CARDIOVASCULAR
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Support And Crossability

The TAD™ Tapered Guide Wire System family of peripheral guide wires (.035 – .018") combines shaft support and a soft tip with shaping ribbon for precise steerability in tight lesions. Features include:

  • Atraumatic guide wire tip with shaping ribbon
  • Maximum distal support designed for a range of anatomies and traversing acute angles
  • Hydrophobic coating that provides excellent lubricity and low friction1

Precise Steerability with Shapeable Tip

  • TAD™ Tapered peripheral guide wire combines a 0.035" proximal shaft support and a 0.018" tip for precise steerability when traversing tight stenoses and negotiating vessels sensitive to spasm
  • The TAD™ II Tapered peripheral guide wire provides enhanced support and trackability for access to acute angles and vessels sensitive to spasm

Versatile Product Offering

  • Multiple length and tip configurations can meet a variety of clinical needs
  • Guide wires come in the following lengths:
    • TAD™: 145 cm, 200 cm, 300 cm
    • TAD™ II: 145 cm, 200 cm, 260 cm

Ordering Information

Product Part Number Diameter Length Tip Style Units Per Package
TAD™ 1012069-03 0.035 in 300 cm Shaping Ribbon 5
TAD™ II 1012069-07 0.035 in 260 cm Shaping Ribbon 5
TAD™ LOC 1012069-01 0.035 in 145 cm Shaping Ribbon 5
TAD™ LOC 1012069-02 0.035 in 200 cm Shaping Ribbon 5
TAD™ LOC 1012069-04 0.035 in 300 cm Shaping Ribbon 5
TAD™ II LOC 1012069-05 0.035 in 145 cm Shaping Ribbon 5
TAD™ II LOC 1012069-06 0.035 in 200 cm Shaping Ribbon 5
LOC Guide Wire Extension 1012068-10 0.035 in 115 cm N/A 5

Tests performed by and data on file at Abbott.

Reference

  1. Tóth GG, Yamane M, Heyndrickx GR. Heart. 2015;101:645–652.

Important Safety Information

Rx Hi-Torque™ Steerable Guide Wires

 

INDICATIONS

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.

 

CONTRAINDICATIONS

The Hi-Torque Steerable Guide Wire is not intended for use in the coronary or cerebral vasculature.

 

WARNINGS

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.

 

PRECAUTIONS

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.

 

ADVERSE EVENTS

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.

Important Safety Information

MAT-2006306 v1.0

DO YOU WISH TO CONTINUE AND EXIT CARDIOVASCULAR.ABBOTT?

CONTENTS OF THE SITE ARE NOT UNDER THE CONTROL OF ABBOTT.

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DO YOU WISH TO CONTINUE AND EXIT CARDIOVASCULAR.ABBOTT?

CONTENTS OF THE SITE ARE NOT UNDER THE CONTROL OF ABBOTT.