Rehearse key EP workflows in a risk-free environment
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This module enables EP fellows to rehearse key workflows in a risk-free environment, offering hands-on experience to accelerate skill development and confidence.
The user will be able to learn how to interpret EGM signals with real-time location-based feedback, develop device coordination, and practice mapping and ablation to build confidence before entering the cath lab and treating real patients.
The platform is fully scalable and easily adaptable to integrate market-specific devices, supporting dedicated training and accelerating device adoption.
Train with real clinical devices across a flexible, compact simulation setup designed for structured procedural practice.
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This module enables EP fellows to rehearse key workflows in a risk-free environment, offering hands-on experience to accelerate skill development and confidence.
The user will be able to learn how to interpret EGM signals with real-time location-based feedback, develop device coordination, and practice mapping and ablation to build confidence before entering the cath lab and treating real patients.
The platform is fully scalable and easily adaptable to integrate market-specific devices, supporting dedicated training and accelerating device adoption.
Practice EP workflows in a safe, risk-free environment
Interpret EGM signals with real-time, location-based feedback
Develop coordination using multiple steerable devices
Build confidence in left atrial mapping and PVI procedures
Customize the platform easily for tools and workflows
Scale training fidelity and portability to any setting
Flow Diverter Case planning in Ankyras®
Import Case directly into VIST® simulator
Practice deployment in patient-specific anatomy
Discuss how this solution fits your simulation program, education initiative, or device-related needs.
Disclaimer & Regulatory Information
VIST® Ankyras® Flow Diverter Rehearsal is a training solution not intended for clinical use or decision making. Ankyras® is a medical device manufactured by Mentice Spain S.L. Mentice Spain S.L. is ISO 13485 certified. Ankyras® complies with the EU Medical Device Regulation (EU CE Mark, MDR 784032). ANKYRAS® is a medical software intended to assist healthcare professionals in the selection of a proper braided device for treatment of intracranial aneurysms. ANKYRAS® is intended for exclusive use by professional users.
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