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FDA approves Medinol drug-eluting coronary stent

October 24, 2023 By Danielle Kirsh

Medinol-Elunir-PerlMedinol this week announced it received FDA approval for its Elunir-Perl drug-eluting stent (DES) for the treatment of coronary artery disease.

Elunir-Perl is the latest evolution in the company’s Elunir DES product portfolio. It has four radiopaque markers, two at each end of the stent, as well as a hybrid polymer-metal radiopaque catheter tip. The features allow for outstanding visualization during PCI procedures, according to Medinol.

“We are pleased to bring technologies to the U.S. that focus both on benefit to patients as well as unique and meaningful advantages to surgeons, allowing for precise stent placement, shorter procedure times and reduced radiation exposure,” CEO Yoram Richter said in a news release.

The DES will be exclusively available in the U.S. through CoSo Health, a healthcare supply and logistics company.

“We are proud to distribute one of the world’s best drug-eluting stents via our intuitive and easy-to-use SaaS+ platform, which reduces layers in the supply chain,” CoSo Health CEO Jae Lee said.

Filed Under: Drug-Device Combinations, Stents Tagged With: medinol

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About Danielle Kirsh

Danielle Kirsh is an award-winning journalist and senior editor for Medical Design & Outsourcing, MassDevice, and Medical Tubing + Extrusion, and the founder of Women in Medtech and lead editor for Big 100. She received her bachelor's degree in broadcast journalism and mass communication from Norfolk State University and is pursuing her master's in global strategic communications at the University of Florida. You can connect with her on Twitter and LinkedIn, or email her at dkirsh@wtwhmedia.com.

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