
ASAHI Hyperion Coronary Guiding Catheter | REF HW60JL350P10000
ASAHI Hyperion Coronary Guiding Catheter (REF HW60JL350P10000) designed to provide stable support and torque response during coronary interventional procedures.

The Boston Scientific MACH1 JL4.5 SH 7F Coronary Guiding Catheter (REF H749343576690) is a single-use guiding catheter designed to facilitate the introduction and placement of interventional devices within the coronary vasculature. The Judkins Left 4.5 short-tip (SH) configuration in a 7F outer diameter is intended to support engagement of the left coronary ostium with predictable handling and a stable platform for device delivery.
Key Features
Judkins Left 4.5 (JL4.5) curve with short tip (SH) geometry for left coronary engagement
7F outer diameter offering a balance between inner lumen capacity and access vessel profile
MACH1 construction designed for torque response, kink resistance and tip-shape retention
Smooth inner lumen intended to support passage of guidewires, balloons and stent systems
Atraumatic soft tip designed to reduce vessel trauma during cannulation
Hydrophilic or lubricious outer treatment per manufacturer specification — Not specified in the located sources
Sterile, single-use device packaged for procedural readiness
Clinical Applications
Selective engagement of the left coronary artery for diagnostic angiography support
Delivery and exchange of interventional devices during percutaneous coronary intervention (PCI)
Procedures requiring predictable backup support and stable coaxial alignment
Use in catheterization laboratory workflows where Judkins Left curve geometry is preferred
Product Information
Brand: Boston Scientific
Product Line: MACH1 Guiding Catheter
Curve: Judkins Left 4.5 (JL4.5)
Tip Length: Short (SH)
Outer Diameter: 7F
Working Length: Not specified in the located sources
Inner Lumen Diameter: Not specified in the located sources
Category: Guiding Catheter
REF/UPN: H749343576690
Sterility: Sterile, single-use
Regulatory status, indications and compatibility should be verified against the current manufacturer Instructions for Use (IFU) prior to procurement or clinical use.
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