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General| Category | Ultrasound System |
|---|---|
| Imaging Modes | 2D, 3D, Color Doppler, Power Doppler |
| Transducer Ports | 4 active ports |
| Applications | Obstetrics, Gynecology, Abdominal, Vascular, Small Parts |
| Data Management | USB ports |
| Advanced Imaging Technologies | HDlive |
| Portability | Cart-based system |
| Operating System | Proprietary |
| Connectivity | Ethernet, USB |
Lists all effective pages in the document, including revision status.
Outlines the topics covered in the manual, organized by chapter.
Provides a general overview of the Ultrasound System's capabilities and architecture.
Lists all the GE Ultrasound system models and products covered by this manual.
Introduces the content of the safety information chapter and its key sections.
Explains conventions, symbols, and safety precaution messages used in the manual.
Describes icons used on the product and in the service information.
Details critical safety precautions for operation, service, and repair of the system.
Provides information on product label locations and their importance for servicing.
Highlights warnings for procedures that may be potentially dangerous.
Explains the requirements and procedures for applying Lockout/Tagout.
Details requirements and procedures for returning probes and repair parts.
Discusses EMC, its impact, and compliance requirements for the Ultrasound System.
Introduces the chapter on site preparation and lists its key sections.
Details the general environmental and electrical requirements for installing the Ultrasound System.
Covers cooling requirements and lighting considerations for the Ultrasound System installation.
Details the electrical requirements, varying by mains voltage and equipment in use.
Lists the contents for console system electrical requirements and provides Invenia ABUS specifications.
Details electrical requirements for LOGIQ laptop models, including adapters and docking carts.
Details electrical requirements for handheld Venue Series systems, including docking stations.
Provides electrical requirements for EchoPAC PC and LOGIQworks workstations.
Specifies site electrical requirements including circuit breaker, outlets, and power cable.
Discusses Ultrasound system susceptibility to Electromagnetic Interference (EMI) and potential sources.
Provides details on preventing and abating EMI, including rules and specific actions.
Outlines the purchaser's responsibilities and facility requirements for site preparation.
Outlines essential facility requirements, including power, door opening, and spacing.
Lists features that are beneficial but not mandatory for the facility.
Outlines mandatory care and maintenance responsibilities and recommended procedures.
Lists critical warnings related to power, board handling, covers, and contamination before repair.
Emphasizes the importance of maintaining records for corrective and routine maintenance.
Explains that the Customer Care Schedule specifies service frequency and items needing attention.
Details preliminary and functional checks, covering operating modes and system components.
Outlines functional checks for GE approved peripherals and hardware options.
Provides instructions for inspecting the mains cable and its connectors for damage and proper attachment.
Describes how to view error logs and run diagnostics for system checks.
Details physical checks of the system, including labeling, covers, panel, and display.
Refers to the User Manual for instructions on system cleaning and air filter cleaning.
Provides warnings and cautions for probe maintenance, cleaning, and disinfection.
States that Phantom use is not required for Care and Maintenance, but can be used for QA tests.
Lists the topics and measurements covered in the Electrical Safety Tests section.
Explains electrical safety tests based on IEC standards and LOTO procedures.
Summarizes acceptance limits and test conditions for leakage currents based on IEC standards.
Describes testing outlets for proper grounding and wiring using an outlet tester.
Details the procedure for measuring ground wire resistance from the plug to exposed metal parts.
Defines Enclosure Leakage current test and its purpose in verifying power line isolation.
Defines the test measuring current flow to ground from isolated ECG leads, simulating a patient connection.
Refers to a table for recording patient lead to lead leakage current measurements.
Details the procedure for sink leakage-isolation tests for probes.
Defines the test measuring current flow from probes through a grounded patient during scanning.
Provides troubleshooting steps for AC/DC fails, chassis fails, probe fails, and other issues.
Advises contacting a GE Service Representative to perform Equipment and Image Quality Checks.
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