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General| Model Name | ENDOTAK RELIANCE SG |
|---|---|
| Category | Medical Equipment |
| Manufacturer | Boston Scientific |
| Device Type | Implantable Cardioverter Defibrillator (ICD) Lead |
| Compatibility | Compatible with specific Boston Scientific ICDs |
| Length | Varies by model |
| Sterilization | Ethylene Oxide |
| Material | Polyurethane, Silicone |
Lists patient conditions that preclude the use of this active fixation lead.
Highlights potential risks and critical safety information associated with lead use.
Emphasizes using only tested and approved ICD systems with the leads.
Advises against patient exposure to MRI environments due to potential interference.
Warns against diathermy treatment due to risk of patient injury.
Stresses the importance of correct lead connections to the pulse generator.
Outlines procedures for testing the lead's ability to convert arrhythmias.
Mandates that leads are for single patient use only; no reuse or resterilization.
Enlists possible physical effects and complications from lead implantation.
Confirms leads are sterilized with ethylene oxide and should not be resterilized.
Explains how to position the lead tip and electrodes within the heart using fluoroscopy.
Describes the process of electrically fixing the lead's helix into the heart wall.
Describes methods to verify lead stability after fixation using fluoroscopy.
Provides steps for repositioning the lead if necessary, including helix retraction.
Emphasizes verifying lead position and integrity using imaging and electrical tests.
Discusses the importance of proper electrical connections and signal evaluation.
Outlines the process for testing the lead's ability to convert arrhythmias.
Details how to connect the lead terminals to the ICD pulse generator.
