The Winn™ family of specialty guide wires enables crossing of challenging lesions with 3 options for guide wire tip stiffness:
The excellent tactile feedback and deliverability1 are due to the combination of:
Product | Part Number | Diameter | Length | Tip Load | Tip Style | Units Per Package |
---|---|---|---|---|---|---|
Hi-Torque Winn™ 40 | 1012466 | 0.014 in | 190 cm | 5.1 g | Core-To-Tip | 5 |
Hi-Torque Winn™ 40 | 1012467 | 0.014 in | 300 cm | 5.1 g | Core-To-Tip | 5 |
Hi-Torque Winn™ 80 | 1012468 | 0.014 in | 190 cm | 11.3 g | Core-To-Tip | 5 |
Hi-Torque Winn™ 80 | 1012469 | 0.014 in | 300 cm | 11.3 g | Core-To-Tip | 5 |
Hi-Torque Winn™ 200T | 1012474 | 0.014 in | 190 cm | 14.3 g | Core-To-Tip | 5 |
Hi-Torque Winn™ 200T | 1012475 | 0.014 in | 300 cm | 14.3 g | Core-To-Tip | 5 |
Data on file at Abbott.
MAT-2006309 v2.0
This Hi-Torque guide wire is intended to facilitate the placement of balloon dilatation catheters during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA). This guide wire may also be used with compatible stent devices during therapeutic procedures.
Not intended for use in the cerebral vasculature or with atherectomy devices.
This device is designed and intended for ONE-TIME USE ONLY. Do not resterilize and / or reuse.
Carefully observe the instructions under “Do Not” and “Do” below. Failure to do so may result in vessel trauma, guide wire damage, guide wire tip separation, or stent damage. If resistance is observed at any time, determine the cause under fluoroscopy and take remedial action as needed. Use the most suitable guide wire for the lesion being treated.
Do Not:
Do:
For Winn™ family only: The Winn™ family of guide wires have distal ends of varying stiffness. Operate these guide wires carefully so as not to injure the blood vessel, observing the information in these instructions. The higher torque performance, stiffer distal ends, and / or higher advancement force may present a higher risk of perforation or injury than a guide wire with a more pliable distal end. Therefore, use the guide wire with the least stiff distal end that will treat the lesion, and use extreme care to minimize the risk of perforation or other damage to blood vessels.
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 guide wires. Using a damaged guide 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.
Never attach the torque device to the modified portion of the proximal end of the extendible guide wire; otherwise, guide wire damage may occur, preventing the ability to attach the DOC™ Guide Wire Extension.
Hi-Torque Guide Wires with Hydrophilic Coating: Avoid abrasion of the hydrophilic coating. Do not withdraw or manipulate the hydrophilic-coated wire through a metal cannula or sharp-edged object.
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.
MAT-2306605 v1.0
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