Guidewires

VSI Torque Device

by Vascular Solutions, Inc.

A sterile hand-operated device intended to be attached to the proximal end of an invasive device (e.g., a catheter, a needle, or a guidewire) to provide the operator with the ability to manually manipulate and control the directional torque (rotation) of the device to which it is attached. This device may be made of plastic or metal materials. This is a single-use device.

Ask about this device Where to buy Compare similar devices

Find similar guidewires

Where to buy VSI Torque Device

We do not have contact details for Vascular Solutions, Inc. yet. Send a request and we will route it to the right person for your country.

Request this device

Is this your product? Claim Vascular Solutions, Inc. to list your reps and distributors by country and receive buyer requests from your territories.

VSI Torque Device models and sizes

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

Model / catalog no.SizeMRIStatus
8181— Not statedAvailable

FDA clearances

  • 510(k) K100093 April 2010

Procedures that use guidewires

Frequently asked questions

What is VSI Torque Device used for?

A sterile hand-operated device intended to be attached to the proximal end of an invasive device (e.g., a catheter, a needle, or a guidewire) to provide the operator with the ability to manually manipulate and control the directional torque (rotation) of the device to which it is attached. This device may be made of plastic or metal materials. This is a single-use device.

Who makes VSI Torque Device?

VSI Torque Device is made by Vascular Solutions, Inc.. It is listed under guidewires in our device library.

What sizes does VSI Torque Device come in?

The FDA device database does not list sizes for VSI Torque Device. Check the instructions for use or ask a Vascular Solutions, Inc. representative.

Is VSI Torque Device MRI safe?

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

Is VSI Torque Device FDA cleared?

VSI Torque Device is covered by FDA submission K100093.

How do I contact a Vascular Solutions, Inc. sales representative?

Vascular Solutions, Inc. has not listed representatives on LA Vascular yet. Visit the Vascular Solutions, 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.

📬 The IR Device Brief

One email a month: new FDA clearances, recalls and device pages in vascular & interventional radiology.

We'll email you a link to confirm. Unsubscribe any time.

Suggest edits

For manufacturers and their teams. Each field shows what the page says now: add, remove or rewrite anything, and leave the rest as is. LA Vascular reviews every change before it goes live.

About you