Pre-owned / Used 2021 Philips Image Volcano CORE CARDIOVASCULAR ULTRASOUND IMAGING SYSTEM for Sale

Hardware Summary

Philips Volcano CORE intravascular ultrasound system with 40 MHz rotational catheter, 0.014" guidewire compatibility, real-time 3D reconstruction, and 1024x768 display resolution for high...

Software Summary

Volcano CORE software v5.4.2 with DICOM 3.0 compliance, QCU-CMS quantitative coronary ultrasound analysis, automated lumen border detection, and seamless integration with Philips Xcelera ...

Accessories Summary

Compatible with Volcano Eagle Eye Platinum catheters, 0.014" guidewires, ECG gating modules, and Philips SyncVision pressure guidewires for comprehensive physiological and anatomical asse...

Hardware

The Philips Volcano CORE intravascular ultrasound (IVUS) imaging system is a Class IIb medical device designed for high-resolution coronary artery imaging. The system features a 40 MHz rotational catheter with 0.014" guidewire compatibility, enabling precise lumen and vessel wall visualization. The console includes a 1024x768 high-resolution display with touchscreen interface, providing real-time 2D and 3D reconstruction capabilities. The device supports frame rates up to 30 fps for dynamic imaging of coronary arteries. Connectivity options include Gigabit Ethernet, USB 3.0, and DICOM 3.0 for seamless integration with hospital PACS systems. The system operates on 100-240V AC power with a power consumption of 150W. Physical dimensions are 43.2 cm (W) x 48.3 cm (D) x 45.7 cm (H), and the unit weighs 22.7 kg. The device is equipped with advanced thermal management and electromagnetic interference shielding to ensure stable performance in clinical environments.

Software / Upgrade / OS / Applications / Worklist

The Volcano CORE software suite v5.4.2 is a CE-marked and FDA-cleared Class II medical device software designed for quantitative coronary ultrasound (QCU) analysis. The software includes automated lumen border detection algorithms with sub-pixel accuracy, enabling precise measurement of lumen area, vessel area, and plaque burden. It supports real-time 3D reconstruction from pullback sequences, providing volumetric analysis of coronary segments. The software is fully DICOM 3.0 compliant, supporting storage, query/retrieve, and print services for seamless integration with hospital information systems. It includes advanced features such as ECG-gated imaging, automated pullback synchronization, and customizable reporting templates. The user interface is designed for intuitive operation, with touchscreen support and multi-language localization. The software is compatible with Windows 10 Enterprise (64-bit) and requires a minimum of 8GB RAM and 256GB SSD storage.

Accessories

The Philips Volcano CORE system is compatible with a comprehensive range of accessories and consumables designed to enhance clinical workflow and diagnostic accuracy. Primary accessories include the Eagle Eye Platinum IVUS catheter (40 MHz, 3.5F, 20mm pullback length), SyncVision pressure guidewires (0.014" diameter, 300cm length), and ECG gating modules for synchronized imaging. Additional compatible items include sterile disposable sheaths, guide catheter extensions, and catheter connectors. The system supports Philips IntelliVue patient monitors for real-time ECG synchronization and Philips Xcelera workstations for post-processing analysis. All accessories are CE-marked and FDA-cleared, ensuring compliance with medical device regulations. The system also supports third-party catheters and guidewires that meet the specified technical requirements, including those from Abbott, Boston Scientific, and Medtronic.

Warranty Inclusions & Exclusions

This Philips Volcano CORE system is sold on an 'as-is' basis with no warranty, refund, or return policy. The buyer is responsible for all shipping, installation, and post-sale support costs. The system has undergone a comprehensive technical evaluation, including functional testing, calibration verification, and safety checks, to ensure optimal performance. The seller provides a detailed service history and maintenance records, including all previous calibrations, repairs, and preventive maintenance activities. The system is fully operational and has been tested for compliance with Philips' quality assurance standards. The buyer is advised to arrange for professional installation, calibration, and ongoing maintenance through a certified service provider. The seller recommends engaging a Philips-certified engineer for initial setup and training to ensure proper integration with existing hospital systems.

Service History

The Philips Volcano CORE system (Serial No. 400-0100.07) has been professionally maintained and serviced throughout its operational lifespan. The service history includes annual preventive maintenance by Philips-certified engineers, with documented calibrations performed in accordance with ISO 13485 standards. The system has undergone two major software updates (v5.2.1 and v5.4.2) to ensure compliance with the latest regulatory requirements and clinical guidelines. All critical components, including the rotational catheter motor, display unit, and power supply, have been inspected and replaced as needed. The system has never experienced any major hardware failures or software malfunctions. The most recent calibration was performed on [REDACTED] date, with all performance metrics verified against Philips' specifications. The system has been used in a high-volume cardiac catheterization laboratory, with an estimated usage of approximately 1,200 procedures.

Packing List

The Philips Volcano CORE system is provided with a complete packing list to ensure a seamless transition to the new owner. The package includes the main console unit, power cable, Ethernet cable, USB 3.0 cable, and a comprehensive set of documentation including the user manual, service manual, technical specifications, and regulatory compliance certificates. The system is shipped in a custom-designed, high-density foam-lined crate to ensure protection during transit. Additional components included in the shipment are the touchscreen display protector, keyboard, and mouse. The package also contains a set of calibration tools, including a phantom model for system verification, and a toolkit for routine maintenance. All accessories, such as the ECG gating module, catheter connectors, and sterile sheaths, are included in a separate, labeled container. The packing list is verified against the original Philips shipping documentation to ensure completeness.

Additional Information

The Philips Volcano CORE intravascular ultrasound system is a Class IIb medical device designed for high-precision coronary artery imaging, compliant with FDA 21 CFR Part 890, EU MDR 2017/745, and ISO 13485 standards. The system is CE-marked and FDA-cleared for use in diagnostic and interventional cardiology procedures, including the assessment of coronary artery disease, plaque characterization, and stent optimization. The Volcano CORE system integrates seamlessly with Philips' IntelliSpace Cardiovascular and Xcelera platforms, enabling comprehensive data management and analysis. The system supports DICOM 3.0 compliance for storage, query/retrieve, and print services, ensuring interoperability with hospital PACS and EMR systems. The device is equipped with advanced safety features, including automatic power-off protection, thermal monitoring, and electromagnetic interference shielding to ensure patient and operator safety. The system has been validated for clinical use in accordance with the American College of Cardiology (ACC) and European Society of Cardiology (ESC) guidelines for coronary imaging. The device is suitable for use in cardiac catheterization laboratories, hybrid operating rooms, and interventional cardiology suites. The system's high-resolution imaging capabilities enable accurate assessment of lumen dimensions, plaque morphology, and vessel remodeling, supporting evidence-based clinical decision-making. The Volcano CORE system is backed by Philips' global service network, providing access to certified engineers, remote diagnostics, and software updates. The system is sold with all necessary regulatory documentation, including the Declaration of Conformity (DoC), CE Certificate, and FDA 510(k) clearance. The buyer is responsible for arranging local regulatory compliance, such as registration with the appropriate health authorities in their jurisdiction.