Venous stents
Abre
A non-bioabsorbable, tubular device made of metal intended to be implanted in a peripheral (typically the iliac and/or femoral) vein to maintain patency in patients with constrained venous outflow; it is not intended for coronary or intracranial venous stenting. It is inserted and advanced to the site of implantation with a dedicated catheter where it self-expands upon release. It is typically made of nickel-titanium alloy (Nitinol) and has radiopaque marker(s) for visualization; it is available in a variety of diameters and lengths. Disposable devices associated with implantation may be included.
FDA clearances
- PMA P200026 November 2021
Procedures that use venous stents
Frequently asked questions
What is Abre used for?
A non-bioabsorbable, tubular device made of metal intended to be implanted in a peripheral (typically the iliac and/or femoral) vein to maintain patency in patients with constrained venous outflow; it is not intended for coronary or intracranial venous stenting. It is inserted and advanced to the site of implantation with a dedicated catheter where it self-expands upon release. It is typically made of nickel-titanium alloy (Nitinol) and has radiopaque marker(s) for visualization; it is available in a variety of diameters and lengths. Disposable devices associated with implantation may be included.
Who makes Abre?
Abre is made by Medtronic, Inc.. It is listed under venous stents in our device library.
What sizes does Abre come in?
Sizes listed for Abre: Stent Length: 40–150 mm. Confirm availability with the manufacturer's instructions for use.
Is Abre MRI safe?
The FDA device database lists Abre as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Abre FDA cleared?
Abre is covered by FDA submission P200026.
How do I contact a Medtronic, Inc. sales representative?
Medtronic, Inc. has not listed representatives on LA Vascular yet. Visit the Medtronic, Inc. company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.