Guidewires
VASSALLO GT 018 Hybrid
by Filmec K.k.
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.
VASSALLO GT 018 Hybrid 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 |
|---|---|---|---|
| VGT18190HYB | Length 190 cm; Outer Diameter 0.018 in | Not stated | Available |
| VGT18300HYB | Length 300 cm; Outer Diameter 0.018 in | Not stated | Available |
FDA clearances
- 510(k) K223432 March 2023
Procedures that use guidewires
Frequently asked questions
What is VASSALLO GT 018 Hybrid 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 VASSALLO GT 018 Hybrid?
VASSALLO GT 018 Hybrid is made by Filmec K.k.. It is listed under guidewires in our device library.
What sizes does VASSALLO GT 018 Hybrid come in?
Sizes listed for VASSALLO GT 018 Hybrid: Length: 190–300 cm; Outer Diameter: 0.02 in. Confirm availability with the manufacturer's instructions for use.
Is VASSALLO GT 018 Hybrid MRI safe?
The FDA device database entry for VASSALLO GT 018 Hybrid does not state its MRI safety status. Check the labeling before MRI.
Is VASSALLO GT 018 Hybrid FDA cleared?
VASSALLO GT 018 Hybrid is covered by FDA submission K223432.
How do I contact a Filmec K.k. sales representative?
Filmec K.k. has not listed representatives on LA Vascular yet. Visit the Filmec K.k. 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.