Healthcare Professionals

EverFlex Self-expanding Peripheral Stent  

Vascular Stenting

Overview

Choose the EverFlex™ self-expanding peripheral stent system for its combined benefits of durability and deployment accuracy — all in a broad range of sizes. Treat lesions in either the SFA, proximal popliteal, or common and/or external iliac arteries with confidence, knowing that the DURABILITY trial series demonstrated safety and efficacy of the EverFlex stent in complex patient populations.


U.S. Indications

The EverFlex Self-Expanding Peripheral Stent System is intended to improve luminal diameter in the treatment of symptamotic de novo or restenotic lesions up to 180 mm in length in the native superficial femoral artery and/or proximal popliteal arteries with reference vessel diameters ranging from 4.5 mm – 7.5 mm.

The EverFlex Self-Expanding Peripheral Stent System is indicated for improving luminal diameter in patients with atherosclerotic disease of the common and/or external iliac arteries up to and including 100 mm in length, with a reference vessel diameter of 4.5 mm - 7.5 mm.


Product Details

The EverFlex self-expanding peripheral stent is deliverable through a 6 F catheter. Its broad size matrix (20 mm – 200 mm) allows physicians to choose the most appropriate single-stent fit.

Pin-Pull Delivery System

EverFlex system

The stent is mounted on a traditional "pin-pull" style delivery system.

Design of EverFlex Self-expanding Peripheral Stent

Design of EverFlex Self-expanding Peripheral Stent

  1. Spiral cell connection pattern enhances flexibility.
  2. Three-wave peak design produces expansion force that resists compression and provides excellent wall apposition.
  3. Peak-to-peak connection nodes help to disperse force uniformly among four struts.
  4. Tantalum markers for enhanced visibility and easier, more precise positioning.
  5. Flexible design improves fracture resistance and restores vessel patency.

MANUALS AND TECHNICAL GUIDES

Instructions for Use
Find this technical manual in the product labeling supplied with each device or by calling technical support for cardiovascular services: (877) 526-7890.


Model Specifications

Catheter Length Stent Size Compatibility
80 cm
Reference Number
120 cm
Reference Number
Diameter
(mm)
Length
(mm)
Recommended
Introducer
Sheath
(F)
Guidewire
(in)
Recommended
Lumen Size
mm)
PRB35-06-020-080 PRB35-06-020-120 6 20 6 0.035 4.5-5.5
PRB35-06-030-080 PRB35-06-030-120 6 30 6 0.035 4.5-5.5
PRB35-06-040-080 PRB35-06-040-120 6 40 6 0.035 4.5-5.5
PRB35-06-060-080 PRB35-06-060-120 6 60 6 0.035 4.5-5.5
PRB35-06-080-080 PRB35-06-080-120 6 80 6 0.035 4.5-5.5
PRB35-06-100-080 PRB35-06-100-120 6 100 6 0.035 4.5-5.5
PRB35-06-120-080 PRB35-06-120-120 6 120 6 0.035 4.5-5.5
PRB35-06-150-080 PRB35-06-150-120 6 150 6 0.035 4.5-5.5
N/A PRB35-06-200-120 6 200 6 0.035 4.5-5.5
PRB35-07-020-080 PRB35-07-020-120 7 20 6 0.035 5.5-6.5
PRB35-07-030-080 PRB35-07-030-120 7 30 6 0.035 5.5-6.5
PRB35-07-040-080 PRB35-07-040-120 7 40 6 0.035 5.5-6.5
PRB35-07-060-080 PRB35-07-060-120 7 60 6 0.035 5.5-6.5
PRB35-07-080-080 PRB35-07-080-120 7 80 6 0.035 5.5-6.5
PRB35-07-100-080 PRB35-07-100-120 7 100 6 0.035 5.5-6.5
PRB35-07-120-080 PRB35-07-120-120 7 120 6 0.035 5.5-6.5
PRB35-07-150-080 PRB35-07-150-120 7 150 6 0.035 5.5-6.5
N/A PRB35-07-200-120 7 200 6 0.035 5.5-6.5
PRB35-08-020-080 PRB35-08-020-120 8 20 6 0.035 6.5-7.5
PRB35-08-030-080 PRB35-08-030-120 8 30 6 0.035 6.5-7.5
PRB35-08-040-080 PRB35-08-040-120 8 40 6 0.035 6.5-7.5
PRB35-08-060-080 PRB35-08-060-120 8 60 6 0.035 6.5-7.5
PRB35-08-080-080 PRB35-08-080-120 8 80 6 0.035 6.5-7.5
PRB35-08-100-080 PRB35-08-100-120 8 100 6 0.035 6.5-7.5
PRB35-08-120-080 PRB35-08-120-120 8 120 6 0.035 6.5-7.5
PRB35-08-150-080 PRB35-08-150-120 8 150 6 0.035 6.5-7.5
N/A PRB35-08-200-120 8 200 6 0.035 6.5-7.5