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CARDIOVASCULAR
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GUIDING THROUGH ACCESS

GuideRight™ guide wire is a stainless steel access guide wire, designed for standard clinical situations.

Stainless steel core

  • Ideal for general needle access, sheath introduction, and catheter delivery

PTFE (Teflon) pre-coating

  • Provides a superior finish with increased lubricity and reduces friction between catheter and guide wire

Versatile product offering

  • Multiple lengths, tip configurations, and diameters to meet a variety of clinical needs


Data on file at Abbott

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

PRODUCT INFO

Our online product catalogs provide the very latest information available, right at your fingertips. Download catalogs by product family in PDF format, or view the entire Abbott Vascular inventory in Excel. Product barcodes enable direct scanning for easy reordering.

IMPORTANT SAFETY INFORMATION

rx-only-logo 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

AP2947347-WBU Rev. A

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.