
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 Medtronic Launcher 5Fr SR35 Coronary Guiding Catheter (REF LA5SR35) is a single-lumen, braided shaft guiding catheter designed to provide consistent coaxial engagement, smooth torque response and reliable backup support during percutaneous coronary access. The Launcher family is recognized for its three-layer construction that combines a lubricious inner liner, a stainless steel braided mid-layer and a customized outer jacket to balance pushability, kink resistance and tip softness in a 5 French profile.
Key Features
Three-layer braided shaft for predictable torque transmission and shape retention
Soft, atraumatic tip designed to reduce the risk of ostial trauma during engagement
Lubricious inner lumen to facilitate smooth device tracking and contrast delivery
SR35 curve geometry intended to support coaxial alignment in selected coronary anatomies
5 French outer diameter to support radial and femoral access strategies
Compatible with standard 0.038 inch guidewires (confirm with current IFU)
Clinical Applications
Selective coronary angiography and contrast injection
Delivery platform for guidewires, balloons and other interventional devices into the coronary vasculature
Procedures where a specialized SR35 curve shape is preferred by the operator
Use as part of standard cath lab inventory for diagnostic and interventional coronary workflows
Product Information
Brand: Medtronic
Product Line: Launcher Coronary Guiding Catheter
Category: Guiding Catheter
REF / UPN: LA5SR35
French Size: 5Fr
Curve / Shape: SR35
Working Length: Not specified in the located sources
Inner Lumen Diameter: Not specified in the located sources
Sterility: Supplied sterile, single use (confirm with current IFU and product labeling)
Packaging: Not specified in the located sources
Note: Specifications, regional availability and regulatory clearances should be verified against the current Medtronic Instructions for Use and local regulatory documentation prior to purchase.
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