CARDIOVASCULAR
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The Engage™ TR Introducer is designed for excellent radial insertion performance and vascular access.

THOUGHTFUL DESIGN FOR
PROCEDURAL PERFORMANCE*

  • Robust hemostatic valves to minimize backbleeding and air aspiration
  • Smooth transitions and gradual tapers designed for seamless insertion and reduced insertion force*
  • Flexible strain relief aids in kink resistance
  • Designed with an atraumatic tip
  • Reliable seal designed to balance pass-through friction while maintaining reliable hemostasis with devices up to 6F

EASE OF USE

  • Snap-lock feature secures dilator in sheath during insertion
  • Innovative flexible rotating suture ring for easy manipulation and convenient suture placement
  • Multiple wire and needle configurations to meet a wide range of needs in radial access

Engage Introducer Sheath

*Data on file at Abbott

Reorder Number French Size (F) (ACT) Guide Wire Material Needle Type Sheath Length (cm) Guide Wire Diameter (in)
C408541 4 SS Standard 8.5 0.025
C408543 5 SS Standard 8.5 0.025
C408545 6 SS Standard 8.5 0.025
C408525 4 SS Standard 12 0.025
C408526 5 SS Standard 12 0.025
C408527 6 SS Standard 12 0.025
C408528 4 SS Standard 25 0.025
C408529 5 SS Standard 25 0.025
C408530 6 SS Standard 25 0.025
C408540 4 Coated Cannula 8.5 0.025
C408542 5 Coated Cannula 8.5 0.025
C408544 6 Coated Cannula 8.5 0.025
C408534 4 Coated Cannula 12 0.025
C408535 5 Coated Cannula 12 0.025
C408536 6 Coated Cannula 12 0.025
C408537 4 Coated Cannula 25 0.025
C408538 5 Coated Cannula 25 0.025
C408539 6 Coated Cannula 25 0.025
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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 ENGAGE™ INTRODUCER / ENGAGE™ TR INTRODUCER Hemostasis Introducer

APPLICATIONS

The Engage™ Introducer is indicated for the introduction of angiographic catheters, closed end catheters, balloon catheters, and electrodes into a blood vessel (including but not limited to femoral, radial, and brachial access) where minimizing blood loss is essential.

The Engage™ TR Introducer is indicated for the introduction of angiographic catheters, closed end catheters, balloon catheters, and electrodes into a radial vessel where minimizing blood loss is essential.

CAUTIONS

  • DO NOT alter this device.
  • Federal law (U.S.) restricts this device to sale by or on the order of a physician.
  • Do not attempt to insert a catheter having a distal tip or body size larger than the introducer size indicated.
  • Do not attempt to use a guidewire over maximum diameter specified on package label.
  • This device should only be used by physicians thoroughly trained in the technique of angiography and/or the use of St. Jude Medical catheter delivery systems. catheters
  • Individual patient anatomy and physician technique may require procedural variations.
  • The closing force of the hemostasis valve may alter or impair the function of some catheters.
  • Damage to guidewire may result if with-drawn through a metal needle cannula. Metal needle must be removed first.
  • Do not attempt to advance or withdraw guidewire if resistance is felt. Use fluoroscopy to determine cause.
  • Damage to the valve assembly may occur if inner catheter is withdrawn rapidly.
  • Advance dilator/sheath assembly with a twisting motion to avoid damage to the sheath or vessel.
  • 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 repro-cessing 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-St. Jude Medical packaging may compromise device functionality and sterility due to com-promised 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 impair-ment, or death

POTENTIAL ADVERSE EVENTS

Potential complications which may be encountered during all catheterization procedures include, but are not limited to: acute myocardial infarction or unstable angina, allergic reaction to the contrast media, arterial dissection, injury, or per-foration, cardiac arrhythmias, coronary artery spasm, embolism, thrombus formation, or death.

IMPORTANT SAFETY INFORMATION

AP2947349-WBU Rev. A

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