The Boston Scientific ENDOTAK RELIANCE DF1 Defibrillation Lead (REF 175) is a transvenous endocardial lead designed for chronic implantation in the right ventricle as part of an implantable cardioverter defibrillator (ICD) system. Engineered for reliable sensing, pacing, and high-voltage defibrillation therapy delivery, the ENDOTAK RELIANCE platform incorporates Boston Scientific's GORE coating intended to support extraction characteristics and lead handling. This catalog listing is intended for qualified B2B procurement by hospitals, cardiology centers, and authorized medical distributors.
Key Features
- Transvenous defibrillation lead from the ENDOTAK RELIANCE family
- DF-1 high-voltage connector with IS-1 pace/sense connector configuration
- Designed for right ventricular placement with active or passive fixation per model
- Engineered for compatibility with Boston Scientific ICD and CRT-D pulse generators using DF-1/IS-1 ports
- Silicone and polyurethane lead body construction with GORE expanded PTFE covering on shocking coil(s) per family specification
- Steroid-eluting tip intended to support stable chronic pacing thresholds
- Reference number: REF 175
Clinical Applications
- Sensing of intracardiac electrograms for tachyarrhythmia detection
- Delivery of high-voltage defibrillation and cardioversion therapy
- Bradycardia and antitachycardia pacing as part of an ICD system
- Use in patients indicated for ICD therapy in accordance with the device Instructions for Use
Product Information
Brand: Boston Scientific
Product Line: ENDOTAK RELIANCE
Model / REF: 175
Category: ICD Leads for Implantable Cardioverter Defibrillators
Connector: DF-1 (high voltage) / IS-1 (pace-sense)
Lead Type: Transvenous right ventricular defibrillation lead
Coil Configuration: Not specified in the located sources
Fixation: Not specified in the located sources
Lead Length: Not specified in the located sources
Sterility: Supplied sterile for single use
Intended Users: Licensed implanting physicians and authorized healthcare facilities
Note: Buyers must verify current model specifications, fixation type, length, and pulse generator compatibility against the official Boston Scientific Instructions for Use and product matrix prior to clinical use.