Disclaimer: AI results are provided by external regulatory-approved AI solutions/partners. deepcOS communicates and displays clinical information to end-users. All medical devices available on deepcOS are regulatory cleared for use in the EU under the MDR/MDD. Only selected medical devices available on deepcOS are regulatory cleared for use in the US under the FDA. The worklist and DICOM viewer components are part of the deepcOS AIDA (v2.1) product, which is classified as software as a medical device under the MDR and is CE-marked. Please contact our support team for further information (
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