurement capabilities within a guided workflow for the disease progression assessment and quantification of COVID-19 and other lung related illness.*
Emergency Lung Suite

LungAI Workflow Key Features

The LungAI workflow leverages TeraRecon's data science expertise to rapidly deliver an automated lung experience that delivers zero-click segmentation and histogram results based on physician-customized thresholds. The results of these studies are available for review and adjustment prior to image archival - maintaining physician control. 
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Web-Based Upload and Anonymization
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Web-based, Responsive Design
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Mobile Support**
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Automatic lung assessment (segmentation & classification)
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AI Results Explorer: Review, Adjust & Re-Run Capabilities
Option
Email notification of available results (HIPAA compliant)
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Our rapid response platform allows physicians to upload cases and receive fast quantification results, regardless of where they sit - the emergency department, radiology, pulmonology, or at home.

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*The following are important statements regarding the use of this tool:

  • Volumetric histogram and lung segmentation functionality are FDA cleared features of Intuition. This functionality is not FDA cleared specifically for COVID-19. It must only be used as an aid and that final interpretation should be performed by a licensed healthcare practitioner with the appropriate training.
  • The results should not be used for screening and the software does not provide specific disease detection and should not be solely or primarily relied upon to diagnose or treat COVID-19.
  • This device is not indicated for the diagnosis of COVID-19 and that in vitro diagnostic testing is currently the only definitive method to diagnose COVID-19.
  • This tool is available by specific licenses only.
  • The default thresholds are generalized recommendations and limits for device performance when used in an U.S. population. The image analysis should only be used as an aid and the final interpretation should be performed by a licensed healthcare practitioner with the appropriate training.
  • Research use only in Europe

**Not for diagnose use on mobile device​