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General| Brand | GE |
|---|---|
| Model | Vivid q |
| Category | Medical Equipment |
| Language | English |
Details the reasons for each revision of the document.
Lists all effective pages in the document and their revision numbers.
Lists the topics covered in the manual, organized by chapter.
Describes the Ultrasound System, its architecture, and signal flow.
Lists all the specific Ultrasound system models covered by this manual.
Provides a brief overview of the Safety Information chapter.
Lists the sections and their corresponding page numbers within the Safety Information chapter.
Explains conventions used throughout the document for clarity.
Explains the use of pictures and icons to reinforce printed messages.
Indicates severe hazards that can cause death or severe injury if ignored.
Indicates hazards that can cause severe personal injury or property damage.
Indicates hazards that can cause minor injury or property damage.
Lists common hazard icons and their meanings (Electrical, Mechanical, Radiation, Laser, Heat, Pinch).
Lists icons indicating special procedures like Avoid Static Electricity, Tag and Lock Out, Hand/Foot/Eye Protection.
Refers to the User's Manual for descriptions and locations of system icons.
Instructs on how to secure the Operator Panel for safe transport.
Introduces the safety precautions to be observed during operation, service, and repair.
Details safety precautions related to personnel and their interaction with the equipment.
Provides guidelines to minimize shock hazards when using the Ultrasound System.
Refers to the User Manual for a full list of product labels.
Precedes potentially dangerous procedures and lists instructions that must be followed.
Outlines the steps and requirements for applying Lockout/Tagout procedures.
Specifies cleaning and decontamination requirements for returned parts.
Defines the customer's responsibility regarding data backup and equipment cleaning.
Explains what Electromagnetic Compatibility (EMC) is and its importance.
States the system's compliance with EMC standards and requirements.
Provides an overview of the Site Preparations chapter.
Lists the sections within the Site Preparations chapter.
Lists the topics covered within the General Ultrasound system requirements section.
Details environmental conditions for system operation and acclimation.
Specifies the cooling requirements for the Ultrasound system.
Discusses lighting requirements for installation, updates, and repairs.
Outlines general requirements for power and ground for system operation.
Details the electrical requirements for different types of Ultrasound systems.
Details electrical requirements for console models.
Lists electrical requirements for the Invenia ABUS Scan Station.
Lists electrical requirements for various LOGIQ console models.
Provides electrical specifications for LOGIQ C Series and C3/C5 Premium models.
Lists electrical requirements for various Vivid console models.
Lists electrical requirements for various Voluson console models.
Details electrical requirements for laptop models.
Lists electrical requirements for LOGIQ laptop models.
Lists electrical requirements for Vivid laptop models.
Lists electrical requirements for Voluson laptop models.
Details power requirements for specific docking carts.
Details power requirements for specific docking carts.
Lists input/output specifications for isolation carts.
Lists input/output specifications for isolation carts.
Lists input/output specifications for E-Isolation Carts for LOGIQ e.
Lists input/output specifications for Advanced Isolation Carts.
Details electrical requirements for handheld systems.
Lists electrical requirements for Venue Series handheld systems.
Details electrical requirements for workstation models.
Lists electrical requirements for EchoPAC PC Turnkey Workstations.
Lists electrical requirements for LOGIQworks Workstations.
Details methods for preventing and abating Electromagnetic Interference (EMI).
Refers to user manuals for probe temperature information.
Discusses the time and personnel needed for site preparation.
Lists the sections within the Facility Needs chapter.
Details the responsibilities of the purchaser for site preparation.
Provides an overview of the Care and Maintenance chapter.
Outlines mandatory care and maintenance responsibilities and tasks.
Lists the sections within the Care and Maintenance chapter.
Explains the importance of maintaining records for maintenance and quality checks.
Details the customer's responsibility for a quality assurance program and testing.
Discusses the frequency of maintenance tasks based on system usage.
Lists initial checks to perform before system maintenance.
Details the steps for performing preliminary system checks.
Outlines functional checks for various system modes and components.
Details the steps and items for performing functional system checks.
Lists functional checks for GE approved peripherals and hardware options.
Provides a procedure for inspecting the mains power cable and connectors.
Instructs on how to view error and temperature logs for troubleshooting.
Details physical checks for various system components like labeling, covers, and displays.
Explains the use of Phantoms in Care and Maintenance, except for Invenia ABUS.
Lists the topics and measurements covered in the Electrical safety tests section.
Provides leakage current limits for 100-130V mains for specific system types.
Provides leakage current limits for 220-240V mains for specific system types.
Lists ISO and Mains Applied limits for probe types.
Defines equipment types and tests related to leakage current.
Defines the Chassis Leakage Current test.
Provides a generic procedure for performing chassis leakage current tests.
Offers a format for recording enclosure/chassis leakage data.
Provides a typical data format for recording enclosure/chassis leakage.
Defines the test for current flow from ECG leads to ground.
Details the procedure for testing leakage current from patient leads to ground.
Refers to a table for recording patient lead to lead leakage current.
Provides a typical data format for recording patient lead to lead leakage.
Offers a format for recording patient lead to lead leakage.
Refers to tables for recording isolated patient lead sink leakage current.
Provides a format for recording isolated patient lead sink leakage.
Offers a format for recording isolated patient lead sink leakage.
Defines the test for current flow from probes through a patient to ground.
Describes the common method for measuring probe leakage using a saline bath.
Provides a data format for recording probe source leakage current.
Offers a data format for recording probe source leakage current.
Provides a data format for recording isolated probe sink leakage.
Offers a data format for recording isolated probe sink leakage.
Describes troubleshooting steps for AC/DC adapter and cable failures.
Details checks for ground continuity, wiring, and outlet integrity for chassis issues.
Discusses troubleshooting steps for probe failures and connector issues.
Guides on troubleshooting peripheral failures and ground connections.
Outlines isolation steps for troubleshooting when other methods fail.
Addresses actions for new systems failing leakage current tests.
Suggests inspecting cables for damage or poor connections in case of ECG failures.
Refers to GE Service Representative for performing Equipment and Image Quality Checks.
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