Venous stents
Duo Hybrid Venous Stent System
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.
Duo Hybrid Venous Stent System models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| N1101410009120 | Length 120 cm | MR Conditional | Available |
| N1101412009120 | Length 120 cm | MR Conditional | Available |
| N1101414009120 | Length 120 cm | MR Conditional | Available |
| N1101416009120 | Length 120 cm | MR Conditional | Available |
| N1101610010120 | Length 120 cm | MR Conditional | Available |
| N1101612010120 | Length 120 cm | MR Conditional | Available |
| N1101614010120 | Length 120 cm | MR Conditional | Available |
| N1101616010120 | Length 120 cm | MR Conditional | Available |
| N1101812010120 | Length 120 cm | MR Conditional | Available |
Procedures that use venous stents
Frequently asked questions
What is Duo Hybrid Venous Stent System 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 Duo Hybrid Venous Stent System?
Duo Hybrid Venous Stent System is made by Vesper Medical, Inc.. It is listed under venous stents in our device library.
What sizes does Duo Hybrid Venous Stent System come in?
Sizes listed for Duo Hybrid Venous Stent System: Length: 120 cm. Confirm availability with the manufacturer's instructions for use.
Is Duo Hybrid Venous Stent System MRI safe?
The FDA device database lists Duo Hybrid Venous Stent System as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Duo Hybrid Venous Stent System FDA cleared?
Duo Hybrid Venous Stent System is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Vesper Medical, Inc. sales representative?
Vesper Medical, Inc. has not listed representatives on LA Vascular yet. Visit the Vesper Medical, 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.