System Model: G BB CHATTANOOGA 2776 - Serial numbers 1000 and above ISO 13485 CERTIFIEDFOREWORD Inset Moe Uasound Tey St Read, understand, and follow the safety precautions and all other information contained in this manual. This manval contains the necessary safety and field service information for thase field service technicians, certified by Chattanooga Group, to perform field service on Intelect Mobile Ultrasound Therapy System. At the time of publication, the information contained herein was current and up- to-date, However, due to continual technological improvements and increased clinical knowledge in the field of ultrasound therapy, as well as Chattanooga Groups policy of continual improvement, Chattanooga Group reserves the right to make periodic changes and Improvements to thei ‘equipment and documentation without any obligation on the part af Chattanooga Group. AS significant changes occur to Intelect Mobile Ultrasound Therapy System, service bulletins will be made available on our website (chattgroup.com) in lieu of reprinted manuals. Technicians repairing Intelect Mobile Ultrasound Therapy System agree to assume all risk and liabilit assoclated with this process, This system Is to be used only under the supervision of a licensed practitioner.SAFETY PRECAUTIONS Ieee” abe Utraound Therapy Stem 1.1 PRECAUTIONARY SYMBOL DEFINITIONS. ‘The precautionary instructions found in this manual 21 indicated by specific symbols. Understand these symbols and therr definitions before operating or Servicing this equipment. The definitions of these symbols ae a fllows: ‘A. CAUTION. Text with a CAUTION’ indicator will exolain possible safety infractions that have the potential to cause minor to moderate injury or damage to equipment, B.WARNING Text with a WARNING’ indicator will explain possible safety infractions that will potentially Cause serious injury and equipment damage. \ DANGER DANGER Text with a"DANGER’ indicator wall explain possible safety infactions that are imminently hazardous situations that would result in death or serious injury EXPLOSION HAZARD Donot useihis equbmentinthe QI) presonce of fammable anesthetics, This ‘symbol is also prominently displayed on focal rumberfine othe une DANGEROUS VOLTAGE Text with a*Dangerous Voltage" indicator serves to inform the Service Technician of possible hazards resuiting in the electrical Charge retained by faulty power supplies F CORROSIVE HAZARD (NiMH Battery) Text with a"Comosive Hazard indicator will explain possible safety infactions if the chemical components of this product ae exposed to alt, skin or other materials Note: Throughout this manual ‘NOTE’ may be found. “The Notes are helpful information to aid in the particular area or function being described 1.2 PRECAUTIONARY INSTRUCTIONS ead, understand, and follow all safety precautions found in this manual Below are general safety precautions that must be read and understood before attempting any service techniques on these systems. * Read, understand and practice the precautionary and operating instructions. Know the limitations and hazards associated ‘with using any ultrasound device. Observe the precautionary and operational decals placed on the unit + Do nat operate the unit in an envitonment of short-wave diathermy use. + The Ukrasound modality should be routinely checked to datermine that all controls function normally using the information provided within this manual Use of controls or adjustments or performance of procedures other than. ‘those specified herein may result in hazardous exposure to ultrasonic eneray. + Do Not use sharp objects such as a pencil point or ballpoint pen to operate the buttons on the control panel as damage may result + Operate, transport and store this unt temperatures between 15 °C and 40 °C (69 °F and 104 *F), wit Relative Huri ranging from 3055-603, Inappropriate handling of, and subjecting the ultrasound applicator to physical abuse, may adversely affect its characteristics, + Inspect Applicator for cracks, which may allow the ingress of conductive fluid before each use, + Inspect all cables, and associated connectors before each use.1- SAFETY PRECAUTIONS Inaet” Noi rasound Therapy Spt 1.2 PRECAUTIONARY INSTRUCTIONS (CONTINUED) |. Do not apply the Ultrasound Applicator to the Patient during the Head Warming period. |- Applicator must remain in Applicator Hook during the Head Warming period use only degassed water in power meter for testing Ultrasound Applicators. Use of other types ‘of watar will cause false test results. see page 12 for degassed water recipes. |- Use of other brands or types of tools, equipment, fixtures, materials, and supplies other than those specifically listed on page 12 will give bad test and libration result. |} foroper equipment is not available or cannot be ‘obtained, send the Uitrasound Applicators tothe factory for calibration |. Donotaerate water when filing power meter. - Unplug the unit ftom the power source and/or remove Battery before attempting any removal or replacement procedures to prevent electrical shock |- Dielectric Withstand Test must alvays be performed aftr a Power Supply has been replaced. Field technicians unequipped to preform the Dielectric Wititand Test should contact the manufacturer for Power Supply replacement ANGER + Handle Power Supply shield with caution, Penetration ofthe shield may result damage fo the unit and/or personal injury. +The Power Supply will retain high voltage in the Power Supply Capacitor C4. Discharge Capacitor using a muttimater prior to any service of the Power Supply + Applicator must be calibrated after removal and replacement of any part, using an Ohmic UPM DT 10 or UPMDT 100. Failure to calibrate a repaired Applicator, Using the proper equipment, may result in setious injury or haim to the patient.2- THEORY OF OPERATION Ina” Noble Uasuné Therap Som 2.1 OVERVIEW ‘The ntelect Mobile Ultrasound Therapy System ate comprised of sevetal PC board assemblies housed within, ‘common enclosure. These assemblies each support a distinct function in the product. The basi elements ‘ate User Interface, Control Board, Ultrasound Board, Ultrasound Applicator, and Power Supply 2.2 POWER SUPPLY ‘A.universl input Power Supply provides al parts ofthe system with 24 VDC The sunply is connected to the tains at all times when the cord is attached. The power switch on the top ofthe unit, switches the 24 VDC ‘output of the Power Supply to the different components in the system. The 24 VDC supply is regulated locally ‘at each PC Board as required 2.3 CONTROL BOARD. ‘The Control Board serves just as is name implies. t controls the operation ofthe Ultrasound Board, User Interface and optional accessories. The Control Board cornmunicates to the Ultrasound Board. The Control Board dives the Display. The Control Board reads the menu buttons. The Control Board also reads the amplitude and the Contrast Cantal an the system, Sound output is generated by the Control Board and routed to an intemal speaker. 2.4 ULTRASOUND BOARD AND APPLICATOR ‘The Ultrasound Board generates the or 3 MHz output to drive the Sound Head. The Ultrasound Board is accessed much like an /O port by the Control Board. It can provide current and voltage information ‘about the ultrasound output of the board, The calibration data for the Sound Head is passed through the Ultrasound Board from the Applicator up to the Control Board. By storing the calibration data in the Applicator there is no calibration necessary for the Ultrasound Board, Calibrated Chattanooga Group Ultrasound Applicators, designed for the Intelect Mobile Ultrasound Therapy System or the Intelect ‘Advanced Therapy System, can be connected and operated on ary Intelect Mobile Ultrasound Therapy System to provide accurate coupling and output, 2.5 USER INTERFACE AND ACCESSORIES The LCD display panel provides the operator visible feedback in the way of menu choices. Pressing the menu buttons makes selections from the menus, The Control Board interprets these user inputs {and responds accordingly. Audible feedback is given as well for events such as key presses and end of treatment ‘The Optional Battery maunts in the system bottom and supplies 24 VDC to the Power Supply. The Power Supply distributes the power required to the system as needad. The charging circuit for the Battery is incorporated on the Control Board, An icon on the display reflects the avallable amount of charge in the Battery. When the system is connected to an approved power outlet and a Battery is installed in the system, the system wil charge the Battery to full capacity, The incorporated charger will not overcharge the Battery3- NOMENCLATURE tna bie Usd Tea Sit | INTELECT MOBILE ULTRASOUND. Know the components and theit functions before ‘THERAPY SYSTEM. performing any operation on or service to the ‘The nomenclature graphics below, Figure Intelect Mobile Ultrasound Therapy System, 3.1, Indicates the general locations ofthe exterior ‘components of the Intelect Mobile Ultrasound Therapy System, FIGURE 3.13- NOMENCLATURE Inlet” Mabe ascund Therap Sen 3.2 HARDWARE AND SOFTWARE SYMBOL DEFINITIONS “The symbols below are found on the system as Therapy System, Wells within the software. These symbols aro kaw the symbols and theft definitions before delined for the purpose of recognition and performing any operation of or service to the ntelect functionality when operating or performing Mobile Ultrasound Taerapy System, service on the Intelect Mobile Ultrasound Intelect Mobile Ultrasound Therapy System Hardware Symbols 0 Power On/Off “The Power OrvOff button contoks the flow of electricity to the unit. luminates steady when system 1s On. Flashes when power is avaiable. Leo “The LCD (Liquid Crystal Display allows the user to view and monitor the information displayed before, during, and after therapy, Wetinical brary Select hsb. n to access the flowing factions: “Retire Ue otacl “Restore Facto Stings “este Facto Protas “anne: “Mew Unttrmation Time ess the Up or Down attow buttonsto se ttl teatent tine of therapy <= Back Use ths burton to return to the previous window @ stop Select this button to stop a testment seston Y down arrow Wien the widow dpays ls of otions press the Down Aow button to srl down te st Pause ress this button to pause and estar therapy sessions Sound Head ec ake Nha oF pats cnc wie pana vasa rest cn that cers ect natoy to mechani energy inthe fam of a vbvatng cya LED Indicator (Output Power) Whe Harare hs Greer op igs tat uta ety bei eed orth Sound Head Applicator “The hand held assernbly used to deliver ultrasonic energy. The Applicator includes the Sound Head, Transducer, and related electronics.3- NOMENCLATURE Inet” Mabie Utasund Therapy Stem 3.2 HARDWARE AND SOFTWARE SYMBOL DEFINITIONS (CONTINUED) °Uteasound Applicator Connection C This part serves asthe connection point between the unit and the Ultrasound Applicator. stant ° Select Start to begin a treatment session. <= Acceptand Return Seco acta men selection and ore tothe home screen va INTENT Use the up or dow sow onthe tent button toads Utasoud Intent the prexabed evel WL nsyojte Press to select and display the Duty Cycle ofthe Ultrasound as prescribed. Options available are: 10%, 20% 50% oF Continuous (10036 Up Arrow When the window displays list of options press the Up Arrow button to scroll up thelist. Battery Indicator When displayed on the LCD, this symbol indicates the Battery pack option is present on the uit This symbol also displays the charge status ofthe Baten LCD Intensity/Contrast Dial Ifthe intensity ofthe LCD display diminishes, turn the dal unt the Display contrast i optimal o 4H Charge indicator ww > This symbol displays when the units connected to Mains Power and the Battery Pack i charging. Frequency Press to change Frequency to 3 MHz or 1 MHz Intensity Display Press to display "Watts or "Wats per ci forthe output ofthe ultrasound. Head Warming FN Press to tum Of or On the Head Warming feature ofthe system Increase A Found in two locations on the system, press to increase session time and/or ultrasound intent respectively Decrease Faund in two locations on the system, press to decrease session time and/or ultrasound imensity respectively. NOTE: During Battery operation, ifthe unit is left on, but is not active for more than five minutes, i will power off to conserve Battery power. To restore power, press the Power OrvOf button4- SPECIFICATIONS. Inlet WobieVrsound Therapy stem 4.1 INTELECT MOBILE ULTRASOUND THERAPY SYSTEM Figure 4.1 below provides physical derail of the Refer to this section when performing Intelect Mobile Ultrasound Therapy System. This troubleshooting, replacement, and repair of the section aso provides ultrasound specications taaid —_Intelect Mobile Ultrasound Therapy System. in roubleshooting. ‘Aintolect Mobile Ultrasound Therapy Systems Physical Specifications |= tan an oe Oe. — ~ eas Atmospheric Pressure. fete tee enn: SOTO PS = ‘Complies with: Me tenance 26H = QD), coms ioc sonton ects ee sommcsineng “SY See weiter era ie on Usa. ae ee Battery Tyo, [Nickel Metal Hyco (NIMH) Fes CRESTS ES AN, 04136060 7-1, EC ed60T-1-2, (12Ve20szeAa) ene4.2 INTELECT MOBILE THERAPY SYSTEM ULTRASOUND SPECIFICATIONS Thissection provides the necessary Uresound specications to dn youbleshooting. Refer to these specications asnecesary when toubleshotng the Uasound PC Board and Applicators ‘A.Ultrasound, Frequency T MHz, 596 3 Miz, 536 Dury Cycles... 10%, 20%, 503%, and Continuous Pulse Frequency 16,48, and 100 Hz Pulse Duration... mec, + 20%; 2 mSec,-+ 20% 5 msec 20% (Output Fower TOM? Crystal (0-20 Warts at 1 MHz, ‘O10 Waits at 3 MHZ 5 cm? Crystal (0-10 Watts, 1 and 3 MHz 2am? Crystal 0-4 Watts, and 3 MHZ 1 a? Giystal (0-2 Watts 3 MHZ Only ‘Ampltude..0-25 w/cm? in Continuous mode, (03 w/em? in Duty Cycle modes Output accuracy. 20% above 10% of ‘Temporal Peak to Average Ratios 21, 203% at 50% Dury Cycle 541, 208% at 20% Dury Cycle 91, = 20% at 10% Duty Cycle ‘Beam Non uniformity Ratio 50:4 maximum Beam Type. Colimating Effective Radiating Areas 10 cm? Crystal-68 cm2- 10.0. em? 5 em? Ciystal-3.5 cen? -50cm? 2m? Crystal - 14 cm? -20.cm2 1 em? Crystal-0.7 cm? -1.0cen? Treatment Time. 130 Minutes Do not apply the Ultrasound Applicator tothe patient during the Head Warming petiod. Applicator must remain in applicator hook during the Head Warming period £8. Head Warming Feature Specifications ‘The Head Waimning feature ofan intelect Mobile Ultrasound Therapy System utilizes Uiasound output resulting in warming of the Applicator to increase patient comfort With Head Warming enabled, uitrasound is emitted without pressing the Start button. The ‘Apolicator LED will not iluminate during the Head Warming period, Ultrasound Display wll Indicate "Warming? ‘Our... 50% Cycling of maximum power Frequency 3Miiz Sound Head Temperature ...29.4°C-433°C BF-TOF5- TROUBLESHOOTING 5.1 INTELECT MOBILE ULTRASOUND THERAPY SYSTEM ERROR MESSAGES ‘A The following information is provided as an ald No component level troubleshooting in defiing the Software Eror Messages ofthe information is or will be provided by Intelect Moblie Ultrasound Therapy ‘Chattanooga Group for field troubleshooting of System. Oncea particular eror message is board components defined, the information will asa list probable B.Once a paticular PC board has been determined causes and possible remedies. Once the ‘25 bad, refer to the appropriate removal and problem area is determined, subsequent tests replacernent section for the board affected and for verification will be necessary to determine a follow the instructions for replacement of the "Bad Board” boned AllTroubleshocting and tests wil be to validate a°ad Boar" only, Be | pec Se [agua ae ieeee =P rae re a Tne vectra Waning appears egg wi a2 neyo a we of una coat dak Catena Gp sevice Es ad Marans ese eons nd an mttaer wit nhl mst eee y Chane lou oa ed ‘Seve Tian ceed Cataooga Gop betare ay utr peatonor we ote uit Use faut tha nda an Ea er Waring in hes ages may oso ryote pate se orm caeexense mera damage he5- TROUBLESHOOTING obi Utasund They Stem 5.3 ELECTRICAL SAFETY Theinielect Mobile Ultrasound Therapy System has been tested to |EC/EN 6060-1, Standard for Safety for Medical Equipment. NOTE: This device complies with current leakage, (ground continuity, and dielectric withstand {Hi.Pot)limitsas prescribed by IEC/ENAIL 60601-1 and CSAVCAN 601.1 Medial Electrical, Part 1: General Requirements for Saft Faclty, local and national limits and test methods may vary. Power Requirements Model: 2776 Input: 100-240VAC (Gerial rumbers 1000 and above) 75 VA, 50/60 He 5.4 LEAKAGE Conduct all necessary leakage tess as required [er IEC/EN 60601-1, Standard for Safety for Medical Equipment ‘Unit faling Dvelectric Withstand or Leakage tests could Indicate serious intemal problems, Dont place unit back into service! Send w for repair Do not attempt to renal! @. Listed by Intertek Testing Services NA Inc. Conforms to UL Standard 606011 Certified to CAN/CSA Standard C22.2 Na, {601.1-M190 w/A2 Meets Directive 93/42/ EEC. Compliant to IECEN 6601-1, EC 60601-1-2, 6601-255,5: TROUBLESHOOTING Inlet” Mabie Urasaund Therap Stem 5.5 VISUAL INSPECTION, Visually inspect the Intelect Mobile Ultrasound Therapy System. A visual inspection can, to an experienced technician indicate possible abuse of the unit and internal problems. 5.6 UNIT STARTUP AND FAN TESTING. ATest 1. Place unit face up on work surface. 2. Connect Power Cord to unit and plug into proper power receptacle 3. Connect an Applicator tothe unt. 4 Tum system on, Adjust the Intensity up and ess Start. The fan wil begin to run, ater the audible beep tones. 5. Place hand atthe back of system, near Contrast Contro, to vetfy Fan is blowing out Refer to Figure 5.1. B.Test Results 1. Unit wll not start, unit alec test. 2) Possible bad Main Power Switch, b)Possible bad Power Supply Possible bad power outlet or Mains Power Cou. )Possble bad Ultrasound Board 2. Treatment will not start up. 23} Applicator not connected. bb) Possible bad Ultrasound Board Possible bad Control Board, 3. Screen does not display, unit failed test. a} Contrast Control needs adjusting by Possible bad Display Possible bad Control Boar. Possible bad Power Supply. ©) Visually check power LED Ifflashing, the Power Supply is good. Replace the Control Boat f) If not flashing perform the Ultrasound Board test to check the Ultsound Boar. Refer to section 5.7 page 15. th= Power Supply functions replace the Ultrasound Board 4. Fan not blowing outward, uni fled test a) Fan blowing inward. Fan wired wrong. Rewire or replace Fan. 5.Fan not blowing, NOTE: The Fan only functions when Ultrasound is being emitted from the Sound Head, 2) Possible bad Fan. by Possible bad Power Supply, €) Possible bad Control Board. FIGURES.15- TROUBLESHOOTING tne” Hebe Uund Thay Stem 5.9 ULTRASOUND TESTS. ‘A. Equipment Required for 5.9 and 5.10 + Degassed Water, Refer to page 12 for degassed water recipes + Ohmic Instruments UPM DT 10 or UPM DT 100 Uttrasound Power Meter + Known good Ultrasound Applicator NOTE: Use any Ultrasound Applicator supplied with a Chattancoga Group unit for ths test B. Ultrasound Applicator Identification neues Test Procedures 1. Without Ultrasound Applicator installed, twin uniton, 2. Look at the Display center. The Applicator ‘not detected icon should appear. Refer to f Figure 5.4 3. Connect the Applicator into Applicator Receptacle Refer to Figure 5.5. Watch Applicator LED while connecting to syste ‘The LED should flash green five times. i NOTE: “The flashing gfeon light indicates that the ‘Applicator is programmed and calibrated, 4. Look at the display center. The Applicator FIGURE 5.5 detected icon should appear. Refer to Figure 5.6. Ultrasound Applicator Identification. Test Results 1. Unit operates as described in steps 2 and 4 2) Unit passed test 2'NO CAL"icon displays center of system Display. 23) Applicator not calibrated. +b) Possible bad Applicator Cable, Re-test with kerown good Applicator. (¢ Possible bad Ultrasound Board. 3.Not detected icon displayed after ton FIGURE 5.6 seconds of Applicator being plugged in, 2) Possible bad Applicator or Applicator Cable, Re-tost with known good Applicator ) Possible bad Ultrasound Board6.1 SEPARATING TOP FROM BOTTOM [Unplug the unt from the power source and/or remove battery before attempting any rernoval or replacement procedures to prevent electrical shock A. Part Numbers "Top ssc iat Base ooo 7252 8. Tools & Equipment Required + #1 Philips Screwdriver . Separating Top from Bottom |. Remove the Plt from the bottom ofthe systom Refer to Figure 6.1 2. Remove the Mains Power cord from the system. Refer to Figure6.1. 3 Remene the rear Fan Gillam the sysern ta (gan accesso the two rear mounting screws. Refer to Figure 6.2. 4, Remove the two front fet from the sistem to {gan accesso the two font sows Refer to Figure 63 5. Remove the four mounting sce from the bottom housing using the #1 Philips scewtive Refer to Figure 6.3. 6 Caeflly separate the upper and lower housings ofthe stem. 7. Disconnect the Power Supply and Fan Harnesses om the Contol Board ofthe system, " SUPT AND FA Refer to Figure 63 SAAN {8 Reassemble the unitby reversing the steps FIGURE 6.3, above. NOTE: Do not ovenighten the screws Overightening will damage the treads ofthe bras inserts6.8 APPLICATOR SOUND HEAD A. Part Numbers (Applicators) Vom, 27333 2am oceanic Som CDRS locm 27336 Sound Heads VT enn NIG 2m. - 22 Som 27128 10cm ian d710 8. Tools and Equipment Required + None .Sound Head Removal and Replacement NOTE: ‘The Transducer is contained within the Sound Head of the Applicator. 1. Unscrew the Sound Head flom the body of the Applicator, Refer to Figure 6.21. 2.Alter moving the Sound Head inspect the plastic Probe Spring Holder in the top of, the Applicator Assembly fr eracks or discoloration. Rafer to Figure 6.22. NoTE: Ifthe Probe Spring Holder is dark or contains crackit should be replaced. Refer to Section 69, part c. 3. Reverse stops 1 and 2 to installa replacement Sound Head, 4. Recalibrate the Applicator following the calibration procedure in Section 7, part B. pyc ‘Applicator must be calibrated after removal and replacement of any part, using an Ohmic UPM DT 10.0rUPM DT 100, Failure to calibrate repaired Applicator using the proper equipment, may result in serious injury to the patient FIGURE 6.21 FIGURE 6.226- REMOVAL & REPLACEMENT elect” Moi Utrasound Tarp Syste 6.9 APPLICATOR PROBE SPRING HOLDER A. Part Number 27040 8B. Tools and Equipment Required + #1 Philips Screwdriver CC. Probe Spring Holder Removal and Replacement | Remove the Sound Head per Section 6.8 part C. 2. Romowe the brass Probe Spring and inspect for damage. Retain the Probe Spring for installation if undamaged Refer to Figure 6.23. 3. Using a # 1 Philips screwdriver remove the screw Securing the Probe Spring Holder to the Applicator housing. Refer to Figure 6.23. 4 Reverse steps 1 through 3 for installation of the replacement spring. 5. Rocalbeate the Applicator. Nore: Do not over tighten the screw holding the Probe Spring Helder. cracked or damaged Probe Spring Holder will affect the ‘operation of the Applicator. DANGER ‘Applicator must be calibrated after removal and replacement of any par, using an Ohmic UPM DT 10 or UPM DI 100. allure to cal brate a repaired Applicator using the proper squipment, may result serious injury to the patient FIGURE 6.236- REMOVAL & REPLACEMENT 6.10 APPLICATOR PC BOARD A. Part Numbers Vom 2TEOD 2am nn 7 27071 Sm. 27073 10cn 27075 B8.Tools and Equipment Required + #1 Philips Screwdriver €.PC Board Removal and Replacement 1. Remove the Sound Head per Section 6.8, part. 2.lemove the Probe Spring and Probe Spring Holder per Section 69, part C FIGURE 6.24 3 Remove the Applicator Cable per Section 6.11, part. 4, Pull the PC Board from the Applicator housing Refer to Figure 6.24. Note: If necessary needle nose plies can be used To grasp the edge of the PC Board for removal Revetse steps 1 through 4 for installation of the replacement PC Board, Recalibrate the Applicator. NoTE: \When replacing the PC Board it should be oriented with the Cable Connector toward the inside ofthe Applicator Handle. Push the PC Board as far into the Applicator Handle as possible, with the Cable end iting into the FIGURE 6.25 ‘hyo PC Eoard slots Refer to Figure 6.25. The Sound Head end ofthe PC Board fits against the screw standoff fr the Probe Spring Holder Refer to Figure 6.26. PRORESPRNG UDERSTaNDOF PACY.W esa) ‘Applicator must be calibrated after removal ‘and replacement of any part, using an Ohmic UPM DT 10 or UPMDT 100, Fallure to calibrate a repaired Applicator using the proper equipment, may result in serious injury to the patient- NT Inca Mi tsend Thay Sten 6.11 APPLICATOR CABLE A. Part Number ‘ 27106 B.Tools and Equipment Required + #1 Philips Screwdriver .PC Board Removal and Replacement 1. Using a counterclockwise motion, turn the ‘end of the Applicator to remove the Applicator Cable Refer to Figure 6.27. 2. Once the end of the cables fee from the Applicator housing, grasp the wires of the ‘able and gently pul the applicator connector from the holder on the PC Board 3.Toinstall position the two black tabs of the replacement Cable away from the inside of the Applicator. Using astral screwdriver FIGURE 6.27 push the Connector onto the pins of the ‘Connector Holder. Gently push the sides of the Connector to very that it is well seated. 4,Once the Cable Connector i well seated, hold the Cable and twist the wires 2 172 turns counterclockwise. Refer to Figure 6.28. NOTE: Twisting the Cable wires prior to screwing the Cable onto the Apalicator housing will low the wires to untwist and straighten aut when the Cable Is screwed into place 5. Verify the operation of the Applicator FIGURE 6.288- PARTS 8.1 TOP ASSEMBLY Inlet” Mabie Urascund Therap Sto a) 1 27244 [TOP ASSEMBLY 1 2 [SEE CONTROL | CONTROL ASSEMALY 1 BOARD ASSY DRAWING, 3 727255 | KEYMAT T 4 NWA] PART OF KEYIMAT, PART NUMBER 27255 5 DTVAD__ | NB GMM SCREW PAN HEAD 178: PARTS Ince” Mabie asunder St ‘8.2 ULTRASOUND ASSEMBLY8- PARTS Inlet” Mobile Uraseund Therapy stem 8.3 CONTROL BOARD ASSEMBLY __-— NOTEINSERT#4 THROUGH TOPROWOFSOCET CONNECTOR OF 1 — CONTOLEOND 7 2 | 2s | DECETS 2 [a [eer 7 [ae [e 7 S| a re 7‘8.4 BASE ASSEMBLY COPPERTAPE Nore: LOCATIONS THE COPPER TAPE, PART 12, SECURES THE SHIELD, PART 411 TOTHEPOWER SUPPLY HOUSING. co)8- PARTS Intel Noble trasound Therapy tem, 8.4 BASE ASSEMBLY (CONTINUED) CONNECTOR INFILL PANEL 1 FAN SEAL T 27265 __ | POWER SUPPLY T 77158 [FAN T 27152_ | UNIVERSAL SNAP-ININLET (EC SOCKET) T 27136 _ | M4 X 35MM SCREW PAN HEAD 2 27142, M3 XMM SCREW PAN HEAD 2 SHELDT PORT POWER SUPPLY T 28152__ | COPPERTAPE 172 OST8- PARTS Intel” Moi Ut asund Therapy Syston 8.5 FINAL ASSEMBLY i a vuwoen mone T | sEroPassY RAWING Top Assembly cry SY [Base Assembly8- PARTS Insect” Nobile Urasound Therapy tem 18.5 FINAL ASSEMBLY (CONTINUED) ar cr 2 27410 _ [BATTER COMPARTMENT COVER ASSEMBLY 4 27253 [PLYNTH 1 5 T7263 [REARVENT T 6 27368 T 27365 1 7 27478 | BATTERY PACK T 9 27373 [FOAM BAFFLE 1 70 D7V42__ [MB KGW PANHEAD SCREW 4 1 27150 | FEET DX 1/4 HBLK 2 2 27a2|__[TAPESM vr10- WARRANTY Inlet obit UtasoundToeap Siem Chattanooga Group, 2 division of Encore Medical L. P. [Company”) warrants thatthe intelect Mobile Ultrasound Therapy System (Product) i fee of defects in material and workmanship. This warranty shal remain in effect fortwo years (24 months) from the date of original consumer purchase. IF these Product fail to function during the two year warranty period due to a defect in material or workmanship, at the Company's ‘option, the Company or sling dealer wil repair or replace this Product without charge within a period of tity (G0) days from the date on which the Product Is returned to the Company or the dealer. All repairs to the Product must be performed by a service center authorized by the Company. Any macifications or repairs performed by unauthorized centers or aroun will vid ths warranty. ‘The warranty period for the applicators is one year (12 month) ‘This Warranty Does Not Cover: + Replacement parts or labor furnished by anyone other than the Compary, the selling dealer, ora certified Company service technican, + Defector damage cused by abr furished by someone the than Company the sling dealer ra certfed ‘ompany service technician. + Any malfunction o failure in the Product caused by product misuse, including, but not limited to, the fllure to provide reasonable and required maintenance or any use that i inconsistent with the Product User's Manual COMPANY SHALL NOT BE LIABLE IN ANY EVENT FOR INCIDENTAL OR CONSEQUENTIAL DAMAGES. ‘Some lacations do not allow the exclusion or limitation of incidental or consequential damages, so the above limitation or exclusion may not apply to you. To obtain service from Company or the selling dealer under this warranty: 1 Aiton claim must be made within the warranty period to the Company or the selling dealer. Written claims made to the Company should be sent to: Chattanooga Group 4717 Adams Road Hinson, IN 37343 USA +#1-473.870-7200 1-423-870-2046 FAX. 1-800-361-6661 CANADA chattgroupcom and 2.The Product must be returned to the Company or the selling dealer by the owner, ARetun Authorization (RA) Number must be obtained before returning any product to the Company, Zs waranty aves you speci egal nghtsand youray abo ave other hts which vary fom location to location. ‘The Company does not authorize any person or representative to create for it any other obligation or ability in connection with the sale ofthe Product. ‘Aly representative or agreement not contained in the warranty shall be vold and of no effect. "THE FOREGOING WARRANTY IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESSED OR IMPLIED, INCLUDING ANY WARRANTY OR MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE.Nene ee Cl CHATTANOOGA GROUP rete 150 13485 cote it ren RIBS Semeen