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Braided Device Sizing Support Application
Convert 3D DICOM images (3DRA, MRA) or 3D vessel models to extract the vessel morphological description to predict the device foreshortening and apposition at the target zone
Start the simulation by using the threshold segmentation method to create the 3D vessel model from the 3D DICOM image (3DRA/MRA).
Explore the patient's anatomy in deeper detail: Ankyras measures the morphology considering the 3-dimensional space, providing a detailed analysis of the changing diameter values over the artery, and the segment length to be treated.
Diameter (mm)
Inscribed Diameter (mm)
Area (mm)
Ankyras uses its unique simulation algorithm to assess commercially available flow diverter's final length and position. This method uses device design and detailed morphological descriptors of the treated vessel to show the fitting and position of the device to provide a 95% accurate position and length of the implanted device.
Selecting a flow diverter with good apposition to the vessel wall is possible thanks to the expansion representation over the device surface and the expansion chart. Simulated expansion is colored upon the device's simulated surface, indicating those areas on which the device is fully expanded and not completely attached to the vessel wall based on the device maximum diameter.
Ankyras Porosity characterizes and predicts the local porosity of the flow diverter after implantation. It is intended to help understand differences in local porosity compared to other device brands and sizes and to evaluate the final coverage and expansion in the desired region.
Ankyras allows the user to prepare a simulation offline - checking the results on-site - to preparing a simulation
Require internet:
View Simulation:
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Create & edit simulation:
Share Simulation:
Ranging from pure visualization to full workflow control, enabling the workflow to run before the intervention with diagnostic 3D images
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Disclaimer & Regulatory Information
Ankyras is manufactured by Mentice Spain S.L.
ANKYRAS is intended to be used by physicians trained in medical procedures involving percutaneous and intravascular interventions.
Ankyras is 510(k) cleared by FDA.
Mentice Spain SL: Mentice Spain SL has obtained the ISO 13485 certification with number MD 784027
Ankyras certifications: The Ankyras product complies with the Medical Device Regulation (EU CE Mark, MDR 784032) and the UK Conformity Assessed (UKCA 784033)
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