Spex®
Maximum Support Microcatheter that Shapes to Hold Your Preferred Angle
SpexLP®
Low Profile and Shapeable with Optimal Support and Pushability to Cross the Tightest Lesions
Shape to Your Choice
Cross Complex and Tight Lesions
Optimal Trackability and Pushability
Shape to Your Choice. Optimal Trackability and Pushability to Cross Complex and Tight Lesions.
Shapeable Metal Tip with Superior Radiopaque Visibility
Telescopes with Spex LP 14/18 and Wingman™ 14/14C CTO Crossing Catheter
Braid Reinforced Microcatheter Body to Maximize Support and Pushability
Customizable Tip Maintains the Desired Angle
Shapes to the preferred angle and holds it throughout the procedure
Shape to Your Choice. Optimal Trackability and Pushability to Cross Complex and Tight Lesions.
Maximum Shape Versatility Provided by Reinforced Microcatheter Body Construction
100mm long shapeable distal tip
Spex LP 35 compatible with Spex LP 14/18 and Wingman 14/14C CTO Crossing Catheter
Lowest Profile Shapeable Support Microcatheter Compatible with Your Preferred Guidewire Size
Three radiopaque markers 50mm apart
Braid reinforced microcatheter body
35
Model Number – Effective Length
SPN35050CE
SPN35050CE-5P*
SPN35090CE
SPN35090CE-5P*
SPN35135CE
SPN35135CE-5P*
SPN35150CE
SPN35150CE-5P*
Effective Length (cm)
50,90,135,150
Guidewire Compatability (in)
0.035
Max Outer Diameter (in/F)
0.06/4.6
Max Pressure (psi/kpa)
300/2068
Shapeable Tip Zone (in/mm)
.75/19
Sheath Compatibility (F/mm)
5/1.7
Hydrophilic Coating (cm)
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. This device is restricted to use by or on the order of a physician. Refer to the Instructions for Use for a complete listing of the Indications, Contraindications, Warnings, Precautions, Adverse Events, and Procedural Steps
14
18
35
Model Number
SLP14090CE
SLP14090CE-5P*
SLP14135CE
SLP14135CE-5P*
SLP14150CE
SLP14150CE-5P*
SLP18090CE
SLP18090CE-5P*
SLP18135CE
SLP18135CE-5P*
SLP18150CE
SLP18150CE-5P*
SLP35090CE
SLP35090CE-5P*
SLP35135CE
SLP35135CE-5P*
SLP35150CE
SLP35150CE-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
©2025 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: This device is restricted to use by or on the order of a physician. Refer to the Instructions for Use for a complete listing of the Indications, Contraindications, Warnings, Precautions, Adverse Events, and Procedural Steps.
Intended Use
The Spex Shapeable Support Microcatheter is intended to treat peripheral artery disease (PAD).
Indications for Use
The Spex Shapeable Support Microcatheter is intended to treat peripheral artery disease (PAD).
Contraindications
The Spex™ Shapeable Support Microcatheter is intended to be used in conjunction with steerable guidewires to access discrete regions of the peripheral vasculature. To facilitate access in conjunction with a guidewire, it may be desired to shape the tip of the microcatheter. 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/ therapeutic agents.
Warnings
• Single Use only. Do not reuse/resterilize. Reusing the device could result in compromised device performance, cross-infection and other safety related hazards including patient injury.
• 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
• 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.
Precautions
• Store in a cool, dry, dark place. Storage of the device in extreme conditions may damage the device and/or affect device performance that could lead to patient injury.
• Use only appropriately sized ancillary device, as shown in the Specifications above.
• Maximum Injection 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 microcatheter during procedure to reduce the possibly of accidental damage, kinking or bending.
• Manipulation of the microcatheter should only occur under fluoroscopy.
©2025 Reflow Medical, Inc. All rights reserved. Reflow Medical, Spex and The Pulse of Medical Ingenuity are registered trademarks or trademarks of Reflow Medical, Inc. This device is restricted to use by or on the order of a physician. Refer to the Instructions for Use for a complete listing of the Indications, Contraindications, Warnings, Precautions, Adverse Events, and Procedural Steps.
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