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General| Brand | GE |
|---|---|
| Model | LOGIQ 3 |
| Category | Medical Equipment |
| Language | English |
Details the reasons for changes made in document revisions.
Lists all pages that are effective in the current revision of the document.
Outlines the topics covered in the current manual, referencing chapters.
Provides a description of the Ultrasound System, its architecture, and signal flow.
Lists the specific GE Ultrasound products for which this manual is effective.
Introduces important safety issues related to servicing the Ultrasound System.
Provides a summary of the contents within the Safety Information chapter.
Explains important conventions, including safety precaution messages and hazard symbols.
Details common hazard icons used to indicate potential risks and the need for caution.
Explains icons that signify specific procedures that must be followed for safety.
Refers to descriptions and locations of Ultrasound System icons in the User Manual.
Details crucial safety precautions for human, mechanical, and electrical aspects of the system.
Covers safety precautions related to the mechanical handling and operation of the Ultrasound System.
Details safe practices and guidelines for electrical handling and operation of the Ultrasound System.
Provides guidelines for connecting and handling ultrasound probes safely.
Refers to peripheral isolation information found in the User's Manual.
Emphasizes referring to the User Manual for a list of product labels and their locations.
Highlights warnings that precede potentially dangerous procedures within the manual.
Details the requirements and procedures for applying Lockout/Tagout (LOTO) for safety.
Outlines requirements for cleaning and returning parts, and user responsibilities for data handling.
Explains electromagnetic compatibility and the system's compliance with emission and immunity limits.
Provides precautions and procedures to prevent damage from electrostatic discharge.
Provides information required to plan and prepare for the setup of an Ultrasound system.
Summarizes the contents of the Site Preparations chapter.
Details general requirements for the Ultrasound system, including environmental and electrical specifications.
Covers cooling and lighting requirements for the Ultrasound System installation environment.
Outlines the general and specific electrical requirements for various Ultrasound system models.
Details electrical specifications for console Ultrasound Systems, including specific models.
Details electrical specifications for laptop Ultrasound Systems, including adapters and docking carts.
Details electrical specifications for handheld Ultrasound Systems, specifically the Venue Series.
Details electrical requirements for EchoPAC PC Turnkey and LOGIQworks Workstations.
Recommends that the branch circuit breaker for the system be readily accessible.
Specifies requirements for dedicated AC power outlets and their proximity to the system.
Instructs on contacting GE for power cables if the system arrives without one or with the wrong one.
Discusses susceptibility to Electromagnetic Interference (EMI) and potential sources.
Provides details on preventing and abating Electromagnetic Interference (EMI).
Refers to user manuals for probe operation and storage temperature information.
Advises starting site preparation checks early and recommends two people for delivery/unpacking.
Outlines general facility requirements and purchaser responsibilities for site preparation.
Details the purchaser's responsibilities in preparing the site, including procuring materials and completing preparations.
Lists essential facility requirements, including power, door opening, and space for cooling.
Lists features that are beneficial but not strictly required for the Ultrasound system installation.
Describes procedures intended to maintain the quality and performance of the Ultrasound system.
Summarizes the contents and scope of the Care and Maintenance chapter.
Presents critical warnings related to system operation, maintenance, and safety.
Explains the importance of maintaining records and having a quality assurance program for Ultrasound systems.
Addresses how often maintenance tasks should be performed based on system usage.
Details system maintenance steps including preliminary checks, functional checks, and inspections.
Details the functional checks for various system components and modes of operation.
Describes functional checks for GE-approved peripherals and hardware options.
Provides instructions for inspecting the mains power cable and its connectors.
Suggests reviewing error logs and running diagnostics to complete system checks.
Guides through a physical inspection of the system's labeling, covers, controls, and components.
Refers to the User Manual for instructions on cleaning the Ultrasound console.
Refers to the User Manual for instructions on cleaning the air filter.
Provides guidance on probe maintenance, checks, cleaning, and disinfecting procedures.
Explains the use of a Phantom for Quality Assurance Program tests, except for Invenia ABUS Scan Station.
Introduces the topics and measurements covered in electrical safety testing.
Discusses terms and precautions related to using an Uninterrupted Power Supply (UPS).
Provides an overview of electrical safety tests based on IEC60601 and IEC62353 standards.
Summarizes acceptance limits and test conditions for leakage currents according to international standards.
Lists leakage current limits for specific Ultrasound system series based on voltage mains.
Details how to test outlets for proper grounding and wiring arrangement using an outlet tester.
Explains how to measure resistance to ensure proper grounding continuity of the Ultrasound system.
Describes the test for enclosure/chassis leakage current to verify power line isolation from the chassis.
Provides a generic procedure for performing chassis leakage current tests.
Offers a typical format for recording enclosure/chassis leakage current data.
Details the test to measure current flowing to ground from isolated ECG leads.
Provides a generic procedure for testing isolated patient lead (source) leakage to ground.
Explains how to test leakage current between patient lead positions.
Refers to a table format for recording patient lead to lead leakage current.
Describes the test for isolated patient lead (sink) leakage and isolation.
Refers to a table format for recording isolated patient lead (sink) leakage current.
Details the test for current flow from probes through a patient to ground.
Describes the common method for measuring probe leakage using a saline bath.
Details the test for isolated probe (sink) leakage and isolation.
Explains the sink leakage test where mains voltage is applied to the part.
Illustrates a test setup for TEE probes and refers to other setups for non-TEE probes.
Provides troubleshooting steps for common issues when excessive leakage current is detected.
Advises on performing Equipment and Image Quality Checks with a GE Service Representative.
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