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GE LOGIQ 7 Pro Quick Manual

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GE Healthcare
Technical
Publications
Direction 5307393-100
Rev. 1
LOGIQ 7/LOGIQ 7 Pro
Quick Guide
R8.x.x
Copyright 2008 By General Electric Co.
Operating Documentation

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Summary of Contents for GE LOGIQ 7 Pro

  • Page 1 GE Healthcare Technical Publications Direction 5307393-100 Rev. 1 LOGIQ 7/LOGIQ 7 Pro Quick Guide R8.x.x Copyright 2008 By General Electric Co. Operating Documentation...

  • Page 2: Regulatory Requirement

    LOGIQ 7/LOGIQ 7 Pro complies with regulatory requirements of the following European Directive 93/42/EEC concerning medical devices. This manual is a reference for the LOGIQ 7/LOGIQ 7 Pro. It applies to all versions of the R8.x.x software and later for the LOGIQ 7/LOGIQ 7 Pro ultrasound systems.

  • Page 3: Revision History

    Please verify that you are using the latest revision of this document. Information pertaining to this document is maintained on ePDM/ MyWorkshop (GE Healthcare Electronic Product Data Management). If you need to know the latest revision, contact your distributor, local GE...
  • Page 4 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 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/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 System Power Power On Unwrap the power cable. Make sure to allow Press the Power switch to turn the power on. The circuit sufficient slack in the cable so that the plug is not breaker must also be in the on position.
  • Page 6 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Power Off Standby Mode Starting an Exam To power down the system: Standby Mode pauses the system without completely You need to select a pre-configured dataflow that sets up shutting down and restarting the system. This is...

  • Page 7: Probe Selection

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Starting an Exam New Patient Probe Selection Function Selection Window [2] New Patient is used to clear the patient entry screen to To start a new patient’s exam, Select a probe from the Touch Panel (the system input a new patient’s data into the database.
  • Page 8 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 LOGIQ 7/LOGIQ 7 Pro Control Panel Tour Additional Feature Keys. Patient, LOGIQView, 3D/ 13. Freeze and Print Keys. Press Freeze to 4D, Contrast, Harmonics. Press to activate these freeze the image; press the P keys to archive, print, Touch Panel.
  • Page 9 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 LOGIQ 7/LOGIQ 7 Pro Touch Panel Tour In general, the key name is indicated at the top of the key. Press knob below the Touch Panel to select There are different types of Touch Panel keys: additional control, then rotate the knob to set values.
  • Page 10 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 LOGIQ 7/LOGIQ 7 Pro Monitor Display Tour Institution/Hospital Name, Date, Time, Operator 10. Measurement. 20. Current date/time, Caps Lock (lit when on), network Identification. connection indicator (PC=connected, PC with X=not 11.

  • Page 11: B/M-Mode Image Optimize

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 B/M-Mode Image Optimize SRI-HD (Option) B Softener SRI-HD (High Detection Speckle Reduction Imaging) is Affects amount of lateral smoothing. an adaptive algorithm to reduce the unwanted effects of Power Output speckle in the ultrasound image.
  • Page 12 Display Format position the Zoom ROI. Changes the horizontal/vertical display layout between B- Reverse Mode and M-Mode. Flips the image left/right. The GE symbol flips B-Flow (Option) accordingly. Provides a more intuitive representation of non- Multi Image quantitative hemodynamics in vascular structures.
  • Page 13 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Color Flow/Doppler Image Optimize Angle Correct Invert Trace Method Estimates the flow velocity in a direction at an angle to Allows blood flow to be viewed from a different Specify Max, Mean, or Off.

  • Page 14: Color Flow Control Panel Control

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Color Flow/Doppler Image Optimize (continued) PW/CF Ratio Continuous Wave Doppler To decrease motion artifact. Increase the PRF, and increase the Wall Filter. The PW/CF Ratio is active when “Depend Triplex” is on in Allows examination of blood flow data all along the triplex mode.

  • Page 15: Basic Measurements

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Basic Measurements Circumference/Area (Ellipse) Measurement Circumference/Area (Trace) Measurement NOTE: The following instructions assume that you first scan the patient and then press Freeze. Press Measure once; an active caliper displays.
  • Page 16 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Circumference and area (Spline trace) Echo Level measurement measurement To make an echo level measurement; To trace the circumference of a portion of the anatomy Press Measure three times to enable the echo level and calculate its area: measurement.
  • Page 17 This would be V for PI, peak velocity Time Interval Measurement For more information, see the LOGIQ 7/LOGIQ 7 Pro for RI, systole for PS/ED ratio, “A” velocity for A/B Basic User Manual Chapter 14 “ReportWriter”. Press Measure twice; and active caliper with a ratio or diastole for ED/PS ratio.

  • Page 18: Using Probes

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Using Probes Connecting a probe Deactivating the probe Place the probe's carrying case on a stable surface When deactivating the probe, the probe is automatically and open the case. placed in standby mode.
  • Page 19 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Probe Application Table 1: Probe Indications for Use Probe Application 3.5C 3.5CS M7C* BE9C 3CRF i12L M12L T739 Abdomen Small Parts Periph. Vasc. Obstetrics Gynecology Pediatrics Neonatal Urology Surgery Cardiac...
  • Page 20 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Probe Application (continued) Table 2: Probe Indications for Use Probe Application P2D P6D 4D10L 4D3C-L 4DE7C Abdomen Small Parts Periph. Vasc. Obstetrics Gynecology Pediatrics Neonatal Urology Surgery Cardiac Transcranial Transesophageal...

  • Page 21: Probe Features

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Probe Features Table 3: Probe Features Probe Feature 3.5C 3.5CS M7C* BE9C 3CRF i12L M12L T739 Coded Excitation Coded Harmonics B-Flow SRI-HD Coded Contrast LOGIQ View Virtual Convex Easy 3D...
  • Page 22 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Probe Features Table 4: Probe Features Probe Feature M3S* 4D10L 4D3C-L 4DE7C Coded Excitation Coded Harmonics B-Flow SRI-HD Coded Contrast LOGIQ View Virtual Convex Easy 3D Advanced 3D Volume 3D/4D...

  • Page 23: Probe Cleaning And Disinfection Instructions

    • DO NOT kink, tightly coil, or apply excessive force on the probe cable. Insulation failure may result. • Electrical leakage checks should be performed on a routine basis by GE Service or qualified hospital personnel. Refer to the service manual for leakage check procedures.
  • Page 24 Probe Cleaning, After Each Use Probe Immersion Levels You MUST disconnect the probe from the LOGIQ 7/ LOGIQ 7 Pro prior to cleaning/disinfecting the probe. Disconnect probe from ultrasound console and Failure to do so could damage the system. remove all coupling gel from probe by wiping with a BE9C soft cloth and rinsing with flowing water.

  • Page 25: Image Management

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Image Management Clipboard Formatting a storage medium Backing Up Patient Information As images are saved by pressing any of the print keys Insert the backup media. Format the backup media.
  • Page 26 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Moving Data Between Ultrasound Systems Query/Retrieve (Q/R) Send To the DICOM device There are 5 options (Import, Export, Q/R, Worklist and MPEGvue) under Data Transfer. Press Patient and select Data Transfer.
  • Page 27 NOTE: Time line image can be saved as multi frames • RawDICOM: saves the still image or CINE Loop image with SaveAs. 3D/4D images can't be saved with in both GE raw format and DICOM format. WMV format. Image/ Patient Management and Connectivity...
  • Page 28 Services Type in the Computer’s Name. Identify the Ultrasound To add the services, Connectivity on the LOGIQ 7/LOGIQ 7 Pro is based on system to the rest of the network by filling in its IP the Dataflow concept. Select the destination device.
  • Page 29 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Dataflow Buttons Miscellaneous A dataflow is a set of pre-configured services. For You can assign print buttons to a device or to a dataflow. Set up Patient/Exam menu options and Printer and Store...
  • Page 30 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 DICOM Status Status Description To check the status of all DICOM jobs or redirect DICOM FAILED Failed. It stays in spooler. Select Retry or jobs, press F4. delete for the job to complete.

  • Page 31: Using Cine

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Using CINE Start Frame/End Frame Cine Capture Turn the Start Frame dial to the left to move to the Selecting Cine Capture will search through all images beginning of the CINE Loop. Turn the dial to the right to...
  • Page 32 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Easy 3D Acquiring a 3D Scan Adjusting the 3D Volume of Interest Optimize the B-Mode image. Ensure even gel You can colorize the 3D volume of interest. coverage. You can resize the VOI by adjusting the scan distance.
  • Page 33 TEL: 0 800 11733 toll free EUROPE FAX: +32 0 3 320 12 59 Service Questions TLX: 72722 GE Ultraschall For service in the United States, call GE CARES Deutschland GmbH & Co. KG BRAZIL TEL: (1) 800-437-1171 Beethovenstraße 239 Postfach 11 05 60 GE Sistemas Médicos...
  • Page 34 Poligono Industrial I TEL: +45 4348 5400 -- FAX: +45 4348 5399 E-28850 TORREJON DE ARDOZ GE Sistemas Médicos de Mexico S.A. de C.V. TEL:900 95 3349 free -- FAX: +34 1 675 3364 Rio Lerma #302, 1º y 2º Pisos...

  • Page 35: Using Online Help Via F1

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 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 36 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 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 37 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Accessing Documentation Via a PC 3. Press Utilities and insert the CD-ROM. 5. Select Scanner Documentation Interface. To view user documentation on a PC, 1. Insert the CD into the CD drive.

  • Page 38: Precaution Levels

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 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 39: Hazard Symbols - Icon Description

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 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.

  • Page 40: Important Safety Considerations

    Applications training is available through the local GE representative. Added confidence in the equipment operation can be gained by establishing a quality assurance program.
  • Page 41 This equipment does not have a defibrillator approved applied part. Training It is recommended that all users receive proper training in applications before performing them in a clinical setting. Please contact the local GE representative for training assistance. ALARA training is provided by GE Application Specialists. The ALARA education program for the clinical end-user covers basic ultrasound principles, possible biological effects, the derivation and meaning of the indices, ALARA principles, and examples of specific applications of the ALARA principle.

  • Page 42: 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/LOGIQ 7 Pro AC power outlet.
  • Page 43 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 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 44 Archived data is managed at the individual sites. Performing data backup (to any device) is recommended on a daily basis. CAUTION Do not unpack the LOGIQ 7/LOGIQ 7 Pro. This must be performed by qualified service personnel only. CAUTION Do not use the LOGIQ 7/LOGIQ 7 Pro Ultrasound system ECG wave for diagnosis and monitoring.

  • Page 45: Device Labels

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 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...
  • Page 46 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Table 1-2: Label Icons Label/Icon Purpose/Meaning Location “Mains ON” indicates the power on position of the mains power breaker. Refer to Chapter 3 in the Basic User Manual for location information.
  • Page 47 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Table 1-2: Label Icons Label/Icon Purpose/Meaning Location Indicates the presence of hazardous substance(s) above the maximum concentration value. Maximum Rear Panel concentration values for electronic information products, as set by the People’s Republic of China Electronic Industry Standard SJ/T11364-2006, include the hazardous substances of lead, mercury, hexavalent chromium, cadmium, polybrominated biphenyl (PBB), and polybrominated diphenyl ether (PBDE).
  • Page 48 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 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 49 NOTE: Do not use devices which intentionally transmit RF Signals (cellular phones, transceivers, or radio controlled products) other than those supplied by GE (wireless microphone, for example) in the vicinity of the equipment as it may cause performance outside the published specifications. Keep the power to these type devices turned off when near this equipment.

  • Page 50: Emc Performance

    Portable and mobile radio communications equipment (e.g. two-way radio, cellular/cordless telephones, wireless computer networks) other than those supplied by GE (wireless microphone, for example) should be used no closer to any part of this system, including cables, than determined according to the following method:...
  • Page 51 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 52 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/LOGIQ 7 Pro and are used simultaneously, must be less than or equal to the rated supply of the LOGIQ 7/LOGIQ 7 Pro.

  • Page 53: Declaration Of Emissions

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 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 54: Declaration Of Immunity

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 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 55: Patient Environmental Devices

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Patient Environmental Devices Figure 1. Patient Environmental Devices 1. Peripheral Device (Signals I/O Port, Power In) 11. Signals I/O Port 20. Power Telephone Line 2. Front Panel (Signal I/O Port, Power Out) 12.

  • Page 56: Acceptable Devices

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

  • Page 57: Acoustic Output

    LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 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 58: Controls Affecting Output

    Acoustic Output Default Levels In order to assure that an exam may not start at a high output level, the LOGIQ 7/LOGIQ 7 Pro 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 59 LOGIQ 7/LOGIQ 7 Pro Quick Guide Direction 5307393-100 Rev. 1 Warning Label and Caution Label Locations (21) (17) (10) Label for China 100‑120V〜 Japan/USA/Asia Console(100V) 220‑2 4 0V〜 CAUTION (18) (11) (12) 제품명 : 초음파영상진단장치 (13) 형 명 : L OGIQ 7 수입자...
  • Page 60 5. The CE Mark of Conformity indicates this equipment conforms with the Council Directive 93/42/EEC. 6. WEEE symbol 7. CISPR CAUTION: The LOGIQ 7/LOGIQ 7 Pro conforms to the CISPR11, Group 1, Class A of the international standard for Electromagnetic disturbance characteristics. 8. Voltage Range (Indication label) 9. Signal ground point label CAUTION: This is only for “FUNCTIONAL GROUNDING”, NOT “PROTECTIVE EARTH”.

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