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GE Medical Systems LOGIQ 7 Quick Manual

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Download this manual See also: Reference Manual
GE Medical Systems
Technical
Publications
Direction 2291859-100
Rev. 1
LOGIQ 7
0459
Quick Guide
Copyright© 2002 By General Electric Co.
Operating Documentation

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Summary of Contents for GE Medical Systems LOGIQ 7

  • Page 1 GE Medical Systems Technical Publications Direction 2291859-100 Rev. 1 LOGIQ 7 0459 Quick Guide Copyright© 2002 By General Electric Co. Operating Documentation...

  • Page 2: Regulatory Requirement

    Regulatory Requirement GE Medical Systems GE Medical System: Telex 3797371 P. O. Box 414, Milwaukee, Wisconsin 53201 U.S.A. (Asia, Pacific, Latin America, North America) GE Ultraschall TEL: 0130 81 6370 toll free Deutschland GmbH & Co. KG TEL: (49)(0) 212.28.02.207 Beethovenstraße 239, Postfach 11 05 60, D-42655 Solingen...

  • Page 3: Revision History

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Revision History DATE REASON FOR CHANGE November 1, 2001 Initial Release November 15, 2002 R2.1.0 Release List of Effective Page PAGE REVISION NUMBER HISTORY Title Rev. 1 A and B Rev. 1 1-54 Rev.
  • Page 4 LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 FOR USA ONLY CAUTION “United Sates law restricts this device to sale or use by or on the order of a physician” if sold in the United States.

  • Page 5: System Power

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 System Power 3. Unwrap the power cable. Make sure to allow Press the Power switch to turn the power on. The sufficient slack in the cable so that the plug is circuit breaker must also be in the on position.

  • Page 6: Power Off

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Power Off Starting an Exam To power down the system: You need to select a pre-configured dataflow that sets up the ultrasound system to work according to 1. Press the Power switch at the front of the the services associated to the dataflow.

  • Page 7: New Patient

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Starting an Exam New Patient Probe Selection Category Selection Window [2] Select the appropriate exam application. To start a new patient’s exam, Select a probe from the Touch Panel (the system automatically selects the last-used application for Function Selection Window [3] 1.

  • Page 8: Logiq 7 Control Panel Tour

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 LOGIQ 7 Control Panel Tour 4. Audio Volume. Press to turn microphone on/off; 10. Imaging/Measurement Keys: Clear, Comment, rotate to adjust speaker volume. Body Pattern, Ellipse, Measure, Zoom, M/D 1. Touch Panel. Touch the Touch Panel to adjust Cursor, Scan Area, Set.

  • Page 9: Logiq 7 Touch Panel Tour

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 LOGIQ 7 Touch Panel Tour In general, the key status is indicated at the top of 3. Progress/Select keys are used for controls that 6. Press to move to the next Touch Panel page.

  • Page 10: Logiq 7 Monitor Display Tour

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 LOGIQ 7 Monitor Display Tour 1. Institution/Hospital Name, Date, Time, Operator 8. Measurement Summary Window. 17. Depth Scale. Identification. 9. Image. 18. Image Management Menu: Menu, Delete, and 2. Patient Name, Patient Identification.
  • Page 11 LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 B/M-Mode Image Optimize Edge Enhance B Softener Edge Enhance brings out subtle tissue differences Affects amount of lateral smoothing. Power Output and boundaries by enhancing the gray scale Suppression differences corresponding to the edges of Optimizes image quality and allows user to reduce structures.

  • Page 12: B-Mode Control Panel Controls

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 B/M-Mode Image Optimize (continued) Anatomical M Mode Reverse Frequency. Changes system parameters to best optimize for a particular patient type. Allows you to rotate or move the M line in order to Flips the image left/right.

  • Page 13: Color Flow/Pw Doppler Image Optimize

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Color Flow/PW Doppler Image Optimize PRF/Wall Filter Velocity scale determines pulse repetition Allows a specific color map to be selected. After a Angle Correct frequency. If the sample volume gate range selection has been made, the color bar displays the exceeds single gate PRF capability, the system resultant map.

  • Page 14: Color Flow Control Panel Control

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Color Flow/PW Doppler Image Optimize (continued) Modify Auto Calcs Compression To decrease motion artifact. Increase the PRF, and increase the Wall Filter. Press to select desired Auto Calcs. Increase to make frozen image appear more To eliminate aliasing.

  • Page 15: Basic Measurements

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Basic Measurements NOTE: The following instructions assume that you Circumference/Area (Ellipse) Measurement Circumference/Area (Trace) Measurement first scan the patient and then press Freeze. 1. Press Measure once; an active caliper 1. Press Measure twice; a trace caliper displays.

  • Page 16: Time Interval Measurement

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Volume Velocity Measurement Worksheets 1. To make a volume calculation, do one of the 1. Press Measure; an active caliper with a vertical Measurement/Calculation worksheets are available following: dotted line displays. to display and edit measurements and calculations.

  • Page 17: Using Probes

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Using Probes Connecting a probe Activating the probe Ensure that the probe is placed gently in the probe holder. 1. Place the probe's carrying case on a stable Select the appropriate probe from the probe Disconnecting the probe surface and open the case.

  • Page 18: Probe Features

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Probe Features Table 1-2: Probe Features Probe Feature 3.5C i12L M12L Coded Excitation Coded Harmonics B-Flow Coded Contrast LOGIQ View Virtual Convex Easy 3D Advanced 3D Anatomical M Mode M Color Flow...

  • Page 19: Probe Safety

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Probe Cleaning and Disinfection Instructions Probe Safety Ultrasound probes are highly sensitive medical instruments that can easily be damaged by improper handling. Use care when handling and protect from damage when not WARNING in use.

  • Page 20: Probe Cleaning, After Each Use

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Probe Cleaning, After Each Use Probe Immersion Levels Probe Disinfection Agents 1. Disconnect probe from ultrasound console and The following high level disinfectant agents have remove all coupling gel from probe by wiping been approved for use with all probes: 3.5C...

  • Page 21: Image Management

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Image Management Formatting a CD/MOD Backing Up Patient Information 1. Insert the backup media. Format the backup Format a CD/MOD prior to following these steps. Clipboard media, CD-ROM or MOD. Select the Utility tab 1.

  • Page 22: Moving (Archiving) Images

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Saving Images as JPEG files and CINE Moving (Archiving) Images 2. Fill in the From Date, then press Recalculate. Specify to Keep days together. Check that you Loops as AVI files Format a CD/MOD prior to following these steps.

  • Page 23: Dataflow Concept

    Importing Patient Data/Images Connectivity Format a CD/MOD prior to following these steps. 1. At another Ultrasound system, insert the MOD Connectivity on the LOGIQ 7 is based on the or CD-ROM. Dataflow concept. 1. Press Patient. Deselect any selected patient(s) 2.

  • Page 24: Configuring Connectivity

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Configuring Connectivity Services (better known as Destinations) Login as Administrator. Press the left Utility tab. Select the Connectivity tab. Configure the menus from right to left, starting with TCP/IP first. 1. Select the Server from the pull-down menu.
  • Page 25 LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Buttons Dataflow NOTE: Remember to specify each service Role as Primary or Secondary. The primary service You can assign print buttons (P1-P4) to a device or Creates a Dataflow, (‘WL-LA-DServ -- Worklist, specifies what always happens first to incoming or to a dataflow.

  • Page 26: Verifying A Device

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Verifying a Device Views Pinging a Device (DICOM Echo) Select the device, press DICOM Verify. Views a snapshot of this ultrasound system’s Select the device, press Check. connectivity architecture (onboard network +...
  • Page 27 LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 DICOM Status To check the status of all DICOM jobs or redirect DICOM jobs, press F4. Image/ Patient Management and Connectivity...

  • Page 28: Using Cine

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Using CINE Start Frame/End Frame Disconnecting B-Mode CINE from Timeline CINE Turn the Start Frame dial to the left to move to the Activating CINE beginning of the CINE Loop. Turn the dial to the To review the B-Mode CINE Loop only, press Cine right to move forward through the CINE Loop.

  • Page 29: Manipulating The 3D Scan

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Easy 3D Acquiring a 3D Scan Manipulating the 3D Scan Performing a Surface Render 1. Optimize the B-Mode image. Ensure even gel Imagine you are able to manipulate the 3D volume From the 3D Touch Panel, press 3D, then press coverage.
  • Page 30 LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Contact Information Placing an Order INTERNET ASIA http://www.gemedicalsystems.com To place an order, order supplies or ask an GE Medical Systems Asia accesory-related question in the United States, call Asia Support Center the GE Access Center: TEL: (1) 800-472-3666...
  • Page 31 LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 DENMARK LUXEMBOURG SPAIN GE Medical Systems TEL: 0800 2603 toll free GE Medical Systems España Fabriksparken 20 Hierro 1 Arturo Gimeno DK-2600 GLOSTRUP MEXICO Poligono Industrial I TEL: +45 4348 5400 -- FAX: +45 4348 5399 E-28850 TORREJON DE ARDOZ GE Sistemas Médicos de Mexico S.A.

  • Page 32: Paperless Documentation

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Paperless Documentation Introduction Using Online Help Via F1 Navigating Through Help Documentation is being provided via: Online Help is available via the F1 key. Online Help is organized like a manual, with individual chapters, sections, and pages.

  • Page 33: Help Links

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Help Links Creating a List of Favorite Topics in Help Using the Help Index After you click on a blue, underlined portion of text, You may find that there are topics you need to refer Or, you can look for topics by using the Index.

  • Page 34: Accessing Documentation Via A Pc

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Accessing Documentation Via a PC Accessing Documentation on the 3. Select Scanner Utilities. Ultrasound Scanner Via the CD-ROM To view user documentation on a PC, To access documentation via the CD-ROM, 1. Insert the CD into the CD drive.
  • Page 35 LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Precaution Levels Icon description Various levels of safety precautions may be found on the equipment and different levels of concern are identified by one of the following flag words and icons which precede the precautionary statement .

  • Page 36: Hazard Symbols - Icon Description

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Hazard Symbols - Icon Description Potential hazards are indicated by the following icons: Table 1-1: Potential Hazards Icon Potential Hazard Usage Source Biological • Patient/user infection due to contaminated equipment. • Cleaning and care instructions ISO 7000 •...

  • Page 37: Important Safety Considerations

    Improper use can result in serious injury. The user must be thoroughly familiar with the instructions and potential hazards involving CAUTION ultrasound examination before attempting to use the device. Training assistance is available from GE Medical Systems if needed. The equipment user is obligated to be familiar with these concerns and avoid conditions that could result in injury.

  • Page 38: Mechanical Hazards

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Related Hazards (continued) Mechanical hazards The use of damaged probes or improper use and manipulation of intracavity probes can result in injury or increased risk of infection. Inspect probes often for sharp, pointed, or rough surface damage that could cause injury or tear protective barriers.

  • Page 39: Equipment And Personnel Safety

    Never use any adaptor or converter of a three-prong-to-two-prong type to connect with a mains power plug. The protective earth connection will loosen. • Do not place liquids on or above the console. Spilled liquid may contact live parts and increase the risk of shock. • Plug any peripherals into the LOGIQ 7 AC power outlet. Safety...
  • Page 40 LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Related Hazards (continued) Do not use this equipment if a safety problem is known to exist. Have the unit repaired and performance verified by qualified service CAUTION personnel before returning to use.
  • Page 41 Archived data is managed at the individual sites. Performing data backup (to any device) is recommended on a daily basis. CAUTION CAUTION Do not unpack the LOGIQ 7. This must be performed by qualified service personnel only. CAUTION Do not use the LOGIQ 7 Ultrasound system ECG wave for diagnosis and monitoring.

  • Page 42: Device Labels

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Device Labels Label Icon Description The following table describes the purpose and location of safety labels and other important information provided on the equipment. Table 1-2: Label Icons Label/Icon Purpose/Meaning Location Identification and Rating Plate Manufacture’s name and address...
  • Page 43 LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Table 1-2: Label Icons Label/Icon Purpose/Meaning Location “ON” indicates the power on position of the power switch. Refer to Chapter 3 in the Basic User Manual for CAUTION: This Power Switch DOES NOT ISOLATE Mains Supply.
  • Page 44 LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Classifications Type of protection against electric shock Class I Equipment (*1) Degree of protection against electric shock Type BF Applied part (*2) (for PCG, Probes marked with BF symbol) Type CF Applied part (*3)
  • Page 45 LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 EMC (Electromagnetic Compatibility) NOTE: This equipment generates, uses and can radiate radio frequency energy. The equipment may cause radio frequency interference to other medical and non- medical devices and radio communications. To provide reasonable protection against such interference, this product complies with emissions limits for a Group 1, Class A Medical Devices Directive as stated in EN 60601-1-2.

  • Page 46: Emc Performance

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 (continued) EMC Performance All types of electronic equipment may characteristically cause electromagnetic interference with other equipment, either transmitted through air or connecting cables. The term EMC (Electromagnetic Compatibility) indicates the capability of equipment to curb electromagnetic influence from other equipment and at the same time not affect other equipment with similar electromagnetic radiation from itself.

  • Page 47: Notice Upon Installation Of Product

    2. Locate the equipment as far away as possible from other electronic equipment. 3. Be sure to use only the cables provided by or designated by GE Medical Systems. Connect these cables following the installation procedures (i.e. wire power cables separately from signal cables).

  • Page 48: Peripheral Update For Ec Countries

    1. The added device must have appropriate safety standard conformance and CE Marking. 2. The total power consumption of the added devices, which connect to the LOGIQ 7 and are used simultaneously, must be less than or equal to the rated supply of the LOGIQ 7.

  • Page 49: Declaration Of Emissions

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Peripheral Update for EC countries (continued) General precautions for installing an alternate off-board, remote device or a network would include: 1. The added device(s) must have appropriate safety standard conformance and CE Marking.

  • Page 50: Declaration Of Immunity

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Declaration of Immunity This system is suitable for use in the following environment. The user must assure that the system is used according to the specified guidance and only in the electromagnetic environment listed.

  • Page 51: Patient Environmental Devices

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Patient Environmental Devices Figure 1-1. Patient Environmental Devices 1. Peripheral Device (Signals I/O Port, Power In) 10. Signals I/O Port 19. Power Telephone Line 2. Front Panel (Signal I/O Port, Power Out) 11.

  • Page 52: Acceptable Devices

    If devices are connected without the approval of GE, the warranty will be INVALID. Any device connected to the LOGIQ 7 must conform to one or more of the requirements listed below: 1. IEC standard or equivalent standards appropriate to devices.

  • Page 53: Acoustic Output

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Acoustic Output Located on the upper right section of the system display monitor, the acoustic output display provides the operator with real-time indication of acoustic levels being generated by the system. See the Acoustic Output chapter in the Advanced Reference Manual for more information. This display is based on NEMA/AIUM Standards for Real-time Display of Thermal and Mechanic Acoustic Output Indices on Diagnostic Ultrasound Equipment.

  • Page 54: Best Practices While Scanning

    Acoustic Output Default Levels In order to assure that an exam may not start at a high output level, the LOGIQ 7 may initiate scanning at a reduced default output level. This reduced level is preset programmable and depends upon the exam category and probe selected. It takes effect when the system is powered on or New Patient is selected.

  • Page 55: Warning Label Locations

    5. The CE Mark of Conformity indicates this equipment conforms with the Council Directive 93/42/EEC. 6. CISPR CAUTION: The LOGIQ 7 conforms to the CISPR11, Group 1, Class A of the international standard for Electromagnetic disturbance characteristics. 7. Voltage Range (Indication label) 8.
  • Page 56 LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Console Labels (continued) 1.ETL Label: NRTL Listing and Certification Mark is used to designate conformance to nationally recognized product safety standards. The Mark bears the name and/or logo of the testing laboratory, product category, safety standard to which conformity is assessed, and a control number.

  • Page 57: Mailing Address

    LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 Fax Back Form You can order printed documentation by faxing this form to Coakley-Tech. Customer Name Telephone Number Mailing Address Quantity Publication Direction Number Basic User Manual 2286866-100, 101, 106, 127 Quick Guide...
  • Page 58 LOGIQ 7 Quick Guide Direction 2291859-100 Rev. 1 This page intentionally left blank.

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