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Alert Indications, Safety, and Warnings

Abre™ Venous Self-expanding Stent System for symptomatic venous outflow obstruction

  

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Abre stent and delivery system on white background
Alert Indications, Safety, and Warnings

Overview

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

 

Simplicity for you.
Durability for them.

Watch the Abre™ Stent mechanism of action.

Indications

The Abre™ Stent System is intended for use in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction.

Clinical evidence

Clinically meaningful impact on quality of life through 36 months — in even the most complex patients.

36-month primary patency*1:

  • 81.6% overall
  • 97.1% NIVL
  • 76.5% aDVT
  • 70.4% PTS
View full evidence

Product details



Simplicity for you.1,2

Hear it from the expert.

Easy deployment to let you focus on your patient.1,2

The AbreTM 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
Abre system triaxial shaft design zoomed illustration with numbered callouts



Durability for them.1,2

Hear it from the expert.

Demonstrated endurance to give your patients freedom of movement.1,2

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 in 50 years in bench testing1
  • 0% fracture rate in clinical trial with 44% of stents extending below inguinal ligament into the CFV†1
  • 0% migration rate in clinical trial1

Model specifications



Product code guide

Abre stent in different sizes and its ordering code components

 Stent diameters

Stent lengths and product numbers 

 

40 mm

60 mm

80 mm

100 mm 

120 mm

150 mm 

10 mm

AB9G10040090

AB9G10060090

AB9G10080090

AB9G10100090

AB9G10120090

AB9G10150090

12 mm

—

AB9G12060090

AB9G12080090

AB9G12100090

AB9G12120090

AB9G12150090

14 mm

—

AB9G14060090

AB9G14080090

AB9G14100090

AB9G14120090

AB9G14150090

16 mm

—

AB9G16060090

AB9G16080090

AB9G16100090

AB9G16120090

AB9G16150090

18 mm

—

AB9G18060090

AB9G18080090

AB9G18100090

AB9G18120090

AB9G18150090

20 mm

—

AB9G20060090

AB9G20080090

AB9G20100090

AB9G20120090

AB9G20150090

Additional resources

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Review
clinical
evidence

Clinical evidence
*

Primary patency was defined as meeting all of the following: freedom from occlusion or restenosis ≥ 50% of the stented segment of the target lesion and freedom from clinically driven target lesion revascularization.

†

Site and core lab data were used.

References

1

AbreTM Stent Instructions for Use.

2

Test data on file at Medtronic. Report 10558227DOC_Rev A. Bench test results may not be indicative of clinical performance.