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Coronary stent Nano+™

Coronary stent Nano+™

Coronary stent Nano+™

Product catalog summary
Product Overview
The document provides detailed information about the Nano+™ Polymer-Free Sirolimus-Eluting Coronary Stent System, highlighting its features, benefits, technical specifications, and efficacy.

Features
  • Polymer-free drug-eluting stent (DES) with a nanoporous drug carrier on the abluminal surface.
  • Balanced strut thickness and high radial force for optimal performance.
  • Innovative design with sine wave + 3-3-3 link and double helix structure.
  • Large open cell design with precise positioning markers.
  • Effective drug delivery using Sirolimus and vacuum drug coating technology for a 90-day release period.

Benefits
  • Significantly reduces dual antiplatelet therapy (DAPT) time.
  • Promotes earlier and better endothelialization, reducing thrombosis risk.
  • Offers great deliverability, easy positioning, and placement.
  • Provides optimal tissue scaffolding and excellent side branch access.

Technical Specifications
  • Stent material: 316L Stainless Steel with nanoporous drug carrier.
  • Strut thickness: 91 microns, Metal-artery ratio: 15%.
  • Recoil ratio: < 2%, Shorting ratio: < 1%.
  • Lowest crossing profile: 0.035" (0.90mm), Balloon tip profile: 0.017".
  • Available in diameters ranging from 2.5 to 4.0 mm and lengths from 12 to 36 mm.

Efficacy and Safety
  • Animal studies show effective DES efficacy and BMS safety.
  • OCT study in Europe indicates no binary restenosis and no stent thrombosis at 24 months.

Contact Information
Lepu Medical Technology (Beijing) Co., Ltd, 37 Chaoqian Road, Changping District, Beijing, China 102200. Tel: +86 10 80120666, Email: [email protected], Web: en.lepumedical.com
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Catalog excerpts

Coronary stent Nano+™-1

Nano+™ Polymer-Free Sirolimus-Eluting Coronary Stent System Product Information Nothing Beats Free New Delivery System 0.017" soft tapered tip Short and round shoulder Hydrosurf ™ hydrophilic coating • olymer-free DES P • anoporous drug carrier on N abluminal surface • Balanced strut thickness • igh radial force H • ine wave + 3-3-3 link S • ouble helix structure D • arge open cell L • recise positioning markers P • Effective drug of Sirolimus • acuum drug coating technology V • 0-day drug releasing period 9 • ew delivery system N Vacuum Drug Coating Technology Ensure complete drug dosage and coating stability Nanoporous Drug Carrier on Abluminal Surface Nanoporous After Drug Loaded Ave. Pore Diameter: 400nm Ave. Pore Depth: 150nm • Significantly shorten DAPT time • Earlier & better endothelialization • Highly reduced risk of thrombosis • Great deliverability • Easy positioning and placement • Optimal tissue scaffolding • Excellent side branch access • Scientific drug releasing period Smaller cavity has stronger adhesion of drug Ranges Normal Drug Coating Technology • Ø 2.5 - 4.0 mm • 12 - 36 mm multi stent lengths Lumen Loss of Nano+ TM Lumen Loss of Durable Polymer SES Inflammation of Durable Polymer SES 1 Month Animal Experiment Result: HE Staining of Nano+ TM Sten

 Open the catalog to page 1
Coronary stent Nano+™-2

Nano+™ OCT Study [3] An OCT Study in Europe Shows Nano+™ A Great Combination of DES Efficacy and BMS Safety No binary restenosis in-stent and in-segment at 6 months No malapposed struts at 6 months Covered struts at 6 months No definite, probable or possible stent thrombosis at 24 months Technical Parameters Stent Material Strut Design Strut Thickness Metal-artery Ratio Recoil Ratio Shorting Ratio Lowest Crossing Profile Balloon Tip Profile Delivery System 316L Stainless Steel Nanoporous drug carrier on abluminal surface 91 15% < 2% < 1% 0.035" (0.90mm) 0.017" RX [3] Suwannasom, P., et al. "Evaluation...

 Open the catalog to page 2

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