Guidewires

VASSALLO GT Crossing30

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.

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VASSALLO GT Crossing30 models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
VGT18190G30Length 190 cm; Outer Diameter 0.018 in Not statedAvailable
VGT18300G30Length 300 cm; Outer Diameter 0.018 in Not statedAvailable

FDA clearances

  • 510(k) K232578 October 2023

Procedures that use guidewires

Frequently asked questions

What is VASSALLO GT Crossing30 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 Crossing30?

VASSALLO GT Crossing30 is made by Filmec K.k.. It is listed under guidewires in our device library.

What sizes does VASSALLO GT Crossing30 come in?

Sizes listed for VASSALLO GT Crossing30: Length: 190–300 cm; Outer Diameter: 0.02 in. Confirm availability with the manufacturer's instructions for use.

Is VASSALLO GT Crossing30 MRI safe?

The FDA device database entry for VASSALLO GT Crossing30 does not state its MRI safety status. Check the labeling before MRI.

Is VASSALLO GT Crossing30 FDA cleared?

VASSALLO GT Crossing30 is covered by FDA submission K232578.

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.

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