PSCIC101: Medtronic PulseSelect Cable for Pulse Field Ablation Catheter System (No Box)

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Additional Details
Medtronic PSCIC101 PulseSelect PFA Catheter Interface Cable
The Medtronic PSCIC101 PulseSelect PFA Catheter Interface Cable is a sterile, single-use component of the PulseSelect Pulsed Field Ablation system. Manufactured by Medtronic, this cable provides the essential connection between the PulseSelect PFA loop catheter and the PulseSelect PFA generator. It facilitates the delivery of pulsed electric fields for cardiac tissue ablation in the treatment of atrial fibrillation. The cable utilizes a custom locking connector to ensure a secure interface during the procedure.
Product Code: PSCIC101
- System Compatibility: Medtronic PulseSelect PFA System
- Connection Type: Catheter-to-Generator Interface
- Connector: Custom Locking Connector
Contents
- 1 Catheter Interface Cable
Features
- Connects PulseSelect PFA catheter to PulseSelect PFA generator
- Features custom locking connector for secure attachment
- Facilitates pulsed field ablation energy delivery
Sterilization
- Device Packaged as Sterile: Yes
- Requires Sterilization Prior to Use: No
- Single-Use, Disposable
Additional Details
- Brand: Medtronic
- Category: Electrophysiology Accessories
- Type: Catheter Interface Cable
- FDA Product Code: QZI
- FDA Product Code Name: Percutaneous Cardiac Ablation Catheter for Treatment of Atrial Fibrillation with Irreversible Electroporation
- GMDN Term Code: 47143
- GMDN Term Name: Electrical-only medical device connection cable, single-use
- GMDN Term Definition: A non-patient-contact, insulated, electrical cord with a connector (plug) at both ends designed to transmit electrical power and/or signal (data) between medical devices (e.g., to connect a lead, electrical catheter, handpiece, or monitor to a parent device). It is not intended to connect directly to patient-worn electrodes (i.e., it is not a lead), is not intended to connect to the mains (i.e., not a mains power cable), does not generate any type of power and/or signal, and has no additional non-electrical conducting or processing functionality. Some types may include an electrical isolator to prevent electrical shocks, and/or a cable cover. This is a single-use device.
AccessGUDID Info
- FDA Product Code: QZI
- FDA Product Code Name: Percutaneous Cardiac Ablation Catheter for Treatment of Atrial Fibrillation with Irreversible Electroporation
- GMDN Term Code: 47143
- GMDN Term Name: Electrical-only medical device connection cable, single-use
- GMDN Term Description: A non-patient-contact, insulated, electrical cord with a connector (plug) at both ends designed to transmit electrical power and/or signal (data) between medical devices (e.g., to connect a lead, electrical catheter, handpiece, or monitor to a parent device). It is not intended to connect directly to patient-worn electrodes (i.e., it is not a lead), is not intended to connect to the mains (i.e., not a mains power cable), does not generate any type of power and/or signal, and has no additional non-electrical conducting or processing functionality. Some types may include an electrical isolator to prevent electrical shocks, and/or a cable cover. This is a single-use device.
More on Ablation | Cryo
Cryoablation is a catheter-based technique used to treat atrial fibrillation by applying extreme cold to targeted areas of heart tissue. This freezing process creates scar tissue that blocks the abnormal electrical signals responsible for triggering arrhythmia. Unlike heat-based methods like radiofrequency ablation, cryoablation uses a balloon catheter to deliver cold energy in a more uniform, circumferential manner—often around the pulmonary veins. The approach is valued for its procedural consistency, controlled lesion formation, and lower risk of certain complications, making it a widely used option in the treatment of AF.
Manufacturer
Medtronic Cardiovascular Therapies offers a broad range of solutions for treating peripheral artery disease, aortic aneurysms, deep vein thrombosis, and other vascular conditions. Key technologies include the Endurant II and Endurant IIs stent graft systems for abdominal aortic aneurysms, the IN.PACT Admiral drug-coated balloon for femoropopliteal disease, and the Abre venous self-expanding stent system for iliofemoral venous outflow obstruction. With a commitment to advancing minimally invasive therapies, Medtronic’s vascular innovations help restore blood flow, reduce procedural risk, and improve quality of life for patients with complex vascular disease.
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