IVC filters

Gunther Tulip

by William Cook Europe ApS

A vascular device intended to be percutaneously implanted in the inferior vena cava (IVC) to prevent pulmonary embolism (PE); it can be retrieved before a threshold period or remain as a permanent implant after the period. It 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 designs (e.g., conical, basket). This is a single-use device.

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Gunther Tulip models and sizes

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

Model / catalog no.SizeMRIStatus
G03766— MR ConditionalAvailable
G52916— MR ConditionalAvailable
G52917— MR ConditionalAvailable
G52918— MR ConditionalAvailable

Procedures that use ivc filters

Frequently asked questions

What is Gunther Tulip used for?

A vascular device intended to be percutaneously implanted in the inferior vena cava (IVC) to prevent pulmonary embolism (PE); it can be retrieved before a threshold period or remain as a permanent implant after the period. It 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 designs (e.g., conical, basket). This is a single-use device.

Who makes Gunther Tulip?

Gunther Tulip is made by William Cook Europe ApS. It is listed under ivc filters in our device library.

What sizes does Gunther Tulip come in?

The FDA device database does not list sizes for Gunther Tulip. Check the instructions for use or ask a William Cook Europe ApS representative.

Is Gunther Tulip MRI safe?

The FDA device database lists Gunther Tulip as MR Conditional. Always follow the specific MRI conditions in the labeling.

Is Gunther Tulip FDA cleared?

Gunther Tulip is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a William Cook Europe ApS sales representative?

William Cook Europe ApS has not listed representatives on LA Vascular yet. Visit the William Cook Europe ApS 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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