IVC filters

Vena Tech

by B Braun Interventional Systems, Inc

A permanently implanted vascular device intended to be percutaneously placed in the inferior vena cava (IVC) to prevent pulmonary embolism (PE). The device achieves its unconstrained diameter upon deployment in the IVC and imparts an outward radial force on the luminal surface of the vena cava to ensure proper positioning and stability. It is designed for blood clot capture while maintaining caval patency. It is made of metal alloys [e.g., stainless steel, titanium (Ti), nickel-titanium alloy (Nitinol)] and is available in various self-expanding, wire designs (e.g., conical, basket).

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Vena Tech models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
4439985Catheter Gauge 9 Fr Not statedAvailable
5010024Catheter Gauge 9 Fr MR ConditionalAvailable
5010028Catheter Gauge 12.90 Fr MR ConditionalAvailable

FDA clearances

Procedures that use ivc filters

Frequently asked questions

What is Vena Tech used for?

A permanently implanted vascular device intended to be percutaneously placed in the inferior vena cava (IVC) to prevent pulmonary embolism (PE). The device achieves its unconstrained diameter upon deployment in the IVC and imparts an outward radial force on the luminal surface of the vena cava to ensure proper positioning and stability. It is designed for blood clot capture while maintaining caval patency. It is made of metal alloys [e.g., stainless steel, titanium (Ti), nickel-titanium alloy (Nitinol)] and is available in various self-expanding, wire designs (e.g., conical, basket).

Who makes Vena Tech?

Vena Tech is made by B Braun Interventional Systems, Inc. It is listed under ivc filters in our device library.

What sizes does Vena Tech come in?

Sizes listed for Vena Tech: Catheter Gauge: 9–12.9 Fr. Confirm availability with the manufacturer's instructions for use.

Is Vena Tech MRI safe?

The FDA device database entry for Vena Tech does not state its MRI safety status. Check the labeling before MRI.

Is Vena Tech FDA cleared?

Vena Tech is covered by FDA submissions K063217, K152765.

How do I contact a B Braun Interventional Systems, Inc sales representative?

B Braun Interventional Systems, Inc has not listed representatives on LA Vascular yet. Visit the B Braun Interventional Systems, 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.

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