Fukuda Denshi Co DS7100 Patient Monitor User Manual DS71v1 1 FA 10 Maintenance 012

Fukuda Denshi Co Ltd Patient Monitor DS71v1 1 FA 10 Maintenance 012

Manual 9

10−1MaintenanceChapter 10− Handling − After Use / Display Panel ･････ 2Handling After Use ･･･････････････････････････ 2Handling the Display Panel ････････････････････ 2− Storage −Device / Recording Paper ････････ 3Storing the Device････････････････････････････ 3Storing the Recording Paper ･･･････････････････ 3− Cleaning −Display Panel and Housing ･･････ 4Cleaning the Display Panel ････････････････････ 4Cleaning the Housing ･････････････････････････ 5Disinfecting the Blood Pressure Transducers ･････ 5Disinfecting the Temperature Probes････････････ 5Disinfecting the CO2 Filter Line ･････････････････ 5Cleaning and Disinfecting the SpO2 Transducer･･･ 5Cleaning and Disinfecting the NIBP Cuff ･････････ 5Cleaning and Disinfecting the ECG lead Cable ･･･ 5− Battery −Handling the Battery Pack･････ 6Handling the Battery ･･････････････････････････ 6Storing the Battery････････････････････････････ 6− Maintenance Check −Daily and Periodic Check ･7About the Maintenance Check ･････････････････ 7●Daily Check ･･･････････････････････････････7●Periodic Check ････････････････････････････7Time-Change Components ････････････････････ 7− Troubleshooting −･･･････････････････････････ 9ECG････････････････････････････････････････ 9Respiration ･････････････････････････････････11Invasive Blood Pressure･･････････････････････ 11SpO2･･････････････････････････････････････12Non-Invasive Blood Pressure ･････････････････13Temperature････････････････････････････････14CO2 Concentration･･･････････････････････････15Recorder ･･･････････････････････････････････16Telemetry ･･････････････････････････････････16General ････････････････････････････････････17Battery･････････････････････････････････････ 1810Maintenance
10−2− Handling − After Use / Display PanelThis section describes precautions for handling the equipment.Handling After Use? Do not apply excessive force when disconnecting the cables. Always pull on the connectorhousing and not on the cable.? Clean the unit, accessories, and cables, and keep them together in one place for next use.? Always check for adequate supply of disposable accessories such as ECG electrodes. If anyshortage, contact our service representative and supply as necessary.Handling the Display Panel? The display panel utilizes exclusive fluorescent light for the backlight.As this fluorescent light tube has product life cycle, it needs to be replaced periodically. If thedisplay becomes dark, scintillates, or does not light, contact your nearest service representative.? The LCD used for the display panel utilizes highly accurate picture elements of pixels over99.99%, but there may be an absence (less than 0.01%) or constant lighting of pixels.
10−3− Storage −Device / Recording PaperThis section describes about the storage of the device and recording paper.Storing the Device? Store in a place where the device will not be exposed to splashing water.? Store in a place where the device will not be adversely affected by atmospheric pressure,temperature, humidity, ventilation, sunlight, dust or atmosphere containing salt or sulfur.? Store in a level area where the device is not exposed to vibration and shock (including duringtransportation).? The following environmental conditions should be observed when storing the device.Storage Temperature :−10∼60?CStorage Humidity :10∼95% (at 60?C)Storing the Recording PaperThe DS-7100 system utilizes heat sensitive recording paper. If placed in a high temperature forlong period of time, the print may become indistinct, and unable to read. When storing, follow theprecautions below.? Store in a place where light is shut off and avoid direct sunlight.? Do not leave the paper in a high temperature (50 °C or 122 °F or above).? Do not store the paper in polyvinyl chloride bag.? Do not expose the paper to alcohol, hydrochloric acid, or ester ketone.? Avoid using adhesive agents other than water based glue.10Storage
10−4− Cleaning −Display Panel and HousingThis chapter explains about the cleaning of the device and sensors.Cleaning the Display PanelSince this device incorporates a touch screen, finger prints and other stains are likely to appear onthe display panel.Follow the procedure below to clean the display panel.1. Press the Key Lock key for more than 2 seconds.ReferenceThe Key Lock key needs to be preprogrammed as user key.Refer to ” 8. System Configuration Ward Setup” for user key setup.2. Clean the touch panel.While the “Touch key OFF" message is displayed, the touch panel key will be deactivated.If “LEAD OFF” or other message is displayed, the key lock message will not be displayed.3. Wipe the touch panel using cleaning cloth.4. Press again the Key Lock key for more than 2 seconds.The message will disappear and the keys will be activate again.CAUTION? Do not clean the touch panel using strong acid.? A special coating is applied to the surface of the touch panel. Wipe thesurface with the soft cleaning cloth provided as optional accessory orwith commercially available eyeglass cleaning cloth.
10−5Cleaning the HousingClean the housing using tightly squeezed gauze or an absorbent cotton cloth dampened withalcohol or a neutral cleanser.CAUTION? Clean the equipment frequently so stains can be removed easily.? To prevent injury, it is recommended to wear gloves when cleaning theequipment.? Do not allow liquids or cleaning solution to enter the monitor orconnectors.? Do not use organic solvents, thinner, toluene and benzene to avoiddamaging the resin case.? Do not polish the housing with abrasive or chemical cleaner.? When sterilizing the entire room using a spray solution, pay closeattention not to have liquids get into the monitor or connectors.? Use only neutral detergent to clean the housing. Do not use chemicalcloth, scrub brush, abrasive, polishing powder, hot water, volatilesolvent and chemicals (cleanser, thinner, benzine, benzol, andsynthetic detergent for house and furniture), or sharp-edged tools.The surface resin coating may be damaged, resulting in discoloration,scratches, and other problems.Disinfecting the Blood Pressure Transducers Disinfect the blood pressure transducers according to the manufacturer’s guidelines.Disinfecting the Temperature Probes Disinfect the Temperature Probes according to the manufacturer’s guidelines.Disinfecting the CO2 Filter Line Disinfect the Filter Line/Capno Line according to the manufacturer’s guidelines.Cleaning and Disinfecting the SpO2 Transducer? Do not soak the sensor in water or antiseptic solution.? Wipe the DURASENSOR with disinfectant such as 70% alcohol. Do not disinfect by applyingradioactive rays, steam, or ethylene oxide.? OXISENSOR is a disposable sensor. Do not reuse or attempt resterilization.Cleaning and Disinfecting the NIBP Cuff? Do not soak the sensor in water or antiseptic solution.? Wipe the NIBP cuff with disinfectant such as 70% alcohol. Do not disinfect by applyingradioactive rays, steam, or ethylene oxide.Cleaning and Disinfecting the ECG lead Cable? Do not soak the sensor in water or antiseptic solution.? Wipe the ECG lead cable with disinfectant such as 70% alcohol. Do not disinfect by applyingradioactive rays, steam, or ethylene oxide.10Cleaning10Cleaning10Cleaning
10−6− Battery −Handling the Battery PackThis section describes about the handling and storage of the battery pack.Handling the Battery? The battery pack can be continually used for more than 300 times (or about 1 year) under normaltemperature, but the continuous use will degrade the battery and shortens the usable time.? When the battery operation time becomes short even after it is fully charged, the battery packneeds to be replaced.? When the charge time of the battery pack becomes short, the battery pack needs to be replaced.? When the battery pack level becomes low, charge the battery well in advance for the next use.Storing the BatteryTo take advantage of the characteristic of battery pack, pay attention to the following when storing.Storage Temperature and Humidity? Store in an environment specified below without corrosive gas.Storage Period StorageTemperature StorageHumidityWithin 30days −20∼60?C30 days∼90 days −20∼45?C90 days∼1year −20∼35?C65?20%? Do not store in an environment outside the specified temperature range or excessive highhumidity. This may result in leakage caused by expansion/contraction inside the battery pack,or rusting of the metal part.Long-term Storage? If left installed in the monitor for long period of time, the electrolyte may leak, or inactivate thebattery which degrades the capacity recovery after storage. Therefore, always remove thebattery from the monitor when storing for long period of time. Contact our servicerepresentative when removing the battery.
10−7− Maintenance Check −Daily and Periodic CheckThis section explains the daily check and periodic check items of the device.About the Maintenance CheckPeriodic inspection must be performed. When reusing the device which was left unused for awhile, always check that the device operates properly and safely before use.To ensure safety, reliability, and high performance, a “Daily Check” and “Periodic Inspection” mustbe performed. We are not liable for any accident arising from lack of maintenance.CAUTION ? Do not open the housing of this device.? Avoid alcohol or other liquids from getting into the equipment.●Daily CheckPerform daily inspection using the “Daily Check List” on the next page.●Periodic CheckPeriodic inspection of medical electronic equipment is mandatory to prevent failures and accidentsand to ensure safety and reliability.Periodic maintenance may be performed by each medical institution or by a third party byconcluding a “Maintenance Contract”.For more details, contact your nearest service representative.Time-Change ComponentsTo ensure reliability of safety, function, and performance of this device, the time-changecomponents must be replaced periodically. When replacing, contact our service representative.EtCO2 Unit Replacing Period: 7,000 hours (approx. 10 months ofcontinuous use）LCD Unit, Inverter Unit Replacing Period: 50,000 hours or 6 yearsNIBP Unit Replacing Period: 100,000 times of use or 6 yearsShort Term Backup Battery Replacing Period: 4 years∼6 years according to the usedfrequencyLong Term Backup Battery Replacing Period: 6 yearsBattery Pack Replacing Period: 1 year or 300 times of charging /discharging.CAUTION The time-change components must be replaced at specified period.10Maintenance Check
10−8Daily Check ListNo.Inspected Date Inspected by LocationDevice Type Serial No. Date of PurchaseItem Details Criteria JudgementAppearance Visually check the exterior forscratches, cracks, deformation,and rust.No abnormality should befound. □OK / □NGCheck whether the unit isinstalled on a level surface.The installation area must belevel and free from vibrationand shock. □OK / □NGInstallation Check whether the unit isinstalled in a place susceptible toadverse environment.The environmental condition(ex. temperature, humidity) ofthe installed place should beas specified.The unit should not besubjected to splashing water.□OK / □NGThe home display appears,and the lamp located at theright side of the display panellights.□OK / □NGFunctions Turn ON the monitor, and checkwhether it operates normally.The date and time should becorrect. □OK / □NGCables Visually check all cables for anydamage. No damage should be found. □OK / □NGPeriodic Inspection Check the date of previousperiodic inspection. Should be within 1 year. □OK / □NGCO2 Calibration(DS-7141)Check the date of previouscalibration date.Previous DateDay Year MonthShould be within 6 months. □OK / □NGComment
10−9− Troubleshooting −This section explains the troubleshooting for each case.ECGThe “LEAD OFF” message is displayed.Cause :The electrode is detached, or is not making good electrical contact with the skin.Solution :・Check if the electrodes are properly attached.・Replace the electrode, or check the lead cable.The “ECG failed” message is displayed.Cause 1 :The ECG amplitude is 0.25mV or below for the waveform size of ×1, ×1/2, ×1/4,and 0.150mV or below for the waveform size of ×2, ×4.Solution :Change the electrode attachment site, or select the lead with higher QRS amplitude.Note :Using 4-electrode or 5-electrode instead of 3-electrode allows more accurate QRSdetection.Cause 2 :The electrode contact is poor.Electrical blanket or other noise source is near the patient.Solution :Attach the electrode firmly.・Replace the lead cable if defective.・If any noise source is near the patient, locate it away from the patient as much as possible.ECG waveform contains noise.The “Artifact” message is displayed.Cause 1 :The electrode contact is poor.Electrical blanket or other noise source is near the patient.Solution :Attach the electrodes firmly.・Replace the lead cable if defective.・If any noise source is near the patient, locate it away from the patient as much as possible.Cause 2 :EMG is interfering.Solution :・Change the electrode site to a location where EMG will less likely to interfere.・Select ESIS mode for the filter mode.Note :Selecting a ESIS mode for the filter mode will decrease the QRS amplitude and mayresult in not counting the heart rate.The “Check electrode” message is displayed.Cause :The electrode contact with the skin is poor. There is substantial contact resistancebetween the electrodes.Solution :Replace all the electrodes.Use the electrodes of the same type.The “ECG unit error” message is displayed.Cause :A communication error with the ECG measuring unit exists.Solution :The breakage of wire or failure of the ECG unit can be considered.Contact our service representative.10Troubleshooting
10−10The measured data is displayed as “×××”.Cause :The heart rate is outside the measurement range.Solution :・Check the electrode application.・Replace the electrode, or check the lead cable.Heart rate is not counted. Heart rate is low.Cause :The ECG waveform amplitude is below the QRS detection level (0.3mV).Solution :Change the electrode site, or select a lead with higher QRS amplitude.Note :Using 4-electrode or 5-electrode instead of 3-electrode allows more accurate QRSdetection.Also, if large amount of noise is interfering, the noise may be erroneously detected asQRS. It is recommended to change the electrode site and increase the ECGamplitude.Heart rate is not counted, and “LEAD OFF” message is displayed.Cause :The electrode of the displayed lead type is detached, or is not making good electricalcontact with the skin.Solution :・Check the electrode application.・Replace the electrode, or check the lead cable.Artificial pacemaker is not displayed.Cause :On the admit / discharge menu, Not used is selected for the pacemaker use.Solution :Select Used for the pacemaker use.The “Pacemaker error” message is displayed.Cause :The pacemaker pulse is detected 16 pulses or more per second.Solution 1 :Attach the electrodes firmly.・Replace the lead cable if defective.・If any noise source is near the patient, locate it away from the patient as much as possible.Solution 2 :If the patient is not wearing a pacemaker, set to Not used for the pacemaker usein the patient admit/discharge menu.The “ECG not connected” message is displayed.Cause :When the ECG relay cable is disconnected during ECG monitoring, this message willbe displayed.Solution 1 :To cease monitoring, press the Alarm Silence key to clear the message andsilence the alarm.Solution 2 :To continue monitoring, plug in the ECG relay cable. This will clear the message andsilence the alarm.
10−11RespirationThe “CVA detected” message is displayed.Cause :Heartbeat is interfering and superimposed on the respiration waveform.Solution :Place the electrode as shown below where the heartbeat will be less likely to interfere.“0” is displayed for respiration rate, or apnea alarm is generated.Cause :The respiration waveform amplitude is below the detection level (0.2O).Solution :Change the electrode site.The respiration waveform and respiration rate is not displayed.Cause 1 :The ECG relay cable designed for electrosurgical knife is used.Solution :The impedance respiration can not be measured if the cable designed forelectrosurgical knife is used. Use the standard ECG relay cable if not using theelectrosurgical knife.Cause 2 :The impedance respiration measurement is ceased.Solution :Turn ON the impedance respiration measurement on the admit / discharge menu orRESP configuration menu.Note :If the pacemaker with the minute ventilation measuring function is used, turn OFF theimpedance respiration measurement. Otherwise, both the pacemaker and the monitorwill not be able to perform accurate measurement.The measured data is displayed as “×××”.Cause :The respiration rate is outside the measurement range.Solution :・Check the electrode application.・Replace the electrode, or check the lead cable.Invasive Blood PressureThe “BP1 Transducer OFF”, “BP2 Transducer OFF” message is displayed.Cause :The transducer for BP1 or BP2 is not connected.Solution :Connect the transducer.The “BP1 not zero balanced”, “BP2 not zero balanced” message is displayed.Cause :The BP zero balance has not been performed since the power is turned ON.Solution :Open the three-way cock of the transducer to air and perform zero balance.The measured data is displayed as “ｰ ｰ ｰ”.Cause :The BP zero balance has not been performed since the power is turned ON.Solution :Open the three-way cock of the transducer to air and perform zero balance.10TroubleshootingRedWhite Black
10−12BP value and waveform are not displayed properly.Cause :Blood pressure line has not been zero balanced.Solution :Open the three-way cock of the transducer to air and perform zero balance.The measured data is displayed as “×××”.Cause :The BP value is outside the measurement range.Solution :Perform zero balance again.The “BP not connected” message is displayed.Cause :When the BP interface cable or 2ch BP conversion cable is disconnected during BPmonitoring, this message will be displayed.Solution 1 :To cease monitoring, press the Alarm Silence key to clear the message andsilence the alarm.Solution 2 :To continue monitoring, plug in the BP interface cable or 2ch BP conversion cable.This will clear the message and silence the alarm.The “Incorr. BP cable” message is displayed.Cause :The cable other than 2ch BP conversion cable is plugged in to the BP connector.Solution :Use the 2ch BP conversion cable.SpO2The “Check SpO2 sensor” message is displayed.Cause :Sensor is detached from the patient.Solution 1 :Check if the sensor part is properly attached to the patient.Solution 2 :Check if the light emitting part and light receiving part of the sensor LED is aligned.The “Pulse search” message is displayed.Cause :The amplitude of the pulse waveform is low, or the sensor is not positioned correctly.Solution :Check if the light emitting part and light receiving part of the sensor LED is aligned.The “No pulse detect” message is displayed.Cause :The amplitude of the pulse waveform is low, or the sensor is not positioned correctly.Solution :Check if the light emitting part and light receiving part of the sensor LED is aligned.The “Motion Artifact” message is displayed.Cause :There is excessive body motion of the patient.Solution :Change the sensor position where the body motion will have less effect.The pulse waveform is not displayed, or interruptedSituation :“Check SpO2 sensor” is displayed.Cause 1 :The amplitude of the pulse waveform is low, or the sensor is not positioned correctly.Solution :Check if the light emitting part and light receiving part of the sensor LED is aligned.Cause 2 :Sensor is defective.Solution :Replace the sensor.Cause 3 :SpO2 sensor is not firmly connected to the SpO2 input connector.Solution :Make sure the SpO2 sensor is securely connected.Cause 4 :Sensor is exposed to light.Solution :Place a black or dark cloth over the sensor to avoid direct sunlight. Also when notused, avoid placing the sensor in light or unplug the sensor from the connector.
10−13The SpO2 measurement is unstable.Cause :There is excessive body motion of the patient which disables correct measurement.Solution :1. Have the patient lie still as much as possible.2. Relocate the sensor, or change the sensor to which the body motion will have less influence.The “SpO2 unit error” message is displayed.Cause 1 :There is a failure of communication with the SpO2 measurement unit.Solution :Breaking of wire or SpO2 unit failure can be considered.Contact our service representative.Cause 2 :Sensor is defective.Solution :Replace the sensor.The “SpO2 sensor fault” message is displayed.Cause :Sensor is defective.Solution :Replace the sensor.The “SpO2 not connected” message is displayed.Cause :When the SpO2 relay cable is disconnected during SpO2 monitoring, this message willbe displayed.Solution 1 :To cease monitoring, press the Alarm Silence key to clear the message andsilence the alarm.Solution 2 :To continue monitoring, plug in the SpO2 relay cable. This will clear the messageand silence the alarm.Non-Invasive Blood PressureThe cuff is not inflated although the pump is operating.Cause1 :The air hose is not firmly connected, and the air is leaking.Solution :Check if the air hose is properly connected.Cause 2 :The cuff size is not corresponded to the selected patient type.Solution :Check if the cuff size is corresponded to the selected patient type.The monitor repeats the measurement, or “ｰ ｰ ｰ” is displayed for the numeric data.Cause 1 :The measurement accuracy is not reliable due to body motion artifact.Solution :Have the patient stay still as much as possible during the measurement.Cause 2 :The pulse is too small to acquire reliable measurement accuracy.Solution :Check if the cuff application is proper, and if the cuff size is corresponded to theselected patient type.The “Check NIBP hose” message is displayed.Cause :The applied pressure to the cuff has exceeded the maximum limit. The measurementtime has exceeded the maximum limit.Solution :Check if the cuff application is proper, if the cuff size is corresponded to the selectedpatient type, or if the air hose is not bent. After checking the above, perform themeasurement again.If the same message is displayed again, a failure of the equipment can be considered.Cease the measurement, and contact our service representative.10Troubleshooting
10−14The “NIBP unit error” message is displayed.Cause :The zero balancing before the measurement has failed, and measurement could not bestarted.Solution :The body movement or other artifact may cause zero balance failure. During themeasurement, have the patient stay still as much as possible.If the same message is displayed again, the failure of the equipment can be considered.Cease the measurement, and contact our service representative.The time of measurement disappears and the numeric data is displayed as “ｰ ｰ ｰ”.Cause :The NIBP data will be erased when the preprogrammed NIBP erase time has elapsed.Solution :Select the appropriate time for NIBP data erase time from 10min, 30min, 60min, 24hrswhich best fits the monitoring purpose.TemperatureThe “Wrong Temp Probe” message is displayed.Cause 1 :The YSI-700 is used.Solution :Use the YSI-400 temperature probe for measurement. The YSI-700 can not be usedwith the DS-7100 series.Cause 2 :There is a contact failure of the temperature probe.Solution :Check if the temperature probe is properly inserted.The numeric data is displayed as “×××”.Cause :The temperature measurement is outside the measurement range.Solution :Check if the temperature probe is properly inserted.The “TEMP not connected” message is displayed.Cause : When the temperature sensor is disconnected during temperature monitoring, thismessage will be displayed.Solution 1 :To cease monitoring, press the Alarm Silence key to clear the message andsilence the alarm.Solution 2 :To continue monitoring, plug in the temperature sensor. This will clear the messageand silence the alarm.The “TEMP auto check” message is displayed. The numeric data is displayed as “ｰ ｰ ｰ”.Cause :The temperature is calibrated once every hour on this monitor. During calibration, thenumeric data will be displayed as “ｰ ｰ ｰ”.Solution :The calibration will complete in 10 seconds. If the calibration does not complete within10 seconds, cease the measurement and contact our service representative.The “TEMP unit check” message is displayed.Cause :Error is detected during temperature calibration.Solution :A unit failure can be considered. Cease the measurement and contact our servicerepresentative.
10−15CO2 ConcentrationThe “Check filter line” message is displayed.Cause :The sampling tube is clogged.Solution :Replace the sampling tube.The “Self-diag CO2” message remains displayed.Cause :An error has occurred to the self-check procedure at power ON.Solution :The CO2 unit failure can be considered.The “Initializing CO2” message does not disappear.Cause :An error has occurred during the initialization at power ON.Solution :The CO2 unit failure can be considered.The “Check CO2 unit” message is displayed.Cause 1 :The exhaust connector is clogged.Solution :After checking the exhaust system and removing the clog, press the “Restart CO2” keyon the CO2 configuration menu.Cause 2 :The sampling tube or nasal prong is clogged.Solution :After checking the inhalation system and removing the clog, press the “Restart CO2”key on the CO2 configuration menu.Cause 3 :The CO2 unit needs to be replaced.Solution :Contact our service representative.The “CO2 unit error” message is displayed.Cause :There is a communication error with the CO2 unit.Solution :The break of wire or CO2 unit failure can be considered.Contact our service representative.There is substantial measurement error.Cause 1 :20 minutes have not yet elapsed since the power is turned ON.Solution :For 20 minutes from turning ON the power, there will be a substantial measurementerror.Cause 2 :The calibration is not properly performed.Solution :Perform CO2 calibration again.The “CO2 not connected” message is displayed.Cause :When the filter line is disconnected during CO2 monitoring, this message will bedisplayed.Solution 1 :To cease monitoring, press the Alarm Silence key to clear the message andsilence the alarm.Solution 2 :To continue monitoring, plug in the filter line. This will clear the message and silencethe alarm.10Troubleshooting
10−16RecorderNo recording is performed.Situation :The “Paper Out” message is displayed on the upper left of the screen.The “Paper Out” message is displayed on the Rec. START/STOP key.Cause :There is no recording paper in the recorder magazine.Solution :Install a new pad of paper into the paper magazine.Situation :The “Magazine Open” message is displayed.Cause :The paper magazine is open.Solution :Close the magazine.Situation :The “Paper jammed” message is displayed.Cause :The paper is jammed.Solution :Open the magazine and install the paper correctly.Situation :No message is displayed, but recording can not be performed.Cause :The recording paper is not correctly installed. The front and backside of the paper isset oppositely.Solution :The “END” printed side of the paper should be facing down in the magazine.The second waveform and third waveform are not recorded.Situation :The second waveform and third waveform are not recorded for manual recording oralarm recording.Cause :The second waveform and third waveform are not set on the recording setup menu.Solution :Set the second waveform and the third waveform on each recording setup menu.The “Recorder error” message is displayed.Cause :The thermal head temperature has increased.Solution :A damage to the thermal head can be considered.Contact our service representative.TelemetryThe “Telemetry unit error” message is displayed.Cause :There is a communication error with the telemetry transmission unit.Solution :The breaking of wire or telemetry transmission unit failure can be considered.Contact our service representative.There is no reception at the telemetry center.Cause :The channel ID or group ID is not corresponded with the telemetry receiver.Solution :Set the correct channel ID and group ID.The BP waveform of 100mmHg or above can not be properly received.Cause :The BP waveform and scale is not corresponded.Solution :When BP waveform is above 100mmHg, set the BP scale above 100mmHg.
10−17GeneralNothing is displayed but the main power indicator is lighted.Cause :A system error has occurred.Solution :Turn off the power, unplug the power cable, and contact our service representative.The “Adjusting” message is displayed. Numbers are displayed large on the display.Cause :This is the test mode. Stop using the device immediately.Solution :Restart the system. The test mode will be cancelled.If the same situation is observed again, contact our service representative.Turn off the DIP switch No.1.The data is initialized each time the power is turned ON.Cause 1 :The internal switch is set to initialize.Solution :The internal switch setting needs to be changed. Contact our service representative.Set the rotary switch to 0.Cause 2 :The battery for backup memory is depleted.Solution :The battery needs to be replaced. Contact our service representative.The display is not clear.Cause 1 :The display brightness is not adjusted.Solution :Due to the LCD display characteristic, the visible range is limited. Adjust to theappropriate brightness.Cause 2 :The monitor is set to the night mode.Solution :Cancel the night mode.The system does not start although the power switch is turned ON.Cause 1 :The power cable is not connected.The battery is not charged.Solution :Turn off the power and connect the power cable. If the battery is not charged, use thepower cable until the battery charging is complete.Cause 2 :Incorrect IC card is inserted.Solution :Turn off the DIP switch No.8.The clock is often delayed.Cause :The battery for the backup memory is depleted. Check if the time is delayed when thepower is turned off.Solution :The battery needs to be replaced. Contact our service representative.10Troubleshooting
10−18BatteryThe operation time is short although the battery is charged.Cause 1 :The battery life has expired.Solution :The battery pack is a consumable product. Replace it once a year.Cause 2 :The ambient temperature is too high or too low.Solution :For safety, the charging operation will be in a standby mode when the battery packtemperature becomes excessively high or low.The charging will automatically resume when appropriate temperature is reached.Charge the battery in an ambient temperature of 10∼30?C.The charge lamp on the patient monitor does not light.Cause 1 :The AC power cable is disconnected.Solution :Plug in the AC power cable.The battery pack can be charged only during the AC operation.Cause 2 :The battery pack is not installed.Solution :The battery pack is optional. If a battery pack is required, contact our servicerepresentative and install the battery pack.Cause 3 :The battery life has expired.Solution :The battery pack is a consumable product. Replace it once a year.During the charging procedure, the charge lamp (orange) does not switch to chargecomplete status (green) and extinguishes.Cause 1 :The battery pack temperature is too high or too low.Solution :For safety, the charging operation will be in a standby mode when the battery packtemperature becomes excessively high or low.The charging will automatically resume when appropriate temperature is reached.Cause 2 :The breakdown of battery pack can be considered.Solution :If the charging operation does not complete within the specified charging time, thecharging operation will cease for safety purpose.Contact our service representative and replace the battery pack.Cause 3 :The battery life has expired.Solution :The battery pack is a consumable product. Replace it once a year.The “Charge battery” message is displayed.Cause :The AC power cable is disconnected.Solution :Plug in the AC power cable.The battery pack can be charged only during the AC operation.
11−1Technical InformationChapter 11− Specification/Performance −･･････････････････ 2Specification･････････････････････････････････ 2Performance･････････････････････････････････ 3− Setup Item −Default and Backup･･･････････ 5Patient Admit / Discharge･･････････････････････ 5Alarm Setup ･････････････････････････････････ 5Parameter Setup ･････････････････････････････ 6Review Function Setup････････････････････････ 7System Configuration Setup ･･･････････････････ 8Display Mode Setup ･････････････････････････12Alarm Mode Setup･･･････････････････････････13− External Connection −Pin Assignments･･･14Serial Connector Output Signal････････････････14Status I/O Signal ････････････････････････････ 1411Technical Information
11−2− Specification/Performance − This section states the specification and performance of this equipment.SpecificationSize260 (W) ×197 (D) ×264 (H) mm (not including the protrusion)Weight (not including the battery)DS-7141 :5.3kgDS-7101L :5.1kgDS-7101LT :5.2kgEnvironmental ConditionOperating Temperature :10∼40?COperating Humidity :30∼85% (without condensation)Transport / Storage Temperature :−10∼60?CTransport / Storage Temperature :10∼95% (at 60?C)SafetyGeneral Standard :EN60601-1:1990(Medical electrical equipment – Part 1: General requirements forsafety)Amendment A1 to EN 60601-1:1993Amendment A2 to EN 60601-1:1995EMC Standard : IEC 60601-1-2:1993(Medical electrical equipment−Part 1: General requirements for safety−2.Collateral standard:Electromagnetic compatibility −requirements andtests. IEC 601-1-2:1993 )Withstand Voltage :Class I, Type CFPower RequirementsVoltage AC100∼240V ?10% DC14V ?10%Frequency 50/60Hz ?PowerConsumption 82VA 60W
11−3PerformanceDisplayDevice :8.4 inch TFT Color LCDControl :Touch Screen TypeWaveform Trace :Stationary TraceWaveform Speed :ECG / SpO2 / BP (6.25mm/s, 12.5mm/s, 25mm/s)RESP / CO2 (6.25mm/s, 12.5mm/s, 25mm/ s)Parameter :ECG, RESP, TEMP, SpO2 (Arterial Oxygen Saturation), BP1, BP2,NIBP, CO2 concentrationRecordingRecording Method :Thermal Array TypeRecording Speed :25mm/sRecording Waveform :Max. 3 waveformsRecording Width :50mmOperationTouch Screen :Eight-Wire Resistive Analog Touch ScreenECGLead Type :Wired 3-electrode, 4-electrode, 5-electrodeFrequency Characteristic :40Hz / 15HzInput Impedance : 5M? or aboveMax. Input Voltage :±10mVPolarization Voltage :±825mV or aboveCommon ModeRejection Ratio :80 dB or aboveHR Measurement Range :Adult 0, 12∼300bpm±3% or ±5bpmNeonate 0, 30∼300bpm±3% or ±5bpmWaveform Size Selection :1/4, 1/2, 1, 2, 4Defibrillation Proof :Provided RespirationMethod :Impedance MethodFrequency Characteristic :1.5Hz (adult, child) / 2.5Hz (neonate)Current :100μA or lowerMeasurement Range :0, 4∼150Bpm±5BpmTemperatureMethod :Thermistor MethodProbe :only YSI-400 seriesMeasurement Range :0∼50?C±0.2?CNo. of Channel : 1 channelSpO2 (Arterial Oxygen Saturation)Method :2 Wavelength Pulse Wave MethodMeasurement Range :0%∼100%Resolution :1%Accuracy :Adult at 70∼100% ±2%at 0∼69% not specifiedNeonate at 70∼100% ±3%at 0∼69% not specifiedMeasurement Range :20∼250bpm±3bpm11Specification / Performance
11−4Blood PressureTransducer Sensitivity :5μV / V / mmHgMeasurement Range :−50∼300mmHgFrequency Characteristic :DC∼6Hz / 8Hz / 12Hz / 40HzAccuracy :±2% of full scale or within ±1mmHgZero Balance Range :within ±150mmHgMeasurement Range :Adult 20∼300bpm±3%Neonate 30∼300bpm±3%Channel :2 channelsNon-Invasive Blood PressureMethod :Oscillometric MethodMeasurement Range :10∼280mmHgResolution :1mmHgAccuracy :±4mmHgMeasurement Range : 40∼240bpm±5%CO2 Concentration (DS-7141)Method :Infra-Red Solid-State Method, Microstream MethodMeasurement Range :0∼99mmHg0-20min 0∼38mmHg:±4mmHg 39∼99mmHg:±12%20min. and up 0∼38mmHg:±2mmHg 39∼99mmHg:±5%RR Measurement Range :0∼150bpm0∼40bpm:±1bpm41∼70bpm:±2bpm71∼100bpm:±3%101∼150bpm:±5%Flow Rate :50±7.5 ml/minSystem Response Time :2.9 seconds (Typical)Delay Time :2.7 seconds (Typical)Rise Time :190 msec (maximum)Telemetry (DS-7141, DS-7101LT)Transmission Freq. :608~614 MHzExact frequency depends on the destination.RF Output Power :-15dBm Standard, 0dBm MAXChannel Spacing :12.5 kHzModulation Mode :Digital, Frequency Shift Keying (FSK)
11−5− Setup Item −Default and BackupThis section lists selection, default setting, and backup status for each setup item.Backup Item“○” : Setup item will be retained even when the power is turned OFF.“△” : Setup item will be retained even when the power is turned OFF. When dischargingprocedure is performed, the value will be reset to initial setting.The alarm setup will be reset to initial setting with the selected alarm mode.“−” : Setup item will be reset to initial setting when the power is turned OFF.Patient Admit / DischargeItem Selection Default BackupPatient Name Numeric, Alphabet, Symbol (16characters) Blank △Sex Male, Female Undetermined △Age 0∼150 years or 0∼999 days 0 year △Birth Date Birth Date (Year, Month, Day) Blank △ID Numeric, Alphabet, Symbol (10characters) Blank △Patient Type Adult, Child, Neonate Adult ○Pacemaker Used, Not used Not used △Impedance Measurement ON, OFF ON △Filter Mode Monitor, ST Display, ESIS Monitor ○Bed ID 0∼999 0○Room/Bed ID Room ID Numeric, Alphabet, Symbol(4 characters) BED− ○Alarm SetupItem Selection Default BackupSystem Alarm Suspend, ON SuspendHR ON, OFF 20−300bpm ON 40−120AYSTOLE ON, OFF 3−10 sec. ON 5 sec.VF ON, OFF ONVT ON, OFF ONSLOW_VT ON, OFF ONRUN ON, OFF 2−8 beats ON 3 beatsCOUPLET ON, OFF OFFPAUSE ON, OFF 1.5−5 sec. OFF 2 sec.BIGEMINY ON, OFF OFFTRIGEMINY ON, OFF OFFFREQUENT ON, OFF 1−50 beats / min. OFF, 10 beatsTACHY ON, OFF 20−300 ONBRADY ON, OFF 20−300 ONSTON, OFFST1 ±2.0mV / ±20mmST2 ±2.0mV / ±20mmOFFBP1 (mmHg) ON, OFF 0−300mmHgONSYS 80−180DIA OFF−OFFMEAN OFF−OFFBP1 (kPa) ON, OFF 0−40.0kPaONSYS 10.0−24.0DIA OFF−OFFMEAN OFF−OFF○/△11Setup Item
11−6Item Selection Default BackupBP2（mmHg）ON, OFF 0−300mmHgONSYS OFF−OFFDIA OFF−OFFMEAN OFF−OFFBP2（kPa）ON, OFF 0−40.0kPaONSYS OFF−OFFDIA OFF−OFFMEAN OFF−OFFRR ON, OFF 5−150Bpm ON 5−30APNEA ON, OFF 5−20sec. ON 15sec.SpO2ON, OFF 50−100% ON 90−OFFNIBP (mmHg) ON, OFF 10−300mmHgONSYS 80−180DIA OFF−OFFMEAN OFF−OFFNIBP (kPa) ON, OFF 1.5−40.0kPaONSYS 10.0−24.0DIA OFF−OFFMEAN OFF−OFFTEMP ON, OFF 30−50?COFF OFF−OFFEtCO2 (mmHg) ON, OFF 1−100mmHg ON 30−45mmHgEtCO2 (kPa) ON, OFF 0.1−13.3kPa ON 4.0−6.0kPaEtCO2 (%) ON, OFF 0.1−13.3% ON 4.0−6.0%InspCO2 (mmHg) ON, OFF 1−4mmHg ON 3mmHgInspCO2 (kPa) ON, OFF 0.1−0.4kPa ON 0.4kPaInspCO2 (%) ON, OFF 0.1−0.4% ON 0.4%○/△NOTE The alarm setup will be retained even after the power is turned OFF.If discharging procedure is performed, the alarm setup will be initialized with theselected alarm mode.Parameter SetupItem Selection Default BackupLead Ⅰ, Ⅱ, Ⅲ, aVR, aVL, aVF,VECG1 Lead ⅡECG2 Lead V ○/△Waveform Size ×1/4, ×1/2, ×1, ×2, ×4ECG1 ×1ECG2 ×1△Filter Selection Monitor, ST Display, ESIS Monitor ○HR Source Auto, ECG, SpO2, BP Auto ○Automatic Lead Switch ON, OFF OFF ○Pacemaker Pulse ON, OFF ON ○HR Average ON, OFF, Instant, Average Average ○HR Sync. Indicator ON, OFF ON ○Pace Pulse Mask Time Auto, 10ms, 20ms, 40ms,OFF Auto ○ECGECG Drift Filter ON, OFF OFF ○Waveform Size ×1/4, ×1/2, ×1, ×2, ×4×1△RR Sync. Indicator ON, OFF ON ○CVA ON, OFF OFF △RR Source Auto, Impedance, CO2Auto ○RESPImpedance Meas. ON, OFF ON ○
11−7Item Selection Default BackupWaveform Size ×1/4, ×1/2, ×1, ×2, ×4×1△SpO2 SEC Alarm OFF, 10, 25, 50, 100 OFF ○SpO2Ignore NIBP ON, OFF ON ○Auto Mode ON, OFF OFF △End Tone ON, OFF ON ○Quick SYS List ON, OFF ON ○PR ON, OFF OFF ○Quick SYS 3, 5, 10 min. 10 min. ○1-Min. Auto 10, 20 min. 20 min. ○NIBPMean ON, OFF OFF ○Scale20, 50, 75, 100, 150, 200,250, 300mmHg4, 8, 12, 16, 20, 24, 32,40kPa150mmHg20kPa ○/△Filter 6, 8, 12, 40Hz 12Hz ○BP1Mean ON, OFF OFF ○Scale20, 50, 75, 100, 150, 200,250, 300mmHg4, 8, 12, 16, 20, 24, 32,40kPa50mmHg8kPa ○/△Filter 6, 8, 12, 40Hz 12Hz ○BP2Mean ON, OFF OFF ○Meas. Unit mmHg, kPa, % mmHg ○EtCO2 Average 10, 20, 30 sec., OFF 10 sec. ○／△CO2Scale 50, 100mmHg4, 8, 10kPa4, 8, 10%50mmHg4kPa4% ○／△Review Function SetupItem Selection Default BackupParameter HR, PR, VPC, ST1/ST2, RR, APNEA,SpO2, BP, NIBP, TEMP,EtCO2 / InspCO2, EVENT1, EVENT2 HR ○Duration 1, 2, 4, 8, 12, 24 hours 4 hours ○GraphicTrendScaleHR :100, 200, 300bpmST :±0.2, ±0.5, ±1.0,±2.0mV±2, ±5, ±10, ±20mmVPC :20, 50, 100 beatsBP1 :20, 50, 100, 150, 200, 300mmHg4, 8, 16, 20, 24, 40kPaBP2 :20, 50, 100, 150, 200, 300mmHg4, 8, 16, 20, 24, 40kPaNIBP :100, 150, 200, 300mmHg16, 20, 24, 40kPaTEMP :20-45, 30-40?CSpO2:0-100, 50-100, 80-100%RR :100, 200, 300bpmAPNEA :15, 30 sec.CO2:50, 100mmHg4, 8, 10kPa4, 8, 10%HR :100bpmST :±0.5mV±5mmVPC :20 beatsBP1 :150mmHg20kPaBP2 :50mmHg8kPaNIBP :150mmHg20kPaTEMP : 30-40?CSpO2: 80-100%RR :50bpmAPNEA :15 sec.CO2:50mmHg4.0kPa4.0%○11Setup Item
11−8Item Selection Default BackupTabularTrend Duration 1, 5, 10, 15, 30, 60 min. 60 min. ○Display Time 4, 8 min. 8 min. ○OCRG Waveform Impedance Resp., CO2Impedance Resp. ○Parameter ECG1, ECG2, BP, SpO2, RESP, CO2ECG1, ECG2 ○Alarm FactorHR/PR/BPR :ON, OFFST :ON, OFFRR :ON, OFFAPNEA :ON, OFFSpO2:ON, OFFBP1 :ON, OFFBP2 :ON, OFFNIBP :ON, OFFTEMP :ON, OFFCO2:ON, OFFHR/PR/BPR :ONST :ONRR :ONAPNEA :ONSpO2:ONBP1 :ONBP2 :ONNIBP :ONTEMP :ONCO2:ON○RecallArrhythmiaFactorASYSTOLE :ON, OFFVF :ON, OFFVT :ON, OFFSLOW_VT :ON, OFFRUN :ON, OFFCOUPLET :ON, OFFPAUSE :ON, OFFBIGEMINY :ON, OFFTRIGEMINY :ON, OFFFREQUENT :ON, OFFTACHY :ON, OFFBRADY :ON, OFFASYSTOLE :ONVF :ONVT :ONSLOW_VT :ONRUN :ONCOUPLET :ONPAUSE :ONBIGEMINY :ONTRIGEMINY :ONFREQUENT :ONTACHY :ONBRADY : ON○Meas. Point 0∼560ms 120ms ○STMeas. Ref. Point 0∼−240ms −80ms ○NOTE? The graphic trend data, tabular trend data will be retained even after thepower is turned OFF.? The ST data, OCRG data, recall data will be retained until 5 minutes after thepower is turned OFF.System Configuration Setup●Volume SetupItem Selection Default BackupPulse 16 levels Level 8 from left ○Key 16 levels Level 10 from left ○Alarm 16 levels Level 10 from left ○Other Bed 16 levels Level 10 from left ○VolumeOthers 16 levels Level 8 from left ○
11−9●Display ConfigurationItem Selection Default BackupNo. of waveforms 0∼6 waveforms 3 waveformsNo. of numericdata 0∼7 numeric data 4 numeric dataDisplayedwaveform ECG1, ECG2, BP, SpO2RESP, CO2ECG1, SpO2, RESPDisplayed numericdata HR, BP, NIBP, SpO2RESP, RR, CO2, VPC/ST HR, NIBP, SpO2, RREnlarged Display ON, OFF OFFDisplayConfigurationShort Trend ON, OFF, Overlap OFF○／△NOTEBy selecting ON for backup at discharge, the setup item will be storedeven after discharge.Selecting OFF will initialize the display configuration to the initial setting ofthe selected display mode.●System Configuration MenuItem Selection Default BackupWave Select ECG1, ECG2, BP, SpO2RESP, CO2ECG1, BP, RESP ○Rec. Duration 24 sec., Continuous 24 sec. ○ManualRecordingDelay Time None, 8sec., 16 sec. 8 sec. ○Alarm Record ON, OFF, Center OFF ○Wave Select ECG1, ECG2, BP, SpO2RESP, CO2, Alarm Factor ECG1, Alarm Factor ○Rec. Duration 12, 24 sec. 12 sec. ○Alarm Factor HR (HR / PR / BPR)Numeric Data, Arrhythmia HR (HR / PR / BPR)Arrhythmia ○AlarmRecordingArrhythmia RecordASYSTOLE, VF, VT,SLOW_VT, RUN,COUPLET, PAUSE,BIGEMINY, TRIGEMINY,FREQUENT, TACHY,BRADYASYSTOLE, VF, VT,SLOW_VT, RUN,TACHY, BRADY ○Periodic Record ON, OFF, Center OFF ○Wave Select ECG1, ECG2, BP, SpO2,RESP, CO2ECG1, BP, RESP ○Rec. Duration 6, 12, 24 sec. 12 sec. ○PeriodicRecordingPeriodic Interval 5, 10, 15, 30, 60 min. 60 min. ○Paper Feed to Top ON, OFF OFF ○Paper Feed to End ON, OFF ON ○Rec.Operation QRS Classification ON, OFF ON ○ECG, BP, SpO225, 12.5, 6.25mm/s 25mm/s ○SweepSpeed RESP, CO225, 12.5, 6.25mm/s 6.25mm/s ○Mode Manual, Auto Manual ○Start Time 00:00∼23:59 22:00 ○Complete Time 00:00∼23:59 7:00 ○Display Time Disp. Only, SlightlyDark, Dark Dark ○Volume No change, Quiet, Veryquiet, Silence Very quiet ○Night ModeAlarm Pole ON, OFF OFF ○11Setup Item
11−10Item Selection Default BackupECG Green ○ST Green ○VPC White ○PACE White ○BP1 Red ○BP2 Cyan ○NIBP Cyan ○SpO2Yellow ○TEMP Orange ○RESP White ○CO2Cyan ○ColorST2 (Trend)32 colorsOrange FixedAlarm Suspend 1, 3, 5 min. 3 min. ○Alarm Setup Alarm Silence 1, 3, 5 min. 3 min. ○●Hospital SetupItem Selection Default BackupAC filter 50, 60Hz According to Dip_SW ○Date 07/19, Jul.19, 19.Jul Jul.19 ○Alarm Mute ON, OFF OFF ○Home Key Function Home / Enlarge, Home Home ○Night Mode Cancel Any Key, Night Mode Key Any Key ○Asystole,VF,VT ON,ON/OFF ON ○BP mmHg, kPa mmHg ○TEMP ?C, ?F?C○UnitST mm, mV mV ○Channel 0801~0879, 0900~0979,1000~1079, 1100~1179,1200~1279, 1300~1379 1100 ○TelemeterGroup 00∼63 00 ○●Ward SetupItem Selection Default BackupTrend Clip ON, OFF ON ○BP Record Scale 20, 40mm 40mm ○HR Low Limit for VT 120, 140bpm 120bpm ○Password ON, OFF OFF ○Discharge Mode Admit, Cease Admit ○Event Key ON, OFF ON ○Mean Calculation Waveform, Calculation Waveform ○Menu All Key(excluding system config.) All Key ○System Config. All Key(excluding pre-set) All Key ○Key MaskPre-Set Menu All Key(excluding ward setup) All Key ○
11−11Item Selection Default BackupUser Key SelectionRec. START/STOP,Alarm Silence, Alarm, KeyLock, NIBP List, GraphicTrend, Tabular Trend,Recall, OCRG, Freeze,NIBP Auto Mode,Size/Lead, HR Source, BPZero, Admit/Discharge,Night Mode, DisplayConfig., Record,Tone/Volume, Other Bed,ST Display, Cease,Enlarged DisplayAlarm Silence, Rec.START/STOP,Size/Lead,Admit/Discharge(from left of display)○Alarm Pole ON, OFF ON ○Alarm Level Level１, Level 1 and 2,Level 1, 2, and 3 Level１ ○Alarm PolePattern Setup Pattern 1∼10Level 1：Pattern 1Level 2：Pattern 10Level 3：Pattern 4○NIBP Data Erase Time 10, 30, 60min, 24hourr 60min ○●Monitor SetupItem Selection Default BackupBattery Operation Normal, Power Save Normal ○Message Icon ON, OFF OFF ○Parameter Key Frame ON, OFF ON ○Wide AC Filter ON, OFF OFF ○Check Discharge at Power ON ON, OFF ON ○Backup at Discharge ON, OFF OFF ○HR, RR HR ○Sync. SygnalOutput Positive Logic, NegativeLogic Positive Logic ○OFF, APNEA, Level 1,Level 1 and 2,Level 1, 2 and 3Level 1 ○StatusOutput SetupAlarm OutputPositive Logic, NegativeLogic, Pulse Positive Logic ○11Setup Item
11−12Display Mode SetupItem Default BackupMode Selection 1○No. of Waveforms 3 Waveform ○No. of Numeric Data 4 Numeric Data ○Displayed Waveforms ECG1, SpO2, RESP ○Displayed Numeric Data HR, NIBP, SpO2, RR ○Enlarged Display OFF ○Short Trend OFF ○Mode 1Comment CONFIG. 1 ○No. of Waveforms 3 Waveforms ○No. of Numeric Data 4 Numeric Data ○Displayed Waveforms ECG1, SpO2, RESP ○Displayed Numeric Data HR, NIBP, SpO2, RR ○Enlarged Display OＮ ○Short Trend OFF ○Mode 2Comment CONFIG. 2 ○No. of Waveforms 4 Waveforms ○No. of Numeric Data 6 Numeric Data ○Displayed Waveforms ECG1, BP1/2 (overlap), SpO2, RESP ○Displayed Numeric Data HR, BP1,BP2, NIBP, SpO2, TEMP, RR ○Enlarged Display OFF ○Short Trend OFF ○Mode 3Comment CONFIG. 3 ○No. of Waveforms 4 Waveforms ○No. of Numeric Data 6 Numeric Data ○Displayed Waveforms Cascade, BP1/2 (overlap), SpO2, RESP ○Displayed Numeric Data HR, BP1, BP2, NIBP, SpO2, TEMP, RR ○Enlarged Display OFF ○Short Trend OFF ○Mode 4Comment CONFIG. 4 ○No. of Waveforms 6 Waveforms ○No. of Numeric Data 7 Numeric Data ○Displayed Waveforms ECG1, BP1/2 (overlap),, SpO2, CO2○Displayed Numeric Data HR, BP1, BP2, NIBP, SpO2, TEMP/ RR,CO2○Enlarged Display OFF ○Short Trend OFF ○Mode 5Comment CONFIG. 5 ○
11−13Alarm Mode SetupItem Default BackupAlarm Mode 1○HR ON 40−120 ○AYSTOLE ON 5 sec. ○VF ON ○VT ON ○SLOW_VT ON ○RUN ON 3 beats ○COUPLET OFF ○PAUSE OFF 2 sec. ○BIGEMINY OFF ○TRIGEMINY OFF ○FREQUENT OFF 10 beats ○TACHY ON ○BRADY ON ○ST OFF ○BP1 (mmHg)ONSYS 80−180DIA OFF−OFFMEAN OFF−OFF○BP1 (kPa)ONSYS 10.0−24.0DIA OFF−OFFMEAN OFF−OFF○BP2 (mmHg)OFFSYS OFF−OFFDIA OFF−OFFMEAN OFF−OFF○BP2 (kPa)OFFSYS OFF−OFFDIA OFF−OFFMEAN OFF−OFF○APNEA ON 15 sec. ○SpO2ON 90−OFF ○NIBP (mmHg)ONSYS 80−180DIA OFF−OFFMEAN OFF−OFF○NIBP (%)ONSYS 10.0−24.0DIA OFF−OFFMEAN OFF−OFF○EtCO2 (mmHg) ON 30‐45 ○EtCO2 (kPa) ON 4.0‐6.0 ○EtCO2 (%) ON 4.0‐6.0 ○InspCO2 (mmHg) ON 3○InspCO2 (kPa) ON 0.4 ○Alarm Mode 1∼5InspCO2 (%) ON 0.4 ○11Setup Item
11−14− External Connection −Pin AssignmentsThis section explains the connector pin assignments.Serial Connector Output SignalNo. Signal Type Description Signal Level1RESET Port Reset TTL Hi Level Reset2RSV Reserved ――3TxD Serial Transmit Data Output RS232C4SG Signal GND5RxD Serial Receive Data Input RS232C6+5V +5V ＋5V power supply (150mA)7RSV Reserved ――8NC No Connection ――Status I/O SignalNo. Signal Type Description Signal Level1QRS SYNC QRS SYNC Output Logic TTL2ALM_OUT+Alarm Output ＋(Isolation）Photo MOS Relay Contact3RSV Reserved ――4RSV Reserved ――5RSV Reserved ――6RSV Reserved ――7＋5V +5V ＋5V power supply (150mA)8ALM_OUT-Alarm Output −(Isolation) Photo MOS Relay Contact9GND Power Supply Digital GND ――※As the serial connector and status I/O connector uses the same isolation power supply, thetotal power supply capacity for ＋5V should be up to 200mA.
12−1AccessoriesChapter 12− Accessories −･･･････････････････････････ 2− Optional Accessories −･･････････････････････ 3ECG, Impedance Respiration Measurement･･････ 3Invasive Blood Pressure Measurement ･･････････ 3Non-Invasive Blood Pressure Measurement･･････ 3Temperature Measurement ････････････････････ 4SpO2 Measurement･･･････････････････････････ 4CO2 Concentration Measurement ･･･････････････ 4Others ･･････････････････････････････････････ 412Accessories
12−2− Accessories −This section lists the accessories for the DS-7100 system.CAUTION? Use only the accessories specified for this device. Otherwise, properfunction cannot be executed.? For quality improvement, specifications are subject to change withoutprior notice.Power Cable :CS-34 (3m)ECG Lead Cable (5-lead) :#3380.0661.13ECG Relay Cable (5-lead) : CI-700D-52ch BP Conversion Cable :CJ-7546NIBP Air Hose :OA-7109B (3.5m)Adult Cuff (Medium) :CUF-7102ASpO2 Interface Cable :DOC-10Recording Paper :OP-124TEThis Operation Manual
12−3− Optional Accessories − The following products are available as optional accessories for the DS-7100 system. Purchasethem as required.CAUTION? Use only the accessories specified for this device. Otherwise, properfunction cannot be executed.? For quality improvement, specifications are subject to change withoutprior notice.ECG, Impedance Respiration MeasurementItem Model Type Q’ty NoteECG Lead Cable 3380.0648.13 13-electrode (hook type)ECG Lead Cable 3380.0661.13 15-electrode (hook type)ECG Lead Cable 500308800 14-electrode (hook type)ECG Relay Cable CI-700D-3 13-electrode (defibrillation-proof)ECG Relay Cable CI-700E-3 13-electrode (electrosurgery-proof) ※ECG Relay Cable CI-700D-4 14-electrode (defibrillation-proof)ECG Relay Cable CI-700E-4 14-electrode (electrosurgery-proof) ※ECG Relay Cable CI-700D-5 15-electrode (defibrillation-proof)ECG Relay Cable CI-700E-5 15-electrode (electrosurgery-proof) ※CAUTION ※ When using the electrosurgery-proof type ECG relay cable, respirationmeasurement can not be performed.Invasive Blood Pressure MeasurementItem Model Type Q’ty NoteInterface Cable (for Gambro) CJ-369 1Interface Cable (for Becton Dichinson) CJ-410 12ch BP Conversion Cable CJ-7546 1Non-Invasive Blood Pressure MeasurementItem Model Type Q’ty NoteAdult Cuff (Large) CUF-7101 1Adult Cuff (Medium)CUF-7102A 1Adult Cuff (Small) CUF-7103 1Pediatric Cuff CUF-7104 1Infant Cuff CUF-7105 1NIBP Air Hose (1.5m) OA-7109A 1NIBP Air Hose (3.5m) OA-7109B 1NIBP Extension Hose (1.5m)OA-7110A 1NIBP Extension Hose (3.5m)OA-7110B 1BP Conversion Socket CUFJ-MO1 1for connection to neonatecuff12Optional Accessories
12−4Temperature MeasurementItem Model Type Q’ty NoteRectal Temperature Probe (for adult) 401J 1Rectal Temperature Probe (for pediatric)402J 1Body Surface Temperature Probe 409J 1Probe Cover 70 14 616 10SpO2 MeasurementItem Model Type Q’ty NoteSpO2 DURASENSOR®DS-100A 1SpO2 OXISENSOR® ⅢD-25 124 per boxSpO2 OXISENSOR® ⅢD-20 124 per boxSpO2 OXISENSOR® ⅢI-20 124 per boxSpO2 OXISENSOR® ⅢN-25 124 per boxSpO2 OXISENSOR® ⅢR-15 124 per boxSpO2 Relay Cable DOC-10 1MAX-FAST MAX-FAST 124 per boxCO2 Concentration MeasurementItem Model Type Q’ty NoteFilterLine H Set (Adult / Pediatric)XS04624 1with Nafion, adapter (25 per box)FilterLine H Set (Infant / Neonate) 006324 1with Nafion, adapter (25 per box)Capno Line H (Adult) 008177 1for nasal, with Nafion (25 per box)Capno Line H (Pediatric) 008178 1for nasal, with Nafion (25 per box)CapnoLine H (Baby / Neonate) 008179 1for nasal, with Nafion (25 per box)CapnoLine H / O2 (Adult) 008180 1for nasal, with Nafion,oxygen delivery (25 per box)CapnoLine H / O2 (Pediatric) 008181 1for nasal, with Nafion,oxygen delivery (25 per box)Calibration Gas Kit (5% CO2)GR08081 1OthersItem Model Type Q’ty NoteGround Cable CE-12 1Battery Pack T4UR18650F-2-4644 1DS-7100 Mount Kit OA-451 1Recording Paper OP-124TE 1Cleaning Cloth OA-57 1

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