Venous stents
Zilver Vena
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.
Zilver Vena 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 |
|---|---|---|---|
| G57428 | — | MR Conditional | Available |
| G57429 | — | MR Conditional | Available |
| G57430 | — | MR Conditional | Available |
| G57431 | — | MR Conditional | Available |
| G57432 | — | MR Conditional | Available |
| G57433 | — | MR Conditional | Available |
| G57434 | — | MR Conditional | Available |
| G57435 | — | MR Conditional | Available |
| G57436 | — | MR Conditional | Available |
| G57437 | — | MR Conditional | Available |
| G57438 | — | MR Conditional | Available |
| G57439 | — | MR Conditional | Available |
| G57440 | — | MR Conditional | Available |
| G57441 | — | MR Conditional | Available |
| G57442 | — | MR Conditional | Available |
| G57443 | — | MR Conditional | Available |
| G57444 | — | MR Conditional | Available |
| G57445 | — | MR Conditional | Available |
| G57446 | — | MR Conditional | Available |
| G57447 | — | MR Conditional | Available |
| G57448 | — | MR Conditional | Available |
| G57449 | — | MR Conditional | Available |
| G57450 | — | MR Conditional | Available |
| G57451 | — | MR Conditional | Available |
| G57452 | — | MR Conditional | Available |
| G57453 | — | MR Conditional | Available |
| G57454 | — | MR Conditional | Available |
| G57455 | — | MR Conditional | Available |
Procedures that use venous stents
Frequently asked questions
What is Zilver Vena 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 Zilver Vena?
Zilver Vena is made by Cook Ireland Ltd. It is listed under venous stents in our device library.
What sizes does Zilver Vena come in?
The FDA device database does not list sizes for Zilver Vena. Check the instructions for use or ask a Cook Ireland Ltd representative.
Is Zilver Vena MRI safe?
The FDA device database lists Zilver Vena as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Zilver Vena FDA cleared?
Zilver Vena is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Cook Ireland Ltd sales representative?
Cook Ireland Ltd has not listed representatives on LA Vascular yet. Visit the Cook Ireland Ltd 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.