Driving cardiovascular innovation together ESC Congress 2025
Madrid, Spain and online
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MM/DD/YYYY
08/29/2025 12:30 PM
08/29/2025 01:30 PM
Europe/Amsterdam
Latest innovations in device therapy for cardiac rhythm management
CRM Satellite Symposium at ESC Congress 2025
Room: Budapest 0 TRANSPARENT
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08/30/2025 10:00 AM
08/30/2025 10:45 AM
Europe/Amsterdam
Hypertension care, reimagined: The Symplicity™ blood pressure procedure
Renal Denervation Satellite Symposium at ESC Congress 2025
Room: Sarajevo 0 TRANSPARENT
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08/30/2025 03:15 PM
08/30/2025 04:00 PM
Europe/Amsterdam
Transforming the care of female and low-risk younger patients with aortic stenosis through guidelines
TAVI Satellite Symposium at ESC Congress 2025
Room: Algiers 0 TRANSPARENT
Tutorials E12Latest innovations in Cardiac Rhythm Management, Renal Denervation & TAVI
Meet the experts for hands-on experience with our simulators!
- Dive into cutting-edge innovations with the extravascular ICD system, leadless and conduction system pacing.
- Learn about renal denervation procedure tips and tricks.
- Develop practical expertise in Transcatheter Aortic Valve Implantation (TAVI) through hands-on simulation training, designed to enhance procedural understanding and refine decision-making skills.
No registration required, join us any time during these time slots:
| Tutorial date | Tutorial time (CEST) |
|---|---|
|
Friday, 29 August |
16:00 - 18:00 |
|
Saturday, 30 August |
16:00 - 18:00 |
|
Sunday, 31 August |
16:00 - 18:00 |
|
Monday, 1 September |
09:30 - 13:00 |
Cardiac Rhythm Management
Renal Denervation
TAVI
Cardiac Ablation Solutions
* For distribution only in markets where the Symplicity Spyral™ multi-electrode renal denervation catheter and Symplicity G3™ renal denervation RF generator have been approved. Not for distribution in the USA, Japan or France.
The material on this website should not be considered the exclusive source of information, it does not replace or supersede information contained in the device manual(s). Please note that the intended use of a product may vary depending on geographical approvals. See the device manual(s) for detailed information regarding the intended use, the (implant) procedure, indications, contraindications, warnings, precautions, and potential adverse events.
For a MRI compatible device(s), consult the MRI information in the device manual(s) before performing a MRI. If a device is eligible for eIFU usage, instructions for use can be found at Medtronic’s website manuals.medtronic.com. Manuals can be viewed using a current version of any major internet browser. For best results, use Adobe Acrobat® Reader with the browser. Medtronic products placed on European markets bear the CE mark and the UKCA mark (if applicable). For any further information, contact your local Medtronic representative.