The Medtronic Launcher 5Fr CHAMP10 Coronary Guiding Catheter (REF LA5CHAMP10) is a single-use percutaneous coronary guiding catheter engineered to provide responsive torque, stable ostial engagement and consistent backup support across a broad range of coronary anatomies. The Launcher platform combines a stainless steel braided shaft with a soft, atraumatic distal tip and a lubricious inner lining intended to facilitate smooth device delivery during diagnostic angiography and percutaneous coronary intervention (PCI).

Key Features
- Pre-shaped CHAMP10 curve designed for predictable, reproducible coronary ostial engagement.
- 5 French outer diameter for radial or femoral access workflows.
- 100 cm usable length consistent with the standard Launcher guiding catheter platform.
- Stainless steel braided shaft for 1:1 torque response and kink resistance.
- Lubricious inner lumen coating to support smooth passage of guidewires, balloons and interventional devices.
- Soft atraumatic distal tip intended to reduce vessel trauma during engagement.
- Radiopaque marker to support fluoroscopic visualization.
- Sterile, single-use packaging configuration.

Clinical Applications
- Selective coronary angiography requiring a CHAMP-style backup support curve.
- Conduit for delivery of guidewires, balloon catheters, stents and adjunctive PCI devices.
- Procedures where stable coaxial engagement and predictable backup support are required by the operator.
- Suitable for use in cardiac catheterization labs performing diagnostic and interventional coronary workflows.

Product Information
- Brand: Medtronic
- Product Family: Launcher Coronary Guiding Catheter
- Reference / REF: LA5CHAMP10
- Curve: CHAMP10
- French Size: 5Fr
- Usable Length: 100 cm (standard Launcher configuration)
- Category: Guiding Catheter
- Use: Single-use, sterile
- Inner Diameter / Minimum Guide Compatibility: Not specified in the located sources
- Country of Origin / GTIN: Not specified in the located sources
- Regulatory status and clinical suitability: Refer to the manufacturer's current Instructions for Use (IFU) and local regulatory documentation prior to procurement or clinical use.