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C. R. Bard Fluency Plus Vascular Stent for Dissection Restenosis after PTA in Peripheral Arteries​​

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C. R. Bard Fluency Plus Vascular Stent for Dissection Restenosis after PTA in Peripheral Arteries​​

C. R. Bard Fluency Plus Vascular Stent for Dissection Restenosis after PTA in Peripheral Arteries​​
C. R. Bard Fluency Plus Vascular Stent for Dissection Restenosis after PTA in Peripheral Arteries​​ C. R. Bard Fluency Plus Vascular Stent for Dissection Restenosis after PTA in Peripheral Arteries​​

Large Image :  C. R. Bard Fluency Plus Vascular Stent for Dissection Restenosis after PTA in Peripheral Arteries​​

Product Details:
Place of Origin: CHINA
Brand Name: C. R. Bard
Certification: ce
Model Number: FVM10100
Payment & Shipping Terms:
Minimum Order Quantity: 1000pcs
Price: Negotiable
Packaging Details: Carton
Delivery Time: 10-15days
Payment Terms: L/C,T/T,Westen Union,Money Gram,Paypal/VTB
Supply Ability: 100000pc/month
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C. R. Bard Fluency Plus Vascular Stent for Dissection Restenosis after PTA in Peripheral Arteries​​

Description
Product Name: C. R. Bard Fluency Plus Vascular Stent Diameter: 12mm
Outer Diameter: 13.5mm Length: 20/30/40/60/80MM
Conveyor Rod: 80/117cm Feature: Disposable
Highlight:

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C. R. Bard Fluency Plus Vascular Stent for Dissection Restenosis after PTA in Peripheral Arteries
The C. R. Bard Fluency Plus Vascular Stent (Model: FVM10100) is a self-expanding endovascular prosthesis designed for the treatment of stenotic or occlusive lesions in the iliac and femoral arteries.
Product Overview
The Fluency Plus Vascular Stent consists of a nitinol stent framework encapsulated between an inner and outer layer of expanded polytetrafluoroethylene (ePTFE), creating a durable, blood-tight lumen. Pre-mounted on a low-profile delivery system for precise deployment during minimally invasive procedures.
Primary Functions
  • Scaffolding: Providing mechanical support to counteract elastic recoil and compression in atherosclerotic arteries.
  • Barrier Function: The ePTFE covering acts as a physical barrier to prevent tissue prolapse and plaque intrusion into the vessel lumen.
  • Sealing: Managing dissections or post-balloon angioplasty flaps by apposing the vessel wall and creating a smooth flow surface.
Key Features and Advantages
  • Advanced Stent Design: Self-expanding nitinol stent with chronic outward force and four radiopaque tantalum markers at each end for precise fluoroscopic visualization.
  • Proven Graft Material: ePTFE covering designed for rapid endothelialization with carbon-coated inner surface for enhanced hemocompatibility.
  • Precise Delivery: Integrated delivery system (80/117 cm lengths) allows controlled deployment in tortuous anatomy.
  • Comprehensive Size Range: Available in diameters of 12 mm and 13.5 mm, with lengths from 20 mm to 80 mm.
  • Clinical Versatility: Addresses flow-limiting dissections, restenosis, and vessel obstruction following angioplasty or atherectomy.
Indications for Use
The stent is indicated for use in the iliac and femoral arteries for:
  • Treatment of residual stenosis after balloon angioplasty (particularly in Fontaine Stage III/IV patients)
  • Management of arterial dissections
  • Addressing plaque disruption or lumen compromise post-angioplasty
  • Treatment of stenosis or re-occlusion, including after thrombolysis or thrombectomy
  • Treatment of in-stent restenosis or re-occlusion
Application Scenarios
  • Peripheral Artery Disease (PAD): Revascularization of iliac and femoral arteries in patients with claudication or critical limb ischemia.
  • Post-Angioplasty Complications: As a bail-out device for suboptimal results from plain balloon angioplasty.
  • Complex Lesions: Used in calcified, tortuous, or recurrent lesions where a covered stent offers superior patency.
Clinical Value
The Bard Fluency Plus Stent provides a critical solution for maintaining long-term vessel patency in challenging peripheral lesions. Its covered design is particularly beneficial in preventing restenosis caused by neointimal hyperplasia and in managing complications that bare-metal stents cannot effectively address. The combination of flexibility, radial strength, and biocompatible barrier supports positive patient outcomes in complex endovascular interventions.

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