The Johnson & Johnson Celsius Catheter Connection Cable, REF CA5400162, is a dedicated interface accessory designed to enable connection of a Celsius diagnostic and ablation catheter to a compatible foreign (non-Biosense Webster) radiofrequency generator. It supports electrophysiology (EP) laboratories that operate mixed-vendor capital equipment by providing a standardized link between the catheter handle and a third-party RF energy source.
Key Features
Purpose-built interconnect cable for the Celsius Catheter family.
Designed for use with a foreign RF generator where compatibility is established by the generator manufacturer.
Engineered to transmit RF energy and electrogram signals between the catheter and the generator.
Single-reference SKU (REF CA5400162) for simplified procurement and inventory control.
Manufactured by Johnson & Johnson MedTech (Biosense Webster) under standardized quality processes.
Supports streamlined cath-lab workflow for centers using multi-vendor EP capital equipment.
Clinical Applications
Cardiac electrophysiology mapping and radiofrequency ablation procedures using the Celsius Catheter.
EP laboratory configurations where the installed RF generator is not a native Biosense Webster unit.
Hospital and ambulatory cardiac centers performing arrhythmia treatment workflows that require flexible generator-to-catheter interfacing.
Use is limited to qualified electrophysiologists and trained cath-lab personnel in accordance with the device Instructions for Use.
Product Information
Brand: Johnson & Johnson (Biosense Webster)
Category: EP Ablation Catheters — Accessories / Connection Cables
REF / UPN: CA5400162
Product Type: Connection cable for Celsius Catheter to foreign RF generator
Compatibility: Celsius Catheter family; foreign RF generator as defined by the generator manufacturer’s compatibility documentation
Sterility: Not specified in the located sources
Single-use / Reusable: Not specified in the located sources
Latex Information: Not specified in the located sources
Country of Origin: Not specified in the located sources
Regulatory Status: Refer to the manufacturer Instructions for Use and local regulatory documentation prior to clinical use.
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