Home

LOGIQ P5/A5/A5Pro Quick Guide

Contents

1. 1 kV differential 2 kV common lt 5 gt 95 dip for 0 5 cycle 40 60 dip for 5 cycles 70 30 dip for 25 cycles lt 5 U1 gt 95 dip for 5 sec Floors should be wood concrete or ceramic tile If floors are covered with synthetic material the relative humidity should be at least 30 Mains power quality should be that of a typical commercial and or hospital environment If the user requires continued operation during power mains interruptions it is recommended that the system be powered from an uninterruptable power source UPS NOTE UT is the a c mains voltage prior to application of the test level Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial and or hospital environment Separation distance to radio communication equipment must be maintained according to the Table 1 5 on page 42 Interference may occur in the vicinity of equipment marked with the symbol icd NOTE These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people LOGIQ P5 A5 A5Pro Quick Guide Patient Environmental Devices Peripheral Device Signals I O Port Power In Front Panel Signal I O Port Power Out Non Imaging Probes Imaging Probes Probe Port ECG Cable Physio Signal Input Panel Rear Panel eS Direction 5137113 100
2. 17 Depth Scale 18 Image Management Menu Menu Delete and Image Manager 19 Caps Lock On or Off 20 iLing icon and system messages display not shown on the image 21 Trackball Functionality Status Scroll M amp A Measurement and Analysis Position size Scan Area Width and Tilt 22 Sub menu 12 B5 2 LOGIQ P5 A5 A5Pro Quick Guide B M Mode Image Optimize Power Output Optimizes image quality and allows user to reduce beam intensity 10 increments between 0 100 Values greater than 0 1 are displayed Dynamic Range Dynamic Range controls how echo intensities are converted to shades of gray thereby increasing the adjustable range of contrast Focus Number and Position Increases the number of transmit focal zones or moves the focal zone s so that you can tighten up the beam for a specific area A graphic caret corresponding to the focal zone position s appears on the right edge of the image NOTE Push key to toggle between Focus Number and Focus Position Rejection Selects a level below which echoes will not be amplified an echo must have a certain minimum amplitude before it will be processed Edge Enhance Edge Enhance brings out subtle tissue differences and boundaries by enhancing the gray scale differences corresponding to the edges of structures Adjustments to M Mode s edge enhancement affects the M Mode Preparing for an Exam Direction 5137113
3. 1 Ensure that the wall outlet is of the appropriate type Figure 1 1 Example Plug and Outlet Configurations 1 100 120 VAC 950VA Plug and Outlet Configuration USA 2 220 240 VAC 950VA Plug and Outlet Configuration Europe 2 Ensure that the power switch is turned off Preparing for an Exam 4 Attach the power plug to the system and secure Direction 5137113 100 Rev 3 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 not pulled out of the wall if the system is moved slightly it in place by using the retaining clamp Figure 1 2 Power Plug a Retaining clamp for power plug CAUTION Ensure that the retaining clamp for the power plug is fixed firmly Use caution to ensure that the power cable does not disconnect during system use If the system is Figure 1 3 Power On Switch Location accidentally unplugged data may be lost LOGIQ P5 A5 A5Pro Quick Guide Power Off To power down the system 1 Press the Power On switch at the front of the system once SYSTEM EXIT Logon Information 3 Using the Trackball select Shutdown The shutdown process takes a few seconds and is completed when the control panel illumination is power switch is turned off 4 Disconnect the probes Clean or disinfect all probes as necessary Store them in their s
4. 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 LOGIQ P5 A5 A5Pro Quick Guide Probe Cleaning After Each Use 4 Disconnect probe from ultrasound console and remove all coupling gel from probe by wiping with a soft cloth and rinsing with flowing water Wash the probe with mild soap in lukewarm water Scrub the probe as needed using a soft sponge gauze or cloth to remove all visible residue from the probe surface Prolonged soaking or scrubbing with a soft bristle brush such as a toothbrush may be necessary if material has dried onto the probe surface Rinse the probe with enough clean potable water to remove all visible soap residue Air dry or dry with a soft cloth Probe Disinfection After Each Use LE Prepare the germicide solution according to the manufacturer s instructions Be sure to follow all precautions for storage use and disposal Place the cleaned and dried probe in contact with the germicide for the time specified by the germicide manufacturer High level disinfection is recommended for surface probes and is required for endocavitary and intraoperative probes follow the germicide manufacturer s recommended time Probes for neuro surgical intra operative use must NOT be sterilized with liquid chemical sterilants because of the possibility of neuro toxic residues remaini
5. 0 1 and accuracy is 5096 Controls Affecting Output The potential for producing mechanical bioeffects MI or thermal bioeffects TI can be influenced by certain controls The Acoustic Output control has the most significant effect on Acoustic Output Indirect effects may occur when adjusting other controls Controls that can influence MI and are detailed under the Bioeffects portion of each control in the Modes chapter of the Basic User Manual Always observe the acoustic output display for possible effects LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 50 Best practices while scanning HINTS Raise the Acoustic Output only after attempting image optimization with controls that have no effect on Acoustic Output such as Gain and TGC NOTE Refer to the Optimization sections of the Modes chapter for a complete discussion of each control WARNING Be Sure to have read and understood control explanations for each Mode used before attempting to adjust the Acoustic Output control any control that can effect Acoustic Output Acoustic Use the minimum necessary acoustic output to get the best diagnostic image or measurement during an examination Begin the exam with Output the probe that provides an optimum focal depth and penetration Hazard Acoustic Output Default Levels In order to assure that an exam may not start at a high output level the LOGIQ P5 A5 A5Pro may initiate scanning at a reduced default ou
6. Technical Publications Direction 5137113 100 Rev 3 LOGIQ P5 A5 A5Pro C 0459 Quick Guide Copyright 2008 By General Electric Co Operating Documentation GE Healthcare Regulatory Requirement This product complies with regulatory requirements of the following European Directive 93 42 EEC concerning medical devices 0459 This manual is reference for the LOGIQ P5 A5 A5Pro It applies all versions of the R 3 0 x software for the LOGIQ P5 A5 A5Pro ultrasound system GE Healthcare GE Healthcare Telex 3797371 Box 414 Milwaukee Wisconsin 53201 U S A Asia Pacific Latin America North America GE Ultraschall TEL 49 212 28 02 207 Deutschland GmbH amp Co KG FAX 49 212 28 02 431 BeethovenstraBe 239 Postfach 11 05 60 D 42655 Solingen GERMANY LOGIQ P5 A5 A5Pro Quick Guide REV 2 3 PAGE NUMBER Title A and B 1 52 REVISION HISTORY Rev 3 Rev 3 Rev 3 Direction 5137113 100 Rev 3 Revision History DATE April 18 2007 May 22 2008 Dec 10 2008 List of Effective Page REASON FOR CHANGE Initial Release BTO7 SW Release BTO9 SW Release LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 CAUTION FOR USA ONLY N United Sates law restricts this device to sale or use by or on the order of a physician if sold in the United States LOGIQ P5 A5 A5Pro Quick Guide System Power Power On To connect the system to the electrical supply
7. To add a service 1 Select the destination device 2 Select the service to add and press Add 3 Type the name in the Name Field 4 Specify criteria in the Properties boxes located in the upper right hand side and lower left hand side 5 Press Verify then Save There are two service types that pertain to printers e Standard Printer is used for digital peripherals e Video Capture Device is used for devices that are triggered by a contact closure typically analog devices Service Properties Deon Storage E Properties SSS 2 og 30 Direction 5137113 100 Hev 3 Dataflow The Dataflow page allows you to add services to the selected dataflow For example DICOM services may be for storage worklist verify etc In addition there are other service types like video print or standard color print Set up dataflows for the services 1 Press Add and type the dataflow name in the name field 2 Select the service you want to use under My Computer and press gt gt to add to Dataflow view 3 Press Verify then Save NOTE Query Retrieve MUST be the only service in a dataflow NOTE Set Query Retrieve to Hidden so that it cannot be selected from the Patient Menu 23 Buttons You can assign print buttons to a device or to a dataflow 1 Select the print button to configure and the properties on the left of the screen Select the serv
8. O o e i o o e lt 8 6 2 B Preparing for an Exam 8 11 12 13 14 15 Direction 5137113 100 Rev 3 Imaging Measurement Keys Clear Comment Body Pattern Ellipse Measure Zoom M D Cursor Scan Area Set Press or rotate these keys as necessary Depth Rotate to adjust the Depth Imaging Feature Keys Auto Optimize On Off THI Multi Image Left Right Select Print Keys Press P Keys to archive print or send the image Probe and Cord Holder Gel Holder Patient Enter Patient screen Reports Activates default report and Measurement Selection Menu of report choices 20 21 22 23 24 SI OP do End Exam Activates Image Management and Touch Panel with end of exam options User Assigned Utility keys Activates the configuration system Probe Preset keys Select the application to use and Probe select Mode Paramenters To toggle between the Primary menus of different modes Top menu Controls Activates the changes of functions in the Top menu Sub menu controls Activates Sub Menu for Modes and toggles changes functions Gain Key Utility key o LOGIQ A5 cta 6 T0454 444 E T4 P P Pn ERE E E JERE ERE ig Ta eet 7 e 22 e Oc 9 o a 4 Freeze key Press Freeze to freeze the image LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Re
9. See Buttons on page 22 Browsing an Exam s Stored Images Mouse over the image in the clipboard then double click Set to view an enlarged thumbnail image Managing an Exam s Stored Images From the Display press Active Images from the New Patient menu open Active Images Deleting an Image Select the image on the clipboard then press the onscreen Delete shortcut Or go to Active Images lower right hand portion of the display Highlight all the images that need to be deleted and press Delete All Temp Images Direction 5137113 100 Rev 3 Formatting a CD DVD 1 Insert the backup media Format the backup media Go to the Utility page by pressing Ins Key Select Connectivity then Removable Media Label the media appropriately Press Format DO NOT use DVD RW or CD RW media CAUTION Storiage media includes CD R DVD R NDL 256MByte 066E0690 USB Flash Drive The Ultrasound system displays a pop up menu when the formatting has been completed Press Ok to continue Verify that the format was successful Image Patient Management and Connectivity 20 Backing Up Patient Information Format the media prior to performing these steps 1 Go to the Utility tab Select System then Backup Restore 2 Select the media 3 Select the parameter under Backup by placing a check mark Then press Backup 4 Answer OK to the Back Up pop up message NOTE The detailed sec
10. Select the Query Retrieve server from the Transfer From pull down menu 4 Press Query in the Transfer From section The server s patient list displays 5 Select the patient s or exam s to retrieve from the patient list 6 Press Transfer The data is retrieved from the server as the progress bar displays Worklist 1 Press Patient and select Worklist The last Worklist used displays on the monitor 2 Press Refresh to refresh the list or select another Worklist server from the transfer From pull down menu 3 Select the patient s or exam s from the list 4 Press Transfer The progress bar displays during the transfer MPEGvue Save the data to CD R to view on PC 1 Format and label the media insert the USB Flash Hard Drive into the front USB Port 2 Press Patient and select Data Transfer 3 Select MPEGvue The patient list in the Local Archive Int HD displays in the Transfer From section 21 4 Select the media from the Transfer To pull down menu 5 Select the patient s or exam s from the list 6 Press Transfer The progress bar displays during the transfer Files are saved in mpeg format Send To the DICOM device 1 Press Patient 2 Search and select the patient and press Exam The Patient Exam screen displays 3 Select the exam which has the images and press Send To NOTE You can only select the Local Archive Int HD for Workflow 4 The Send To dialogue box displays
11. Quick Guide DENMARK GE Medical Systems Fabriksparken 20 DK 2600 GLOSTRUP TEL 45 4348 5400 FAX 45 4348 5399 FRANCE GE Medical Systems 738 rue Yves Carmen F 92658 BOULOGNE CEDEX TEL 05 49 33 71 toll free FAX 33 1 46 10 01 20 GERMANY GE Ultraschall Deutschland GmbH amp Co KG BeethovenstraDe 239 Postfach 11 05 60 D 42655 Solingen TEL 0130 81 6370 toll free TEL 49 212 28 02 207 FAX 49 212 28 02 431 GREECE GE Medical Systems Hellas 41 Nikolaou Plastira Street G 171 21 NEA SMYRNI TEL 30 1 93 24 582 FAX 30 1 93 58 414 ITALY GE Medical Systems Italia Via Monte Albenza 9 20052 MONZA TEL 1678 744 73 toll free FAX 39 39 73 37 86 TLX 3333 28 Direction 5137113 100 Rev 3 LUXEMBOURG TEL 0800 2603 toll free MEXICO GE Sistemas M dicos de Mexico S A de C V Rio Lerma 302 1 y 2 Pisos Colonia Cuauht moc 06500 M xico D F TEL 5 228 9600 FAX 5 211 4631 NETHERLANDS GE Medical Systems Nederland B V Atoomweg 512 NL 3542 AB UTRECHT TEL 06 022 3797 toll free FAX 31 304 11702 POLAND GE Medical Systems Polska Krzywickiego 34 P 02 078 WARSZAWA TEL 48 2 625 59 62 FAX 48 2 615 59 66 PORTUGAL GE Medical Systems Portuguesa S A Rua Sa da Bandeira 585 Apartado 4094 TL X 22804 P 4002 PORTO CODEX TEL 05 05 33 7313 toll free FAX 351 2 2084494 RUSSIA GE VNIIEM Mantulinskaya Ul 5A 123100 MOSCOW TEL 7
12. a new patient s data into the database Register is used to enter new 1 Press Patient Press the New Patient button on the AA nb GE Se W Fall u idis You can preset a per application an patient information into the database prior to performing application per probe via Utility the actual exam Details displays exam details and 2 Select the Exam Category additional patient information 3 Type the Patient ID Patient Name Birthdate etc Patient Entry Menu Refer to Illustration a e V 4 Press the Register button on the Patient menu DO Image Management Window 1 m D m dais eon NOT press Register if you are automatically Access to this patient s exam history and image Se D E Se e SES generating a patient ID management features H 5 Press Scan B Mode Esc or Exit Select the probe Dataflow 4 Selects this exam s dataflow preference Iv Exit 5 Patient Data Transfer Exits the Patient Menu and returns to scanning JH CARD VAS UR SMP PED Patient Information 6 Patient ID Name Birthdate Age and Sex Category Selection and Exam Information 7 amp 8 Select the appropriate category and enter the exam information Patient View and Exam View 9 Patient View lists the patients in the database Search Key enables searching list by Patient ID Last Name M First Name Birthdate Sex and Last
13. 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 Acoustic Output Display Specifications The display consists of three parts Thermal Index TI Mechanical Index MI and a relative Acoustic Output AO value Although not part of the NEMA AIUM standard the AO value informs the user of where the system is operating within the range of available output Depending on the examination and type of tissue involved the parameter will be one of three types e Soft Tissue Thermal Index TIS Used when imaging soft tissue only it provides an estimate of potential temperature increase in soft tissue e Bone Thermal Index Used when bone is near the focus of the image as in the third trimester OB examination it provides an estimate of potential temperature increase in the bone or adjacent soft tissue e Cranial Bone Thermal Index TIC Used when bone is near the skin surface as in transcranial examination it provides an estimate of potential temperature increase in the bone or adjacent soft tissue The TI and MI is displayed at all times The MI and TI displays start at a value of 0 0 and increments in steps of 0 1 Display precision is
14. 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 P5 A5 A5Pro AC power outlet LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 36 Related Hazards continued CAUTION Smoke amp m Fire Hazard Biological Hazard A A A CAUTION CAUTION CAUTION Do not use this equipment if a safety problem is known to exist Have the unit repaired and performance verified by qualified service personnel before returning to use The system must be supplied from an adequately rated electrical circuit The capacity of the supply circuit must be as specified in Chapter 3 of the Basic User Manual For patient and personnel safety be aware of biological hazards while performing invasive procedures To avoid the risk of disease transmission e Use protective barriers gloves and probe sheaths whenever possible Follow sterile procedures when appropriate Thoroughly clean probes and reusable accessories after each patient examination and disinfect or sterilize as needed Refer to Probes and Biopsy in the Basic User Manual for probe use and care instructions e Follow all infection control policies established by your office department or institution as they apply to personnel and equipment Contact with natural rubber latex may cause a severe anaphylactic reaction in persons sensitive to the natural l
15. of your equipment p Direction 5137113 100 Hev 3 51 CISPR CAUTION The LOGIQ P5 A5 A5Pro conforms to the CISPR11 Group 1 Class A of the international standard for Electromagnetic disturbance characteristics Grounding reliability can only be achieved when this equipment is connected to a receptacle marked Hospital Only or Hospital Grade For U S A Canada Japan Power Indication label Optional Flexible LCD monitor may rotate in transporting bind the system securely not to cause the damage in transportation there is a pinch point in the LCD monitor Need care for injury on hands or fingers in flipping down the LCD monitor of Circuit Breaker Circuit Breaker LAMP DEFOR COMDINO 16 Eres OCA cm mr MMC Zeta CONDO TO Fe LAR d LM III nesso A A A A gt 2 4 AOM A A Kid United States law restricts this device to sale or use by or on the order of a physician C 0459 X CISPR 11 EN 55011 CLASS GROUP 1 CLASSE B GROUPE 1 For Proper grounding connect to hospital grade receptacle For Proper grounding connect to hospital grade receptacie LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 Warning Label Locations continued 6 GE DLIRASOUND DREL al SAMPDAENUD 1 Identification and Rating Plate USA Asia 120V Console CLASS IT 2 dent
16. possible from other electronic equipment 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 4 Lay out the main equipment and other peripherals following the installation procedures described in the Option Installation manuals General Notice 1 Designation of Peripheral Equipment Connectable to This Product The equipment indicated on Chapter 15 of the Basic User Manual can be hooked up to the product without compromising its EMC performance Avoid using equipment not designated in the list Failure to comply with this instruction may result in poor EMC performance of the product 2 Notice against User Modification The user should never modify this product User modifications may cause degradation in EMC performance Modification of the product includes changes in a Cables length material wiring etc b System installation layout c System configuration components d Securing system parts cover open close cover screwing 3 Operate the system with all covers closed If a cover is opened for some reason be sure to shut it before starting resuming operation 4 Operating the system with any cover open may affect EMC performance LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 44 Peripheral Update for EC countries The following is intended to provide the users in EC countri
17. the enclosure per IEC60 529 Can be used in operating room Foot Switch environment Mo Type CF Applied Part heart in the box symbol is in accordance with IEC 878 02 03 ECG marked Type CF ATTENTION Consult accompanying documents is intended to alert the user to refer to the operator manual Various or other instructions when complete information cannot be provided on the label CAUTION Dangerous voltage the lightning flash with arrowhead is used to indicate electric shock Inside of console hazards Mains OFF indicates the power off position of the mains power breaker Refer to Chapter 3 in the Basic User Manual for location information Mains ON indicates the power on position of the mains power breaker Refer to Chapter 3 in the Basic User Manual for location information 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 location information LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 39 Table 1 2 Label Icons Protective Earth indicates the protective earth grounding terminal Equipotentiality indicates the terminal to be used for connecting equipotential conductors when interconnecting grounding with other equipment Rear of console This symbol indicates that the waste of electrical and electronic equipment must not be disposed as unsorted munic
18. 095 956 7037 FAX 7 502 220 32 59 TLX 613020 GEMED SU 30 SPAIN GE Healthcare TEL 34 91 663 25 00 Avda Europa 22 FAX 34 91 663 25 01 E 28108 Alcobendas Madrid SWEDEN GE Medical Systems PO BOX 1243 16428 KISTA TEL 020 795 433 toll free FAX 46 87 51 30 90 TLX 12228 CGRSWES SWITZERLAND GE Medical Systems Schweiz AG oternmattweg 1 CH 6010 KRIENS TEL 155 5306 FAX 41 41 421859 TURKEY GE Med Sys Turkiye A S Mevluk Pehliran Sodak Yilmaz Han No 24 Kat 1 Gayretteppe ISTANBUL TEL 90 212 75 5552 FAX 90 212 211 2571 UNITED KINGDOM GE Medical Systems Coolidge House 352 Buckingham Avenue SLOUGH Berkshire SL1 4ER TEL 0800 89 7905 toll free FAX 44 753 696067 LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 31 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 DANGER Indicates that a specific hazard is known to exist which through inappropriate conditions or actions will cause e Severe or fatal personal injury e Substantial property damage Severe personal injury WARNING Indicates that a specific hazard is known to exist which through inappropriate conditions or actions may cause e Substantial property damage CAUTION Indicates that a potential haza
19. 100 Rev 3 Frame Average Temporal filter that averages frames together This has the effect of presenting a smoother softer image Colorize Enables gray scale image colorization To deactivate reselect a Gray Map Gray Map Determines how the echo intensity levels received are presented as shades of gray Rotation Up Down Rotates the image by selecting the value from the pop up menu Frequency Multi Frequency mode lets you downshift to the probe s next lower frequency or shift up to a higher frequency Frame Rate Resolution Optimizes B Mode frame rate or spatial resolution for the best possible image Anatomical M Mode Allows you to move the M Mode trace in order to Image difficult to reach anatomy Sweep Speed Changes the speed at which the time line is swept B Mode Control Panel Controls Auto Optimize Automatic Tissue Optimization optimizes the image based upon a specified Region of Interest ROI or anatomy within the display Zoom Magnifies a zoom region of interest which is magnified to approximately the size of a full sized image An un zoomed reference image 15 displayed adjacent to the zoom window The system adjusts all imaging parameters accordingly Press Zoom key to activate Press right zoom key again to deactivate Use the Trackball to position the Zoom ROI Reverse Flips the image left right LOGIQ P5 A5 A5Pro Quick Guide B M Mode Image Optimize continued B M M
20. 5137113 100 Rev 3 LOGIQ P5 A5 A5Pro Features continued Table 1 4 Probe Features continued SE eee wem x Wa pw ee __ _ ee ee __ __ w s mew NEN pw T s __ _ qp Inm iw Wee I e 11 e 1e ee mem I _ Je De Ee wx Ii Dx D gy _____ __ Ja I x _ pw Ix x 1m e ge xus wea __ IE ____ _ __ __ itm IX _ _ px I 1 Jl _ _ ee _ a _ E IK x lt X XxX XxX KI X Xx xX Xx X X X X X X X XxX XxX X X x lt X XxX X X X XxX XxX X X X X X X x lt BRL a e 1 Using Probes 17 LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 18 Probe Cleaning and Disinfection Instructions Probe Safety WARNING 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 in use DO NOT use a damaged or defective probe Failure to follow these precautions can result in serious injury and equipment damage Ultrasound transducers can easily be damaged by improper handling and b
21. Choose the destination device and select OK NOTE The destination device is configured in the Utility screen Multiple devices are able to be configured 5 successful unsuccessful message is displayed at the bottom of the screen NOTE If you press the Clear button in the Transfer From and Transfer To section all the search criteria is cleared and the list is refreshed accordingly NOTE ALWAYS exit to scanning after any Data Transfer function to ensure that the operation has completed LOGIQ P5 A5 A5Pro Quick Guide EZBackup Move NOTE EZBackup EZMove allows you to manage hard disk space move images off the hard drive while maintaining the patient database on the scanner as well as to back up the patient database and images NOTE EZBackup EZMove can take up to 20 minutes Make sure to schedule this at the same time daily when no patients are scheduled 1 To start the EZBackup EZMove procedure go to the Patient menu and select the EZBackup EZMove button at the bottom of the Patient list The EZBackup EZMove Wizard starts 2 Verify the information on the first page of the EZBackup EZMove Wizard then press Next NOTE If the EZBackup EZMove presets need to be modified those requirements are specified on the Utility gt System gt Backup Restore page 3 Verify the information on the EZBackup EZMove Wizard Page 2 This page tells you how many medias you need to do this backup After you have gat
22. Exam date Search ide key and string fields help define the search parameters 2005 02 18 15 13 0 16 1 MB Exam View lists the exams of the selected patient Select 2005 03 09 12 54 5 14 3 MB e 2005 02 18 14 02 51 12 2 MB the patient or the exam in Patient View and press Exam 2005 02 25 15 11 1 9 59 MB me Tu 2005 03 14 11 59 5t 8 28 MB View or Review 2005 03 14 11 41 2 7 28 MB 2005 02 18 13 58 42 6 15 MB 2005 02 23 16 42 3 5 80 MB 2005 03 14 12 14 0 5 79 MB 2005 02 25 11 46 14 5 78 MB 2005 05 16 11 53 5 5 52 MB 2005 02 25 16 54 5 4 59 MB C 0737982 KIM SA ju ju 11 0739189 PARK SY 0722577 wan 0707982 oms COLOR 0738764 SU JH 0740051 lee is 0731751 LEEMH 0533968 0593653 JUNG SY T nmzzmzmmmzmzlis Preparing for an Exam LOGIQ P5 A5 A5Pro Quick Guide LOGIQ P5 A5 A5Pro Control Panel Tour oe oS de Record Press to activate recording devices Audio On Off and Volume TGC Move slide pots left right to adjust TGC Reverse Press to invert the image left right Additional Feature Keys Keyboard Use the keyboard to enter patient information and annotations Mode Keys M Mode Continuous Wave CW and Pulsed Wave Doppler PW Modes Power Doppler Image Mode PDI Color Flow CF Mode B Mode and B Flow CW PW PDI CF keys are for LOGIQ P5 only LOGIQ 5 We Eg T amp rr KE A tm a nmn rrr rra 16 1 S 7
23. Guide Direction 5137113 100 Rev 3 41 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 However there is no guarantee that interference will not occur in a particular installation NOTE If this equipment is found to cause interference which may be determined by turning the equipment on and off the user or qualified service personnel should attempt to correct the problem by one or more of the following measure s e reorient or relocate the affected device s e increase the separation between the equipment and the affected device power the equipment from a source different from that of the affected device e consult the point of purchase or service representative for further suggestions NOTE The manufacturer is not responsible for any interference caused by using other than recommended interconnect cables or by unauthorized changes or modifications to this equipment Unauthorized changes or modifications could void the users authority to operate the equipment NOTE To comply with the regulations on electromagnetic interference for a Class A FCC Device all interconnect cables to per
24. Packet Size 3 Select the appropriate probe for very superficial structure Select two focal zones Adjust the depth to the anatomy to be imaged Maintain a low gain setting for gray scale MI0 8 Tis 0 1 9L ume ag GE Healthcare i Carotid 0 08 12108 16 53 54 CF Mode Line Density 0 Transparency Map 0 Flash Suppression 1 Focus Position Frame Average 3 Power Output 100 0 693 183 6 164 4 5 PW CF Rat Carotid 31 Transfer E Prox Mid Dist 100 Lt 3 2 kHz 344 Hz 312 Accumulation or Map Compress 6 AO PRF WF S P Z CCA x BULB ICA B ECA VERT SUBC Ves Worksheet Direct Rep SV Length 2 Wall Filter Frequency Pos Angle Steer Fine Angle Steer Activate Color Flow Maintain the PRF at a lower setting Increase Frame Averaging for more persistence MI 0 20 Tis 0 0 9L N pa Carotid l Angle Correct Auto Angle Wall Filter Pos PWD Mode Top and Sub Menu LOGIQ P5 AS A5Pro Quick Guide Basic Measurements NOTE The following instructions assume that you first scan the patient and then press Freeze Distance and Tissue Depth Measurements 1 Press Measure once an active caliper displays 2 To position the active caliper at the start point distance or the most anterior point tissue depth move the Trackball To fix the start point press Set The system fixes the first caliper and displays a second activ
25. Rev 3 MT MT Figure 1 1 Patient Environmental Devices Signals I O Port Power Out Signals I O Port Footswitch Connector Power In Peripheral Devices Signals I O Port Power In 17 Footswitch 18 Power Line AC 19 Ground Line 20 Power Cable with Protective Earth 21 DVD Drive 47 LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 48 Acceptable Devices The devices shown in Patient Environmental Devices on page 1 47 are specified to be suitable for use within the PATIENT ENVIRONMENT CAUTION DO NOT connect any probes or accessories without approval by GE within the PATIENT ENVIRONMENT See Peripheral Update for EC countries on page 44 Unapproved Devices If devices are connected without the approval of GE the warranty will be INVALID CAUTION Unapproved devices shall not be used in the patient environment Any device connected to the LOGIQ P5 A5 A5Pro must conform to one or more of the requirements listed below 1 IEC standard or equivalent standards appropriate to devices 2 he devices shall be connected to PROTECTIVE EARTH GROUND Accessories Options Supplies CAUTION Unsafe operation or malfunction may result Use only the accessories options and supplies approved or recommended in these instructions for use LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 49 Acoustic Output Located on the upper right section of the system display monitor the
26. ansp MAX highlights High Intensity echoes for fetal skeleton or echogenic structures e Transp MIN highlights Low Intensity echoes for vascular structures or cystic areas e Transp X RAY used with color power Doppler to show vessels within the volume e Gradient Light more shadows better depth perception e Light brighter near field structures darker far field structures Mix Combination of two Render Modes 100 LOGIQ P5 AS A5Pro Quick Guide Contact Information INTERNET http www gemedicalsystems com USA GE Healthcare Ultrasound Service Engineering 9900 Innovation Drive Wauwatosa WI 53226 TEL 1 800 437 1171 or FAX 1 414 721 3865 Clinical Questions For information in the United States Canada Mexico and parts of the Caribbean call the Customer Answer Center TEL 1 800 682 5327 or 1 262 524 5698 In other locations contact your local Applications Sales or Service Representative Service Questions For service in the United States call GE CARES TEL 1 800 437 1171 Accessories Catalog Requests To request the latest GE Accessories catalog or equipment brochures in the United States call the Response Center TEL 1 800 643 6439 In other locations contact your local Applications Sales or Service Representative Preparing for an Exam Direction 5137113 100 Hev 3 Placing an Order To place an order order supplies or ask an accesory related question in the United Sta
27. anufacturer is not responsible for any interference caused by using other than recommended interconnect cables or by unauthorized changes or modifications to this equipment Unauthorized changes or modifications could void the users authority to operate the equipment CAUTION Do not use devices which intentionally transmit RF signals cellular phones transceivers or radio controlled products in the vicinity of this equipment as it may cause performance outside the published specifications Keep the power to these type devices turned off when near this equipment Keep power to these devices turned off when near this equipment Medical staff in charge of this equipment is required to instruct technicians patients and other people who may be around this equipment to fully comply with the above regulation Portable and mobile radio communications equipment e g two way radio cellular cordless telephones wireless computer networks should be used no closer to any part of this system including cables than determined according to the following method Table 1 5 Portable and mobile radio communications equipment distance requirements Frequency Range 150 kHz 80 MHz 80 MHz 800 MHz 800 MHz 2 5 GHz Calculation Method d 3 5 V square root of P d 3 5 E square root of P d 7 E square root of P Where d separation distance in meters P rated power of the transmitter V compliance value for conducted RF compliance value fo
28. atex protein Sensitive users and patients must avoid contact with these items Refer to package labeling to determine latex content and FDA s March 29 1991 Medical Alert on latex products The system is equipped with an Auto Freeze feature which disables acoustic output and freezes the image when the system is not in use Take care when deactivating this feature Never put any device onto the monitor LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 Related Hazards continued i CAUTION 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 P5 A5 A5Pro This must be performed by qualified service personnel only CAUTION Do not use the LOGIQ P5 A5 A5Pro Ultrasound system ECG wave for diagnosis and monitoring 37 LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 38 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 Identification and Rating Plate Manufacture s name and address Date of manufacture See Warning Label Locations on page 51 Model and serial numbers Electrical ratings Volts Amps phase and frequency Type Class Label Used to indicate the degree of safety or protection IP Code IPX8 Indicates the degree of protection provided by
29. capability the system automatically switches to high PRF mode Multiple gates appear and is indicated on the display Wall Filter insulates the Doppler signal from excessive noise caused from vessel movement NOTE Push key to toggle between PHF and Wall Filter Angle Correct Estimates the flow velocity in a direction at an angle to the Doppler vector by computing the angle between the Doppler vector and the flow to be measured Auto Angle Adjuste the angle to the direction of the Flow Angle Steer Slants the Color Flow region of interest or the Dopple M Line to obtain a better doppler angle Threshold Threshold assigns the gray scale level at which color information stops Preparing for an Exam Direction 5137113 100 Rev 3 Doppler Display Formats Display layout can be preset to have B Mode and Time motion side by side or over under Sample Volume Gate Length Sizes the sample volume gate Map Allows a specific color map to be selected After a selection has been made the color bar displays the resultant map Packet Size Controls the number of samples gathered for a single color flow vector Invert Allows blood flow to be viewed from a different perspective i e red away negative velocities and blue toward positive velocities The real time or frozen image can be inverted Color Flow Control Panel Control Scan Area Toggles between the CFM window size and position Con
30. dow S D Ratio D S Ratio or Ratio Select PI RI S D Ratio A B Ratio or D S Ratio from the Doppler Primary amp Secondary Controls Perform velocity measurements 1 The first caliper is the start point on the Doppler waveform This would be Vmax for Pl peak velocity for RI systole for S D ratio A velocity for A B ratio or diastole for D S ratio 2 he second caliper is the end point caliper to the end point of the Doppler waveform This would be for Pl minimum velocity for RI diastole for S D ratio B velocity for A B ratio or systole for D S ratio NOTE For the PI calculation if Trace Auto is not selected manually trace the waveform between VMAX and Va NOTE For the PI calculation if Trace Auto is on the system automatically traces the waveform when Set is pressed to fix Vg 12 Worksheets Measurement Calculation worksheets are available to display and edit measurements and calculations There are generic worksheets as well as Application specific worksheets The worksheets are selected from the worksheet button on the screen LOGIQ P5 A5 A5Pro Quick Guide Using Probes Connecting a probe 1 Place the probe s carrying case on a stable surface and open the case 2 Carefully remove the probe and unwrap the probe cable 3 DO NOT allow the probe head to hang free Impact to the probe head could result in irreparable damage 4 Turn the connector locking handle counter cl
31. e caliper 4 To position the second active caliper at the end point distance or the most posterior point tissue depth move the Trackball 5 complete the measurement press Set The system displays the distance or tissue depth value in the measurement results window NOTE Before you complete a measurement To toggle between active calipers press Measure To erase the second caliper and the current data measured and start the measurement again press Clear once NOTE After you complete the measurement to erase all data that has been measured to this point but not data entered onto worksheets press Clear Preparing for an Exam Direction 5137113 100 Rev 3 Circumference Area Ellipse Measurement 1 Press Measure once an active caliper displays 2 To position the active caliper move the Trackball 3 To fix the start point press Set The system fixes the first caliper and displays a second active caliper 4 To position the second caliper move the Trackball 5 Turn the Ellipse control an ellipse with an initial circle shape appears NOTE Be careful not to press the Ellipse control as this activates the Body Pattern 6 To position the ellipse and to size the measured axes move the calipers move the Trackball 7 increase the size Turn the Ellipse control in a clockwise direction To decrease the size turn the Ellipse control in a counterclockwise direction 8 To toggle be
32. eclaration of Emissions Emission Type Electromagnetic Environment CISPR 11 Group 1 This system uses HF energy only for its internal function Therefore RF emissions are very low and are not likely to cause any interference in nearby electronic HF Emissions Class B equipment It is suitable for use in all establishments IEC 61000 3 2 Class B 230V 50Hz Harmonic Disturbanc Emissions IEC 61000 3 3 Complies Voltage Fluctuations Flicker Emissions LOGIQ P5 AS A5Pro Quick Guide Declaration of Immunity Direction 5137113 100 Hev 3 46 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 IEC 61000 4 2 Static discharge ESD IEC 61000 4 4 Electrical fast transient burst IEC 61000 4 5 Surge Immunity IEC 61000 4 11 Voltage dips short interruptions and voltage variations on mains supply IEC 61000 4 8 Power frequency 50 60 Hz magnetic field IEC 61000 4 6 TBD VRMS Conducted RF 150 kHz 80 MHz IEC 61000 4 3 3 V m 3 V m Radiated RF 80 MHz 2 5 GHz 80 MHz 2 5 GHz Table 1 7 Declaration of Immunity Immunity Type Test Level EMC Environment and Guidance 8 kV contact 8 kV air 1 5 kV for mains 1 5 kV differential 2 5 kV common lt 5 gt 95 dip for 0 5 cycle 6 kV contact 8 kV air 2 kV for mains 1 kV for SIP SOP
33. es with updated information concerning the connection of the LOGIQ P5 A5 ABPro to image recording and other devices or communication networks The LOGIQ P5 A5 A5Pro has been verified for overall safety compatibility and compliance with the following on board image recording devices Sony Color Printer UP D23MD Sony B W Printer Model UP D897MD Sony Color Printer Model UP 50 51MD Panasonic DVD Video LQ MD800 800P 800E Mitsubishi VCR HS MD3000 3000E 3000U The LOGIQ P5 A5 A5Pro has also been verified for compatibility and compliance for connection to a local area network LAN via the rear panel Ethernet connection provided the LAN components are IEC EN 60950 compliant Connection may also be made to a CE Marked and IEC EN 60950 compliant modem using one of the serial ports at the rear panel The LOGIQ P5 A5 A5Pro may also be used safely while connected to devices other than those recommended above if the devices and their specifications installation and interconnection with the system conform to the requirements of IEC EN 60601 1 1 General precautions for installing an alternate on board device would include 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 P5 A5 A5Pro and are used simultaneously must be less than or equal to the rated supply of the LOGIQ P5 A5 A5Pro There must be adequate heat dissipation and ventilation
34. hered the media you are ready to begin the backup Press Next 4 pop up message appears that provides you with the media label Label the media then insert the media Press OK 5 The status menu appears NOTE When if you need to insert the next media a message appears providing you with the media label a well Label the media then insert the media and press OK 6 When the backup is complete the Backup completed page appears To view the media do so via the Patient menu by selecting the patient and loading the appropriate media or via Import or via DICOM CD View Direction 5137113 100 Hev 3 Connectivity Connectivity on the LOGIQ P5 A5 A5Pro is based on the Dataflow concept Login as Administrator Select Utility Select Connectivity Configure the menus from left to right starting with TCP IP first When finished making connectivity changes to the utility menus restart the system TCP IP Type in the Computer s Name better known as the AE Title Identify the Ultrasound system to the rest of the network by filling in its IP Address Subnet Mask and Gateway if applicable Press Save Image Patient Management and Connectivity 22 Device Use the Device tab to add DICOM destinations 1 Press Add 2 the name of the device and its IP address 3 Press Ping then Save MyComputer Properties ycompuer Ezmg5188 io ooo LOGIQ P5 A5 A5Pro Quick Guide Services
35. hipping cases to avoid damage Direction 5137113 100 Rev 3 Starting an Exam You need to select a pre configured dataflow that sets up the ultrasound system to work according to the services associated to the dataflow 1 Select your Operator Login and type in your Password TitleLogin 7 STE e d 5 Se Ser L s 1 ape ECG aee a an NC d s IT MA PIE 44 k M 1 D r Pa Ne e ge 5 el op ate 3 e SH vex DESMET ee aa T Ze T wr 1 leie e xti CR a e vb i mna Rx Sai ee SC Ve nun ur a ae a ac iere D Pm CR i zu be se AU 4 CN 1 e a eis EXT D 1 m 8 a1 Vr Zens si LA Tr r AR ssa T R T WI i n 4 d ET Tg 2 Press Log on 3 Fill in the New Patient menu as described on Page 3 OR If the patient name is on the patient record list 1 Trackball to the patient s name to highlight the name or perform a search to locate the patient then press Select Patient LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 3 Starting an Exam New Patient Probe Selection Function Selection Window 2 Select a probe the system automatically selects the last Worklist displays a Worklist screen New Patient is used To start a new patient s exam used application for this probe to clear the patient entry screen to input
36. ice you want to use under My Computer and press to add to Printflow view NOTE Select the Standard Print under Active Images Page as necessary Press Save NOTE You can configure each print key to multiple output devices workflow LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 24 Removable Media Saving Images as JPEG files and CINE DICOM Status Loops as AVI files Format and verify media To check the status of all DICOM jobs or redirect Format the media prior to following these steps DICOM jobs press F4 E 1 Insert a media into the drive or an USB Drive into the USB Port 2 Press Menu on the lower right hand portion of the display and select Save As The SAVE AS menu appears For Transfer To E lmage_115649 jpg E Image 115655 jpg E Image 115658 jpg E Image 115702 jpg E Image_115705 jpg Miscellaneous Set up Patient Exam menu options and Printer and Store Options 3 Specify Compression and Save As Type and press Save The image is saved to the media 4 Finalize the media by selecting Yes The media is ejected from the system NOTE If you want to add more images to the media select No and do not finalize the media LD S NM NUM Image Patient Management and Connectivity LOGIQ P5 A5 A5Pro Quick Guide Using CINE Activating CINE Press Freeze then roll the Trackball to activate CINE To start CINE Loop playback press Run S
37. ification and Rating Plate Europe Asia Latin America 220V Console 3 ldentification and Rating Plate Japan 120V Console 4 ldentification and Rating Plate Korea 220V Console 5 Identification and Rating Plate China 220V Console 6 IUL Label L PLIERS DOEL n sl b Pepp 2 SESERUM AT DEET E SEA EA 55a SEDO TE ATTO ES Japan 100v Console ee re A E yta dtdd Y w bOGKPS yadta FERAE GHE EELEE zo EIERE LAYS Ysa s SR Be ede sss vue eS dg 51 Ere IT 0 23008 RETS DENKS Ah CLEE j China 220v Console
38. ipal waste and must be collected separately Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment Rear of console LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 40 Classifications Type of protection against electric shock Class Equipment 1 Degree of protection against electric shock Type CF Applied part 3 for ECG Probes marked with CF symbol Continuous Operation System is Ordinary Equipment IPXO Footswitch is IPX8 1 Class EQUIPMENT EQUIPMENT in which protection against electric shock does not rely on BASIC INSULATION only but includes an earth ground This additional safety precaution prevents exposed metal parts from becoming LIVE in the event of an insulation failure 2 Type BF APPLIED PART TYPE BF APPLIED PART providing a specified degree of protection against electric shock with particular regard to allowable LEAKAGE CURRENT Table 1 3 Type BF Equipment Normal Mode Single fault condition Patient leakage current Less than 100 microA Less than 500 microA 3 Type CF APPLIED PART Type CF Applied Part providing a degree of protection higher than that for TYPE BF Applied Part against electric shock particularly regarding allowable LEAKAGE CURRENTS Table 1 4 Type CF Equipment Normal Mode Single fault condition Patient leakage current Less than 10 microA Less than 50 microA LOGIQ P5 A5 A5Pro Quick
39. ipheral devices must be shielded and properly grounded Use of cables not properly shielded and grounded may result in the equipment causing radio frequency interference in violation of the FCC regulations NOTE Do not use devices which intentionally transmit RF Signals cellular phones transceivers or radio controlled products in the vicinity of the equipment as it may cause performance outside the published specifications Keep the power to these types of devices turned off when near this equipment The medical staff in charge of this equipment is required to instruct technicians patients and other people who maybe around this equipment to fully comply with the above requirement 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 Proper installation following the service manual is required in order to achieve the full EMC performance of the product The product must be installed as stipulated in 4 2 Notice upon Installation of Product In case of issues related to EMC please call your service personnel LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 42 The m
40. ivation and meaning of the indices ALARA principles and examples of specific applications of the ALARA principle LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 35 Equipment and Personnel Safety Related Hazards WARNING _ This equipment contains dangerous voltages that are capable of serious injury or death If any defects are observed or malfunctions occur stop operating the equipment and perform the proper action for the patient Inform a qualified service person and contact a Service Representative for information There no user serviceable components inside the console Refer all servicing to qualified service personnel only mounted to the LOGIQ P5 A5 A5Pro DANGER The concerns listed below can seriously affect the safety of equipment and personnel during a diagnostic ultrasound examination WARNING Only approved and recommended peripherals and accessories should be used All peripherals and accessories must be securely Hazard a Explosion Risk of explosion if used in the presence of flammable anesthetics ni A Hazard Electrical To avoid injury Do not remove protective covers No user serviceable parts are inside Refer servicing to qualified service personnel To assure adequate grounding connect the attachment plug to a reliable hospital grade grounding outlet Never use any adaptor or converter of a three prong to two prong type to connect with a mains power plug The protective earth
41. ng on the probe Neurological procedures must be done with the use of legally marketed sterile pyrogen free probe sheaths After removing from the germicide rinse the probe following the germicide manufacturer s rinsing instructions Flush all visible germicide residue from the probe and allow to air dry Using Probes Direction 5137113 100 Hev 3 Probe Immersion Levels y m m ins V J dat SS w6N TL d ac TT oft 7 4DEXC TE V a 4 A j ASCS x AEE A r Cx id EI m UT A gt A 2 1 Fluid Level 2 Aperture 3 Contact face within patient environment 19 Probe Disinfection Agents Ultrasound probes can be disinfected using liquid chemical germicides The level of disinfection is directly related to the duration of contact with the germicide Increased contact time produces a higher level of disinfection Refer to the Probe Care Card http www gemedicalsystems com rad us probe care html LOGIQ P5 A5 A5Pro Quick Guide Image Management Clipboard As images are saved by pressing any of the print keys P1 P2 or Print Screen the images appear at the bottom of the display on the clipboard as thumbnails of the images saved during the exam These images remain on the clipboard until the end of the exam Printing Images Press the appropriate print key P1 P2 or Print Screen For more information on programming the Print buttons
42. ockwise 5 Align the connector with the probe port and carefully push into place 6 Turn the connector locking handle clockwise to secure the probe connector 7 Carefully position the probe cable in the probe cord holder spot so it is free to move but not resting on the floor Activating the probe Press the Probe Preset button on the front panel Move the cursor to the probe icon displayed on the monitor screen and press SET The probe activates in the currently selected operating mode The probe s default settings for the mode and selected exam are used automatically Using Probes Direction 5137113 100 Hev 3 Deactivating the probe When deactivating the probe the probe is automatically placed in standby mode 1 Press the Freeze key 2 Gently wipe the excess gel from the face of the probe 3 Carefully slide the probe around the right side of the keyboard toward the probe holder Ensure that the probe is placed gently in the probe holder Disconnecting the probe Probes can be disconnected at any time However the probe should not be selected as the active probe 1 Move the probe locking handle counterclockwise Pull the probe and connector straight out of the probe port 2 Carefully slide the probe and connector away from the probe port and around the right side of the keyboard Ensure the cable is free Be sure that the probe head is clean before placing the probe in its storage box D
43. ode Scanning Hints Auto Optimize Improves imaging performance while reducing optimization time Frequency Changes system parameters to best optimize for a particular patient type 13126 Carotid Rt Lt DW 2 Stenosis X Volume C Angle rv IMT jj AB Ratio Worksheet Direct Rep Virtual Convox Direction 5137113 100 Rev 3 Maps There is an inter dependency between gray maps gain and dynamic range If you change a map revisit gain and dynamic range settings Dynamic Range Affects the amount of gray scale information displayed If you increase the gain you may want to decrease the dynamic range Frequency CrossHaam 4 Dynamic Range SHI HD CrossHeam Gray Map Rotation B Mode Top Menu and Sub Menu 1 Edge Enhance Better delineates the amount of border crispness Frame Average Smooths the image by averaging frames Affects the amount of speckle reduction Caroud B Mode None Biopsy Kit Frame Average Middle Line Density Focus Width Low 100 0 B Softener Power Output Suppression Edge Enhance 0 Rejection 0 Calorize Steer Diff Focus Position Fo cus Number LOGIQ P5 A5 A5Pro Quick Guide Color Flow Doppler Image Optimize Baseline Adjusts the baseline to accommodate faster or slower blood flows to eliminate aliasing PRF Wall Filter Velocity scale determines pulse repetition frequency If the sample volume gate range exceeds single gate PRF
44. ol pem ___ __ p 1 0 00 1 LL jp __ went __ p p P j Lj wowacenie 0000 o po p P P P jo 2 0 o p p P P PP Lj 2 Ww ILL TI ITT Ir JILL LI TI TTT HER L LL ITT NEN o d do _ Using Probes 15 LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 LOGIQ P5 A5 A5Pro Features Table 1 3 Probe Features Probe Applicaton ascs ac scs ec eec oc ot im m va vo vo Gem D OD I fx x x X X X DS mE X X X SRI X X X X EES ix x x hows X x xe de x x eee ES xxx xx fe ee x ke ES px xe de xx fe ee x ES Deme p qx x x x x x x x x x x x x Wwe x x xx x x x x x x x x x x p x x x x x x xx x x x x x x kee egen omm X X m X X LN LN exe EES ki n wey yey i T E n i i x X X X X X K X XJ X xX xX X X X X X X X XIXI X X XJ X Xx Xx Xx X X XJ X X X XJ X X X XxX X X XJ X X X K X X X mmm BEER mmm mmm rmm i mmm mmm EHE Will x x TI THT E LOGIQ P5 A5 A5Pro Quick Guide Direction
45. probe A defective probe or excessive force can cause patient injury or probe damage Observe depth markings and do not apply excessive force when inserting or manipulating intercavity probes Inspect probes for sharp edges or rough surfaces that could injure sensitive tissue In order for liquid chemical germicides to be effective all visible residue must be removed during the cleaning process Thoroughly clean the probe as described on the following page before attempting disinfection CREUTZFIELD JACOB DISEASE Neurological use on patients with this disease must be avoided If a probe becomes contaminated there is no adequate disinfecting means EP Electrical The probe is driven with electrical energy that can injure the patient or user if live internal parts are contacted by conductive solution Hazard DO NOT immerse the probe into any liquid beyond the level indicated by the immersion level diagram Never immerse the probe connector or probe adaptors into any liquid DO NOT drop the probes or subject them to other types of mechanical shock or impact Degraded performance or damage such as cracks or chips in the housing may result Inspect the probe before and after each use for damage or degradation to the housing strain relief lens and seal A thorough inspection should be conducted during the cleaning process DO NOT kink tightly coil or apply excessive force on the probe cable Insulation failure may result
46. r press Clear once To clear the trace caliper and the current data measured press Clear twice LOGIQ P5 A5 A5Pro Quick Guide Volume 1 make a volume calculation do one of the following e one distance measurement Make two distance measurements Make three distance measurements NOTE Three distances should be done in the dual format mode side by side images One measurement is usually made in the sagittal plane and two measurements in the axial plane e one distance and one ellipse measurement e one ellipse measurement 2 Select Volume Time Interval Measurement 1 Press Measure twice and active caliper with a vertical dotted line displays 2 To position the active caliper at the start point move the Trackball 3 To fix the start point press Set The system fixes the first caliper and displays a second active caliper 4 To position the second caliper at the end point move the Trackball 5 complete the measurement press Set The system displays the time interval between the two calipers in the measurement results window Direction 5137113 100 Rev 3 Velocity Measurement 1 Press Measure an active caliper with a vertical dotted line displays 2 To position the caliper at the desired measurement point move the Trackball complete the measurement press Set The system displays the velocity measurement in the measurement results win
47. r radiated RF If the maximum transmitter power in watts is rated The separation distance in meters should be LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 43 Notice upon Installation of Product Separation distance and effect from fixed radio communications equipment field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile radios amateur radio AM and FM radio broadcast and TV broadcast transmitter cannot be predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the ultrasound system is used exceeds the applicable RF compliance level as stated in the immunity declaration the ultrasound system should be observed to verify normal operation If abnormal operation is observed additional measures may be necessary such as re orienting or relocating the ultrasound system or using an RF shielded examination room may be necessary 1 Use either power supply cords provided by GE Medical Systems or ones designated by GE Medical Systems Products equipped with a power source plug should be plugged into the fixed power socket which has the protective grounding conductor Never use any adaptor or converter to connect with a power source plug i e three prong to two prong converter 2 Locate the equipment as far away as
48. rd may exist which through inappropriate conditions or actions will or can cause e Minor injury Property damage NOTE Indicates precautions or recommendations that should be used in the operation of the ultrasound system specifically e Maintaining an optimum system environment e Using this Manual e Notes to emphasize or clarify a point LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 32 Hazard Symbols Icon Description Potential hazards are indicated by the following icons Table 1 1 Potential Hazards EN IE esi cis EN NENNEN 585 Biological Patient user infection due to contaminated equipment Cleaning and care instructions ISO 7000 Hazard Sheath and glove guidelines No 0659 a Electrical Electrical micro shock to patient e g ventricular Probes e ECG A Hazard e Connections to back panel Moving e Console accessories or optional storage devices that can fall on patient user or others e Moving Hazard e Collision with persons or objects result in injury while maneuvering or during system e Using brakes transport e Transporting e Injury to user from moving the console Acoustic e Patient injury or tissue damage from ultrasound radiation e ALARA the use of power output following Output the as low as reasonably achievable Hazard principle Explosion e Risk of explosion if used in the presence of flammable anesthetics e Flammable anesthetic Hazard Smoke amp e Patient user injury or adver
49. se reaction from fire or smoke e Replacing fuses Fire Hazard e Patient use injury from explosion and fire e Outlet guidelines LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 33 Important Safety Considerations The following topic headings Patient Safety and Equipment and Personnel Safety are intended to make the equipment user aware of particular hazards associated with the use of this equipment and the extent to which injury can occur if precautions are not observed Additional precautions may be provided throughout the manual CAUTION Improper use can result in serious injury The user must be thoroughly familiar with the instructions and potential hazards involving 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 Patient Safety Related Hazards WARNING The concerns listed can seriously affect the safety of patients undergoing a diagnostic ultrasound examination Patient identification Always include proper identification with all patient data and verify the accuracy of the patient s name or ID numbers when entering such data Make sure correct patient ID is provided on all recorded data and hard copy prints Identification errors could result in an incorrect diagnosis Diagnostic information Equipment malfunction or incorrec
50. ss LU the left split screen key 4 To perform a parallel scan scan evenly perform a sweep fan scan rock the probe once Note the distance of the scan 5 The 3D volume of interest is dynamically assembled on the right side of the screen NOTE If the image stops before you re done scanning start acquiring the SD volume of interest again 6 complete the 3D scan press R the right split screen key NOTE You can also press Freeze but then you need to also press the 3D key to obtain the final render Direction 5137113 100 Hev 3 Manipulating the 3D Scan Imagine you are able to manipulate the 3D volume of interest VOI in your hand You can rotate it left to right or right to left You can rotate it forward backward white hand Then imagine that you can view the volume of interest one slice at a time through the anatomy red hand Also imagine that you are able to pull back tissue to view specific portions of anatomy yellow and green hands The 3D volume of interest is a tangible anatomical object that you can see and manipulate easily using the Trackball and Set control panel keys Practice positioning the pointer at different places within the 3D volume of interest Highlight different colors press Set to select this volume for manipulation Use the hand to move the 3D volume Adjusting the 3D Volume of Interest You can colorize the 3D volume of interest You can resize
51. t settings can result in measurement errors or failure to detect details within the image The equipment user must become thoroughly familiar with the equipment operation in order to optimize its performance and recognize possible malfunctions Applications training is available through the local GE representative Added confidence in the equipment operation can be gained by establishing a quality assurance program CAUTION The system s acoustic output remains transmitting when the user controls are being used Allowing the system to transmit acoustic output with the probe not in use or in its holder can cause the probe to build up heat Always turn off acoustic output or freeze the image when not in use LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 34 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 Never use excessive force when manipulating intracavity probes Become familiar with all instructions and precautions provided with special purpose probes Electrical A damaged probe can also increase the risk of electric shock if conductive solutions come in contact with internal live parts Inspect probes A Hazard often for cracks or openings in the housing and holes in and around
52. tation adjustment may be needed depending on the anatomy being scanned For example if the fetus is in the breech position the top of the baby s head is facing up However if the fetus is vertex the top of the head faces down and the orientation needs to be flipped 180 degrees Use the 3D Orient button to change the orientation TIP Any fluid interface provides the best results For example for a 3D 4D view of the fetal face first obtain the best profile view 2 Press 3D 3 Press Real Time 4D Preparing for an Exam LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 Optimizing the 4D Rendered Image Orientation Rotations when on full screen mode Rotates Image Up and Down Rotate Y E Tranzwerzal Rotates Image Clockwise and p Counterclockwise Rotate Z 28 Tools to Improve 4D Image Quality TIP When scanning in 4D use slow movements to keep the ROI in the field of view Select the Render Setting tab Quality High Quality best resolution but slower acquisition rates Lower Quality fastest acquisition speeds but less resolution of 3D AD image Lower Threshold The higher numbers effectively make the image brighter by taking away the low level echoes Typical range for OB 10 45 Render Modes Rend Mode 1 amp 2 e Surface Texture better for older fetuses more detail e Surface Smooth better for younger fetuses smoother rendered image e Tr
53. tes call the GE Access Center TEL 1 800 472 3666 In other locations contact your local Applications Sales or Service Representative OTHER COUNTRIES NO TOLL FREE TEL international code 33 1 39 20 0007 CANADA GE Healthcare Ultrasound Svc Engineering TEL 1 800 664 0732 9900 Innovation Drive Wauwatosa WI 53226 Customer Answer Center TEL 1 262 524 5698 LATIN amp SOUTH AMERICA GE Healthcare Ultrasound Svc Engineering TEL 1 262 524 5300 9900 Innovation Drive Wauwatosa WI 53226 Customer Answer Center TEL 1 262 524 5698 EUROPE GE Ultraschall Deutschland GmbH amp Co KG BeethovenstraDe 239 Postfach 11 05 60 D 42655 Solingen TEL 0130 81 6370 toll free TEL 49 212 28 02 207 FAX 49 212 28 02 431 29 ASIA GE Medical Systems Asia Asia Support Center 67 4 Takakura cho Hachiouji shi Tokyo 192 0033 TEL 81 426 48 2940 FAX 81 426 48 2905 ARGENTINA GEME S A Miranda 5237 Buenos Aires 1407 TEL 1 639 1619 FAX 1 567 2678 AUSTRIA GE GesmbH Medical Systems Austria Prinz Eugen Strasse 8 8 A 1040 WIEN TLX 136314 TEL 0660 8459 toll free FAX 43 1 505 38 74 BELGIUM GE Medical Systems Benelux Gulkenrodestraat 3 B 2160 WOMMELGEM TEL 0 800 11733 toll free FAX 32 0 3 320 12 59 TLX 72722 BRAZIL GE Sistemas M dicos Av Nove de Julho 5229 01407 907 Sao Paulo SP TEL 0800 122345 FAX 011 3067 8298 LOGIQ P5 A5 A5Pro
54. the VOI by adjusting the scan distance 26 Performing a Surface Render From the 3D Top Menu press Texture to add a photorealistic clay like quality to the render Adjust the opacity and density via Threshold Opacity press the key to adjust opacity This adjusts what grays the system recognizes allowing you to emphasize de emphasize grays as necessary Scalpel To scalpel away portions of the anatomy 1 Press Scalpel A caliper appears on the 3D VOI 2 Press Set to set the caliper Trackball around the portion to be cut away 3 Double click and apply the scalpel 4 Change the projection and scalpel again NOTE You can undo one scalpel 3DView Scanning Hints oet the appropriate values for the 3D Acq Mode and Scan Plane It is advisable to set the scan distance before the scan begins LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 27 Basic 4D 1 Scan in 2D and obtain the best possible view of your 4 Adjust the size and position of the ROI box using the 6 To start 4D acquisition press SET button Region of Interest ROI Scan Area button and Trackball 7 Use the Tile button change the display between the rci Press the Scan Area button ONCE to resize the following screens ROI move the Trackball left right or up down Quad Split Full Press Scan Area AGAIN to re position the ROI using the Trackball to move the ROI DA SH POUL 96 Medicu Systems 030 S TIP Orien
55. the acoustic lens or other damage that could allow liquid entry Become familiar with the probe s use and care precautions outlined in Probes and Biopsy CAUTION Ultrasound transducers are sensitive instruments which can easily be damaged by rough handling Take extra care not to drop transducers and avoid contact with sharp or abrasive surfaces A damaged housing lens or cable can result in patient injury or serious impairment or operation CAUTION Ultrasound can produce harmful effects in tissue and potentially result in patient injury Always minimize exposure time and keep ultrasound levels low when there is no medical benefit Use the principle of ALARA As Low As Reasonably Achievable increasing output only when needed to obtain diagnostic image quality Observe the acoustic output display and be familiar with all controls affecting the output level See the Bioeffects section of the Acoustic Output chapter in the Advanced Reference Manual for more information CAUTION Do not use with Defibrillator 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 der
56. tion of this menu decouples the user defined configuration above This allows you to selectively restore what you want to restore across multiple machines NOTE DO NOT restore service back ups across systems from one LOGIQ P5 A5 A5Pro system to another LOGIQ P5 A5 A5Pro system LOGIQ P5 A5 A5Pro Quick Guide Moving Data Between Ultrasound Systems There are 5 options Import Export Q R Worklist and MPEGvue under Data Transfer Import 1 Atthe other Ultrasound system insert the removable media 2 Press Patient and select Data Transfer 3 Select Import 4 Select Local Archive Int HD from the Transfer To pull down menu 5 Select the patient s or exam s from the Transfer From Search field for import 6 Press Transfer 7 Wait until the patient information is copied and press F3 when finished to eject the media Export 1 Insert format and label the removable media 2 Press Patient and select Data Transfer 3 Select Export 4 Select the patient s or exam s to export in the Transfer From Search field the top portion 5 Select the destination at the Transfer To pull down menu 6 Press Transfer The progress bar displays during the transfer 7 Press F3 to eject the media Specify that you want to finalize the media Direction 5137113 100 Rev 3 Query Retrieve Q R 1 Press Patient and select Data Transfer 2 Select Q R The local archive is enabled for the transfer process 3
57. to prevent overheating of the device There must be adequate mechanical mounting of the device and stability of the combination Risk and leakage current of the combination must comply with IEC EN 60601 1 Electromagnetic emissions and immunity of the combination must conform to IEC EN 60601 1 2 Qn e LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 45 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 2 The added device s must be used for their intended purpose having a compatible interface 3 Signal or mains isolation devices and additional protective earth may be needed to assure compliance with IEC EN 60601 1 1 CAUTION The connection of equipment or transmission networks other than as specified in the user instructions can result in an electric shock hazard or equipment malfunction Substitute or alternate equipment and connections requires verification of compatibility and conformity to IEC EN 60601 1 1 by the installer Equipment modifications and possible resulting malfunctions and electromagnetic interference are the responsibility of the owner Declaration of Emissions This system is suitable for use in the following environment The user must assure that it is used only in the electromagnetic environment as specified Table 1 6 D
58. top To stop CINE Loop playback press Run Stop To activate Timeline CINE press Freeze press Scan Area then roll the Trackball to activate CINE Quickly Move to Start End Frame Press First to move to the first CINE frame press Last to move to the last CINE frame Start Frame End Frame Turn the Start Frame dial to the left to move to the beginning of the CINE Loop Turn the dial to the right to move forward through the CINE Loop Turn the End Frame dial to the right to move to the end of the CINE Loop Turn the dial to the left to move backward through the CINE Loop Adjusting the CINE Loop Playback Speed Turn the Loop Speed dial clockwise counter clockwise to increase decrease the CINE Loop playback speed Preparing for an Exam Direction 5137113 100 Rev 3 Disconnecting B Mode CINE from Timeline CINE To review the B Mode CINE Loop only press Cine Mode Selection and select B Only To review the Timeline CINE Loop only press Cine Mode Selection and select TL Only To return to linked B Mode and Timeline CINE Loop review press Cine Mode Selection and select B TL Moving through a CINE Loop Frame By Frame Turn Frame by Frame to move through CINE memory one frame at a time 25 LOGIQ P5 A5 A5Pro Quick Guide Easy 3D option Acquiring a 3D Scan 1 Optimize the B Mode image Ensure even gel coverage 2 Press the 3D control panel key Two screens appear To start acquiring the image pre
59. tput 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 LOGIQ P5 A5 A5Pro Quick Guide Warning Label Locations Console Labels 1 Possible shock hazard Do not remove 7 covers or panels No user serviceable parts are inside Refer servicing to qualified service personnel 2 Do not use the following devices near this equipment cellular phone radio receiver mobile radio transimitter 8 radio controlled toy etc Use of these devices near this equipment could cause this equipment to perform outside the published specifications Keep power to these devices turned off when near this equipment 10 3 The equipment weighs approximately 80 kg 176 lbs To avoid possible injury and equipment damage when transporting from one area of use to another Be sure the pathway is clear Limit movement to a slow careful walk Use two or more persons to move the equipment on inclines or long distance Prescription Device For U S A Only 5 The CE Mark of Conformity indicates this equipment conforms with the Council Directive 93 42 EEC 6 WEEE label indicates that the waste of electrical and electronic equipment must not be disposed as unsorted municipal waste and must be collected separately Please contact an authorized representative of the manufacturer for information concerning the decommissioning
60. trols in Common with B Mode For more information on Focal Zone Power Output FR RES Frame Averaging Dynamic Range Map and Colorize refer to the B M Mode Image Optimize section in this Quick Guide on Page 6 Scanning Hints Line Density Trades frame rate for sensitivity and spatial resolution If the frame rate is too slow reduce the size of the region of interest select a different line density setting or reduce the packet size Wall Filter Affects low flow sensitivity versus motion artifact To improve sensitivity Increase the Gain Decrease the PRF Increase the Power Output Adjust the Line Density Decrease the Wall Filter Increase Frame Averaging Increase the Packet Size Reduce the ROI to the smallest reasonable Size 9 Position the Focal Zones properly po DUO e cue To decrease motion artifact 1 Increase the PHF 2 Increase the Wall Filter To eliminate aliasing 1 Increase the PRF 2 Lower the Baseline Color Flow Doppler Image Optimize continued For venous imaging 1 Ensure that you have selected the small parts exam category 2 Select a venous application Healthcare 6 7 08 12 08 16 50 13 1679 1679 26 0 25 7 5 Carotid Kn Rt Lt Won Stenosis X Volume C Angle IMT i A B Ratio Worksheet Direct Angle Steer E Spatial Filter Frequency a Threshold Map Invert CFM Mode and Sub Menu
61. tween active calipers press Measure 9 complete the measurement press Set The system displays the circumference and area in the measurement results window NOTE Before you complete a measurement To erase the ellipse and the current data measured press Clear once The original caliper is displayed to restart the measurement To exit the measurement function without completing the measurement press Clear a second time 17 Circumference Area Trace Measurement 1 Press Measure twice a trace caliper displays 2 To position the trace caliper at the start point move the Trackball To fix the trace start point press Set The trace caliper changes to an active caliper 4 To trace the measurement area move the Trackball around the anatomy A dotted line shows the traced area NOTE To erase the dotted line but not the trace caliper press Clear once To clear the trace caliper and the current data measured press Clear twice NOTE To erase the line bit by bit back from its current point move the Trackball or turn the Ellipse control counterclockwise 5 complete the measurement press Set The system displays the circumference and the area in the measurement results window NOTE Before you complete a measurement To erase the line bit by bit back from its current point move the Trackball or turn the Ellipse control counterclockwise To erase the dotted line but not the trace calipe
62. u 13 LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 LOGIQ P5 A5 A5Pro Probe Applications Table 1 1 Probe Indications for Use Probe Application 352 3505 4C ses ac EsCS e 9L im Wie ws 35 ss w pepe eee AIC ____ ___ mox x x x __ uw I wx x mel _ m1 _ _ __ ix on __ 111i e wo r nds eal x x qx x ee NN mn LL j III TI LL Te Is real O 0 0 pq P j jx _ 0 p p p p p p Bene 000 0 j L LL essel ___ _ E j J j j p Transesophageal ewe __ j J j j LL l1 l1 1 1 1 nm X X XJ X 14 LOGIQ P5 A5 A5Pro Quick Guide Direction 5137113 100 Rev 3 LOGIQ P5 A5 A5Pro Probe Applications continued Table 1 2 Probe Indications for Use continued n I 131 8 _ __ E E 2 __ __ o x 0 0 __ ewe __ p p P p owes o J p P P _ j LL wm __ ___ ___ _ __ _ j j me o o Ix x gp fx fx xe _ sew LI ILL ll Ll Ll L
63. v 3 LOGIQ P5 A5 A5Pro Top and Sub Menu Controls In general Top Menu Controls are of two types Sub Menu key functions they are Push amp Turn Knobs Sub Menu is of Up Paddle Switch type mE Increase Value Next Page 1 The Paddle Switch is used to select Sub Menu Decrease Value Previous Page Controls 2 he Push is used to select Top Menu Controls 3 Rotate is used to turn on off or change the parameter selected through Top Menu Controls Top Menu Controls LOGIQ P5 A5 A5Pro Quick Guide LOGIQ P5 A5 A5Pro Monitor Display Tour L Institution Hospital Name Date Time Operator Identification Patient Name Patient Identification Acoustic Output Readout System status real time or frozen GE Symbol Probe Orientation Marker Coincides with a probe orientation marking on the probe Image Preview Gray Color Bar Cine Gauge di ER 1059 AD ee RI JE SR Ete DET ich Vole jc Angle Renal Volume 1 1 AH 11 Rend Leger Wink ob Ag Ei Preparing for an Exam fap GE Healthcare Direction 5137113 100 Rev 3 8 Measurement Summary Window 9 Image 10 Measurement 11 Results Window 12 Probe Identifier Exam Study 13 Imaging Parameters by Mode current mode highlighted 14 Focus Marker 15 TGC not shown on the image 16 Body Pattern 1 2 da VONGE 11 3343 AM 3 1 0 Tis 0 1 46
64. y contact with certain chemicals Failure to follow these precautions can result in serious injury and equipment damage Do not immerse the probe into any liquid beyond the level specified for that probe Never immerse the transducer connector or probe adapters into any liquid Avoid mechanical shock or impact to the transducer and do not apply excessive bending or pulling force to the cable Transducer damage can result from contact with inappropriate coupling or cleaning agents Do not soak or saturate transducers with solutions containing alcohol bleach ammonium chloride compounds or hydrogen peroxide Avoid contact with solutions or coupling gels containing mineral oil or lanolin Avoid temperatures above 60 C Inspect the probe prior to use for damage or degeneration to the housing strain relief lens and seal Do not use a damaged or defective probe CAUTION Adequate cleaning and disinfection are necessary to prevent disease transmission It is the responsibility of the equipment user to verify and maintain the effectiveness of the infection control procedures in use Always use sterile legally marketed probe sheaths for intra cavitary and intra operative procedures For neurological intra operative procedures use of a legally marketed sterile pyrogen free probe sheath is REQUIRED Probes for neuro surgical use must not be sterilized with liquid chemical sterilants because of the possibility of neuro toxic residues remaining on the

Download Pdf Manuals

Related Search

Related Contents

INSTRUCTION MANUAL Audioart  MANUAL DE INSTRUÇÕES  Watt Meter and Power Analyzer User`s Manual    Annexe A.5 - PHPNET - Nom de domaine gipsa  TDS-BD-APX500 Hardware User Manual  Friedrich Heat Pump 920-087-09 User's Manual  Quicken 2004 Home & Business Users Guide  

Copyright © All rights reserved. Failed to retrieve file