Guidewires
Peripheral Guidewire
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.
Peripheral Guidewire models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| OEM BTK GW #1, 4G 195-014 | β | Not stated | Available |
| OEM BTK GW #1, 4G 195-018 | β | Not stated | Available |
| OEM BTK GW #1, 4G 300-014 | β | Not stated | Available |
| OEM BTK GW #1, 4G 300-018 | β | Not stated | Available |
| OEM BTK GW #2, 12G 195-014 | β | Not stated | Available |
| OEM BTK GW #2, 12G 195-018 | β | Not stated | Available |
| OEM BTK GW #2, 12G 300-014 | β | Not stated | Available |
| OEM BTK GW #2, 12G 300-018 | β | Not stated | Available |
| OEM BTK GW #3, 30G 195-014 | β | Not stated | Available |
| OEM BTK GW #3, 30G 195-018 | β | Not stated | Available |
| OEM BTK GW #3, 30G 300-014 | β | Not stated | Available |
| OEM BTK GW #3, 30G 300-018 | β | Not stated | Available |
| OEM BTK GW #4, 6G 195-014 | β | Not stated | Available |
| OEM BTK GW #4, 6G 195-018 | β | Not stated | Available |
| OEM BTK GW #4, 6G 300-014 | β | Not stated | Available |
| OEM BTK GW #4, 6G 300-018 | β | Not stated | Available |
Procedures that use guidewires
Frequently asked questions
What is Peripheral Guidewire 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 Peripheral Guidewire?
Peripheral Guidewire is made by Brivant Limited. It is listed under guidewires in our device library.
What sizes does Peripheral Guidewire come in?
The FDA device database does not list sizes for Peripheral Guidewire. Check the instructions for use or ask a Brivant Limited representative.
Is Peripheral Guidewire MRI safe?
The FDA device database entry for Peripheral Guidewire does not state its MRI safety status. Check the labeling before MRI.
Is Peripheral Guidewire FDA cleared?
Peripheral Guidewire is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Brivant Limited sales representative?
Brivant Limited has not listed representatives on LA Vascular yet. Visit the Brivant Limited 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.