Guidewires
VASSALLO GT 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 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 |
|---|---|---|---|
| VGT14190HYB | Length 190 cm; Outer Diameter 0.014 in | Not stated | Available |
| VGT14300HYB | Length 300 cm; Outer Diameter 0.014 in | Not stated | Available |
FDA clearances
- 510(k) K203529 May 2021
Procedures that use guidewires
Frequently asked questions
What is VASSALLO GT 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 Hybrid?
VASSALLO GT Hybrid is made by Filmec K.k.. It is listed under guidewires in our device library.
What sizes does VASSALLO GT Hybrid come in?
Sizes listed for VASSALLO GT Hybrid: Length: 190–300 cm; Outer Diameter: 0.01 in. Confirm availability with the manufacturer's instructions for use.
Is VASSALLO GT Hybrid MRI safe?
The FDA device database entry for VASSALLO GT Hybrid does not state its MRI safety status. Check the labeling before MRI.
Is VASSALLO GT Hybrid FDA cleared?
VASSALLO GT Hybrid is covered by FDA submission K203529.
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.