Quick Specs
Simpleware Medical delivers comprehensive tools for segmentation, meshing, measurement, and 3D printing from medical imaging data. Automate workflows, ensure regulatory compliance, and export simulation-ready models with confidence.
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Gli studenti hanno accesso gratuito a software di simulazione di livello mondiale.
Connettiti a Ansys per scoprire come la simulazione può potenziare la tua prossima innovazione.
FDA 510(k) cleared and CE marked 3D image processing software that converts medical scan data into accurate, patient-specific models to support clinical decision-making.
Ansys Simpleware Medical provides a complete image-to-simulation workflow for clinical applications. Transform CT and MRI data into reliable 3D models for pre-surgical planning, patient-specific device design inputs, and anatomical analysis. Regulatory-ready workflows integrate directly with design, simulation, and medical 3D printing environments.
Simpleware Medical delivers comprehensive tools for segmentation, meshing, measurement, and 3D printing from medical imaging data. Automate workflows, ensure regulatory compliance, and export simulation-ready models with confidence.
*Not part of the regulatory clearance
CLINICAL WORKFLOWS
Simpleware Medical enables engineers and clinical teams to create accurate, simulation-ready models from CT and MRI data through structured, automated workflows. Segmentation, automation, and industry-leading meshing capabilities reduce manual effort while improving consistency and reproducibility. Regulatory-ready processes support FDA 510(k), EEA CE marking requirements, and medical device workflows in Australia and Japan. Seamlessly integrate imaging, design, and simulation into a unified environment for faster insights and improved collaboration.
Simpleware Medical delivers end-to-end capabilities from image import to patient-specific, clinically actionable model generation.
It's vital to Ansys that all users, including those with disabilities, can access our products. As such, we endeavor to follow accessibility requirements based on the US Access Board (Section 508), Web Content Accessibility Guidelines (WCAG), and the current format of the Voluntary Product Accessibility Template (VPAT).
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