Do you have a question about the GE LOGIQ C5 and is the answer not in the manual?
Brand | GE |
---|---|
Model | LOGIQ C5 |
Category | Medical Equipment |
Language | English |
Identifies and explains the function of each control on the system's panel.
Details menu keys, function keys, and programming custom functions.
Describes the various information and indicators shown on the system monitor.
Instructions for system power-up and understanding LED status indicators.
Steps to safely shut down and power off the ultrasound system.
Guides on operator selection, login, and entering new patient data.
Details controls for optimizing B/M mode image quality.
Explains parameters for enhancing Doppler and Color Flow image quality.
Instructions for distance, area, and depth measurements using calipers.
Details Doppler velocity and ratio calculations (PI, RI, S/D).
Instructions on activating, playing, and controlling CINE loops for image review.
Steps for acquiring, manipulating, and rendering 3D ultrasound volumes.
Procedures for connecting, activating, and disconnecting ultrasound probes safely.
Lists recommended applications for various ultrasound probes.
Provides technical details for system probes, including frequencies.
Essential safety guidelines for handling ultrasound probes to prevent damage and hazards.
Step-by-step instructions for cleaning and disinfecting ultrasound probes after use.
Explains the meaning of precaution levels (DANGER, WARNING, CAUTION) and icons.
Describes potential hazards like biological, electrical, explosion, and fire.
Emphasizes patient safety, proper identification, and diagnostic data integrity.
Covers electrical safety, voltages, and proper grounding procedures.
Explains protection classes (I, II) and applied part types (BF, CF).
Covers clipboard, printing, browsing, managing, and deleting images.
Instructions for saving ultrasound images and data to a USB memory stick.
Guides setting up TCP/IP and network parameters for system connectivity.
Details configuring DICOM services, destinations, and verifying connections.
Explains how to create and configure dataflows for system operations.
Discusses EMI, its effects, and measures to mitigate interference.
Guidelines for installing the system and maintaining separation from RF sources.
Lists peripherals verified for safety and compatibility within the patient environment.
Declares compliance with RF emissions standards for the system's intended use.
Details the system's compliance with electromagnetic immunity standards.
Identifies the location and meaning of warning labels on the equipment console.
Form for ordering printed manuals by fax.