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GE Dinamap ProCare Service manual

1. 2 5 Compatible Parts Reorder Codes Product Code ECAT DINAMAP ProCare Monitor Operations Manual 2009360 001 DINAMAP ProCare Monitor Service Manual 2009381 001 Battery 633178CR Power Cord 316579 Printer Paper box of 10 089100 E9050KP DINAMAP Rolling Stand 003215 E9050JB Pole Mounting Option 2009762 001 Wall Mounting Option 2009763 001 Hose Management Option 2009764 001 Bed Rail Option 2009765 001 Nurse Call 487208CR NIBP OPTIONS Airhose 12 ft Adult Pediatric Screw Connector 107365 E9050LH Airhose 24 ft Adult Pediatric Screw Connector 107366 E9050LJ Airhose 12 ft Neonatal Quick Disconnect 107368 E9050LK Airhose 12 ft Adult Pediatric Quick Disconnect 88847 E9050KN CUFF ASSORTMENT PACKS CLASSIC CUF Assortment pack 2692 E2692J Includes 1 each Infant Child Small Adult Adult Large Adult Thigh Cuff CLASSIC CUF Assortment Pack Neonate 2693 E2693J Includes 2 Neo 1 3 Neo 2 5 Neo 3 5 Neo 4 5 Neo 3 SOFT CUF Assortment Pack 2695 E2695J Includes 1 each Infant Child Small Adult Adult Large Adult Thigh Cuff SOFT CUF Assortment Neonate 2694 E2694J Includes 2 Neo 1 3 Neo 2 5 neo 3 5 Neo 4 5 Neo 5 DURA CUF Assortment Pack 2699 E2699J Includes 1 each Infant Child Small Adult Adult Large Adult Thigh Cuff DURA CUF Assortment Pack Adult 2698 E2698J Includes 1 each Infant CHild Small Adu
2. 2010532 001 Spanish 100 P N 001 Language Model Is Printer Installed Method of NIBP Determination Auscultatory is labeled on left keypad 2010534 001 Italian 400 Printer Installed 2010535 001 Italian 300 Printer Installed 2010536 001 Italian 200 Printer Installed 2010537 001 Italian 100 Printer Installed 2010538 001 Italian 400 2010539 001 Italian 300 2010540 001 Italian 200 2010541 001 Italian 100 2010542 001 Swedish 400 Printer Installed 2010543 001 Swedish 300 Printer Installed 2010544 001 Swedish 200 Printer Installed 2010545 001 Swedish 100 Printer Installed 2010546 001 Swedish 400 2010547 001 Swedish 300 2010552 001 Swedish 200 2010553 001 Swedish 100 2010554 001 Dutch 400 Printer Installed 2010555 001 Dutch 300 Printer Installed 2010556 001 Dutch 200 Printer Installed 2010557 001 Dutch 100 Printer Installed 2010588 001 Dutch 400 2010559 001 Dutch 300 2010560 001 Dutch 200 2010561 001 Dutch 100 2010578 001 Chinese 400 Printer Installed 2010589 001 Chinese 300 Printer Installed 2010590 001 Chinese 200 Printer Installed 2010592 001 Chinese 100 Printer Installed 2010593 001 Chinese 400 Revision B ProCare Patient Monitor Service Manual 2009381 001 Calibration amp Maintenance Appendix D Replacement Parts and Assemblies 2010594 001 Chinese 300 P
3. FL3 Love R LED IR LED CATHODE n 2A RCAL RETURN Are mm 4 5 5 gt DET A EN SEDIPS Sm INNER SHIELD INNER SHIELD GND oe e Lamm DET ANODE DET CATHODE 5 m LED RED LED CATHODE DIGICAL HERE o ma DET C i RCAL QURE EE DIGICAL On m a c C 3 NIC Nc Z gt 200 100MHZ em ANALOG GND OUTER SHIELD LED oe e m EE DET CATHODE DET ANODE GND m e FL2 Ae mm Y Rand mm 4 1 Z 200 100MHZ DET A oo DET C mm P5VSP INNER SHIELD MENI gt INNER SHIELD ME NC mm NC OUTER SHIELD mm e k IRLED CATH D35 OUTER SHIELD MEME A BAV199 RED LED CATH MN 3 NIC Nc 3 P3V3 P5VSP R183 Ve g Q19 us P3V3 DTA143XKA 4N35 10K0 FIVI Logic x 3M da ok SpO2 Module Connector 14 pin 249 3 fe 2 CTH E 4 R129 N5VSP P5VSP 10K0 V Ve J12 NELLCOR P5VSP A mm cock P5D EE ND Pov oe Hem ov oF Hcp zr oo e WEN RESET 100nF 25V R142 m on 3 m SPO2_RST 01 w c 3K01 M v 0 V f AN 016 SN umm ANALOG OUT N A 8 M WEN TRANSMIT MP5060UT TO J2 ON NELLCOR MP506 e 5 in Eus MMBT3904LT1 A B 5 NEEE RECEIVE MP506 IN E e E EE 5ANALOG e aen CTS MP506 IN 12 m GND D FROM SPO2 3 V R136 e Semm ev DIGITAL 499 Amm ov R184 P5VSP Ms 1K00 P3V3 gt sp SP J17 C120 R139 U26 D TO SPO2 ZE Q20 SUE N MASIMO XN DIARI fan ey 1K00 A EE o R145 le e 1 249 En Ve ej oo 3 cm vo S 5 TO J3 ON MASIMO MS 5 GND en GND Ln RESET
4. 3 IN NES ep e e U16 BYG22 cap CBS EN FB R27 C96 C97 C76 100NF 100NF R65 E 1K00 R33 t C25 2K87 1U0 16V PROGRAM CONNECTOR V V J1 ma PGM PS_ON 0 Em mm mm 5 5 0 V SUPPLY PSD V MIC39101 5V e e 2 VIN vout e U5 c38 1 072 1 EN la 1 C73 C4 H FLG H 202 100NF GND 100NF 40U0 16V 25V ji 8 25V RESET TEST 0 I Schematic Main Board SCHEMATIC PWA MAIN BOARD PROCARE P N 2008855 Rev B 5 of 10 page 5 13 14 P3V3 Printer Connector c c Schematic Main Board fuc E wt cr PP PRINTER INTERFACE R1235R59 SR58 SR57 sg SR55 SR SR122 mm 100K gt 100K lt 100K 100K 2 400 100K 100K 100K 2 19 VCC 20E U11 V PR DI i 2 hao nz PR ST6 4 A1 1Y 16 6 haz malt PR_ST5 e S A3 m G PR_ST4 sba mi 13 7 PR_ST3 e np Nig PR_ST2 e A3 NIS PR_ST1 Pre TOE GND PR CLK 7 L e V P5A P5A ES EB R91 R60 R97 20K0 30K1 PR EOP lt 1M00 more 8 5 1 7 2 P3v3 AE o 3 4 U13 R89 7 ENQ 30K1 6 EREE E DTA143XKA V 7 Logic 8 R73 V 100R
5. 3 Principles of Operation evision Pro Care Patient Monitor Service Manual 2009381 001 For your notes 3 2 ProCare Patient Monitor Service Manual Revision B 2009381 001 Principles of Operation 3 1 Introduction 3 1 Introduction This section provides overall theory of operation and functional description of the ProCare Monitor The ProCare Monitor comes in six different configurations ProCare 100 Capable of monitoring Blood Pressure BP and Pulse ProCare 200 Capable of monitoring Blood Pressure BP Pulse and Temperature ProCare 300 Nellcor Capable of monitoring Blood Pressure BP Pulse and SPO2 Nellcor technology ProCare 300 Masimo Capable of monitoring Blood Pressure BP Pulse and SPO2 Masimo technology ProCare 400 Nellcor Capable of monitoring Blood Pressure BP Pulse SPO2 Nellcor technology and Temperature ProCare 400 Masimo Capable of monitoring Blood Pressure BP Pulse SPO2 Masimo technology and Temperature The model of your monitor determines which parameters are in your monitor Using the ProCare monitor a clinician can view print and recall data that is derived from each parameter The Monitor is also capable of alerting the clinician to changes in the patient s condition All of the main operations of the ProCare Monitor are easy to use and only a button touch away Please review the factory default settings and where applicable enter setting
6. Assembly Drawings amp ProCare Schematics Appendix D Replacement Parts and Assemblies 9 A Assembly Drawings amp ProCare Schematics ProCare Patient Monitor Service Manual Revision B 2009381 001 see Appendix C in Section 4 for Display Cover removal instructions Exploded Assembly Drawing ProCare Monitor 1 of 2 page 5 1 2 l KEN h N NL i NI N NI ANON NSS a EX EA EE Em Exploded Assembly Drawing ProCare Monitor front case page 5 3 4 PNEUMATIC TUBING ROUTING MAIN PROCESSOR P3V3 P5A C47 C45 C50 100nF cas C44 100nF 25V P3V3 P3V3 LE toont 25V C46 100nF 25V e R1 SR117 100nF 25V 100 100K V V 13 22 97 V PR TH a 8 8 S 8 R104 R84 S Z ggg ln CHG 78 pou into 42 PUMP
7. Diastolic 197 203 Pressure reading at 150mmHg top display Systolic 147 153 Pressure reading at 150mmHg bottom display Diastolic 147 153 Pressure reading at 100mmHg top display Systolic 97 103 Pressure reading at 100mmHg bottom display Diastolic 97 103 Pressure reading at 50mmHg top display Systolic 47 53 Pressure reading at 50mmHg bottom display Diastolic 47 53 4 6 5 Overpressure Verification Overpressure threshold Adult mmHg 305 325 Overpressure threshold Neonate mmHg 155 159 4 6 6 Buttons Software revision in systolic display top on off Software revision in systolic display bottom NIBP alarm initiated E80 displayed on SYSTOLIC display Audible alarm can be silenced Silenced LEDs flash Overpressure alarm can be cleared Alarm button is functioning 4 6 7 Display All 7 Segment LEDs Light Correct Color All Discrete LEDs Light Correct Color 4 6 8 4 6 8 External DC Detection Charging indicator LED illuminated 4 6 9 NIBP Determination Systolic reading mmHg 107 133 Revision B ProCare Patient Monitor Service Manual 4 21 2009381 001 Calibration amp Maintenance Appendix A Test Results Form Step Description Min Max Actual Pass Fail N A 4 6 9 NIBP Determination continued Diastolic reading mmHg 67 93 MAP reading mmHg 85 95 Heart rate reading bpm 76 84 Systo
8. If Discharge ESD floors are covered with synthetic material the relative EN 61000 4 2 8 KV air 8 kV air humidity should be at least 30 Electrical Fast 2 kV for power supply lines 2 kV for power supply Mains power should be that of a typical commercial Transient Burst lines or hospital environment EN 61000 4 4 1 kV for input output lines 1 kV for input output lines Surge X 1 kV differential mode X 1 kV differential mode Mains power should be that of a typical commercial EN 61000 4 5 or hospital environment 2 kV common mode 2 kV common mode Voltage dips short interruptions and voltage variations on power supply input lines EN 61000 4 11 5 Ur 29596 dip in Up for 0 5 cycles lt 40 U 260 dip in U for 5 cycles lt 70 U 230 dip in U for 25 cycles lt 5 U 295 dip in UU for 5 s lt 5 U 295 dip in Uy for 0 5 cycles lt 40 U 260 dip in Ug for 5 cycles lt 70 U 23096 dip in Uy for 25 cycles lt 5 U 29596 dip in Uy for5s Mains power should be that of a typical commercial or hospital environment If the user of the equipment requires continued operation during power mains interruptions it is recommended that the equipment be powered from an uninterruptible power supply or a battery PowerFrequency 3 A m 3 A m Power frequency magnetic fields should be at levels 50 60 Hz characteristics of a typical location in a typical Magnetic F
9. ON 10K0 TL poat inti 20 gt DUMP ON V DC MON 76 pou int 93 LATCHED OVP PUMP 75 paas ints 58 gt DUMP2 ON PH c 74 Paso U9 INTA 97 e gt ADULT 0 PT2 73 posi ints 8 r PNEU RESET FPT 72 pape MMC2107 inte 90 o TP34 R116 V BAT MON PRI 1 TH pags inr o TP33 400K 1koo 22 8 yry 1 1K00 VRL pag H gt PR DI D FROM COMM 1 n 48 RxD pat O C DR CLK D FROM SPO2 1 0 46 Rxp2 paz 9 c PR ST D TO COMM lt gt e 27 ot pas 4 c PR_ST2 D TO SPO2 ca 45 TXp2 pag C PR_ST3 1K00 PAS H PR_ST4 SPI MISO e S 63 miso PA6 gt PR STB SP MOSI lt k NDS R206 2 Mosi pA 00 C PR ST6 SPI CLK lt 65 scx d R201 TSRO TP260 9 s TP39 TP40 TP41 75R0 a PBO Le gt PR VHON TDE c3 DE PB1 gt PR M4 T CLK lt gt ek pB2 LIS gt PR M2 T TDI lt 93 rbi ppg 14 gt PR M3 T IDO lt gt 94 Too ppg gt PR_M1 T IMS lt gt 95 Tus pps HO gt PR EOP EN T TRST lt 98 TRST PB6 3 PR LAT Place near U9 C32 FB7 PR_EOP 1K00 R103 10P i 30 cLkouT 1 SHDN_TO_PRI RESET_TEST 0 MA ix R62 C ee rd STR K c3 somHz 10M0 ae 96 TAL pci P6 YS 1 SW MUX V 1K00 pp 002 2 RTC DATA 84 PC3 O RESET PRI Q RAN ao pca 2 c RTC CLK 1K00 Icocto pcs 20 c SPO2 RST 0 P3V3 R120 4 icoc11 pce HS gt IPS ON aj ICOC12 pc 18 e c CS SEC 0 e g115100K zo coc R112 38 C0020 35 1K00 ADC PWM 100K 37 1C0C21 PDO fo e gt FSP FROM PRI CS DISPLAY e 39 160022 PD1 fea FAST_OVP 0 PWM VOL ICOC23 PD2 55 1 DUMP ON MON PW
10. 1 Unpack and identify the contents of all shipping materials 2 Remove the ProCare monitor 3 Unpack the external DC Power Input 4 Insert the external DC Power Input connector into the DC input on the lower right side of the monitor 5 Plug the DC Power Input transformer into a Hospital Grounded AC receptacle The word CHARGING will illuminate green on the front of the monitor indicating that an external power source is available Prior to usage it is necessary to charge the monitor for 12 hours 4 2 2 Set the Date and the Clock Setting the Date and Time To set the date and time on the ProCare Monitor you must first access the configuration mode The following table illustrates the menus and the corresponding LCD display graphics Setting Window Text in Window SpO Averaging Pulse Rate and SpO gt Nad SpO SAE Temp Unit of Measure Temperature G or F Year Systolic Ur Month MAP Cuff NEH Day Diastolic JAY Hour min Hr Minute min Nin Procedures 1 With the Monitor off press and hold the Menu button at the same time as pressing the On Off button for 3 seconds 4 4 ProCare Patient Monitor Service Manual Revision B 2009381 001 Calibration amp Maintenance 4 2 Configuring Your ProCare Monitor 2 The Monitor automatically switches on in configuration mode 3 To set the date and time press the Menu button to move from one setting to another You will need to press the M
11. A PBAT m 13 e 14 R14 Q5 i 10K0 12307DS m R15 18 19 40K0 PBAT PR 4 E al t C6 22 PR VHON t Y yos T 33U0 E DTC143ZKA P5A N Lade 25V a V R26 a V 15K0 PR TH P5D V R53 2K0 e PR LAT LON os e ER DTC143ZKA em P3V3 e A P gt 100nF 25V V 100nF 2 t34 s V PR M1 VCC VS2 P L E LB1831M PR M3t Lina ouT4 PR M2 i N3 U4 ouri PR MA 11 14 ouT412 17 19 FG5 FG7 Bros ros 2 o FG FG2 FG3 FG4 LE V SCHEMATIC PWA MAIN BOARD PROCARE P N 2008855 Rev B 6 of 10 page 5 15 16 PWM_VOL PWM PITCH t SEC ALARM D TO COMM D FROM COMM lt REM ALARM AUDIO ALARMS P5D R49 BRD 1R00 o SIC C7 R82 LEN oer T 10U0 10K0 Bu MMBT3904LT1 LAT C26 R24 c10 p V d n 1U0 9 C42 16V 100K 10N0 4K99 7 e hmm Zi a 220U0 2 wo qm WTS v m m C8 C86 Speaker Connector 10U0 100NF 16V 25V V R94 V V V V 49K9 PSD cm SONO R124 10K0 ab R46 PED 1K00 R178 1K00 R179 20 Y M A D16 Div PSD Q26 P5D DTC143ZKA 2 yA N DTC143ZKA C85 V SS DTC143ZKA soak al e 18 Comms Connector Loge oo N V HOST COMM V 15 12 116 C84 GND 1 nd C83 2 4 VCC FON FOFF TTL_TX V 100NF
12. BYG22 L1 BYG22 T 100nF U17 H L C69 1 L C70 R96 D8 C29 100nF MES GND di 4 D4 C40 po 301K SMGT39CA 33U0 516 17 18 A 220U0 25V NN i 25V y BYS10 25V R25 V DC MON c3 e V 49K9 d V L C90 R87 T 100nF 100K L BC 5V PBAT iud MCT8LOS 301K N OU U2 R149 GND 668 VR1 e OR10 2131617 25V 50K cw ve R150 Mw OR10 V V V V R42 V 10K0 V BC 5V Battery Connector _PBAT da e5 J2 n 10K0 100nF 25V mess gt amp e e V mm a B 3 4 B OPA2340 D12 cos a 3 a CR R72 ae l SUM a 3 U A 4K99 BAS16 S V e e V R11 R81 200K e R1 38 5 i OPA2340 1 0 K0 10K0 us De C116 R148 6 R92 R147 V 0 191 V 75mA 400nF 25V 150K 100K 100K R76 R182 OR10 OR10 R61 9 N 9 MT ag ge ET 249K V WA C117 Q15 R93 CA R146 O18 SAS 49K9 25V 100K 25V 100nF 25V R64 4K99 V BAT MON SEC V V V BAT MON PRI lt gt I CHG lt a pat SCHEMATIC PWA MAIN BOARD PROCARE P N 2008855 Rev B 4 of 10 page 5 11 12 3 3 V SUPPLY PBAT P3V3 MIC4680 3V3 68U0 e e e e 2 VIN sw3 inn e U12 L2 1 SHDN Fel 4 030 c GND 041 Ez wa R101 330 d wa IR T 22000 a 25V 1 10K0 D6 25V BYG22 V V 0 V PON 10 9 T Ti TNA ANALOG VOLTAGE SUPPLY 6 5 V 68U0 V L3 0 MIC3172 D7
13. Electromagnetic Compatibility EMC ProCare Monitor Compliant Cables and Accessories WARNING The use of accessories transducers and cables other than those specified may result in increased emissions or decreased immunity performance of the equipment or system The table below lists cables transducers and other applicable accessories with which GE Medical Systems claims EMC compliance NOTE Any supplied accessories that do not affect EMC compliance are not included Part No Description Maximum Lengths Temperature Cables and Probes 2008774 001 Turbo Temp Oral Probe Blue 3 0m 10ft 2008775 001 Turbo Temp Rectal Probe Red 3 6 m 12 ft 2016998 001 Dual Temp Cable 20 cm 8 in Pulse Oximetry Cables and Sensors 407705 006 Nellcor DuraS ensor Reusable Finger Probe 0 9 m 3 ft DS 100A 2008773 001 Nellcor Interface Cable OxiSmart DOC 10 Cable 33m 11ft 2009743 001 Masimo P C08 Cable 25m 8 2ft 2009745 001 Masimo Finger Sensor Adult Reusable N A Accessories 316579 001 AC Cable Hospital Grade AHA 3 6m 12ft 2013057 001 Universal AC DC Adapter N A ILC 1926 Isolated Level Converter N A Revision B ProCare Patient Monitor Service Manual 4 43 2009381 001 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ILC 1926 Electromagnetic Compatibility EMC ILC 1926 Changes or modifications to this system not expressly approved by GE Medical Syst
14. F 7 Record and verify the reading in the TEMP display is 102 F 0 2 F 8 Set the probe simulator to B P and verify reading is 106 0 F x 0 2 F Press broken probe button down and verify the Monitor displays E6 I 4 16 ProCare Patient Monitor Service Manual Revision B 2009381 001 Calibration amp Maintenance 4 6 ProCare Patient Monitor Parameter Tests 9 Calibration verification is complete Disconnect the probe simulator and install the temperature probe If the Monitor does not pass the calibration verification then the Monitor needs repair 4 6 12 SpO Perform only if equipped with SpO module Note for Monitors equipped with Nellcor SpO2 Nellcor is aware that various Nellcor oximetry platforms have some interesting behaviors when used with various pulse simulators On occasion when testing the integrity of the Nellcor oximetry system abnormal results may occur when introducing large changes in the pulse rate and or pulse amplitude Extreme changes in rate sent to the Nellcor sensor by the SpOs simulator may cause the SpO algorithm to completely miss in finding the pulse rate This is an expected result To workaround this incrementally step up or down the settings on your SpO simulator and allow for the Monitor to detect and display the new pulse rate or saturation Nellcor recommends use of the SRCmax Portable Tester for use with ProCare Monitors equipped with the Nellcor SpO system Masimo rec
15. French 100 Traditional P N 001 Language Model Is Printer Installed Method of NIBP Determination Auscultatory is labeled on left keypad 2010505 001 French 400 Auscultatory 2010506 001 French 300 Auscultatory 2010507 001 French 200 Auscultatory 2010508 001 French 100 Auscultatory 2010509 001 German 400 Printer Installed Traditional 2010510 001 German 300 Printer Installed Traditional 201051 1 001 German 200 Printer Installed Traditional 2010512 001 German 100 Printer Installed Traditional 2010513 001 German 400 Printer Installed Auscultatory 2010514 001 German 300 Printer Installed Auscultatory 2010515 001 German 200 Printer Installed Auscultatory 2010516 001 German 100 Printer Installed Auscultatory 2010517 001 German 400 Traditional 2010518 001 German 300 Traditional 2010519 001 German 200 Traditional 2010520 001 German 100 Traditional 2010521 001 German 400 Auscultatory 2010522 001 German 300 Auscultatory 2010523 001 German 200 Auscultatory 2010524 001 German 100 Auscultatory 2010525 001 Spanish 400 Printer Installed 2010526 001 Spanish 300 Printer Installed 2010527 001 Spanish 200 Printer Installed 2010528 001 Spanish 100 Printer Installed 2010529 001 Spanish 400 2010530 001 Spanish 300 2010531 001 Spanish 200 4 30 ProCare Patient Monitor Service Manual 2009381 001 Revision B Calibration amp Maintenance Appendix D Replacement Parts and Assemblies
16. Installed 2010658 001 Hungarian 200 Printer Installed 2010659 001 Hungarian 100 Printer Installed 2010660 001 Hungarian 400 2010661 001 Hungarian 300 2010662 001 Hungarian 200 2010663 001 Hungarian 100 2010664 001 Czech 400 Printer Installed 2010665 001 Czech 300 Printer Installed 2010666 001 Czech 200 Printer Installed 2010667 001 Czech 100 Printer Installed 2010668 001 Czech 400 2010669 001 Czech 300 2010670 001 Czech 200 2010671 001 Czech 100 2010672 001 Slovak 400 Printer Installed 2010673 001 Slovak 300 Printer Installed 2010674 001 Slovak 200 Printer Installed 2010675 001 Slovak 100 Printer Installed 2010676 001 Slovak 400 2010677 001 Slovak 300 2010678 001 Slovak 200 2010679 001 Slovak 100 2010680 001 Polish 400 Printer Installed 2010681 001 Polish 300 Printer Installed 2010682 001 Polish 200 Printer Installed 2010683 001 Polish 100 Printer Installed 2010684 001 Polish 400 4 34 ProCare Patient Monitor Service Manual 2009381 001 Revision B Calibration amp Maintenance Appendix D Replacement Parts and Assemblies P N 001 Language Model Is Printer Installed Method of NIBP Determination Auscultatory is labeled on left keypad 2010685 001 Polish 300 2010686 001 Polish 200 2010687 001 Polish 100 2010688 001 Greek 400 Printer Installed 2010689 001 Greek 300 Printer Installed 2010690 001 Greek 200 Printer Installed 20106
17. Nurse Call System is triggered Uses a Nurse Call Cable to attach to the System P N 487208CR Compatible Monitors Compact PRO 100 400 Series ProCare Series and PRO 1000 Alarm View Wireless transmitter attached to the Monitor Sends alarms and vital signs results to a pager Compatible Monitors Compact MPS Select and Portable PRO 100 400 series ProCare Series and PRO 1000 CIC Provides Central Alarm Notification amp Data Management Compatible with StatView for paging Compatible Monitors PRO 1000 Version 2 and Dash 2000 both hardwired ApexPro Provides Central Alarm Notification and data management Transmits data wirelessly Pro 100 400 Series and ProCare requires P N IPC 1931 PatientNet Provides central alarm notification and data management Lethal arrhythmia at the Central Station WMTS frequency hopping spread spectrum Note Dash 2000 is incompatible with PatientNet ILC 1926 Interfaces the PRO 100 400 series or ProCare monitor to ANY hardwired connection Revision B ProCare Patient Monitor Service Manual 4 23 2009381 001 Calibration amp Maintenance Appendix B Connectivity Requires Cables PRO 100 400 ProCare Series Compact Plus cable p n 683235 XL monitor series p n 682234 ILC 1927 Interfaces the PRO 1000 monitor to any hardwire connection Installs into the Communications bay at the rear of the monitor IPC1928 nterfaces the PRO 1
18. The model of the Monitor determines which symbols appear on it T Attention consult accompanying documents Silence Alarms Menu Inflate Stop Cycle History Print On Off Battery Power External Communications Port Connector Charging og LD LU W LD 2 amp E Defibrillator proof type BF equipment Class Il equipment according to IEC 60536 O 500hPa Packaging label depicting the transportation and storage atmospheric pressure range of 500 to 1060 hPa 1060hPa 2 8 ProCare Partient Monitor Service Manual Revision B 2009381 001 Product Description 2 4 Host Communications Connector 2 4 Host Communications Connector All host port signals are NON ISOLATED and should be connected to equipment conforming to IEC 601 1 ONLY Where isolation of data communication is required the isolated level converter should be used If external alarm control is required p n 487208 Isolated Remote Alarm Cable Assembly should ALWAYS be used Please refer to the Information Sheet included with the isolated remote alarm cable for operational details Note When using remote alarm the ProCare Monitor should be considered the primary alarm source The secondary alarm is used for secondary purposes only 2 4 1 DB15 Connector Pin Assignments Connection Details Host Port Connector rear panel Pin 15 WARNING Auxiliary equipment connected to the DINAMAP ProCare Pin 1 Monitor will result in the formati
19. V V N e RECEIVE MS 5 IN mn TRANSMIT MS 5 OUT ISOLATION BARRIER SCHEMATIC PWA MAIN BOARD PROCARE Ve Schematic Main Board P N 2008855 Rev B 9 of 10 page 5 21 22 Temperature Probe Connector e 14 PSTEMP PWA MAIN BOARD PROCARE P5TEMP R166 1K00 C137 e t U36 la TL431 S V A go ain exp Temp PGM Connector ZEE Soi til apo pu 2 D TO T ADC ins Ee AE Ea AD scuk 22 pios onpvo 23 DRDY FROM T ADC p 4 R172 15 ancom U34 csoH DONG POPULATE PSTEMP PSTEMP EXT e e 3 ner ADS1240 Rr 5 13K7 o REF 01 CLK TAD aus penal RE e PSTEMP Ps X IN POL 5 10K0 R193 pi Seles 10K0 A 5 RESET 0 10K0 DGND1 L14 giao cota ISOLATION BARRIER e R157 V THERM BLM11B221SB 1K00 Vi Lo C152 C136 T 100NF T 100NF ARO A 25V 25V BLM11B221SB PSTEMP paus V Vi C138 100nF 25V R1 54 V PSTEMP y anos 10K0 PSTEMP C133 i STEN ON cB e C D FROM TEMP PSTEMP 400nF 25V R168 a
20. accuracy in human blood studies on healthy adult volunteers in induced hypoxia studies while performing rubbing and tapping motions at 2 to 4 Hz at an amplitude of 1 to 2 cm and a nonrepetitive motion between 1 to 5 Hz at an amplitude of 2 to 3 cm in induced hypoxia studies in the range of 70 100 SpO2 against a laboratory co oximeter and ECG monitor This variation equals plus or minus one standard deviation Plus or minus one standard deviation encompasses 68 of the population TThe Masimo SET SpO parameter with LNOP Neo Pt sensors has been validated for neonatal motion accuracy in human blood studies on neonates while moving the neonate s foot at 2 to 4 cm against a laboratory co oximeter and ECG monitor This variation equals plus or minus one standard deviation Plus or minus one standard deviation encompasses 68 of the population The Masimo SET SpO parameter with has been validated for low perfusion accuracy in bench top testing against a Biotek Index 2 stimulator and Masimo s simulator with signal strengths of greater than 0 02 and a Yo transmission of greater than 596 for saturations ranging from 70 to 10096 This variation equals plus or minus one standard deviation Plus or minus one standard deviation encompasses 68 of the population Revision B ProCare Partient Monitor Service Manual 2 15 2009381 001 Product Description 2 6 Specifications ProCare Partient Monitor Service Manual 2009381 001 Revision B
21. component Refer servicing to qualified service personnel CAUTION Only qualified technicians should perform repairs to this equipment For information about operating the Monitor in a clinical environment refer to the separate Operations Manual This Service Manual consists of the following five sections Section 1 describes this volume and tells you how to use it Information is also provided about the physical and functional characteristics of the Monitor and how to get assistance in the event the unit fails to function properly Section 2 provides a general overview of the ProCare Monitor including the user controls external connections and product parameter specification Section 3 presents principles of operation for the Monitor including an overall system description and principles of operation at the component level Section 4 provides information about periodic and corrective maintenance of the Monitor and part list replacement part lists Procedures include module performance testing and calibration procedures Information is also provided to facilitate isolating faults to the subassembly level Section 5 provides component information about the Monitor including assembly drawings and electrical schematics ProCare Patient Monitor Service Manual Revision B 2009381 001 Introduction 1 2 Manual Changes 1 2 Manual Changes If in the normal course of using this manual you notice errors omissions incor
22. e V 2 CTH E 4 i R191 2K0 R194 R195 R196 gt R197 gt R164 siz307Ds D28 15 14 2K21 Q23 N L7 ind S LA 18 NoD S iE ria A DTO TEMP 3 4 MCLRO RB5 e e i RB4 PGM T R169 BLM11B221SB 1 RAANG s T E js D29 d RAVAN RB2TX R188 Z gaste RA2IAN2IVREF RBAIRX sl Aw R160 MON HTR RA3 AN3 CMP1 RBO INT 100K In m RA4ITOCKIICMP2 aje cm T C134 18 osci U35 S V C 100NF PIC16F628 X R187 V PSTEMP ex Y oscojour 10K0 Sh VSS1 VSS2 V C132 5 6 e T D22 22P0 R162 Ll X4 A BAS16 omz ORO T i L10 C131 e o e e BLM11B221SB 290 A 2 gt TEMP PROBE IN iN e 2 P3V3 Temp Probe Switch Connector R158 R189 R132 PSD 10K0 V EN_HTR 10K0 a 13 499K C142 d V JUMPER toys L 16V R165 499K V y V P N 2008855 Rev B 10 of 10 page 5 23 24 P5D ial PBAT gt PSD 100NF n 2 V PDG L 0 12 100NF vec Yo 11 PDG LO V yi pmen e e e e e e e e e e e e e e e e e e e L VOC gq DIG_MUXO 21 19 yo ZO PDG 12 VS 3 par 01 3 DIG MUXT nm ya PD RI R13 R4 R5 R6 R7 Ro R10 RH R12 100R 4 ax op 6 DIG_MUX2 Al ap va 7 PDG 14 190 100 T oko 1040 do 190
23. error message and report the failure to Customer Support Refer to the Operation Manual for information about patient alarms and general procedural alarms When a system failure is encountered the error code is displayed on the screen for five seconds and the system enters failsafe mode The error code is logged in the history log General system error codes are listed below Alarm Conditions and Error Codes When responding to a Monitor alarm always CHECK THE PATIENT FIRST and then check the Monitor cuff hose and sensors Press SILENCE to reset patient alarm conditions NIBP Alarm Definition Possible Cause E89 NIBP No Determination Unable to make an NIBP determination due to insufficient signal E84 Timeout Determination time gt 2 minutes Motion Artifact E85 Timeout One cuff pressure at gt 1 minute Motion artifact E83 Timeout Inflation Inflation time is gt 40 seconds Possible air leak is being detected E82 Excess Air in Cuff Residual air in cuff above threshold for successful auto zero E80 Overpressure Overpressure condition detected SpO Alarm Definition Possible Cause E20 SpOz No Sensor SpO sensor not connected No sensor code detected Sensor failure E21 SpO Replace Sensor SpO2 sensor or cable possibly defective Cable not connected properly Revision B ProCare Patient Monitor Service Manual 4 19 2009381 001 C
24. on Electrical Safety Testing of the ProCare Monitor The DINAMAP ProCare Monitor is designed and tested to meet electrical safety standard IEC 601 1 Requirements in this standard parallel requirements in NFPA99 relating to electrical safety This product meets the requirements of NFPA99 section 7 5 1 2 2 grounding of appliances through the use of double insulation in the external power supply module Power Brick The absence of a ground connection on the power brick obviates the need for any ground resistance test such as that described in NFPA99 section 7 5 1 3 2 Some non USA Power bricks are equipped with a non conductive Revision B ProCare Patient Monitor Service Manual 4 9 2009381 001 Calibration amp Maintenance 4 5 Safety Testing pin at the ground pin location to aid mechanical retention of the Power Brick into the receptacle Dielectric strength Hi Pot testing of the double reinforced mains insulation 4000 V RMS 60 Hz may be done by disconnecting the Power Brick from the Monitor and applying the Hi Pot tester as follows Connect one lead to the two mains power prongs Connect the other lead to the conductive sleeve on the DC output connector at the end of the cord Hi Pot testing of the patient connections 1500 VRMS 60 Hz may be done by connecting one lead of the Hi Pot tester to the outer shell of a spare DC connector plug inserted into the DC input connector on the Monitor The other lead
25. power supply network that supplies buildings used for domestic purposes Voltage Fluctuations Complies Flicker Emissions EN 61000 3 3 4 44 ProCare Patient Monitor Service Manual Revision B 2009381 001 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ILC 1926 Guidance and Manufacturer s Declaration Electromagnetic Immunity The ILC 1926 is intended for use in the electromagnetic environment specified below It is the responsibility of the customer or user to assure that the ILC 1926 is used in such an environment Immunity Test EN 60601 Test Level Compliance Level Electromagnetic Environment Guidance Electrostatic 6 kV contact 6 kV contact Floors should be wood concrete or ceramic tile If Discharge ESD floors are covered with synthetic material the relative EN 61000 4 2 8kV air 8kV air humidity should be at least 30 Electrical Fast 2 kV for power supply lines No AC Input No AC Input Transient Burst EN 61000 4 4 El kV for input output lines Surge X 1 kV differential mode No AC Input Mains power should be that of a typical commercial EN 61000 4 5 or hospital environment 2 kV common mode Voltage dips short interruptions and voltage variations on power supply input lines EN 61000 4 11 lt 5 U 295 dip in Uy for 0 5 cycles lt 40 U 26096 dip in U for 5 cycles 1096 U 53096 dip in U for 25 cycles lt 5 U 29596 dip in Up fo
26. printer paper presence When the printer is out of paper it sends a PAPER OUT signal to the primary processor 3 3 5 Pneumatic Valve Manifold PVM The PVM assembly consists of a pump a deflate valve and a dump valve The PVM inflates deflates the cuff during BP determinations During normal operation the PVM is controlled by the primary processor If a failsafe mode or overpressure condition occurs the secondary processor provides the appropriate control signals to insure a safe condition where the cuff vents to ambient atmosphere pressure 3 3 6 Optical Switch The optical switch indicates whether the temperature probe is inserted in the probe holder or not The Main Board powers the switch Revsion B ProCare Partient Monitor Service Manual 3 7 2009381 001 Principles of Operation 3 3 Functional Description ProCare Patient Monitor Service Manual 2008381 001 Revision B Optical Switch Main Board Isolated DC Power Supply Tubing f BP Cuff tubing Pump Valve PT1 PT2 Pneumatic Manifold Control NIBP Data Control UI Board Temp Probe Temp Control Data T mp Optional Control Switches Interface Ef SpO2 Probe un Optional SpO2 Circuit External DC gt Regulated Display 6V Battery gt DC Power LEDs Control Data Real Time OO Clock Port rear Remote Alarm Audio Printer Driver Control gg c 6 ol UV i i ProCare Vital Signs Monitor Sy
27. 000 Monitor to the Unity network hardwire Installs into the Communications bay at the rear of the monitor IPC 1931 Connects DINAMAP Monitors to the CIC system Transfers vital signs results from the Monitor to the CIC Requirements for use Plug DINAMAP into ApexPro using the DINALINK cable 4 24 ProCare Patient Monitor Service Manual Revision B 2009381 001 Calibration amp Maintenance Appendix B Connectivity Apex version 2 CIC version 3 Revision B ProCare Patient Monitor Service Manual 4 25 2009381 001 Calibration amp Maintenance Appendix C Display Cover Removal Installation Appendix C Display Cover Removal Installation To remove the plastic display cover 1 Place the Monitor on a stable surface 2 Insert a flat head screwdriver between the top of the display cover and the body of the monitor 3 Twist the screwdriver so that the display cover is slightly separated from the body of the monitor 4 Using two hands grasp the top middle edge of the display cover and pull away and down 4 26 ProCare Patient Monitor Service Manual Revision B 2009381 001 Calibration amp Maintenance Appendix C Display Cover Removal Installation 5 The fascia and displays are now visible Installing the Display Cover 1 Place the Monitor on a flat stable surface 2 Insert the tabs at the base of the display cover into the slots underneath the bottom row of LEDs 3 Us
28. 1 English 300 Printer Installed Traditional 2010479 001 English 200 Printer Installed Traditional 2010480 001 English 100 Printer Installed Traditional 2010481 001 English 400 Printer Installed Auscultatory 2010482 001 English 300 Printer Installed Auscultatory 2010483 001 English 200 Printer Installed Auscultatory 2010484 001 English 100 Printer Installed Auscultatory 2010485 001 English 400 Traditional 2010486 001 English 300 Traditional 2010487 001 English 200 Traditional 2010488 001 English 100 Traditional 2010489 001 English 400 Auscultatory 2010490 001 English 300 Auscultatory 2010491 001 English 200 Auscultatory 2010492 001 English 100 Auscultatory 2010493 001 French 400 Printer Installed Traditional 2010494 001 French 300 Printer Installed Traditional 2010495 001 French 200 Printer Installed Traditional 2010496 001 French 100 Printer Installed Traditional 2010497 001 French 400 Printer Installed Auscultatory 2010498 001 French 300 Printer Installed Auscultatory 2010499 001 French 200 Printer Installed Auscultatory 2010500 001 French 100 Printer Installed Auscultatory 2010501 001 French 400 Traditional 2010502 001 French 300 Traditional Revision B ProCare Patient Monitor Service Manual 2009381 001 Calibration amp Maintenance Appendix D Replacement Parts and Assemblies 2010503 001 French 200 Traditional 2010504 001
29. 112 Table 1 in range specified Predictive Mode Accuracy 0 6 C 1 0 F Determination Time Less then 60 seconds SpO Nellcor Pulse Oximetry Sp0O Range and Accuracy ad ult neonate 70 100 3 5 digits Pulse Rate Range and Accuracy 30 250 BPM 3 BPM Saturation Pitch Indicator Pitch changes with saturation Sensor Connect Disconnect from Patient se The Monitor detects the connection or disconnection or a nsor to the patient within 15 seconds Revision B ProCare Partient Monitor Service Manual 2009381 001 Product Description 2 6 Specifications SpO Nellcor Pulse Oximetry The monitor detects the attachment or disconnection of a Sensor Connect Disconnect from Monitor sensor from the Monitor within 5 seconds The Monitor detects a pulse of enters a no signal state Fuse Detection within 15 seconds of being attached to a patient the monitor detects loss of pulse from patient and enters a kossor Pulse no signal state within 10 seconds Nellcor Sensors SpO Range 70 to 100 OxiMAX Sensor Models Single Patient Use MAX A MAX AL 2 MAX NT 2 MAX P 2 MAX I 2 MAX R 3 5 OxiClig Sensor Models Single Patient Use OxiCliq A 25 OxiCliq P 125 OxiCliq NT 12 5 Reusable Sensor Models D YS 3 D YS amp D YSE 3 5 D YS 8 DYSPD 3 5 DS 100A 3 OXI A N 3 OXI P
30. 2 VIN vous e leu MCB1608S102E baet m U29 Da T 330P 1 EN dE R200 du T A j T 1000 YS 7 e e e e V ISOLATION BARRIER e e C126 10U0 C124 L C149 N5VSP _PBAT Ve ido foun Tr MIC5270 5 0 Ve GE eno U28vourif e i e e VIN T M t a DO NOT POPULATE L C151 HE C129 EE 3300 c128 exe TOt PSVSP 25V 25V r680P ci D20 MIC39101 5V y 7 E e 2p He e 24 vIn usb vout e V R153 i L11 gias C150 y C125 T 75RO a 0123 our LEN ne 10U0 10U0 25V GND VIN L13 MCB1608S102E IPS_ON 18 sp swt e 5 Sp u R sync PNE R151 MMZ2O12RIOZA 7 d d e e vc Roc H4 ad Ms INOS Ire Rcc H3 De V n R152 LT1425CS 3K01 U31 3 G3 G1 H e V e 9 64 G2 8 e C101 C102 SG PG 1N0 1NO E Ve e V 1NO NO 3K15V 3k15V V i ISOLATION BARRIER usse Schematic Main Board P N 2008855 Rev B 8 of 10 page 5 19 20 PWA MAIN BOARD PROCARE SpO2 Module Connector 10 pin TO J1 ON NELLCOR MP506 END TO J1 ON MASIMO MS 5 Allow 4mm clearance between these signal and all other board signals SpO2 Pat ient Connector EUM NELLCOR MASIMO
31. 6 11 Temperature Perform if equipped with Temp module 4 16 4 6 12 SpO2 Perform only if equipped with SpO2 module 4 17 4 6 13 Printer Output Test 4 18 4 6 14 Communication Port Test 4 18 4 7 Alarm Code Interpretation 4 19 4 7 1 System Failures aren eer enen 4 19 Appendix A Test Results Form oane eeen 4 21 Appendix B Connectivity oee II 4 23 Appendix C Display Cover Removal Installation 4 25 Appendix D Replacement Parts and Assemblies nnn 4 27 Appendix E Electromagnetic Compatibility 4 37 5 Assembly Drawings 8 ProCare Schematics sasaa 00010 3 1 Revsion B ProCare Patient Monitor Service Manual 2009381 001 Table of Contents ProCare Patient Monitor Service Manual Revision B 2009381 001 1 Introduction Revision B ProCare Patient Monitor Service Manual 2009381 001 1 1 ProCare Patient Monitor Service Manual 2009381 001 Revision B 1 1 Scope of Manual This Service Manual provides service and parts repair information about the DINAMAP ProCare Monitor This manual is intended for use by trained service technicians who are familiar with electromechanical devices and analog circuit techniques WARNING To reduce the risk of electric shock do not remove cover or back of any
32. 8 ProCare Patient Monitor Service Manual Revision B 2009381 001 Calibration amp Maintenance 4 5 Safety Testing 4 5 Safety Testing To adequately test the safety and integrity of the ProCare Monitor the following test equipment is recommended e 12VDC Power Supply e DMM Fluke 8842 or equivalent e NIBP Analyzer DNI Nevada Cufflink or Equivalent e Adult BP Cuff Neonate BP Cuff hose inflation bulb and mandrel e Inflation bulb and associated tubing e Calibration Kit p n 320246 available through GE Medical Systems e SPO Simulator for appropriate SPO type if SPO is installed e SPO Cable for appropriate SPO type if SPO is installed e TE 1811 Temperature Probe Simulator if TEMP is installed The Temperature Simulator for the Alaris System is available from Alaris Medical Systems Inc 619 458 7000 e Printer Paper if PRINTER is installed CAUTION Calibration equipment should always be kept dry and free of particulate matter Moisture or foreign substances introduced to the pneumatic system will likely cause damage to the monitor and or the accessories Complete the Test Record Appendix A as tests are performed Note This test is written so that a knowledgeable technician who is familiar with the ProCare monitor and the test equipment and will be able to follow the test procedure Note To enter service mode press and hold the CYCLE buttons while pressing the ON OFF button for 3 seconds Notes
33. 91 001 Greek 100 Printer Installed 2010692 001 Greek 400 2010693 001 Greek 300 2010694 001 Greek 200 2010695 001 Greek 100 Revision B ProCare Patient Monitor Service Manual 2009381 001 Appendix E Electromagnetic Compatibility evision e Patient Monitor Service M 2009381 001 4 38 ProCare Patient Monitor Service Manual Revision B 2009381 001 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ProCare Monitor Electromagnetic Compatibility EMC ProCare Monitor Changes or modifications to this system not expressly approved by GE Medical Systems can cause EMC issues with this or other equipment This system is designed and tested to comply with applicable regulation regarding EMC and must be installed and put into service according to the EMC information stated in this appendix WARNING Use of portable phones or other radio frequency RF emitting equipment near the system may cause unexpected or adverse operation WARNING The equipment or system should not be used adjacent to or stacked with other equipment If adjacent or stacked use is necessary the equipment or system should be tested to verify normal operation in the configuration in which it is being used Guidance and Manufacturer s Declaration Electromagnetic Emissions The DINAMAP ProCare Monitor is intended for use in the electromagnetic environment speci
34. AL e RTC DATA R174 P3V3SEC 4 10K2 P3V3SEC e 055 Y R176 R43 100nF 25V 20K0 1K00 L 20 y 1 luas VDD 2 RAO ANO RB7 28 lt gt FAST CHG V BAT MON SEQ 3 RATAN RB6 HL gt LATCHED OVP L_CHG 41 RAZIAN2 as 28 P5A2 sm A hei Ee P lt gt FAST OVP 0 F Sano R175 m TK pn 40K2 RBO INTO 21 e 1 SW PWR 0 B C35 R177 9 osct U3 20K0 ED A XL PIC16LC73B C34 4 0MHZ YA V V e 10 Gac 22P0 ORO eco Hi FSP TO PRI C3 1 RC1 CCP2 RC7IRX HE SEC ALARM lt gt RC2ICCP1 RC6 TX i hien T FSP_FROM_PRI RC3 SCK H4 PNEU_RESET RAS AN4 SSZ ADULT O PU ee as 1 CS SECO V gt gt SHDN TO PRI gt PS ON lt gt SPI MISO Schematic Main Board SCHEMATIC PWA MAIN BOARD PROCARE P N 2008855 Rev B 2 of 10 page 5 7 8 P6VMIN C66 PSA 100nF 25V LP2980 5V PNEUMATI CS V eN 5 e o P5D PBAT U7 vou 3 ON OFF Pump Connector PSD WA mn Sg c37 J7 2 203 220U0 D9 16v PBAT BAS16 me SUMP V y C65 TP37 TP38 PSD e UP hd Xo Us PBACK IN PBACK OUT EE pn e P5D XFPM 050 DUMP d n V C28 i EM R36 R51 PTI T 33U0 5V1 vour 2 A 5 140 25V Mot oo
35. ARD SWITCH LOCATIONS PBAT F ALARM Op CYCLE e Ld e cr cn co Lg 407 otr HO 100NF 100NF C 100NF 47U0 ne mo lt I PRINT 50V 50V 50V 16V e e e MENU T O ON OFF VIN BANS DG 0 12 e DG3 NW 037 DG4 PDG_L 0 1 la 1 hd GREEN CHARGING R126 e q 065 10K0 R135 Ny o Ik io Y aPTD3216QYC GREEN Ny uoo V Y aPTD3216SYCK LEDs m swo V YELLOW APTD32160YC Y aPTb32t6Qvc SW_PWR A A B m BATT GREEN GREEN S Ad LOW tow BATTERY ON OFF Y aPrD3216QYC E RIGHT GREEN B Ty cs NW Eoo NW 055 LEDST LEDS AP3216SURC NN LED69 x xy NS LED68 CHARGING RED V asser F APTD32165YCK F APSD16SURC VW serpatsove YL APTD32160YC F aPTb32t6Qvc degF degC Eon YELLOW GREEN GREEN GREEN V NSW 1055 Y aPTD3216QYC GREEN R18 R75 Sw MuX 3883 R133 E R134 RIG RA 38R3 38R3 DOR DR oon P swo V s15 a S EE S15 C A B PDG LO J T HISTORY V a SW1 BAT54C A B PDG L1 ALARM y E DG12 SW2 A B x LEDS3 Ny e082 NS A LED46 LED44 LED42 D6 SILENCE PDG L2 AS v LED67 AP3216SURC Y AP3216SURC Y AP3216SURC L AP3216SURC AP3216SURC Y AP3216SURC RC APS218SURC RED RED RED RED RED RED RED PULSE PULSE Sp02 502 DIA HIGH LOW HGH Low d R125 40KQ NN LED38 xy LED
36. AT NS LEDS LEDAT LED45 LED43 BAT54C swa 1 Y APS2I6SURC L AP3216SURC Y AP3216SURC Y AP3D168URC AP3216SURC Y AP32168URC n x PDG La R64 RED RED RED RED RED RED CYCLE IRI SW4 R79 R63 R38 R19 R17 R15 A B 22R 22R 22R 22R 22R 22R D5 MENU POG 14 S7 S6 S5 ERI ES E a g e ta SW5 BAT54C A GE B INFLATE PDG L5 DGO e SW6 e o n DG2 D4 1 MINUS PDG 18 e e ee e Q LED2 SEN APIS REO YO xy LED64 LED7 LED22 xy be LED26 LED25 IN Aon BAT54C m n vo GREEN ALVOL APTD3216QYC Y PTD3216QYC APTD3216QYC GREEN L APTD3216QYC APTD32160YC L APTD3216QYC RIGHT MIDDLE LEFT GREEN PULVOL GREEN GREEN GREEN GREEN GREEN o AB PDG L7 MIDDLE PUL VOL AUTO AUTO is RIGHT unos RIGHT LEFT PLUS LEDS Ny eos LED59 x C LED7O NSW ee APTD3216QYC Y aPTD3216QYC APTD3216QYC ys LED2O LEDS aevo NW APTDSHGON Y aPTD3216QYC LEDS1 LEDI2 ey iai sw8 GREEN GREEN GREEN APTD32160YC Y aPTD3216QYC APTD32160YC GREEN L APTD3216QYC YL aPTD3216QYC AN GREEN GREEN GREEN GREEN GREEN GREEN aeTb32160YC A 8 GREEN PDG L8 p PRINT 9 R70 R72 R22 WA a Res Re R82 22R 22R 22R J 22R 22R 22R pi pua D 22R BATS4C CIA m 35 a E P PER S14 a S m0 PROCARE USER INTERFACE BOARD Schematic User Interface Board P N 2008741 Rev B 2 of 2 page 5 27 28 CE GE Medical Systems 0086 Information Technologies 2009381 001 B gemedical com World Headquarters GE Medical Systems Information Technologies Inc 8200 West Tower Avenue Milwaukee WI 53223 USA
37. D ORO 2K0 T 33U0 3 Ri80 1 067 YA T 100NF 25V y 3 1K00 680P 25V D10 D27 V BAS16 A BAS16 V V kd Spare Parts DUMP ON MON Y14 PSA P5A ET Be B R9 C60 Q7 U14 10K0 SI2306DS e AcT y 100nF 25V DUMP ON m V i U14 y FPT hora R10 MOT MR 10K0 4 DUMP2_ON MON R203 i Bt Ufa 100K Hero o V 017 R6 DUMP2_ON U14 10NO 10K0 R83 hcr o 649K R204 SR205 SR173 R121 C64 100K 100K 2100K 100K V ONO V HA ET C61 PNEU OVERRIDE 0 4K99 400nF 25V P6VMIN voc 14 R28 a 1 ADC PWM C58 o lt ficrod S 4K99 oT 14 V S 100nF 25V L C43 1 SI9410DY 7 nl A70N PUMP_ON S y mt HA LP2980 5V V V e vin U6 Vou e e g 3 ON OFF C36 GND 2U2 Q8 SI9410DY gt 2 ABN FAST_OVP 0 A A m y R44 Aa V V C63 E 2 3 1K00 L C59 100nF 25V R5 R99 R100 R75 Ik Po XFPM 050 V 40K0 10K0 10K0 OR10 PT2 we 18 PT2 O VOUT e T 1 c57 V V n R181 C21 wr PUMP K00 680P lt lt V V d SCHEMATIC Schematic be Main Board PWA MAIN BOARD PROCARE P N 2008855 Rev B 3 of 10 page 5 9 10 BATTERY CHARGER DC Input Power J3 V_IN PBAT m e pal La S im e e 2 VIN aa p e Z e LL Lc1o4 245 900NH_0A7
38. GE Medical Systems Information Technologies We bring good things to life DINAMAP ProCare Monitor Service Manual Stolig ALARM ve PULSE yo E IN ME PL LATE Press Hse Rat E Ang Ry Low CHARGING Pera ME n nmm DINAMAP ProCare Monitor Service Manual This manual is for DINAMAP ProCare Monitors models 100 200 300 and 400 with or without printers ProCare 100 BP Pulse ProCare 200 BP Pulse and Temp e ProCare 300 BP Pulse and SpO5 e ProCare 400 BP Pulse Temp and SpO The model of the Monitor determines which parameters are in your monitor Please refer to applicable sections Reissues and Updates Changes occurring between issues are addressed through Change Information Sheets Addendums and replacement pages If a Change Information Sheet does not accompany this manual it is correct as printed Errors and Omissions If errors or omissions are found in this manual please notify GE Medical Systems nformation Technologies Technical Publications 4502 Woodland Corporate Boulevard Tampa FL 33614 1 877 274 8456 Part No 2009381 001 B The content of this document including all figures and drawings is proprietary information of GE Medical Systems nformation Technologies provided solely for purposes of operation maintenance or repair and dissemination for other purposes or copying thereof is prohibited without prior written consent by GE Medical Systems nformatio
39. M PITCH 3 PD3 D FROM TEMP 59 vp pn 2 gt D TO TEMP P5D 70 pnn pps 29 gt REM ALARM 0 I 82 VODA poe 22 TEMP PROBE IN VSSA por 2 DUMP2_ON_MON e C49 51 VDDF aL 0 VSSF R107 L C12 F ww 85 VDDSYN pes FSP_TO_PRI 10NO 2w PSD P3V3 P3V3 ii VSSSYN PE6 o TP30 1K00 44 VSTBY PE7 PT HU 454595 te en c3 fo low REC EE Am R98 D US HS 1 Er L T 100NF Mu a q00NF 10U0 FENO RR _P5A 10NO 2w 10U07110N0 pes R95 12 Jat 54 Jeo Jo 10K0 pe 1K00 PE7 needs to be high at start up V V V c2 LC5 tou Tr V V v SCHEMATIC P N 2008855 Rev B PWA MAIN BOARD PROCARE 1 of 10 page 5 5 6 3 3V SECONDARY POWER PBAT RESET T T 1 P3V3SEC VIN C141 3 U22 5 ea U27 JP NIOFFL ipoggs VOUTP e 100nF 25V de zii Y Q14 C106 YPASS C105 REAL TIME CLOCK 2 DTC143ZKA 2U2 10U0 Z SL 9 oscour2 anii e m ONO 1 R137 100nF 25 ar015 10 13 10K0 i NA as V V SE P3V3 OSCIN Q7 gt R141 d ops C56 T 8 de ae 25V 100nF is SECONDARY PROCESSOR eS 7 d deo Tan i Le y p xs 3 PCF8563T 1K00 32 768KHZ 1 osci CLKOUTH EEE OSCO sci 6 e RTC CLK E gt V ART gg SD
40. N 001 Language Model Is Printer Installed Method of NIBP Determination Auscultatory is labeled on left keypad 2010595 001 Chinese 200 2010596 001 Chinese 100 2010597 001 Japanese 400 Printer Installed 2010598 001 Japanese 300 Printer Installed 2010599 001 Japanese 200 Printer Installed 2010600 001 Japanese 100 Printer Installed 2010601 001 Japanese 400 2010602 001 Japanese 300 2010603 001 Japanese 200 2010604 001 Japanese 100 2010605 001 Danish 400 Printer Installed 2010606 001 Danish 300 Printer Installed 2010607 001 Danish 200 Printer Installed 2010608 001 Danish 100 Printer Installed 2010609 001 Danish 400 2010610 001 Danish 300 2010611 001 Danish 200 2010612 001 Danish 100 2010613 001 Norwegian 400 Printer Installed 2010614 001 Norwegian 300 Printer Installed 2010615 001 Norwegian 200 Printer Installed 2010616 001 Norwegian 100 Printer Installed 2010617 001 Norwegian 400 2010618 001 Norwegian 300 2010619 001 Norwegian 200 2010620 001 Norwegian 100 2010621 001 Korean 400 Printer Installed 2010622 001 Korean 300 Printer Installed 2010623 001 Korean 200 Printer Installed 4 32 ProCare Patient Monitor Service Manual 2009381 001 Revision B Calibration amp Maintenance Appendix D Replacement Parts and Assemblies P N 001 Language Model Is Printer Installed Method of NIBP Determination Auscultat
41. P button Verify an NIBP determination has been initiated Block pump port and verify E80 alarm Press SILENCE button verify alarm has been silenced Verify flashing red indicator of Silence Press the SILENCE button verify alarm condition is removed Press ALARM button several times verify unit cycles through all alarm settings i e SYS DIA SPO2 10 Turn the Monitor off 4 14 ProCare Patient Monitor Service Manual Revision B 2009381 001 Calibration amp Maintenance 4 6 ProCare Patient Monitor Parameter Tests 4 6 7 LED Tests 1 Power on the ProCare Monitor 2 During the power up self test verify all 7 segment LED display segments and all discrete LEDs except CHARGING LEDs illuminate and are the correct color LED COLOR MATRIX RED YELLOW GREEN NOT LIT Systolic Pulse Rate AUTO CYCLE CHARGING Diastolic LOW HISTORY F BATTERY C BATTERY ICON HIGH all ALARM VOLUME LOW all PULSE VOLUME Alarm Bell Icon INFLATE PRESSURE SpO Strength Meter 3 Repeat power up cycle until all LEDs are checked 4 6 8 External DC Verification 1 Plug the DC power cable into the monitor 2 Verify that the CHARGING indicator is illuminated 4 6 9 NIBP Determination 1 Set NIBP Analyzer to Adult Mode SYS DIA 120 80 MAP 90 BPM 80 2 Press START STOP button on the Monitor to begin determination 3 Record and verify systolic diastolic map a
42. P determination 8 Temperature probe holster Temperature probe is stored here 9 Cycle button Press to start Auto Cycle or STAT mode 10 Temperature probe cover storage Box of probe covers is stored here 11 History button Press to activate the history mode When activated it displays the most recent entries stored Press and hold the button for 2 seconds to clear all entries stored 12 Print button Press to print currently displayed values or all stored entries when in history mode 13 On Off button Controls on off state of monitor push for power on and push again for power off 14 Temperature probe connector Temperature probe cable attaches here C M Revision B ProCare Partient Monitor Service Manual 2 5 2009381 001 Product Description 2 3 Controls Indicators and Connectors 15 24 16 17 25 18 26 3 i Front Panel 15 Silence icon when Silence button is pressed after alarm sounds silence active silence icon bell lights to indicate that audible alarms have been silenced for 2 minutes 16 Systolic window 3 digit red LED indicates measured systolic Blood Pressure in mmHg 17 Diastolic window 3 digit red LED indicates measured diastolic Blood Pressure in mmHg 18 Alarm volume indicator lights to indicate you are making a change to the alarm volume 19 Pulse volume illuminates to indicate you are making a change to the pulse volume 20 I
43. S SAS 31 Ld S sud 620 R101 7 G S6 200 R108 2 VIN ue SAG jo SAG LEN SAG LEN 620 3 La S 200 cm S cm S Kr n 10 10 10 Dco 2 BAT El oP or pp V 4 4 4 Det 5 SPI CLK P5D Ut COM COM COM mm Hcr2 T 12 com 12 com 12 com DG2 138 ENE Hcr 2D 7 A A TT com 17 com 17 com SW PWR Le R131 TL so 14 SA0 3 ar mm CS DISPLAY PO A Gl Tl a 8 8 5 psp psp HR B S st 3 330 SAI um EET V so y 2 i C 3 GND V 3 5 330 SA3 ES s DCN LEDS curxiop RED wm ss DES m DIASTOLIC LED17 LED18 LED19 8 J S6 330 SAG DMR20A 1 RED DMR20A RED DMR20A RED eel V 330 LTC4624JD SAO 2 A SAO 2 A SAO 2 A SA1 15 B SA1 15 B E SA1 15 B PSD SA2 13 6 SA2 13 6 SA2 13 6 needs pull up on main board SA3 4 Di SA3 1 Di SA3 11 Di 31 31 2 31 100NF Fam 5 le Shei V SM 7 E2 SA4 7 E2 SA4 7 E2 R56 T SA5 31 SAS EM La B SAS 3 100R PSD vee zi 1 PS0 SAG 14 6 SA6 14 G SAG 14 G u 13 PS1 lop 0 pp _10 pp DSO 101 F 4 4 e Hia KRE PS2 COM COM COM 8 oo 103 E PS3 121 com 121 com 121 com LL2L3 2 Horas PS4 TI com 17 com 17 com bug e OFT ug B 5 sel Sl 15 PS5 8 8 8 0 E 105 ss 106 Bs o7 H AUTO TIME 17 Ver m LED30 TEME E CLR DS7 LTC2623JD RED GND P5 LTC4627 D RED 0 se R36 R29 330 z E V S10 330 R35 R30 T U U PED sii C5 s12 39 31 S13 ARP L 100NF EN 330 a YA s15 R32 3 cm vec 7 PS8 E B P5D 100 330 por Fic 4 13 PS9 DSO 101 pcs 14 ay 102 5 PS10 aes 8 14 PS11 TAL vero Detd
44. T 400nF 25V T ol 25V U8 Vv SV FUSED 4 wa 4 E GND 5 L ICL3221 C81 REMOTE ALARM 6 j C82 kanas 100nF 25V RS 232 TX 7 a 6 C2 RS 232 RX 8 P 14 TUN gt S External DB15 onnector Mappin fear lt Conne pping J6 NAME DB15 LEN 1 INVALID 2 AD 1 GND 1 P5D u 2 TTL TX 2 V 3 TTL RX 3 Q13 AN V eig 4 5V FUSED 4 DTA143XKA 7 5 GND 7 T od 6 REMOTE ALARM 8 10K0 T RS 232 TX 11 Q6 e 8 RS 232_RX 13 V NDT3055L D2 L a SM6T15CA wle Schematic Main Board PWA MAIN BOARD PROCARE P N 2008855 Rev B 7 of 10 page 5 17 18 T TDI i T TDO TCLK r RESET TEST 0 T TMS 1 TDE 1 T TRST 1 Test Connector P3V3 e 6 e r e L C92 R22 SRI9 lt R18 lt RI7 Tr 10K0 10K0 lt 10K0 10KO s P3V3 P5D PBAT Display Connector o 1 as 2 Be R125 i 10K0 e 5 e EE ed J5 2 e e Dn SW_MUX lt gt e 3 m Lem i e Zn CS_DISPLAY Dn SW PWR 0 3 e 4 SPI MOSI e m SPI CLK e A mm ke VIN 1 R133 R134 R135 CHARGING LED ol Sm 1K00 499 499 499 V V R127 R126 100K 100K V ISOLATED POWER SUPPLY x Y P5TEMP 112 D19 MIC39101 5V e DOON 2 p Ho e
45. Tel 1 414 355 5000 1 800 558 5120 US only Fax 1414 355 3790 European Representative GE Medical Systems Information Technologies GmbH Munzinger Stra e 3 5 D 79111 Freiburg Germany Tel 49 761 45 43 0 Fax 49 761 45 43 233 Asia Headquarters GE Medical Systems Information Technologies Asia GE China Co Ltd 24th Floor Shanghai MAXDO Center 8 Xing Yi Road Hong Qiao Development Zone Shanghai 200336 P R China Tel 86 21 5257 4650 Fax 86 21 5208 2008
46. Width 9 8 in 24 8 cm Depth 6 9 in 17 5 cm Weight including battery 7 8 lb 3 5 Kg Mountings Self Supporting on rubber feet Portability Carried by built in handle 2 12 ProCare Partient Monitor Service Manual Revision B 200938 1 001 Product Description 2 6 Specifications Mechanical Classification Information Mode of Operation Continuous degree of Protection against harmful ingress of water Drip Proof IPX1 NIBP CUFF PRESSURE RANGE Adult 0 mmHg to 290 mmHg Neonate 0 mmHg to 145 mmHg DEFAULT TARGET Adult 150 15 mmHg CUFF INFLATION Neonate 110 x 15 mmHg TARGET CUFF INFLATION Adult 100 250 mmHg 5mmHg Steps ADJUSTMENT RANGE Neonate 100 140 mmHg 5 mmHg Steps BLOOD PRESSURE Adult 120 seconds maximum DETERMINATION TIME Neonate 85 seconds maximum PULSE RATE RANGE Adult 30 200 BPM 3 Neonate 30 220 BPM 3 BLOOD PRESSURE Systolic MAP Diastolic MEASUREMENT RANGES mmHg mmHg mmHg Adult 30 290 20 260 10 220 Neonate 30 140 20 125 10 110 NIBP ACCURACY Meets AAMI ANSI standard SP 10 AAMI ANSI standard 5 mmHg mean error Intra arterial method 8 mmHg standard dev Temperature Alaris Thermometry SCALES Fahrenheit Celsius RANGE Max 42 2 Celsius 108 0 Fahrenheit Min 31 6 Celsius 88 9 Fahrenheit Monitor Mode Accuracy 20 17 C 0 2 F when tested in a calibrated liquid bath meets ASTM E1
47. acid storage battery When external DC power becomes available the system rapidly switches from battery power to external power 1 8 ProCare Patient Monitor Service Manual Revision B 2009381 001 2 Product Description Pro Care Pa Service Manual rtient Monitor Se 2009381 001 For your notes 2 2 ProCare Partient Monitor Service Manual Revision B 2009381 001 Product Description 2 1 Introduction 2 1 Introduction DINAMAP ProCare Monitors provide non invasive determination of systolic blood pressure diastolic blood pressure mean arterial pressure pulse rate temperature and oxygen saturation 2 2 Product Configurations Each ProCare Monitor is supplied with an accessory pack The contents of the pack vary according to model Unpack the items carefully and check them against the checklists enclosed within the accessory boxes If an accessory is missing or if an item is in a nonworking condition contact General Electric Medical Systems Information Technologies Customer Service immediately It is recommended that all the packaging be retained in case the ProCare Monitor must be returned for service in the future Revision B ProCare Partient Monitor Service Manual 2 3 2009381 001 Product Description 2 3 Controls Indicators and Connectors 2 3 Controls Indicators and Connectors Descriptions of the items shown are listed on the pages that follow For symbol definitions refer to page 2 8 o
48. alibration amp Maintenance 4 7 Alarm Code Interpretation E23 SpOz Sensor off finger No SpO signal check or reposition the sensor E25 SpOs No Signal No or very low SpO signal reposition sensor Temperature Printer Miscellaneous Alarm Definition Possible Cause E63 Temp Disconnected or Incorrect type of temperature probe use Wrong Probe Type TurboTemp type temperature probe E61 Temp Probe Broken Bad temperature probe Temp probe not properly connected E66 Temp probe Too Hot Bad temperature probe Verify monitor with known good accessories E10 Printer No Paper Printer is out of paper Printer door open Printer may be defective E11 Printer Too Hot E12 Recorder cannot print Main battery voltage is too low to operate E00 Memory Lost Refer Monitor to Customer Service 900 999 Internal Memory Errors Refer Monitor to Customer Service 4 20 ProCare Patient Monitor Service Manual Revision B 2009381 001 Calibration amp Maintenance Appendix A Test Results Form Appendix A Test Results Form Step Description Min Max Actual Pass Fail N A 4 6 2 Leakage Leakage Result mmHg 0 6 4 6 3 Pressure Transducer Verification Pressure reading at 200mmHg top display Systolic 197 203 Pressure reading at 200mmHg bottom display
49. ance 4 3 Periodic Maintenance 4 3 1 As Required Perform the following maintenance procedures as required 4 3 1 1 Integrity of Hoses and Cuffs When the pneumatic integrity of any NIBP cuff and hose is in doubt replace the cuff and hose and discard the questionable accessories 4 3 1 2 Cleaning of Monitor CAUTION Do not clean Monitor with isopropyl alcohol or other solvents Wipe the exterior of the Monitor with a cloth slightly dampened with mild detergent or normal hospital bactericides Use dishwashing detergents such as IVORY and JOY registered trademarks of Procter amp Gamble Corp or PALMOLIVE registered trademark of Colgate Palmolive Corp Do not immerse unit 4 3 1 3 Cleaning of Accessories Clean the adult cuffs supplied for use with the monitor by hand washing in warm soapy water However take care to avoid entry of water into the cuff and hoses at any time If water enters the cuff dry the cuff by passing air through it The neonatal cuffs are for single patient use discard if they become soiled Clean cuffs and hoses with a cloth slightly dampened with mild detergent Do not immerse hoses Do not immerse cuffs without prior application of cuff hose caps Clean SpO2 sensor surface before and after each patient use Clean SpO2 sensor with a cloth slightly dampened with a mild detergent Wipe SpO2 sensor to ensure all detergent residue has been removed Compatible cleaning and disinfecting solutio
50. are routed to the SpO PWA Nellcor or Masimo The analog signals are analyzed on the SpO PWA The results are digitized and sent to the Main Board via opto couplers The couplers provide patient isolation as well as serial data interface The Main Board temporarily stores the data and routes it to the UI Board for display and or printer A reset signal to the SpO PWA is also provided so that the power up sequencing is corrected If the SpO circuit quits communicating to the Main Board the Main Board will attempt to reset the SpO2 PWA 3 2 2 Cuff Blood Pressure BP and Pulse When the cuff and hose are attached to the ProCare Monitor and a Non Invasive Blood Pressure NIBP determination is initiated the pump inflates the cuff Pressure transducers PT1 and PT2 monitor pressure information The pneumatic manifold has one valve which is used to deflate the cuff Valve control is through the Main Board Once determinations are made for the systolic BP and diastolic BP the Main Board calculates the pulse rate Mean Arterial Pressure MAP The results are then displayed on the UI Board and sent to the printer if specified The Pneumatic Valve Manifold PVM device is controlled by the secondary processor The secondary processor monitors pressure information from PT2 If an over inflation condition occurs the OVERPRESSURE signal is routed to the PVM to release the air pressure The Main Board also generates an alarm condition with the sp
51. ate and the Clock 4 4 4 2 3 Parameter Level Functional Testing 4 5 4 3 Periodic Maintenance 0 ccc cece eee eee II 4 6 43 1 As Requited ore stars abate deese Oe b S BOtesg iod bed 4 6 4 3 2 Annual Procedures 4 7 4 4 Care of the Storage Battery ooo eenen e 4 8 44 1 Battery Charging aaneen e e nen 4 8 4 5 Safety Testing venen eene eneen nn 4 9 Notes on Electrical Safety Testing of the ProCare Monitor 4 9 4 5 1 Temp Circuit Leakage Test o 4 10 4 5 2 SpO2 Circuit Leakage Test 4 10 4 6 ProCare Patient Monitor Parameter Tests 4 11 4o SETUP Arin rai en eot pne e in dia 4 14 4 6 2 Leakage Testing ennen mI 4 12 4 6 3 Pressure Transducer Verification 4 12 4 6 4 Pressure Transducer Calibration 4 13 4 6 5 Overpressure Verification 4 14 4 6 6 Button Tasting iceri eneen 4 14 ANG T LED TOS ias ER RA a 4 15 4 6 8 External DC Verification 4 15 4 6 9 NIBP Determination 4 15 4 6 10 NIBP Overpressure Verification 4 16 ProCare Patient Monitor Service Manual Revision B 2009381 001 Table of Contents 4
52. ber 6 is displayed in the min window Note the number of remaining changes to the flash memory available are displayed in the MAP Cuff window Following each true calibration the Monitor decrements by 1 the number of remaining calibrations available If the MAP Cuff window is displaying a figure of less than 10 and the accuracy of the Monitor is in doubt contact General Electric Medical Systems Information Technologies Technical Support at 1 877 274 8456 b Press and hold the MENU button until two beeps are heard one when Revision B ProCare Patient Monitor Service Manual 4 13 2009381 001 Calibration amp Maintenance 4 6 ProCare Patient Monitor Parameter Tests the button is pressed and another after the button has been depressed long enough for the process to complete 9 Turn the ProCare Monitor off 4 6 5 Overpressure Verification Note To enter service mode press and hold the CYCLE button while pressing the ON OFF button 1 2 4 6 6 Button Testing 8 9 Remain in service mode Use the inflation bulb to inflate pressure until valve opens Record and verify pressure at which valve opens Press CYCLE button so that the min window changes to a 2 Use the inflation bulb to inflate pressure until valve opens Record and verify pressure at which valve opens Turn unit off Turn the Monitor on Record software revision as shown in the systolic and diastolic display Press START STO
53. cations made to the Monitor s settings configuration must be saved prior to placing the Monitor into service The Monitor must be in service mode for any changes to be saved Events that require you to manually save to the Monitor s memory include calibration attempts and enabling disabling the Monitor s parameters refer to section 4 6 4 It is not necessary to manually save following a pressure transducer calibration verification or simple calibration check The number of times the flash memory can be saved is limited The fatal alarm error 975 may be issued after this process is performed more than 90 times Following issuance of this fatal alarm the monitor must be returned to the GE Medical Systems nformation Technologies Service Center to have the flash memory reset so that future saves can be performed 1 Connect your NIBP Analyzer to the ProCare Monitor 2 T an inflation bulb into the pneumatic setup 3 Consult the following diagram for pneumatic setup guidelines Secure the NIBP cuff around a 2 diameter rigid unbreakable object NIST CALIBRATED DIGITAL MANOMETER INFLATION BULB CALIBRATION KIT P N320246 12 AIR HOSE Revision B ProCare Patient Monitor Service Manual 4 11 2009381 001 Calibration amp Maintenance 4 6 ProCare Patient Monitor Parameter Tests 4 6 2 Leakage Testing Note To enter service mode press and hold the CYCLE button while pressing
54. ce relationship The ProCare Monitor contains a number of electrical amp electro mechanical assemblies These assemblies are Main Board PWA User Interface UI Board PWA SPO2 PWA optional Printer optional Pneumatic Valve Manifold PVM Optical Switch optional Revsion B ProCare Partient Monitor Service Manual 3 5 2009381 001 Principles of Operation 3 3 Functional Description 3 3 1 Main Board PWA The ProCare Main Board is based on the Motorola MMC2107 integrated microprocessor The microprocessor integrates Flash ROM RAM A D converter with input multiplexor SPI interface and timers into one chip This microprocessor is the primary processor for the ProCare Monitor It services and controls the Patient Parameter Interface PPI devices printer UI Board Real Time Clock audio circuit and host communication The secondary processor controls the watchdog pneumatic safety interlock timing check primary processor reset and power supply control The secondary processor is powered at all times Independent software in the primary and secondary processor periodically communicate when the software systems are operating properly When either system stops processing or detects an error it stops communicating with the other Either system upon detecting a failure can assert a safe state herein called FAILSAFE of the hardware Upon entering a FAILSAFE condition the Main Board will perform the followi
55. d be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as re orienting or relocating the equipment DO ver the frequency range 150 KHz to 80 MHz field strengths should be less than 3 V m Revision B ProCare Patient Monitor Service Manual 4 51 2009381 001 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ILC 1931 Recommended Separation Distances The table below provides the recommended separation distances in meters between portable and mobile RF communications equipment and the ILC 1931 The ILC 1931 is intended for use in the electromagnetic environment on which radiated RF disturbances are controlled The customer or the user of the ILC 1931 can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the ILC 1931 as recommended below according to the maximum output power of the communications equipment Separation Distance in Meters m According to Frequency of Transmitter Rated m Output 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz Power o RAT in m me 4223 VP 0 01 0 12 0 12 0 23 0 1 0 38 0 38 0 73 1 1 2 1 2 2 3 10 3 8 3 8 7 3 100 12 12 23 At 80 MHz and 800 MHz the separation distance for the higher frequency range applies For transmitters rated at a maximum outpu
56. d separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance Conducted RF 3 Vrms 3V rms EN 61000 4 6 150 KHz to 80 MHz d 1 2 VP Radiated RF 3 V m 3 V m JP EN 61000 4 3 80 MHz to 2 5 GHz d 1 2 80 MHz to 800 MHz d 23VP 800 MHz to 2 5 GHz where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and dis the recommended separation distance in meters m Field strengths from fixed RF transmitters as determined by an electromagnetic site survey should be less than the compliance level in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol al Note 1 At 80 MHz and 800 MHz the higher frequency range applies Note 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by reflection from structures objects and people Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile radio AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the equipment is used exceeds the applicable RF compliance level above the equipment shoul
57. eaker sounding and error code message on the UI Board 3 4 ProCare Patient Monitor Service Manual Revision B 2008381 001 Principles of Operation 3 3 Functional Description 3 2 3 Temperature Model 200 and 400 The ProCare Monitor uses Alaris Turbo Temp technology to measure patient temperature The Turbo Temp probe contains a heating element that pre heats the probe to reduce determination time The heating function is controlled by the Main Board The Turbo Temp probe also contains a thermistor that indicates the temperature When the probe is attached to the temperature connector and patient the signal generated by the thermistor is routed to the Main Board The Main Board converts the thermistor signal along with status information i e ORAL or RECTAL probe indicators to a DIGITAL signal The Main Board then processes the DIGITAL signal and displays the patient temperature on the UI Board and printer in Celsius or Fahrenheit 3 2 4 Host Communication Port The Host Comm Port is used to interface the ProCare Monitor with other electronic devices a central nurse s station or remote alarm device Signals can be sent to the ProCare Monitor to initiate blood pressure determinations and other functions Patient data can also be retrieved through this port For further information reference the Dinamap ProCare Series Host Communication manual 3 3 Functional Description The following paragraphs provide the functional interfa
58. ems can cause EMC issues with this or other equipment This system is designed and tested to comply with applicable regulation regarding EMC and must be installed and put into service according to the EMC information stated in this appendix WARNING Use of portable phones or other radio frequency RF emitting equipment near the system may cause unexpected or adverse operation WARNING The equipment or system should not be used adjacent to or stacked with other equipment If adjacent or stacked use is necessary the equipment or system should be tested to verify normal operation in the configuration in which it is being used Guidance and Manufacturer s Declaration Electromagnetic Emissions The ILC 1926 is intended for use in the electromagnetic environment specified below It is the responsibility of the customer or user to assure that the ILC 1926 is used in such an environment Emissions Test Compliance Electromagnetic Environment Guidance RF Emissions Group 1 The equipment uses RF energy only for its internal function Therefore its RF EN 55011 emissions are very low and are not likely to cause any interference in nearby electronic equipment RF Emissions Class B EN 55011 Harmonic Emissions Not Applicable The equipment is suitable for use in all establishments including domestic EN 61000 3 2 establishments and those directly connected to the public low voltage
59. enu button several times until the year setting appears Use the buttons to increment or decrement the individual settings Once you are finished changing a setting press the Menu button again to move to the next setting Note For the date and time to be saved you must advance the menu through the min setting 4 To exit config mode press the On Off button 4 2 3 Parameter Level Functional Testing After the initial configuration is complete perform functional testing of each of the parameters using the accessories supplied with the ProCare Monitor Refer to the ProCare Operator s Manual for more detailed parameter specific instructions Perform a blood pressure by connecting the supplied hose and cuff together then attaching to the front of the ProCare Monitor Press the Inflate Stop on the front to begin the NIBP cycle Connect the supplied temperature probe to it s corresponding connection A predictive temperature will begin once the probe is removed from its holster Replace the probe after completion of the Temp cycle The SpOs sensor is an assembly consisting of two parts the DS 100A and the extender cable DOC 10 Connect the cables prior to attaching to the monitor An SpO reading will be displayed within moments of attaching the sensor to either a Nellcor simulator or to your finger Revision B ProCare Patient Monitor Service Manual 4 5 2009381 001 Calibration amp Maintenance 4 3 Periodic Mainten
60. er Revsion B ProCare Patient Monitor Service Manual 1 5 2009381 001 Introduction 1 3 Service Policy Contact General Electric Medical Systems Information Technologies at 1 877 274 8456 Monday through Friday 8 00 a m to 6 00 p m EST excluding holidays Packing Instructions Follow these recommended packing instructions m Remove all hoses cables sensors and power cords from the monitor before packing m Pack only the accessories you are requested to return place them in a separate bag and insert the bag and the product inside the shipping carton m Use the original shipping carton and packing materials if available If the original shipping carton is not available m Place the product in a plastic bag and tie or tape the bag to prevent loose particles or materials from entering openings such as hose ports Use a sturdy corrugated container to ship the product Pack with 4 to 6 in of padding on all sides of the product Tape securely to seal the container for shipping Insurance Insurance is at the customer s discretion The shipper must initiate claims for damage to the product incurred during shipping Shipping damage is not covered under warranty 1 3 4 Service Loaners Loaner units can be provided at no charge during the warranty period if your product needs to be returned for factory service If requested loaner units will be shipped within 48 hours to your facility General Electric Medical System
61. f this section 2 3 1 ProCare Monitor Rear Panel Connections 1 Speaker Grille 2 Data interface connector Host communications port 15 pin D type RS 232 serial port for use only with equipment conforming to IEC 601 1 configured to comply with IEC 601 1 3 Printer Door optional 2 4 ProCare Partient Monitor Service Manual Revision B 2009381 001 Product Description 2 3 Controls Indicators and Connectors 2 3 2 Front Panel Controls and Indicators Buttons 1 Silence button Press to mute audible alarms Any alarm active that is acknowledgeable is also removed whenever this key is pressed When pressed after alarm sounds silence active the silence icon bell lights to indicate that audible alarms have been silenced for 2 minutes Alarms button Press to view or adjust parameter alarm settings button Plus Minus Press the button to increment an adjustable setting and the button to decrement an adjustable setting This button is active only when a user setting mode limit or menu is active 4 Menu button Press to access menu settings that can be adjusted while in clinical mode i e ALARM VOLUME PULSE VOLUME INFLATE PRESSURE refer to Operating Modes in this section for a description of clinical mode 5 SpO sensor connector SpO sensor cable attaches here 6 BP connector BP cuff hose attaches here 7 Inflate Stop button Press to start a manual BP determination or stop any B
62. fied below It is the responsibility of the customer or user to assure that the DINAMAP ProCare Monitor is used in such an environment Emissions Test Compliance Electromagnetic Environment Guidance RF Emissions Group 1 The equipment uses RF energy only for its internal function Therefore its RF EN 55011 emissions are very low and are not likely to cause any interference in nearby electronic equipment RF Emissions Class B EN 55011 Harmonic E missions Class A The equipment is suitable for use in all establishments including domestic EN 61000 3 2 establishments and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes Voltage Fluctuations Complies Flicker Emissions EN 61000 3 3 Revision B ProCare Patient Monitor Service Manual 4 39 2009381 001 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ProCare Monitor Guidance and Manufacturer s Declaration Electromagnetic Immunity The DINAMAP ProCare Monitor is intended for use in the electromagnetic environment specified below It is the responsibility of the customer or user to assure that the DINAMAP ProCare Monitor is used in such an environment Immunity Test EN 60601 Test Level Compliance Level Electromagnetic Environment Guidance Electrostatic 6 kV contact 6 kV contact Floors should be wood concrete or ceramic tile
63. figured for use with either a Nellcor or Masimo SPO2 PWA The SPO2 PWA provides continuous readings of oxygen saturation and pulse rate Additional circuitry on the Main Board provides power data communications and isolation between SPO2 PWA and primary processor Patient data received from the finger sensor is filtered amplified and analyzed on the SPO2 PWA The information is sent to the Main Board via the optically coupled electrically isolated serial connection The primary processor receives the data and routes it to the UI board for display The data is also sent to the printer if specified 3 3 4 Printer The printer receives power from the Main Board and communicates with the primary processor Printer presence and print head temperature is indicated by PR TH signal to the primary processor When a print command is sent to the printer from primary processor the following will occur PR CLK signal transfer the data into print head PR Di signal serial dot to be printed PR LAT signal latch the data stream into the head PR ST1 6 cause the head to print various sections PR M1 4 signals control power sequentially to the two stepper motor windings Together these signal CONTROL DATA cause the printer to print a graphic hardcopy of the patient vital sign values and trend data It also causes the printer to print a hardcopy of error logging and service record data The printer has a built in sensor to monitor the
64. ield commercial or hospital environment EN 61000 4 8 NOTE U is the AC mains voltage prior to application of the test level 4 40 ProCare Patient Monitor Service Manual Revision B 2009381 001 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ProCare Monitor Guidance and Manufacturer s Declaration Electromagnetic Immunity The DINAMAP ProCare Monitor is intended for use in the electromagnetic environment specified below It is the responsibility of the customer or user to assure that the DINAMAP ProCare Monitor is used in such an environment Immunity Test EN 60601 TestLevel Compliance Level Electromagnetic Environment Guidance Portable and mobile RF communications equipment should not be used closer to any part of the equipment including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance Conducted RF 3 Vrms 3V rms EN 61000 4 6 150 KHz to 80 MHz d 12 VP Radiated RF 3 V m 3 V m JP EN 61000 4 3 80 MHz to 2 5 GHz dz12 80 MHz to 800 MHz d 23 VP 800 MHz to 2 5 GHz where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and dis the recommended separation distance in meters m Field strengths from fixed RF transmitters as determined by an electromagnetic site survey should be less than the compliance le
65. ing two hands apply firm pressure to the outside edges while flexing the upper middle edge of the display cover away from the monitor It is imperative that even pressure is applied as the plastic retention tabs can break free from the display cover 4 Apply steady even pressure to the opposite sides of the display cover until an audible click is heard Revision B ProCare Patient Monitor Service Manual 4 27 2009381 001 Calibration amp Maintenance Appendix D Replacement Parts and Assemblies Appendix D Replacement Parts and Assemblies ID numbers reference the explode drawings in Section 5 ID FRU Number Description Content comments 1 2009910 001 Main PWA Supplied with Arterial ref product s w 2 200991 1 001 Main PWA Ausc Supplied with Auscultatory version of Monitor 3 2009912 001 UI PWA 4 2009913 001 Nellcor Module Supplied with mounting spacers 5 2009914 001 Masimo Module Supplied with mounting spacers 6 2009915 001 Plastics kit 1 Case front amp rear 2 Handle front amp rear with h w 3 Bulkheads 4 types amp NIBP insert 4 Nellcor amp Masimo inside labels 5 Std labels DC input No temp side label 6 Battery door amp foam 7 Help card guide and rubber feet 8 Printer door and blanking plate when available 9 Cable tie hardware 2009916 001 Screw kit All internal hardware screws washers etc 7 2009918 001 Te
66. l 3 The accuracy specification under motion conditions is 3 For a definition of motion contact GE Medical Services Technical Support T The MAX N and the OxiCliq N were tested on patients gt 40 kg t The accuracy specification has been determined between saturations of 80 100 SpO Masimo Oximetry Saturation Range 1 100 Pulse Rate and Accuracy 25 240 BPM 3 digits Perfusion Range 0 02 to 20 2 14 ProCare Partient Monitor Service Manual Revision B 200938 1 001 Product Description 2 6 Specifications SpO Masimo Oximetry Accuracy and Motion Tolerance Without Motion Adult Ped 70 to 100 x2 digits Without Motion Neonate 70 to 100 3 digits With Motion Adult Ped Neo 70 to 100 3 digits Low Perfusiont 70 to 100 2 digits 0 to 69 unspecified Pulse Rate Without Motion 25 to 240 beats min 3 digits With Motion normal physiologic range 25 to 240 beats min 5 digits The Masimo SET SpO parameter with LNOP Adt sensors has been validated for no motion accuracy in human blood studies on healthy adult volunteers in induced hypoxia studies in the range of 70 100 SpO against a laboratory co oximeter and ECG monitor This variation equals plus or minus one standard deviation Plus or minus one standard deviation encompasses 68 of the population The Masimo SET SpO parameter with LNOP Adt sensors has been validated for motion
67. lic reading mmHg 107 133 Diastolic reading mmHg 67 93 MAP reading mmHg 85 95 Heart rate reading bpm 76 84 Systolic reading mmHg 107 133 Diastolic reading mmHg 67 93 MAP reading mmHg 85 95 Heart rate reading bpm 76 84 4 6 10 NIBP Overpressure E80 displayed on SYSTOLIC display Pump will not start Overpressure alarm can be cleared 4 6 11 Temperature Test 80 0 F 80 4 F Temperature reading at 80 2 F 79 9 F 80 5 F Temperature reading at 102 0 F 101 8 F 102 2 F Temperature reading at BP verify reads E61 N A N A 46 12 SpO gt Pulse Value Displayed Saturation Value Displayed Signal Strength Bar Graph Displayed E23 displayed on SpO display Alarm is silenced error display remains Pulse Value Saturation Value Displayed Signal Strength Bar Graph Displayed 4 6 13 Printer Test Printout is generated cleanly 4 6 14 Communication Port Test _NC 0 is displayed on terminal Pump stops 4 22 ProCare Patient Monitor Service Manual Revision B 2009381 001 Calibration amp Maintenance Appendix B Connectivity Appendix B Connectivity CHANT Provides HL7 output for electronic Patient Medical Records Uses ILCs Isolated Level Convertors where required along with the CHANT software to communicate with the HIS System Compatible Monitors DINAMAP XL Compact MPS Select and Portable PRO 100 400 series ProCare Series and PRO 1000 Nurse Call System When the DINAMAP monitor alarms the
68. lt Adult Large Adult Thigh Cuff 2 10 ProCare Partient Monitor Service Manual Revision B 2009381 001 Product Description 2 5 Compatible Parts Reorder Codes Product Code ECAT DURA CUF Assortment Pack Child 2697 E2697J Includes 2 Infant 3 Child and 1 Small Adult Cuff Additional Blood Pressure Cuffs are available through http www gemedicalsystems com TEMPERATURE IVAC Turbo Temp Oral Temperature Probe Long Cord 2008774 001 IVAC Turbo Temp Rectal Temperature Probe Long Cord 2008775 001 IVAC Temperature Probe Covers 88015 E9050KK Sp0 Nellcor Pulse Oximeter Cable DOC 10 2008773 001 DuraSensor Adult Oxygen Sensor DS100A Masimo Adult Reusable Sensor 1 Bx NR125 2009745 001 Cable PC08 2009743 001 VAC is a trademark of Alaris Medical Systems NELLCOR is a trademark of Mallinckrodt Masimo is a trademark of Masimo Corporation Revision B ProCare Partient Monitor Service Manual 2 11 2009381 001 Product Description 2 6 Specifications 2 6 Specifications LE This product conforms with the essential requirements of the Medical Device Directive Accessories without the CE Mark are not guaranteed to meet the Essential requirements of 0086 the Medical Device Directive The ProCare Monitor is protected against vertically falling drops of water and conforms to IPX1 the IEC 529 standard at level IPX1 Vertically falling d
69. mperature 1 Housing front amp rear 2 Mounting bracket and plastic guide 3 Sensor and cable 4 Mounting hardware 8 2009917 001 Printer 1 Printer 2 Printer chassis and screw 3 Printer door with roller and label 9 2009919 001 Printer door Door with label and roller 10 2009920 001 Pneumatics Pump assembly 11 2009921 001 Dump valve Dump valve and adhesive tape to apply 12 2011645 001 Kit Keypads Set left and right keypads 13 2009922 001 Speaker Include mounting bracket 14 2009923 001 Host comms cable With mounting h w 2008538 001 Power brick UK UK plug 240V input 2008539 001 Power brick EUR Euro plug 230V input 2009460 001 Power brick US US plug 120V input 15 2010429 001 English 400 Ibi kit 1 keypad labels set LH amp RH 2010478 001 English 300 Ibl kit 2 Fascia 2010479 001 English 200 Ibl kit 3 Display cover 2010480 001 English 100 Ibl kit For language variants reference following pages 16 Help card guides All 3 guides and for each language 4 28 ProCare Patient Monitor Service Manual Revision B 2009381 001 Calibration amp Maintenance Appendix D Replacement Parts and Assemblies 2010429 001 Label Kit English 400 printer P N 001 Language Model Is Printer Installed Method of NIBP Determination Auscultatory is labeled on left keypad 2010429 001 English 400 Printer Installed Traditional 2010478 00
70. n Technologies Tampa Florida Illustrations may show design models production units may incorporate changes Hierarchy of Warnings and Cautions A general warning is a statement that alerts the user to the possibility of injury death or other serious adverse reactions associated with the misuse of the device A warning relates to steps in a procedure A general caution is a statement that alerts the user to the possibility of a problem with the device associated with its use or misuse Such problems include device malfunction device failure damage to the device or damage to other property A caution relates to steps in a procedure GE Medical Systems Information Technologies 2002 2004 TAMPA FL All rights reserved Revision B ProCare Patient Monitor Service Manual 2009381 001 World Headquarters GE Medical Systems Information Technologies Inc 8200 West Tower Avenue Milwaukee WI 53223 USA Tel e 1 414 355 5000 1 800 558 5120 US only Fax e 1 414 355 3790 European Representative GE Medical Systems Information Technologies GmbH Munzinger StraBe 3 5 D 79111 Freiburg Germany Tel 49 761 45 43 0 Fax 49 761 45 43 233 Asia Headquarters GE Medical Systems Information Technologies Asia GE China Co Ltd 24th Floor Shanghai MAXDO Center 8 Xing Yi Road Hong Qiao Development Zone Shanghai 200336 P R China Tel 86 21 5257 4650 Fax 86 21 5208 2008 ProCare Patient M
71. nd heart rate from the monitor display 4 Press CYCLE button to initiate a determination in Auto BP mode Revision B ProCare Patient Monitor Service Manual 4 15 2009381 001 Calibration amp Maintenance 4 6 ProCare Patient Monitor Parameter Tests 5 Record and verify systolic diastolic map and heart rate from the monitor display 6 Press CYCLE button until SEBE is displayed on the HISTORY LED to initiate a determination in STAT mode 7 Record and verify systolic diastolic map and heart rate from the monitor display 8 Press Start Stop button end STAT mode 4 6 10 NIBP Overpressure Verification 1 Restrict airflow through cuff hose port 2 Press Inflate Stop to begin NIBP determination 3 Verify that E80 is displayed on the SYSTOLIC display and an audible alarm sounds 4 Remove the air restriction 5 Press Inflate Stop and verify that the pump does not start 6 Press the Silence button 7 Press the Silence button again 8 Verify the alarm condition is cleared from the SYSTOLIC display 4 6 11 Temperature Perform if equipped with Temp module The Temperature Simulator for the Alaris System is available from Alaris Medical Systems Inc 619 458 7000 1 Disconnect the temp probe from the Monitor 2 Connect the probe simulator to the Monitor 4 Set the probe simulator to 80 2 F 5 Record and verify the reading in the TEMP display is 80 2 F 0 2 F 6 Set the probe simulator to 102
72. nded separation distance d in meters m can be estimated using the equitation applicable to the frequency of the transmitter where Pis the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer NOTE These guidelines may not apply in all instances Electromagnetic propagation is affected by absorption and reflection from structures objects and people Revision B ProCare Patient Monitor Service Manual 2009381 001 4 47 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ILC 1926 Compliant Cables and Accessories WARNING The use of accessories transducers and cables other than those specified may result in increased emissions or decreased immunity performance of the equipment or system not included The table below lists cables transducers and other applicable accessories with which GE Medical Systems claims EMC compliance NOTE Any supplied accessories that do not affect EMC compliance are Part No Description Maximum Lengths Accessories N A RJ 45 series Category 5 cable N A 683235 Adapter Cable RJ 45 to DB15 600 mm 2 ft 683236 Adapter Cable RJ 45 to DB25 460 mm 18 in 683242 Adapter Cable RJ 45 to DB9 3 0m 10ft 4 48 ProCare Patient Monitor Service Manual Revision B 2009381 001 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ILC 1931 Elect
73. nflate pressure illuminates to indicate you are making a change to the inflation pressure 21 Pulse Rate window 3 digit yellow LED shows the pulse rate in beats per minute 22 SpO pulse indicator Red LED bar flashes to indicate that real time pulse rate measurements are being derived from SpO signals 23 SpO window 3 digit red LED indicates oxygen saturation in 96 24 MAP Cuff window 3 digit red LED indicates measured MAP in mmHg and shows instantaneous cuff pressure during BP determination 25 Min window Displays the BP mode if manual or STAT is the cycle time when in Auto Cycle mode 26 Battery power indicator Green LED indicates the Monitor is operating on battery power 27 Low battery power indicator Yellow LED indicates LOW charge status of internal battery 28 Charging indicator Green LED indicates presence of external power Source and battery charging 29 Temperature window 4 digit red LED indicates measured temperature ProCare Partient Monitor Service Manual Revision B 2009381 001 Product Description 2 3 Controls Indicators and Connectors Right Side Panel 30 External power socket To be used with approved GE Medical Systems Information Technologies AC DC power converter ONLY Revision B ProCare Partient Monitor Service Manual 2009381 001 2 7 Product Description 2 3 Controls Indicators and Connectors Symbols The following symbols are associated with the ProCare Monitor Note
74. ng tasks Parameter monitoring disabled Alarm tone sounding from speaker Pneumatic FAILSAFE deflate the cuff pump off Normal communications interface disabled Remote alarm control inactive Hard keys except ON OFF key inactive The ON OFF key can reset the Monitor and end the FAILSAFE condition The FAILSAFE condition will terminate automatically after 10 minutes to preserve battery power All regulated DC power isolated and non isolated is generated on the Main Board from Battery supply The external DC input is used to charge the battery via charging circuitry on the Main Board 3 3 2 User Interface UI Board PWA The UI Board is used as a message center It displays patient vital signs alarms status monitor set up limit violation BP cycle and the time the data was received The primary processor on the Main Board controls the UI Board When the primary processor reads the parameter signals it decodes the signals and routes the display information to the UI Board The Ul assembly also provides hardkey switches for the ProCare Main Board The primary processor asserts a HIGH on the 16 outputs of the 1 of 16 decoder demultiplexer one at a time and then reads at the signal on SW MUX ALOW on SW MUX indicates that the switch is asserted 3 6 ProCare Patient Monitor Service Manual Revision B 2008381 001 Principles of Operation 3 3 Functional Description 3 3 3 SPO2 PWA The ProCare monitor can be con
75. ns are Chlorine bleach disinfectant 5 2596 0 75 cup per gallon of water CAUTION Do not apply isopropyl alcohol to the Monitor some parts can become marred and cracked 4 6 ProCare Patient Monitor Service Manual Revision B 2009381 001 Calibration amp Maintenance 4 3 Periodic Maintenance Cidex Formula 7 registered trademark of Johnson amp Johnson Medical Products Inc or pHisoHex registered trademark of Winthrop Breon Laboratories Quaternary based germicidal detergents like VESTAL INSURANCE registered trademark of the Vestal Corp HI TOR PLUS registered trademark of the Huntington Corp or VIREX registered trademark of S C Johnson amp Son Corp For the above follow manufacturers recommendations for dilution rate and use These recommendations are not an endorsement of the manufacturers or of the effectiveness of these materials for cleaning or disinfecting 4 3 1 4 Long Term Storage If it becomes necessary to store the Monitor for an extended period of time remove all attached accessories Attach the original packing inserts and place the monitor into the original shipping container Long term storage of a discharged lead acid battery can permanently degrade its storage capacity Therefore the battery should be fully charged before storage Batteries in storage should be charged every six months to maintain their capacity Elevated temperatures will shorten battery life and can lead to pe
76. ntacting Customer Support it is helpful to attempt to duplicate the problem and to check all accessories to ensure that they are not the cause of the problem If you are unable to resolve the problem after checking these items contact General Electric Medical Systems Information Technologies at 1 877 274 8456 Prior to calling please be prepared to provide m product name and model number m a complete description of the problem If repair parts or service are necessary you will also be asked to provide the product serial number the facility s complete name and address a purchase order number if the product is in need of non warranty repair or to order spare parts m the facility s General Electric Medical Systems Information Technologies account number m the appropriate part number for spare or replacement parts 1 3 3 Return to Factory Repair Service If your product requires warranty extended warranty or non warranty repair service call Customer Support and a representative will assist you Estimates for non warranty repairs are provided pre set flat rates to facilitate prompt service In cases where the product has external chassis or case damage please advise the Customer Support representative when you call The Customer Support representative will record all necessary information and will provide you with a Return Merchandise Authorization Number RMA Prior to returning any product for repair you must have a RMA numb
77. of the tester should be connected to the patient connection being tested WARNING Don t electrocute yourself or anyone else when performing Hi Pot testing NOTE Hi Pot testing is done on every unit at the factory and should not be repeated unnecessarily nor performed more often than required 4 5 1 Temp Circuit Leakage Test 1 Setup an IEC 601 1 approved leakage tester to apply 240 VAC to an isolated circuit 2 Plug temp probe Hi Pot adapter into the temp jack 3 Record and verify the temp circuit leakage current 4 5 2 SpO Circuit Leakage Test 1 Setup an IEC 601 1 approved leakage tester to apply 240 VAC to an isolated circuit 2 Plug an SpO cable into the SpO connector on the front of the unit 3 Plug SpO probe Hi Pot adapter in to the DB9 jack at the end of the SpO cable 4 Record and verify the SpO circuit leakage current 4 10 ProCare Patient Monitor Service Manual Revision B 2009381 001 Calibration amp Maintenance 4 6 ProCare Patient Monitor Parameter Tests 4 6 ProCare Patient Monitor Parameter Tests 4 6 1 SETUP Complete the Test Record Appendix A as tests are performed Note This test is written so that a technician who is familiar with the ProCare monitor and the test equipment will be able to successfully complete the test procedures To enter service mode press and hold the CYCLE button while pressing the ON OFF button for 3 seconds Saving Changes into Flash Memory Modifi
78. ommends BIO TEK SpO simulators 1 Connect the appropriate SpO simulator and cable to the SpO connector 2 Verify the unit displays a Pulse value Saturation value Signal Strength Bar Graph 3 Disconnect the SpO cable 4 Verify the unit generates a E23 alarm and speaker is sounding 5 Press the SILENCE button 6 Verify the sound has stopped but the error display remains 7 Re connect the SpO sensor 8 Verify the unit displays a Pulse Value Saturation value Signal Strength bar Graph Revision B ProCare Patient Monitor Service Manual 4 17 2009381 001 Calibration amp Maintenance 4 6 ProCare Patient Monitor Parameter Tests 4 6 13 Printer Output Test 1 Load Thermal Paper into the print mechanism 2 Press PRINT button 3 Verify the printer outputs a record and print quality is good 4 6 14 Communication Port Test Connect unit to a PC terminal emulator 2 Turn unit on Co Type NCO E press Enter 4 Verify response from unit NC al Verify that within 40 seconds the pump starts O Type ND 5 press Enter N Verify response from unit ND A 00 Verify the pump stops 4 18 ProCare Patient Monitor Service Manual Revision B 2009381 001 Calibration amp Maintenance 4 7 Alarm Code Interpretation 4 7 Alarm Code Interpretation 4 7 1 System Failures If any other alarms appear that are not listed in the paragraphs that follow record the
79. on If abnormal performance is observed additional measures may be necessary such as re orienting or relocating the equipment DO ver the frequency range 150 KHz to 80 MHz field strengths should be less than 3 V m 4 46 ProCare Patient Monitor Service Manual Revision B 2009381 001 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ILC 1926 Recommended Separation Distances The table below provides the recommended separation distances in meters between portable and mobile RF communications equipment and the ILC 1926 The ILC 1926 is intended for use in the electromagnetic environment on which radiated RF disturbances are controlled The customer or the user of the ILC 1926 can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the ILC 1926 as recommended below according to the maximum output power of the communications equipment Separation Distance in Meters m According to Frequency of Transmitter Rated m Output 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz Power o RAT in m me 4223 VP 0 01 0 12 0 12 0 23 0 1 0 38 0 38 0 73 1 1 2 1 2 2 3 10 3 8 3 8 7 3 100 12 12 23 At 80 MHz and 800 MHz the separation distance for the higher frequency range applies For transmitters rated at a maximum output power not listed above the recomme
80. on of an electromedical system and thus must comply with the requirements of EN 60601 1 1 IEC 601 1 All host port signals are NON ISOLATED and should be connected to equipment conforming to IEC 601 1 configured to comply with IEC 601 1 1 ONLY Where isolation of data communication is required GE Medical Systems Information Technologies part number ILC1926 should be used If external alarm control is required GE Medical Systems Information Technologies part number 487208 Isolated Remote Alarm Cable Assembly should ALWAYS be used When a high priority condition is displayed on the Monitor the remote alarm signal becomes active within 0 5 seconds The active state of the alarm signal is an open circuit In the inactive state the alarm signal is connected to ground Please refer to the Information Sheet included with the isolated remote alarm cable for operational details Note When using remote alarm the ProCare Monitor should be considered the primary alarm source The secondary alarm is used for secondary purposes only Pin Function 1 Common 2 Inverted TTL Transmit Data 3 Inverted TTL Receive Data 4 5 volts 5 No connection 6 No connection 7 Common 8 Remote Alarm 9 No connection 10 No connection 11 RS232 Transmit Data TxD 12 No connection 13 RS232 Receive Data RxD 14 No connection 15 No connection Revision B ProCare Partient Monitor Service Manual 2 9 2009381 001 Product Description 2 5 Compatible Parts
81. onitor Service Manual 2009381 001 Revision B DINAMAP ProCare Monitor Service Manual 2009381 001 Revision B GE Medical Systems Information Technologies gemedical com NOTE The information in this manual only applies to ProCare Monitor It does not apply to earlier Monitors Due to continuing product innovation specifications in this manual are subject to change without notice GE Medical Systems Information Technologies 2002 2004 All rights reserved T 2 ProCare Monitor Revision B 2009381 001 Table of Contents 1 Introduction eus ore neve MEO pore x 1 1 1 1 Scope of Manual aaneen nnn 1 3 1 2 Manual Changes senden ene nn 14 1 3 Service Poligy oren eer eren Re n e KR Rr RER eee ee 1 5 1 3 1 Service Contracts oee 1 5 e ned et d aha Al Att 1 5 1 3 3 Return to Factory Repair Service 1 5 1 34 Service Loaners ennen 1 6 1 3 5 Repalt ParlS cias ao 1 6 1 3 6 Replacement Accessories 1 7 1 4 Product Description oee 1 8 1 4 1 General Description 1 8 2 Product Description 2 1 2 41Introduction vereri EE veeteelt el ee 2 3 2 2 Product Configurations ss xx x x x K x K K K eneen een 2 3 2 3 Controls Indicators and Connectors ansanaamanasa 2 4 2 3 1 ProCare Monitor Rear Panel Connections nananana 2 4 2 3 2 F
82. or 25 cycles lt 5 U 29596 dip in Up for 5 s lt 5 U 295 dip in Uy for 0 5 cycles lt 40 Ux 260 dip in U for 5 cycles lt 70 U 230 dip in U for 25 cycles lt 5 U 295 dip in Uy for 5 s Mains power should be that of a typical commercial or hospital environment If the user of the ILC 1931 requires continued operation during power mains interruptions itis recommended that the Host monitor be powered from an uninterruptible power supply or a battery Power Frequency 3 A m 3 A m Power frequency magnetic fields should be at levels 50 60 Hz characteristics of a typical location in a typical Magnetic Field commercial or hospital environment EN 61000 4 8 NOTE U is the AC mains voltage prior to application of the test level 4 50 ProCare Patient Monitor Service Manual Revision B 2009381 001 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ILC 1931 Guidance and Manufacturer s Declaration Electromagnetic Immunity The ILC 1931 is intended for use in the electromagnetic environment specified below It is the responsibility of the customer or user to assure that the ILC 1931 is used in such an environment Immunity Test EN 60601 TestLevel Compliance Level Electromagnetic Environment Guidance Portable and mobile RF communications equipment should not be used closer to any part of the equipment including cables than the recommende
83. ory is labeled on left keypad 2010624 001 Korean 100 Printer Installed 2010625 001 Korean 400 2010626 001 Korean 300 2010627 001 Korean 200 2010628 001 Korean 100 2010629 001 Finnish 400 Printer Installed 2010630 001 Finnish 300 Printer Installed 2010631 001 Finnish 200 Printer Installed 2010632 001 Finnish 100 Printer Installed 2010633 001 Finnish 400 2010634 001 Finnish 300 2010635 001 Finnish 200 2010636 001 Finnish 100 2010638 001 Portuguese 400 Printer Installed 2010639 001 Portuguese 300 Printer Installed 2010640 001 Portuguese 200 Printer Installed 2010641 001 Portuguese 100 Printer Installed 2010642 001 Portuguese 400 2010643 001 Portuguese 300 2010644 001 Portuguese 200 2010645 001 Portuguese 100 2010646 001 Russian 400 Printer Installed 2010647 001 Russian 300 Printer Installed 2010648 001 Russian 200 Printer Installed 2010649 001 Russian 100 Printer Installed 2010650 001 Russian 400 2010651 001 Russian 300 2010652 001 Russian 200 2010653 001 Russian 100 Revision B ProCare Patient Monitor Service Manual 2009381 001 Calibration amp Maintenance Appendix D Replacement Parts and Assemblies P N 001 Language Model Is Printer Installed Method of NIBP Determination Auscultatory is labeled on left keypad 2010656 001 Hungarian 400 Printer Installed 2010657 001 Hungarian 300 Printer
84. pressure to 100mmHg 4 12 ProCare Patient Monitor Service Manual Revision B 2009381 001 Calibration amp Maintenance 4 6 ProCare Patient Monitor Parameter Tests 12 Record and verify the pressure reading on the top LED display SYSTOLIC 13 Record and verify the pressure reading on the bottom LED display DIASTOLIC 14 Use the valve on the bulb to reduce pressure to 50mmHg 15 Record and verify the pressure reading on the top LED display SYSTOLIC 16 Record and verify the pressure reading on the bottom LED display DIASTOLIC If any of the tests fail continue to section 4 6 4 Otherwise continue to section 4 6 5 4 6 4 Pressure Transducer Calibration Perform only if Pressure Transducer Verification is out of tolerance as specified in Appendix A Note To enter service mode press and hold the CYCLE button while pressing the ON OFF button 1 Turn the ProCare Monitor ON and enter Service Mode 2 The min window should display 0 3 Open valve on bulb to open pressure system to atmosphere 4 Set NIBP Analyzer to Manometer function and press Zero Pressure 5 Press CYCLE button until the min window shows 1 6 Close valve on bulb and manually inflate pressure to 200 mmHg using the CuffLink manometer as reference 7 Press MENU button when pressure reads 200 mmHg to save calibration setting 8 Two steps are necessary for burning changes into flash a Press the CYCLE button repeatedly until the num
85. r 5 s lt 5 U 295 dip in Uy for 0 5 cycles lt 40 Ux 260 dip in Ug for 5 cycles lt 70 U 23096 dip in U for 25 cycles lt 5 U 295 dip in Uy for5 s Mains power should be that of a typical commercial or hospital environment If the user of the DINAMAP ILC 1926 requires continued operation during power mains interruptions it is recommended that the Host monitor be powered from an uninterruptible power supply or a battery PowerFrequency 3 A m 3 A m Power frequency magnetic fields should be at levels 50 60 Hz characteristics of a typical location in a typical Magnetic Field commercial or hospital environment EN 61000 4 8 NOTE U is the AC mains voltage prior to application of the test level Revision B ProCare Patient Monitor Service Manual 4 45 2009381 001 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ILC 1926 Guidance and Manufacturer s Declaration Electromagnetic Immunity The ILC 1926 is intended for use in the electromagnetic environment specified below It is the responsibility of the customer or user to assure that the ILC 1926 is used in such an environment Immunity Test EN 60601 TestLevel Compliance Level Electromagnetic Environment Guidance Portable and mobile RF communications equipment should not be used closer to any part of the equipment including cables than the recommended separation distance calculated from
86. re Monitor The DINAMAP ProCare Monitor is intended for use in the electromagnetic environment on which radiated RF disturbances are controlled The customer or the user of the DINAMAP ProCare Monitor can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the DINAMAP ProCare Monitor as recommended below according to the maximum output power of the communications equipment Separation Distance in Meters m According to Frequency of Transmitter neee 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz Watts d 12VP d 12VP d 23 VP 0 01 0 12 0 12 0 23 0 1 0 38 0 38 0 73 1 1 2 1 2 2 3 10 3 8 3 8 7 33 100 12 12 23 At 80 MHz and 800 MHz the separation distance for the higher frequency range applies For transmitters rated at a maximum output power not listed above the recommended separation distance d in meters m can be estimated using the equitation applicable to the frequency of the transmitter where Pis the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer NOTE These guidelines may not apply in all instances Electromagnetic propagation is affected by absorption and reflection from structures objects and people 4 42 ProCare Patient Monitor Service Manual Revision B 2009381 001 Appendix E Electromagnetic Compatibility
87. rect data or if you can suggest comments that may help improve this manual please send suggestion to General Electric Medical Systems nformation Technologies Technical Publications 4502 Woodland Corporate Boulevard Tampa Florida 33614 Changes to the Service Manual either in response to user input or to reflect continuing product improvements are accomplished through reissue Changes occurring between reissues are addressed through Change Information Sheets and replacement pages If a Change Information Sheet does not accompany your manual the manual is correct as printed ProCare Patient Monitor Service Manual Revision B 2009381 001 Introduction 1 3 Service Policy 1 3 Service Policy The warranty for this product is two years Parts and Labor In the event of a monitor malfunction the monitor must be returned to General Electric Medical Systems Information Technologies to be covered under warranty All repairs on products under warranty must be performed or approved by Product Service personnel Unauthorized repairs will void the warranty Only qualified electronics service personnel should repair products not covered by warranty 1 3 1 Service Contracts 1 3 2 Assistance Service contracts may be purchased on most products Contact your Sales Representative for details and pricing If the product fails to function properly or if assistance service or spare parts are required contact Customer Support Before co
88. rmanent battery damage 4 3 2 Annual Procedures Perform the test procedures described in section 4 6 every twelve months or whenever the accuracy of of the monitor is in doubt Revision B ProCare Patient Monitor Service Manual 4 7 2009381 001 Calibration amp Maintenance 4 4 Care of the Storage Battery 4 4 Care of the Storage Battery The Monitor uses one Lead Acid storage battery The battery can be charged at any time without reducing the charging capacity 4 4 1 Battery Charging The Monitor charges the Lead Acid battery whenever the AC power supply is in use The Monitor automatically senses if the battery needs recharging Battery charging will continue as long as the Monitor is connected to the AC power supply even when the Monitor is turned off Batteries should be charged before first use or after long periods of storage The battery should be charged for 8 hours before use as a charged battery loses some charge when left in storage It is possible to use the Monitor while the Monitor is charging The battery should be charged at room temperature 59 F 86 F 16 C 30 C It is normal for the battery to become warm during charging or after use Batteries can be charged or topped off at any time It is not necessary to wait until they are fully discharged If the monitor is idle for extended periods it should be fully charged once a month to ensure optimum performance 4
89. romagnetic Compatibility EMC ILC 1931 Changes or modifications to this system not expressly approved by GE Medical Systems can cause EMC issues with this or other equipment This system is designed and tested to comply with applicable regulation regarding EMC and must be installed and put into service according to the EMC information stated in this appendix WARNING Use of portable phones or other radio frequency RF emitting equipment near the system may cause unexpected or adverse operation WARNING The equipment or system should not be used adjacent to or stacked with other equipment If adjacent or stacked use is necessary the equipment or system should be tested to verify normal operation in the configuration in which it is being used Guidance and Manufacturer s Declaration Electromagnetic Emissions The ILC 1931 is intended for use in the electromagnetic environment specified below It is the responsibility of the customer or user to assure that the ILC 1931 is used in such an environment Emissions Test Compliance Electromagnetic Environment Guidance RF Emissions Group 1 The equipment uses RF energy only for its internal function Therefore its RF EN 55011 emissions are very low and are not likely to cause any interference in nearby electronic equipment RF Emissions Class A EN 55011 Harmonic Emissions EN 61000 3 2 Not Applicable The equipment is suitable for use in all e
90. ront Panel Controls and Indicators 2 5 2 4 Host Communications Connector aa eeen 2 9 2 4 1 DB15 Connector Pin Assignments 2 9 2 5 Compatible Parts oee eeen 2 10 2 6 Specifications aa ELER REER RTE eneen 2 12 3 Principles of Operation 3 1 3 T Introduction nrs an arena ent weiden hd E EERE 3 3 3 2 Overall Principles of Operation 3 4 3 2 1 SpO2 Model 300 and 400 3 4 Revsion B ProCare Patient Monitor Service Manual 2009381 001 Table of Contents 3 2 2 Cuff Blood Pressure BP and Pulse 3 4 3 2 3 Temperature Model 200 and 400 oo 3 5 3 24 Host Communication Port 3 5 3 3 Functional Description eneen III 3 5 3 3 1 Main Board PWA neee 3 6 3 3 2 User Interface UI Board PWA 3 6 POO OD PW Aah nb Los I etit Ttt eM CHEER 3 7 S34 Prihter wis de bebe Z ana reb eb bios Pt giat stage hala od 3 7 3 3 5 Pneumatic Valve Manifold PVM oo 3 7 3 3 6 Optical Swit esie en rta I e hol sede ORE 3 7 Calibration amp Maintenance 4 1 4 1 Introduction eene eneen nnn 4 3 4 2 Configuring Your ProCare Monitor oee 4 4 4 2 1 Unpacking and Preparation for Installation ss 4 4 4 2 2 Set the D
91. rops shall have no harmful effects to the monitor Power Requirements MAINS Protection against electrical shock Class II AC INPUT VOLTAGE 120 VAC 60 Hz 24W Alternate Sources Protection against electrical shock Class lI DC INPUT VOLTAGE 24 VDC nominal at 1A The AC Mains adapter contains a nonresettable and nonreplaceable fuse Battery 6 volt 3 3 amp hours Protected by internal auto resetting fuse and thermal protection Minimum Operation Time 2 hrs 5 min cycle with adult cuff at 25 C SpO2 active at 60 bpm temp in monitor mode printout of current values every 5 minutes from full charge Fuses The Monitor contains four fuses The fuses are auto resettable and mounted within the Monitor The fuses protect the low voltage DC input the battery the remote alarm output and the 5V output on the host port connector Environmental Operating Temperature 5 C to 40 C 41 F to 104 F Storage Temperature 20 C to 50 C 4 F to 122 F Operating Atmospheric Pressure Range 700 to 1060 hecto Pascal Humidity Range 0 to 95 non condensing Radio Frequency Complies with IEC Publication 601 1 2 April 1993 Medical Electrical Equipment Electromagnetic Compatibility Requirements and Tests and CISPR 11 Group1 Class A for radiated and conducted emissions Mechanical Dimensions Height 9 8 in 25 0 cm
92. s appropriate for your use Revsion B ProCare Partient Monitor Service Manual 3 3 2009381 001 Principles of Operation 3 2 Overall Principles of Operation 3 2 Overall Principles of Operation The following paragraphs provide a general system interface relationship The general block diagram is located in Figure 3 1 The ProCare Monitor is a portable unit that receives input power from an internal rechargeable battery When the ON OFF button is pressed the Main Board is brought out of a sleep mode and turns on the power regulators The power regulators provide conditioned power from the Lead Acid Battery The external DC source is used only to charge the Lead Acid Battery Once the ProCare Monitor is energized a self test is performed The self test automatically tests the main functions of the ProCare Monitor Failure of the self test will set the ProCare Monitor into a fail safe mode with an audio alarm Under normal operating condition the ProCare Monitor is ready to record the patient vital signs using three external attachments the temperature probe SPO2 sensor and cuff Interface with a central station or other device is accomplished through the host communication port on the back of the ProCare Monitor 3 2 1 SpO Model 300 and 400 The SpO probe has a built in sensor When the SpO sensor is attached to the SpO connector and patient the probe senses the heart rate and oxygen saturation The analog signals
93. s Information Technologies will pay outgoing charges for a loaner sent for product repairs under warranty The customer is responsible for shipping charges to return the loaner unit to General Electric Medical Systems nformation Technologies All loaner units must be returned within 5 business days after receipt of your repaired unit Loaner and or Rental products are available to meet your needs in non warranty situations 1 3 5 Repair Parts Repair parts can be ordered from General Electric Medical Systems Information Technologies Via phone 1 877 274 8456 or Via FAX 1 800 421 6841 Exchange replacement assemblies such as Circuit Board Assemblies are also available ask your Customer Support representative for details 1 6 ProCare Patient Monitor Service Manual Revision B 2009381 001 Introduction 1 3 Service Policy Most orders ship on the same day if received before 3PM Eastern Time Overnight freight options are available to meet your critical needs All orders must include the following information Facility s complete name address and phone number FAX number Your purchase order number Your General Electric Medical Systems nformation Technologies account number if available 1 3 6 Replacement Accessories Replacements such as hoses sensors etc must be purchased from General Electric Medical Systems nformation Technologies at 1 800 558 5102 Please have the Product Code of the item you wish to order
94. stablishments other than domestic and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes Voltage Fluctuations Flicker Emissions EN 61000 3 3 Not Applicable Revision B ProCare Patient Monitor Service Manual 4 49 2009381 001 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ILC 1931 Guidance and Manufacturer s Declaration Electromagnetic Immunity The ILC 1931 is intended for use in the electromagnetic environment specified below It is the responsibility of the customer or user to assure that the ILC 1931 is used in such an environment Immunity Test EN 60601 Test Level Compliance Level Electromagnetic Environment Guidance Electrostatic 6 kV contact 6 kV contact Floors should be wood concrete or ceramic tile If Discharge ESD floors are covered with synthetic material the relative EN 61000 4 2 8kV air 8kV air humidity should be at least 30 Electrical Fast 2 kV for power supply lines N A No AC Input Transient Burst EN 61000 4 4 1 kV for input output lines Surge X 1 kV differential mode N A No AC Input EN 61000 4 5 2 kV common mode Voltage dips short interruptions and voltage variations on power supply input lines EN 61000 4 11 lt 5 U 295 dip in Uy for 0 5 cycles lt 40 U 26096 dip in U for 5 cycles 1096 U 53096 dip in U f
95. stem Block Diagram 1 of 2 page 3 9 10 Isolated Power C97 Ea as Ek RE B e pz Bises a aja aig S f BBH Printer e EBE js 55 EN Los 3 Lo c Es Drivers External DC 6Volt Battery FONTS Regulated DC speaker Audio Speaker Pneumatic Valve Control PT1 PT2 NIBP Data Host SpO Interface Communications BEBEBSBE s L E EE gt j o PLUG ENTRY amp Temp Probe Temperature bei ai optional Control Data ontro ProCare Vital Signs Monitor Main Board Diagram 2 of 2 page 3 11 12 VIEWED FROM TOP COMPONENT SIDE A Calibration amp Maintenance evision Pro Care Patient Monitor Service Manual 2009381 001 For your notes ProCare Patient Monitor Service Manual 2009381 001 Revision B Calibration amp Maintenance 4 1 Introduction 4 1 Introduction This section contains general Monitor service procedures including alarm code interpretation service mode operation and periodic maintenance and battery care Refer to Section 5 for disassembly and reassembly procedures and related component service information Revision B ProCare Patient Monitor Service Manual 4 3 2009381 001 Calibration amp Maintenance 4 2 Configuring Your ProCare Monitor 4 2 Configuring Your ProCare Monitor 4 2 1 Unpacking and Preparation for Installation
96. t power not listed above the recommended separation distance d in meters m can be estimated using the equitation applicable to the frequency of the transmitter where Pis the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer NOTE These guidelines may not apply in all instances Electromagnetic propagation is affected by absorption and reflection from structures objects and people 4 52 ProCare Patient Monitor Service Manual 2009381 001 Revision B Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ILC 1931 Compliant Cables and Accessories WARNING The use of accessories transducers and cables other than those specified may result in increased emissions or decreased immunity performance of the equipment or system The table below lists cables transducers and other applicable accessories with which GE Medical Systems claims EMC compliance NOTE Any supplied accessories that do not affect EMC compliance are not included Part No Description Maximum Lengths Accessories 683235 Adapter Cable RJ 45 to DB15 600 mm 2 ft 418497 002 Apex Pro Cable 1 8m 6 ft Revision B ProCare Patient Monitor Service Manual 4 53 2009381 001 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ILC 1931 4 54 ProCare Patient Monitor Service Manual 2009381 001 Revision B
97. the equation applicable to the frequency of the transmitter Recommended separation distance Conducted RF 3 Vrms 3V rms EN 61000 4 6 150 KHz to 80 MHz d 1 2 VP Radiated RF 3 V m 3 V m JP EN 61000 4 3 80 MHz to 2 5 GHz d 1 2 80 MHz to 800 MHz d 23VP 800 MHz to 2 5 GHz where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and dis the recommended separation distance in meters m Field strengths from fixed RF transmitters as determined by an electromagnetic site survey should be less than the compliance level in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol al Note 1 At 80 MHz and 800 MHz the higher frequency range applies Note 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by reflection from structures objects and people Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile radio AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the equipment is used exceeds the applicable RF compliance level above the equipment should be observed to verify normal operati
98. the ON OFF button 1 Turn the Monitor ON and enter Service Mode 2 Press CYCLE button and the min display should change to a 1 3 Close the valve on the inflation bulb 4 Set the NIBP Analyzer to Leak test function 5 Press the Pump button on the NIBP Analyzer 6 After the system inflates to 200mmHg wait for the Wait on the NIBP analyzer message to be cleared 7 Press the Start button on the NIBP Analyzer to begin the leakage test 8 After 60 seconds the NIBP Analyzer will display the leakage rate 9 Record and verify the leakage rate 10 Turn the ProCare Monitor off 4 6 3 Pressure Transducer Verification Note To enter service mode press and hold the CYCLE button while pressing the ON OFF button 1 Turn the Monitor ON and enter Service Mode 2 The HISTORY LED should display 0 3 Set NIBP Analyzer to Manometer function and press Zero Pressure 4 Press CYCLE button HISTORY display should change to a 1 5 Use the inflation bulb to inflate the cuff hose and pressure indicator setup to 200mmHg 6 Record and verify the pressure reading on the top LED display SYSTOLIC 7 Record and verify the pressure reading on the bottom LED display DIASTOLIC 8 Use the valve on the bulb to reduce pressure to 150mmHg 9 Record and verify the pressure reading on the top LED display SYSTOLIC 10 Record and verify the pressure reading on the bottom LED display DIASTOLIC 11 Use the valve on the bulb to reduce
99. vel in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol al and people Note 1 At 80 MHz and 800 MHz the higher frequency range applies Note 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by reflection from structures objects Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile radio AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the equipment is used exceeds the applicable RF compliance level above the equipment should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as re orienting or relocating the equipment bOver the frequency range 150 KHz to 80 MHz field strengths should be less than 3 V m Revision B ProCare Patient Monitor Service Manual 4 41 2009381 001 Appendix E Electromagnetic Compatibility Electromagnetic Compatibility EMC ProCare Monitor Recommended Separation Distances The table below provides the recommended separation distances in meters between portable and mobile RF communications equipment and the DINAMAP ProCa
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101. your purchase order and account number available Revsion B ProCare Patient Monitor Service Manual 2009381 001 1 7 Introduction 1 4 Product Description 1 4 Product Description The Monitor is described below Refer to Table 1 1 for specifications 1 4 1 General Description The ProCare Monitor provides a small portable easy to use monitoring alternative for sub acute hospital and non hospital settings The DC operated Monitor offers noninvasive determination of systolic blood pressure diastolic blood pressure mean arterial pressure pulse rate oxygen saturation and temperature Monitors are available with or without integrated printers ProCare Monitors are intended for use in various markets from the physician s office to sub acute triage and medical surgical units Indicators for external DC operation from AC mains battery operation and battery charging are at the front of the unit At the time of publication the available functioning parameters included the following NIBP Nellcor Pulse oximetry SpO2 Masimo Pulse oximetry SpO2 Alaris Oral and Rectal thermometry thermal recorder printer Other DINAMAP ProCare features include The ability to uses industry standard accessories Remote alarm capability Function keys for quick access to Alarm Silence Monitor Menus Print and NIBP Inflate Stop The ProCare Monitor operates from either an external DC power supply or from the internal lead
102. zls l PS12 al RES PS13 As mE PS14 191 IE PS15 ar HL CLR 18 LR DST V PS GND 9 0 PS 0 15 RE DIC143 js a digital transistor witt 7 base resistor and a 47K base pull down resistor DTD123EK is a digital transist r AR e UR dial resistor and DAB BG aw resistor P S 0 15 8 5 a al zi sal 4 7 El 2 3 8 8 5 3 5 5 5 5 5 2 E Schematic L 028 y 029 LY Q30 y Q31 LY 032 y 033 y 034 y 035 y 036 LY 037 A 039 LN Q40 LN Q41 VN L DUE DTD123EK DTD123EK DTD123EK DTD123EK DTD123EK DTD123EK DTD123EK DTD123EK DTD123EK DTD123EK EK V DTD123EK DTD123EK DTD123EK Vh DTD123EK ser n e al se Oar re PROCARE USER INTERFACE BOARD P N 2008741 Rev B page 5 25 26 1 of 2 PCB BO

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