The Lowest Profile Reinforced Support Catheter
- Promotes improved and predictable access to the vasculature
- Features three radiopaque markers that enhance visibility on imaging
- Increases lubricity with a seamless, low-profile hydrophilic coating
- Designed to fill a specific need based on clinical feedback
- Advance engineered for treating complex critical limb ischemia (CLI)
- Optimizes pushability and access through lesions
NEW AND IMPROVED LUER AND STRAIN RELIEF FOR UNMATCHED PERFORMANCE
Access and cross difficult lesions with the lowest profile reinforced catheter.
BRAID-REINFORCED MICROCATHETER BODY
Provides added column strength and pushability to cross difficult lesions.
CUSTOMIZABLE TIP MAINTAINS THE DESIRED ANGLE
Allows the physician to straighten and reshape to the preferred angle and holds it throughout the procedure
COMPATIBLE WITH YOUR PREFERRED GUIDEWIRE AND PROCEDURAL TECHNIQUE
Telescope SpexLP 18/ SpexLP 14 into the SpexLP 35 to maximize support.
14
18
35
Model Number
SLP14090US
SLP14090US-5P*
SLP141135US
SLP141135US-5P*
SLP14150US
SLP14150US-5P*
SLP18090US
SLP18090US-5P*
SLP18135US
SLP18135US-5P*
SLP18150US
SLP18150US-5P*
SLP35090US
SLP35090US-5P*
SLP35135US
SLP35135US-5P*
SLP35150US
SLP35150US-5P*
Effective Length (cm)
90, 135,150
90, 135,150
90,135,150
Guidewire Compatability (in)
0.014″
0.018″
0.035”
Tip Profile
1.4F
1.6F
2.9F
Max Outer Diameter (F)
2.2F
2.5F
4.0F
Max Pressure (psi/kpa)
360/ 2482
360/ 2482
360/ 2482
Shapeable Tip Zone (in/mm)
3.94/ 100
3.94/ 100
3.94/ 100
Sheath Compatibility (F/mm)
4/ 1.3
4/ 1.3
5 / 1.7
Hydrophilic Coating (cm)
40
40
40
*(-5P) Indicates 5 pack availability
©2024 Reflow Medical, Inc. All rights reserved. Reflow Medical, Spex, and The Pulse of Medical Ingenuity are registered trademarks or trademarks of Reflow Medical, Inc. Federal law (USA) restricts these devices to sale by or on the order of a physician. Refer to the Instructions for Use for a complete listing of the Indications, Contraindications, Warnings, Precautions, Complications, and Directions for Use.
Indications, Safety, & Warnings
CAUTION: Federal law (USA) restricts these devices to sale by or on the order of a physician. Refer to the Instructions for Use for a complete listing of the Indications, Contraindications, Warnings, Precautions, Complications, and Directions for Use.
Indications for Use
Spex LP Support Catheters are intended to be used in conjunction with steerable guidewires to access discrete regions of the peripheral vasculature. They may be used to facilitate placement and exchange of guidewires and other interventional devices, and provide a conduit for delivery of saline solutions or diagnostic/ therapeutics agents.
Contraindications
The spex LP Support Catheter is contraindicated for use in the coronary and cerebral vasculature.
Warnings
Single Use only. Do not reuse/resterilize. Reusing the device could result in compromised device performance, cross-infection and other safety related hazards.
Do not use if device is open or packaging is damaged.
Never advance, withdraw or rotate an intravascular device against resistance until the cause is determined by fluoroscopy.
Precautions
Store in a cool, dry place. Protect from direct sunlight and high temperature.
Use only appropriately sized ancillary device, as shown in the Specifications below.
Maximum Infusion Pressure: 360 psi (2482kpa)
Use the catheter prior to the “Use By” date specified on the package
The catheter should only be used by physicians qualified to perform percutaneous, vascular interventions.
Precautions to prevent or reduce clotting should be taken when any catheter is used in the vascular system. Use of systemic heparinization and heparinized saline solution should be considered.
Exercise care while handling the catheter during procedure to reduce the possibly of accidental damage, kinking or bending.
Manipulation of the catheter should only occur under fluoroscopy.
Complications
Vascular catheterization and/or vascular intervention may result in complications including but not limited to:
• Vessel dissection, perforation, rupture or total occlusion
• Infection
• Hematoma
• Unstable angina
• Embolism
• Hypo/hypertension
• Acute myocardial infarction
• Arrhythmia, including ventricular fibrillation
• Death
• If the catheter is damaged, this product may cut into a blood vessel wall. Extreme caution needs to be taken when removing a damaged device. In the case of complications resulting from the removal of the entire system, stop immediately the procedure, and perform appropriate treatment at the discretion of the physician.
©2024 Reflow Medical, Inc. All rights reserved. Reflow Medical, Spex, and The Pulse of Medical Ingenuity are registered trademarks or trademarks of Reflow Medical, Inc. Federal law (USA) restricts these devices to sale by or on the order of a physician. Refer to the Instructions for Use for a complete listing of the Indications, Contraindications, Warnings, Precautions, Complications, and Directions for Use.
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