Boston Scientific EKOS Control Unit 4.0 EKOS Endovascular | REF H74939590106120

The Boston Scientific EKOS Control Unit 4.0 (REF H74939590106120) is the dedicated electronic drive console used with the EKOS Endovascular System to deliver controlled ultrasonic energy through compatible EKOS catheters during ultrasound-facilitated, catheter-directed thrombolysis. The Control Unit 4.0 generates and regulates the ultrasound output and monitors core temperature feedback from the treatment zone, supporting consistent and reproducible therapy delivery in a hospital interventional setting.

Key Features
Fourth-generation EKOS drive console designed for the EKOS Endovascular System.
Delivers and regulates ultrasonic energy to compatible EKOS Intelligent Drug Delivery Catheters.
Integrated touchscreen user interface for procedure setup, monitoring and status indication.
Real-time monitoring of catheter feedback, including treatment zone temperature.
Designed to be mounted on the dedicated EKOS cart for use in interventional suites.
Reusable capital equipment intended to support multiple single-use catheter procedures.

Clinical Applications
Used as the control console component of the EKOS Endovascular System for ultrasound-facilitated, catheter-directed thrombolysis.
Supports interventional procedures performed by trained vascular and interventional specialists in hospital cath lab, IR and hybrid OR environments.
Indications, contraindications and patient selection are defined by the EKOS Endovascular System Instructions for Use and applicable local regulatory clearances.

Product Information
Brand: Boston Scientific
Product Line: EKOS Endovascular System
Model: EKOS Control Unit 4.0
REF / UPN: H74939590106120
Category: Accessories and Other — Capital Equipment / Console
Device Type: Reusable electronic control unit (drive console)
Compatibility: EKOS Endovascular System catheters and connector cables
Power Requirements: Not specified in the located sources
Dimensions and Weight: Not specified in the located sources
Regulatory Status: Not specified in the located sources — refer to the manufacturer IFU and local regulatory documentation.

REF / UPNH74939590106120
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