The Abbott Optisure Defibrillation Lead (REF LDA210Q) is a transvenous, dual-coil high-voltage lead engineered for chronic implantation in the right ventricle as part of an implantable cardioverter defibrillator (ICD) system. Optisure leads are part of Abbott's high-voltage lead portfolio and are intended to deliver defibrillation and cardioversion therapy while providing reliable bradycardia pacing and sensing.
Key Features
- Dual-coil high-voltage configuration (RV and SVC shocking coils) for defibrillation therapy delivery
- DF4/IS-1 connector family compatible with Abbott ICD pulse generators (verify connector standard against device labeling)
- Active fixation design with extendable/retractable helix for stable RV apical or septal placement
- Silicone insulation with Optim copolymer outer layer engineered to enhance abrasion and tear resistance
- Steroid-eluting tip intended to mitigate acute pacing threshold rise
- 7F lead body designed to support transvenous delivery through standard introducers
Clinical Applications
- High-voltage defibrillation and cardioversion in patients indicated for ICD or CRT-D therapy
- Right ventricular sensing and bradycardia pacing as part of an implanted ICD system
- Use with compatible Abbott ICD/CRT-D pulse generators per device labeling and the lead's Instructions for Use
Product Information
- Brand: Abbott
- Product line: Optisure High Voltage Lead
- REF / UPN: LDA210Q
- Category: ICD Leads for Implantable Cardioverter Defibrillators
- Configuration: Dual-coil, active fixation transvenous defibrillation lead
- Lead body diameter: Not specified in the located sources
- Usable length: Not specified in the located sources
- Connector: Not specified in the located sources — confirm DF4 vs DF-1/IS-1 from product labeling
- Sterility: Supplied sterile, single-use; refer to package labeling
- Regulatory status / indications: Refer to the official Abbott Instructions for Use and regional regulatory clearances applicable to your market
This listing is intended for qualified B2B procurement by licensed healthcare facilities. Implantation must be performed by trained electrophysiology professionals in accordance with the manufacturer's Instructions for Use.
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