Guidewires
Regalia XS 1.0
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.
Regalia XS 1.0 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 |
|---|---|---|---|
| PAGP140000 | Length 180 cm; Outer Diameter 0.014 in | Not stated | Available |
| PAGP140300 | Length 300 cm; Outer Diameter 0.014 in | Not stated | Available |
Procedures that use guidewires
Frequently asked questions
What is Regalia XS 1.0 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 Regalia XS 1.0?
Regalia XS 1.0 is made by Asahi Intecc Co., Ltd.. It is listed under guidewires in our device library.
What sizes does Regalia XS 1.0 come in?
Sizes listed for Regalia XS 1.0: Length: 180–300 cm; Outer Diameter: 0.01 in. Confirm availability with the manufacturer's instructions for use.
Is Regalia XS 1.0 MRI safe?
The FDA device database entry for Regalia XS 1.0 does not state its MRI safety status. Check the labeling before MRI.
Is Regalia XS 1.0 FDA cleared?
Regalia XS 1.0 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.