• Myval
  • myval
  • myval
  • 0% Permanent Pacemakers post procedure upto 6months.

  • 700+ Patients to be studied under Myval Global Clinical Trial Program

  • No Stroke/TIA post procedure

  • Zero Device related Mortality

Myval

  • Balloon expandable TAVR system with bovine pericardium tri-leaflet valve on a Nickel Cobalt alloy frame with Hybrid-Honey comb design.
  • The unique hybrid design of Myval, post crimping, has a unique appearance of alternating light and dark bands under fluoroscence, supporting ease of positioning on the annular plane.
  • Unique crimping pattern with MyvalTM, due to the geometry of design ensures precise orthotopic device placement without any deep throating into the LVOT.
  • Precise annular placement ensures that there is no conduction system disturbances thus eliminating need for a new pace maker as seen with previous technologies.
  • MyvalTM comes with a Navigator Balloon with a Dual-Stopper System for precision in positioning & deployment.

 

For detailed information on Myval product, please click here

www.myval.com

Benefits

  • 01

    NAVIGATOR BALLOON DUAL-STOPPER SYSTEM FOR PRECISE DEPLOYMENT FOR PRECISE DEPLOYMENT

  • 02

    UNIQUE BANDING PATTERN UNDER FLUORO FOR GUIDED PRECISION PLACEMENT

  • 03

    UNPRECEDENTED HYBRID HONEYCOMB DESIGN FOR INTUITIVE PRECISION & Orthotopic placement

Product Specifications

Valve mechanism Balloon Expandable
Valve material Bovine pericardium tri-leaflet on a Nickel-Cobalt alloy frame
Valve architecture Hybrid Honeycomb cell design
Delivery System 14F NavigatorTM Delivery system with MyvalTM prepared and crimped in the cathlab
0.035" Guidewire compatible and Usable catheter length of 120 cm

For Information regarding Size Chart, please click here

www.myval.com

Clinical Data

Study Name Type of Study Total Patients Status Link
Sponsor Initiated Studies
MyVal-1 Study First-in-man 30 Ongoing Know more