Hi-Torque Versacore™ family of peripheral workhorse guide wires are designed to meet an array of clinical needs, from start to finish.
|Product||Part Number||Diameter||Length||Tip Style||Units Per Package|
|Hi-Torque Versacore™ Modified J||1012068-01||0.035 in||145 cm||Core-To-Tip||5|
|Hi-Torque Versacore™ Modified J||1012068-05||0.035 in||175 cm||Core-To-Tip||5|
|Hi-Torque Versacore™ Modified J||1012068-09||0.035 in||260 cm||Core-To-Tip||5|
|Hi-Torque Versacore™ Modified J||1012068-07||0.035 in||300 cm||Core-To-Tip||5|
|Hi-Torque Versacore™ Floppy||1012068-02||0.035 in||145 cm||Core-To-Tip||5|
|Hi-Torque Versacore™ Floppy||1012068-04||0.035 in||175 cm||Core-To-Tip||5|
|Hi-Torque Versacore™ Floppy||1012068-06||0.035 in||260 cm||Core-To-Tip||5|
|Hi-Torque Versacore™ Standard||1012068-03||0.035 in||145 cm||Core-To-Tip||5|
|Hi-Torque Versacore™ Standard||1012068-08||0.035 in||300 cm||Core-To-Tip||5|
|LOC Guide Wire Extension||1012068-10||0.035 in||115 cm||N/A||5|
Tests performed by and data on file at Abbott.
The Hi-Torque Steerable Guide Wire is intended for use in angiographic procedures to introduce and position diagnostic and interventional devices within the peripheral vasculature during percutaneous procedures. The wire can be torqued to facilitate navigation through tortuous vessels.
The Hi-Torque Steerable Guide Wire is not intended for use in the coronary or neurovasculature.
The Hi-Torque Steerable Guide Wire is not intended for use in the coronary or cerebral vasculature.
This device is designed and intended for ONE-TIME USE ONLY. DO NOT RESTERILIZE AND / OR REUSE.
Observe all guide wire movement in the vessels. Before a guide wire is moved or torqued, the tip movement should be examined under fluoroscopy. Do not torque a guide wire without observing corresponding movement of the tip; otherwise, vessel trauma may occur.
Torquing a guide wire against resistance may cause guide wire damage and / or guide wire tip separation.
Always advance or withdraw the guide wire slowly. Never push, auger, withdraw, or torque a guide wire which meets resistance. Resistance may be felt and / or observed under fluoroscopy by noting any buckling of the guide wire tip. Determine the cause of resistance under fluoroscopy and take any necessary remedial action.
If the wire tip becomes entrapped within the vasculature, DO NOT TORQUE THE GUIDE WIRE.
Maintain continuous flush while removing and reinserting the guide wire to prevent air from entering the catheter system. Perform all exchanges slowly to prevent air entry and / or trauma. Wipe the wire before all exchanges.
When reintroducing the guide wire, confirm that the interventional device tip is free within the vessel lumen and not against the vessel wall. Failure to do so may result in vessel trauma upon guide wire exit from the device. Use the radiopaque marker of the interventional device to confirm position.
Guide wires are delicate instruments and should be handled carefully. Prior to use and when possible during the procedure, inspect the guide wire carefully for bends, kinks, or other damage. Do not use damaged wires. Using a damaged wire may result in vessel damage and / or inaccurate torque response. Confirm the compatibility of the guide wire diameter with the interventional device before actual use. Free movement of the guide wire within the interventional device is an important feature of a steerable guide wire system because it gives the user valuable tactile information. Test the system for any resistance prior to use. Adjust or replace the hemostatic valve with an adjustable valve if it is found to inhibit guide wire movement.
Potential Adverse Events associated with use of this device may include the following but not limited to perforation, dissection, occlusion, myocardial infarction, embolism and infection.