Home

Patient Data Module (PDM) - Frank`s Hospital Workshop

1. Category Description Maximum Lengths Masimo reusable sensor finger N A Masimo sensor LNCS Adtx adult adhesive N A Masimo sensor LNCS Pdtx PED adhesive N A Masimo sensor LNGS Inf L infant adhesive N A Masimo sensor LNCS Neo L neonatal adhesive N A Masimo sensor LNCS NeoPt L NEOPT neonatal N A adhesive Masimo sensor LNCS DCI adult reusable N A Masimo sensor LNCS DCIP ped reusable N A Masimo sensor LNCS Y1 multisite reusable N A Masimo sensor LNCS TC I TIP CLIP ear reusable N A Masimo sensor LNCS TF I reusable forehead N A Masimo sensor LNOP DC_195 reusable finger sensor N A Masimo sensor LNOP DCSC reusable spot check N A sensor Masimo sensor LNOP DC 12 reusable spot check N A sensor Masimo sensor LNOPTF I reusable forehead sensor N A Masimo sensor LNOP NEO L neonate adhesive sensor N A Masimo sensor LNOP NEOPT L sensitive skin neo N A adhesive sensor Masimo sensor LNOP INF L infant adhesive sensor N A Masimo sensor LNOP NEO bridge neonate adhesive N A sensor Masimo sensor LNOP NEOPT sensitive skin bridge N A neonate adhesive sensor Masimo sensor LNOPv In disposable infant sensor N A Masimo sensor LNOPv Ne disposable neonate sensor N A Masimo sensor LNOPv Ad disposable adult sensor N A Masimo adult adhesive LNOP sensors N A Masimo pediatric adhesive LNOP sensors N A Masimo infant pediatric LNOP HiFi sensor N A Masimo neonatal adult LNOP HiFi sensor N A Masimo infant pediatric LNOP th
2. WARNING PHYSICAL INJURY Do not hang articles on the IV pole that are not related to the Patient Data Module s use Do not place the Patient Data Module more than 147 cm 58 in from the floor when mounting on an IV pole with a base not less than 58 cm 23 in in diameter WARNING To reduce the ingress of water into the equipment do not mount the Patient Data Module in a vertical position with the patient cables facing up or down 2030047 001A Patient Data Module 3 3 Installation 482A Mounting options include mounting to a bed headboard or footboard an IV pole or a roll stand using one of the docking stations Mounting kits include all necessary hardware and installation instructions me 2021963 001 2021968 001 Pole Rail Clamp Mou O cet Mount PDM Mini Dock Adapter Plate a Mount PRC W L Bracket 2022676 001 Mount PDM GCX Rollstand Wall Channel 2022677 001 Mount PDM M Arm Down Post 2034357 001 Mount PDM Slide 483A Patient Data Module 2030047 001A Installation Connect to host patient monitor Connect to transport bedside monitor If using the Patient Data Module with a transport bedside monitor 1 Guide the mounting rails of the Patient Data Module onto the transport dock mounting rails 2 Slide the Patient Data Module toward the ePort until the locking key secures it to the transport dock Connect to bedside monitor If using the
3. 2030047 001A Patient Data Module 7 5 Field Replaceable Units Labels Apply labels as shown 404B 464A Battery door and tray 1 Remove 1 screw that holds the battery door to the housing and remove the door and washer 462A 2 Remove the battery if one is in the tray 3 Use a flathead screw driver to lift the catch tab on the tray as you pull it out of the housing 7 6 Patient Data Module 2030047 001A Field Replaceable Units AR tab 468A Mount rail and pull tab 1 Remove 2 screws on the latch stop Remove the latch stop Latch stop screws M 463A 2 Grasp the pull tab between thumb and index finger as shown and gently pull it straight out about a half inch Lift the assembly out of the rail slot 2030047 001A Patient Data Module 7 7 Field Replaceable Units 469A NOTE In the event that the pull tab assembly comes apart when pulled from the rail slot reassemble as shown below 470A 471A 3 Remove 2 short screws at the rear of the mount rail and 2 long screws at the front of the mount rail Long screws Short screws PS 464A 4 Unseat the mount rail by twisting it slightly Lift mount rail off the top housing 7 8 Patient Data Module 2030047 001A Field Replaceable Units NOTE When reassembling make sure there are not gaps between the mount rail and the housing when re seating Top housing 1 Remove the mount rail
4. Output specifications Parameters displayed T1 T2 Error independent of source 0 1 C with series 400 probes 0 3 C with series 700 probes Alarms User selectable upper and lower limits 2030047 001A Patient Data Module A 5 Appendix A Technical Specifications Invasive blood pressure Number of channels Up to 4 with appropriate cables Transducer sites site name arterial ART systolic diastolic mean and rate and displayed values femoral FEM systolic diastolic mean and rate pulmonary artery PA systolic diastolic and mean central venous pressure CVP mean left atrial LA mean right atrial RA mean intracranial pressure ICP mean umbilical artery UAC systolic diastolic mean and rate umbilical vein UVC mean special pressure SP mean Transducer requirements Transducers meeting the following specifications can be used however have not been evaluated by UL NOTE Note UL Classification covers the following invasive blood pressure transducers m Utah Deltran IV CPT 400 m Edwards PX600 m Bekton Dikinson P23XL 1 m Abbot 42582 08 Accuracy 2 or 1 mmHg whichever is greater exclusive of transducer 2 or 3 mmHg whichever is greater exclusive of Patient Data Module Over pressure rating 500 kPa 4000 mmHg above atmospheric pressure all except catheter tip transducers Under pressure rating 50 kPa 400 mmHg below atmospheric
5. 4 2 Change the PC S IP address 0 00 c cee e een 4 4 Disable firewall and networking services one 4 4 Enter the Patient Data Module service tool 4 6 Service tool MOAU ES ooooccccocnnn eee eens 4 7 Device Information oenen eneen 4 7 Configuration sr oe ira tene den o ticas Td 4 8 DIAghOSUCS erneer ere ee Sadly a le a 4 10 Calibr ON ee os ans zaten cig ordende erdee nend wed da und bok gd deelen 4 10 Maintenance schedule oaeen eee een 5 2 Manufacturer recommendations ann 5 2 Manufacturer responsibility Lk 5 2 Inspections ts ee a T aera eee eee Brahe 5 2 Gleanings ie cease vernederde benk sarod di 5 3 PreCautlons isis Merten er Gein eine eaten Wee Rte Med Reh are Pee 5 3 Cleaning procedures eneen 5 3 SOTO Le smash wh na Pade dins its shea yan ee ideale 5 4 Consequences of using improper cleaning product 5 4 Cleaning products to avoid oen 5 4 Expansion interface cleaning een 5 5 Battery compartment cleaning aaneen 5 6 oterilizati N asc a oee aa atd ates eg ae cea Re a aden eh Bee WSE 5 6 Battery Cale Soccer a neten tend 5 7 Use recommendations 0 0 c cece ects 5 7 Storage recommendations ennen eeen 5 7 Charge the battery eeen 5 8 Condition the battery eenen 5 8 Checkout procedures and NBP calibration 5 9 Patient Data Module 2030047 001A 6 Troubleshooting san ineen
6. 6 Calibrate analog out Go to Calibration on page 4 10 for instructions 2030047 001A Patient Data Module 7 11 Field Replaceable Units 7 Licensing information must be re entered Contact GE technical support and provide the Patient Data Module serial number and MAC address to proceed See the How to Reach Us page included with this manual for contact information Go to Licensing on page 4 9 for instructions on entering the new activation code 8 Manufacturer s serial number must be re entered Go to Asset Settings on page 4 8 for instructions on entering the manufacturer s serial number 9 Go to the Solar 8000M i patient monitor service manual and complete checkout procedures NBP hose coupling and elbow 1 Remove the top housing and main board per above steps 2 Disconnect the front panel connector Main board flex pump connector Front panel connector W a hose NBP hose at and coupling manifold 3 Disconnect the main board flex pump connector 477A 4 Hold flex out of the way and disconnect the NBP hose from the coupling 5 Remove hose from the manifold NOTE When reassembling slide hose all the way onto the manifold fitting so that the hose lays flat 6 Go to the Solar 8000M patient monitor service manual and complete checkout procedures 7 12 Patient Data Module 2030047 001A Field Replaceable Units NBP assembly with manifold hose 1 Remove the top ho
7. Flashing amber indicates communication failure Alternately flashing with the power LED indicates software transfer The following LED condition identifies the power status No light indicates no power applied Solid amber indicates software booting up Solid green indicates powered by AC derived mains or battery Flashing amber indicates approximately five minutes battery power remaining Alternately flashing with the communication LED indicates software transfer Patient Data Modules connect to a bedside or transport patient monitor using the host interface connector It carries power communication and analog output signals to the display device 2 4 Patient Data Module 2030047 001A Equipment Overview Basic components Battery The Patient Data Module is designed to operate on battery power when used with a transport monitor or whenever AC power is interrupted A complete battery management system allows you to obtain maximum battery performance When connected to a bedside monitor audible and visual alarms alert you when loss of power is imminent and on screen capacity gauges on the transport monitor indicate battery charge condition and capacity Patient Data Module ePort host interface cable The Patient Data Module ePort host interface cable provides external power and communication between the Patient Data Module and a patient or transport monitor Docking stations There are three versions of docking
8. 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 Power Frequency 50 60 Hz Magnetic Field EN 61000 4 8 3 A m 3 A m Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment NOTE U is the AC mains voltage prior to application of the test level 2030047 001A Patient Data Module B 3 Appendix B Electromagnetic Compatibility Immunity Test EN 60601 Test Level Compliance Level Electromagnetic Environment Guidance Conducted RF EN 61000 4 6 Radiated RF EN 61000 4 3 3 Vrms 150 KHz to 80 MHz 3 V m 80 MHz to 2 5 GHz 3 Vrms 3 V m 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 d 12 4P d 1 2 80 MHz to 800 MHz d 2 3 NE 800 MHz to 2 5 GHz where Pis 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
9. but may be required for cables and leadwires Frequent sterilization will reduce the useful life of cables and leadwires Sterilize with ethylene oxide gas EtO at a maximum temperature of 50 C 122 F After EtO sterilization follow the recommendations from the sterilizer manufacturer for required aeration 5 6 Patient Data Module 2030047 001A Maintenance Battery care The Lithium Ion battery is a rechargeable battery containing Lithium Ion cells Each battery contains an integrated electronic fuel gauge and a safety protection circuit The processor within the equipment communicates with both the battery and the charger The following are facts about Lithium Ion battery technology m The battery discharges on its own even when it is not installed in the equipment This discharge is the result of the Lithium Ion cells and the bias current required for the integrated electronics The self discharge rate doubles for every 10 C 18 F rise in temperature The capacity loss of the battery degrades significantly at higher temperatures As the battery ages the full charge capacity of the battery degrades and is permanently lost As a result the amount of charge that is stored and available for use is reduced The following terms are used to define the battery capacity m Design capacity The theoretical capacity of the battery cells when the battery is new m Full charge capacity The actual amount of charge
10. 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 claims EMC compliance NOTE Any supplied accessories that do not affect EMC compliance are not included Maximum Lengths Category Description ECG Cables Cable ECG 3 5 lead Multi Link 6 m 20 ft Compatible ECG trunk cable 5 lead 3 m 10 ft 3 m 10 ft Compatible ECG trunk cable 3 lead B 5 2030047 001A Patient Data Module Appendix B Electromagnetic Compatibility Category Description Maximum Lengths Care cable ECG 3 lead Multi Link w grabber 3 6 m 12 ft Care cable ECG 3 5 lead Multi Link 3 6 m 12 ft Care cable ECG 3 lead Multi Link din neonatal 3 6 m 12 ft Care cable ECG 6 lead Multi Link 3 6 m 12 ft Care cable ECG 12 lead Multi Link 3 6 m 12 ft Care cable ECG 12 lead ESU Multi Link 3 6 m 12 ft Care cable ECG 3 5 lead ESU Multi Link 3 6 m 12 ft ECG Multi link Leadwires Lead wire set 5 lead Multi Link group grabber 130 cm 51 in Lead wire set 3 lead Multi Link group grabber 130 cm 51 in Lead wire set 5 lead Multi Link grabber 130 cm 51 in Lead wire set 5 lead Multi Link grabber V2 V6 130 cm 51 in Lead wire set 3 lead M
11. 10ft ePort to host interface cable 15 ft ePort to host interface cable 20ft ePort to host interface cable 25 ft 2021968 001 Fixed mount adapter Mini dock 2030340 001 Bedside dock 2030341 001 Transport dock 7 2 Patient Data Module 2030047 001A Field Replaceable Units Disassembly quidelines WARNING REPAIR TO THE FRU LEVEL Field repairs are recommended to the field replaceable unit FRU only Attempting a field repair on a pcb or a factory sealed component or assembly could jeopardize the safe and effective operation of the Patient Data Module NOTE GE recommends using the new fasteners screws washers etc provided in the FRU kits rather than re using the old fasteners Some fasteners are not intended to be re used more than three times Take advantage of existing thread pattern cut by turning the screw counterclockwise until it drops into the existing thread pattern Tools required A T10 TORX style screwdriver and a standard set of hand tools are required for disassembly and assembly Wearing safety glasses is recommended Before disassembly Before disassembling the Patient Data Module always do the following Remove all cables Remove the battery Provide appropriate electrostatic discharge protection to prevent damaging the Patient Data Module See Electrostatic discharge ESD precautions below for details Hardware precautions Obs
12. 2030047 001A Patient Data Module B 9 Appendix B Electromagnetic Compatibility B 10 Patient Data Module 2030047 001A World Headquarters European Representative Asia Headquarters GE Medical Systems GE Medical Systems GE Medical Systems Information Technologies Inc Information Technologies GmbH Information Technologies Asia GE China Co Ltd 8200 West Tower Avenue Munzinger StraBe 3 5 24th Floor Shanghai MAXDO Center Milwaukee WI 53223 USA D 79111 Freiburg 8 xing Yi Road Hong Qiao Development Zone Tel 1414 355 5000 Germany Shanghai 200336 P R China 1 800 558 5120 US only Tel 4976145 43 0 Tel 86 21 5257 4650 Fax 1414 355 3790 Fax 49 76145 43 233 Fax 86 215208 2008 GE Medical Systems Information Technologies a General Electric Company going to market as GE Healthcare www gehealthcare com
13. 8 Ibs with optional battery Environmental Power requirements Input voltage 8 to 17 Vde Input current 0 3A nominal at 16 75 V Power consumption 4 5 Watts nominal Cooling Natural convection Operating heat dissipation 10 2 Btu Hr NOTE System may not meet its performance specifications if stored or used outside the manufacturer s specified temperature and humidity ranges Operating temperature and 10 C to 35 C 50 F to 95 F humidity 15 to 95 RH non condensing Storage temperature and 40 C to 60 C 40 F to 140 F humidity 15 to 95 RH non condensing Battery Type Exchangeable lithium ion Quantity One Voltage 11 1 V nominal Capacity 1 8 Amp hour nominal Run time Approximately 3 5 hours with new fully charged battery Charge time Approximately 2 hours Battery life 500 cycles to 50 capacity A 2 Patient Data Module 2030047 001A Appendix A Technical Specifications ECG Standard leads available I II III V1 to V6 aVR aVL and aVF Leads analyzed simultaneously Twelve I Il Ill V1 to V6 aVR aVL and aVF Lead fail Identifies failed electrodes and switches to those intact Lead fail sensing current Active electrodes lt 30 nA each Reference electrode lt 270 nA Input specifications QRS detection range Signal width Heart rate range Common mode reje
14. ECG Config Filter Check that the Patient Data Module power frequency setting matches the patient monitor s power frequency setting Check that ECG Config Filter is enabled If this does not correct the problem follow steps in the No parameter section in this table Patient Data Module will not dock 1 2 Check for damage to mounting rails If damaged replace the mounting rails Check for damage to the docking station bedside dock transport dock or mini dock If damaged replace the docking station GEHC MS service tool red values If the following values in are highlighted red they are out of specification See chapter 4 Service Tool and Configuration Diagnostics gt Service Metrics Under TEMPERATURE amp VOLTAGE RAILS if Main DSP voltage and temperature is red out of specification replace the Main cpu board See chapter 7 Field Replaceable Units for ordering parts and replacement procedures Under TEMPERATURE amp VOLTAGE RAILS if ARM and ECG voltage is red out of specification contact GE technical support to service the Patient Data Module See the How to Reach Us page included with this manual for contact information 6 4 Patient Data Module 2030047 001A Troubleshooting Error messages The following error messages display at the patient monitor if there is a serious problem with the Patient Data Module Error message Action COMMUNICATIO
15. Intended use GE is responsible for the effects of safety reliability and performance only if m Assembly operations extensions readjustments modifications or repairs are carried out by persons authorized by GE m The electrical installation of the relevant room complies with the requirements of the appropriate regulations m The equipment is used in accordance with the instructions for use This device is intended for use under the direct supervision of a licensed health care practitioner This device is not intended for home use Federal law restricts this device to be sold by or on the order of a physician 1 2 Patient Data Module 2030047 001A Introduction Hazard definitions Contact GE for information before connecting any devices to the equipment that are not recommended in this manual Parts and accessories used must meet the requirements of the applicable IEC 60601 series safety standards and or the system configuration must meet the requirements of the IEC 60601 medical electrical systems standard Periodically and whenever the integrity of the device is in doubt test all functions The use of accessory equipment not complying with the equivalent safety requirements of this equipment may lead to a reduced level of safety of the resulting system Consideration relating to the choice shall include use of the accessory in the patient vicinity and evidence that the safety certification of the acces
16. Patient Data Module with a bedside monitor 1 Connect one end of the ePort host interface cable to the Patient Data Module ePort connector 2 Connect the other end of the ePort host interface cable to the Solar to Patient Data Module adapter on the back of the Solar 8000M 1 patient monitor 2030047 001A Patient Data Module 3 5 Installation 3 6 Patient Data Module 2030047 001A 4 service Tool and Configuration 2030047 001A Patient Data Module Service Tool and Configuration Overview The Patient Data Module service tool provides the following Device information Configuration including asset setting ECG filter configuration licensing and software transfer m Diagnostics m Calibration All service functions for the Patient Data Module are performed through a service laptop Required equipment Set up the PC The following is a list of equipment to use with the GEHC MS service tool If servicing the Patient Data Module using a Solar 8000M I patient monitor m PC with Microsoft Windows XP or 2000 operating system a CD ROM drive and a network card Category 5 crossover cable 2028822 001 ePort to host interface cable 2017098 002 Solar 8000M i patient monitor with PDM service adapter 2028845 002 Patient Data Module software CD with GEHC MS Service Tool If servicing the Patient Data Module without a host patient monitor m PDM Service Tool Kit 2030924 001 Connect the PC to
17. a bedside transport or surgical monitor for further processing and display The data that it collects converts and sends includes the patient s vital signs and physiological waveforms It also stores patient history including trends and special events and setup information such as blood pressure zero points and alarm limit settings The patient history is stored so that the collected information is transferred when a patient is transferred to a different monitor TRANSPORT PRO HOST V2 1 A gt gt ETHERNET WI POWER SYSTEM POWER BATTERY BATTERY BATTERY SLOTA BATTERY SLOTS SERVICE PORT ETHERNET NEONATAL SOLAR 8000M i HOST V5 T POWER TRAMNET gt TRAMRAC yw power POWER POWERED RAC ETHERNET NOT REQUIRED UNITY NETWORK ETHERNET MPORT ETHERNET A ETHERNET A MPORT N swircHeo power ANCILLARY MODULE PRESENT Toewces he MPORT BATTERY USER INTERFACE INTERFACE CABLE TO EXTERNAL DEFIB INTRA AORTIC BALLOON PUMP OR VENTILATOR A A SWITCHED POWER MODULE PRESENT y EXPANSION MODULE future USB amp USB POWER SYSTEM POWER TRAY ECGIRESP PATIENT DATA MODULE v1 POWER ON SWITCH NEP BP ZERO ALL SWITCH SpO POWERBATTERY COMMUNICATION LED STATUS DUAL BP 1 BP 2 DEFIB SYNC DUAL TEMPICO ANALOG OUT PDM DOCKING STATION PATIENT CABLE MULTILINK ECG CABLE LEADWIRES AND ELECTR
18. and pull tab per above steps 2 Remove 4 machine screws that hold the top and bottom housing together O O 3 Turn the Patient Data Module right side up and lift off the top housing 464A 4 Install the top housing as follows a Inspect the gasket in the top housing to be sure it is securely placed in the groove Gasket 472A b Make sure the flex connector to the front panel board is connected securely 2030047 001A Patient Data Module 7 9 Field Replaceable Units connector 473A c Starting at the rear of the module position alignment pins of the top housing into the bottom housing holes then close the housing straight down 474A d Squeeze the top and bottom housings together to eliminate gaps Install the screw near the Power ON button first 7 10 Patient Data Module 2030047 001A Field Replaceable Units Main board 1 Remove the top housing per above steps 2 Disconnect the NIBP cable from the connector without pulling on the wires Alignment pins NIBP cable 465A 3 Remove 6 screws on the main board 4 Remove the main board NOTE When installing the main board position it into the alignment pins See figures above and below fold the flex material over the top of the board and hold in place while installing screws Alignment pin 5 Load new software from the CD included in the Main board FRU kit Go to Software Transfer on page 4 9 for instructions
19. for contact information Enter the activation code and click Activate to complete the installation Click Remove to remove a license NOTE After installation perform the checkout procedures provided in the host patient monitor service manual A new activation code must be requested and entered if the main cpu board is replaced Software Transfer The Software Transfer module is used for installing Patient Data Module software Follow the instructions displayed on the screen To power cycle the Patient Data Module disconnect and reconnect the ePort host interface connector CAUTION Do not disconnect the power during software transfer The Patient Data Module could be damaged NOTE After installation perform the checkout procedures provided in the host patient monitor service manual 2030047 001A Patient Data Module 4 9 Service Tool and Configuration Diagnostics The Diagnostics category consists of Log Files and Service Metrics modules Log Files The Log Files module allows viewing and downloading log files Messages and errors in log files provide useful information to a trained technician Click View Log to view or Download Log to download the log file Service Metrics The Service Metrics module displays various Patient Data Module statistics NBP STATISTICS can be useful in determining NBP usage Click REFRESH ALL to refresh the data The following buttons clear NBP data m NBP Pump Ru
20. stations m Bedside dock for use with Solar 8000M i patient monitor m Transport dock for use with Transport Pro patient monitor m Fixed mount adapter mini dock for use with mounting hardware Patient Data Module bedside dock The Patient Data Module bedside dock is used for mounting the Patient Data Module to a bedside patient monitor It has a host interface connection which delivers power provides communication and allows easy connection with a patient monitor Patient Data Module transport dock The Patient Data Module transport dock is attached to a transport patient monitor when it ships from the factory It is fastened to the back of the transport patient monitor and delivers power provides communication and allows easy connection and disconnection Patient Data Module fixed mount adapter mini dock The Patient Data Module fixed mount adapter provides a mechanical connection between the Patient Data Module and mounting hardware There are no electrical connections on the mini dock 2030047 001A Patient Data Module 2 5 Equipment Overview Views Patient Data Module bedside dock 480A Patient Data Module fixed mount adapter mini dock 481A 2 6 Patient Data Module 2030047 001A Equipment Overview Theory of operation Overview The Patient Data Module is a portable acquisition device It collects data from a patient converts the data to a digital form for processing and sends the data to
21. the battery can store and deliver m Remaining charge capacity The amount of full charge capacity currently remaining in the battery This is a percent of full charge capacity Use recommendations GE recommends the following methods to improve battery performance m Location Position the equipment in a location that does not artificially increase the operating temperature of the batteries m Charging method Whenever possible use the Cadex SMart Two charger to charge the battery The Cadex SMart Two charger maintains a lower battery cell temperature during the charge cycle This reduction in temperature can extend the life of the battery m Conditioning guideline Remove the batteries from the equipment every six months and condition it using the Cadex SMart Two charger This condition cycle recalibrates the electronic fuel gauge Storage recommendations Store the battery outside of the device at a temperature between 20 C to 25 C 68 F to 77 F Storing the battery inside the Patient Data Module is not recommended for the following reasons m Ina device that is powered by an AC power source the battery cell temperature increases by 10 C to 15 C 18 F to 27 F above the room s ambient temperature This reduces the life of the battery 2030047 001A Patient Data Module 5 7 Maintenance m na device that is powered by an AC power source floating the battery self discharges to less than
22. 0 mmHg Pediatric 30 to 240 mmHg Neonatal 30 to 140 mmHg Adult 10 to 220 mmHg Pediatric 10 to 200 mmHg Neonatal 10 to 110 mmHg Adult 20 to 260 mmHg Pediatric 20 to 215 mmHg Neonatal 20 to 125 mmHg Adult 0 to 290 mmHg Pediatric 0 to 250 mmHg Neonatal 0 to 150 mmHg Pressure accuracy Automatic cycle times Auto zero Tubing length Automatic cuff deflation Static 2 or 3 mmHg whichever is greater Clinical 5 mmHg average error 8 mmHg standard deviation 0 to 24 hours Zero pressure reference prior to each cuff inflation Variable Cycle time exceeding 3 minutes 85 seconds neonatal power off or cuff pressure exceeds 290 mmHg 6 mmHg for adult 250 mmHg 5mmHg for pediatric or 150 mmHg 3mmHg for neonatal Cuff sizes Disposable Large adult adult small adult pediatric child and neonatal Reusable Adult thigh large adult adult small adult small adult child child and infant Alarms User selectable upper and lower limits for systolic diastolic and mean pressures A 8 Patient Data Module 2030047 001A Appendix A Technical Specifications Pulse oximetry Sp02 Parameters monitored Arterial oxygen saturation SpO2 and peripheral pulse rate PPR Probe types Masimo reusable single use Nellcor reusable single use Masimo range SpO2 1 to 100 Pulse rate 25 to 240 beats per minute Masimo accuracy Mas
23. 25 49 9 of full charge capacity m One LED illuminated 10 24 9 of full charge capacity m One LED flashing lt 10 of full charge capacity remaining Install or change the battery 1 Open the battery door by gently pulling on the battery door pull tab 862A 2 Pull the battery tray out of the Patient Data Module using the battery tray strap and remove the battery 3 Insert the new battery with the test button facing up and the arrow pointing into the Patient Data Module 855A 3 2 Patient Data Module 2030047 001A Installation 4 5 6 Software Press the battery door closed until it seals the battery compartment WARNING PHYSICAL INJURY Make sure the battery is completely inserted and that the battery door is securely sealed Falling batteries could seriously or fatally injure neonatal or other vulnerable patients Press the Power button on the Patient Data Module Verify that the Power indicator illuminates amber while the Patient Data Module boots up then illuminates green The Patient Data Module leaves the factory with software installed If you need to install the software contact your GE representative Mounting options WARNING For safety reasons all connectors for patient cables and sensor leads are designed to prevent inadvertent disconnection should someone pull on the leads Do not route cables in a way that they may present a stumbling hazard
24. 90 of its full charge capacity after approximately two weeks The battery is then recharged to 100 resulting in a 95 average state of charge Storing the battery at a high state of charge also reduces the life of the battery GE recommends that you remove the battery and store it near the Patient Data Module until it is needed Charge the battery The battery can be charged by one of two methods m Inside a Patient Data Module that is connected to a powered host m Outside the Patient Data Module using a Cadex Smart2 Battery Charger Charge with a Cadex Smart2 battery charger 1 Insert the battery into the battery charger The RUN LED lights 2 Leave the battery in the charger until the READY LED lights NOTE If the FAIL LED lights remove the battery from the battery charger and reinsert it This corrects any battery charger time out errors If the FAIL LED still lights replace the battery Charge inside the Patient Data Module The battery charges whenever the Patient Data Module is connected to an AC powered host Condition the battery Remove or replace the battery 1 Open the battery door at the rear of the Patient Data Module 2 Remove the battery 3 Insert a new battery with the connection pins inserted first and facing down 4 Close the battery door 5 Connect Patient Data Module to a host patient monitor and confirm that the battery LED lights green and the battery icon displays in the lower corner of the pa
25. Data Module 4 5 Service Tool and Configuration Security Accounts Manager Properties Local Computer General Log On Recovery Dependencies Service name SamSs Display pame Security Accounts Manager Description Stores security information for local user accounts Path to executable CAWINDOWS system32 isass exe Verify 6 sored T Disabled y Service status Stopped You can specify the start parameters that apply when you start the service from here 432A To disable the Security Accounts Manager select Disable from the Startup type drop down list Select Apply to disable the Security Accounts Manager Select Ok and close all windows Repeat these steps for all VPN wireless network cards or any firewall protection programs running on your PC NOTE If you are unsure of the firewall and networking services on your PC contact your local IT administrator for details Windows 2000 and XP PC s allow you to send a list of services to your IT administrator Enter the Patient Data Module service tool Properly connect and configure the Patient Data Module and service laptop as described in Set up the PC on page 4 2 Insert the Patient Data Module software CD in the CD ROM drive The GEHC MS Tool application opens automatically If the GEHC MS Tool application does not launch open the CD ROM drive and double click ShellExecute js Type the username and password and click logi
26. GE Healthcare Patient Data Module PDM Service Manual Software version 1 Patient Data Module English 2030048 001 cd 2030046 001A paper 2007 General Electric Company All rights reserved NOTE Due to continuing product innovation specifications in this manual are subject to change without notice Listed below are GE Medical Systems Information Technologies trademarks used in this manual All other trademarks contained herein are the property of their respective owners UNITY NETWORK DASH SOLAR TRAM and TRIM KNOB are trademarks of GE Medical Systems Information Technologies registered in the United States Patent and Trademark Office CARESCAPE is a trademark of GE Medical Systems Information Technologies For technical documentation purposes the abbreviation GE is used for the legal entity name GE Medical Systems Information Technologies T 2 Patient Data Module 2030047 001A 6 April 2007 Contents INTO UCI atra 1 1 Manual information 00 cece eee eee ee 1 2 Revision NISTO cise cc teed ote eta ete e EA 1 2 Manual Purpose cai dias 1 2 Intended audience LL 1 2 Ordering manuals nnee 1 2 Safety information venen eenen eenen 1 2 Responsibility of the manufacturer een 1 2 Intended USE kak a Einu s ad eh bane Aras a E ek De a ss 1 2 Hazard definitions eneen 1 3 Patient Data Module hazards lt 1 4 Equipment symbols oe 1 4 Service information uus
27. N Go to See Problems and solutions on page 6 3 FAILURE BATTERY FAIL Go to See Battery care on page 5 7 SERVICE THE PDM Contact GE technical support 2030047 001A Patient Data Module 6 5 Troubleshooting 6 6 Patient Data Module 2030047 001A f Field Replaceable Units 2030047 001A Patient Data Module Field Replaceable Units Ordering Parts Parts The parts lists in this chapter supply enough detail for you to order replaceable parts If you require additional information or troubleshooting assistance contact GE Technical Support To order parts contact Service Parts at the address or telephone number listed on the How to Reach Us page included with this manual The table below lists replaceable assemblies that can be ordered Item Number Description 2031069 002 Battery door and tray 2031069 003 Battery 2031069 004 Patient Data Module mount rail and pull tab 2031069 005 Label kit Nellcor 2031069 006 Label kit Masimo 2031069 007 NBP assembly with MFLD hose 2031069 008 NBP MELD hose coup elbow only 2031069 009 Top housing 2031069 010 Main cpu includes software CD 2031069 011 Expansion cover 2028783 001 Solar to Patient Data Module adapter 2017098 001 2017098 002 2017098 003 2017098 004 2017098 005 ePort to host interface cable 5 ft ePort to host interface cable
28. ODES NBP TUBING AND CUFF PULSE OXIMETRY CABLE AND MASIMO OR NELLCOR PROSES TEMP CABLE AND PROBE OR CARDIAC OUTPUT CABLE AND PROBE OR INV PRESSURE CABLE AND TRANSOUCER 413B The Patient Data Module shares power and communicates with host devices through the host interface connection called the ePort The Patient Data Module connects directly to a transport patient monitor through a docking station The Patient Data Module connects to a bedside host patient monitor through the host interface cable and docking station The Patient Data Module contains software and hardware to monitor the following parameters m ECG respiration m Noninvasive blood pressure m Pulse oximetry 2030047 001A Patient Data Module 2 7 Equipment Overview Up to four channels of invasive blood pressure and cardiac output or two channels of temperature m Defibrillator sync analog out interface 2 8 Patient Data Module 2030047 001A 3 Installation 2030047 001A Patient Data Module 3 1 Installation Battery Test the battery charge Before installing a battery verify the battery s state of charge Press the green TEST button on the battery The number of charge level indicator LEDs that illuminate measures the approximate charge remaining in the battery m Four LEDs illuminated 75 100 of full charge capacity m Three LEDs illuminated 50 74 9 of full charge capacity m Two LEDs illuminated
29. Patient Data Module is intended for use in the electromagnetic environment specified below It is the responsibility of the customer or user to assure that the Patient Data Module is used in such an environment Immunity Test EN 60601 Test Level Compliance Level Electromagnetic Environment Guidance Electrostatic Discharge ESD EN 61000 4 2 6 kV contact 8 kV air 6 kV contact 8 kV air Floors should be wood concrete or ceramic tile If floors are covered with synthetic material the relative humidity should be at least 30 Electrical Fast Transient Burst 2 kV for power supply lines 1 kV for input output lines 2 kV for power supply lines Mains power should be that of a typical commercial or hospital environment EN 61000 4 4 1 kV for input output lines Surge 1 kV differential mode 1 kV differential mode Mains power should be that of a typical commercial or hospital environment EN 61000 4 5 2 kV common mode 2 kV common mode Voltage dips short interruptions and voltage variations on power supply input lines EN 61000 4 11 lt 5 U gt 95 dip in U for 0 5 cycles lt 40 U gt 60 dip in Uy for 5 cycles lt 70 U gt 30 dip in U for 25 cycles lt 5 U 295 dip in U for 5 s lt 5 U 295 dip in U 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 gt 95 dip in U
30. URN To calibrate Analog Out IP measure voltage across the following pins Pin Wire color Signal name 2 Red BP_ANALOG_OUT 6 Green ANALOG_RETURN 5 Type in or use the scroll buttons to enter the measured voltage from the digital voltmeter 6 Click OK to confirm the measured voltage NOTE Perform calibration if the main cpu board is replaced After calibration perform the checkout procedures provided in the host patient monitor service manual 2030047 001A Patient Data Module 4 11 Service Tool and Configuration 4 12 Patient Data Module 2030047 001A 5 Maintenance 2030047 001A Patient Data Module Maintenance Maintenance schedule Manufacturer recommendations To help ensure the equipment remains in proper operational and functional order adhere to a good maintenance schedule The manufacturer recommends that the following be performed by service personnel upon receipt of the equipment every 12 months thereafter and every time the unit is serviced Visual inspection Cleaning Battery maintenance Electrical safety tests See the Solar 8000M i patient monitor v5 service manual Maintenance and checkout chapter for system tests Checkout procedures See the Solar 8000M 1 patient monitor v5 service manual Maintenance and checkout chapter for system tests Manufacturer responsibility Inspection WARNING Failure on the part of all responsible individuals hosp
31. acquired leads Lead label ST deviation current complex superimposed over a reference complex J point indicator and 15 minute mini trends are shown for all acquired leads Measured at user selectable measurement points 0 30 40 50 60 and 80 ms following the J point 12 0 mm to 12 0 mm 0 1 mm 16 beats 12 mm high limit gt low limit for any event within a lead group inferior lateral or anterior that exceeds the alarm limit for that group Pace detection rejection Input voltage range Input pulse width Rise time Over under shoot Mode Standard leads available 2 mV to 700 mV 0 1 ms to 2 ms 10 us to 100 us 2 mV maximum Pacemaker artifact rejection On or Off I II RL LL A 4 Patient Data Module 2030047 001A Appendix A Technical Specifications Respiration Respiration range limit 1 to 200 breaths minute Respiration rate accuracy 0 to 120 breaths minute 1 121 to 200 breaths minute 3 Impedance range 100 to 1500 Ohms at 52 6 KHz Detection sensitivity range 0 4 to 10 Ohms impedance variation Respiration rate alarm 1 to 200 breaths minute range No breath alarm range 3 to 30 seconds Temperature Number of channels Up to 2 with Y adapter cable Input specifications Probe type Series 400 or 700 determined by input cable Temperature range 0 C to 45 C 32 F to 113 F Resolution 0 01 C internal
32. atient processes the patient data signals and stores a limited amount of patient data 24 hours captured at 1 minute resolution for seamless transport Front view 5 6 4 4048 1 Expansion cover expansion mount for future expansion modules 2 Communication icon and indicator 3 Power icon and indicator 4 Power ON IBP Zero All button 5 Patient cable connectors 6 Defib Sync for auxiliary equipment 2 2 Patient Data Module 2030047 001A Equipment Overview Rear view aia a 1 ePort host interface connection 405B 2 Battery door Side view 406A 1 Expansion cover 2 Docking station 3 Pull tab 2030047 001A Patient Data Module 2 3 Equipment Overview Controls Indicators Communication Power Connector The power zero all key has a dual role as a power on and zero all Power on Turns the data acquisition function ON Power is derived from a battery or patient monitor When turned on the function changes to the zero all function Zero all Zeros all invasive pressure lines which are open to atmosphere Each pressure can also be zeroed if desired with a menu option in the pressure menu The following LED condition identifies the communication status with a bedside or transport patient monitor No light indicates no communication Solid amber indicates an application reset Solid green indicates communication
33. ces Local Sy Alerter Notifies sel Manual LocalSyster Sa Application Manage Provides s Manual LocalSyster By Ati HotKey Poller Started Automatic LocalSyste Sy Automatic Updates Enables th Started Automatic LocalSyster By Background Intellig Transfers f Manual LocalSyster BlackICE t Automatic Ba Cisco Systems Inc Started Automatic LocalSyster a ClipBook Supports C Manual LocalSyster By com Event System Provides a Started Manual LocalSyster Sy Computer Browser Maintains a Started Automatic LocalSyster Bs Def Watch Started Automatic LocalSyster Bs DHCP Client Manages n Started Automatic LocalSyster Sy Distributed Link Tra Sends notif Started Automatic LocalSyster Bs Distributed Transac Coordinate Manual LocalSyster AAA AA A 455A 3 Inthe specific service e g BlackICE and Security Accounts Manager properties window select Stop BlackICE Properties Local Computer General Log On Recovery Dependencies Service name BlackICE Display name BlackICE Description Path to executable C Program Files Network ICE BlackICE blackd exe Click Stop Startup type Automatic y Started tus Start from here Start parameters 4 Verify that the Service status reads Stopped Stop Pause Resume You can specify the start parameters that apply when you start the service 456A 2030047 001A Patient
34. ction Gain accuracy Linearity deviation Noise 0 5 mV to 5 mV 40 ms to 120 ms Q to S 30 to 300 beats per minute 90 dB minimum at 60 Hz 5 diagnostic mode 5 lt 30 uV referred to input Output specifications Frequency response Monitoring mode 0 05 to 100 Hz 0 05 to 40 Hz 0 05 to 25 Hz Diagnostic mode 0 05 to 150 Hz Analog output Selectable at 1V mV Defibrillator sync analog out delay lt 35 ms Sampling rate Monitoring mode 240 samples second Diagnostic mode 500 samples second 2030047 001A Patient Data Module A 3 Appendix A Technical Specifications Heart rate Heart rate averaging 8 4 beats Display update interval 2 seconds Heart rate accuracy 1 or 1 beat minute whichever is greater Response time lt 6 seconds Limit alarm delay lt 10 seconds after limit alarm condition exceeded Heart rate alarm range 0 to 300 beats minute high limit gt low limit Arrhythmia analysis 1 to 100 PVCs minute Method QRS morphology classification and timing based on single or multiple lead analysis Arrhythmia calls Full lethal only or no arrhythmia PVC alarm limit range 1 to 100 PVCs minute ST Segment analysis Measurement description ST display Measurement point Measurement range Display resolution ST measurement averaging ST alarm limits ST segment deviation is measured and displayed for all
35. cy 0 5 C 17 C to 30 C Injectate temperature range 0 C to 30 C 32 F to 86 F Injectate temperature accuracy 0 3 C Cardiac output review Accept reject individual measurements and store average Catheter sizes 5 6 7 7 5 or 8 French Injuectate volume selections 3 5 or 10 IEC EN UL 60601 1 CAN CSA C22 2 No 601 1 IEC EN 60601 1 2 IEC EN 60601 2 27 IEC EN 60601 2 30 IEC EN 60601 2 34 IEC EN 60601 2 49 IEC EN 60601 2 51 EN 12470 4 EN ISO 9919 ANSI AAMI SP10 ANSI AAMI EC11 ANSI AAMI EC13 CE Marking Medical Devices Directive 93 42 EEC JJG 760 YY 91079 Patient Data Module 2030047 001A Appendix A Technical Specifications Warranty One year warranty 2030047 001A Patient Data Module A 11 Appendix A Technical Specifications A 12 Patient Data Module 2030047 001A Appendix B Electromagnetic Compatibility 2030047 001A Appendix B Electromagnetic Compatibility Electromagnetic compatibility EMC Changes or modifications to this system not expressly approved by GE 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 e
36. e avoided NOTE For additional information refer to the How the Reach Us page in the manual for contact information 5 4 Patient Data Module 2030047 001A Maintenance Expansion interface cleaning Under normal operation the expansion interface should not require cleaning If the expansion interface does require cleaning follow these instructions CAUTION m The expansion interface is not waterproof Do not let fluids enter the electronics through the expansion interface Do not spray fluid into the expansion interface Cleaning the expansion interface in a manner other than that specified below may cause the unit to malfunction and void the warranty 1 Use a cellular urethane cleaning swab lightly moistened with one of the following solutions recommended in the APIC Guidelines for Selection and Use of Disinfectants 1996 m Sodium hypochlorite 5 2 household bleach minimum 1 500 dilution minimum 100 ppm free chlorine and maximum 1 10 dilution m Any sodium hypochlorite wipe product that meets the above guidelines NOTE Wring excess disinfectant from cloth before using Contact of disinfectant solutions with metal parts may cause corrosion Do not damage or bend connector pins when cleaning or drying 2 Insert the swab under the expansion interface to clean 484A NOTE Avoid inserting the swab toward the rear of the expansion interface where connector pins can be damaged 3 Do n
37. eenen ennen 1 5 Service requirements eene eeen 1 5 Equipment Identification LL 1 6 Equipment Overview 2 020ee eee eeeee 2 1 Oveni ew En As Aerde dee Da ee eek eee tls a ai a eed 2 2 Front VIEW Ai 4 arne dere ner aa a aA earn atl Bice ie wee 2 2 REAM VIEW tnt edt amen aa ae 2 3 Sd MEW rn eten er a Baren tra dee ee legden 2 3 COMO ES ns ansi a E a al Ole AR bek a A it tee 2 4 indicators Lai i are ir eer an Aa a a aed 2 4 CONECO cer T AEF cur 2 4 Basic components 5 soan oeren erva a a a a a ia per 2 5 BAON cake latvia A dank Oe er A 2 5 Patient Data Module ePort host interface cable 2 5 Docking Stations unt toer a asi a i e A as i a eed 2 5 Theory of operatio kits er oreert skai ee 2 7 O zi Zr aard retard suede edet A aa ka aki Means 2 7 Installation Ziet wrr ebde benee mad 3 1 Battery znne A tienes dea 3 2 Test the battery charge _ oes ven sane ern ws eaten an 3 2 Install or change the battery 00 eee eee 3 2 Software saneren A dee ded 3 3 Mounting options ooooococconccoon ainas 3 3 2030047 001A Patient Data Module Connect to host patient monitor ooo 3 5 Connect to transport bedside monitor cece eee eee 3 5 Connect to bedside monitor 000 c eee e eee eee 3 5 Service Tool and Configuration 4 1 OVERVIEW serene a a 4 2 Required equipment LL iii 4 2 Setup the PC ostia eae we een een o A EE 4 2 Connect the PC to the Patient Data Module
38. efore using the equipment Defibrillator proof type CF equipment type CF equipment is specifically designed for applications where a conductive connection directly to the heart is established The paddles indicate the equipment is defibrillator proof Defibrillator proof type BF equipment type BF equipment is specifically designed for applications intentional external and internal application to the patient excluding direct cardiac application Type BF equipment is type B equipment with an F type isolated floating part The paddles indicate the equipment is defibrillator proof Medical Equipment With respect to electric shock fire and mechanical hazards only in accordance with UL 60601 1 CAN CSA C22 2 NO 601 1 IEC 60601 1 IEC 60601 2 27 IEC 60601 2 30 IEC 60601 2 34 and IEC 60601 2 49 This symbol indicates that the waste of electrical and electronic equipment must not be disposed as unsorted municipal waste and must be collected separately Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment This symbol indicates the date of manufacture of this device The first four digits identify the year and the last two digits identify the month 1 4 Patient Data Module 2030047 001A Introduction Battery Communication Power A ePort connection f Zero all Service information Service requirements Refer e
39. electromagnetic environment on which radiated RF disturbances are controlled The customer or the user of the Patient Data Module can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment B 4 Patient Data Module 2030047 001A Appendix B Electromagnetic Compatibility transmitters and the Patient Data Module as recommended below according to the maximum output power of the communications equipment Separation Distance in Meters m According to Frequency of Transmitter Rated Maximum Output Power of Transmitter in 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz W 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 aAt 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 P is 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 Compliant cables and accessories WARNING The use of accessories
40. erve the following guidelines when disassembling the Patient Data Module m Note the positions of wires cables and different sized screws marking them if necessary to ensure they are replaced correctly m Do not kink pinch stretch twist or tightly fold a flex cable Electrostatic discharge ESD precautions All external connectors of the Patient Data Module are designed with protection from ESD damage However if the module requires service exposed components and assemblies inside are susceptible to ESD damage This includes human hands non ESD protected work stations or improperly grounded test equipment 2030047 001A Patient Data Module 7 3 Field Replaceable Units The following guidelines may not guaranty a 100 static free workstation but can greatly reduce the potential for failure of any electronic assemblies being serviced m Discharge any static charge you may have built up before handling semiconductors or assemblies containing semiconductors m A grounded antistatic wristband 3M part number 2046 or equivalent or heel strap should be worn at all times while handling or repairing assemblies containing semiconductors Use properly grounded soldering and test equipment Use a static free work surface 3M part number 8210 or equivalent while handling or working on assemblies containing semiconductors m Do not remove semiconductors or assemblies containing semiconductors from antistatic containers Velo sta
41. imo patents 70 to 100 SpO2 2 lt 69 SpO2 Unspecified 3 beats per minute without motion 5 beats per minute with motion This device is covered under one or more of the following U S A patents 5 758 644 5 823 950 6 011 986 6 157 850 6 263 222 6 501 975 and other applicable patents listed at http www masimo com patents htm Nellcor range SpO2 1 to 100 Pulse rate 20 to 250 beats per minute Nellcor accuracy 70 to 100 SpO2 Adult 2 neonatal 3 lt 69 SpO2 Unspecified Pulse rate 3 beats per minute without motion Analog output Selectable saturation 0 to 100 equivalent 0 to 1V Alarm limit range SpO2 0 to 100 PPR 0 to 350 beats per minute Messages NO SENSOR DEFECTIVE SENSOR SENSOR OFF UNRECOGNIZED SENSOR LOW PERFUSION PULSE SEARCH INTERFERENCE DETECTED AMBIENT LIGHT LOW SIGNAL IQ Nellcor PROBE OFF PATIENT LOW QUALITY PULSE SEARCH TRefer to manufacturer s specifications for probe accuracy statement 2030047 001A Patient Data Module A 9 Appendix A Technical Specifications Cardiac output Certifications Method Thermodilution Parameters Displayed Cardiac output blood temperature injectate temperature real time cardiac output washout curve last average CO Cardiac output range 0 2 to 15 liters per minute Blood temperature range 17 C to 42 C 62 F to 107 F Blood temperature accura
42. ion Check for damage to the ePort interface on the Patient Data Module If damaged contact GE technical support to service the Patient Data Module See the How to Reach Us page included with this manual for contact information Check the Patient Data Module s battery following steps in the Battery is not charging section in this table No communication indicators LEDs not illuminated O At the patient monitor check the M Port status LED If it is not green go to the Solar 8000M i patient monitor service manual Troubleshooting chapter for further information Follow steps in the No power section in this table No parameters 4 Check for damage to the parameter cable s If damaged replace cables Check for damage to the parameter interface lf damaged contact GE technical support to service the Patient Data Module See the How to Reach Us page included with this manual for contact information Check for licensing using the GEHC MS service tool See chapter 4 Service Tool and Configuration Go to Configuration gt Licensing If license is not activated install the license s Check that the patient monitor is configured to display the parameter Noisy waveforms missing markers or inaccurate patient data Check for ECG configuration filter using the GEHC MS service tool See chapter 4 Service Tool and Configuration as follows 1 2 3 Go to Configuration gt
43. itals or institutions employing the use of this device to implement the recommended maintenance schedule may cause equipment failure and possible health hazards The manufacturer does not in any manner assume the responsibility for performing the recommended maintenance schedule unless an Equipment Maintenance Agreement exists The sole responsibility rests with the individuals hospitals or institutions utilizing the device Remove power and all cables before inspecting or cleaning the equipment Inspect the equipment and its components carefully prior to installation once every 12 months thereafter and each time the equipment is serviced Do not use the equipment if damage is determined Refer damaged equipment to qualified service personnel m Inspect the case for cracks or other physical damage m Inspect cables for fraying or other damage m Inspect all plugs and connectors for bent pins or other damage m Check for loose or missing screws on the mounting hardware NOTE Damaged cables or equipment should be replaced by service personnel 5 2 Patient Data Module 2030047 001A Maintenance Cleaning Precautions Improper cleaning methods can result in degradation of the equipment performance and or failure To avoid damage to the equipment Cleaning procedures Never use conductive solutions solutions that contain chlorides wax or wax compounds to clean the equipment Never immerse equipment in any
44. liquid Never pour or spray any liquid on the equipment or permit fluid to seep into connections or openings Never autoclave or steam clean the equipment Never use the following solutions acetone Bentadine ketone alcohol based cleaners sodium salts abrasive cleaners or any type of Ammonium Chloride such as Dimethyl Benzyl Ammonium Chloride or Quaternary Ammonium Chloride Never connect the device to a patient until it is thoroughly dry CAUTION Failure to follow these rules may melt distort or dull the finish of the case blur lettering on the labels or cause equipment failures Remove power all cables and batteries Close the battery door Wipe the exterior with a soft lint free cloth using one of the following solutions recommended in the APIC Guidelines for Selection and Use of Disinfectants 1996 m Sodium hypochlorite 5 2 household bleach minimum 1 500 dilution minimum 100 ppm free chlorine and maximum 1 10 dilution m Any sodium hypochlorite wipe product that meets the above guidelines NOTE Wring excess disinfectant from cloth before using Contact of disinfectant solutions with metal parts may cause corrosion Do not damage or bend connector pins when cleaning or drying Allow solution to remain on device for a minimum of one minute or per hospital guidelines Do not let fluid pool around connection pins If this happens blot dry with a cotton swab or soft cloth Shake out e
45. mitting 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 Patient Data Module is intended for use in the electromagnetic environment specified below It is the responsibility of the customer or user to assure that the Patient Data Module is used in such an environment Flicker Emissions EN 61000 3 3 Emissions Test Compliance Electromagnetic Environment Guidance RF Emissions Group 1 The equipment uses RF energy only for its internal function Therefore its RF emissions are very low and are not likely to cause any interference in nearby EN 55011 electronic equipment RF Emissions Class A EN 55011 Harmonic Emissions Class A The equipment is suitable for use in all establishments other than domestic and those directly connected to the public low voltage power supply network that EN 61000 3 2 supplies buildings used for domestic purposes Voltage Fluctuations Complies B 2 Patient Data Module 2030047 001A Appendix B Electromagnetic Compatibility Guidance and manufacturer s declaration electromagnetic immunity The
46. n Asset Settings 434A The Configuration category consists of Asset Settings ECG Filter Config Licensing and Software Transfer modules The Asset Settings module displays the manufacturer s serial number and the user assigned asset number 1 Enter the serial number and click Submit NOTE The manufacturer s serial number must follow the specific format found on the serial number label on the Patient Data Module The manufacturer s serial number must be edited if the main cpu board is replaced serial number Ei 464A 2 Enter the user assigned asset number and click Submit NOTE The user assigned asset number can be up to 13 alphanumeric characters 4 8 Patient Data Module 2030047 001A Service Tool and Configuration ECG Filter Config The ECG Filter Config module allows configuration of the power frequency and ECG filter The power frequency of the Patient Data Module must match the power frequency of the host patient monitor The ECG filter is always enabled It can be disabled temporarily but it will always default to Enabled after a power cycle or reboot CAUTION Do not disable ECG Filter during clinical use Licensing The Licensing module is used for activating or removing license s To obtain a license contact GE technical support and provide the Patient Data Module serial number and MAC address See the How to Reach Us page included with this manual
47. n or press Enter on the keyboard Username biomed Password ChangeMe 4 6 Patient Data Module 2030047 001A Service Tool and Configuration NOTE Username and password are case sensitive Username and password cannot be created edited or deleted 433A Service tool modules The GEHC MS Service Tool has four categories Device Information Configuration Diagnostics and Calibration Each category contains module s for servicing the Patient Data Module Click on the category tab then the module The following is a brief overview of these modules NOTE Some information displayed in the module only updates in 30 second intervals The GEHC MS Service Tool provides a basic description of each module in the Help file From the toolbar in the module click Help gt Help Device Information The Device Information module displays general information about the Patient Data Module and calibration information It also displays the last date and times that NBP calibration analog out IP calibration and analog out ECG calibration was performed NOTE To print the Device Information page connect a parallel printer or enable a network port that has connectivity to a network printer Click File gt Print After printing disconnect or disable the network port used for printing to prevent inadvertent access to the Patient Data Module 2030047 001A Patient Data Module 4 7 Service Tool and Configuration Configuratio
48. n time m NBP Deflate Valve Cycle Count m NBP Dump Valve Cycle Count m NBP Pump Cycle Count NOTE Some Patient Data Module statistics only update every 30 seconds After replacing the NBP pump assembly clear all NBP statistics and perform the checkout procedures provided in the host patient monitor service manual If a value in the Service Metrics module is out of specification the data field will be highlighted red Contact GE technical support See the How to Reach Us page included with this manual for contact information Calibration The Calibration category consists of Analog Out ECG Calibration and Analog Out IP Calibration The following additional equipment in required to perform this calibration m Unterminated defib sync cable 2017842 001 part of the Patient Data Module Service Tool Kit m Digital voltmeter 1 Connect the unterminated cable to the Defib Sync connector on the front of the Patient Data Module 2 Click Start Calibration to begin the calibration process 3 Follow instructions displayed on screen NOTE To abort the calibration process with no changes press Stop Calibration 4 10 Patient Data Module 2030047 001A Service Tool and Configuration 4 Measure voltages indicated below using the digital voltmeter 435A To calibrate Analog Out ECG measure voltage across the following pins Pin Wire color Signal name 1 Brown ECG_ANALOG_OUT 6 Green ANALOG_RET
49. ot let fluid pool around connection pins If this happens blot dry with a cotton swab or soft cloth Shake out excess liquids from connector recesses 2030047 001A Patient Data Module 5 5 Maintenance Wipe off cleaning solution with a clean moist swab Dry thoroughly with a clean dry swab and let air dry for at least 30 minutes Do not apply heat NOTE Drying times may vary based on the environmental conditions Battery compartment cleaning Sterilization Under normal operation the battery compartment should not require cleaning If the battery compartment does require cleaning follow these instructions CAUTION m The battery compartment is not waterproof m Do not let fluids enter the electronics through the air holes in the battery compartment floor m Cleaning the battery compartment in a manner other than that specified below may cause the unit to malfunction and void the warranty Remove the battery from the battery compartment Clean the device with a gauze pad or cloth lightly moistened with one of the following m Water m Soap Use a cloth lightly moistened with distilled water to rinse away the cleaning solution Make sure moisture does not enter the electronics area below the battery compartment floor Dry thoroughly with a lint free cloth Allow the battery compartment to air dry completely prior to closing the compartment door NOTE EtO sterilization is not recommended
50. ow to Reach Us page included with this manual for contact information Check that the battery is charging by inserting a known good battery in the Patient Data Module If not charging contact GE technical support to service the Patient Data Module See the How to Reach Us page included with this manual for contact information Check that the battery is fully charged by pressing the TEST button on the battery If the LED is not at 100 go to Battery care on page 5 7 for further charging and conditioning procedures Check for damage to the battery connector and external surfaces If damaged replace the battery Check that the battery is charging with the GE approved battery charger See Battery care on page 5 7 for procedures If not charging replace the battery External surface is damaged Check the Patient Data Module s top housing as follows 1 Check for cracks or other damage to the top housing If damaged replace the top housing See chapter 7 Field Replaceable Units for ordering parts and replacement procedures Check for cracks or other damage to the bottom housing If damaged contact GE technical support to service the Patient Data Module See the How to Reach Us page included with this manual for contact information NBP is not functioning Check the NBP calibration date and time as follows 1 Check the NBP performance as follows 1 Use the GEHC MS service tool See cha
51. pressure all except catheter tip transducers Excitation voltage 2 5 V dc 0 1 Transducer output 50 uV V cm Hg Input specifications Range 25 mmHg to 349 mmHg Offset 150 mmHg A 6 Patient Data Module 2030047 001A Appendix A Technical Specifications Output specifications Frequency response Zero balance range Zero balance accuracy Accuracy Displayed frequency response Display scale selections Analog output Alarms Alarm range dc to 40 Hz 0 3 dB 150 mmHg 1 mmHg 2 or 1 mmHg which ever is greater exclusive of transducer 0 to 12 Hz or 0 to 40 Hz 3dB user selectable 0 30 0 40 0 60 0 100 0 160 0 200 0 300 mmHg 1 V 100 mmHg User selectable upper and lower limits for systolic diastolic and mean pressures 99 to 350 mmHg Non invasive blood pressure Measurement technique Oscillometric Displayed parameters Systolic diastolic and mean pressures pulse rate time of last measurement Measurement modes Manual Auto and Stat Heart rate detection Adult pediatric and neonate 30 to 240 beats per minute Total cycle time 20 to 40 seconds typical dependent on heart rate and motion artifact 2030047 001A Patient Data Module A 7 Appendix A Technical Specifications Systolic pressure range Diastolic pressure range Mean pressure range Cuff pressure range Adult 30 to 29
52. pter 4 Service Tool and Configuration and go to the Device Information module If NBP is not calibrated perform the NBP calibration according to the procedures in the Solar 8000M i service manual Maintenance and checkout chapter Go to the Solar 8000M i patient monitor service manual Maintenance and checkout chapter and perform the NBP calibration check If NBP pressure is leaking not maintaining CUFF pressure for at least one minute check for leakage on the NBP cuff Listen for hissing as air escapes If the cuff is not leaking use the GEHC MS service tool See chapter 4 Service Tool and Configuration and go to Diagnostics gt Service Metrics See Diagnostics on page 4 10 Record the NBP statistics information for trending Replace the NBP assembly with manifold See chapter 7 Field Replaceable Units for ordering parts and replacement procedures 2030047 001A Patient Data Module 6 3 Troubleshooting Problem Solution No power Check for damage to the ePort to host interface cable If damaged replace the cable Check for damage to the Tram net port on the patient monitor If damaged go to the Solar 8000M i patient monitor service manual Field replaceable units chapter for ordering parts Connect a known good Patient Data Module to the patient monitor If the Patient Data Module is not powering go to the Solar 8000M i patient monitor service manual Troubleshooting chapter for further informat
53. quipment servicing to GE s authorized service personnel only Any unauthorized attempt to repair equipment under warranty voids that warranty m tis the user s responsibility to report the need for service to GE Medical Systems Information Technologies or to one of their authorized agents m Failure on the part of the responsible individual hospital or institution using this equipment to implement a satisfactory maintenance schedule may cause undue equipment failure and possible health hazards m Regular maintenance irrespective of usage is essential to ensure that the equipment is always functional when required 2030047 001A Patient Data Module 1 5 Introduction Equipment Identification Every GE Medical Systems Information Technologies device has a unique serial number for identification A sample of the information found on a serial number label is shown below HHH HH HH HHH H H rel T Description Product code Year manufactured Fiscal week manufactured Production sequence number 5 Manufacturing site 6 Miscellaneous characteristic Product code for the Patient Data Module is SA3 1 6 Patient Data Module 2030047 001A 2 Eguipment Overview 2030047 001A Patient Data Module Equipment Overview Overview The Patient Data Module is a data acquisition device for a GE modular system It provides a connection from the host monitor to the p
54. rtifications rte entel ante Meente eed A 10 Warranty aardnesten Ar T A 11 2030047 001A Patient Data Module i iii Appendix B Electromagnetic Compatibility B 1 Electromagnetic compatibility EMC Guidance and manufacturer s declaration electromagnetic emissions B 2 Guidance and manufacturer s declaration electromagnetic immunity B 3 Recommended separation distances Compliant cables and accessories L aaa eee nen B 5 I IV Patient Data Module 2030047 001A 1 Introduction 2030047 001A Patient Data Module Introduction Manual information Revision history Manual purpose Intended audience Ordering manuals Each page of this manual has the document part number and revision letter at the bottom of the page The revision letter identifies the document s update level The revision history of this document is summarized below Revision Comments A Initial release This manual provides technical information for service representatives and technical personnel for maintaining the equipment This manual is intended for service representatives and technical personnel who install configure maintain administer troubleshoot or repair this equipment A paper copy of this manual will be provided upon request Contact your local GE representative and request the part number on the first page of the manual Safety information Responsibility of the manufacturer
55. sory has been performed in accordance to the appropriate IEC 60601 1 and or IEC 60601 1 1 harmonized national standard If the installation of the equipment in the USA will use 240V rather than 120V the source must be a center tapped 240V single phase circuit Warnings and Cautions are used throughout this manual and designate a degree or level of hazardous situations A hazard is defined as a source of potential injury to a person DANGER DANGER indicates an imminent hazard which if not avoided will result in death or serious injury WARNING WARNING indicates a potential hazard or unsafe practice which if not avoided could result in death or serious injury CAUTION CAUTION indicates a potential hazard or unsafe practice which if not avoided could result in minor personal injury or product property damage NOTE A NOTE provides application tips or other useful information 2030047 001A Patient Data Module 1 3 Introduction Patient Data Module hazards WARNING ACCIDENTAL SPILLS To avoid electric shock or device malfunction liquids must not be allowed to enter the device If liquids have entered a device take it out of service and have it checked by a service technician before it is used again Equipment symbols The following symbols appear on the equipment 109 EN c US 4P41 2006 08 ATTENTION Consult accompanying documents b
56. strengths from fixed RF transmitters as determined by an electromagnetic site surveys should be less than the compliance level in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol V Note 1 At 80 MHz and 800 MHz the higher freguency 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 eguipment 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 Over the frequency range 150 KHz to 80 MHz field strengths should be less than 3 V m Recommended separation distances The following table provides the recommended separation distances in meters between portable and mobile RF communications equipment and the Patient Data Module The Patient Data Module is intended for use in the
57. t Start gt Settings gt Control Panel gt Control Panel gt Network Network and Dial up Connections Connections 6 Right click Local Area Connection Te Select Properties 8 Select Internet protocol TCP IP 9 Click Properties 10 Select Use the following IP address 11 In the IP address field type 192 168 252 95 12 In the Subnet mask field type 255 255 255 0 13 If prompted to restart the PC select Yes 18 Continue with the instructions Disable firewall and networking services on page 4 4 Disable firewall and networking services If your PC is running any firewall protection or networking services such as Cisco Systems VPN BlackICE Security Accounts Manager or a wireless network card perform the following procedure to disable these services on the PC 1 Select one of the following from the toolbar m In Windows XP select Start gt Control Panel gt Administrative Tools gt Services m In Windows 2000 select Start gt Settings gt Control Panel gt Administrative Tools gt Services 2 In the list of available firewall and networking services double click the service e g Black ICE and Security Accounts Manager to be disabled 4 4 Patient Data Module 2030047 001A Service Tool and Configuration E e lO x Action View Les eme BB 2 nm Tree Name Description status startup Type togonas Servi
58. t bags until absolutely necessary m Make sure power to an assembly is turned off before removing or inserting a semiconductor m Do not slide semiconductors or electrical electronic assemblies across any surface Do not touch semiconductor leads unless absolutely necessary Semiconductors and electronic assemblies should be stored only in antistatic bags or boxes Handle all PCB assemblies by their edges Do not flex or twist a circuit board Replacement procedures Battery Unless otherwise stated reassemble the Patient Data Module in reverse order of disassembly 1 Open the battery door by gently pulling on the battery door pull tab 862A 2 Pull the battery tray out of the Patient Data Module using the battery tray strap and remove the battery 3 Insert the new battery with the test button facing up and the arrow pointing into the Patient Data Module 74 Patient Data Module 2030047 001A Field Replaceable Units 855A 4 Press the battery door closed until it seals the battery compartment WARNING PHYSICAL INJURY Make sure the battery is completely inserted and that the battery door is securely sealed Falling batteries could seriously or fatally injure neonatal or other vulnerable patients 5 Press the Power button on the Patient Data Module 6 Verify that the Power LED illuminates amber while the Patient Data Module boots up then illuminates green Power LED 404B
59. the Patient Data Module There are two ways to connect the PC to the Patient Data Module One method uses power from the Solar 8000M i patient monitor the other method uses an external power supply 4 2 Patient Data Module 2030047 001A Service Tool and Configuration crossover cable ePort to host cable 430A ePort to host cable external power supply 431A Power from external power supply 1 Connect the category 5 crossover cable between the PC network port and the PDM service adapter 2 Connect the ePort to host interface cable between the ePort on the Patient Data Module and the ePort connector on the PDM service adapter 3 Ifthe PDM service adapter is not connected to a Solar 8000M i patient monitor connect the external power supply to the PDM service adapter 4 Remove the Patient Data Module battery 5 Press the power button on the Patient Data Module 6 Power on the PC 2030047 001A Patient Data Module 4 3 Service Tool and Configuration Change the PC s IP address NOTE Disable all network ports on the PC except the Patient Data Module connection Windows XP Windows 2000 1 From the toolbar select Start gt Run 2 Type cmd and press Enter 3 Type ipconfig lt space gt all and press Enter 4 If the IP address and subnet mask are defined record them m IP address m Subnet mask 5 From the toolbar select Start gt From the toolbar selec
60. tient monitor 5 8 Patient Data Module 2030047 001A Maintenance Recycle the battery Recycle the battery when it no longer holds a charge Remove the battery from the Patient Data Module and follow your local recycling guidelines WARNING EXPLOSION HAZARD Do not incinerate the battery or store at high temperatures Serious injury or death could result In the United States and Canada the Rechargeable Battery Recycling Corporation RBRC can help locate your nearest rechargeable battery collection site Contact them by m telephone 1 800 8 BATTERY 800 822 8837 m internet www rbrc org Checkout procedures and NBP calibration GE recommends that qualified service personnel perform system checkout procedures including electrical safety tests parameter tests and NBP calibration found in the Solar 8000M i patient monitor service manual upon receipt of the equipment every 12 months thereafter any time the equipment is serviced or any time the validity of the NBP pressure readings is in doubt 2030047 001A Patient Data Module 5 9 Maintenance 5 10 Patient Data Module 2030047 001A 6 Troubleshooting 2030047 001A Patient Data Module Troubleshooting Overview The problems and solutions in this chapter represent only a few of the faults that you may encounter and are not intended to cover every possible problem that may occur Required tools and equipment Before
61. ulti Link MiniGrab Ld 74cm 29 in Lead wire set 3 lead Multi Link adult graber Ld II 74 cm 29 in Lead wire set Multi Link individual grabber 130 cm 51 in Lead wire set Multi Link individual snap 130 cm 51 in Lead wire set Multi Link individual grabber V2 V6 130 cm 51 in Lead wire set 5 lead Multi Link snap 130 cm 51 in Lead wire set 5 lead Multi Link group snap 130 cm 51 in Lead wire set 3 lead Multi Link group snap 130 cm 51 in Lead wire set Multi Link neonatal mini clip DIN 60 cm 24 in Lead wire set Multi Link banana limb leads 130 cm 51 in Lead wire set Multi Link banana V leads C leads 130 cm 51 in Lead wire set Multi Link radiotranslucent grabber 1 6 m 60 in Lead wire set 6 lead Multi Link snap 130 cm 51 in Lead wire set 6 lead Multi Link grab 130 cm 51 in 10 lead banana AHA RL V6 130 cm 51 in Invasive BP Cables and Transducers IP cable Utah 3 6 m 12 ft IP cable Spectramed 3 6 m 12 ft IP cable Abbott Transpac lll 3 6 m 12 ft IP cable bifurcated dual BP adapter 30 cm 12 in Care IP cable Utah 3 6 m 12 ft Care dual IP cable Utah 3 6 m 12 ft B 6 Patient Data Module 2030047 001A Appendix B Electromagnetic Compatibility Category Description Maximum Lengths Care IP cable Abbott Transpac IV 36m 12ft Care dual IP cable Abbott Transpac IV 36m 12ft Care IP Edwards Life Sciences Truwave adapter cable 36m 12ft Care dual IP Ed
62. umb toe sensor N A Nellcor OxiMax MaxFast forehead sensor N A Nellcor OxiMax adhesive sensor adult N A Nellcor OxiMax adhesive sensor adult long N A B 8 Patient Data Module 2030047 001A Appendix B Electromagnetic Compatibility Category Description Maximum Lengths Nellcor OxiMax adhesive sensor pediatric N A Nellcor OxiMax adhesive sensor infant N A Nellcor OxiMax adhesive sensor neonatal N A Nellcor OxiMax adhesive sensor nasal N A SC PR N A Nellcor SoftCare nonadhesive sensor neonate N A Nellcor SoftCare nonadhesive sensor adult N A Nellcor Durasensor DS 100A finger clip sensor reusable N A adult Nellcor Oxiband OXI A N adult neonatal reusable N A Nellcor Oxiband OXI P l pediatric infant reusable N A Nellcor Dura Y D YS multi site sensor N A Nellcor D YSE ear clip for Dura_Y sensor N A Nellcor PediCheck D YSPD pediatric spot check sensor N A Nellcor OxiClig adhesive sensor adult N A Nellcor OxiClig adhesive sensor neonatal adult N A Nellcor OxiClig adhesive sensor infant N A Nellcor OxiCliq adhesive sensor pediatric N A Accessories Cable defib sync to unterminated end 15 4 6m 15 ft Cable defib sync to Physio Control 15 4 6m 15 ft Cable defib sync to DataScp 95 31 9 5m 31 ft Cable defib sync to AAMI 6P ECG 4 6 m 4 6m 15 ft Cable defib sync to HP Philips 18 5 5m 18 ft ePort cable 7 6 m 25 ft
63. using main board NBP hose coupling and elbow per above steps 2 Remove 4 screws from the battery cover Battery cover Front panel board connector Main board flex pump connector 467A 3 Grasp and slide the battery cover out to the rear 4 Remove screw under the pump tube connection 466A 5 Lift off the manifold with pump 6 Remove the interface gasket 2030047 001A Patient Data Module 7 13 Field Replaceable Units Interface gasket 478A 7 Before installing the NBP assembly with manifold a Make sure the pump and manifold are fully seated together b Make sure the gasket is in place c Position the manifold and pump in the bottom housing and carefully press to seat connector d Install the screw then connect the hose Slide hose all the way onto the manifold fitting so that the hose lays flat e Make sure the pump is resting between the positioning protrusions 8 After replacing the NBP assembly with manifold use the GEHC MS service tool to clear all NBP statistics and perform the checkout procedures in the Solar 8000M i service manual Maintenance and checkout chapter 7 14 Patient Data Module 2030047 001A A Appendix A Technical Specifications Appendix A Technical Specifications Technical Specifications Physical Height 7 0 cm 2 75 in Width 14 6 cm 5 75 in Depth 21 6 cm 8 5 in Weight 1 1 kg 2 5 Ibs without optional battery 1 3 kg 2
64. wards Life Sciences Truwave adapter 3 6 m 12 ft cable Care IP Spectramed cable 3 6 m 12 ft Care dual IP Spectramed cable 3 6 m 12 ft Utah Disposable transducers N A Spectramed transducers N A Abbott Transpac lll transducers N A Edwards Truwave transducers N A Cardiac Output Cables and Probes Cardiac Output Cable 3 6 m 12 ft Cardiac Output Probe 2 4m 8 ft Temperature Cables and Probes Dual Temp Cable 20 cm 8 in Dual Temp Cable 1 2m 4ft Temp Probe Interconnect cable 400 series 3 6 m 12 ft Care cable dual temp 400 700 series 0 5m 1 6 ft Care cable temp 400 700 series 0 5m 1 6 ft Care cable temp single to disp 400 700 series 3 6 m 12 ft SpO2 cables and sensors Cable Masimo LNC 10 GE connector 3 0 m 9 8 ft Patient adapter cable Nellcor DIGICAL 3m one wire 3 0 m 0 8 ft removed Care SpO2 patient adapter cable Masimo 3 6 m 12 ft Care SpO2 patient adapter cable Nellcor DIGICAL 3 6 m 12 ft Masimo disposable adhesive sensor LNOP ADT adult N A Masimo disposable adhesive sensor LNOP PDT N A pediatric Masimo disposable adhesive sensor bridge LNOP Neo N A neonatal Masimo disposable adhesive sensor LNOP NeoPt L N A neonatal Masimo reusable multsite sensor LNOP YI N A Masimo reusable sensor pediatric N A 2030047 001A Patient Data Module B 7 Appendix B Electromagnetic Compatibility
65. waren aen 6 1 e a la nnn ener eene ene een an enn ee 6 2 Required tools and equipment en 6 2 Before you begin erisera rare aaiae aai a e eeen 6 2 Problems and solutions oocooocccooo o 6 3 ErrOor MeSSAadeS cc enne nere eaten et ee 6 5 7 Field Replaceable Units 7 1 Ordering PartS Ziemia asa i entente iS 7 2 PariSi is are ae eg A ii 7 2 Disassembly guidelines oooooocoorrcaraaa 7 3 Tools requir d oia ci A ere ee a 7 3 Before disassembly eneen 7 3 Hardware precautions eee 7 3 Electrostatic discharge ESD precautions Ls 7 3 Replacement procedures oaeen 7 4 Battery on nennen TT 7 4 La ek ne sanat Werben eee eee 7 5 Battery door and tray Lk 7 6 Mount rail and pUlltAD cars ea oer weaker dan eben ele eld 7 7 Top HOUSING artnr severe heat heme At 7 9 Main DOIG REE 7 11 NBP hose coupling and elbow lt 7 12 NBP assembly with manifold hose 0 0c eee eee eee ee 7 12 A Appendix A Technical Specifications A 1 Technical Specifications evene eee A 2 PAYSICAU A tenten E RULET can A 2 Environmental oer ea ete voe eed eae ei ee A 2 Batterien o er Oot tenir S A 2 ECG ian iai ia a aa ai ai a a a A A 3 ROSPITALON rn Petre vaa teln er an re aj aa lara A 5 Temperatuf tc eee wende ee eee A 5 Invasive blood pressure oo A 6 Non invasive blood pressure onee A 7 Pulse oximetry Sp02 eenen A 9 Cardiac Output unir eren eee A 10 Ce
66. xcess liquids from connector recesses Wipe off cleaning solution with a clean moist cloth 2030047 001A Patient Data Module 5 3 Maintenance Storage Dry thoroughly with a clean dry lint free cloth and let air dry for at least 30 minutes Do not apply heat NOTE Drying times may vary based on the environmental conditions Remove batteries when the device is not in use even for short periods of time Store in a dry well ventilated area Hang the device using a holder if available If leadwires or cables are attached hang them straight Do not coil leadwires or cables tightly around the device Consequences of using improper cleaning product Appearance of waveforms when the device is not connected to a patient causing false alarms instead of a leads fail alarm and possibly not providing a visual or audible leads fail alarm Brittle and breaking device case Overall system performance degradation Melting dulling or distorting the case Total medical device failure requiring replacement Unit malfunction Void warranty Cleaning products to avoid Cleaning products known to cause the types of problems listed above include but are not limited to Sani Cloth Wipes Ascepti Wipes HB Quat Clorox Wipes they do not contain bleach Over the counter detergents e g Fantastic Tilex etc Products that contain active ingredients and solutions similar to these products should also b
67. you begin The following lists necessary tools for troubleshooting m Patient Data Module software CD with GEHC MS service tool shipped with Patient Data Module Solar 8000M i patient monitor with PDM service adapter 2028845 002 PC with Microsoft Windows XP or 2000 operating system a CDROM drive and a network card Category 5 crossover cable 2028822 001 ePort to host interface cable 2017098 002 If troubleshooting the Patient Data Module without a host patient monitor m PDM Service Tool Kit 2030924 001 Before beginning any detailed troubleshooting complete a thorough visual inspection to be sure All I O cable connections are secured All patient devices are properly powered PC with GEHC MS Service Tool is properly connected to the Patient Data Module See Connect the PC to the Patient Data Module on page 4 2 for details 6 2 Patient Data Module 2030047 001A Troubleshooting Problems and solutions Problem Solution Battery is not charging Check the Patient Data Module s battery interface as follows 1 Check the Patient Data Module s battery as follows 1 Check for damage to the battery tray If damaged replace the battery tray See chapter 7 Field Replaceable Units for ordering parts and replacement procedures Check for damage to the battery connector inside the battery compartment If damaged contact GE technical support to service the Patient Data Module See the H

Patient Data Module (PDM) - Frank`s Hospital Workshop

Contents

Download Pdf Manuals

Related Search

Related Contents