Guidewires

Transend

by Boston Scientific Corporation

A long, thin wire intended to be percutaneously placed into the peripheral vasculature (not heart or central nervous system) to function as a guide for the introduction of devices (e.g., catheters). It is made of metal (e.g., stainless steel, Nitinol), with or without coating, and is available in a variety of distal tip designs. It is intended to be used for percutaneous angiography, angioplasty, rotational atherectomy and thrombectomy, drainage, and other diagnostic and interventional procedures. It may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.

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Transend models and sizes

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

Model / catalog no.SizeMRIStatus
M001468010— Not statedAvailable
M001468100— Not statedAvailable
M001468110— Not statedAvailable
M001468120— Not statedAvailable
M001468130— Not statedAvailable
M003468020— Not statedAvailable

Procedures that use guidewires

Frequently asked questions

What is Transend used for?

A long, thin wire intended to be percutaneously placed into the peripheral vasculature (not heart or central nervous system) to function as a guide for the introduction of devices (e.g., catheters). It is made of metal (e.g., stainless steel, Nitinol), with or without coating, and is available in a variety of distal tip designs. It is intended to be used for percutaneous angiography, angioplasty, rotational atherectomy and thrombectomy, drainage, and other diagnostic and interventional procedures. It may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.

Who makes Transend?

Transend is made by Boston Scientific Corporation. It is listed under guidewires in our device library.

What sizes does Transend come in?

The FDA device database does not list sizes for Transend. Check the instructions for use or ask a Boston Scientific Corporation representative.

Is Transend MRI safe?

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

Is Transend FDA cleared?

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

How do I contact a Boston Scientific Corporation sales representative?

Boston Scientific Corporation has not listed representatives on LA Vascular yet. Visit the Boston Scientific Corporation 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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