Temporary dialysis catheters

Turbo-Flo HD

by Cook Incorporated

A flexible, double-lumen tube intended to be used for short-term (< 30 days) central venous (jugular, subclavian vein) and/or femoral vein access, primarily during haemodialysis, to conduct blood from a patient and returning it after extracorporeal circulation; it may also be used during haemoperfusion and/or apheresis. It is intended for coaxial flow of blood and may be radiopaque; devices dedicated to catheter introduction/function (e.g., introducer needle) may be included. This is a single-use device.

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Where to buy Turbo-Flo HD

Contact Cook Incorporated directly; they can quote, ship, or point you to the distributor for your country.

From cookmedical.com, checked October 2026.

No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.

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Procedures that use temporary dialysis catheters

Frequently asked questions

What is Turbo-Flo HD used for?

A flexible, double-lumen tube intended to be used for short-term (< 30 days) central venous (jugular, subclavian vein) and/or femoral vein access, primarily during haemodialysis, to conduct blood from a patient and returning it after extracorporeal circulation; it may also be used during haemoperfusion and/or apheresis. It is intended for coaxial flow of blood and may be radiopaque; devices dedicated to catheter introduction/function (e.g., introducer needle) may be included. This is a single-use device.

Who makes Turbo-Flo HD?

Turbo-Flo HD is made by Cook Incorporated. It is listed under non-tunneled dialysis catheters (vascath) in our device library.

What sizes does Turbo-Flo HD come in?

The FDA device database does not list sizes for Turbo-Flo HD. Check the instructions for use or ask a Cook Incorporated representative.

Is Turbo-Flo HD MRI safe?

The FDA device database entry for Turbo-Flo HD does not state its MRI safety status. Check the labeling before MRI.

Is Turbo-Flo HD FDA cleared?

Turbo-Flo HD is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Cook Incorporated sales representative?

Cook Incorporated has not listed representatives on LA Vascular yet. Visit the Cook Incorporated 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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