Guidewires

ClosureFast Guidewire

by Argon Medical Devices, Inc.

A long, thin, sterile wire intended to be percutaneously placed into the cardiac vasculature (ventricles or coronary vessels) to function as a guide for the introduction, positioning, and/or operation of a device (e.g., catheter, pacing lead); it may also be used in the peripheral vasculature. It may be made of metal (e.g., stainless steel, Nitinol), or polymer and/or glass materials to provide MRI-compatibility, with or without coating, and is available in a variety of distal tip designs. It is used for various diagnostic and interventional procedures, and may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.

Contact a rep Compare similar devices

ClosureFast Guidewire models and sizes

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

Model / catalog no.SizeMRIStatus
GW-018-45-SS— Not statedAvailable
GW-025-150-DE1.5J— Not statedAvailable
GW-025-260-1.5J— Not statedAvailable
GW-035-45— Not statedAvailable

Procedures that use guidewires

Frequently asked questions

What is ClosureFast Guidewire used for?

A long, thin, sterile wire intended to be percutaneously placed into the cardiac vasculature (ventricles or coronary vessels) to function as a guide for the introduction, positioning, and/or operation of a device (e.g., catheter, pacing lead); it may also be used in the peripheral vasculature. It may be made of metal (e.g., stainless steel, Nitinol), or polymer and/or glass materials to provide MRI-compatibility, with or without coating, and is available in a variety of distal tip designs. It is used for various diagnostic and interventional procedures, and may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.

Who makes ClosureFast Guidewire?

ClosureFast Guidewire is made by Argon Medical Devices, Inc.. It is listed under guidewires in our device library.

What sizes does ClosureFast Guidewire come in?

The FDA device database does not list sizes for ClosureFast Guidewire. Check the instructions for use or ask a Argon Medical Devices, Inc. representative.

Is ClosureFast Guidewire MRI safe?

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

Is ClosureFast Guidewire FDA cleared?

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

How do I contact a Argon Medical Devices, Inc. sales representative?

Argon Medical Devices, Inc. has not listed representatives on LA Vascular yet. Visit the Argon Medical Devices, 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