Guidewires
CROSSLEAD Pro 018
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.
CROSSLEAD Pro 018 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 |
|---|---|---|---|
| CPR01810P | Outer Diameter 0.018 in; Length 100 cm | Not stated | Available |
| CPR01810S | Outer Diameter 0.018 in; Length 100 cm | Not stated | Available |
| CPR01820P | Length 200 cm; Outer Diameter 0.018 in | Not stated | Available |
| CPR01820S | Length 200 cm; Outer Diameter 0.018 in | Not stated | Available |
| CPR01823P | Outer Diameter 0.018 in; Length 235 cm | Not stated | Available |
| CPR01823S | Length 235 cm; Outer Diameter 0.018 in | Not stated | Available |
| CPR01830P | Outer Diameter 0.018 in; Length 300 cm | Not stated | Available |
| CPR01830S | Length 300 cm; Outer Diameter 0.018 in | Not stated | Available |
Procedures that use guidewires
Frequently asked questions
What is CROSSLEAD Pro 018 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 CROSSLEAD Pro 018?
CROSSLEAD Pro 018 is made by Asahi Intecc Co., Ltd.. It is listed under guidewires in our device library.
What sizes does CROSSLEAD Pro 018 come in?
Sizes listed for CROSSLEAD Pro 018: Length: 100–300 cm; Outer Diameter: 0.02 in. Confirm availability with the manufacturer's instructions for use.
Is CROSSLEAD Pro 018 MRI safe?
The FDA device database entry for CROSSLEAD Pro 018 does not state its MRI safety status. Check the labeling before MRI.
Is CROSSLEAD Pro 018 FDA cleared?
CROSSLEAD Pro 018 is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Asahi Intecc Co., Ltd. sales representative?
Asahi Intecc Co., Ltd. has not listed representatives on LA Vascular yet. Visit the Asahi Intecc Co., Ltd. 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.