CARDIOVASCULAR
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Guiding Through Access

Stainless Steel Guide Wire Core

  • Is ideal for needle access, sheath introduction, and catheter delivery1

PTFE Pre-Coating

  • Provides a superior finish with increased lubricity to reduce friction between the catheter and guide wire

Versatile Product and Options

  • Multiple lengths, tip configurations, and diameters to meet a variety of clinical needs
  • Various tip configurations including standard, straight, exchange, super stiff, firm, Bentson, and J
  • Guide wire lengths of 150 cm, 180 cm and 260 cm

Ordering Information

Product Part Number Diameter Length Description “J” Radius Flexible
Tip Length
GuideRight™ 404555 0.035 in 150 cm Standard Straight “J” 3 5 cm
GuideRight™ 404560 0.032 in 180 cm Super Stiff, “J” 3 8 cm
GuideRight™ 404568 0.025 in 150 cm Standard, “J” 3 5 cm
GuideRight™ 404569 0.032 in 150 cm Standard, “J” 3 5 cm
GuideRight™ 404570 0.035 in 150 cm Standard, “J” 3 5 cm
GuideRight™ 404571 0.035 in 180 cm Standard, “J” 3 5 cm
GuideRight™ 404577 0.035 in 260 cm Standard, Exchange, “J” 3 5 cm
GuideRight™ 404578 0.035 in 150 cm Firm, “J” 3 3 cm
GuideRight™ 404610 0.038 in 150 cm Standard, “J” 3 5 cm
GuideRight™ 404617 0.038 in 260 cm Standard, Exchange, “J” 3 5 cm
GuideRight™ 404840 0.035 in 150 cm Standard, Straight N/A 6 cm
GuideRight™ 404843 0.035 in 150 cm Bentson, Straight N/A 15 cm
GuideRight™ 404844 0.035 in 260 cm Standard, Exchange, Straight
N/A 6 cm
GuideRight™ 404878 0.032 in 260 cm Standard, Exchange, “J”
3 5 cm

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 GuideRight™ GUIDEWIRES

 

INDICATIONS FOR USE

Abbott Medical Guidewires are intended for use in the percutaneous introduction of catheters.

 

CONTRAINDICATIONS

There are no known contraindications for this device.

 

WARNINGS

For Single Use Only! Single-use devices are designed and tested for only one patient application. These are disposable devices and are not designed for reprocessing and reuse. Reuse of designated “single-use” devices creates a risk of patient or user infections due to prior patient use and the difficulty in cleaning the narrow structures at material interfaces following direct blood contact. Contamination or reprocessing cleaning agent residues may lead to adverse patient reactions and may damage the device. Use of non-Abbott Medical packaging may compromise device functionality and sterility due to compromised protection from shipping and handling damage. The absence of labeling after reprocessing, may lead to misuse of the device and impaired traceability. Reprocessing and reuse may result in patient or user injury, permanent impairment or death.

 

COMPLICATIONS

Procedures requiring percutaneous catheter/guidewire introduction should not be attempted by physicians unfamiliar with the possible complications. Complications may occur during certain procedures but may not be limited to air embolism, hematoma formation, sepsis/infection, excessive bleeding, vessel damage.

Important Safety Information

MAT-2006303 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.