Abre Venous Self-expanding Stent System

The Abre™ venous self-expanding stent system is designed for the unique challenges of venous disease. It offers easy deployment, to let physicians focus on their patient, and delivers demonstrated endurance, to give patients freedom of movement.1,2

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Overview

Simplicity  For You. Durability  For Them.

Indications

The Abre stent system is intended for use in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction. 

CLINICAL EVIDENCE

The ABRE clinical study demonstrates the safety and effectiveness of the Abre venous stent.1 Learn more about the study and the 12-months results.

88% Primary patency
at 12 months*

98.6% NIVL 87.1% aDVT 79.8% PTS Primary patency by patient population

98% Freedom from MAEs at 30 days

Product Details

Simplicity  For You1,2

Easy Deployment, to Let You Focus on Your Patient1,2

The Abre stent minimizes jumping and foreshortening, landing precisely where you need it.2

Rotating thumbwheel offers predictable placement and auditory feedback.2

Abre stent and delivery system and zoom on handle with rotating thumbwheel

Triaxial shaft design controls friction and stabilizes stent.2

  1. Isolation sheath
  2. Hemostatic valve
  3. Introducer sheath
  4. Retractable sheath
  5. Inner shaft
Triaxial shaft design of Abre delivery system

Durability For Them1,2

Demonstrated Endurance, to Give Your Patients Freedom of Movement1,2

Animation showing Abre stent bending and rotating

The nitinol Abre stent maintains lumen integrity and flow in diverse patients and anatomies.1  

It ensures radial strength and crush resistance, without compromising flexibility.2  

Unique technology:

  • Open-cell design with three offset connection points.
  • Struts customized to each size.

Consistent behavior across a broad range of diameters and lengths.2

Bench evidence shows long-term durability.2

Clinical evidence shows real-world dependability, even in challenging cases.1

0% fracture rate at 50 years in bench testing2

0% fracture rate in clinical trial with 44% of stents extending
below inguinal
ligament into 
the CFV1

0% migration rate  in clinical trial1

  

Model Specifications

Product Code Guide

Abre stent in different sizes and its ordering code components
 

Stent Lengths and Product Numbers

Stent Diameters

40 mm

60 mm

80 mm

100 mm

120 mm

150 mm

10 mm

AB9U10040090

AB9U10060090

AB9U10080090

AB9U10100090

AB9U10120090

AB9U10150090

12 mm

AB9U12060090

AB9U12080090

AB9U12100090

AB9U12120090

AB9U12150090

14 mm

AB9U14060090

AB9U14080090

AB9U14100090

AB9U14120090

AB9U14150090

16 mm

AB9U16060090

AB9U16080090

AB9U16100090

AB9U16120090

AB9U16150090

18 mm

AB9U18060090

AB9U18080090

AB9U18100090

AB9U18120090

AB9U18150090

20 mm

AB9U20060090

AB9U20080090

AB9U20100090

AB9U20120090

AB9U20150090

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Review Clinical Evidence

Clinical Evidence
*

Primary Patency was defined as meeting all of the following criteria at 12 months post-procedure: Freedom from occlusion or restenosis ≥ 50% of the stented segment of the target lesion and freedom from clinically driven target lesion revascularization. 

MAEs included all-cause death, clinically significant pulmonary embolism, procedural major bleeding complication, stent thrombosis, and stent migration. MAEs were adjudicated by a Clinical Events Committee, except stent thrombosis and stent migration, which were assessed by an imaging core laboratory. 

References

1

ABRE CSR v1.2 30/JUL/2020. 

2

Test data on file at Medtronic. Bench test results may not be indicative of clinical performance.