Bioresorbability

   

Bioresorbability

   

FANTOM® Encore Tyrocore Bioresorbable Scaffold - The Most Advanced Bioresorbable Scaffold for PCI Therapy

FANTOM® Encore Tyrocore Bioresorbable Scaffold

The Most Advanced Bioresorbable Scaffold for PCI Therapy

FANTOM® Encore Tyrocore Bioresorbable Scaffold is a drug-eluting bioresorbable vascular scaffold developed as an alternative to metallic stents for the treatment of coronary artery disease. It is made from Tyrocore, Reva’s proprietary polymer designed specifically for vascular scaffolds. Tyrocore is the First Polymer Invented for BRS, it was Invented in Collaboration between REVA Medical & Rutgers University

After restoration of blood flow, scaffolds support the artery through the healing process and then disappear (or “resorb”) from the body over a period of time. This resorption is intended to allow the return of natural movement and function of the artery.

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MOTIV® Tyrocore Bioresorbable Scaffold - The only BRS Approved for BTK Therapy

MOTIV® Tyrocore Bioresorbable Scaffold

The only BRS Approved for BTK Therapy

Motiv® is a sirolimus – Eluting Bioresorbable Vascular Scaffold System.

It Is the First & Only BRS Approved for Below-the-Knee (BTK) Revascularization Therapy and is made from Tyrocore, Reva’s proprietary polymer designed specifically for vascular scaffolds. Tyrocore is the First Polymer Invented for BRS, it was Invented in Collaboration between REVA Medical & Rutgers University

  • Tyrocore is derived from the naturally occurring tyrosine amino acid

  • Low inflammation, irritation, during degradation
  • No formation of calcification during degradation
  • Tyrocore enables MOTIV® to be the World’s Thinnest BRS
  • Tyrocore is inherently radiopaque, making Motiv® visible under x-ray to ensure accurate placement in the artery.

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A NEW CLASS IN PERCUTANEOUS CLOSURE SYSTEM - Designed specifically for large arteriotomies

A NEW CLASS IN PERCUTANEOUS CLOSURE SYSTEM
Designed specifically for large arteriotomies

PerQseal®️ is a percutaneous closure system, delivered over-the-wire, at the end of the primary procedure, and positioned at the arteriotomy site, using visual and tactile position indicators. Once hemostasis has been confirmed, the wire is removed and the device is deployed.

The PerQseal®️ closure device shall be indicated:

  • For the percutaneous sealing of a common femoral arteriotomy in patients following endovascular procedure
  • For closing arteriostomies created with sheath sizes 12-20 F
  • Large holes up to 24F arteriostomies

CLINICAL DATA
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CLINICAL DATA
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