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Cordis (manufactured by Tryton Medical)

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Stents / Coronary Side Branch Stents

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Company Name Product Name Material Catheter System Strut Wall Thickness Maximum Guidewire Size (inch) Recommended Guide Catheter Stent Diameter (mm) Stent Length (mm) Delivery System Length (cm) US FDA Indicated Use
Cordis (manufactured by Tryton Medical) Tryton Side Branch Stent Cobalt chromium (balloon-expandable stent) Rapid exchange (Rx) 85 μm 0.014 6 F (0.068-inch minimum ID, kissing-balloon technique) 2.5–2.5, 2.5–3, 2.5–3.5, 3–3.5, 3.5–4 (side branch–main branch) 19 (2.5-mm side branch), 15 (3–3.5-mm side branch) 140 Indicated for improving the side branch luminal diameter of de novo native coronary artery bifurcation lesions (Medina classification 1.1.1; 0.1.1; 1.0.1) with a side branch diameter stenosis of ≥ 50% and a lesion length ≤ 5 mm, along with reference vessel diameters ≥ 2.5 to ≤ 3.5 mm in the side branch and ≥ 2.5 to ≤ 4 mm in the main branch; intended for use in conjunction with commercially available balloon-expandable drug-eluting coronary stents in the main branch

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CTO DES Hypertension Imaging Modalities PCI Pharmacology PE Radial Regulatory Structural Disease Valvular Interventions
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Cardiac Interventions Today (ISSN 2572-5955 print and ISSN 2572-5963 online) is a publication dedicated to providing coverage of the latest developments in technology, techniques, clinical studies, and regulatory and reimbursement issues in the field of coronary and cardiac interventions.



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