EVOLUT PRO+ SYSTEM Transcatheter Aortic Valve Implantation (TAVI)
The next generation EvolutTM PRO+ transcatheter aortic valve system provides industry-leading hemodynamics — allowing your patients to return to activity faster.1,2,3
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Overview
Meet the Evolut PRO+ SYSTEM
ADVANCED
SEALING
LOW DELIVERY
PROFILE
HEMODYNAMIC
PERFORMANCE
PRODUCT DETAILS
Treat more
Patients
Leadership
In Valve Design
Control
During Deployment
EXPECT MORE OPTIMIZE PRO STUDY
8.8%
PERMANENT PACEMAKER RATE AT 30 DAYS3
0%
MODERATE/SEVERE PVL AT DISCHARGE3
0 DEATHS
AND DISABLING STROKES AT 30 DAYS3
8.1% mm Hg
GRADIENT AT DISCHARGE
EXPERTS CORNER
RESOURCES
MANUALS AND TECHNICAL GUIDES
Access instructions for use and other technical manuals in the Medtronic Manual Library. Search by the product name (e.g., Evolut) or model number.
EVOLUT PRO+ PLATFORM RESOURCES
How Evolut can treat more patients?
CONTACT US
Low risk
Indication
Learn More
Bicuspid
Indication
Learn More
*
Broadest annulus range based on CT derived diameters.
1
Bleiziffer S, Eichinger WB, Hettich I, et al. Impact of patient-prosthesis mismatch on exercise capacity in patients after bioprosthesis aortic valve replacement. Heart. May 2008;94(5):637-641.
2
van Slooten YJ, van Melle JP, Freling HG, et al. Aortic valve prosthesis-patient mismatch and exercise capacity in adult patients with congenital heart disease. Heart. January 2016;102(2):107-113.
3
Pibarot P, Dumesnil JG, Jobin J, Cartier P, Honos G, Durand LG. Hemodynamic and physical performance during maximal exercise in patients with an aortic bioprosthetic valve: comparison of stentless versus stented bioprostheses. J Am Coll Cardiol. November 1, 1999;34(5):1609-1617.
4
Up to 80% deployment. The valve can be partially or fully recaptured up to three times prior to the point of no recapture. Third attempt must be a complete recapture and retrieval from patient.
DISCLAIMER
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.
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