1. Manuals
  2. Brands
  3. Lepu Medical Manuals
  4. Medical Equipment
  5. K10
  6. Operator's manual

Lepu Medical K10 Operator's Manual

Patient monitor
Hide thumbs
Table of Contents

Advertisement

Quick Links

Advertisement

Table of Contents
loading
Need help?

Need help?

Do you have a question about the K10 and is the answer not in the manual?

Questions and answers

otieno stephen
April 7, 2025

my k15 is not measuring pressure

0
1 comments:
Mr. Anderson
April 9, 2025

Your Lepu Medical K10 may not be measuring pressure due to one of the following reasons:

1. The IBP transducer kit may not be properly connected or may be faulty.
2. The disposable pressure sensor may not be functioning correctly.
3. The built-in pressure verification function or calibration may not have been performed properly.
4. There could be air leakage in the pneumatic system.
5. The monitor only supports 2 channels of IBP waveforms, so the issue could be with channel selection or configuration.

Check the transducer kit, ensure proper connection, and perform pressure verification as described in the operator’s manual.

This answer is automatically generated

0

Subscribe to Our Youtube Channel

Related Manuals for Lepu Medical K10

Summary of Contents for Lepu Medical K10

  • Page 4         ...

  • Page 5: Table Of Contents

    Safety ..............................1 1.1 Safety Information ............................1 1.1.1 Warnings ............................1 1.1.2 Cautions ............................2 1.1.3 Notes ..............................2 1.2 Equipment Symbols ............................. 3 1.2.1 Symbol/Icon on the Device ....................... 3 1.2.2 Icons List on the Screen ........................4 1.2.3 Symbol/Icon on the Package ......................
  • Page 6 3.4.2 Buttons and Keyboard ........................25 3.5 Using the Touchscreen ..........................26 3.6 Setting the Screens ............................ 27 3.7 Using the Main Menu ..........................28 3.8 Changing System Settings .......................... 28 3.8.1 Changing General Settings ......................28 3.8.2 Setting the Date and Time ......................30 3.8.3 Network Settings..........................
  • Page 7 Alarms ..............................45 6.1 Alarm Categories ............................45 6.2 Physiological and Technical Alarms ......................45 6.3 Alarm Indicators ............................49 6.3.1 Alarm lamp............................49 6.3.2 Alarm message ..........................49 6.3.3 Highlighting Numeric ........................49 6.3.4 Audible Alarm Tones ........................49 6.3.5 Alarm Status Symbols ........................
  • Page 8 8.3 Understanding the RESP Display ........................ 68 8.4 Changing RESP Settings ..........................69 Monitoring NIBP........................... 71 9.1 Introduction ............................... 71 9.1.1 The Oscillometric Blood Pressure Measurement ................71 9.1.2 The Oscillometric method vs. the Korotkoff Sound Method ............71 9.2 Safety Information ............................. 71 9.3 Measurement Limitations ..........................
  • Page 9 12.3.1 Understanding IBP Icon ......................... 90 12.3.2 IBP Transducer Kit Connection ...................... 90 12.4 Understanding the IBP Display......................... 91 12.5 Changing IBP Settings ..........................92 Monitoring Carbon Dioxide (CO ) ...................... 93 13.1 Introduction ............................. 93 13.2 Safety Information ........................... 93 13.3 CO Sensor Connection ..........................
  • Page 10 16.2 Safety Information ..........................113 16.3 Medication Calculation (Medicine Dosage Calculation) ................ 113 16.4 Oxygenation Calculation ........................117 16.5 Ventilation Calculation ........................... 120 16.6 Renal Function Calculation ........................123 16.7 HEMO.(Hemodynamic Calculation) ....................... 126 Tourniquet ............................129 Printing ............................130 18.1 Using a Printer ............................
  • Page 11 23.2 Temp Accessories ........................... 148 23.3 SpO Accessories ............................ 148 23.4 NIBP Accessories ............................ 149 23.5 CO Accessories............................149 23.6 IBP Accessories ............................150 23.7 CSM Accessories ............................ 150 23.8 Other Accessories ..........................150 Technical Specifications ........................151 24.1 ECG ................................. 151 24.2 RESP ...............................

  • Page 12: Safety

    1.1 Safety Information ☞ WARNING for PACEMAKER PATIENTS: Although the pacemaker pulse inhibition function is available in this device, the heart rate meter may continue to count the pacemaker rate during occurrences of cardiac arrest or some arrhythmias. Do not rely entirely upon rate meter ALARMS.

  • Page 13: Cautions

    single area. Do not silence the audible alarm if patient safety may be compromised. Do not use the monitor to those patients who have a severe hemorrhagic tendency or who have sickle cell disease, for they may develop partial bleeding when this monitor is used to take the blood pressure measurement.

  • Page 14: Equipment Symbols

     All combinations of equipment must comply with the standard IEC 60601-1.  DO NOT position the device so that it is difficult to connect the plug of the power cord.  If the user requests more information such as circuit diagrams, parts list, and product descriptions for repairs carried out by qualified technical personnel, please contact us.

  • Page 16: Symbol/Icon On The Package

     Some symbols may not appear on your equipment.

  • Page 17: The Basics

    2.1 Monitor Description  The CE-certified patient monitors have the functions of recording and displaying parameters in real-time of ECG, heart rate (HR), non-invasive blood pressure (NIBP, age≥ 3 years old), functional oxygen saturation (SpO ), respiration rate (RESP), body temperature (TEMP), and end-tidal CO concentration (EtCO ) for monitoring the...

  • Page 18: Features

     ECG arrhythmia analysis function and S-T segment monitoring have not been CE-certified.  SpO2 monitoring with Nellcor module and NIBP measurement with SunTech module have not been CE-certified. This equipment is applicable for use in hospitals and clinical institutions. The operation should be performed by qualified professionals only.

  • Page 19: Main Unit

         This patient monitor is configurable with different parameters; the monitor you purchase may not cover all the functions described above. 2.2 Main Unit...
  • Page 21 Extended Module  The only difference among K10, K12, and K15 is the display screen size of the monitor.
  • Page 23             ＜        ...

  • Page 24: Display Screen

      。 。 2.3 Display Screen...

  • Page 25: Message Indication Area

    Message indication area Parameter area Waveform 1 Parameter 1 Waveform 2 Parameter 2 Waveform 3 Waveform area Parameter 3 Waveform 4 Parameter 4 Parameter 5 Waveform 5 Statusbar Gender PID Patient type Patient name Physiological alarm information Alarm status Extended module info ...
  • Page 26    If you purchased the monitor with extended module, then the corresponding module icon(s) will also appear on the upper right screen. "Menu" button "Alarm" button "Review" button Power supply Technical alarm event Printer Beep volume System time ...
  • Page 27            Operating key to move the cursor on status bar and focus on the icon of printer, beep volume, power supply, system time or on the information area, then the corresponding setting window pops up, that's, Printer setting window, Beep volume setting window, power supply setting window, System time setting window.

  • Page 28: Parameter Area And Waveform Area

     Please be cautious when using this option. It's not recommended to set the alarm sound volume to 0.

  • Page 29: Views Management

    ECG panel: enter into ECG setting window panel: quick to enter into setting window NIBP panel: quick to enter into NIBP setting window Respiration panel: quick to enter into RESP setting window Temperature panel: quick to enter into TEMP setting window 2.4 Views Management...
  • Page 31  ...

  • Page 32: Operating Instructions

    3.1 Installation Devices connected to the equipment must meet the requirements of the applicable IEC standards. The system configuration must meet the requirements of the IEC 60601-1-1 medical electrical systems standard. Any personnel who connect devices to the equipment’s signal input/output port are responsible for providing evidence that the safety certification of the devices has been performed in accordance with IEC 60601-1-1.

  • Page 33: Environmental Requirements

     Save the packing case and packaging material as they can for reuse if the equipment must is returned.  The user can customize the module configuration by choosing the necessary modules to meet your own needs. Therefore, your monitor may not have all the monitoring functions and accessories.

  • Page 34: Turning The Monitor On

    built-in battery to power the monitor. After the mains power supply has been interrupted while power switch remains in the “on” status and is restored after for longer than 30 seconds, the monitor runs with the last settings when the monitor restarts. The monitor is applicable to connect to the public mains power network.

  • Page 35: Starting Monitoring

    The battery-powered monitor continues to run without interruption when the AC mains power is lost. Start the monitor again 1 minute later after it is switched off. When the monitor is switched off, allow one minute before switching it back on so that the monitor powers off correctly. 3.3 Turning the Monitor Off Although not recommended, you can press and hold the Power on/off key for 10 seconds to forcibly shut down the monitor when it does not follow a normal shut down.

  • Page 36: Buttons And Keyboard

           In this monitor, the button functions noted above are similar.

  • Page 37: Using The Touchscreen

     →        3.5 Using the Touchscreen...

  • Page 38: Setting The Screens

    3.6 Setting the Screens  ...

  • Page 39: Using The Main Menu

    3.7 Using the Main Menu    3.8 Changing System Settings → →  The default required password in the monitor is “8989”.  The selected language is applied after the monitor is restarted. → →...
  • Page 40  If your monitor has the “Spot-check Mode” function option, then the setting options for Alarm Volume is “Spot Check”, “0 -10”. → →      This function is not available for the ECG waveform.   ...

  • Page 41: Setting The Date And Time

         → →    → →  ...
  • Page 42       If DHCP fails (that’s to say, no DHCP server or no network is connected), then the IP address will be changed as “0.0.0.0”, and the network icon “ ” will be displayed on the lower right of the screen. If IP address is automatically configured by DHCP successfully, then the IP address will be displayed and network icon will be changed as “...

  • Page 43: Printer Settings

    → →     → →      The setting for Wave 1, Wave 2 and Wave 3 should be different (eg. Wave 2 and Wave 3 can not be set as "ECG III" at the same time). Only 2 ECG waveforms at most can be printed simultaneously.

  • Page 44: Operating Modes

    3.9 Operating Modes The Demo mode is for demonstration purposes only. To avoid stimulated data being mistaken for a monitored patient’s data, you must not change into Demo mode during monitoring. Otherwise, improper monitoring and delayed treatment could result. → →...

  • Page 45: Standby Mode

     “ ” → ” ” → “ ” → “ ” → “ ”  You cannot enter the private mode if a low battery alarm occurs.  Private mode is only available when the monitor is connected with the central monitrong system (CMS) and the patient is admitted by the CMS.

  • Page 46: Patient Data Management

    → 4.1 Apply an existed patient’s document → → 4.2 Create a new patient’s document → →     ≤    ...

  • Page 47: Edit A Patient Document

    4.3 Edit a patient document → →  No password is needed to edit the default patient document. In the default patient document, only the patient type can be modified, and other items are not editable. 4.4 Delete a patient document →...

  • Page 48: User Screens

    5.1 Tailoring/Setting Your Screens ：   →     ...

  • Page 49: Display Views

            5.2 Display Views      ...

  • Page 50: General View

       → →  If "3-lead wires" is selected, then in all view settings (including general view, big font view, all ECG trace view, NIBP list view and so on), the user can only be set it as the current displayed ECG waveform (that's "ECGII", "ECGI"...

  • Page 51: Big Font View

      Waveform 1- 5 and Parameter 1 - 5 are corresponding to the waveform 1- 5 and Parameter 1- 5. Similarly, in other views, the waveform 1- 5 and Parameter 1- 5 corresponds to that in the View settings window. ...

  • Page 52: All Ecg Trace View

           ...

  • Page 53: Oxycrg View

               ...

  • Page 54: Csm View

            ...

  • Page 56: Alarms

    Before monitoring a new patient, always check that the monitor can work properly, the alarm system works properly, and the alarm settings are appropriate for the patient before starting the monitoring. In order to ensure that the operator can accurately identify the alarms, it is recommended that the distance between the operator and monitor should not exceed 4 meters.
  • Page 59 ...

  • Page 60: Alarm Indicators

      6.3 Alarm Indicators    When multiple alarms of different levels coincide, the monitor selects the alarm that has the highest level and gives visual and audible alarm indications accordingly.

  • Page 61: Alarm Status Symbols

        Alarm reset key: pressing this key can perform alarm reset for the current activated alarm event (the audible alarm silences, but the visual alarming is active), then the icon “ ” displays on the upper right corner of the screen. The monitor can respond to a new alarm event during the alarm reset status, both visual and audible alarming are active when there is a new alarm condition, and the icon “...

  • Page 62: Understanding The Alarm Setting

       → When the alarm sound is switched off, the monitor will give no audible alarm tones even if a new alarm occurs. Therefore the user should be very careful about whether to switch off the alarm sound or not. Do not rely exclusively on the audible alarm system for monitoring.
  • Page 63        If the parameter alarm switch is set to “OFF”, then icon ” ” will be displayed on the corresponding parameter panel. If the parameter panel has two or more related parameters, once one alarm switch for these related parameters set as “OFF”, icon “ ”...

  • Page 64: High And Low Alarm Setting Range

    alarm limits, and alarm level for these parameters can be set here.  Alarm settings are saved when power off, which means the previous settings continue even the patient monitor is powered off. Repower includes unexpected power failure and manual reboot. →...

  • Page 65: Factory Default Alarm Limit Setting Value

     The following parameters are optional. （ ） （ ） （ ） （ ） （ ） （ ） （ ） （ ） （ ） （ ） （ ） （ ） （ ） （ ） （ ） （ ） （ ） （...
  • Page 66 ℃ ℃ ℃ ℃ ℃ ℃ ％ ％ ％ ％ ％ ％ ℃ ℃ ℃...

  • Page 67: Verify Alarm Function

    A hazard can exist if different alarm presets are used for the same or similar device in a single area. 6.5 Verify Alarm Function 6.6 When an Alarm Occurs     ...

  • Page 68: Ecg Monitoring

    7.1 Introduction 7.2 Safety Information This patient monitor can only be equipped with ECG cable and lead wires provided by the manufacturer; using those from other suppliers may cause improper performance or inadequate protection while using a defibrillator. Use authorized electrodes on the same patient. DO NOT use the electrodes on other patients, to avoid the potential of contamination.

  • Page 69: Preparing To Monitor Ecg

    imaging, which may cause electromagnetic interference to the monitor or harm the monitor’s operator. DO not contact any other conductive parts (including ground) with any conductive parts of electrodes, lead wires, and cable. This patient monitor can withstand the discharge of a defibrillator and the interference from the electrosurgical unit.

  • Page 70: Ecg Electrodes Placement

       If any side-effect such as allergic or itchy reaction is noted, remove the electrodes from the patient immediately.  The symbol indicates that the cable and accessories are “CF” type levels for protection against electric shocks and with defibrillation-proof capability.

  • Page 72: Understanding The Ecg Display

    7.4 Understanding the ECG Display       Heart rate label and unit Heart beat symbol High and low alarm limit setting for Heart rate Heart rate value Arrhythmia symbol     ...

  • Page 73: Changing Ecg Settings

    7.5 Changing ECG Settings →  According to the different function configuration, the ECG parameter setting window may be different, please refer to the monitor in your hand.        For different ECG related setting window, and when the ECG filtering mode is set as “OPER”, then items like “Wires”, “Lead,”...

  • Page 74: About Arrhythmia Detection And Template Learning

     If your monitor is configured with 12-lead ECG function, then you can set “Wires” as “5-leadwire” or “10-leadwire” to obtain ECG signals. When “10-leadwire” is chosen, then the waveform of lead I, II, III, aVR, aVL, aVF, V1-V6 will be displayed on the All ECG Trace view.

  • Page 75: Understand The Arr Type

     Because Arrhythmia detection needs a template ECG waveform as reference which is a piece of normal ECG waveform with regular rhythm and stable amplitude, it is necessary to re-activate the template learning when the patient is changed, or the Arrhythmia detection is incorrect.

  • Page 76: About S-T Segment Monitoring

    7.7 About S-T Segment Monitoring...

  • Page 77: Freezing Waveform

    The S-T segment measuring algorithm has been tested for accuracy of the ST segment data. The significance of the ST segment changes need to be determined by a clinician. 7.8 Freezing Waveform 7.9 Factors Affecting ECG signal    ...
  • Page 78  The 12-lead ECG acquisition can only be conducted in the All ECG Trace view.  Once the ECG is acquired, the ECG data automatically stored in the review records. If the monitor fails to upload the ECG data to the AI-ECG system due to network connection, you can upload it again by selecting the records in Review –...

  • Page 79: Monitoring Respiration (Resp)

    8.1 Introduction 8.2 Safety Information When monitoring the patient’s respiration, it is recommended to use the so-called “non-OR” ECG cable which has no built-in resistors to prevent the energy loss of defibrillator discharge. Otherwise the performance of respiration monitoring is degraded. The respiration measurement does not recognize the cause of Apnea.

  • Page 80: Changing Resp Settings

    Label and unit of respiration Respiratory Sync mark The high and low alarm Respiration rate limit setting of RR     8.4 Changing RESP Settings →         When “Wires” is set as “10-leadwire” in ECG related settings, then “Apnea” can be set as off, 10, 15, 20, 25, 30, 35 and 40.
  • Page 81     In RESP settings window, CO Settings are entered if your monitor is configured with CO monitoring.

  • Page 82: Monitoring Nibp

    9.1 Introduction 9.2 Safety Information When taking the blood pressure measurement on a neonate patient. DO NOT operate in the Adult mode. The high inflation pressure may cause lesion or even body putrescence. Even though the monitor can identify the cuff type so it will stop inflation and indicate "Cuff error"...

  • Page 83: Measurement Limitations

    time of inflatable balloon to run longer, which may not only prolong the measurement time but also result in the cuff wrapped area to suffer purpura, hypoxemia, or neuralgia because of the friction. Before the measurement is carried out, select an appropriate measuring mode depending on the patient type.

  • Page 84: Measurement Mode

         9.4 Measurement Mode     9.5 Setting Up the NIBP Measurement  ...

  • Page 85: Starting And Stopping Measurements

        Too frequently, blood pressure measurements may cause purpura, ischemia, and neuropathy in the limb with the cuff. Inspect the application site regularly to ensure skin quality and inspect the extremity of the cuffed limb for normal color, warmth, and sensitivity. If any abnormity occurs, move the cuff to another site or stop the blood pressure measurements immediately.
  • Page 86             ...

  • Page 87: Understanding The Nibp Numerics

    9.6 Understanding the NIBP Numerics NIBP measurement mode NIBP label and unit Diastolic pressure value Systolic pressure value Pulse rate value     9.7 Changing NIBP Settings →    ...
  • Page 88   STAT mode can only be used for an adult.  When changing the patient, the default NIBP measuring mode is “Manual”.  For “Adult”, if the NIBP measuring mode is set as “STAT”, then the monitor does not save this setting when you shut down the monitor.
  • Page 89  if your monitor is configured with SunTech NIBP module, then the initial cuff pressure range for adult is 120-200mmHg, the initial cuff pressure range for pediatric is 80- 200 mmHg, the initial cuff pressure range for neonate is 60 – 80 mmHg. ...

  • Page 90: Monitoring Oxygen Saturation (Spo 2 )

    10.1 Introduction 10.2 Safety Information Continuous use of fingertip SpO sensors may result in discomfort or pain, especially for those patients with microcirculatory problems. The sensor should NOT be applied to the same site for over two hours, please inspect the monitoring site every 1-2 hours for skin integrity, and change the measuring site periodically if necessary.
  • Page 91 Excessive ambient light may also affect the measurements. The light sources include fluorescent lamps, dual ruby light, infrared heater, and direct sunlight. As the SpO value serves as a reference value for judgment of anemic anoxia and toxic anoxia, the measurement result of some patients with acute anemia may also present as good SpO value.

  • Page 92: Apply The Sensor

     A clinical study for SpO measurement accuracy was completed on human subjects according to Standard ISO 80601-2-61.  A functional tester or SpO simulator cannot be used to assess the accuracy of the oximeter or a SpO sensor. However, it can be used to check how accurately a particular oximeter is reproducing the given calibration curve.

  • Page 93: Understanding The Spo2 And Pr Display

    10.5 Understanding the SpO2 and PR Display  label Label of pulse rate Pulse rate value Pulse intensity bar graph value High and low alarm limit for SpO...

  • Page 94: Changing Spo 2 And Pr Settings

         10.6 Changing SpO and PR Settings →    10.1 Nellcor SpO Module  The SpO monitoring with Nellcor module is not CE-certified.  If your monitor is configured with Nellcor SpO Module, then the SpO related setting window is as shown in below figure.
  • Page 95   “Interference” icon SatSeconds icon and sensitivity setting  When inserting finger into the probe cushion, then searching pulse icon “ ” appears on the upper side of the SpO panel. However, once the SpO /PR readings appear, or probe/ finger is off, then icon “...

  • Page 97: Monitoring Temperature

    11.1 Introduction 11.2 Safety Information Verify that the probe detecting function works correctly before monitoring. Unplug the temperature probe cable from the T1 or T2 connector, and the monitor displays the message [T1 Sensor Off] or [T2 Sensor Off] and gives alarm tones. Make the correct choice in the setup menu for “KRK”...

  • Page 98: Understanding The Temp Display

     Pediatric patients are generally more active, pay close attention when affixing the sensor.  The TEMP sensor is designed for use with the specific patient monitor, which cannot be used as applied part to other products.  The operator is responsible for checking the compatibility of the patient monitor and sensor type, including cable before use.
  • Page 99   ...

  • Page 100: Monitoring Ibp

    12.1 Introduction 12.2 Safety Information The pressure tube which connects the catheter and the pressure transducer should be straightway without any tangle. Use the pressure transducer kit specified in this manual. Never reuse disposable pressure transducers. Make sure that the applied parts never contact other conductive parts. To reduce the hazard of burns during high-frequency surgical procedures, ensure that the monitor’s cables and transducers never come into contact with the high-frequency surgical units.

  • Page 101: Setting Up The Ibp Measurement

    Each time when connecting transducer kit or using a new transducer kit, zero calibration to the IBP transducer must be carried out. Before using the tube, cable and/or transducer, make sure that all accessories meet the performance requirements which is not changed by aging or environmental conditions. 12.3 Setting Up the IBP Measurement...

  • Page 102: Understanding The Ibp Display

    IBP transducer kit with disposable pressure sensor 12.4 Understanding the IBP Display “IBP1”    For K10 and K12 monitors, it only show 2 channels of waveforms.  For K15 monitor, it shows 4 channels of waveforms. IBP mark and unit Measuring position Systolic pressure...

  • Page 103: Changing Ibp Settings

       12.5 Changing IBP Settings →                ...

  • Page 104: Monitoring Carbon Dioxide (Co 2 )

    13.1 Introduction 13.2 Safety Information Sensor is a precision measuring part, please use it correctly and store it properly; Precautions for electrostatic discharge (ESD) and electromagnetic interference (EMI) to...
  • Page 105 and from other equipment. Failure of Operation: If the CO Sensor fails to respond as described in this user manual, DO NOT use it until approved for use by qualified personnel. Do not position the sensor cables or tubing in any manner that may cause entanglement or strangulation.
  • Page 106 flammable gasses. The use of the CO Sensor in an environment may present an explosion hazard. Electrical Shock Hazard: Always disconnect the CO Sensor before cleaning. Do NOT use it if it appears to have been damaged. Refer servicing to qualified service personnel. The power voltage over monitor working voltage may cause damage to the CO sensor.

  • Page 107: Co Sensor Connection

    13.3 CO Sensor Connection Sampling Dehumidification Sampling Sampling cell Filter adapter tubing tubing...

  • Page 108: Mainstream Co Sensor Connection

    On-air Connector Adapter Sensor cable Adapter sensor...

  • Page 109: Measurement Limitations

     Always position the sensor with the adapter in an upright position to avoid a collection of fluids on the windows of the adapter. Large concentrations of fluids at this point obstruct gas analysis. 13.4 Measurement Limitations    ...

  • Page 110: Understanding The Co 2 Display

    13.6 Understanding the CO Display Unit of EtCO Label of Fi CO Label of Respiration rate Label of CO and EtCO Value of Respiration rate Value of EtCO Value of Inspired CO      13.7 Changing CO Settings →...
  • Page 111           ℃...
  • Page 112 ℃ ℃ ℃     The information prompts during Zero calibration, but there is no audible and visual alarm. When performing a zero calibration during normal patient measurement operations, disconnect the transducer from the patient’s airway first. DO not rely on the measurement readings taken during zeroing.

  • Page 113: Monitoring Csm

    14.1 Introduction 14.2 Safety Information If used with High Frequency (HF) surgery please pay attention to the positioning of CSM electrodes. In order to reduce the hazard of burns, the electrodes should not be located between the surgical site and the electro-surgical unit return sensor. The conductive parts of sensors and their connectors, including the neutral sensor, should not contact other conductive parts including earth and ground.
  • Page 114 α =ln(E 30-42.5Hz 6-12Hz ratio β =ln(E 30-42.5Hz 11-21Hz ratio...
  • Page 115    ...

  • Page 116: Csm Processes

    14.4 CSM Processes    Middle of forehead Left side of forehead Mastoid left side...

  • Page 117: Changing Csm Settings

     Once the electrodes have been secured on the skin, attach the color-coded wires on the patient cable to appropriate electrode.  Shown above is a left sided setup; right sided is also acceptable.  Place electrodes at the side farthest from the surgical area. 14.5 Changing CSM Settings →...

  • Page 118: Review

      15.1 ARR Events  All event list can be searched by date, we will not cover it later again.

  • Page 119: Trend Graph

    15.2 Trend Graph      On the Short Trends view, the general waveform is on the left of the waveform area and the short trend view on the right. 15.3 NIBP List ...

  • Page 120: Ecg Waveforms

     15.4 ECG Waveforms 15.5 Alarm Event...

  • Page 121: Spo 2 Event

    15.6 SpO Event 15.7 CSM Records CSM trend graph recall CSM record---by Trends  ...

  • Page 122: Exporting Data

             CSM record---by Events 15.8 Exporting Data →...
  • Page 123  If no USB disk is detected, then “Refresh”, “Export”, and “Unmount” buttons are displayed in grey and unavailable.      Do not unplug the USB disk from the monitor during exporting, or the exported data will be in disorder, and the history record files will be corrupted.

  • Page 124: Calculations

    16.1 Introduction      16.2 Safety Information After the calculation is finished, verify the entered values are correct and the calculated values are appropriate. We assume no responsibility for any consequences caused by wrong entries and improper operations. The calculation feature is independent of other monitoring functions and can be therefore used for patients being monitored by other monitors.
  • Page 125 Medicine Dosage Calculation window...
  • Page 126       The medicine applies the fixed unit, or a fixed family of units. The operator must select the appropriate unit according to doctor’s advices. In a unit family, the carry between 2 adjacent units performs automatically along with the current inputs. When the space on screen for an item is not enough to display all digits of the item in a certain unit, it will be displayed as “…”.
  • Page 127  The patient here has nothing to do with the current patient monitoring right now, and only for Medicine Calculation. Titration window    ...

  • Page 128: Oxygenation Calculation

    16.4 Oxygenation Calculation Oxygenation calculation window —...
  • Page 129 — — — － — －...
  • Page 130 — — — － — —  The result for each parameter will be shown as “---” before click “Calculate” button.  The calculation result will be shown in yellow if the result is beyond the reference range. Result Unit Oxygenation calculation---Calculate result...

  • Page 131: Ventilation Calculation

    Range Oxygenation calculation---Reference range 16.5 Ventilation Calculation Ventilation calculation window...
  • Page 132 — — － — — — — －...
  • Page 133 — —  The result for each parameter will be shown as “---” before click “Calculate” button.  The calculate result will be shown in yellow if the result is beyond the reference range. Result Unit Ventilation calculation---Calculate result...

  • Page 134: Renal Function Calculation

    Range Ventilation calculation---Reference range 16.6 Renal Function Calculation Renal function calculation window...
  • Page 135 — — — －...
  • Page 136 — — — — —  The result for each parameter will be shown as “---” before click “Calculate” button.  The calculate result will be shown in yellow if the result is beyond the reference range. Result Unit Renal function calculation---Calculate result...

  • Page 137: Hemo.(Hemodynamic Calculation)

    Range Renal function calculation---Reference range 16.7 HEMO.(Hemodynamic Calculation) → Hemodynamics Setting ...
  • Page 138         · · ·...
  • Page 139 · Note：BSA (Body Surface Area) = 0.006*height+0.0128*weight-0.1529 t = ( 7.0 / ( 2.4 + lv_d/10 ) ) * lv_d * lv_d * lv_d / 1000 (lv_d：left ventricle diameter)

  • Page 140: Tourniquet

    → Tourniquet Settings Count-down      The lasted time that cuff pressure maintained with the specified value for adult and pediatric is fixed to be 170s and nonadjustable, and for neonate is fixed to be 85s and nonadjustable.

  • Page 141: Printing

    18.1 Using a Printer  The built-in printer may be used due to the configuration.   Power Indicator Open button Error Indicator Paper cartridge 18.2 Loading Printing Paper...

  • Page 143: Attentions

    Printing paper 18.3 Attentions Use only specified thermal paper. Otherwise, it may cause damage to the recorder’s print head, the recorder may be unable to print, or poor print quality may result. Never pull the recorder paper with force when a recording is in process. Otherwise, it may cause damage to the recorder.

  • Page 147: Cleaning The Printing Head Of Printer

    18.5 Cleaning the Printing Head of Printer...

  • Page 148: Other Functions

    19.1 System Information → 19.2 Nurse Call Settings    Do not rely exclusively on the nurse call system for alarm notification. Remember that the most reliable alarm notification combines audible and visual alarm indications with the patient’s clinical condition.

  • Page 149: Battery

    20.1 Overview 20.2 Battery Maintenance Please pay attention to the battery polarities. Do not insert it into the battery compartment with reversed polarities. Do not use the batteries manufactured by other companies. Using batteries other than those recommended may damage the device. To avoid damaging the battery, Do not use any other power supply than the power supplied with the monitor.

  • Page 150: Battery Recycling

    Do not use this battery on other devices. Do not use this battery below -10° C or above 40° C. Dispose of the battery in accordance with local law. To avoid battery damage always remove battery(s) before shipping or storage. To maintain battery supply time and prolong battery life, please charge the battery every one or two months if the battery is not used for an extended period.

  • Page 151: Cleaning And Disinfection

                        ...

  • Page 152: Disinfecting The Device And Accessories

      21.1 Disinfecting the Device and Accessories   Do not use damaged accessories. Accessories cannot be entirely immerged into water, liquor or cleanser. Do not use radiation, steam or EO to disinfect accessories. Do wipe off the remained Ethanol or isopropanol on the accessories after disinfection, for good maintenance can extend the life of accessories.

  • Page 153: Maintenance

    22.1 Daily Examination      22.2 Routine Maintenance If the hospital fails to carry out a satisfactory maintenance program with the monitor, the monitor may not function properly and present the potential to jeopardize the patient’s safety and health. Perform protective grounding impedance, leakage current and insulation resistance test.

  • Page 154: Ecg Verification

    The Monitor is calibrated in the factory before sale, so there is no need to calibrate it during its life cycle. Any patient simulators should not be used to validate the accuracy of blood pressure and oxygen saturation measurement, they can only be used as functional testers to verify its precision.
  • Page 155 Mercury blood pressure meter NIBP cuff with dual air tube Air tube Air tube Air tube Air tube Air vent Increase the pressure manually Manual valve Module testing through the inflatable balloon NIBP software Inflation balloon module This belongs to the monitor...

  • Page 156: Ibp Calibration

     After the verification, press the button again to return to the normal working mode to continue other operations, or the NIBP key is invalid.  Pressure accuracy verification must be performed by a technician or equipment manager. Doctors and nurses are not qualified to perform the verification. Accuracy verification performed while the pressure cuff is still on the patient may cause patient injury.

  • Page 157: Co Test

       22.6 CO Test...
  • Page 158 Use accessories specified in this chapter. Using other accessories may cause damage to the patient monitor or not meet the claimed specifications in this manual. Check the accessories and their packages for any sign of damage. Do not use them if any damage is detected.

  • Page 159: Accessories

    23.1 ECG Accessories 23.2 Temp Accessories 23.3 SpO Accessories...

  • Page 160: Nibp Accessories

    23.4 NIBP Accessories – 23.5 CO Accessories...

  • Page 161: Ibp Accessories

    φ 23.6 IBP Accessories 23.7 CSM Accessories 23.8 Other Accessories...

  • Page 162: Technical Specifications

    24.1 ECG    μ     ≥  ≥  ≥ ± ≤...
  • Page 163 ≤   ...

  • Page 164: Resp

          24.2 RESP  ...

  • Page 165: Temp

    24.3 TEMP ℃ ℃ ℃ ℃ ℃ ℃ ℃ ℃ ℃ ℃ 24.4 NIBP     ...
  • Page 166          ...

  • Page 167: Spo

    24.5 SpO    ≤    ≤  Arms is the accuracy defined as the root-mean-square value of deviation according to ISO 80601-2-61.

  • Page 168: Pulse Rate

    24.6 Pulse Rate ± ± ± ± ±  The pulse rate ACCURACY is tested by an electronic pulse simulator.
  • Page 169 24.7 CO     ±      ...

  • Page 170: Csm

      ± 24.8 CSM 24.9 IBP...

  • Page 171: Wi-Fi Specifications

    24.10 Wi-Fi Specifications 24.11 Signal Outputs Specifications ± ≤ Ω...

  • Page 172: Classification

    24.12 Classification 24.13 Operating Environment        ...

  • Page 173: Storage

      24.14 Storage    24.15 Transportation    24.16 Packaging      ...

  • Page 174: Other Technical Specifications

    24.17 Other Technical Specifications      ≤...

  • Page 175: Troubleshooting

    ： Do not open the monitor cabinet without permission. In case of problems while this device is in service, follow the instructions below to eliminate the problem first. If the attempt fails, contact the dealer in your local area or the manufacturer.
  • Page 177 ℃...

  • Page 178: Common Faults

    25.2 Common Faults...
  • Page 179      “ ”    ...
  • Page 180      ...
  • Page 181        ...
  • Page 182  Facial muscles will recover sooner than skeletal muscles.  When these artifacts are present, the CSI should be interpreted with caution.
  • Page 184     Use of the monitor adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and other equipment should be observed to verify that they are operating normally. Use of accessories, transducers and cables other than those specified or provided by the manufacturer of the monitor could result in increased electromagnetic emissions or decreased electromagnetic immunity of the monitor and result in improper operation.
  • Page 185  The EMISSIONS characteristics of the monitor make it suitable for use in industrial areas and hospitals (CISPR 11 class A). If it is used in a residential environment (for which CISPR 11 class B is normally required), the monitor might not offer adequate protection to radio-frequency communication services.
  • Page 187    ...
  • Page 189    ...

This manual is also suitable for:

K12K15

Table of Contents