The Medtronic Launcher 6Fr AL10 Coronary Guiding Catheter (REF LA6AL10) is a single-lumen percutaneous guiding catheter designed to facilitate the introduction and positioning of interventional devices within the coronary vasculature. The Amplatz Left 1.0 (AL1.0) curve is intended for selective engagement of coronary ostia where additional backup support and a coaxial seating profile are clinically required.

Key Features
Three-layer construction combining a stainless-steel braid with an inner PTFE liner and a nylon-blend outer jacket for torque response and kink resistance.
Large lumen relative to outer diameter to support contemporary interventional devices and contrast injection.
Atraumatic, smoothly tapered soft tip designed to reduce vessel trauma during ostial engagement.
Pre-shaped AL1.0 (Amplatz Left 1.0) curve providing strong passive backup support.
Hydrophobic outer coating to assist navigation through the introducer and vasculature.
Radiopaque construction to aid fluoroscopic visualization.

Clinical Applications
Selective cannulation of coronary artery ostia during diagnostic and interventional procedures.
Delivery of guidewires, balloon catheters, stents, and other compatible interventional devices.
Procedures requiring enhanced backup support, including selected right coronary artery (RCA) anatomies, anomalous take-offs, and shepherd's-crook configurations where standard Judkins curves provide insufficient support.
Use in transfemoral and, where clinically appropriate, transradial percutaneous coronary access.

Product Information
Brand: Medtronic
Product Line: Launcher Coronary Guide Catheter
REF / UPN: LA6AL10
French Size: 6Fr
Curve: AL1.0 (Amplatz Left 1.0)
Configuration: Single lumen, pre-shaped, non-side-hole (verify side-hole variant against manufacturer matrix if required)
Working Length: Not specified in the located sources
Inner Diameter: Not specified in the located sources
Sterility: Sterile, single-use device
Category: Guiding Catheter / Interventional Cardiology
Buyers should verify country-specific regulatory status, lot, expiry, and full IFU details against current Medtronic documentation prior to procurement.