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    Del DRVIndico 100Operators Manual

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    I II III

    Indico 100

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    This manual contains informationFor the operation of the Indico 100

    X-Ray generator

    Del Medical Imaging Corp.11550 W. King StreetFranklin Park, IL 60131Technical Support: 847-288-7000Fax: 847-288-7911Email: [email protected]

    Manual Part Number: 8000-DRVOPR Revision: A May 23, 2003

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    2003 Del Medical Imaging Corp. Revision A Page 3

    INTRODUCTION 1

    Del DRVINDICOOPERATOR

    SAFETY AND SPECIFICATIONS 2

    MANUALCONSOLE CONTROLS 3

    REMOTE FLUORO CONTROLLER 4

    kV -mAs REDUCTION FORPERIPHERAL ANGIOGRAPHY 5

    PROGRAMMING THE CONSOLE 6

    ERROR CODES AND MESSAGES 7

    GENERATOR EXPOSURE TABLES 8

    MAINTENANCE SCHEDULE 9

    X-RAY TUBE DATA 10

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    2003 Del Medical Imaging Corp. Revision A Page 5

    INTRODUCTION 1

    Congratulations!

    You have acquired the Del Indico 100 series high frequency X-ray generator. This generator features stateof-the-art computer-based control to ensure minimum patient dose, excellent repeatability, and superior

    contrast. The operator control functions are designed to be simple and user-friendly.

    The AEC (Automatic Exposure Control) and APR (Anatomical Programming) features give you controlledexposure factors, automatically optimized for the radiological study selected.

    INDICO 100 MAIN FEATURES

    Models available in maximum output power of 32 to 80 kW, in both radiographic and fluoroscopic modelsA radiographic-only 100 kW model is also available.

    Full 150 kV capability for all models.

    Smaller, lighter modular design.

    Constant dose output due to kV and mA regulation during exposures.

    User-friendly controls. Large LCD panel display for APR and utility routines.

    User-friendly system configuration.

    APR techniques may be modified by the operator.

    ms and mAs limits for AEC may be operator set.

    Provisions for APR / tube downloading.

    Extensive self-diagnostics with operator prompt messages.

    Serial RS232 communications interface.

    May be programmed for APR operation only or both APR and manual technique selection.

    Time and mA / mAs selections are to IEC standards.

    Programmable setup, calibration and APR routines (using an external computer).

    Choice of ten fluoro kV to rad kV transfer curves (R & F units only).

    Choice of four kV vs. mA curves for ABS (automatic brightness stabilization) circuits (R & F units only).

    OPTIONS

    Dual speed starter for automatic high / low speed selection.

    Two-tube capability.

    Pedestal mount or wall mount bracket for operator control console.

    Automatic brightness stabilization (ABS) for consistent imaging (AUTO kV / mA or kV only).

    Remote fluoro controller for R & F tableside operation.

    Digital imaging interface.

    Remote exposure hand switch.

    High level fluoro for therapy simulators.

    Pulsed fluoro with last image hold.

    kV / mAs reduction for peripheral angiography.

    DAP (Dose Area Product).

    SAFETY NOTICE: This manual contains important operating and safety information. An understandingof this information is critical to the safe operation and long term reliability of yourequipment. Please ensure that you read the warning notices before using thisequipment.

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    1 Introduction

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    GENERATOR DUTY CYCLE LIMIT

    NOTE: THE FOLLOWING SECTION CONTAINS IMPORTANT INFORMATION. PLEASE READ ANDUNDERSTAND THIS MATERIAL BEFORE CONTINUING.

    Internal X-ray generator components will heat up during normal use of the generator. This is similar to X-ray tubeheating during normal generator operation. The amount of heat produced is proportional to the product of kV, mA,and time

    Modern X-ray generators are designed to operate with the majority of X-ray tubes over their rated power ranges.They are designed for operating duty cycles consistent with practical patient examination routines that allowfor reasonable cooling intervals between X-ray exposures. Insufficient cooling time between exposures maylead to excessive heat build - up in the generator, which may cause serious generator damage.

    This X-ray generator has internal duty cycle monitoring to warn of excessive heat build - up. If the generatorcalculates that the next exposure will exceed the rated generator duty cycle limit, a warning message GEN DUTYWARNING will be displayed. Exposures will not be inhibited when this message is displayed, but it should beunderstood that continuing to make exposures might cause generator damage due to overheating. If possible, thegenerator should be allowed to cool sufficiently such that this message is no longer displayed.

    DAILY X-RAY TUBE WARM-UP PROCEDURE

    CAUTION: THE FOLLOWING PROCEDURE PRODUCES X-RAYS. OBSERVE ALL SAFETYPRECAUTIONS TO PROTECT PERSONNEL.

    Use this procedure when the generator is first turned on for the day, or when it has not been used for severalhours. This procedure provides for exposures at medium power before the tube is used at maximum mA or kVvalues. This will reduce the possibility of damaging the anode and high voltage components. No test setup isrequired.

    For maximum stability and reliability, use the following techniques at start up:Select the following:

    Large focal spot

    80 kV

    Normal 50/60 Hz anode rotation

    For a 300 kHU to a 400 kHU tube, use approximately 200 mAs per exposure. For a 200 kHU to 300 kHU tubeuse approximately 150 mAs per exposure.

    Depending on the X-ray tube power rating, select either 100 mA or 200 mA.

    Make one (1) to three (3) exposures (depending on tube loading) at 30 second intervals.

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    SAFETY AN D SPECIFICAT IONS 2

    Keep this operators manual with the equipment at all times, and periodically review the operating and safetyinstructions.

    SAFETY / WARNING SYMBOLS

    Warning symbol used to indicate a potential hazardto operators, service personnel or to the equipment.It indicates a requirement to refer to theaccompanying documentation for details.

    Radiation exposure symbol used on operatorconsole. Lights to indicate that an exposure is inprogress. This is accompanied by an audible tonefrom the console.

    Fluoro radiation exposure symbol used on operator

    console and on optional remote fluoro control unit.Lights to indicate that a fluoro exposure is inprogress. This is accompanied by an audible tonefrom the console.

    WARNING THIS X-RAYUNIT MAY BEDANGEROUS TO PATIENT ANDOPERATOR UNLESS SAFEEXPOSURE FACTORS ANDOPERATING INSTRUCTIONSARE OBSERVED.

    Radiation warning label on console, used in certainjurisdictions.

    Never allow unqualified personnel to operate the X-ray generator.

    WARNING: PROPER USE AND SAFE OPERATING PRACTICES WITH RESPECT TO X-RAYGENERATORS ARE THE RESPONSIBILITY OF THE USERS OF SUCH GENERATORS. DELMEDICAL IMAGING CORP. PROVIDES INFORMATION ON ITS PRODUCTS ANDASSOCIATED HAZARDS, BUT ASSUMES NO RESPONSIBILITIES FOR AFTER-SALEOPERATING AND SAFETY PRACTICES.

    DEL ACCEPTS NO RESPONSIBILITY FOR ANY GENERATOR NOT MAINTAINED ORSERVICED ACCORDING TO THE SERVICE AND INSTALLATION MANUAL OR ANYGENERATOR THAT HAS BEEN MODIFIED IN ANY WAY.

    DEL ALSO ASSUMES NO RESPONSIBILITY FOR X-RAY RADIATION OVEREXPOSURE OFPATIENTS OR PERSONNEL RESULTING FROM POOR OPERATING TECHNIQUES ORPROCEDURES.

    WARNING: THIS X-RAY UNIT MAY BE DANGEROUS TO PATIENT AND OPERATOR UNLESS SAFEEXPOSURE FACTORS AND OPERATING INSTRUCTIONS ARE OBSERVED.

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    2 Safety and Specifications

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    X-ray radiation exposure may be damaging to health, with some effects being cumulative and extending overperiods of many months or even years. X-ray operators should avoid any exposure to the primary beam andtake protective measures to safeguard against scatter radiation. Scatter radiation is caused by any object in thepath of the primary beam and may be of equal or less intensity than the primary beam that exposes the film.

    No practical design can incorporate complete protection for operators or service personnel who do not takeadequate safety precautions. Only authorized and properly trained service and operating personnel should

    be allowed to work with this X-ray generator equipment. The appropriate personnel must be made aware ofthe inherent dangers associated with the servicing of high voltage equipment and the danger of excessiveexposure to X-ray radiation during system operation.

    Wear protective clothing. Protective aprons with an equivalent of a minimum of 1/64 (0.35 mm) of lead arerecommended.

    To protect the patient against radiation, always use radiation protection accessories in addition to deviceswhich are fitted to the X-ray equipment.

    Keep as large a distance as possible away from the object being exposed and the X-ray tube assembly.

    This X-ray equipment may only be operated in medical rooms which meet IEC requirements.

    Never operate this X-ray equipment in areas where there is a risk of explosion. Detergents and disinfectants,including those used on patients, may create explosive mixtures of gases. Please observe the relevantregulations.

    The operator console, or anything electrically connected to it, must never be used within 6 ft (1.8 m) of thepatient environment.

    Only trained maintenance staff may remove the covers of the generator cabinet and the control console.

    Do not connect unapproved equipment to the rear of the console: J5 is for the interconnectcable to the generator main cabinet, J2 is a serial port for use by an external computer, andJ13 is for connection of an external hand switch and / or foot switch. INCORRECTCONNECTIONS OR USE OF UNAPPROVED EQUIPMENT MAY RESULT IN INJURY OREQUIPMENT DAMAGE.

    CONSULT YOUR SERVICE REPRESENTATIVE IF EXTERNAL EQUIPMENT IS TOBE CONNECTED TO THIS SYSTEM. PERIPHERAL DEVICES SHOULD BE IEC 601-1APPROVED IF LOCATED IN THE PATIENT AREA, AND IEC 950 APPROVED IF OUTSIDETHE PATIENT AREA.

    CAUTION: DO NOT EXCEED THE TUBE MAXIMUM OPERATING LIMITS SHOWN IN THE SECTION X-RAY TUBE DATA AT THE END OF THE OPERATORS MANUAL. INTENDED LIFE AND

    RELIABILITY WILL NOT BE OBTAINED UNLESS GENERATORS ARE OPERATED WITHINPUBLISHED SPECIFICATIONS.

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    Safety and Specifications 2

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    APPLICABLE STANDARDS

    The Indico 100 family of generators complies with the following regulatory requirements and design standards:

    FDA Center for Devices & Radiological Health (CDRH) - 21 CFR title 21 subchapter J (USA).

    Radiation Emitting Devices Act - C34 (Canada).

    Medical Device Regulations (Canada).

    EC Directive 93/42/EEC concerning Medical Devices (European Community).

    IEC 601.1, IEC 601.2.7:1998, CSA 601.1, UL2601.1

    -Type of protection against electric shock: Class I equipment.-Degree of protection against electric shock: Not classified.-Degree of protection against harmful ingress of water: Ordinary equipment.-Mode of operation: Continuous operation with intermittent loading (standby - exposure).-Equipment not suitable for use in presence of a FLAMMABLE ANESTHETIC MIXTURE WITH AIROR WITH OXYGEN OR NITROUS OXIDE.

    IEC 601.1.2Immunity:IEC1000-4-2 Electrostatic dischargeIEC1000-4-3 Radiated RF fieldIEC1000-4-4 Electrical fast transientIEC1000-4-5 SurgeIEC1000-4-6 Conducted RF immunityIEC1000-4-8 Magnetic field immunityIEC1000-4-11 Voltage dips, interrupts and variations

    Emission:EN55011 (CISPR Publications II Emission Standards, Group 1 Class A).

    ELECTROMAGNETIC COMPATIBILITY (EMC)

    In accordance with the intended use, this X-ray generator complies with the European Council Directiveconcerning Medical Devices. The CE marking affixed to this product signifies this. One of the harmonizedstandards of this Directive defines the permitted levels of electromagnetic emission from this equipment and itsrequired immunity from the electromagnetic emissions of other devices.

    It is not possible, however, to exclude with absolute certainty the possibility that other high frequency electronicequipment, which is fully compliant to the EMC regulations, will not adversely affect the operation of this generatorIf the other equipment has a comparatively high level of transmission power and is in close proximity to thegenerator, these EMC concerns (the risk of interference) may be more pronounced. It is therefore recommendedthat the operation of equipment of this type such as mobile telephones, cordless microphones and other similamobile radio equipment be restricted from the vicinity of this X-ray generator.

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    2 Safety and Specifications

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    OUTPUT PARAMETERS

    kV range: Radiography 40 to 150 kV.

    Fluoroscopy 40 to 125 kV.

    kV accuracy: (5% + 1) kVp.

    mA range: Radiography 10 to 400 mA (32 kW), 10 to 500 mA (40 kW), 10 to630 mA (50 kW), 10 to 800 mA (65 kW), and 10 to 1000 mA (80and 100 kW).

    Fluoroscopy 0.5 to 6.0 mA, 0.5 to 20 mA optional. Normally usedfor therapy simulators only.

    mA accuracy: (5% +1.0) mA for all mA values.

    mAs range: Tube dependent, max 1000 mAs.

    Time range: Radiography 1.0 to 6300 ms (40 to 100 kW), 1.25 to 6300ms (32kW).

    Fluoroscopy 0 to 5 or 0 to 10 minutes.

    Lowest current - time

    product: 0.5 mAs.

    Loading factors whichwill allow lowestcurrent - time product: All mA values 500 mA. Refer to table 1 in section 7.

    * 20 mA maximum for fluoroscopy available with high level fluoro option only.

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    Safety and Specifications 2

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    OUTPUT PARAMETERS (Continued)

    OUTPUT PARAMETER MODE GENERATOR SERIES LOADING FACTOR

    Maximum X-ray tubevoltage and highest X-ray

    tube current at that

    voltage

    Radiographic

    (Intermittent)

    100 kW

    80 kW

    65 kW

    50 kW

    40 kW

    32 kW

    150 kV, 630 mA

    150 kV, 500 mA

    150 kV, 400 mA

    150 kV, 320 mA

    150 kV, 250 mA

    150 kV, 200 mA

    Maximum X-ray tubevoltage and highest X-ray

    tube current at thatvoltage

    * See note on previouspage

    Fluoroscopic

    (Continuous)

    80 kW

    65 kW

    50 kW

    40 kW

    32 kW

    125 kV, 6 / 20 mA

    125 kV, 6 / 20 mA

    125 kV, 6 / 20 mA

    125 kV, 6 / 20 mA

    125 kV, 6 / 20 mA

    Maximum X-ray tubecurrent and highest X-ray

    tube voltage at that

    current

    Radiographic

    (Intermittent)

    100 kW

    80 kW

    65 kW

    50 kW

    40 kW

    32 kW

    1000 mA, 80 kV

    1000 mA, 80 kV

    800 mA, 80 kV

    630 mA, 80 kV

    500 mA, 80 kV

    400 mA, 80 kV

    Maximum X-ray tubecurrent and highest X-ray

    tube voltage at thatcurrent

    * See note on previouspage

    Fluoroscopic

    (Continuous)

    80 kW

    65 kW

    50 kW

    40 kW

    32 kW

    6 / 20 mA, 125 kV

    6 / 20 mA, 125 kV

    6 / 20 mA, 125 kV

    6 / 20 mA, 125 kV

    6 / 20 mA, 125 kV

    Combination of X-ray tubecurrent and X-ray tube

    voltage resulting in

    highest output power

    Radiographic

    (Intermittent)

    100 kW

    80 kW

    65 kW

    50 kW

    40 kW

    32 kW

    1000 mA, 100 kV

    1000 mA, 80 kV

    800 mA, 80 kV

    630 mA, 80 kV

    400 mA, 100 kV

    320 mA, 100 kV

    Combination of X-ray tubecurrent and X-ray tube

    voltage resulting inhighest output power

    * See note on previouspage

    Fluoroscopic

    (Continuous)

    80 kW

    65 kW

    50 kW

    40 kW

    32 kW

    6 / 20 mA, 125 kV

    6 / 20 mA, 125 kV

    6 / 20 mA, 125 kV

    6 / 20 mA, 125 kV

    6 / 20 mA, 125 kV

    Highest constant outputpower at 100 kV, 0.1 sec

    Radiographic

    (Intermittent)

    100 kW

    80 kW

    65 kW50 kW

    40 kW

    32 kW

    100 kW (1000 mA, 100 kV, 0.1 s)

    80 kW (800 mA, 100 kV, 0.1 s)

    63 kW (630 mA, 100 kV, 0.1 s)50 kW (500 mA, 100 kV, 0.1 s)

    40 kW (400 mA, 100 kV, 0.1 s)

    32 kW (320 mA, 100 kV, 0.1 s)

    Nominal shortestirradiation time

    (AEC exposures)

    AEC All models 15 ms

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    2 Safety and Specifications

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    ENVIRONMENTAL SPECIFICATIONS

    OPERATING

    Ambient temperature range: 10 to 40 C.

    Relative humidity: 30 to 75%.

    Atmospheric pressure range: 500 to 1060 hPa (375 to 795 mm Hg).

    TRANSPORT AND STORAGE

    Ambient temperature range: -20 to 70 C.

    Relative humidity: 10 to 95%, including condensation.

    Atmospheric pressure range: 500 to 1060 hPa (375 to 795 mm Hg).

    This information is provided to help you establish safe operating conditions for both you and your DEL X-

    ray generator.

    Do not operate this X-ray generator except in accordance with information included in this section, and anyadditional information provided by the X-ray generator manufacturer and/or competent safety authorities.

    Address any questions regarding X-ray generator operation to:

    Del Medical Imaging Corp.11550 W. King StreetFranklin Park, IL 60131Technical Support: (847) 288-7000Fax: (847) 288-7911Email: [email protected]

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    2003 Del Medical Imaging Corp. Revision A Page 13

    CONSOLE CONTROLS 3

    OPERATOR CONTROL PANEL

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    I II III

    Indico 100

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    FILE: IN_CONS.CDR

    1. Power ON, power OFF buttons.

    2. Radiography controls and display.

    3. Image receptor buttons.

    4. Anatomical programming display and control.

    5. Fluoroscopy controls and display.

    6. Prep and exposure buttons and exposure indicator LED.

    NOTE: THIS MANUAL REFERS TO THE INDICO 100 R & F CONSOLE. FOR RAD ONLYUNITS, IGNORE REFERENCES TO THE FLUOROSCOPY FUNCTION.

    NOTE: ICONS ADJACENT TO BUTTONS ARE SHOWN AS THE CONSOLE IS SHIPPEDFROM THE FACTORY. THESE MAY BE ALTERED BY THE INSTALLER TO MATCHTHE ACTUAL CONFIGURATION OF THE GENERATOR.

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    POWER AND EXPOSURE CONTROLS

    Power ON / Power OFF buttons

    Press to switch the X-ray generator on. The

    console will light up and a self-check will beperformed.

    Press to switch the generator off.

    Prep / Exposure Buttons and Exposure Indicator LED

    Press and hold the prep button to spin the rotor.While pressing the prep button, press and hold the

    exposure button to make an X-ray exposure.

    The X-ray exposure indicator will light when anX-ray exposure is being taken.

    Pressing the exposure button only will cycle thegenerator through prep and then exposure.

    When the prep button is pressed, SPINNINGROTOR will be displayed in the APR window.

    When the prep cycle is complete, X-RAY READYwill be displayed in the APR window.

    During the X-ray exposure, X-RAY ON will bedisplayed in the APR window.

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    RADIOGRAPHY CONTROLS AND DISPLAY

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    1. Field select buttons and indicators (for AEC only).2. Film / Screen select button and indicators (for AEC only).3. Technique select button and indicators.4. Focus select button and indicators.5. kV up / down buttons.6. mA and mAs up / down buttons.7. Time (ms) up / down buttons.8. Density up / down buttons.

    9. Radiography display panel: kV, mA / mAs, Post mAs / ms, and density.

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    Field Select Buttons and Indicators (for AEC only)

    Press the appropriate field select button(s) to select thedesired field or combination of fields. The adjacent LED(s)will light to indicate the selected field(s). All three fieldsmay not be deselected.

    Operates only when AEC is selected.

    Film / Screen Select Button and Indicators (for AEC only)

    I II III

    Press the film / screen select button to select the desiredfilm / screen combination. The appropriate LED will light toindicate the desired selection.

    I

    for film / screen I.

    II

    for film / screen II.

    III

    for film / screen III.

    Operates only when AEC is selected.

    Technique Select Button and Indicators

    This function may be disabled in programming.Press the technique select button until the appropriateLED lights to indicate the desired technique.

    for Automatic Exposure Control (1 point technique).

    mAs for mAs technique (2 point technique).

    mA/ms for mA and ms technique (3 point technique).

    Focus Select Button and Indicators

    Press the focus select button until the appropriate LEDlights to indicate the desired focal spot.

    for small focus.

    for large focus.

    This function may be programmed for auto focal spotselection.

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    Note: The rate of scrolling for the kV, mA and time display increases if thebuttons are pressed continuously. To return to the slowest scroll rate,release the button(s) and start again.

    kV up / down buttons and display

    +

    To increase kV, press +.To decrease kV, press -.

    Displays demanded kVp of the exposure.

    mA and mAs up / down buttons and display

    +

    To increase mA or mAs, press +.To decrease mA or mAs, press -.

    Displays mA when AEC or mA/ms selected.Displays mAs when mAs is selected.

    Time (ms) up / down buttons and post-mAs / ms display

    +

    To increase time (ms), press +.To decrease time (ms), press -.

    Displays AEC, or shows backup mAs orbackup ms when AEC selected.

    No display when mAs selected.Displays time (ms) when mA/ms selected.Displays POST mAs after an AEC exposureis completed.

    Density up / down buttons and display

    +

    Buttons operate only in AEC mode.To increase dose, press +.To decrease dose, press -.

    The range is typically -5 to +5. (Installerprogrammable to have a range of up to -8 to+8).This varies the optical density by changing thedose.The % dose change per density step change isinstaller programmable.

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    IMAGE RECEPTOR BUTTONS AND INDICATORS

    1. Table, with Bucky, image receptor select2. Table, no Bucky, image receptor select3. Vertical image receptor select4. Linear tomographic receptor select5. Under-table R/F and remote R/F select6. Auxiliary image receptor select

    Note: Image Receptors (1-6) are depicted as the console is shipped from thefactory. The receptors may have been reprogrammed during installation.As a result, the receptors may contain installer - applied icons that differfrom those shown in this manual.

    Table with Bucky Image Receptor

    Press this button to select over-table X-ray tube with table imagereceptor. The adjacent indicator will light.

    Used for Bucky / AEC techniques.

    Table no Bucky image Receptor

    Press this button to select over-table X-ray tube when no imagereceptor is required. The adjacent indicator will light. Used for tabletop and off table techniques.

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    Vertical Image Receptor

    Press this button to select vertical (wall) image receptor orcassette holder. The adjacent indicator will light. Used for Bucky /AEC or cassette only techniques.

    Linear Tomographic Receptor

    Press this button to select the linear tomographic receptor. Theadjacent indicator will light.This receptor may be programmed to be remotely selected.

    Under-Table R/F and Remote R/F

    Press this button to select the fluoroscopy function (radiographic /fluoroscopic models only). The adjacent indicator will light and thefluoroscopy display will light.

    Auxiliary

    Press this button to select the auxiliary image receptor. The

    adjacent indicator will light. This may be programmed for R & Fapplications and digital applications.This receptor may be programmed to be remotely selected.

    Note: The image receptors may have been reprogrammed for your installation.

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    FLUOROSCOPY CONTROLS AND DISPLAY

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    1. Fluoroscopy display: kV, mA, time (min), PPS2. Fluoro ON indicator3. Fluoro kV up / down buttons4. Fluoro mA up / down buttons5. Time zero and accumulated time buttons6. Pulsed fluoro frame rate buttons7. I.I. magnification select button8. Delta dose select button

    9. Automatic brightness stabilization (ABS) select button10. Pulsed fluoro ON / OFF button (Optionally selects high level fluoro)

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    Fluoro ON Indicator

    When fluoro is on, the fluoro eye symbol will light. This isaccompanied by an audible tone from the console.

    Note: The fluoro kV and fluoro mA buttons are only functional when ABS isswitched OFF.

    Fluoro kV up / down buttons and display

    +

    To increase kV, press +.To decrease kV, push -.

    lit indicates that ABS is selected, manual kV

    control is therefore not available.

    Fluoro mA up / down buttons and display

    +

    To increase mA, press +.To decrease mA, press -.

    lit indicates that ABS is selected, manual mAcontrol is therefore not available.

    Pulsed fluoro mode uses a fixed (not operator -

    adjustable) mA value.

    Time zero and accumulated time buttons and display

    To reset the time display to zero, press .

    To display accumulated time, press once. The

    symbol will light to indicate that accumulatedtime is displayed.

    To reset the accumulated time, press whenthe accumulated time is displayed.

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    Pulsed fluoro frame rate buttons and display

    +

    To increase the PPS (Pulse Per Second) rate,press +. To decrease the PPS rate, press -.Pulse rates are 3, 7.5, 15, and 30 PPS for 60 Hzbased cameras, and 2.5, 6.25, 12.5, and 25 PPS

    for 50 Hz based cameras (6.25 is displayed as 6,and 12.5 is displayed as 12).

    Only active when pulsed fluoro is switched ON.

    I.I. magnification select button

    Press to select I.I. magnification mode. The relative magnificationvalue is shown in the lower right corner of the LCD display window(installer programmable).

    Delta dose select button

    Press to select delta dose control function. The delta dose value isshown in the lower right corner of the LCD display.

    ABS (Automatic Brightness Stabilization) Select button

    Press to select ABS. The adjacent indicator will light. Switching offABS will allow the operator to set the fluoro kV and mA manually.

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    Pulsed fluoro ON / OFF button (Optional high level fluoro ON / OFF button)

    Press to select pulsed fluoro. The adjacent indicator will light.

    This is only active for optional pulsed fluoro.

    For optional high level fluoro (HLF):With ABS off, selects high level fluoro. The adjacent indicator willlight to indicate that HLF is on. The fluoro mA range is 0.5 to 6.0mA if HLF is off, and 5.0 to 20 mA if HLF is on.

    With ABS on, if full HLF mode is programmed, the fluoro mArange will be 0.5 to 20 mA. The generator will automatically switchbetween normal and HLF modes, and the adjacent indicator willlight to indicate that the generator is in HLF mode.

    Manual HLF selection is not available if ABS is on.

    The frequency (pitch) of the tone from the console will increaseduring an exposure when high level fluoro is selected.

    Warning: High Level Fluoroscopy is compatible with therapy simulators only. Highlevel Fluoro must not be used for other applications.

    Exposure Indicator

    The LED adjacent to the prep symbolwill light when the foot-switch is pressedfor fluoroscopy exposure.The APR screen will display X-RAY ON.The operator control panel will alsoindicate the exposure by means of audiblebeeps.The rotor may continue to spin briefly afterthe foot-switch is released (installerprogrammable).

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    ANATOMICAL PROGRAMMING CONTROLS AND DISPLAY

    THE ABOVE IS A TYPICAL DISPLAY. YOUR UNIT MAY DIFFER DEPENDING ON MODEL,SET-UP, AND PROGRAMMING

    1. Anatomical section and anatomical view selection buttons.

    To select an APR technique:

    From the main APR menu (shown in the above figure), press the button next to thedesired anatomical section. The APR display will show anatomical views within thatsection.

    Press the button for the required anatomical view. The radiography display will showthe programmed X-ray technique factors.

    Press the function button again to toggle between normal, large and small patientsizes. The default is normal.

    You may override the programmed techniques by pressing the appropriate selection

    button (the ability to override the / mAs / mA/ms button may be disabled inprogramming). This will not change the programmed parameters. To make permanentchanges to the APR, see CHAPTER 6: PROGRAMMING THE CONSOLE.

    2. Tube 1 / tube 2 selection indicator (two tube units only).

    This will indicate which tube has been programmed for the selected receptor.

    3. Anode heat indicator (%HU) readout.Indicates the tube anode heat for the selected X-ray tube. An anode heat warningmessage will be displayed at an installer-programmable level, typically 80 %. Exposuresthat will exceed a value of typically 90 % will be inhibited (this is also installerprogrammable).

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    4. DAP (Dose Area Product) display. This feature is optional.

    Displays accumulated dose (mGycm2) or dose rate (mGycm

    2 /s). Refer to DAP - DOSE

    AREA PRODUCT at the end of this chapter for further details.

    5. ms/mAs readout.

    Thesignificance of the ms/mAs readout varies depending on mode selected:

    In AEC mode, with fixed backup time selected, the AEC backup time is displayed.

    In AEC mode, with either variable ms or variable mAs backup time, the backup mAs orms value is displayed.

    In mAs mode, the time of the exposure will be displayed.

    In mA/ms mode, the calculated mAs of the exposure will be displayed (based on themA and ms selected).

    6. Status and operator message display area.

    This area shows status, warning, and error messages.

    7. Time readout - 24 hour mode (RAD only). Displays MAG and DOSE selection influoro mode.

    The current time is displayed in 24 hour format when in RAD mode.

    The time display is replaced by a MAG selection indicator when a fluoro receptor isselected (the mag function may be disabled in programming; in this case DOSE will bedisplayed instead of MAG). The MAG number indicates the relative magnification ofthe I.I.

    The MAG display is replaced by the DOSE selection display for approximately 3seconds after pressing the dose button. This indicates the relative dose; the actualdose value at each setting is determined by the installer.

    8. Back () selection buttons.Press the back and next selection buttons to scroll forward or backwards through thedisplay. The symbols > will be displayed when these buttons are active.

    9. Reset button.

    Press the button to return to the main menu when in one of the APR submenus.

    Pressing this button will clear status and error messages.

    When the main APR menu is presented, this button accesses a submenu that allowsRESET and TEST of the DAP function. Refer to DAP - DOSE AREA PRODUCT at the

    end of this chapter for further details.

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    DAP - DOSE AREA PRODUCT (OPTIONAL)

    The DAP function is only available if the optional DAP device is installed in the X-ray system,and if the DAP function has been enabled in programming.Any references made to tube 2 or the ability to switch tubes apply to two tube generators only.

    DAP Overview

    The DAP device(s) must be allowed to stabilize when the generator is switched on,and the first time when switching from tube 1 to tube 2 or from tube 2 to tube 1.

    During this time, when the DAP device is settling, the DAP display will indicate--------. X-Ray exposures may be made during this time, but the DAP function willbe disabled during the settling period. The settling period may last up to a fewminutes after the generator is switched on.

    The DAP device for the tube that is selected when the generator is switched on isautomatically tested by the generator after the settling period. If the DAP devicepasses the self-test, the DAP readout will display its last setting. This indicates thatthe DAP is functional, and ready to measure the dose-area product.

    If the DAP self-test fails, an error message will be presented, and the DAPreadout will display --------. This indicates that the DAP is not functional.

    When switching to the other tube for the first time in that session (from tube 1 totube 2 or from tube 2 to tube 1), the DAP device associated with that tube will betested. As in the previous step, the DAP readout will display its last setting toindicate that the DAP is functional, or

    -------- to indicate that the DAP is not

    functional.

    The installer may program the generator to present an audible warning, along with avisual alarm via the LCD display on the console, to indicate that preset limits foraccumulated DAP or DAP rate have been reached.

    * DAP ACCUM WARN will display to indicate that the accumulated dose exceedsthe programmed accumulated dose-area product limit.

    * DAP RATE WARN will display to indicate that the current dose rate exceedsthe programmed dose rate limit.

    Note: A reading of 0mGycm2

    indicates that the DAP display has been manuallyreset as described later in this section, and that no exposures have beentaken since it was reset.

    Note: Always check local regulations to determine how frequently the DAPdevice must be tested. The procedure to test the DAP follows later in thissection.

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    DAP Display

    Before proceeding with initial dose-area product measurements, ensure that theDAP display is 0mGycm

    2. The DAP display may be manually reset to zero as

    described in DAP Reset / Test, below.

    The DAP measures and displays cumulative dose per unit area when in RAD mode.It may be programmed to measure and display the dose-area product for each tubeindividually, or to sum the readings from both tubes. This is installer programmable.

    In fluoroscopy mode, the DAP may be programmed to display accumulated dose-area product (mGycm

    2), or DAP rate (mGycm

    2 /s). If programmed to display DAP

    rate, the DAP rate display will be in reverse video during fluoroscopic operation.When the fluoro run is finished, the DAP display will revert to normal video, and theaccumulated dose will be displayed. The DAP rate feature for fluoro operation isinstaller programmable.

    The maximum accumulated reading on the DAP display is 9999999. An errormessage will be presented when this limit is reached.

    DAP Reset / Test

    The DAP display(s) may be reset to zero, and a manual DAP functional test may be performedwhen desired, as described below.

    1. In order to select the DAP device to test, select a receptor that is programmed forthe desired tube / DAP device (tube 1 or tube 2). This will also select the DAP toreset if programmed for individual dose-area product readings for each tube.

    If the two DAP readings are summed, the reset function may be performed oneither the tube 1 or tube 2 selection. The DAP display is common to both tubes,therefore the DAP display may be reset at either the tube 1 or tube 2 tube position.

    If the generator is programmed for individual DAP measurements for each tube,and you are intending to reset the DAP display, confirm that the correct tube / DAPdevice is selected before continuing.

    2. Press the button at the main APR menu when DAP is displayed at the bottom

    center of the LCD screen. This will present the DAP reset / test menu. Press RESET to reset the DAP display to zero.

    Press TEST to test the DAP. The message DAP TEST: OK will be presentedif the DAP has passed its test.

    Repeat for the other tube if desired.

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    REMOTE FLUORO 4CONTROLLER (optional)The illustration below shows the remote fluoro controller. This unit allows the operator to selectfluoroscopy functions at a location remote from the operator control console. The remotefluoro controller will be energized only when a fluoro technique is selected.

    1. Fluoroscopy exposure indicator2. Fluoro display: kV, mA, time (min), PPS, MAG3. Remote ON indicator4. Decrease / Increase kV and mA buttons5. Time zero / accum time buttons6. Pulsed fluoro rate control7. Magnification control for image intensifier (I.I.)8. Aux button: selects delta dose9. Automatic brightness stabilization (ABS) select button10. Pulsed fluoro select button

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    Fluoroscopy must be selected at the operator console to enable the remote fluoro control unit.The default kV and mA will display on both the operator control console and on the remotefluoro unit.

    REMOTE FLUORO CONTROLS AND DISPLAY

    There are four modes of operation for the unit:

    Manual: - operator controls the exposure

    ABS (Automatic Brightness Stabilization)

    PF (Pulsed Fluoro) optional PF with ABS (optional).

    kV selector and display

    In manual mode:To increase kV, press +.To decrease kV, push -.

    In ABS mode:The AUTO indicator lights and the kVselect buttons are inactive.The display will indicate the kV during theexposure.

    mA selector and display

    In manual mode:To increase mA, press +.To decrease mA, press -.

    In ABS mode:The AUTO indicator lights and the mAselect buttons are inactive.The display will indicate the mA during theexposure.Pulsed fluoro mode uses a fixed (notoperator - adjustable) mA value.

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    Time zero and accumulated time (minutes) display

    To reset the time display to zero, pressZERO.

    To display accumulated fluoro exposuretime, press ACCUM. The ACC indicatorwill light.

    To reset the accumulated time, pressZERO when the accumulated time isdisplayed.

    Pulsed fluoro frame rate selector and display

    PPS

    To increase the PPS (Pulses Per Second)rate, press +. To decrease the PPS rate,press -.

    Pulse rates are 3, 7.5, 15, and 30 PPS for60 Hz based cameras, and 2.5, 6.25, 12.5,and 25 PPS for 50 Hz based cameras(6.25 is displayed as 6, and 12.5 isdisplayed as 12).

    Mag (magnification) selector and display

    To increase the I.I. (Image Intensifier)magnification, press +.To decrease magnification, press -.

    Aux Button (Delta Dose Selector)

    Press this button to select delta dose when ABS is used.The ABS indicator will indicate the selected dose: No flashindicates dose 0, slow flashing indicates dose 1, and fast flashing

    indicates dose 2.The remote fluoro control will beep at a slow rate on dose 1, andat a fast rate on dose 2 during a fluoroscopy exposure.

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    ABS (Automatic Brightness Stabilization) Selector

    Press this button to select ABS. The adjacent indicator will light.Pressing the button to deselect ABS will extinguish the indicator,allowing fluoro kV and mA to be set manually.

    PF (Pulsed Fluoro) Select Button

    Selects pulsed fluoro.Only active for optional pulsed fluoro function.

    Fluoroscopy Exposure Indicator

    This indicator will light during fluoroscopy exposure. This isaccompanied by an audible tone from the console.

    Remote ON Indicator

    When fluoro mode is selected, REMOTE will light.

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    kV - mAs REDUCTION FOR 5PERIPHERAL ANGIOGRAPHY (optional)

    When interfaced to a special procedures stepping table, this option enables the Indico 100generator to sequentially select varying radiographic techniques as the patient is moved overthe image receptor. The kV and / or the mAs may be set to track changes in the anatomy ofthe patient for each of the table steps.

    When kV / mAs stepping is enabled, five kV / mAs sequences will be available, witheach sequence containing six kV / mAs steps. The kV and mAs is programmable for each stepas described later in this section.

    SELECTING THE TABLE STEPPER FUNCTION

    1. Select the image receptor that is configured for peripheral angiography. The radiographicdisplay will indicate a preselected and possibly arbitrary kV and mAs value. The firstexposure in the exposure sequence will not necessarily use those kV and mAs values.The kV and mAs used for the exposure sequence will be as per steps 1 to 6 in theconsole LCD display window.

    2. The LCD display window will display the first kV - mAs stepping screen (PER. SHIFT1) asshown. The sample screens below do not show the secondary displays i.e. tube number%HU, time etc. Also, the kV and mAs values may differ from the sample screens.

    * PER. SHIFT1 *

    1- 80kV / 25mAs 5- 68kV / 8mAs

    2- 75kV / 25mAs 6- 64kV / 4mAs

    3- 72kV / 16mAs

    4- 72kV / 16mAs

    >>

    3. Press >> to select the second kV - mAs stepping screen (PER. SHIFT2) as shown belowThis may be programmed for different kV / mAs steps from the previous screen.

    * PER. SHIFT2 *

    1- 80kV / 25mAs 5- 68kV / 8mAs

    2- 75kV / 25mAs 6- 64kV / 4mAs

    3- 72kV / 16mAs

    4- 72kV / 16mAs

    >>

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    4 . Press >> to select the remaining kV - mAs stepping screens (PER. SHIFT3 to PER.SHIFT5). These screens may be programmed for different kV / mAs steps from theprevious screens.

    5. Press

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    PROGRAMMING THE CONSOLE 6

    MAKING CHANGES TO PRE-PROGRAMMED APR TECHNIQUES

    The default techniques associated with the anatomical views in the APR display window maybe edited if desired. To do this, follow the steps in this chapter.

    ENTERING INTO PROGRAMMING MODE

    1. Start with the generator switched OFF.

    2. Press and hold the button while pressing the power ON button on the operatorconsole.

    3. When the console finishes its power-on sequence, and the ENTER PASSWORD promp

    is displayed, press the button 4 times to access the following menu:

    * GENERATOR SETUP *

    UTILITY APR EDITOR: DISABLED

    EXIT SETUP

    Access is now provided to the following groups of functions. These will be discussed insequence.

    UTILITY Set Time & Date

    Error Log

    Statistics

    ConsoleAPR EDITOR Enables/disables changes to the APR

    techniques

    EXIT SETUP Returns to normal operation i.e. nonprogramming mode.

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    UTILITY MENU

    To select the UTILITY menu, press the selection button adjacent to UTILITY in the APRdisplay window. This allows access to the following functions:

    * UTILITY *

    SET TIME & DATE

    ERROR LOG

    STATISTICS

    CONSOLE

    EXIT

    SET TIME & DATE Allows setting of the time and date

    ERROR LOG Allows the error log to be reviewedSTATISTICS Allows review of the tube exposure

    counter(s), the fluoro exposure counter ifapplicable, and the generator accumulatedexposure counter.

    CONSOLE Allows console parameters to be setEXIT Returns to the GENERATOR SETUP

    menu (previous page)

    Set Time and Date

    * SET TIME & DATE *

    YEAR: 1997 HOUR: 16

    MONTH: 1 MIN: 35

    DAY: 1 +

    -

    EXIT

    Use these steps to set the time and date.

    1. From the UTILITY menu, select SET TIME & DATE.

    2. Select the parameter to change. Press the + or - buttons to set the desired value. Time isset in 24 hour format.

    3. Select EXIT to return to the UTILITYmenu.

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    Error Log

    * ERROR LOG *

    ERROR # 10 OF 100

    DATE: 09-12-2000 TIME: 13:09

    ERROR CODE: 30 +

    ERROR MESSAGE: ROTOR FAULT -

    EXIT

    Use these steps to view the error log.

    1. From the UTILITYmenu select ERROR LOG.

    2. Select ERROR# and press the + or - buttons to scroll through the error log. The errorcode, error message, date and time of the error will be displayed in the APR displaywindow, and the associated parameters will be displayed on the console displays.

    3. SelectEXIT to return to the UTILITY menu.

    Statistics

    * STATISTICS *

    TUBE 1 EXP: 0

    TUBE 2 EXP: 0

    FLUORO HOURS: 0

    TOTAL EXP: 0EXIT

    The statistics menu shows the tube exposure count, accumulated fluoro hours, andaccumulated generator exposure count.

    1. From the UTILITYmenu select STATISTICS.

    2. The statistics (tube 1 exposures, tube 2 exposures if applicable, fluoro hours if applicabletotal generator exposures) may now be viewed.

    3. Select EXIT to return to the UTILITY menu.

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    Console

    * CONSOLE *

    SLOW KEY REPEAT: 200MS LCD SCREEN

    MED KEY REPEAT: 150MS APR MODE: NO

    FAST KEY REPEAT: 75MS +

    SPEAKER VOLUME: 15 -

    EXIT

    The CONSOLE menu displays console parameters that may be changed to suit operatorpreferences.

    1. From the UTILITYmenu select CONSOLE.

    2. Select SLOW KEY REPEAT. Press the + or - buttonto select the speed at which displayschange while the button is pressed for the first 5 counts.

    3. Select MED KEY REPEAT. Press the + or - buttonto select the speed at which displayschange while the button is pressed for the next 5 counts.

    4. Select FAST KEY REPEAT. Press the + or - buttonto select the speed at which displayschange while the button is pressed after 10 counts.

    5. Select SPEAKER VOLUME. Press the + or - button to set the speaker volume in therange 1 to 15.

    6. Select LCD SCREEN. Press button to toggle between normal and reverse display for theLCD display screen.

    7. Select APR MODE. Press selection button to toggle between NO and YES. Selecting

    YES disallows changes to the / mAs / mA/ms selections when in normal operating

    mode. This must be set to NO to allow switching between / mAs / mA/ms in normaloperating mode.

    8. Select EXIT to return to the UTILITY menu.

    9. Select EXIT to return to the GENERATOR SETUP menu.

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    APR EDITOR

    * GENERATOR SETUP *

    UTILITY APR EDITOR: DISABLED

    EXIT SETUP

    Use these steps to edit the programmed APR techniques.

    NOTE: BEFORE MAKING CHANGES TO THE DEFAULT APR TECHNIQUES, PLEASERECORD ALL CURRENT DEFAULTS. THESE DEFAULTS MAY BE RECORDED INCOPIES OF THE APR PROGRAMMING WORKSHEET AT THE END OF THIS CHAPTER.

    1. From the GENERATOR SETUPmenu select APR EDITOR.

    2. Pressthe APR EDITOR button to toggle between ENABLEDand DISABLED.

    DISABLED does not allow editing and then saving the changed APR technique(s)ENABLED allows the operator to change the default APR techniques, and then save thechanges. The APR will then default to the newly saved techniques.

    The generator stores the last APR editor setting prior to being switched OFF. Ifthe APR editor was previously ENABLED, APR changes may subsequently bemade and then saved in normal operating mode without the need to manually setthe APR editor to ENABLED. To disable this feature, the APR editor must be set toDISABLED.

    3. With the APR EDITOR set to ENABLED, return to normal operation by pressing EXIT

    SETUP.

    4. The following menu is displayed. This is a typical menu, actual anatomical views mayhave been reprogrammed, and the screen may differ slightly depending on generatomodel.

    TUBE 1 0%HU * APR TABLES *

    SKULL LOWER EXTREMITY

    THORAX UPPER EXTREMITY

    ABDOMEN G.I.

    PELVIS SPINE160MS

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    5. Perform the APR technique change as outlined below.

    6. Select the desired APR menu to be edited; for example SKULL.

    7. Select the desired APR view to edit, for example SKULL AP/PA, vertical image receptor.

    8. Select the patient size to edit within that view, for example medium.

    All techniques with the exception of kV will be common to all patient sizes. Thecommon techniques for all patient sizes within that view should be programmedfirst, then the desired kV for the selected patient size. After these techniques aresaved per the remainder of this section, kV values may be programmed if desiredfor the other patient sizes in the same APR view.

    9. The default selections are shown on the console, for example.

    70 kV, 100 mA, 20 ms, technique = mA/ms, large focus.

    10. Change the technique to the desired value(s). Parameters that may be edited are: kV,

    mA/mAs, time (ms), technique select ( / mAs / mA/ms), focus, image receptor, plus

    film screen, density and field selection in AEC mode.The APR view being edited will be highlighted with a rectangular outline as soon as anyparameter is changed within that view. Also the word SAVE will appear in the displaywindow above the reset button.

    11. Continue making all desired APR changes within that view.

    12. When finished, press the button. This is the first step necessary to save the changes.This also allows the option of canceling the changes in the next step.

    13. If you do not wish to save the changes, press EXIT to abort the SAVE function. To savethe changes, press the button under SAVE. The message SAVING DATA... will brieflyappear.

    14. Press to return to the main APR screen.

    15. You may now make changes to other APR techniques if desired by repeating the abovesteps 6 to 14.

    16. It is suggested that the APR editor be set to DISABLED as described earlier in thissection, in order to avoid unintended APR changes in the future.

    MAKING CHANGES TO THE APR TEXT

    The anatomical sections and views as displayed in the APR window may be altered to suit

    your requirements, but you will need to contact your service representative to have this done.Use copies of the worksheet on the next page to record your desired changes. One sheetshould be used per APR view, the master copy should be photocopied as many times asnecessary to record the required changes.

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    APR PROGRAMMING WORKSHEET (THIS IS A MASTER, MAKE WORKING COPIES AS NEEDED)

    kV Table with Bucky Receptor

    Tech Select

    Patient Size Small

    Focus

    FieldSelect

    Table non Bucky Receptor

    mAs

    Medium

    Vertical Image Receptor

    mA/ms

    Large

    Tomography

    Film Screen

    Auxiliary Image Receptor

    R/F (Fluoro)

    mA/mAs

    ms

    DENSITY

    __________________

    __________________

    __________________

    __________________

    __________________

    __________________

    __________________

    __________________

    __________________

    __________________

    __________________

    __________________

    __________________

    __________________

    __________________

    __________________

    MENU 1

    APR TABLES

    MAX 16 CHARACTERS

    MENU 2

    ANATOMICAL VIEW

    MAX 16 CHARACTERS

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    ERROR CODES AND MESSAGES 7

    The Indico 100 console will display status messages on the APR display during normal andabnormal operation of the generator. This chapter contains tables of those messages andsuggests actions to be taken should any malfunctions occur.

    Messages may be cleared by pressing the RESET button.

    Operator Messages

    These messages indicate the status of the generator. No action is required.

    MESSAGE DESCRIPTIONINITIALIZATION Displayed during power up sequence.SPINNING ROTOR Displayed when prep state is active.X-RAY READY Displayed when generator is ready to exposeX-RAY ON Displayed during both a rad and fluoro exposure.

    DAP NOT READY The optional DAP is in its warm up state, and not ready to makeDAP measurements.

    Limit Messages

    These messages indicate that an exposure has been requested that exceeds one or morelimits.

    MESSAGE PROBLEM ACTIONTUBE KV LIMIT Requested kV not allowed as tube kV

    limit has been reached.None.

    GEN KV LIMIT Requested kV not allowed as generatorkV limit has been reached.

    None.

    TUBE MA LIMIT Requested mA not allowed as tube mAlimit has been reached.

    None.

    GEN MA LIMIT Requested mA not allowed asgenerator mA limit has been reached.

    None.

    TUBE KW LIMIT Requested parameter not allowed astube kW limit has been reached.

    None.

    GEN KW LIMIT Requested parameter not allowed asgenerator kW limit has been reached.

    None.

    TUBE MAS LIMIT Requested mAs not allowed as tubemAs limit has been reached. None.

    GEN MAS LIMIT Requested mAs not allowed asgenerator mAs limit has been reached.

    None.

    GEN MS LIMIT Requested ms not allowed asgenerator ms limit has been reached.

    None.

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    MESSAGE PROBLEM ACTIONCAL LIMIT Requested parameter not calibrated. Consult your service

    representative.GEN. PPS LIMIT PPS limit has been reached. None.AEC DENSITY LIM Requested density not programmed. Select another

    density or requestthose steps beprogrammed.Consult your servicerepresentative forthis.

    ANODE HEAT WARN Anode has exceeded programmedwarning level.

    Wait for anode tocool.

    FL TIMER WARN Fluoro interval timer 5.0 mins. Reset fluoro timer.

    INVALID PARAM Generator detected invalid parameter

    within received message, messageignored.

    Select valid

    parameter.

    GEN DUTY WARNING The X-ray generator has reached itsduty warning limit.

    Re-evaluatetechnique factors.Allow generator tocool if possible. Ifexposures arecontinued, seriousgenerator damagemay result due tooverheating.

    DAP ACCUM WARN The accumulated DAP value hasreached the programmed DAP limit. Reset the DAP.

    DAP RATE WARN The current DAP rate exceeds theprogrammed DAP rate limit.

    Reduce the dose.

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    Error Messages

    These messages indicate that an error has occurred.

    ERROR CODE MESSAGE PROBLEM ACTION

    E001 GEN EPROM ERR Consult your service

    representative.E003 GEN NVRAM ERR Consult your service

    representative.

    E004 GEN RTC ERROR Generator CPU real timeclock is not functioning.

    Reset time and date.

    Consult your servicerepresentative.

    E005 PS CONTACT ERR Consult your servicerepresentative.

    E006 ROTOR FAULT Power unit off andretry rotor start.

    Consult your service

    representative.E007 FILAMENT FAULT Consult your service

    representative.

    E008 MA FAULT Consult your servicerepresentative.

    E009 PS NOT READY Power supply is not ready tomake an exposure.

    Retry exposure.

    Consult your servicerepresentative.

    E011 HIGH MA FAULT Consult your servicerepresentative.

    E012 LOW MA FAULT Consult your servicerepresentative.

    E013 MANUAL TERMIN Operator released exposureswitch during exposure. Re-take exposure ifnecessary.

    Consult your servicerepresentative.

    E014 AEC BUT ERROR AEC exposure exceededallowed back up time.

    Check exposuretechnique settings.

    Consult your servicerepresentative.

    E015 AEC BU MAS ERR AEC exposure exceededallowed back up mAs.

    Check exposuretechnique settings.

    Consult your servicerepresentative.

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    ERROR CODE MESSAGE PROBLEM ACTION

    E016 TOMO BUT ERROR Tomo exposure exceededback up time.

    1. Check exposuretechnique settings.

    2. Increase tomoback up time if

    necessary.E017 NOT CALIBRATED Consult your service

    representative.

    E018 PREP TIMEOUT Generator has been in prepstate too long.

    Reduce length oftime in prep state.

    E019 ANODE HEAT LIMIT Selected parameters willcause X-ray tube to exceedits programmed anode heatlimit.

    Reduce parametersor wait for tube tocool.

    E020 THERMAL INT #1 X-ray tube # 1 too hot andits thermal switch hasopened.

    Wait for X-ray tube #1 to cool.

    E021 THERMAL INT #2 X-ray tube # 2 too hot and

    its thermal switch hasopened.

    Wait for X-ray tube #

    2 to cool.

    E022 DOOR INTERLOCK Door is open. Close door.

    E023 COLLIMATOR ERR Collimator is not ready. Check collimator.

    E024 CASSETTE ERROR Cassette is not ready. Check cassette.

    E025 II SAFETY INT II safety is not ready. Check II safety.

    E026 SPARE INT Spare input is not ready. Consult your servicerepresentative.

    E028 PREP SW CLOSED Consult your servicerepresentative.

    E029 X-RAY SW CLOSED Consult your servicerepresentative.

    E030 FLUORO SW CLOSED Consult your service

    representative.E031 REMOTE COMM ERR Communication error

    detected with remote fluorocontrol unit.

    Turn power off andthen on to ResetGenerator.

    Consult your servicerepresentative.

    E032 CONSOLE COMM ERR Generator has detectederror in communication toconsole.

    Turn power off andthen on to resetgenerator.

    Consult your servicerepresentative.

    E033 GEN BATTERY LOW Consult your servicerepresentative.

    E034 +12VDC ERROR Consult your servicerepresentative.

    E035 -12VDC ERROR Consult your servicerepresentative.

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    2003 Del Medical Imaging Corp. Revision A Page 47

    ERROR CODE MESSAGE PROBLEM ACTION

    E036 +15VDC ERROR Consult your servicerepresentative.

    E037 -15VDC ERROR Consult your servicerepresentative.

    E038 CAL DATA ERROR Consult your servicerepresentative.

    E039 AEC DATA ERROR Consult your servicerepresentative.

    E040 FLUORO DATA ERROR Consult your servicerepresentative.

    E041 REC DATA ERROR Consult your servicerepresentative.

    E042 TUBE DATA ERR Consult your servicerepresentative..

    E043 KV ERROR Switch OFF generator.Prevent further use ofgenerator, then.consult your servicerepresentative.

    E044 COMM ERROR Received communicationmessage not valid andignored.

    Reset error.

    E045 NOT SUPPORTED Received message valid,but not supported by thissystem.

    Reset error.

    E046 MODE INHIBITED Received message valid,but not allowed duringpresent state.

    Reset error.

    E047 FL TIMER LIMIT Fluoro Timer has exceededtime limit.

    Reset Fluoro timer.

    E048 FOCUS MISMATCH Consult your service

    representative.E049 NOT ENABLED Requested function has not

    been programmed to beenabled.

    Consult your servicerepresentative.

    E050 GEN DATA ERROR Consult your servicerepresentative.

    E051 AEC DEVICE ERR Generator has detected nofeedback signal from AECdevice.

    Check that X-ray tubeis pointing at correctAEC device.

    Consult your servicerepresentative.

    E052 HIGH SF CURRENT Consult your service

    representative.E053 HIGH LF CURRENT Consult your service

    representative.

    E054 AEC OUT OF RANGE Consult your servicerepresentative.

    E055 NO FIELDS ACTIVE AEC enabled but no fieldsare selected.

    Select AEC field(s).

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    ERROR CODE MESSAGE PROBLEM ACTION

    E056 NO TUBE SELECTED Consult your servicerepresentative.

    E057 AEC STOP ERROR Consult your servicerepresentative.

    E058 CONSOLE BUT ERR Consult your servicerepresentative.

    E059 HOUSE HEAT LIMIT X-ray tube housing hasexceeded limit.

    Wait for tube to cool.

    E060 EXP KV HIGH Consult your servicerepresentative.

    E061 EXP KV LOW Consult your servicerepresentative.

    E062 EXP_ SW ERROR Consult your servicerepresentative.

    E063 FACTORY DEFAULTS Consult your servicerepresentative.

    E066 NO SYNC PULSE Consult your servicerepresentative.

    E070 SOFTWARE KEY ERR Consult your servicerepresentative.

    E071 DAP OVERFLOW The accumulated DAP valueexceeds the display limit.

    Reset the DAP.

    E072 DAP DEVICE ERROR The DAP device is notfunctional.

    Consult your servicerepresentative.

    E073 DAP DATA ERROR Consult your servicerepresentative.

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    2003 Del Medical Imaging Corp. Revision A Page 49

    GENERATOR EXPOSURE 8TABLES

    Table 1 following shows mAs values resulting from preselected mA and ms values (3 pointoperation). This table also shows the range and interrelation of these loading factors. Forexample, if in AEC operation it is known that the preset backup mAs limit is 50 mAs and 100mA is chosen for that technique, then the maximum length of exposure possible (at which timethe backup mAs limit is reached) is 500 ms.

    In the above example, read down the 100 mA column to the 50 mAs value. Then readacross to the left side of the page to the 500 ms value, this will be the maximum time allowedfor the stated conditions.

    Please review the note at the bottom of page 56. This details AEC backup options thatare available.

    IEC 60601-2-7 requires that this information be provided in a form suitable to be displayed at aprominent location on or near the control console of the generator. To this end, an extra copyof table 1 is provided on pages 52 and 53 which may be photocopied as required, or removedfrom this manual and placed in a suitable location as per local requirements.

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    INDICO 100 GENERATOR TECHNIQUE SELECTION(3 Point Selection: mA/TIME & mAs per IEC)

    Time mA Selected

    (ms) 25 32 40 50 63 80 100 125 160 200 250 320 400

    1.0

    1.2 .5 1.6 .5 .63

    2 .5 .63 .8

    2.5 .5 .63 .8 1.0

    3.2 .5 .63 .8 1.0 1.25

    4 .5 .63 .8 1.0 1.25 1.6

    5 .5 .63 .8 1.0 1.25 1.6 2.0

    6.3 .5 .63 .8 1.0 1.25 1.6 2.0 2.5

    8 .5 .63 .8 1.0 1.25 1.6 2.0 2.5 3.2

    10 .5 .63 .8 1.0 1.25 1.6 2.0 2.5 3.2 4.0

    12.5 .5 .63 .8 1.0 1.25 1.6 2.0 2.5 3.2 4.0 5.0

    16 .5 .63 .8 1.0 1.25 1.6 2.0 2.5 3.2 4.0 5.0 6.3

    20 .5 .63 .8 1.0 1.25 1.6 2.0 2.5 3.2 4.0 5.0 6.3 8

    25 .63 .8 1.0 1.25 1.6 2.0 2.5 3.2 4.0 5.0 6.3 8 10

    32 .8 1.0 1.25 1.6 2.0 2.5 3.2 4.0 5.0 6.3 8 10 12.5

    40 1.0 1.25 1.6 2.0 2.5 3.2 4.0 5.0 6.3 8 10 12.5 16

    50 1.25 1.6 2.0 2.5 3.2 4.0 5.0 6.3 8 10 12.5 16 20

    63 1.6 2.0 2.5 3.2 4.0 5.0 6.3 8 10 12.5 16 20 25

    80 2.0 2.5 3.2 4.0 5.0 6.3 8 10 12.5 16 20 25 32

    100 2.5 3.2 4.0 5.0 6.3 8 10 12.5 16 20 25 32 40

    125 3.2 4.0 5.0 6.3 8 10 12.5 16 20 25 32 40 50

    160 4.0 5.0 6.3 8 10 12.5 16 20 25 32 40 50 63

    200 5.0 6.3 8 10 12.5 16 20 25 32 40 50 63 80

    250 6.3 8 10 12.5 16 20 25 32 40 50 63 80 100

    320 8 10 12.5 16 20 25 32 40 50 63 80 100 125

    400 10 12.5 16 20 25 32 40 50 63 80 100 125 160

    500 12.5 16 20 25 32 40 50 63 80 100 125 160 200

    Table 1: mAs values vs. mA & time selected

    Table 1 continued on next page

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    2003 Del Medical Imaging Corp. Revision A Page 51

    Time mA Selected

    (ms) 25 32 40 50 63 80 100 125 160 200 250 320 400

    630 16 20 25 32 40 50 63 80 100 125 160 200 250

    800 20 25 32 40 50 63 80 100 125 160 200 250 320

    1000 25 32 40 50 63 80 100 125 160 200 250 320 400

    1250 32 40 50 63 80 100 125 160 200 250 320 400 500

    1600 40 50 63 80 100 125 160 200 250 320 400 500 630

    2000 50 63 80 100 125 160 200 250 320 400 500 630 800

    2500 63 80 100 125 160 200 250 320 400 500 630 800 1000

    3200 80 100 125 160 200 250 320 400 500 630 800 1000

    4000 100 125 160 200 250 320 400 500 630 800 1000

    5000 125 160 200 250 320 400 500 630 800 1000

    6300 160 200 250 320 400 500 630 800 1000

    Table 1 (Cont): mAs values vs. mA & time selected

    Note: 32 kW Generators Maximum mA = 40040 kW Generators Maximum mA = 50050 kW Generators Maximum mA = 63065 kW Generators Maximum mA = 80080 kW Generators Maximum mA = 1000100 kW Generators Maximum mA = 1000

    Note: 1) mA/TIME values are tube rating dependent. For certain tubes, some mA/TIME shigher kV selections.

    2) The maximum power output of the Indico 100 family of generators is 32 kW, 40 kW, 5respectively. The generator software does not allow a kV and mA combination to be maximum values.

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    2003 Del Medical Imaging Corp. Revision A Page 52

    Time mA Selected

    (ms) 25 32 40 50 63 80 100 125 160 200 250 320 400

    1.0

    1.2 .5

    1.6 .5 .63 2 .5 .63 .8

    2.5 .5 .63 .8 1.0

    3.2 .5 .63 .8 1.0 1.25

    4 .5 .63 .8 1.0 1.25 1.6

    5 .5 .63 .8 1.0 1.25 1.6 2.0

    6.3 .5 .63 .8 1.0 1.25 1.6 2.0 2.5

    8 .5 .63 .8 1.0 1.25 1.6 2.0 2.5 3.2

    10 .5 .63 .8 1.0 1.25 1.6 2.0 2.5 3.2 4.0

    12.5 .5 .63 .8 1.0 1.25 1.6 2.0 2.5 3.2 4.0 5.0

    16 .5 .63 .8 1.0 1.25 1.6 2.0 2.5 3.2 4.0 5.0 6.3

    20 .5 .63 .8 1.0 1.25 1.6 2.0 2.5 3.2 4.0 5.0 6.3 8

    25 .63 .8 1.0 1.25 1.6 2.0 2.5 3.2 4.0 5.0 6.3 8 10

    32 .8 1.0 1.25 1.6 2.0 2.5 3.2 4.0 5.0 6.3 8 10 12.5

    40 1.0 1.25 1.6 2.0 2.5 3.2 4.0 5.0 6.3 8 10 12.5 16

    50 1.25 1.6 2.0 2.5 3.2 4.0 5.0 6.3 8 10 12.5 16 20

    63 1.6 2.0 2.5 3.2 4.0 5.0 6.3 8 10 12.5 16 20 25

    80 2.0 2.5 3.2 4.0 5.0 6.3 8 10 12.5 16 20 25 32

    100 2.5 3.2 4.0 5.0 6.3 8 10 12.5 16 20 25 32 40

    125 3.2 4.0 5.0 6.3 8 10 12.5 16 20 25 32 40 50

    160 4.0 5.0 6.3 8 10 12.5 16 20 25 32 40 50 63

    200 5.0 6.3 8 10 12.5 16 20 25 32 40 50 63 80

    250 6.3 8 10 12.5 16 20 25 32 40 50 63 80 100

    320 8 10 12.5 16 20 25 32 40 50 63 80 100 125

    400 10 12.5 16 20 25 32 40 50 63 80 100 125 160

    500 12.5 16 20 25 32 40 50 63 80 100 125 160 200

    Table 1: mAs values vs. mA & time selected

    Table 1 continued on next page

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    2003 Del Medical Imaging Corp. Revision A Page 53

    Time mA Selected

    (ms) 25 32 40 50 63 80 100 125 160 200 250 320 400

    630 16 20 25 32 40 50 63 80 100 125 160 200 250

    800 20 25 32 40 50 63 80 100 125 160 200 250 320

    1000 25 32 40 50 63 80 100 125 160 200 250 320 400

    1250 32 40 50 63 80 100 125 160 200 250 320 400 500

    1600 40 50 63 80 100 125 160 200 250 320 400 500 630

    2000 50 63 80 100 125 160 200 250 320 400 500 630 800

    2500 63 80 100 125 160 200 250 320 400 500 630 800 1000

    3200 80 100 125 160 200 250 320 400 500 630 800 1000

    4000 100 125 160 200 250 320 400 500 630 800 1000

    5000 125 160 200 250 320 400 500 630 800 1000

    6300 160 200 250 320 400 500 630 800 1000

    Table 1 (Cont): mAs values vs. mA & time selected

    Note: 32 kW Generators Maximum mA = 40040 kW Generators Maximum mA = 50050 kW Generators Maximum mA = 63065 kW Generators Maximum mA = 80080 kW Generators Maximum mA = 1000100 kW Generators Maximum mA = 1000

    Note: 1) mA/TIME values are tube rating dependent. For certain tubes, some mA/TIME shigher kV selections.

    2) The maximum power output of the Indico 100 family of generators is 32 kW, 40 kW, 5

    respectively. The generator software does not allow a kV and mA combination to be maximum values.

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    2003 Del Medical Imaging Corp. Revision A Page 54

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    2003 Del Medical Imaging Corp. Revision A Page 55

    MAINTENANCE SCHEDULE 9

    This section is organized into two parts. The first part of this section details tests by which theoperator can verify that the AEC and ABS circuits are functioning, and that there are noapparent defects in the console or associated equipment.

    These tests should be done monthly as a minimum, or more frequently if required bylocal regulations.

    CAUTION: THE AEC AND ABS VERIFICATION PROCEDURES REQUIRE THE PRODUCTION OF XRAYS. OBSERVE CORRECT OPERATING PROCEDURES, AND TAKE APPROPRIATEPRECAUTIONS AGAINST X-RADIATION.

    The second part of this section is the recommended maintenance schedule for your generator

    This maintenance schedule is recommended for all Indico 100 series X-ray generators.

    WARNING: REFER ALL SERVICING TO APPROPRIATE SERVICE PERSONNEL WHO ARE TRAINED TOSERVICE THIS EQUIPMENT AND WHO ARE FAMILIAR WITH THE POTENTIAL HAZARDSASSOCIATED WITH THIS EQUIPMENT.

    NOTE: MAINTENANCE SCHEDULE FREQUENCY MAY BE DETERMINED BY CERTAINREGULATORY REQUIREMENTS OF THE COUNTRY OR STATE IN WHICH THEINSTALLATION IS LOCATED. ALWAYS CHECK THE LOCAL CODES AND REGULATIONSWHEN DETERMINING A MAINTENANCE SCHEDULE.

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    9 Maintenance Schedule

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    AEC FUNCTIONAL CHECK

    The following procedure may be used to verify that the AEC circuits are functioning ongenerators equipped with AEC (automatic exposure control).

    1. Switch the generator ON, and select an appropriate radiographic image receptor.

    2. Align the X-ray tube and the selected image receptor such that the central ray is directlyover the center field of the AEC pickup device. Set the focal spot to film plane distance to40 in. (1 m).

    3. Select AEC mode of operation. Select center field, large focus.

    MINIMUM EXPOSURE TIME:

    4. With no object in the radiation field, adjust the collimator or beam limiting device to projecta 10 in. X 10 in. (24 cm X 24 cm) field at the image receptor.

    5. Select 80 kVp, 100 mA, and a backup mAs of 50 if it is operator selectable. If this is notoperator selectable, the default AEC backup settings must be used. Refer to the note at

    the end of this page to determine the AEC backup mode that has been programmed.6. Make an exposure and verify that the POST mAs reading is 2 mAs.

    MAXIMUM EXPOSURE TIME:

    7. Close the collimator or beam limiting device completely. Place a folded lead apron overthe image receptor.

    8. Select 60 kVp, 100 mA, and a backup mAs of 50 if it is operator selectable. If this is notoperator selectable, the default backup settings must be used. Refer to the note at theend of this page to determine the AEC backup mode that has been programmed.

    9. Make an exposure and verify that the error message AEC BUT ERROR or AEC BU MAS

    ERR is indicated in the APR display window after the exposure has terminated. Thisconfirms that the exposure has continued until it was terminated by the AEC backuptimer.

    NOTE: The AEC backup mode is installer programmable. Three modes are available, FIXED,MAS, and MS. Only the MAS mode allows the operator to set the backup mAs for an AECexposure.

    FIXED: The generator will determine the maximum AEC backup time, not to exceed presetAEC backup mAs/ms values or system limits. The characters AEC will be displayed in the timewindow of the LED display during AEC operation.

    MAS: Allows the operator to adjust the AEC backup mAs, not to exceed preset AEC backupmAs/ms values or system limits. The mAs value will be displayed in the time window of theLED display during AEC operation.

    MS: Allows the operator to adjust the AEC backup ms, not to exceed preset AEC backupmAs/ms values or system limits. The ms value will be displayed in the time window of the LEDdisplay during AEC operation.

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    2003 Del Medical Imaging Corp. Revision A Page 57

    ABS FUNCTIONAL CHECK

    The following procedure may be used to verify that the ABS circuits are functioning ongenerators equipped with ABS (automatic brightness stabilization).

    1. Switch the generator ON, and select an appropriate fluoroscopic image receptor.

    2. Select ABS mode. The indicator LED adjacent to the ABS selector button on the controconsole or on the remote fluoro control will be lit to indicate that ABS is ON.

    3. Open the collimator or beam limiting device shutters to maximum. With no object in theimage field, press the fluoro footswitch. Confirm that the collimator or beam limitingdevice is fully open by observing the monitor.

    4. While continuing to press the fluoro footswitch, note the fluoro kV display at the controconsole or remote fluoro control. This should be less than 55 kV.

    5. Close the collimator or beam limiting device and press the fluoro footswitch. With noobject in the image field, ensure that the radiation is fully blocked by observing the

    monitor. If necessary, cover the image intensifier with lead aprons to block all radiation.6. While continuing to press the fluoro footswitch, note the fluoro kV display at the contro

    console or remote fluoro control. This should be the maximum available fluoro kV, 110 kVor 125 kV (depending on whether the upper fluoro kV limit has been set to 110 kV or 125kV).

    7. Place an absorber (20 cm of water, or 1.5 in. (3.8 cm) of pure aluminum, or equivalent) inthe center of the image field.

    8. Press the fluoro footswitch. While viewing the absorber on the monitor, open thecollimator or beam limiting device sufficiently to cover as much of the absorber aspossible. Ensure that the X-ray beam does not extend beyond the sides of the absorber

    as stray radiation will adversely affect the kVp reading in the next step.9. While continuing to press the fluoro footswitch, note the fluoro kV display at the contro

    console or remote fluoro control. This should stabilize between 70 and 80 kVp.

    CONSOLE AND MISCELLANEOUS GENERATOR CHECKS

    The user must routinely check the X-ray equipment for apparent defects or damage. Reporany apparent defects or irregular operation of any equipment to service personneimmediately, and discontinue use of the suspected faulty equipment until repairs are madeContinuing operation with faulty equipment may present various safety hazards, including risk

    of increased radiation.

    1. Check all visual displays (warning and status lights, technique displays and indicatorsetc) for normal operation.

    2. Check all audible indicators (speakers, beepers, etc) for normal operation, and check thatthe loudness settings are adequate for the environment.

    3. Check all interconnect cables and connectors for damage.

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    9 Maintenance Schedule

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    MAINTENANCE ACTIVITIES IN THE TABLE BELOW ARE TO BE PERFORMED BYAUTHORIZED SERVICE PERSONNEL ONLY. HOWEVER THE OWNER OR OPERATOROF THE EQUIPMENT MUST SCHEDULE THE SUGGESTED MAINTENANCE ACTIVITYWHEN REQUIRED BY CONTACTING THEIR LOCAL SERVICE AGENCY.

    MaintenanceFrequency

    Description of Preventative Maintenance

    As governed by localregulations

    Check and recalibrate the DAP meter in the generator.

    Every 6 Months ANDwhenever a relatedcertifiable X-raycomponent isreplaced:

    1. Clean and re-grease all HV connections using vapourproof compound.

    2. Clean the control console, remote fluoro control (if used)and main cabinet as needed. REFER TO NEXT PAGE,CLEANING, BEFORE PROCEEDING

    3. Perform the X-ray tube auto calibration routine.

    4. Verify the calibration of the generator.

    5. Perform any additional tests required by laws governingthis installation.

    Every 12 months: 1. Examine the following for any visible damage andreplace any damaged components:

    The exterior of the control console and remote fluorocontrol if used, including the membrane switchassembly.

    The cable between the control console and thegenerator main cabinet and between the remotefluoro control (if used) and generator main cabinet.

    The hand switch and fluoro footswitch (if used) andthe cables connecting these to the console.

    2. Open the generator cabinet and examine the unit for anyvisible damage: missing or loose ground connections, oilleaks, damaged cables etc.

    3. Ensure that there are no obstructions blocking the

    ventilation holes at the top of the cabinet, or the louverson the front door panels.

    Every 5 years: Replace the lithium batteries on the CPU board in the controlconsole and on the generator CPU board in the main cabinetwith the same manufacturer and type as identified on theoriginal batteries.

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    CLEANING

    Never use anything other than soap and water to clean plasticsurfaces. Other cleaners may damage the plastic.

    Never use any corrosive, solvent or abrasive detergents or

    polishes. Ensure that no water or other liquid can enter any equipment. This

    precaution prevents short circuits and corrosion forming oncomponents.

    Methods of disinfection used must conform to legal regulations andguidelines regarding disinfection and explosion protection.

    If disinfectants are used which form explosive mixtures of gases, thesegases must have evaporated before switching on the equipment again

    Disinfection by spraying is not recommended because the disinfectantmay enter the X-ray equipment.

    If room disinfection is done with an atomizer, it is recommended tha

    the equipment be switched OFF, allowed to cool down and coveredwith a plastic sheet. When the disinfectant mist has subsided, theplastic sheet may be removed and the equipment be disinfected bywiping.

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    X-RAY TUBE DATA 10

    CAUTION: NOTE TO THE INSTALLER: THE GENERATOR MUST BE PROGRAMMED NOT TO EXCEEDTHE MAXIMUM OPERATING LIMITS OF THE X-RAY TUBE.

    The following pages contain data for the X-ray tube(s) used with your X-ray generator at thetime of installation.

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    10 X-Ray Tube Data

    2003 Del Medical Imaging Corp. Revision A Page 62

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    X-Ray Tube Data 10

    2003 Del Medical Imaging Corp. Revision A Page 63

    NOTE TO INSTALLER:

    INSERT TUBE DATA HERE.

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    10 X-Ray Tube Data

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