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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
Contact UsAbre Mechanism of Action Animation Video - (02:20)
Watch the Abre venous stent and delivery system mechanism of action animation.
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The AbreTM Stent System is intended for use in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction.
The ABRE clinical study demonstrates the safety and effectiveness of the AbreTM Venous Stent.1 Learn more about the study and the 24-month results.
Hear it from the expert.
Abre Physician Testimonial Video Simplicity - (01:05)
Listen to a physician talk about the ease of use of the Abre venous stent and delivery system.
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The AbreTM Stent minimizes jumping and foreshortening, landing precisely where you need it.2
Rotating thumbwheel offers predictable placement and auditory feedback.2
Triaxial shaft design controls friction and stabilizes stent.2
Hear it from the expert.
Abre Physician Testimonial Video Durability - (01:19)
Learn about the importance of durability in venous stenting from the words of an experienced physician.
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The nitinol AbreTM 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:
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
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 |
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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.
MAEs included all-cause death, clinically significant pulmonary embolism, post-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.
Site and core lab data were used.
ABRE CSR v1.2 July 30, 2020 and ABRE 24M PASR v1.0.
Test data on file at Medtronic. Report 10558227DOC_Rev A. Bench test results may not be indicative of clinical performance.