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User Manual - Mennen Medical

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1. l The LED besides this icon indicates the charging status When the battery is being recharged the LED is bright CHARGE Indicator The LED besides this icon indicates the power status O When the monitor connects to the mains power supply the POWER Indicator LED is bright 20 Introduction MENNMOVE 3 Vital Signs Monitor User Manual Introduction 3 4 Interfaces For the convenience of operator interfaces of different functions are in different sites of the monitor There is a USB port on rear panel for Data storing function Left side of the monitor At the left side of the monitor is the recorder L I m wi TI Figure 3 11 Left Panel Sensor port on the front panel Connectors for cables and sensors are as shown in Figure 3 8 1 SpO sensor connector 2 NIBP cuff connector Right side of the monitor If the monitor has TEMP function there will be TEMP module and thermometer outfitted on the right side Two optional TEMP measurement modules are available T2 module and TH module Infrared Ear Temperature module Refer to Figure 3 12 21 MENNMOVE 3 Vital Signs Monitor User Manual Introduction With T2 TEMP Module T2 TEMP probe T2 TEMP probe well With Infrared Ear Temperature Module thermometer EMP thermometer 22 MENNMOVE 3 Vital Signs Monitor User Manual Introduction With F3000 TEMP Module F3000
2. Medium Mode is beep beep beep which is triggered once every 25 s Low Mode is beep which is triggered once every 30 s The sound pressure range for audible alarm signals is from 45 dB to 84 dB 45 MENNMOVE 3 Vital Signs Monitor User Manual Alarm WARNING Do not rely exclusively on the audible alarm system for patient monitoring Adjustment of alarm volume to a low level or off during patient monitoring may result in patient danger Remember that the most reliable method of patient monitoring combines close personal surveillance with correct operation of monitoring equipment NOTE 1 The monitor does not have alarm condition delay or alarm signal generation delay 2 When alarms of different levels occur at the same time the monitor prompts one of the highest levels 3 If the monitor is powered off and then turned on the alarm setup can resume to the setup which is set before the power off 5 1 3 Alarm Setup Select the ALARM SETUP in the SYSTEM MENU to open the submenu as shown below ALARM SETUP Figure 5 1 Alarm Setup 9 Alarm setup of each parameter You can turn ON or OFF the alarm for each parameter and set the upper and lower alarm limit for each parameter by ALM HI or ALM LO In the ALARM SETUP menu set the alarm limit for each parameter For example Method to set systolic blood pressure alarm limit for SYS alarm 46 MENNMOVE 3 Vital Signs Monitor User Manual Alarm
3. Step 1 Set the SYS alarm to ON Step 2 Select the ALM HI higher alarm limit of SYS ALM LO lower alarm limit of SYS The user can press UP DOWN and OK to set the menu The method for setting the alarm limits of other parameters is the same as SYS alarm ALM REC and ALM REC TIME By configuring ALM REC the function of automatically outputting the alarm information in case of any physiological alarm can be enabled or disabled If the item is ON the monitor will automatically print out the alarm information once any physiological alarm happens If the item is OFF the monitor will not automatically output the alarm information Additionally if ALM REC is ON you can also adjust the recording time of the alarm waveform to be outputted by setting ALM REC TIME Available options are 8s 16s and 32s WARNING If the user set ALM to OFF the monitor will not give alarm prompt when alarm condition is active thus the user should use this function cautiously 5 2 Alarm Cause Alarm occurs when 1 Physiological alarm is evoked 2 Technical alarm is evoked 9 A Conditions that activate the parameter alarms The measurement value exceeds the alarm limit and the alarm is set to ON Alarms will not be activated if the alarm is set to OFF B Conditions that activate the system alarms technical alarm Upon the system error the monitor prompts alarm immediately C General alert In some circumstances alerts will behav
4. again Ambient temp too The Sensor Low high temperature is higher than 40 C Put the sensor into the sensor bracket measure again after the ambient temperature Ambient temp too The Sensor Low f reaches normal value low temperature is lower than 10 C PROBE ERROR The probe cannot be Medium Put the sensor into the sensor identified bracket take it out and measure again If the problem persists stop using measuring function of TEMP module notify biomedical engineer or Manufacturer s service staff sais MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional Message Cause Alarm Level What to do Warm up error Malfunction in the Medium Put the sensor into the sensor warm up circuit bracket take it out and measure again If the problem persists stop using measuring function of TEMP module notify biomedical engineer or Manufacturer s service staff Prompt Message Cause Warm up over The monitor prompts it after taking the sensor out of the bracket and warm up is over Measure over After the Predict measuring is over the data and message display on the interface Measure time out No measuring result after the module entering Predict state for 30s Probe temp too The original temperature of sensor gt 33 O and lt 40 high Temp SENSOR The proble is disconnected from the pa
5. eating food chewing gum or mints brushing teeth smoking or performing strenuous activity may affect temperature readings for up to 20min after activity has ended Do not take an axillary temperature through patient s clothing Direct probe cover to skin contact is required 68 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional WARNING Biting the sensor tip while taking a temperature may result in damage to the sensor Use disposable TEMP sensor covers recommended by MENNEN MEDICAL LTD to limit patient cross contamination The use of any other probe cover may produce temperature measurement errors or result in inaccurate readings Temp measurement isn t suitable for use during defibrillation 10 1 2 Measuring Procedure 1 Ensure the sensor is well installed The icon indicating measuring position flashes in TEMP parameter area on the main interface If necessary change the MEASURE MODE and MEASURE POS measure position in menu Take out the sensor from the sensor bracket After warm up it beeps and displays WARM UP OVER in information area Load a sensor cover by inserting the sensor into a sensor cover and press the sensor handle firmly The sensor handle will move slightly to engage the sensor cover Holding the sensor handle with your thumb and two fingers insert it to the measuring position For measuring oral TEMP place the sensor tip under the patient s tongue on either side of the m
6. transmitters and the MENNMOVE 3 as recommended below according to the maximum output power of the communications equipment Separation distance according to frequency of transmitter m Rated masinii 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz output power of transmitter W J2 3 5 JP d 3 5 JP d T JP Y E E 0 01 0 12 0 12 0 23 0 1 0 37 0 37 0 73 1 1 2 1 2 2 3 10 3 7 3 7 7 3 100 12 12 23 For transmitters rated at a maximum output power not listed above the recommended separation distance d in meters m can be estimated using the equation 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 1 At 80 MHz and 800 MHz the separation distance for the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people
7. 200 and 550 during transportation and storage Before use the equipment patient cable and sensor should be checked Replacement should be taken if there is any evident defectiveness or aging symptom which may impair the safety or performance If the monitor gets damp put it in dry circumstance to dry it until it can work normally If liquid pours on the monitor please contact the service personnel authorized by MENNEN MEDICAL LTD MENNMOVE 3 Vital Signs Monitor User Manual Intended Use and Safety Guidance CAUTION 11 Setting alarm limits to extreme values can render the alarm system useless 12 A potential hazard can exist if different alarm presets are used for the same or similar equipment in any single area NOTE 1 N O oO FB W N Position the device in a location where the operator can easily see the screen and access the operating controls The monitor can only be used on one patient at a time The equipment is calibrated to display functional oxygen saturation This equipment is not intended for family usage If the device is discolored or damaged then discontinue use of the device The pictures and interfaces in this manual are for reference only Regular preventive maintenance should be carried out every two years You are responsible for any requirements specific to your country 1 2 7 Explanation of Symbols on the Monitor This symbol indicates that the equ
8. Mode no measurement site is detected or the temperature does not stabilize 2 When the monitor operates in Predictive Mode or Quick Predictive Mode the ambient temperature is greater than 35 C 95 F Cold Mode Cold Mode is provided for use in applications where body temperatures may be lower than normal such as for patients recently out of surgery The accuracy and measurement time of Cold Mode measurements are equivalent to standard prediction measurements at the respective body sites 80 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional 10 3 6 Measuring Procedure Oral and Axillary Temperature Taking 1 Make certain that the Blue isolation chamber probe unit is attached 2 Withdraw probe and apply a probe cover The thermometer turns on automatically and a beep will be heard when the probe completes warm up 3 For Oral temperatures insert the probe tip deep into the sublingual pocket next to the frenulum linguae vertical fold of tissue in middle of tongue on one side or the other toward the back of the mouth NOTE Accurate body temperature readings can only be obtained in one of these two heat pocket locations as shown Temperatures taken in other mouth locations will result in inaccurate body temperature readings Heat Pockets Patient s mouth must be CLOSED Securely hold the probe in place until the temperature is displayed For Axillary temperatures have the pa
9. TEMP probe F3000 TEMP isolation chamber Figure 3 12 Right Panel WARNING Only connect accessories supplied or recommended by MENNEN MEDICAL LTD to the device Rear Panel FAA ANUN Figure 3 13 Rear Panel of MENNMOVE 3 23 MENNMOVE 3 Vital Signs Monitor User Manual Introduction Sockets on the rear panel are shown in the above figure Equipotential grounding terminal for connection with the hospital s grounding system Power supply socket 100V 240V 50Hz 60Hz USB connecting port for USB storage Network Interface Standard RJ45 Socket for connecting to MFM CMS of MENNEN MEDICAL LTD Bottom panel There are battery compartment and fuse box on the bottom panel Battery compartment cover ebejojs Jo Buidd ys eJojeq 1ayjeq anoulas s emje abewep Jeyeq plone oL S O 29 El lt 3 peas E Q 5 0 go a8 53 as of go 2 E lt gt Fuse box Figure 3 14 Bottom panel 24 MENNMOVE 3 Vital Signs Monitor User Manual Introduction 3 5 Built in Rechargeable Battery 3 5 1 Battery Safety Information WARNING 1 Do not take off the battery when monitoring The unexpected power supply off can not impact the monitor normal working if it has battery for standby 2 Stop using the battery if abnormal heat odor discoloration deformation or ab
10. a eat toe aes alec e a 3 catia lade ae 75 10 24 Replacing the Bator tall educa iR aia 76 A O 1T 10 3 TEMP Monitoring with F3000 Module ooooonoocnncccconcconcconoconcconnnonnnoconoconn cono ncon nono nccnnncnnnno 78 10 31 General Information issenensis aniani tie Gado 78 10 3 2 Safety TONO aaa 78 10 3 3 Probe Covers Applying amp Removing ooooocoocccocnconcconnoconaconnnonncconccconocancnnancconncnns 79 10 3 4 Changing Isolation Chambers and Probes ccccccesecesseeeeeeeseeceeceeeeeeeeeeseeeaeees 79 10 3 5 Measuring Mod a AER esas Aneesh 80 10 3 6 Measuring Procedure cc a aa 81 10 3 7 TEMP Setup for F3000 Modi le ii as 83 LOS AA Ad E EE 83 Chapter 11 Other FUNCHOHS 5 5cssss cascssenksctsaecdosuescoupessacadsavtocbosis gave pavoanasnespacaohusbuatsceignetsparbeesseeatacs 87 111 Nurse Call teeta aaa etl uardastes dec eydenduc nants leek ai aaia a E aa 87 112 Wireless lA e ae O eei EEA O aa Ea Eat 87 Chapter 12 Accessories and Ordering Information soesssesssesssecssocesoossoossssesssesssoossoossoossssssssee 88 Chapter 13 Warranty and ServiCe e sseoessoesssesssesssecssocssoossossssoesssesssoessoosssossssesssesssoessoossoosssssssoee 91 EA neroaren ae aa aca Senda cet aap a a e oa a Ne deed nwo ea taboos Sea 91 13 2 Contact Informations cect lest dace tells ep cance suse au a vat esto w Banc eo eu esos Sacer ake 91 A O tinction 92 AC A a a et So 92 A12 Specifications a 92 A ASE AO OS NR vio 92 AL 2
11. function mentioned above is unavailable O BARCODE SETUP 4 ID Patient ID can maximumly be a three digit number On this precondition you can determine which digit in the barcode is the starting ending digit for the paitent ID via configuration of START and END Take the following barcode for example If you set START to 2 and END to 4 the updated patient ID will begin with the second digit and end with the fourth digit in the barcode namely 787 9787121113260 PAT TYPE You can determine which digit in the barcode indicates the patient type For example if you set PAT TYPE to 1 the first digit in the barcode will be identified as an indication of patient type ON OFF If it is set to ON the patient information is updated automatically by using a barcode scanner If it is set to OFF a message box indicating Confirm to update patient yes will pop up when scanning a barcode Click on YES to automatically update patient information click on NO to quit automatical update ADU PED NEO Select a digit from 0 9 to indicate the patient type For example if ADU is set to 9 PAT TYPE is set to 1 and the first digit in the barcode is 9 the patient type could be updated to ADU NOTE 1 The set value of START END in ID as well as the set value of PAT TYPE must not exceed the length of the barcode 2 If START END is set to 0 the patient ID will not be updated by using barcode scanner 3 If PAT TYPE is set to 0
12. pulses In addition the measurement time will be prolonged Cardiac Arrhythmia s Measurements will be unreliable and may not be possible if the patient s cardiac arrhythmia has caused an irregular heartbeat The measuring time thus will be prolonged Heart lung Machine Measurements will not be possible if the patient is connected to a heart lung machine Pressure Changes Measurements will be unreliable and may not be possible if the patient s blood pressure is changing rapidly over the period of time during which the arterial pressure pulses are being analyzed to obtain the measurement 62 MENNMOVE 3 Vital Signs Monitor User Manual NIBP Monitoring Optional Severe Shock If the patient is in severe shock or hypothermia measurements will be unreliable since reduced blood flow to the peripheries will cause reduced pulsation of the arteries Heart Rate Extremes Measurements can not be made at a heart rate of less than 40 bpm and greater than 300 bpm 9 4 NIBP Setup Select SYSTEM MENU gt NIBP SETUP and you will see the menu below NIBP SETUP EXIT Figure 9 2 NIBP SETUP INTERVAL Set it to MANUAL AVG or 1 2 3 4 5 10 15 30 60 90 120 240 480 min When Interval is set to AVG the monitor provides the result by averaging the values obtained from three or five times of NIBP measurement STAT Once this itme is selected the menu will automatically exit from the screen and the monitor will perfo
13. take place 1 Alarm message displays on the screen as described in alarm mode 2 The monitor beeps in its corresponding alarm class and volume 3 Alarm lamp flashes 5 5 When an Alarm Occurs NOTE When an alarm occurs you should always check the patient s condition first The alarm message appears in Information area of the screen It is needed to identify the alarm and act appropriately according to the cause of the alarm 1 Check the patient s condition 2 Identify the cause of the alarm 3 Identify which parameter is alarming or which alarm is happening 4 When cause of alarm has been over check that the alarm is working properly You will find the alarm messages for the individual parameter in their appropriate parameter chapters of this manual 48 MENNMOVE 3 Vital Signs Monitor User Manual Alarm 5 6 Testing Alarms When you switch the monitor on a selftest is started You must check that the alarm indicator lights and that you hear a single tone This indicates that the visible and audible alarm indicators are functioning correctly For further testing of individual measurement alarms perform the measurement on yourself or use a simulator Adjust alarm limits and check that appropriate alarm behavior is observed 49 MENNMOVE 3 Vital Signs Monitor User Manual Trend and Recording Chapter 6 Trend and Recording In SELECTION submenu the user can set the displayed contents to waveform trend table
14. the patient type will not be updated by using barcode scanner 4 Barcodes containing characters other than digits or containing space will be 40 MENNMOVE 3 Vital Signs Monitor User Manual System Menu considered invalid and cannot be identified If any invalid character is detected a message box indicating Special signs are in code bar will pop up 5 Connect the barcode scanner to the monitor and wait 10 seconds before starting the scanner 6 Refer to the accompanying operator s manual of the scanner for more information about its usage EXIT Exit the menu Factory Maintain Factory maintenance function is only available for the service engineers of MENNEN MEDICAL LTD or representative authorized by MENNEN MEDICAL LTD 4 12 Data Storing The monitor can support the USB storage for the Data Store function Enter the menu by SYSTEM MENU gt DATA STORE to set the data storing function You can set the storing interval browse data search data and delete all the data or single item data DATA STORE Figure 4 22 Data Store ON OFF set the Data Store function to ON or OFF WARNING 1 If you want to stop the data storing function you should set this item to OFF before unplugging the USB disk 2 Do not unplug the USB storage when storing data If the data damaged by unplugging the USB storage during data storing can not be deleted on the monitor the user can delete them on the PC A MENN
15. to the alarm level 44 MENNMOVE 3 Vital Signs Monitor User Manual Alarm Screen Display When the measured parameter exceeds its alarm limits and triggers a physiological alarm the monitor will give alarm prompt on the screen indicating the occurrence of alarm The description will display in Information area such as NS TOO HIGH and A displays beside the parameter to indicate the low medium level alarm Technical alarm will not prompt signal Alarm Level Visual Prompt High 1 ry displays in Parameter area 2 displays in the information area Physiological alarm only Medium 1 rN displays in Parameter area 2 displays in the information area Physiological alarm only Low 1 A displays in Parameter area 2 displays in the information area Physiological alarm only Lamp light The high medium low level alarms are indicated by the system in following different visual ways Alarm Level Visual Prompt High Alarm indicator flashes in red with the frequency of 1 4 2 8 Hz Medium Alarm indicator flashes in yellow with the frequency of 0 4 0 8 Hz Low Alarm indicator lights on in yellow Alarm Sound The high medium low level alarms are indicated by the system in following different audio ways Alarm Level Audio Prompt Mode is beep beep beep beep beep beep beep beep beep beep High fede te e which is triggered once every 5 s
16. 11 36 3 113 77 89 99 60 09 50 1 36 8 118 73 88 99 60 MENNMOVE 3 Vital Signs Monitor User Manual System Menu You can shift the data list to waveform display by pressing the TREND WAVEFORM button on front panel The waveform displays as shown in the following figure hin 118 on rA 364 7 O Figure 4 12 Waveform Display For Single display mode the Selection menus are different see the following menu SELECT ON Sp02 TREND TABI ALARM LIST TREND GRAPH EXIT Figure 4 13 Selection for SpO2 233 MENNMOVE 3 Vital Signs Monitor User Manual System Menu SELECT ION NIBP TREND TAB ALARM LIST TREND GRAPH EXIT Figure 4 14 Selection for NIBP 4 5 Deleting Data If you press the button when a trend list or an alarm list is displayed on the screen the following menu will pop up DELETE DATA YES NO Figure 4 15 Delete Data DELETE ID Entirely delete the trend and alarm data of the current monitored patient DELETE ALL DATA Entirely delete the trend and alarm data of all the monitored patients Select YES to make the operation effective select NO to cancel the operation 4 6 Version Select VERSION in SYSTEM MENU to check the version of the monitor and the configuration of the modules 4 7 Time Setup Select TIME SETUP in SYSTEM MENU to access the submenu of TIME SETUP as shown below System time is in format of Y M D M D Y or D M Y Users can set
17. 22 Environment eei Aa ee n ara E A OE a REEE Ta SER Onia RESAS 92 A123 Display a ted EOR 93 AT 24 BAN A EE AEE EEEE RR a 94 A ee AEE E aaa O E E E 94 AT 26 Data Stora de A O A IS 94 VI Pel 277 NIBP Optional dass penia a A cela A iain 95 Al 28 SpOs Optional A A ad 96 ARZI LEMP Otte cies tec Lou ceases a Scenes a A e eax a obio 97 A1210 WInless NGtW OLK ssl discal 99 Appendixll EMC Information Guidance and Manufacture s Declaration scscsssssseeeees 1 A2 1 Electromagnetic Emissions For all EQUIPMENT and SYSTEMS coocococcccoccnonconcconcnnnonnos 1 A2 2 Electromagnetic Immunity For all EQUIPMENT and SYSTEMS cococcococconcnnnconcconinnnonnos 2 A2 3 Electromagnetic Immunity For EQUIPMENT and SYSTEMS that are not ETFE SUPPORTIN O soja A Aia 3 A2 4 Recommended Separation Distances ns 4 VI MENNMOVE 3 Vital Signs Monitor User Manual Intended Use and Safety Guidance Chapter 1 Intended Use and Safety Guidance 1 1 Intended Use The monitor is intended to be used by qualified physicians or personnel professionally trained and it is for monitoring adults pediatrics and neonates in hospital environments This monitor is used to monitor vital signals for patients and is suitable for use in hospital environments including out patient department wards and NICU Monitored paramenters include NIBP SpO2 pulse rate Quick TEMP Infrared TEMP 1 2 Safety Guidance 1 2 1 Environment Follow the instructions bel
18. 3 5 5 Recycling the Battery When the battery no longer holds a charge it should be replaced Remove the old battery from the monitor and recycle it properly 3 5 6 Maintaining the Battery Batteries should be conditioned regularly to maintain their useful life Remove the batteries from the monitor if they are not used for a longer period of time And recharge the batteries at a minimum of every 6 months when they are stored Discharge the battery completely once every month 26 MENNMOVE 3 Vital Signs Monitor User Manual System Menu Chapter 4 System Menu The monitor features in flexible configurations You can configure various aspects of the monitor including the parameters to be monitored audio signal volume and output content Press MENU on the front panel to open SYSTEM MENU You can perform the following operations in this menu SYSTEM MENU MAINTAIN DEFAULT TIME SETUP SYSTEM SETUP NIBP SETUP SELECTION TEMP SETUP VERSION ALARM SETUP DATA STORE Figure 4 1 System memu 4 1 Patient Setup Click on PATIENT SETUP in SYSTEM MENU to open the following menu PATIENT SETUP EXIT Figure 4 2 Patient Setup You can set the following patient information PAT ID Patient ID 1 1000 PAT TYPE Patient type ADU PED or NEO Press the UP DOWN button on the front panel to select the items then press the OK button to confirm Pick EXIT to return to the previous menu 27 MENNMO
19. 6 MENNMOVE 3 Vital Signs Monitor User Manual Introduction 3 2 3 Single Parameter Mode SpO only measuring mode ID 1 Sp0 gt yy O O A 16 19 08 Figure 3 8 Display in SpOz only mode 17 MENNMOVE 3 Vital Signs Monitor User Manual Introduction NIBP only measuring mode In NIBP only measuring mode the PR from NIBP measurement is also displayed on screen ID 1 mmHg CUFF SYS 118 DIA 13 MAP PR BPM 88 60 L 16317307 Figure 3 9 Display in NIBP only mode 18 MENNMOVE 3 Vital Signs Monitor User Manual Introduction 3 3 Button Functions Figure 3 10 Buttons All the operations to the monitor can be finished by several buttons ON OFF When the monitor is off press this button to switch on the monitor When the monitor is on press this button for less than ls the monitor will enter the sleep mode if STANDBY is set to ON Press this button and hold it for gt 2s to switch off the monitor SILENCE amp Press this button for less than 2s to silence the audible alarm then the icon EJ appears and a message SILENCE XXX S shows in the information area Repress it or wait until the pause time is over and the audible alarm resumes to the normal monitoring status Press this button for gt 2s t
20. Access the NIBP SETUP menu and pick the CONTINUAL item to start a continuous measurement The continuous measurement will last 5 min 5 To stop measuring During measuring press the NIBP START STOP on the front panel at any time to stop measurement WARNING If liquid is inadvertently splashed on the equipment or its accessories or may enter the conduit or inside the monitor contact local Customer Service Center NOTE If you are in doubt about the accuracy of any reading s check the patient s vital signs by an alternative method before checking the functioning of the monitor Initial Inflation Pressure Patient Type ADU PED NEO Inflation Value 160mmHg 140mmHg 100mmHg Measurement Limitations For different patient conditions the oscillometric measurement has certain limitations The measurement is in search of regular arterial pressure pulse In those circumstances when the patient s condition makes it difficult to detect the measurement becomes unreliable and measuring time increases The user should be aware that the following conditions could interfere with the measurement making the measurement unreliable or longer to derive In some cases the patient s condition will make a measurement impossible Patient Movement Measurements will be unreliable or may not be possible if the patient is moving shivering or having convulsions These motions may interfere with the detection of the arterial pressure
21. Accessory equipment connected to the analog and digital interfaces must be certified according to the respective IEC EN standards Furthermore all configurations shall comply with the valid version of the system standard IEC EN60601 1 1 Everybody who connects additional equipment to the signal input connector or signal output connector configures a medical system and is therefore responsible that the system complies with the requirements of the valid version of the system standard IEC EN60601 1 1 If in doubt consult our technical service department or your local distributor The simultaneous use of cardiac pacemaker and other patient connected equipment may cause safety hazard Use the battery only in this monitor Do not connect battery directly to an electric outlet or cigarette lighter charger Do not unplug the battery when monitoring Make sure the monitor is used in the appointed range of voltage so that the effect of power supply can be ignored Do not solder the leading wire and the battery terminal directly If liquid leaking from the battery gets into your eyes onto your skin or clothes do not rub your eyes Wash them well with clean water and go to see a doctor immediately Always keep the battery away from fire Stop using the battery if abnormal heat odor discoloration deformation or abnormal condition is detected during use charge or storage Keep it away from the monitor Do not use a battery with serious scar or d
22. BP 01 57 40020 NIBP Cuff Infant 10cm 19cm reusable CM1201 01 57 40018 NIBP Cuff Pediatric 18cm 26cm reusable CM1202 01 57 40029 NIBP Cuff Adult 25cm 35cm reusable CM1203 01 57 40074 NIBP Cuff Adult 33cm 47cm reusable CM1204 11 57 40097 NIBP Cuff for Neonatal for single patient use 5 4cm 9 1 cm 11 57 40098 NIBP Cuff for Neonatal for single patient use 6 9cm 11 7cm 01 59 036118 NIBP Tube for Adult Pediatric 3m Grey 01 57 040212 NIBP Cuff Infant 10cm 19cm reusable CM1301 01 57 040211 NIBP Cuff Pediatric 18cm 26cm reusable CM1302 01 57 040205 NIBP Cuff Adult 25cm 35cm reusable CM1303 01 57 040210 NIBP Cuff Adult 33cm 47cm reusable CM1304 01 57 471021 Connecting Tube for Neonatal Cuff 3m TEMP For T2 Module 02 04 110140 Oral axillary probe 02 04 110139 Rectal probe 11 57 110159 Probe covers TEMP For TH Module 01 13 036415 TH module communication wire 12 08 208058 Probe covers for TH module 200 pieces package 89 MENNMOVE 3 Vital Signs Monitor User Manual 12 08 208059 Probe cover loader for TH module with 40 pieces probe cover TEMP For F3000 Module 11 57 471312 Filac 3000 Oral Probe 4ft 11 57 471313 Filac 3000 Oral Probe 9ft 11 22 066159 Filac 3000 Oral Isolation Chamber 11 57 471314
23. E AN 2 1 2 7 Explanation of Symbols on the MOnitor ooooooccnocccnocconnoconccona nono nonnnoconocono nono ncon nono nonnnos 5 Chapter 2 Installation Of Monitor ccsccscsscssssccssscccssscecsscecscesccsssscesscssccsssscscssssssssecsessessessees 7 2 1 Opening the Package and Checkin iii 7 2 2 Connecting the Power CAD IG x dada 7 23 Powering on the MOON T 2 4 Connecting Sensor to Patient senec onenian ia 8 2 5 Checking the Recorders AAA AA A a E a ERE EAEE 8 Chapter 3 Mt rode tint sisss ccetuxcevacatsesntasccsesstcosessseieoscduas assess vsahoboscndvscdstheiwosecensesssnesndousconveseassedeucass 9 3 l General Informat ON 23 acts aeae ee a eaaa odes aos eps va Seas aa AEA sas hes ages 9 32 SCTECIM DISPLAY E E AE EEE ETE 10 3 2 1 General DisplaMode uana a aes eee sees 10 3 2 2 Double Parameter Mode viii 15 3 2 3 Single Parameter Mode ns sessesseeseesseeseeseesseesresresstessesersseessesstssressessrsstesseeseesressee 17 3 3 B tton FUNCIONEN a aa T 19 Dee EOIR E O AP E A A R 21 3 5 Built Rechargeable Bateria ta e o Ed 25 3 5 1 Battery Safety OMA id A A a dd id 25 3 5 2 Battery Status on the Main Screen cccssscsssssssscsssccesscssscsscescesseseseccssceessceenasees 25 3 5 3 Checking Battery Peron das 26 3 54 Replacing the Bateria ansauenates 26 Dio R cycling the Bat o e atid cal oda e le ois ro ae oe 26 3 5 6 Maintaining the Bai A A A AA 26 Chapter 4 EMMA e 27 4 1 Patient SUID iras iii 27 4 2 D
24. Filac 3000 Rectal Probe 4ft 11 57 471315 Filac 3000 Rectal Probe 9ft 11 22 066160 Filac 3000 Rectal Isolation Chamber 11 57 471316 Filac 3000 Probe Covers Others 01 57 78035 Printing Paper 03 28 101950 Trolley 01 13 36014 Power Cable IEC Standard 1 8m 01 13 036106 Power cord USA 1 8m 21 21 064167 Rechargeable Lithium Ion Battery TWSLB 008 14 8V 4 4 Ah 21 21 064168 Rechargeable Lithium Ion Battery TWSLB 009 14 8V 2 2 Ah 11 13 01950 Power cord 3C 3m 11 13 114214 Ground Cable 11 23 068003 USB barcode scanner Cipher LAB 1000U USB port conntact CCD scan 90 Accessories and Ordering Information MENNMOVE 3 Vital Signs Monitor User Manual Warranty and Service Chapter 13 Warranty and Service 13 1 Warranty MENNEN MEDICAL LTD warrants that MENNEN MEDICAL LTD s products meet the labeled specifications of the products and will be free from defects in materials and workmanship that occur within warranty period The warranty is void in cases of a damage caused by mishandling during shipping b subsequent damage caused by improper use or maintenance c damage caused by alteration or repair by anyone not authorized by MENNEN MEDICAL LTD d damage caused by accidents e replacement or removal of serial number label and manufacture label If a product covered by this warranty is determined to be defective bec
25. MOVE 3 Vital Signs Monitor User Manual System Menu NOTE If you set the item to ON after restarting the monitor this item will resume OFF automatically INTERVAL set the storing interval by this item it can be set to 1S 5S 10S 30S 1MIN or 5MIN MANAGEMENT select BROWSE to browse data stored before DELETE ALL select this item to delete all the data stored before UP DOWN select this item then turn the page by pressing the UP or DOWN button to browse data SEARCH search data by patient ID date and time RETURN select this item to return to the previous menu Select the single item data in DATA BROWSER menu press OK to display the following menu DELETE TREND TABLE TREND GRAPH ALARM LIST RETURN Figure 4 23 Menu The user can select to browse the TREND TABLE TREND GRAPH or ALARM LIST The user can select DELETE to delete the single item data or select the RETURN to return to the previous menu NOTE The data which is being stored can not be browsed in real time Before searching data you should turn off the Data Store function at first 4 13 Sleep Mode Entering the Sleep Mode Select SYSTEM MENU gt SYSTEM SETUP gt STANDBY and configure the item to ON Then you will see the following dialoge box after pressing the switch for less than 1s 42 MENNMOVE 3 Vital Signs Monitor User Manual System Menu ENTER SLEEP MODE Figure 4 24 Enter Sleep Mode Select YES to enter
26. P 15 09 53 1 114 18 90 15 09 52 1 117 15 89 15 09 52 1 114 19 90 15 09 52 1 112 16 88 Figure 4 6 NIBP Trend Table SpO TREND TAB to display SpO trend table bir 4 12 MAP 84 DIA F 1 CUFF TEMP NJ C o XV A a ll E Sp02 PR BPM TIME ID Sp02 PR 15 09 53 1 99 60 15 09 52 1 99 60 15 09 52 1 99 50 15 09 52 1 99 60 Figure 4 7 SpO Trend Table 30 MENNMOVE 3 Vital Signs Monitor User Manual TEMP TREND TAB to display TEMP trend table kra 1 12 MAP 84 DIA 71 CUFF TEMP EN 36 8 7 E S002 PR BPM TIME ID TEMP 15 09 53 36 8 15 09 52 1 36 0 15 09 52 1 36 7 15 09 52 1 37 0 Figure 4 8 SpO Trend Table ALARM LIST to display alarm list lar 1 4 2 map S DIA 84 7 1 CUFF TEMP EN t 36 8 7 E PR BPM TIME ID ALARM LIST 15 09 53 1 xx TEMP 36 9 15 09 52 1 xx TEMP 36 3 15 09 52 1 xx TEMP 36 3 15 09 52 1 xx TEMP 36 5 Figure 4 9 Alarm List 31 System Menu MENNMOVE 3 Vital Signs Monitor User Manual TREND GRAPH to display the trend graph TREND GRAPH Figure 4 10 Trend Graph PARAMETER TAB to display SpO and NIBP parameters in the area Figure 4 11 Parameter Table SYS 2412 af DIA 71 CUFF TEMP EN C o 368 f E Y Sp02 y PR BPM TIME ID_ TEMP SYS DIA MAP Sp02 PR 09 53 1 36 8 112 71 84 99 60 09 52 1 36 0 111 16 87 99 60 09 5
27. TERVAL item for MANUAL or set the interval for auto measurement or select the CONTINUAL mode 6 Press the NIBP START STOP on the front panel to start a measurement You can also stop this measurement by this button WARNING Prolonged non invasive blood pressure measurements in automatic mode may be associated with purpuric ischemic and neuropathy in the limb wearing the cuff When monitoring a patient examine the extremities of the limb frequently for normal color warmth and sensitivity If any abnormality is observed stop the blood pressure measurements Operation Prompts 1 To start auto measurement Access NIBP SETUP menu and pick the INTERVAL item in which the user may set up the time interval for auto measurement After that press the NIBP START STOP on the front panel to start the auto measurement according to the selected time interval 2 To stop auto measuring During auto measuring press the NIBP START STOP on the front panel at any time to stop the auto measurement in process WARNING If you repeatedly use AUTO measuring in a short term it may lead to inaccurate readings or endanger patient s life 3 To start a manual measuring NH Access NIBP SETUP menu and pick the INTERVAL item Select the MANUAL selection Then press the NIBP START STOP on the front panel to start a manual measurement 61 MENNMOVE 3 Vital Signs Monitor User Manual NIBP Monitoring Optional 4 To start a continuous measuring
28. VE 3 Vital Signs Monitor User Manual System Menu 4 2 Default Setup NOTE Select any item in this submenu to cancel the current setup and use the selected default setup DEFAULT SAVE CURRENT AS USER CONFIG CONF RM Figure 4 3 Default Menu FAC DEF CONFIG factory default configuration USER DEF CONFIG user defined default configuration SAVE CURRENT AS USER CONFIG Save the current setup as the user default configuration 9 0 CONFIRM Confirm your choice exit this submenu and return to the previous menu 4 3 System Setup In this submenu SYSTEM SETUP has a few items to set see the following menu SYSTEM SETUP MED EXIT Figure 4 4 System Setup ALARM VOL Set alarm volume to HIGH MED or LOW 28 MENNMOVE 3 Vital Signs Monitor User Manual System Menu STANDBY Set it to ON or OFF to enable or disable the Sleep Mode function Refer to 4 12 Sleep Mode KEY VOL Set key volume to HIGH MED LOW or OFF SPHY VOL Set sphygmic volume to HIGH MED LOW or OFF WORK MODE Set work mode to MONI monitoring mode or SPOT spot check mode NOTE 1 The work mode will be indicated in the information area 2 In the spot check mode audio and visual prompts for all medium and low technical alarms will be disabled medium and low technical alarms will only be indicated by turns in the information area In the monitoring mode audio and visual prompts for all alarms will be effective an
29. acturer s service staff Stop using measuring function System error during of TEMP module notify Temp Error E03 heater thermistor Medium E biomedical engineer or calibration Manufacturer s service staff 84 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional Message Cause Alarm Level What to do Stop using measuring function ae of TEMP module notif Temp Error E04 System timing error Medium f g ed biomedical engineer or Manufacturer s service staff Stop using measuring function of TEMP dule tif Heater error Heater error Medium a re biomedical engineer or Manufacturer s service staff E es Stop using measuring function irect Mode patient y of TEMP module tif Temp Error P02 thermistor unstable or Low f E aoa biomedical engineer or out of range i Manufacturer s service staff l Stop using measuring function Direct Mode heater of TEMP module notify Temp Error P03 thermistor unstable or Low i biomedical engineer or out of range Manufacturer s service staff Stop using measuring function Predict Mode patient of TEMP module notify Temp Error P04 thermistor unstable or Low i biomedical engineer or out of range f Manufacturer s service staff Stop using measuring function Predict Mode heater of TEMP module notify Temp Error POS thermistor unstable or Low E f biomedi
30. al Signs Monitor User Manual Introduction Chapter 3 Introduction 3 1 General Information The monitor integrates the function of parameter measurement modules display recording and output to compose a compact portable device Its built in replaceable battery provides convenience for patient movement On the LCD display screen SpO2 waveform and all the monitoring parameters can be displayed clearly The monitor is a user friendly device with operations conducted by a few buttons on the front panel Refer to section 3 3 Button Functions for more details D O a ee K Figure 3 1 MENNMOVE 3 Vital Signs Monitor MENNMOVE 3 Vital Signs Monitor can monitor SpO2 Arterial Oxygen Saturation SpO2 Pulse Rate PR SpO2 PLETH Plethysmogram NIBP Systolic Pressure SYS Diastolic Pressure DIA Mean Pressure MAP Pulse Rate PR TEMP Temperature TEMP MENNMOVE 3 Vital Signs Monitor User Manual Introduction 3 2 Screen Display The monitor is equipped with LCD The patient parameters waveforms alarm messages patient ID time monitor status and other information can be reflected from the screen If the monitor is outfitted with the modules SpO2 NIBP and TEMP the three parameters SpO NIBP and TEMP are onscreen in the general display mode If the monitor is configured to the double parameter measuring function as NIBP SpO or NIBP TEMP double parameters will be displayed onscreen Also the monitor can be co
31. all pump by means of a T piece connector and hoses to the pneumatic system Select CALIBRATE in menu Inflate the pneumatic system to 0 mmHg 50 mmHg and 200 mmHg by ball pump separately The difference between the indicated pressure of the reference manometer and the indicated pressure of the monitor will not exceed 3 mmHg Otherwise please contact our customer service Monitor Reference manometer Metal vessel Figure 4 20 NIBP Calibration LEAK TEST This item is used for an air leakage test Select this item to start the air leakage test Then the item will change into STOP LEAK TEST Select it again and the system will stop the air leakage test 38 MENNMOVE 3 Vital Signs Monitor User Manual System Menu WARNING This pneumatic test other than being specified in the IEC EN1060 1 standard is to be used by the user to simply determine whether there are air leaks in the NIBP airway If at the end of the test the system gives the prompt that the NIBP airway has air leaks please contact the manufacturer for repair Procedure of the Air Leakage Test 1 2 3 4 5 6 7 Connect the cuff securely with the socket for NIBP air hole Wrap the cuff around the cylinder of an appropriate size Access the NIBP SETUP menu Select LEAK TEST by pressing UP DOWN It indicates Leak testing in the information area The system will automatically inflate the pneumatic system to about 180mmHg After 20 seconds o
32. arm type SYS DIA MAP PR Cuff Pressure measuring range 0 mmHg 300 mmHg Pressure resolution 1 mmHg Maximum mean error 5 mmHg Maximum standard deviation 8 mmHg Maximum measuring time of single ADU PED 120s measurement NEO 90s Typical measuring period 30s 45s depend on HR motion disturbance 95 MENNMOVE 3 Vital Signs Monitor User Manual Specifications Overpressure protection ADU 29743 mmHg PED 240 3 mmHg NEO 14743 mmHg PR Measuring range 40 bpm 240bpm Accuracy 3bpm or 3 5 whichever is greater A1 2 8 SpO Optional MENNEN MEDICAL LTD module Measuring Range 0 100 Alarm Range 0 100 Resolution 1 Data update period Is Accuracy Adult Pediatric 2 70 100 SpO2 Undefined 0 69 SpO Neonate 3 70 100 SpO Undefined 0 69 SpO Pulse Rate Measuring Range 25 bpm 300 bpm Alarm Range 30 bpm 300 bpm Resolution 1 bpm Accuracy 2bpm Sensor Red light 660 3 nm Infrared light 905 5 nm Emitted light energy lt 15 mW 96 MENNMOVE 3 Vital Signs Monitor User Manual Specifications Nellcor module optional Measuring Range 1 100 Alarm Range 0 100 Resolution 1 Data update period Is Sensor Type Accuracy Accuracy DS 100A OXI A N 3 70 100 SpO When t
33. ause of defective materials components or workmanship and the warranty claim is made within the warranty period MENNEN MEDICAL LTD will at its discretion repair or replace the defective part s free of charge MENNEN MEDICAL LTD will not provide a substitute product for use when the defective product is being repaired 13 2 Contact Information If you have any question about maintenance technical specifications or malfunctions of devices contact your local distributor Alternatively you can send an email to MENNEN MEDICAL LTD service department at support MENNEN MEDICAL LTD com cn 9 MENNMOVE 3 Vital Signs Monitor User Manual Specifications Appendix Specifications A1 1 Classification Anti electroshock type Class equipment and internal powered equipment Anti electroshock degree SpO gt NIBP BF TEMP CF T2 module BF TH module F3000 module Ingress protection IPX1 With T2 or F3000 TEMP module IPX0 Working system Continuous operation equipment Compliant with standards IEC 60601 1 1988 A1 A2 ISO 9919 EN 12470 4 EN12470 5 2003 EN 60601 1 1990 A1 A2 IEC EN 60601 2 30 IEC EN 60601 1 2 2005 A1 ANSI AAMI SP10 IPC610 185013485 A1 2 Specifications A1 2 1 Size and Weight Size 174 mm L x 235 mm H x 189 mm D Weight lt 3 5 kg not including battery A1 2 2 Environment The monitor may not meet the perfo
34. cal engineer or out of range f Manufacturer s service staff Stop using measuring function of TEMP module notify biomedical engineer or Manufacturer s service staff Temp Error P06 meee to pre heat iow probe tip NOTE Measure readings displayed on the screen are unreliable when the monitor indicates Temp Error PO6 85 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional Prompts Message Cause Warm up over The monitor prompts it after the probe is taken out of the probe well and warm up is over Measure over Prediction measurement is completed Quick Predict Over Quick predicton measurement is completed MONITORING The mode is switching to Monitor Mode 86 MENNMOVE 3 Vital Signs Monitor User Manual Other Functions Chapter 11 Other Functions 11 1 Nurse Call The monitor provides dedicated nurse call port which is connected to nurse call system through the nurse call cable to perform the nurse call function 11 2 Wireless Network The monitor can constructs wireless network through AP Access Point Our company arranges the qualified engineers to install and set the wireless network for the user and test the corresponding performance For details please refer to Patient Monitor Wireless Network Installation Guide NOTE 1 Be aware that some network based functions may be limited for monitors on wireless networks in comparison with th
35. changes in the patient s oxygen saturation level but the measurement accuracy will be improved When a critical patient is monitored selecting high sensitivity will help to understand the patient s state O NIBP SETUP AVG INTERVAL Set the average NIBP measurement interval to 1min 2min 3min 4min or 5min AVGTIMES Set the average NIBP measurement times to 3 or 5 37e MENNMOVE 3 Vital Signs Monitor User Manual System Menu RESET Select it to reset the NIBP module Restore measurement status Pick this item to restore initial settings of the pressure pump When the pressure pump does not work properly and the system fails to give message for the problem pick this item to activate self test procedure thus restore the system from abnormal performance CALIBRATE Calibrate the cuff pressure reading with a calibrated reference manometer Select CALIBRATE to start the calibration and the item will change into STOP CAL which if is selected the system will stop calibration WARNING The calibration of the NIBP measurement is necessary every two years or as frequently as dictated by your Hospital Procedures Policy The performance should be checked according to the following details Procedure of the Pressure Transducer Calibration Replace the cuff of the monitor with a rigid metal vessel with a capacity of 500 25 ml Connect a calibrated reference manometer with an error less than 0 8 mmHg and a b
36. cons 55 So Motoring POC dirias 55 SA Limitations of Measurement syccssise sais A A ad 56 PUMA a Sa aN ai Sala leh ht a al OO e E dd 56 8 5 1 Adjutable Range of Alarm Limits 0 dd a dass 56 8 5 2 Alarm Information and Prompts c ccccccessseesseceeceseceeceeescecaeceeeeeneeeseecaeceeeeees 57 8 6 Maintenance and CE A i 58 Chapter 9 NIBP Monitoring Optional esssesssesssesssoossoossosesssesssesssocssoossoossssesssesssoossoossossssssssose 59 9 OVE eW O E 59 9 2 NIBP Safety Information ita 59 eS NIBP MONOT A O A aa eco N 60 9 NIBP Sn a a a dois 63 SA A a aa as cD oe A aa a 64 9 5 1 Adjutable Range of Alarm Limits 0 0 0 0 cc ccecccceccsssceesseceseceseceeeeesseecsaeceeeeeeeeesaeeaeees 64 9 5 2 Alarm Information and Prompts c cccccceseceseceescesseeeeseceeeseeeenseecsaeceseeeeeeensaeeaeees 65 9 6 Maintenance and CIE ATG x snc22 icles died Sees 67 Chapter 10 TEMP Monitoring Optional sesssesssesssoossoossosssssesssesssocssoossoossssesssesssoessoossoossssssssee 68 10 1 TEMP Monitoring with T2 Module SA AN AAA 68 101 1 Mtr dC a 68 10 12 M as ting as e 114 APN A A a a a ey teactineds 69 101 3 TEMP Setup Tor T2 Modales A A ARAN 70 A e Be 70 Me Mg Careand a a o ls e ee Sado o ten 9 72 10 2 TEMP Monitoring with TH Module ooooonoconocccocccnonnconncconcconnnonnnonnnoconocnnn cono nc on coco nocnnncnnnnos 73 LO 2 NS ON 73 10 2 2 Me suring Procedure ici A Ai aia 74 A e loa maaan elec CaRlc
37. d alarms will be indicated by turns in the information area 3 In the spot check mode medium and low technical alarms cannot disable the settings of silencing the alarm Only when a new physiological alarm or a high technical alarm occurs can the monitor automatically exit the alarm silenced status In the monitoring mode if a new alarm of any type occurs the monitor will automatically exit the alarm silenced status 4 In the spot check mode no trend graph will be shown WAVE FORM Set displayed waveforms to UNFILLEDor FILLED FACE SELECT Set NIBP or SpO as the main displayed parameter onscreen FACE SELECT is only available for the monitor with the configured modules NIBP SpO EXIT Return to the previous menu 4 4 Selection For the monitor outfitted with SpO NIBP and TEMP modules you may select SELECTION in SYSTEM MENU to access this submenu in which six selections are available NIBP TREND TAB SpO TREND TAB TEMP TREND TAB ALARM LIST TREND GRAPH and PARAMETER TAB Only one item can be selected to display information on the lower part of the interface SELECTION NIBP TREND TAB TREND GRAPH Sp02 TREND TAB TEMP TREND TAB ALARM LIST EXIT Figure 4 5 Selection 29 MENNMOVE 3 Vital Signs Monitor User Manual System Menu NIBP TREND TAB to display NIBP trend table Ho 1 12 MAP 84 DIA A 7 1 CUFF TEMP NJ te a ll E Sp02 PR BPM TIME ID SYS DIA MA
38. device should be sent to the special agencies according to local regulations for separate collection after its useful life bal E Federal US law restricts this device to sale by or on the neon order of a physician MENNMOVE 3 Vital Signs Monitor User Manual Installation of Monitor Chapter 2 Installation of Monitor NOTE To ensure that the monitor works properly please read Chapter1 Intended Use and Safety Guidance and follow the steps before using the monitor 2 1 Opening the Package and Checking Visually examine the package prior to unpacking If any signs of mishandling or damage are detected contact the carrier to claim for damage Open the package and take out the monitor and accessories carefully Keep the package for possible future transportation or storage Check the components according to the packing list Check for any mechanical damage Check all the cables modules and accessories If there is any problem contact the manufacturer or local representative immediately 2 2 Connecting the Power Cable Connection procedure of the AC power line Make sure the AC power supply complies with following specification 100V 240V 50Hz 60Hz Apply the power line provided with the monitor Plug the power line to input interface of the monitor Connect the other end of the power line to a grounded power output NOTE Connect the power line to the jack special for hospital usage Connect t
39. dio system off Alarm silenced Parameter alarm off Patient type ADU MEMBER lt a lle al Patient type PED Patient type NEO NIBP manual mode NIBP interval mode NIBP continual mode Heart beat 12 MENNMOVE 3 Vital Signs Monitor User Manual Introduction Measuring oral TEMP in ADU mode Measuring axillary TEMP in ADU mode Measuring rectal TEMP in ADU mode g a Measuring oral TEMP in PED mode For device with the le a Measuring axillary TEMP in PED mode T2 or F3000 TEMP module only 2 Measuring rectal TEMP in PED mode Measuring TEMP Measuring value of TEMP is above the upper alarm limit Only for Predictive Mode Measuring value of TEMP is below the lower alarm limit Only for Predictive ar e Mode For device with the Infrared E Measuring ear TEMP aie e Temperature module only ID Current patient ID 09 00 43 Current time Parameter Area 0 Parameter area is on the right of Waveform area and parameters are displayed SpO2 SpO gt Unit PR Pulse Rate Unit BPM NIBP SYS DIA MAP Unit mmHg or kPa Pulse Rate Pulse Rate Unit BPM 13 MENNMOVE 3 Vital Signs Monitor User Manual Introduction NIBP measuring mode TEMP Temperature Unit L or O The PR signal from SpO measuring takes priorit
40. e as physiological alarms in normal senses we do not regard them as real patient health related items 5 3 Silence The user can press SILENCE button on the front panel to silence the audible alarm or turn off the audio system If an alarm occurs during this period the monitor can still give alarm 1 Alarm silenced icon E Press the SILENCE button on the front panel for less than 2s and the audible alarm is mute The alarm silenced icon displays Pressing SILENCE again can resume the audible alarm 47 MENNMOVE 3 Vital Signs Monitor User Manual Alarm 2 Audio system off icon Press the SILENCE button for gt 2s the audio system is turned off including the audible alarm key volume and pulse tone Pressing SILENCE again can turn on the audio system 5 4 Parameter Alarm WARNING 1 Prior to monitoring make sure that the alarm limit settings are appropriate for your patient 2 Setting alarm limits to extreme values may cause the alarm system to become ineffective The setup for parameter alarms is in the menus In the SYSTEM MENU gt ALARM SETUP you can check and set the alarm limit or alarm status The setup is isolated from each other When a parameter alarm is OFF an icon displays near the parameter If the alarms are turned off individually they must be turned on individually For the parameters whose alarm is set to ON the alarm will be triggered when at least one of them exceeds alarm limit The following actions
41. e dangerous for the children to use an over pressure level 4 Before starting a measurement verify that you have selected a setting appropriate for your patient adult pediatric or neonate 5 Do not apply the cuff to a limb that has an intravenous infusion or catheter in place This could cause tissue damage around the catheter when infusion is slowed or blocked during cuff inflation 6 Make sure that the air conduit connecting the blood pressure cuff and the monitor is neither blocked nor tangled 59 MENNMOVE 3 Vital Signs Monitor User Manual NIBP Monitoring Optional NOTE 1 The equipment is suitable for use in the presence of electrosurgery 2 The continuous measuring automatic measuring and calibration can not be operated on neonate or pediatric patient 3 Please use the proper type of cuff as recommended in this manual or the wrong type may lead to injury on patient especially when measuring neonate 4 Continuous use of the automatic measuring mode for short interval may lead to the discomfort of patient 5 It is suggested that the user should not start NIBP measuring when the low battery displays or the monitor may be turned off automatically 9 3 NIBP Monitoring 1 Plug in the air hose and switch on the system 2 Apply the blood pressure cuff to the patient s arm or leg following the instructions below Ensure that the cuff is completely deflated Apply the appropriate size cuff to the patient and make sur
42. e is beyond the High pressure value is beyond the measurement range measurement range NIBP NOISE Because OF arm motion Make sure that the patient signal noise is too large or Low under monitoring is SIGNAL pulse rate is not regular motionless When the monitor is NIBP Self powered on NIBP module Hish Contact your service Test Error is detected to fail in E personnel calibration Measure again if failure INIT persists stop using PRESSURE ian during measuring 2 module and notify TOO HIGH aii aoa aaa ane a biomedical engineer or manufacturer s service staff Start up measurement NIBP System manometer and leakage iow Contact your service Failure test and NIBP fail in personnel calibration Measure again if failure persists stop using OVER Pressure has exceeded the Low measuring function of NIBP PRESSURE specified upper safety limit module and notify biomedical engineer or manufacturer s service staff NIBP Notify biomedical i SECONDAR Secondary over pressure A Bes S oe a aes High or manufacturer s service Y OVER protection staff PRESSURE i 66 MENNMOVE 3 Vital Signs Monitor User Manual NIBP Monitoring Optional Message Cause Alarm Level What to do CUFF TYPE Cuff type does not comply L lect iate cuff t ERR with the patient type a COS Measuring time 120s adult pediatric mode or Low gt 90s neonatal mode NIBP TIME OUT Measure again or use other measu
43. e monitor or harming the patient Do not touch the patient bed or instrument during defibrillation During monitoring if the power supply is off and there is no battery for standby the monitor will be off and only the patient information and alarm settings can be saved After reconnecting the power supply the user should turn on the monitor for monitoring CAUTION Federal law U S restricts this device to sale by or on the order of a physician Electromagnetic Interference Ensure the environment in which the monitor is installed is not subject to any sources of strong electromagnetic interference such as radio transmitters mobile telephones etc The monitor is designed for continuous operation and is ordinary i e not drip or splash proof Keep the environment clean Avoid vibration Keep it far from corrosive medicine dust area high temperature and humid environment Do not immerse transducers in liquid When using solutions use sterile wipes to avoid pouring fluids directly on the transducer The device and accessories are to be disposed of according to local regulations after their useful lives Alternatively they can be returned to the dealer or the manufacturer for recycling or proper disposal Remove a battery whose life cycle has expired from the monitor immediately Avoid liquid splash and excessive temperature The temperature must be kept between 50 and 400 while working And it should be kept between
44. e that the symbol is over the appropriate artery Ensure that the cuff is not wrapped too tightly around the limb Excessive tightness may cause discoloration and eventual ischemia of the extremity Figure 9 1 Applying Cuff NOTE The width of the cuff is either approximately 40 of the limb circumference or 2 3 of the upper arm length The inflatable part of the cuff should be long enough to encircle 80 100 of the limb The wrong size of cuff can cause erroneous readings If the cuff size is in question use another cuff with suitable size to avoid errors 60 MENNMOVE 3 Vital Signs Monitor User Manual NIBP Monitoring Optional Make sure that the cuff edge falls within the range of mark lt gt If it does not use a larger or smaller cuff that fits better 3 Connect the cuff to the air hose The limb chosen for taking the measurement should be placed at the same level as the patient s heart If this is not possible you should apply the following corrections to the measured values 9 Ifthe cuff is placed higher than the heart level add 0 75 mmHg 0 10 kPa for each inch of difference If it is placed lower than the heart level deduct 0 75 mmHg 0 10 kPa for each inch of difference 4 Check whether the patient mode is appropriately selected Access PATIENT SETUP menu from SYSTEM MENU and pick PAT TYPE item and select the required patient type 5 Select a measurement mode in the NIBP SETUP menu Pick the IN
45. efault O 28 4 3 System A Naas 28 AA SCLC OM ceiien aai i a a a a NA a ata tee 29 as sens Goa II a ou AT 34 O Sale nis 34 4 7 me SOUP esses tas chee los eta le a Pa e 34 DE NIBP SA a ata ee ES 35 A EI CPU ics 40 atscide oi ceod cae aecasedc cli a datos waits se dav otcseede Suteal av E A A 35 4 TO Alarm Pi sn 35 r IEN EEE O LA Yi ad 35 AND Data Storing spaco O 41 AVS Sleep Modei A eee A 42 Chapter AMM a 44 SL AA NOAA 44 A o A O E 44 SoM 2 Alarm Modest A A iii 44 A AN 46 A acta tect Sasa Saati ade cates elena aug Saeed ad vais oN case suse ER 47 A A RA 47 o Asencio Sanaa Aust snes 2 vas aaa ee ae ne eae as 48 5 5 When an Alarm Oc 48 o A O 49 Chapter 6 Trend and Recording siecscscicsacssesssuvecsconstscsosusseassocsducsssussdsbaessoeddesuedscdossssecucsecsuadsansescceaus 50 6 1 General Information on RE do e tea E 4d 50 6 2 Recorder Operati ns a e as e edo to Esa da E 0d 50 Chapter 7 Maintenances Cleaning vs5scs ssseossvesandscvossoosesivousssevansdsedabeseedenouucsenosevdessostenssdeuanesceaceoesuds 52 IV Ste Che daa ed et o ol La ea ota Sura a ea e aloes e 32 T2 G etal Cleanin AD AR AA EA AA AAA AAA 52 A O O 53 TA Replacement OF RUSS sti 53 Chapter 8 SpO2 Monitoring Optional sessseossoossooesossssesssoossoosssosssssssssesssosesoossoosssosssseessosssssesse 54 8 1 What is SpOs Monitor di 54 8 2 Precautions during SpO Pulse Monitoring oooccooccoococonoconocononconncnnncnnnncon nono no conc nnnnccnnnnconn
46. eformation Only patient cable and other accessories supplied by MENNEN MEDICAL LTD can be used Or else the performance and electric shock protection can not be guaranteed and the patient may be injured The user should check the monitor and accessories before use Please set the alarm according to the individual status of patient to avoid delaying treatment Ensure there will be alarm audio prompt when alarming Devices connecting with monitor should be equipotential The monitor is equipped with a wireless AP via network interface to receive RF electromagnetic energy Therefore any other equipment complies with CISPR radiation requirements may also interfere with the wireless communication and make it interrupted Wireless LAN equipment contains an intentional RF radiator that has the potential of interfering with other medical equipment including patient implanted devices MENNMOVE 3 Vital Signs Monitor User Manual Intended Use and Safety Guidance 23 24 25 26 27 28 10 WARNING When the monitor and electrosurgical device are used together the user physician or nurse should guarantee the safety of patient Please disinfect timely to prevent cross infection between patients This monitor is not a device for treatment purposes Only NIBP and SpO applied parts of the monitor are defibrillation proof When a defibrillator is applied keep other accessories away from the patient Otherwise it may result in damaging th
47. egulations regarding disposal of infectious biological medical waste 11 Cleaning frequency and practices must be consistent with institutional policy for cleaning of non sterile devices 12 The F3000 module is not intended for neonatal patients NOTE Even though this device has been designed to minimize the effects of electromagnetic interference it does generate radio frequency energy If not used in accordance with the instructions the device could cause interference in other equipment operating within its vicinity If the device is causing interference the following actions may be taken in an 78 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional attempt to correct the interference e Re orient or re locate the receiving device e Increase the separation between the devices e Consult a customer service representative 10 3 3 Probe Covers Applying amp Removing 1 Open probe cover box by lifting tab at top corner and pulling to remove top panel 2 Insert box of probe covers into top of isolation chamber NOTE To aid infection control never switch boxes between blue and red isolation chambers Also never switch probes between blue and red isolation chambers Keep like colors together 3 Remove probe from the probe well This automatically turns on the thermometer 4 To help remind the user to apply or remove a probe cover a probe icon with flashing probe cover will be displayed when the p
48. for any effect on safety reliability and performance of the equipment if Assembly operations extensions re adjustments modifications or repairs are carried out by persons authorized by MENNEN MEDICAL LTD and The electrical installation of the relevant room complies with national standards and The instrument is used in accordance with the instructions for use Upon request MENNEN MEDICAL LTD may provide with compensation necessary circuit diagrams and other information to help qualified technician to maintain and repair some parts which MENNEN MEDICAL LTD may define as user serviceable Terms Used in this Manual This guide is designed to give key concepts on safety precautions WARNING A WARNING label advises against certain actions or situations that could result in personal injury or death CAUTION A CAUTION label advises against actions or situations that could damage equipment produce inaccurate data or invalidate a procedure NOTE A NOTE provides useful information regarding a function or a procedure II Table of Contents Chapter 1 Intended Use and Safety Guidance se sseessooesoosssosssosesseessoossoossoossssesssecssoossoosssosssoesssose 1 A i ae laa cae Nea ee a a oe eR E oat ne Se ey 1 1 2 Safety UIC eu melnam nuaran base ho eat ee a 1 A O do 1 12 2 Power Source Requirements A i a AE E 1 12 3 Grounding MI e o ls ates 1 1 2 4 Equipotential Grounding AAA A AA AA A Gaeta 2 A O a 0 2 A A A
49. fter changing the displayed language to make the operation effective NURSE CALL Turn on or off the nurse call When the parameter alarm occurs the monitor gives 3s nurse call alarm prompt if the audible alarm or the audio system is off the monitor can also give the nurse call alarm in abnormal condition 36 MENNMOVE 3 Vital Signs Monitor User Manual System Menu The relay contact between pin7 and pin8 of RJ45 is normally open But it is closed when an alarm is audible SERVER IP It can be changed by the user according to the IP of PC installed with MFM CMS of MENNEN MEDICAL LTD SERVER PORT Set server port PRES UNIT Set the pressure unit to mmHg or kPa TEMP UNIT Set the temperature unit to C or F HOT KEY Set the hot key to PATIENT or PRINT COLOR SELECT Set the color of displayed waveforms 16 kinds of colors can be selected Click on DEFAULT to return to the default configuration COLOR SELECT CONF RM Figure 4 19 Color Select OTHER SETUP e SpO SETUP SpO ALARM LEV You can configure the alarm level for SpO SENSOR OFF to HIGH or LOW SENSITIVITY The SpO reading is the average of data collected within a specific time You can set Sensitivity to HIGH MED or LOW via the menu The higher the sensitivity is the quicker the pulse oximeter responds to the changes in the patient s oxygen saturation level Contrarily the lower the sensitivity is the slower the pulse oximeter responds to the
50. h a new fully charged battery at 2511 continuous SpO measuring NIBP automatic measuring mode with the operating interval of 15 minutes automatic recording per 10 minutes Operating time 2 2Ah gt 240 min 4 4Ah gt 480 min Charge time 2 2Ah lt 180 min 4 4Ah lt 360 min The monitor is on or in standby mode A1 2 5 Recorder Record width 48 mm Paper speed 25 mm s Recording types Parameter list recording Trend graph review recording Alarm list recording Real time 8s waveform recording Recording of all the data of current patient ID Real time alarm recording A1 2 6 Data Storage Trend 72 hours at 1 min resolution NIBP trend list 30 000 groups Alarm list 800 groups 94 MENNMOVE 3 Vital Signs Monitor User Manual A1 2 7 NIBP Optional Specifications Mode Manual Auto Continuous Measuring interval in AUTO mode 1 2 3 4 5 10 15 30 60 90 120 240 480 min Measure time in continuous measure mode 5 minutes interval is 5s Measuring type Systolic Pressure Diastolic Pressure Mean Pressure Pulse Rate Measuring range ADU mode SYS 40 mmHg 270 mmHg DIA 10 mmHg 215 mmHg MAP 20 mmHg 235 mmHg PED mode SYS 40 mmHg 200 mmHg DIA 10 mmHg 150 mmHg MAP 20 mmHg 165 mmHg NEO mode SYS 40 mmHg 135 mmHg DIA 10 mmHg 100 mmHg MAP 20 mmHg 110 mmHg Al
51. he last measurement data before the thermometer is powered off 8 Clinical repeatability 0 120 1 5 years old 0 100 gt 5 years old 10 2 3 Alarm 10 2 3 1 Adjutable Range of Alarm Limits Patient Type Measure ALM HI ALM LO Step position ADU PED NEO Ear 42 C 107 6 O 35 5 C 95 9 O 0 1 C 75 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional 10 2 3 2 Alarm Information and Prompts Physiological alarms Message Cause Alarm Level TEMP HIGH Measuring value of TEMP is above upper alarm limit Medium TEMP LOW Measuring value of TEMP is below lower alarm limit Medium Technical alarms Message Cause Alarm Level What to do The TEMP value is Check the integrity of the Tem exceed robe cover make sure it is oe beyond the range of Med P limit clean and take a new 320 43 measurement The infrared ear thermometer will also give error messages on its screen For details about the error messages refer to the accompanying operating instructions of the thermometer NOTE If the infrared ear thermometer frequently signals ERR alarms the insulated board inside the thermometer housing is malfunctioning or the ambient temperature changes the monitor will delete the measurement values onscreen to avoid misoperation 10 2 4 Replacing the Battery The device is supplied with one li
52. he sensor is used on neonates as recommended the specified accuracy range increases by 1 compared with that used on adults Pulse Rate Measuring Range 20bpm 300bpm Alarm Range 30bpm 300bpm Resolution lbpm Accuracy 3bpm 20bpm 250bpm Sensor Wave length approximately 660 and 900nm Emitted light energy lt 15mW A1 2 9 TEMP Optional T2 Module Monitor mode 25 C 45 C Measuring range Predict mode 35 5 C 42 C Working temperature 10 C 40 C Sensor type Oral axillary rectal Alarm range 35 5 C 42 C Resolution 0 186 Accuracy Monitor mode 0 1 C 25 C 45 C not including transducer Response time lt 60s Update time ls 2s 97 MENNMOVE 3 Vital Signs Monitor User Manual Specifications Warm up time lt 10s Time for predicting lt 30s Calibration Self test interval lt 5 minutes TH Module Measuring range 34 C 42 2 C Working temperature 10 C 40 C Alarm range 35 5 C 42 C Resolution 0 1 C Accuracy 0 2 C 35 5 C 42 C 0 3 C out of the range mentioned above Response time Is F3000 Module Measuring range 30 C 43 C Prediction measurement range 35 C 43 C Cold mode prediction measurement range 33 C 43 C Working temperature 10 C 40 C Sensor type Oral axillary rectal Alarm range 33 C 43 C Resolutio
53. ipment is IEC EN60601 1 Type CF equipment The unit displaying this symbol contains an F Type isolated floating patient applied part providing a high degree of protection against shock It is not suitable for use during defibrillation This symbol indicates that the instrument is O IEC EN60601 1 Type BF equipment The unit displaying J H this symbol contains an F Type isolated floating patient applied part providing a high degree of protection against shock and is suitable for use during defibrillation This symbol indicates that the instrument is e IEC EN60601 1 Type BF equipment The unit displaying this symbol contains an F Type isolated floating patient applied part providing a high degree of protection against shock It is not suitable for use during defibrillation VAN Caution MENNMOVE 3 Vital Signs Monitor User Manual Intended Use and Safety Guidance Consult Instructions for Use Equipotentiality Stand by It designates that the switch or switch position which one part of the monitor has been switched on while the monitor is at the status of stand by e 4h Serial number The symbol indicates that the device complies with the European Council Directive 93 42 EEC concerning medical devices oN M 5 Authorized representative in the European community Date of manufacture E EG Manufacturer P N Part Number Recycle The symbol indicates that the
54. is below lower Medium alarm limit e ND HIGH NIBP DIA measuring value is above upper Medium alarm limit IA i lue is below 1 E ND LOW NIBP p measuring value is below lower Medium alarm limit NM HIGN NIBP MAP measuring value is above upper Medium alarm limit NM LOW NIBP Me measuring value is below lower Medium alarm limit Technical alarms display in the area below the NIBP value Message Cause Alarm Level What to do Stop using measuring NIBP COMM NIBP module failure or MnO Sr RE monui ee High notify biomedical engineer ERR communication failure a y or Manufacturer s service staff LOOSE Cuff is no properly wrapped L P 1 the cuff CUFF or no cuff exists os a e ye Check and replace the leaking parts if required ff h t AIR LEAK CU OPES O DONETI Low notify biomedical engineer damaged or manufacturer s service staff 65 MENNMOVE 3 Vital Signs Monitor User Manual NIBP Monitoring Optional Message Cause Alarm Level What to do Check whether the airway is luded NIBP Decline of air pressure is HN ee PRESSURE less than 2 mmHg after 6 Low i a A el il a ERROR deflations ey J still exists contact your service personnel WEAK Cuff is too loose or patient i Use other method to SIGNAL pulse is too weak e measure blood pressure M th tient blood i NIBP Range aybe the patien 00 Maybe the patient blood Exceeded pressure valu
55. itor should be performed by qualified customer service technician The safety and maintenance check can be conducted by personnel from MENNEN MEDICAL LTD WARNING 1 If the hospital or agency that is responding to using the monitor does not follow a satisfactory maintenance schedule the monitor may become invalid and the human health may be endangered 2 Replace batteries according to the instruction of our service engineer NOTE To prolong the life of rechargeable battery it is recommended to charge it at least once every month and it must be done after the electric energy runs out 7 2 General Cleaning WARNING Before cleaning the monitor or the sensor make sure that the equipment is switched off and disconnected from the power line CAUTION 1 Do not use the grinding material such as steel wool etc 2 Do not let the cleaning agent enter into the chassis of the system 3 Do not leave the cleaning agents at any part of the equipment Recommended cleaning agents for cleaning the monitor housing are m Diluted ammonia lt 3 52 MENNMOVE 3 Vital Signs Monitor User Manual Maintenance Cleaning m Ethanol 75 m Isopropanol 70 7 3 Disinfection To avoid extended damage to the equipment disinfection is only recommended when stipulated as necessary in the Hospital Maintenance Schedule Disinfection facilities should be cleaned first Recommended types of disinfectants are m Ethanol 75 m Isopropanol 70
56. itoring Procedure SpO plethysmogram measurement l Switch on the monitor 2 Attach the sensor to the appropriate site of the patient finger 3 Plug the connector of the sensor extension cable into the SpO socket on the SpO module 55 MENNMOVE 3 Vital Signs Monitor User Manual SpO gt 2 Monitoring Optional Figure 8 1 Mounting of the Sensor 8 4 Limitations of Measurement In operation the accuracy of oximetry readings can be affected by 69090909 F High frequency electrical noise including noise created by the host system or noise from external sources such as electrosurgical apparatus which is admitted by the host system Do not use monitor and oximetry sensors during magnetic resonance imaging MRI scanning Induced current could potentially cause burns Intravenous dye Excessive patient movement Outside ray radiation Improper sensor application Sensor temperature maintain between 28 C and 42 C for best operation Placement of the sensor on an extremity that has a blood pressure cuff arterial catheter or intravascular line Significant concentration of dysfunctional hemoglobin such as carboxyhemog lobin and methemoglobin Low SpO2 Circular perfusion is not good for test part It is recommended to use SpO sensors described in Chapter 12 Accessories and Ordering Information 8 5 Alarm 8 5 1 Adjutable Range of Alarm Limits SpO2 PR alarm range Parameter Max Up
57. l TEMP Monitoring Optional 10 3 TEMP Monitoring with F3000 Module 10 3 1 General Information MENNMOVE 3 with the F3000 module measures patient temperatures by oral axillary or rectal means The electromagnetic compatibility of this device has been verified by test according to the EN60601 1 2 2005 requirements 10 3 2 Safety Information WARNING 1 Do not use this device near flammable anesthetics Not suitable for use in the presence of flammable anesthetic mixture with air oxygen or nitrous oxide 2 Do not use this thermometer without first installing a new probe cover 3 Use probe covers supplied by the manufacturer with this thermometer only Use of any other probe cover will result in erroneous temperature readings The thermometer and probe covers are Non sterile Do not use on abraded tissue To limit cross contamination use Blue devices for Oral and Axillary temperature taking only 6 Use RED devices only for RECTAL temperatures 7 Thoroughly dry all electrical contacts on both probe and thermometer after washing or device may fail to function properly 8 For re calibration service or integrity checks refer to a qualified Biomedical Technician or return to the manufacturer 9 Do not open the F3000 module No user serviceable parts inside Opening of the module may affect calibration and voids warranty 10 Disposal of used probe covers must be performed in accordance with current medical practices or local r
58. likely to cause any interference in nearby electronic equipment RF emissions Class A CISPR 11 Harmonic emissions The MENNMOVE 3 is suitable for use in all Class A establishments other than domestic and those directly IEC EN 61000 3 2 connected to the public low voltage power supply network that supplies building used for domestic purposes Voltage fluctuations flicker emissions Complies IEC EN 61000 3 3 A2 2 Electromagnetic Immunity For all EQUIPMENT and SYSTEMS Guidance and manufacture s declaration electromagnetic immunity The MENNMOVE 3 is intended for use in the electromagnetic environment specified below The customer or the user of MENNMOVE 3 should assure that it is used in such an environment Immunity test IEC EN 60601 test level Compliance level Electromagnetic environment guidance Electrostatic discharge ESD IEC EN 61000 4 2 6 kV contact 8 kV air With TH module 2 kV contact 4kV air With module F3000 4 kV contact 6kV air 6 kV contact 8 kV air With TH module 2 kV contact 4kV air With F3000 module 4 kV contact 6kV air Floors should be wood concrete or ceramic tile If floor are covered with synthetic material the relative humidity should be at least 30 Electrical fast transient burst IEC EN 61000 4 4 2kV for power supply lines With TH module 0 5 kV for power supply lines 2 kV f
59. m Glutaraldehyde up to 3 6 WARNING Disinfect the monitor and reusable accessories regularly to avoid patient cross infection 7 4 Replacement of Fuse Unscrew the fuse cap anticlockwise replace the fuse protector tube and screw down the fuse cap clockwise Fuse size D5x20 Rated value T1 6AL 250VP NOTE Switch off the power of the monitor before examining the fuse 53 MENNMOVE 3 Vital Signs Monitor User Manual SpO gt 2 Monitoring Optional Chapter 8 SpO Monitoring Optional 8 1 What is SpO2 Monitoring The monitor uses oximetry to measure functional oxygen saturation in the blood SpO Plethysmogram measurement is employed to determine the functional oxygen saturation of hemoglobin in the arterial blood For example if 97 hemoglobin molecules in the red blood cells of the arterial blood combine with oxygen then the blood has a SpO oxygen saturation of 97 The SpOz numeric on the monitor will read 97 The SpO numeric shows the percentage of hemoglobin molecules which have combined with oxygen molecules to form oxyhemoglobin The SpO2 PLETH parameter can also provide a pulse rate signal and a plethysmogram wave How the SpO PLETH Parameter Works Arterial oxygen saturation is measured by a method called pulse oximetry It is a continuous non invasive method based on the different absorption spectra of reduced hemoglobin and oxyhemoglobin It measures how much light sent from light sources on one side of the senso
60. magnetic Immunity For EQUIPMENT and SYSTEMS that are not LIFE SUPPORTING Guidance and manufacturer s declaration electromagnetic immunity The MENNMOVE 3 is intended for use in the electromagnetic environment specified below The customer or the user of MENNMOVE 3 should assure that it is used in such an environment i 1 test li Panty ECE STILS Compliance Electromagnetic environment guidance test level level Conducted 3 Vrms 3Vrms Portable and mobile RF communications RF IEC EN 150 kHz to 80 MHz equipment should be used no closer to any 61000 4 6 part of the EUS T Ultrasound Scanner Radiated RE including cables than the recommended Svan avon tion distance calculated from th IEC EN separation distance calculated from the 61000 4 3 80 MHz to 2 5 GHz equation applicable to the frequency of the transmitter Recommended separation distance pa EEN LY J 3 5 d ral 80 MHz to 800 MHz 1 d JP 800 MHz to 2 5 GHz 1 Where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and d is the recommended separation distance in metres 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 W NOTE 1 At 80 MHz and 800 MHz the higher frequency ra
61. mennen 49 medical since 1963 MennMove 3 Vital Sign Monitor USER MANUAL DDM 000 015 Rev A April 2014 About this Manual P N DDM 000 015 REV A Release Date April 2014 Copyright MENNEN MEDICAL LTD 2008 2014 All rights reserved Statement This manual will help you understand the operation and maintenance of the product better It is reminded that the product shall be used strictly complying with this manual User s operation failing to comply with this manual may result in malfunction or accident for which MENNEN MEDICAL LTD hereinafter called MENNEN MEDICAL LTD can not be held liable MENNEN MEDICAL LTD owns the copyrights of this manual Without prior written consent of MENNEN MEDICAL LTD any materials contained in this manual shall not be photocopied reproduced or translated into other languages Materials protected by the copyright law including but not limited to confidential information such as technical information and patent information are contained in this manual the user shall not disclose such information to any irrelevant third party The user shall understand that nothing in this manual grants him expressly or implicitly any right or license to use any of the intellectual properties of MENNEN MEDICAL LTD MENNEN MEDICAL LTD holds the rights to modify update and ultimately explain this manual Responsibility of the Manufacturer MENNEN MEDICAL LTD only considers itself responsible
62. mode to PREDICT or MONITOR MEASURE POS Set the measuring position to ORAL AXILLARY or RECTA The axillary sensor can be used for measuring oral axillary temperature while the rectal sensor for measuring rectal temperature 10 1 4 Alarm 10 1 4 1 Adjutable Range of Alarm Limits Patient Type Measure position ALM HI ALM LO Step ADU Oral Axillary Rectal 42 C 107 6 4 35 5 C 95 9 11 0 1 C PED Oral Axillary Rectal 42 C 107 6 F 35 5 C 95 9 F 0 1 C 70 MENNMOVE 3 Vital Signs Monitor User Manual 10 1 4 2 Alarm Information and Prompts Physiological alarms TEMP Monitoring Optional Message Cause Alarm Level TEMP HIGH Measuring value of TEMP is above upper alarm limit Medium TEMP LOW Measuring value of TEMP is below lower alarm limit Medium Technical alarms Message Cause Alarm Level What to do TEMP module Stop using measuring function Temp COMM failure or A of TEMP module notify Ds High l l STOP communication biomedical engineer or failure Manufacturer s service staff The TEMP value is Put the sensor into the sensor Temp exceed limit beyond the range of Medium bracket take it out and 250 45 measure again No TEMP TEMP sensor is not Connect the sensor and the connected to the Low monitor well and measure SENSOR TEMP module
63. monitoring phase Unplug the SpO sensor cable from the socket the screen will display the error message SpO2 SENSOR OFF and the audible alarm is activated 2 If the SpO sensor can not work properly please reconnect the sensor or change a new one 3 Do not use the sterile supplied SpO2 sensors if the packaging or the sensor is damaged and return them to the vendor 4 Prolonged and continuous monitoring may increase the risk of unexpected change of dermal condition such as abnormal sensitivity rubescence vesicle repressive putrescence and so on It is especially important to check the sensor placement of neonate and patient of poor perfusion or immature dermogram by light collimation and proper attaching strictly according to changes of the skin More frequent examinations may be required for different patients 5 Tissue damage may be caused by incorrect application or prolonged measurement duration using the sensor more than 4 hours Inspect the sensor periodically according to sensor user manual 6 The sensor complies with the ISO 10993 1 2009 for biocompatibility NOTE 1 Make sure the nail covers the light window 2 The wire should be on the backside of the hand 3 Hand should not be too cold when measuring and the nail polish should be cleaned before measuring or the data accuracy may be affected 4 SpQOz waveform is not proportional to the pulse volume 5 A functional tester cannot be used to assess SpO accuracy 8 3 Mon
64. n 0 1 C Accuracy Monitoring Mode and Preditive Mode 0 1 C Quick Predictive Mode 0 3 C 98 MENNMOVE 3 Vital Signs Monitor User Manual Specifications Typical measurement time after Oral Quick Predictive Mode 3 5 seconds insertion into measurement site non fever temps 8 10 seconds fever temps Oral Predictive Mode 6 10 seconds Axillary 8 12 seconds Rectal 10 14 seconds Monitoring Mode all sites 60 120 seconds A1 2 10 Wirless Network Compliant with Standard and IEEE802 11b g R amp TTE Directive 99 5 EEC Directive Frequency Range 2 412 GHz 2 462 GHz America 2 412 GHz 2 484 GHz Japan 2 412 GHz 2 472 GHz ETSI Working frequency segment Ch1 11 America Ch1 14 Japan Chl 13 ETSI 99 Appendix EMC Information Guidance and Manufacture s Declaration A2 1 Electromagnetic Emissions For all EQUIPMENT and SYSTEMS Guidance and manufacture s declaration electromagnetic emission The MENNMOVE 3 is intended for use in the electromagnetic environment specified below The customer or the user of the MENNMOVE 3 should assure that it is used in such and environment Emission test Compliance Electromagnetic environment guidance as The MENNMOVE 3 uses RF energy only for its internal RF emissions function Therefore its RF emissions are very low and are Group 1 i y CISPR 11 not
65. ncreases as the pulse breaks through the occlusion in the artery As the cuff pressure decreases further the pulsations increase in amplitude reach a maximum which approximates to the mean pressure and then diminish In adult and pediatric mode the blood pressure measurements determined with this device comply with the American National Standard for Electronic or Automated Sphygmomanometers ANSI AAMI SP10 1992 in relation to mean error and standard deviation when compared to auscultatory measurements in a representative patient population For the auscultatory reference the fifth Korotkoff sound was used to determine the diastolic pressure In neonatal mode the blood pressure measurements determined with this device comply with the American National Standard for Electronic or Automated Sphygmomanometers ANSI AAMI SP10 1992 in relation to mean error and standard deviation when compared to intra arterial measurements in a representative patient population 9 2 NIBP Safety Information WARNING 1 It is forbidden to perform NIBP measurements on patient with sickle cell disease or under any condition where the skin is damaged or expected to be damaged 2 For a thrombasthenia patient it is important to determine whether measurement of the blood pressure shall be done automatically The determination should be based on the clinical evaluation 3 Ensure that the correct setting is selected when performing measurements on children It may b
66. nfigured to single parameter mode with SpO2 measuring only or NIBP measuring only In SpO only or NIBP only measuring mode the single parameter of SpO or NIBP is displayed The configuration is preset by the manufacturer it can not be changed by the user 3 2 1 General Display Mode The screen is divided into three areas 1 Parameter area 2 Waveform Trend list Alarm list area 3 Information area e 4 4 8 MAP 86 Y dd MOI 36 4 Sp0 gt PR BPM 60 3 Figure 3 2 Main display with waveform 10 MENNMOVE 3 Vital Signs Monitor User Manual Introduction The Waveform area can display parameter trend list or alarm list It displays as follows E 368 mo 442 os DIA 84 71 CUFF TEMP EN E PR BPM TIME ID ALARM LIST 15 09 53 1 xx TEMP 36 9 15 09 52 1 x TEMP 36 3 15 09 52 1 x TEMP 36 3 15 09 52 1 x TEMP 36 5 Figure 3 3 Main display with alarm list The display on the screen can be changed to a trend graph as follows TREND GRAPH Figure 3 4 Display trend graph 11 MENNMOVE 3 Vital Signs Monitor User Manual The icons on the interface and their meanings are as follows Introduction Battery status indicator Connected to mains power supply Network connection indicator Network connection off Medium Low alarm High alarm icon Au
67. ng a TEMP Measurement 90 0 9094 Select the correct sensor according to the measuring position and patient type Apply the sensor to the patient You are advised to use a protective rubber cover on sensor Ensure the alarm settings on or off higher alarm or lower alarm limit are appropriate for the patient and the type of temperature measurement Select the correct measuring position in menu Switch on the monitor It takes 2 min 3 min for the body temperature to stabilize WARNING To ensure optimal accuracy always confirm that the correct mode and alarm limit are selected Changing the measure position may lead to the change of alarm limit Verify probe cables fault detection before the beginning of monitoring phase Unplug the temperature probe cable from the socket and then the screen will display the error message TEMP SENSOR OFF and the audible alarm is activated Take the TEMP probe and cable carefully When they are not in use you should coil up the probe and cable into a loose circle If the wire inside the cable is tensely pulled it may cause mechanical damage to the probe and the cable The calibration of the temperature module is necessary every two years or as frequently as dictated by your Hospital Procedures Policy When you need to calibrate the temperature measurement please contact the manufacturer Patient actions may interfere with accurate oral temperature readings Ingesting hot or cold liquids
68. nge applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people a Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile radios amateur radio AM and FM radio broadcast and TV broadcast 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 EUS TUltrasound Scanner is used exceeds the applicable RF compliance level above the EUS T Ultrasound Scanner should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as reorienting or relocating the EUS TUltrasound Scanner j Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m A2 4 Recommended Separation Distances Recommended separation distances between portable and mobile RF communications equipment and the MENNMOVE 3 Vital Signs Monitor The MENNMOVE 3 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of the MENNMOVE 3 can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment
69. normal condition is detected during use recharge or storage Keep it away from the monitor 3 Make sure the monitor is used in the appointed range of voltage so that the effect of power supply can be not noticeable 4 Before using the rechargeable lithium ion battery hereinafter called battery be sure to read the user manual and safety precautions thoroughly 5 Do not place battery in the monitor with the and in the wrong way around 6 Do not connect the positive and negative terminals with metal objects and do not put the battery together with metal objects which can result in short circuit 7 Do not heat or throw battery into fire 8 Do not use leave battery close to fire or other places where temperature may be above 600 Do not immerse throw and wet battery in water seawater 9 Do not destroy the battery do not pierce battery with a sharp object such as a needle do not hit with a hammer step on or throw to cause strong shock do not disassemble or modify the battery 10 Take out the battery before cleaning or storing the monitor for more than 1 month 3 5 2 Battery Status on the Main Screen The monitor is equipped with a built in rechargeable battery When switching on AC power supply the battery will be recharged automatically until full electric energy There is a sign LO or ERA in the bottom right corner of screen When the monitor is working with AC mains power and it has no batter
70. ntainer by pushing top button 82 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional NOTE 1 Probe movement during a measurement can affect the thermometer s ability to measure the site temperature and may lengthen the time required to obtain a reading 2 Ifa beep is not heard 10 seconds after withdrawing the probe from the probe well and starting temperature measurement in Predictive Mode or Quick Predictive Mode check the physical connection of the F3000 module 10 3 7 TEMP Setup for F3000 Module Click TEMP SETUP in the SYSTEM MENU and the following settings are available MEASURE MODE Set the measuring mode to PREDICT QUICK PREDICT or MONITOR MEASURE POS Set the measuring position to ORAL AXILLARY or RECTA COLD MODE Activate deactivate the cold mode by setting it to ON OFF NOTE 1 The QUICK PREDICT mode is for oral measurement only 2 The QUICK PREDICT mode is unavailable when COLD MODE is set to ON 3 Make sure all settings of TEMP Setup are properly set up every time before you withdraw the probe from the probe well If you modify the settings immediately a measurement is completed the new settings will be effective for the next measurement 10 3 8 Alarm 10 3 8 1 Adjutable Range of Alarm Limits Patient Type Measure position ALM HI ALM LO Step 43 C 33 C ADU PED Oral Axillary Rectal 0 1 C 39 C by default 36 C by default 10 3 8 2 Alarm Info
71. nto the paper cassette printing side facing upwards Ensure proper position and tidy margin 50 MENNMOVE 3 Vital Signs Monitor User Manual Trend and Recording Pull about 2cm of the paper out and then close the recorder casing NOTE Be careful when inserting paper Avoid damaging the thermo sensitive print head Unless when inserting paper or shooting troubles do not leave the recorder catch open Removing Paper Jam When the recorder functions or sounds improperly you should open the recorder casing to check for a paper jam Removing the paper jam in the following way Cut the record paper from the feeding edge Open the recorder casing Re insert the paper 51 MENNMOVE 3 Vital Signs Monitor User Manual Maintenance Cleaning Chapter 7 Maintenance Cleaning 7 1 System Check Before using the monitor do the following Check if there is any mechanical damage Check if all the outer cables inserted modules and accessories are in good condition Check all the functions of the monitor to make sure that the monitor is in good condition If you find any damage on the monitor stop using the monitor on patient and contact the biomedical engineer of the hospital or MENNEN MEDICAL LTD immediately The overall check of the monitor including the safety check should be performed only by qualified personnel once every 24 months and each time after fixing up All the checks that need you to open the mon
72. o the ground line if necessary Refer to section1 2 Safety Guidance for details NOTE When the battery configuration is provided after the monitor is transported or stored the battery must be recharged Switch on AC power supply can recharge the battery no matter if the monitor is powered on 2 3 Powering on the Monitor Press the ON OFF button on front panel to power on the monitor LOGO information will be displayed on the screen WARNING Do not use it on any patient if any sign of damage is detected or the monitor displays some error messages Contact biomedical engineer in the hospital or Customer Service Center immediately MENNMOVE 3 Vital Signs Monitor User Manual Installation of Monitor NOTE 1 Check all the functions of the monitor and make sure that the monitor is in good condition 2 If rechargeable batteries are provided recharge them after using the monitor every time to ensure the electric power is enough 3 The interval between double presses of ON OFF button should be more than 1 second 2 4 Connecting Sensor to Patient Connect all the necessary patient sensors between the monitor and the patient NOTE For information on correct connection refer to related chapters 2 5 Checking the Recorder If your monitor is equipped with a recorder open the recorder door to check if paper is properly installed in the slot If no paper is present refer to Chapter 6 Trend and Recording for details MENNMOVE 3 Vit
73. o turn off the audio system including audible alarm key volume and pulse tone Then the icon displays in the information area Pressing the button again can resume the audio system 19 MENNMOVE 3 Vital Signs Monitor User Manual NIBP START STOP To inflate the cuff and start blood measuring During the measuring process press the button to stop measuring m For the monitor with NIBP function ALARM LIMET For SpO only monitor the NIBP STASRT STOP button N is changed to ALARM LIMIT button Press this button to NA set the alarm limit of the parameters of SpO TREND WAVEFORM a Press this button to switch between waveform display ae trend graph and trend list display HOT KEY In the monitoring mode this hot key is configured as the RECORD record button by default Press it and you can print out the SHORTCUT KEY currently displayed waveforms trend graph trend lists or FOR CHANGING alarm lists Pressing it while recording can stop recording PATEN EELEE In the spot check mode this hot key is configured as the y shortcut key for changing the patient type You can rapidly alter the patient type by pressing this button MENU eS Press to open the SYSTEM MENU Refer to Chapter 4 Es System Menu for details cy UP O vw Select the items in menu or decrease or increase the OK items Confirm the selection by pressing OK Y DOWN The icons on the front panel
74. or alarm list which can be printed out via RECORD 6 1 General Information on Recording A thermal dot matrices recorder with printout paper of 48mm wide is used for the monitor Performance of the Recorder Set the displayed content via SYSTEM MENU gt SELECTION trend table or alarm list Then print it via RECORD Press the RECORD to print out the currently displayed content Press the UP DOWN button to page up or down the screen then press RECORD to print it out The real time waveform of 8s can be printed out NOTE 1 You can press the RECORD on the control panel to stop the current recording process 2 It is suggested that the user should not use the recorder when the low battery displays or the monitor may be turned off automatically 6 2 Recorder Operations Record Paper Requirement Only standard thermosensitive record paper can be used otherwise the recorder may not function the recording quality may be poor and the thermosensitive printhead may be damaged Proper Operation When the recorder is working the record paper goes out steadily Do not pull the paper outward with force otherwise the recorder may be damaged Do not operate the recorder without record paper Paper Out When OUT OF PAPER alarm is displayed the recorder can not start Please insert record paper properly Inserting Paper Pull outwards the upper arc part of the recorder casing to release the casing Insert a new roll of paper i
75. or power supply lines With TH module 0 5 kV for power supply lines Mains power quality should be that of a typical commercial or hospital environment Surge IEC EN 61000 4 5 1 kV differential mode 2 kV common mode 1 kV differential mode 2 kV common mode Mains power quality should be that of a typical commercial or hospital environment Power frequency 50 60Hz magnetic field IEC EN 61000 4 8 Voltage dips short interruptions and voltage variations on power supply input lines IEC EN61000 4 11 3A m lt 5 UT gt 95 dip in UT for 0 5 cycle 40 UT 60 dip in UT for 5 cycles 70 UT 30 dip in UT for 25 cycles lt 5 UT 95 dip in UT for 5 sec 3A m lt 5 UT gt 95 dip in UT for 0 5 cycle 40 UT 60 dip in UT for 5 cycles 70 UT 30 dip in UT for 25 cycles lt 5 UT gt 95 dip in UT for 5 sec Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment Mains power quality should be that of a typical commercial or hospital environment If the user of the EUS TUltrasound Scanner requires continued operation during power mains interruptions it is recommended that the EUS T Ultrasound Scanner be powered from an uninterruptible power supply or a battery NOTE UT is the a c mains voltage prior to application of the test level A2 3 Electro
76. ose on wired networks 2 The obstacle may interfere with data transmission and even cause data loss not available in the U S A 87 MENNMOVE 3 Vital Signs Monitor User Manual Chapter 12 Accessories and Ordering Information The specification of accessories recommended is listed below Using other accessories WARNING may damage the monitor The following accessories are recommended when using this monitor MENNEN MEDICAL LTD SpO 12 01 110492 SH3 Neonate resuable SpO2 Warp Sensor 12 01 110515 SH4 adult soft tip SpO2 sensor TPU 02 01 110531 SH4 adult silicone soft tip SpO2 sensor 12 01 110521 SH5 SpO2 Silicone Soft tip Sensor pediatric 12 01 109069 SH1 adult reusable SpO2 Sensor LEMO 12 01 109079 SH1 adult reusable SpO2 finger sensor DB9 01 57 040196 Adult disposable SpO2 sensor 01 57 040197 Pediatric Disposable SpO2 sensor 01 57 040198 Infant Disposable SpO2 sensor 01 57 040199 Neonatal Disposable SpO2 Sensor 01 13 210001 SpO2 extension cable DB9 to LEMO TPU 2m NELLCOR SpO 11 15 30043 Nellcor Reusable Adult SpO2 Sensor DS 100A OxiMax 11 15 40096 Nellcor Reusable Adult Neonate SpO2 Sensor OXI A N OxiMax 11 13 30131 Nellcor SpO2 Extension Cable 88 Accessories and Ordering Information MENNMOVE 3 Vital Signs Monitor User Manual Accessories and Ordering Information NI
77. outh to reach the rear sublingual pocket Have the patient close his lips around the sensor Sublingual Pocket Figure 10 1 Measuring position in mouth For measuring oral TEMP do not take an axillary temperature through patient s clothing 5 The monitor enters PREDICT measuring mode displays in the TEMP parameter area After Predict measuring is over the measuring result displays and MEASURE OVER appears on the interface 69 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional 6 Ifthe predict measuring is successfully finished the monitor enters MONITOR mode after 30s otherwise the monitor enter MONITOR mode immediately after the predict measuring The monitoring state lasts for 10 min and then the monitor enters waiting state displays in the TEMP parameter area on interface Put the sensor back into the sensor bracket 7 Ifnecessary repeat the measurement according to the procedure above NOTE After one measurement the user should put the sensor back to the sensor bracket and then take it out for starting a new measurement The monitor s state can change from the PREDICT mode into the MONITOR mode but it can not change from the MONITOR mode into the PREDICT mode 10 1 3 TEMP Setup for T2 Module Click on the TEMP SETUP in the SYSTEM MENU to display the following figure TEMP SETUP EXIT Figure10 2 TEMP Setup MEASURE MODE Set the measuring
78. ow to ensure completely safe electrical installation The environment where the monitor will be used should be reasonably free from vibration dust corrosive or explosive gases extremes of temperature humidity and so on For a cabinet mounted installation allow sufficient room at the front for operation and sufficient room at the rear for servicing with the cabinet access door open The monitor operates within specifications at ambient temperatures between 5 40 Ambient temperatures that exceed these limits could affect the accuracy of the instrument a a cause damage to the modules and circuits Allow at least 2 inches 5cm clearance around the instrument for proper air circulation 1 2 2 Power Source Requirements Refer to Appendix 1 2 3 Grounding the Monitor To protect the patient and hospital personnel the cabinet of the monitor must be grounded Accordingly the monitor is equipped with a 3 wire cable which grounds the instrument to the power line ground protective earth when plugged into an appropriate 3 wire receptacle If a 3 wire receptacle is not available consult the hospital electrician Connect the grounding wire to the equipotential grounding terminal on the mains system If it is not evident from the instrument specifications whether a particular instrument combination is hazardous or not for example due to summation of leakage currents the user should consult the manufacturers concerned or an exper
79. per Limit Min Lower Limit Step SpO 100 0 1 PR 300 30 1 56 MENNMOVE 3 Vital Signs Monitor User Manual Default SpO alarm limits SpO Monitoring Optional Max Upper Limit Min Lower Limit Step ADU 100 90 1 PED 100 90 1 NEO 95 88 1 Default PR alarm limits Max Upper Limit Min Lower Limit Step ADU 120 50 1 PED 160 75 1 NEO 200 100 1 8 5 2 Alarm Information and Prompts Physiological alarm Message Cause Alarm Level SpO HIGH SpO gt measuring value is above upper alarm limit Medium SpO2 LOW SpO2 measuring value is below lower alarm limit Medium PR HIGH PR measuring value is above upper alarm limit Medium PR LOW PR measuring value is below lower alarm limit Medium Sphygmic signal from the measured position is too NO PULSE weak the monitor does not detect any sphygmic High signal Technical alarms Al Message Cause What to do Level Mak th i The SpO sensor may be High Low ten de da SpO2 SENSOR OFF disconnected from the Configured P finger or another patient by the user ne appropriate position 57 MENNMOVE 3 Vital Signs Monitor User Manual SpO Monitoring Optional Al Message Cause pt What to do Level Stop using measuring function of SpO2 module SpO2 COMM STOP SpO2 module ue High notify biomedical enginee
80. pull the ear back to straighten the ear cannal and snugly fit the probe into the ear canal aiming towards the membrane of the eardrum to obtain an accurate reading lt AS SA NOTE For children over two year old and adults pull the ear straight up and back as shown 74 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional below R Press the Scan button for one second until you hear a long beep sound which signals the end of the measurement and rusults will be shown on the display of the monitor Before starting another measurement wait until all icons stop flashing and two beep sounds are heard WARNING Replace the probe cover after each use to ensure an accurate reading and avoid cross contamination NOTE 1 The thermometer will automatically shut down after one minute pending to extend battery life 2 The device must stay in stable ambient room temperature for 30 minutes before operation 3 Before the measurement please stay in a stable environmrnt for five minutes and avoid exercise or bath for 30 minutes 4 It is recommended that you measure the same ear for three times If the three measurements are different select the highiest temperature 5 Remember to compare the measurement result to the regular temperature of the patient There is no gender and age limitation for using infrared ear thermometer The data saved in the thermometer is t
81. r Check for proper operation and accuracy 5 Holding the thermometer too long may cause a higher ambient temperature reading of the probe which could make the body temperature measurements lower than usual 73 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional 10 CAUTION Check whether the thermometer is damaged once it drops If you cannot make sure of it send the complete device to your local dealer for recalibration Keep the unit dry and away from any liquids and direct sunlight The probe should not be submerged into liquids For more details about using the infrared ear thermometer refer to the accompanying operating instructions of the thermometer The monitor outfitted with the TH module must not be used together with other electrosurgery equipment for example ESU 10 2 2 Measuring Procedure l Align the center of the probe to the center of the probe cover Make sure to place the adhensive side of probe cover upward 2 Insert the probe into the probe cover on the probe cover loader until the probe cover clicks in place T NOTE If the probe cover did not install well the icon gt will flash on the LCD of the thermometer and you cannot take the ear temperature with four beep sounds heard and without reading on the LCD when measuring Press ON MEM button of the thermometer The icon will display on the LCD of the 3 thermometer and you will hear two beep sounds 4 Gently
82. r communication failure 5 or manufacturer s service staff Reconnect the sensor or choose another measured SpO LOW The measured signals position If the problem PERFUSION coming from pulse are too Low remains please notify weak biomedical engineer or manufacturer s service staff qa Er Sp Senge e Reconnect the sensor with disconnected from the de outra Make te NO SpO SENSOR monitor or the sensor is Low a TE the monitor is well not connected well to the connected with the cable device SpO2 NOISY There is interference with Check the condition of SIGNAL SpO2 measurement patient and avoid patient a Low signals and the waveform movement make sure the is abnormal cable is well connected Prompts Message Cause SEARCH PULSE SpO sensor may be disconnected from the patient or the monitor 8 6 Maintenance and Cleaning These reusable sensors should be cleaned and disinfected The validated cleaning agents are listed below Recommended cleaning agents are m Ethanol 75 Isopropanol 70 58 MENNMOVE 3 Vital Signs Monitor User Manual NIBP Monitoring Optional Chapter 9 NIBP Monitoring Optional 9 1 Overview This monitor uses the oscillometric method for measuring NIBP It can be used for adult pediatric and neonatal patients Oscillometric devices measure the amplitude of pressure changes in the occluding cuff as the cuff deflates from above systolic pressure The amplitude suddenly i
83. r is transmitted through patient tissue such as a finger or an ear to a receiver on the other side The amount of light transmitted depends on many factors most of which are constant However one of these factors the blood flow in the arteries varies with time because it is pulsating By measuring the light absorption during a pulsation it is possible to derive the oxygen saturation of the arterial blood Detecting the pulsation gives a PLETH waveform and pulse rate signal The SpO gt value and the PLETH waveform can be displayed on the main interface The sensor contains LEDs that emit red light at a wavelength of approximately 660 nm and infrared light at a wavelength of approximately 905 nm The power of the sensor LED is less than 15 mW WARNING Pulse oximetry can overestimate the SpO value in the presence of Hb CO Met Hb or dye dilution chemicals SpO Pulse Monitoring WARNING 1 ES Electrosurgery equipment wire and SpO cable must not be tangled up 2 Do not put the sensor on extremities with arterial catheter or venous syringe NOTE Do not perform SpO2 measuring and NIBP measuring on a same arm at one time because obstruction of blood flow during NIBP measuring may adversely affect the reading of SpO value 54 MENNMOVE 3 Vital Signs Monitor User Manual SpO gt 2 Monitoring Optional 8 2 Precautions during SpO2 Pulse Monitoring WARNING Verify sensor cable fault detection before beginning of
84. r so the system will automatically open the deflating valve which marks the completion of a pneumatic measurement If no prompt appears on the bottom of the NIBP parameter area it indicates that the airway is in good situation and no air leaks exist However if the prompt AIR LEAK appears in the place it indicates that the airway may have air leaks In this case the user should check for loose connection After confirming secure connections the user should re perform the pneumatic test If the failure prompt still appears please contact the manufacturer for repair Cuff Figure 4 21 Diagram of NIBP Air Leakage Test NIBP MEMORY You can set this item to ON or OFF If the item is ON the monitor will automatically memorize the initial measurements of the patient when measuring his or her blood pressure Then the monitor will inflate the cuff according to the previous memorized measurements This function accelerates the measuring of the patient s blood pressure 39 MENNMOVE 3 Vital Signs Monitor User Manual System Menu O ALARM SETUP ALARM MUTE Set the duration of silencing the audible alarm to 60s 120s or 180s ALARM SILENCE You can set this item to ON or OFF If the item is ON you can turn off the audio system by pressing the SILENCE button on the front panel for gt 2s In this case all sounds including the alarm sound key sound and sphygmic sound coming from the monitor will be mute If the item is OFF the
85. ring method Prompt message display in the prompt area below NIBP value Message Cause Manual measuring During manual measuring mode Continual Measuring In continuous measuring mode Auto measuring During automatic measuring mode Measurement over Measurement over Calibrating During calibrating Calibration over Calibration over Leak testing During leakage test Leak test over Leakage test is over Resetting NIBP module in resetting 9 6 Maintenance and Cleaning If the cover requires more rigorous cleaning remove the air bladder first Allow the cover to thoroughly air dry before use Cuffs have been tested to withstand the following recommended disinfectants isopropanol 70 ethanol 75 67 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional Chapter 10 TEMP Monitoring Optional 10 1 TEMP Monitoring with T2 Module 10 1 1 Introduction MENNMOVE 3 with the T2 module takes a temperature in either Predict or Monitor Mode In the Predict mode the monitor measures oral axillary rectal TEMP in a short time calculates and gets the measuring results In Monitor mode it can monitor patient for 10 min The Oral Axillary sensor and Rectal sensor are of standard configuration The monitor can only measure temperature of adult and pediatric patients If the user measure temperature of neonate patient the monitor will not display data Maki
86. rm continuous measurement immediately 63 MENNMOVE 3 Vital Signs Monitor User Manual NIBP Monitoring Optional 9 5 Alarm 9 5 1 Adjutable Range of Alarm Limits The adjusting range of NIBP alarm limits Adult Mode SYS 40 mmHg 270 mmHg DIA 10 mmHg 215 mmHg MAP 20 mmHg 235 mmHg Pediatric Mode SYS 40 mmHg 200 mmHg DIA 10 mmHg 150 mmHg MAP 20 mmHg 165 mmHg Neonatal Mode SYS 40 mmHg 135 mmHg DIA 10 mmHg 100 mmHg MAP 20 mmHg 110 mmHg Default NIBP alarm limits ADU mmHg PED mmHg NEO mmHg Lower Upper Lower Upper Lower Upper Limit Limit Limit Limit Limit Limit SYS 90 160 70 120 40 90 DIA 50 90 40 70 20 60 MAP 60 110 50 90 25 70 When the monitor is configured to NIBP only measuring mode the PR is displayed in the ALARM SETUP menu The range of PR alarm limit Max Upper Limit BPM Min Lower Limit BPM Step BPM PR 240 40 1 Default PR alarm limit Max Upper Limit BPM Min Lower Limit BPM Step BPM ADU 120 50 1 PED 160 75 1 NEO 200 100 1 64 MENNMOVE 3 Vital Signs Monitor User Manual 9 5 2 Alarm Information and Prompts Physiological alarms NIBP Monitoring Optional Message Cause Alarm Level ue j NS HIGH NIBP SYS measuring value is above upper Medium alarm limit i lue is below l NS LOW NIBP SYS measuring value
87. rmance specifications given here if stored or used outside the specified temperature and humidity ranges When the monitor and related products have differing environmental specifications the effective range for the combined products is that range which is common to the specifications for all products Temperature Working 5 C 40 C With TEMP 10 C 40 C 92 MENNMOVE 3 Vital Signs Monitor User Manual Specifications Transport and storage 20 C 55 C With TH module 20 C 50 C Humidity Working 25 80 non condensing Transport and storage 25 93 non condensing Altitude Working 860hPa 1060hPa Transport and storage 700hPa 1060hPa Power supply Voltage 100V 240V Frequency 50Hz 60Hz FUSE T 1 6AL A1 2 3 Display Device 5 6 inch color TFT Resolution 640x480 Messages 1 Power Supply Indicator LED Green 1 Power On Indicator LED Green 1 Alarm Indicator LED Red Yellow 1 Charge Indicator LED Yellow 1 Alarm Mute Indicator LED Backlight 1 NIBP Working Status Indicator LED Backlight 3 indicating modes correspond to Alarm Mode 93 MENNMOVE 3 Vital Signs Monitor User Manual Specifications A1 2 4 Battery Quantity 1 Type Li battery Capacitance 2 2Ah 4 4Ah optional Working period Wit
88. rmation and Prompts Physiological alarms Message Cause Alarm Level Measuring value of TEMP is above the upper alarm TEMP HIGH te Medium limit 83 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional Message Cause Alarm Level TEMP LOW Measuring value of TEMP is below the lower alarm Medien limit Technical alarms Message Cause Alarm Level What to do TEMP module Stop using measuring function Temp COMM failure or f of TEMP module notify ae High STOP communication biomedical engineer or failure Manufacturer s service staff The TEMP value is Put the probe into the probe Temp exceed A ae out of the range of Medium well take it out and measure limit 300 43 again The probe in use is Measure Site not consistent with Medium Correctly set the measure Error the measure position i position on the monitor set on the monitor Prob figurati No TEMP m 5 am pases on Well connect the probe and the SENSOR P monitor and measure again connected error Stop using measuring function t i f TE a i Tenip Eor EDI System error during Medium of ME module notify synchronization biomedical engineer or Manufacturer s service staff l Stop using measuring function System iver during E of TEMP module notify Temp Error E02 patient thermistor Medium f DD biomedical engineer or calibration Manuf
89. robe is withdrawn from the probe well and following a completed temperature measurement 5 Insert the probe end into a cover in the box Push the handle firmly until you feel the cover snap into place 6 Take appropriate temperature measurement oral axillary or rectal 7 Eject the used cover into bio waste container by pressing top button 8 Remove discard and replace box when empty 10 3 4 Changing Isolation Chambers and Probes NOTE 1 For aiding in infection control use only the Blue probe and Blue isolation chamber for Oral and Axillary temperature taking The Red probe and Red isolation chamber must only be used for Rectal temperature taking 2 Do not attach a Red probe to a Blue isolation chamber or vice versa 1 To remove or replace any isolation chamber probe assembly grasp the isolation chamber from each side as shown Squeeze inward releasing the snaps and slide the isolation chamber up to pull off To replace align probe well finger with opening in the top of the unit Slide the isolation chamber down until the side snaps click into place The probe is connected to the thermometer automatically ON ES a Da To change probes remove the isolation chamber as described previously 79 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional 7 Grasp the sides of the L shaped connector piece with one hand and then using other hand pull backward on the latch holding the end of the L
90. s in danger or the monitor has serious problem in technical respect It is the most serious alarm Medium level alarm means serious warning Low level alarm is a general warning The monitor provides two types of alarm physiological alarms and technical alarms Also the monitor provides prompts Physiological alarms refer to those alarms triggered by patient s physiological situation which could be considered dangerous to his or her life Technical alarm refer to system failure which can make certain monitoring process technically impossible or make monitoring result unbelievable The monitor can give the character indication of monitoring process or other functions And this character is called prompts The alarm levels for technical alarms and some physiological alarms are pre set by the system and cannot be changed by the user in most of the cases But you can alter the alarm level for SpO SENSOR OFF For more information please refer to SoO2 SETUP in 4 11 Maintain 5 1 2 Alarm Modes When alarm occurs the monitor can raise the user s attention in at least three ways which are audio prompt visual prompt and description Audio and visual prompt is given by LCD display device the speaker on the display device and the alarm indicator Physiological alarm Technical Alarm or description is displayed in information area or beside the parameters at the bottom of the screen NOTE The concrete presentation of each alarm prompt is related
91. shaped connector 8 Once free of the latch slide the L shaped connector out of isolation chamber 9 To replace properly align the top of the L shaped connector to the slot on the back of the isolation chamber 10 Then slide the connector up into the slot pressing firmly on the bottom of the connector until it clicks into place 10 3 5 Measuring Mode Predictive Mode When MEASURE MODE is set to PREDICT the monitor operates in Predictive Mode to provide fast and accurate temperature measurements Quick Predictive Mode When MEASURE MODE is set to QUICK PREDICT the monitor operates in Quick Predictive Mode which is an oral predictive measurement mode intended for situations where fast temperature measurements are desired Quick Predictive Mode allows clinicians to rapidly identify patients with normal body temperatures If the patient temperature is outside of the normal range the monitor will automatically switch into its standard predictive mode to provide a more accurate reading Quick Predictive Mode is not available when in Cold Mode Monitoring Mode When MEASURE MODE is set to MONITOR the monitor will perform continual temperature measurement for a maximum of 10 minutes Besides in the following instances the monitor will automatically switch to Monitoring Mode and perform temperature measurement for a maximum of 5 minutes until the temperature stabilizes 1 When the monitor operates in Predictive
92. t in the field to ensure that the necessary safety of all instruments concerned will not be impaired by the proposed combination MENNMOVE 3 Vital Signs Monitor User Manual Intended Use and Safety Guidance 1 2 4 Equipotential Grounding Protection class 1 instruments are already included in the protective grounding protective earth system of the room by way of grounding contacts in the power plug For internal examinations on the heart or the brain the Monitor must have a separate connection to the equipotential grounding system One end of the equipotential grounding cable potential equalization conductor is connected to the equipotential grounding terminal on the rear panel of the instrument and the other end to one point of the equipotential grounding system The equipotential grounding system assumes the safety function of the protective grounding conductor if ever there is a break in the protective grounding system Examinations in or on the heart or brain should only be carried out in medically used rooms incorporating an equipotential grounding system Check each time before use that the instrument is in perfect working order The cable connecting the patient to the instrument must be free of electrolyte WARNING If the protective grounding protective earth system is doubtful the monitor must be supplied by internal power only 1 2 5 Condensation Make sure that during operation the instrument is free of condensation Condensa
93. the Sleep mode NOTE When the SYSTEM SETUP gt STANDBY is OFF or the monitor is in DEMO mode or there is any inputting signal pressing the ON OFF button can not make the monitor enter the sleep mode Quitting the Sleep Mode In the sleep mode if a new signal occurs or you press any button on the front panel the monitor will enter the working mode NOTE 1 If the following situation occurs monitor will return to normal monitoring mode automatically The monitor receives physiological signal of SpO and lasts for 5s If the monitor is powered by battery when the battery electric energy is low it will enter normal monitoring mode and indicates low battery alarm 2 In DEMO mode the monitor can not enter Sleep mode 43 MENNMOVE 3 Vital Signs Monitor User Manual Alarm Chapter 5 Alarm This chapter gives general information about the alarm and measures to be taken accordingly Alarm setup and prompt messages are provided in respective parameter setup sections WARNING A potential hazard can exist if different alarm presets are used for the same or similar equipment in any single area 5 1 Alarm Modes 5 1 1 Alarm Level Each alarm either technical or physiological has its own level For alarm of higher level when the alarm condition is active the system will give a prompt in various ways Alarms in the monitor are divided into three levels high medium and low High level alarm indicates the patient s life i
94. the year month day hour minute and second Pick the item you want to modify and confirm it by pressing OK 34 MENNMOVE 3 Vital Signs Monitor User Manual System Menu Select EXIT item to save the setup and return to the previous menu If you want to exit the menu without saving it press the MENU on front panel TIME SETUP CONF RM Figure 4 16 Time Setup 4 8 NIBP Setup Refer to 9 4 NIBP Setup 4 9 TEMP Setup Refer to 10 1 3 TEMP Setup for T2 Module and 10 3 7 TEMP Setup for F3000 Module 4 10 Alarm Setup Refer to 5 1 3 Alarm Setup 4 11 Maintain Select MAINTAIN item in SYSTEM MENU to open ENTER MAINTAIN PASSWORD dialog box in which you can enter password and then customize maintenance settings Factory maintenance function is only available for the service engineers of MENNEN MEDICAL LTD or representative authorized by MENNEN MEDICAL LTD 35 MENNMOVE 3 Vital Signs Monitor User Manual System Menu ENTER MAINTAIN PASSWORD 3 0 0 _ CONFIRM afol 0 0 _ CONFIRM 3fofafo EXIT Figure 4 17 Enter Maintain Password User Maintain Input the user password 9 9 8 1 in the USER KEY box and press OK USER MAINTAIN menu will pop up in which you can set following items USER MAINTAIN COLOR SELECT EXIT Figure 4 18 User Maintain BED No Set the bedside number to a value from 1 to 64 LANGUAGE Set the displayed language NOTE You should restart the monitor a
95. thium cell CR2032x1 To replacing the battery follow the procedure 1 Open the battery cover by inserting a pointed object into the battery cover pin hole meanwhile use thumb to push battery cover out De 2 Hold the thermometer and flip the battery out with a small screwdriver 76 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional 3 Insert the new battery under the metal hook on the left side and press the right side of the battery down until the it clicks in place pA 2 WARNING 1 Keep the battery away from children 2 Ensure the positive side is up and the negative side down 10 2 5 Maintenance Calibration Mode To switch to calibration mode follow the steps below a Press the ON MEM button to turn the thermometer on The display of the thermometer shows symbols and functions b Keep pressing the ON MEM button for five seconds and you will see the OFF symbol on the display Do not release the button until you see a dot onscreen c The thermometer is now in the Calibration Mode and the display is flashing and showing the CAL symbol NOTE It is suggested that a re test is performed for the device on accuracy after three years Please send the complete device to the dealers or nearest service address However if this device is used according to the operation instructions periodic re calibration is not required Pe MENNMOVE 3 Vital Signs Monitor User Manua
96. tient OFF 10 1 5 Care and Cleaning Recommended cleaning agents are m Ethanol 75 m Isopropanol 70 E MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional 10 2 TEMP Monitoring with TH Module 10 2 1 Introduction MENNMOVE 3 with the TH module Infrared Ear Temperature Module takes a temperature in the ear Diagram of the Infrared Ear Thermometer Probe Cover Probe Cover Cap Scan Button Ejector hie Lens Key Chain Probe Probe Cover Detector LCD ON MEM Button Batter Cover Pin Hole Battery Cover WARNING 1 Keep the probe covers away from children 2 Do not resue the disposable probe covers 3 Only use the disposable probe covers supplied or recommended by MENNEN MEDICAL LTD Use of other manufacturers probe covers reuse of disposable probe covers or absence of probe covers may produce temperature measurement errors and or inaccuraies 4 The infrared ear thermometer is not intended for neonatal patients CAUTION 1 Keep the probe window clean dry and undamaged at times to ensure accuate measurements To protect the probe window always keep the thermometer in the storage cover while transporting or when not in use 2 Proper installation of the probe cover ensures accurate measurements 3 Do not autoclave 4 The thermometer is not waterproof Do not immerse or drip fluids on it Should this occur dry the thermometer with warm ai
97. tient raise the arm then place the probe tip in the axilla Press gently to assure good contact For the most accurate temperature the probe tip should be placed directly against the patient s skin Have the patient then lower the arm and remain as still as possible Hold the probe parallel to the arm as shown 81 MENNMOVE 3 Vital Signs Monitor User Manual TEMP Monitoring Optional 10 If three short beeps are heard it means the unit switched to Monitoring Mode for this temperature only Two beeps are sounded when measurement is complete and the final temperature is displayed Eject the used cover into a bio waste container by pushing top button Rectal Temperature Taking l 2 Make certain that the Red isolation chamber probe unit is attached Withdraw the probe and apply a probe cover Thermometer turns on automatically a beep will be heard when the probe completes warm up Apply lubrication if desired Insert the probe into the patient s rectum To ensure proper tissue contact angle the probe slightly after insertion Depth of insertion is recommended at 1 2 to 3 4 12 mm 19 mm for adults and 1 4 to 1 2 6 mm 13 mm for children If three short beeps are heard it means the unit switched to Monitoring Mode for this temperature only Two beeps are sounded when measurement is complete and the final temperature is displayed Eject the used cover into a bio waste co
98. tion can form when equipment is moved from one building to another thus being exposed to moisture and differences in temperature 1 2 6 Safety Precautions WARNING and CAUTION messages must be observed To avoid the possibility of injury observe the following precautions during the operation of the instrument WARNING 1 If liquid is inadvertently splashed on the equipment or its accessories it may enter the conduit or inside the monitor At this moment contact local Customer Service Center 2 The monitor is intended to be used by qualified physicians or personnel professionally trained And they should be familiar with the contents of this user manual before operation 3 Only qualified service engineers can install this equipment And only service engineers authorized by MENNEN MEDICAL LTD can open the shell 4 EXPLOSION HAZARD Do not use the monitor in a flammable atmosphere where concentrations of flammable anesthetics or other materials may occur 5 SHOCK HAZARD the power receptacle must be a three wire grounded outlet A hospital grade outlet is required Never adapt the three prong plug from the monitor to fit a two slot outlet MENNMOVE 3 Vital Signs Monitor User Manual Intended Use and Safety Guidance 10 11 12 13 14 15 16 17 18 19 20 21 22 WARNING Do not attempt to connect or disconnect a power cord with wet hands Make certain that your hands are clean and dry before touching a power cord
99. y or the battery has full electric energy it displays xo When the monitor is working with AC mains power and the battery is being recharged it displays oEZA When the monitor is working with battery it displays FA If the monitor is off you can see recharging status from the charger indicator Battery status light is yellow when recharging off when full 25 MENNMOVE 3 Vital Signs Monitor User Manual Introduction 3 5 3 Checking Battery Performance The performance of rechargeable batteries may deteriorate over time Battery maintenance as recommended here can help to slow down this process 1 Disconnect the patient from the monitor and stop all monitoring and measurement 2 Switch the monitor power on and charge the battery for more than 6 hours continuously 3 Disconnect monitor from mains power and let the monitor run until there is no battery power left and the monitor shuts off 4 The running time of the battery reflects the battery performance If the running time is obviously less than the specified time in the specification please change the battery or contact the service personnel 3 5 4 Replacing the Battery During monitoring state or communication state when the battery is low or empty the monitor will indicates a BATTERY LOW alarm When the lifespan of battery is over or foul odor and leakage has been detected please contact the manufacturer or local distributor for replacement of battery
100. y to be displayed Waveform Trend List Alarm List Area 0 It can display SpO waveform Trend tab or Alarm list You can select it in the SELECTION of SYSTEM MENU Information Area The information areas are to display operating status of the monitor and condition of the patient including the following data Patient type and ID Signs indicating the net connection status Signs indicating the battery or mains power supply status Current time Alarms and prompts Alarm Indicator and Alarm Status In normal condition the alarm indicator does not light When an alarm is generated the alarm indicator lights or flashes The color of light represents the alarm level Refer to Chapter 3 Alarm for details Refer to relevant content of parameters for Alarm information and prompt Charging Indicator and Charging Status To indicate the status of charging when the battery is being charged the light turns to yellow after the charge is finished the light will be off 14 MENNMOVE 3 Vital Signs Monitor User Manual Introduction 3 2 2 Double Parameter Mode NIBP SpO Interface Figure 3 5 NIBP as the Main Parameter 1 1 3 89 DIA TA ZELETA Figure 3 6 SpO as the Main Parameter 15 MENNMOVE 3 Vital Signs Monitor User Manual Introduction NIBP TEMP Interface ADU mmHg MAP 88 CUFF PR BPM Figure 3 7 NIBP TEMP Interface 1

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