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Braided Device Sizing Support Application
Ankyras predicts the device foreshortening for patient-specific aneurysm treatment planning with 94% average accuracy
The solution, available on Desktop, Web, or Mobile, provides simulated results in a user-friendly interface that promotes communication between healthcare professionals and device manufacturers to support and simplify device sizing.
Supported by various validation studies and a robust algorithm, Ankyras provides users with highly detailed anatomical information and allows the simulation of the user's desired flow diverters (FD) in the target vessel for device sizing and positioning assessment / to accurately assess device sizing and positioning.
A unique sizing concept providing valuable insights about the patients medical case. With Ankyras, physicians can interact with the curves, shapes, and push zones of the vessel, to help define the best treatment strategy for the patient. It also facilitates the communication and understanding between device manufacturers and physicians, maximizing safety and efficiency for patient treatment.
Ankyras is Mentice's first device to receive CE Mark and FDA approvals. With over 25 years of experience, Mentice offers a unique integration of virtual and physical platforms for medical device and procedural training. This includes hands-on possibilities, online simulations, and communication with manufacturers and peers for patient-specific treatment discussion and device feedback.
Accurate visualization of device foreshortening and final position
Ability to share simulation through online portal, enabling collaboration between physicians and device manufacturer
Easy selection of the best suited device and its distal position for the best possible flow diversion effect
Assessment of stent-wall apposition and local porosity to allow for detailed investigations of different flow diverters
Flow diverter telescoping functionality for complex cases
Vessel morphology characterization of the aneurysm region
Ease of implementation
Simple-to-use module to load DICOM images and/or 3D surface models from the patient’s vasculature.
Ankyras facilitates a multi-faceted environment accessed via desktop, web, and mobile providing operating physicians with convenience and immediate access ranging from pure visualization to complete workflow control.
The workflow is run before the intervention with diagnostic 3D images and can be brought to the operating room using standard mobile devices.
Simulate the desired FD devices with a unique foreshortening algorithm and compare the results among the different sizes to predict the most suitable device for the patient.
When the simulated device deployment is saved, the user can share the results among manufacturers, distributors and clinicians for case planning.
Simple-to-use module to load DICOM images and/or 3D surface models from the patient’s vasculature.
Accessed via desktop, web, and mobile providing operating physicians with convenience and immediate access ranging from pure visualization to complete workflow control.
Simulate the desired FD devices with a unique foreshortening algorithm and compare the results among the different sizes to predict the most suitable device for the patient.
When the simulated device deployment is saved, share the results among manufacturers, distributors and clinicians for pre or post-operative case planning.
"Ankyras facilitates patient-specific size selection during endovascular treatment planning. Sharing and interacting with the simulation results allows our team to be highly involved in case preparation, which is key to providing optimal case support. Developed based on our requirements as a device manufacturer and the needs of clinical users, Ankyras substantially adds to the patient’s safety."
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+34 933 28 39 64
Disclaimer & Regulatory Information
Ankyras is manufactured by Mentice Spain S.L. and distributed by Mentice subsidiaries and partners in approved markets.
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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