Guidewires
Cruiser-18
by Biotronik AG
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.
Cruiser-18 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 |
|---|---|---|---|
| Medium 195cm | — | Not stated | Available |
| Medium 300cm | — | Not stated | Available |
| Stiff 195cm | — | Not stated | Available |
| Stiff 300cm | — | Not stated | Available |
Procedures that use guidewires
Frequently asked questions
What is Cruiser-18 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 Cruiser-18?
Cruiser-18 is made by Biotronik AG. It is listed under guidewires in our device library.
What sizes does Cruiser-18 come in?
The FDA device database does not list sizes for Cruiser-18. Check the instructions for use or ask a Biotronik AG representative.
Is Cruiser-18 MRI safe?
The FDA device database entry for Cruiser-18 does not state its MRI safety status. Check the labeling before MRI.
Is Cruiser-18 FDA cleared?
Cruiser-18 is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Biotronik AG sales representative?
Biotronik AG has not listed representatives on LA Vascular yet. Visit the Biotronik AG 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.