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
Contents
Manual 9
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| Document ID | 380411 |
| Application ID | wOVnFJBjOncRtHtUy8lSFQ== |
| Document Description | Manual 9 |
| Short Term Confidential | No |
| Permanent Confidential | No |
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| Document Type | User Manual |
| Display Format | Adobe Acrobat PDF - pdf |
| Filesize | 127.96kB (1599460 bits) |
| Date Submitted | 2003-12-10 00:00:00 |
| Date Available | 2003-12-10 00:00:00 |
| Creation Date | 2003-12-06 12:02:47 |
| Producing Software | Acrobat PDFWriter 4.0 Windows NT |
| Document Lastmod | 2003-12-08 09:45:12 |
| Document Title | DS71v1-1_FA_10_Maintenance_012.PDF |
| Document Creator | Microsoft Word - DS71v1-1_FA_10_Maintenance_012.doc |
| Document Author: | ezashi |
Chapter 10 Maintenance ●Daily Check ･･･････････････････････････････7 ●Periodic Check ････････････････････････････7 Time-Change Components ････････････････････ 7 − Troubleshooting − ･･･････････････････････････ 9 ECG ････････････････････････････････････････ 9 Respiration ･････････････････････････････････ 11 Invasive Blood Pressure･･････････････････････ 11 SpO2 ･･････････････････････････････････････ 12 Non-Invasive Blood Pressure ･････････････････ 13 Temperature････････････････････････････････ 14 CO2 Concentration･･･････････････････････････ 15 Recorder ･･･････････････････････････････････ 16 Telemetry ･･････････････････････････････････ 16 General ････････････････････････････････････ 17 Battery ･････････････････････････････････････ 18 10−1 10 Maintenance After Use / Display Panel ･････ 2 − Handling − Handling After Use ･･･････････････････････････ 2 Handling the Display Panel ････････････････････ 2 Device / Recording Paper ････････ 3 − Storage − Storing the Device ････････････････････････････ 3 Storing the Recording Paper ･･･････････････････ 3 Display Panel and Housing ･･････ 4 − Cleaning − Cleaning the Display Panel ････････････････････ 4 Cleaning the Housing ･････････････････････････ 5 Disinfecting the Blood Pressure Transducers ･････ 5 Disinfecting the Temperature Probes ････････････ 5 Disinfecting the CO2 Filter Line ･････････････････ 5 Cleaning and Disinfecting the SpO2 Transducer･･･ 5 Cleaning and Disinfecting the NIBP Cuff ･････････ 5 Cleaning and Disinfecting the ECG lead Cable ･･･ 5 Handling the Battery Pack･････ 6 − Battery − Handling the Battery ･･････････････････････････ 6 Storing the Battery････････････････････････････ 6 − Maintenance Check − Daily and Periodic Check ･ 7 About the Maintenance Check ･････････････････ 7 − Handling − After Use / Display Panel This section describes precautions for handling the equipment. Handling After Use ?Do not apply excessive force when disconnecting the cables. Always pull on the connector housing 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 any shortage, 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 the display 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 over 99.99%, but there may be an absence (less than 0.01%) or constant lighting of pixels. 10−2 − Storage − Device / Recording Paper This 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 during transportation). ?The following environmental conditions should be observed when storing the device. Storage Temperature : −10∼60?C Storage Humidity : 10∼95% (at 60?C) Storing the Recording Paper The DS-7100 system utilizes heat sensitive recording paper. If placed in a high temperature for long period of time, the print may become indistinct, and unable to read. When storing, follow the precautions 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. 10 Storage 10−3 − Cleaning − Display Panel and Housing This chapter explains about the cleaning of the device and sensors. Cleaning the Display Panel Since this device incorporates a touch screen, finger prints and other stains are likely to appear on the display panel. Follow the procedure below to clean the display panel. 1. Press the Reference Key Lock key for more than 2 seconds. The 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. ? Do not clean the touch panel using strong acid. ? A special coating is applied to the surface of the touch panel. Wipe the CAUTION surface with the soft cleaning cloth provided as optional accessory or with commercially available eyeglass cleaning cloth. 10−4 Cleaning the Housing Clean the housing using tightly squeezed gauze or an absorbent cotton cloth dampened with alcohol or a neutral cleanser. ? Clean the equipment frequently so stains can be removed easily. ? To prevent injury, it is recommended to wear gloves when cleaning the equipment. ? Do not allow liquids or cleaning solution to enter the monitor or connectors. ? Do not use organic solvents, thinner, toluene and benzene to avoid damaging the resin case. ? Do not polish the housing with abrasive or chemical cleaner. C A U T I O N ? When sterilizing the entire room using a spray solution, pay close attention not to have liquids get into the monitor or connectors. ? Use only neutral detergent to clean the housing. Do not use chemical cloth, scrub brush, abrasive, polishing powder, hot water, volatile solvent and chemicals (cleanser, thinner, benzine, benzol, and synthetic 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 10 Disinfect the Temperature Probes according to the manufacturer’s guidelines. Cleaning 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 applying radioactive 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 applying radioactive 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 applying radioactive rays, steam, or ethylene oxide. 10−5 − Battery − Handling the Battery Pack This 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 normal temperature, 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 pack needs 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 Battery To 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 Storage Temperature Storage Humidity Within 30days 30 days∼90 days 90 days∼1year −20∼60?C −20∼45?C −20∼35?C 65? 20% ?Do not store in an environment outside the specified temperature range or excessive high humidity. 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 the battery which degrades the capacity recovery after storage. Therefore, always remove the battery from the monitor when storing for long period of time. Contact our service representative when removing the battery. 10−6 − Maintenance Check − Daily and Periodic Check This section explains the daily check and periodic check items of the device. About the Maintenance Check Periodic inspection must be performed. When reusing the device which was left unused for a while, always check that the device operates properly and safely before use. To ensure safety, reliability, and high performance, a “Daily Check” and “Periodic Inspection” must be performed. We are not liable for any accident arising from lack of maintenance. ? Do not open the housing of this device. C A U T I O N ? Avoid alcohol or other liquids from getting into the equipment. ●Daily Check Perform daily inspection using the “Daily Check List” on the next page. ●Periodic Check Periodic inspection of medical electronic equipment is mandatory to prevent failures and accidents and to ensure safety and reliability. Periodic maintenance may be performed by each medical institution or by a third party by concluding a “Maintenance Contract”. For more details, contact your nearest service representative. 10 Time-Change Components EtCO2 Unit Replacing Period: 7,000 hours (approx. 10 months of continuous use） LCD Unit, Inverter Unit Replacing Period: 50,000 hours or 6 years NIBP Unit Replacing Period: 100,000 times of use or 6 years Short Term Backup Battery Replacing Period: 4 years∼6 years according to the used frequency Long Term Backup Battery Replacing Period: 6 years Battery Pack Replacing Period: 1 year or 300 times of charging / discharging. C A U T I O N The time-change components must be replaced at specified period. 10−7 Maintenance Check To ensure reliability of safety, function, and performance of this device, the time-change components must be replaced periodically. When replacing, contact our service representative. Daily Check List No. Inspected Date Inspected by Location Device Type Serial No. Date of Purchase Item Appearance Installation Functions Details Criteria Judgement Visually check the exterior for scratches, cracks, deformation, and rust. No abnormality should be found. □OK / □NG Check whether the unit is installed on a level surface. The installation area must be level and free from vibration and shock. □OK / □NG The environmental condition (ex. temperature, humidity) of Check whether the unit is the installed place should be installed in a place susceptible to as specified. adverse environment. The unit should not be subjected to splashing water. □OK / □NG The home display appears, and the lamp located at the right side of the display panel lights. □OK / □NG The date and time should be correct. □OK / □NG Turn ON the monitor, and check whether it operates normally. Cables Visually check all cables for any damage. No damage should be found. □OK / □NG Periodic Inspection Check the date of previous periodic inspection. Should be within 1 year. □OK / □NG Should be within 6 months. □OK / □NG CO2 Calibration (DS-7141) Comment 10−8 Check the date of previous calibration date. Previous Date Day Year Month − Troubleshooting − This section explains the troubleshooting for each case. ECG The “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 QRS detection. 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. 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 may result 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 resistance between 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. 10−9 10 Troubleshooting 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. The 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 QRS detection. Also, if large amount of noise is interfering, the noise may be erroneously detected as QRS. It is recommended to change the electrode site and increase the ECG amplitude. 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 electrical contact 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 Solution : Select Used for the pacemaker use. is selected 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 use in 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 will be displayed. Solution 1 : To cease monitoring, press the Alarm Silence key to clear the message and silence the alarm. Solution 2 : To continue monitoring, plug in the ECG relay cable. This will clear the message and silence the alarm. 10−10 Respiration The “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. Red White Black “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 for electrosurgical knife is used. Use the standard ECG relay cable if not using the electrosurgical knife. 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 Pressure The “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. 10−11 10 Troubleshooting Cause 2 : The impedance respiration measurement is ceased. Solution : Turn ON the impedance respiration measurement on the admit / discharge menu or RESP configuration menu. Note : If the pacemaker with the minute ventilation measuring function is used, turn OFF the impedance respiration measurement. Otherwise, both the pacemaker and the monitor will not be able to perform accurate measurement. BP 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 BP monitoring, this message will be displayed. Solution 1 : To cease monitoring, press the Alarm Silence key to clear the message and silence 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. SpO2 The “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 interrupted Situation : “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 not used, avoid placing the sensor in light or unplug the sensor from the connector. 10−12 The 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 will be displayed. Solution 1 : To cease monitoring, press the Alarm Silence key to clear the message and silence the alarm. Solution 2 : To continue monitoring, plug in the SpO2 relay cable. This will clear the message and silence the alarm. Non-Invasive Blood Pressure 10 Troubleshooting The 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 the selected patient type. The “Check NIBP hose” message is displayed. Cause : The applied pressure to the cuff has exceeded the maximum limit. The measurement time has exceeded the maximum limit. Solution : Check if the cuff application is proper, if the cuff size is corresponded to the selected patient type, or if the air hose is not bent. After checking the above, perform the measurement again. If the same message is displayed again, a failure of the equipment can be considered. Cease the measurement, and contact our service representative. 10−13 The “NIBP unit error” message is displayed. Cause : The zero balancing before the measurement has failed, and measurement could not be started. Solution : The body movement or other artifact may cause zero balance failure. During the measurement, 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, 24hrs which best fits the monitoring purpose. Temperature The “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 used with 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, this message will be displayed. Solution 1 : To cease monitoring, press the Alarm Silence key to clear the message and silence the alarm. Solution 2 : To continue monitoring, plug in the temperature sensor. This will clear the message and 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, the numeric data will be displayed as “ｰ ｰ ｰ”. Solution : The calibration will complete in 10 seconds. If the calibration does not complete within 10 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 service representative. 10−14 CO2 Concentration The “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” key on 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. 10 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 be displayed. Solution 1 : To cease monitoring, press the Alarm Silence key to clear the message and silence the alarm. Solution 2 : To continue monitoring, plug in the filter line. This will clear the message and silence the alarm. 10−15 Troubleshooting 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 measurement error. Recorder No 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 is set 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 or alarm 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. Telemetry The “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. 10−16 General Nothing 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 the appropriate brightness. Cause 2 : The monitor is set to the night mode. Solution : Cancel the night mode. 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 the power is turned off. Solution : The battery needs to be replaced. Contact our service representative. 10−17 10 Troubleshooting 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 the power cable until the battery charging is complete. Battery The 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 pack temperature 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 service representative 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 charge complete 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 pack temperature 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, the charging 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. 10−18 Chapter 11 Technical Information − Specification/Performance − ･･････････････････ 2 Specification ･････････････････････････････････ 2 Performance･････････････････････････････････ 3 Default and Backup･･･････････ 5 − Setup Item − Patient Admit / Discharge･･････････････････････ 5 Alarm Setup ･････････････････････････････････ 5 Parameter Setup ･････････････････････････････ 6 Review Function Setup････････････････････････ 7 System Configuration Setup ･･･････････････････ 8 Display Mode Setup ･････････････････････････ 12 Alarm Mode Setup･･･････････････････････････ 13 Pin Assignments･･･ 14 − External Connection − Serial Connector Output Signal････････････････ 14 Status I/O Signal ････････････････････････････ 14 11 Technical Information 11−1 − Specification/Performance − This section states the specification and performance of this equipment. Specification Size 260 (W) ×197 (D) ×264 (H) mm (not including the protrusion) Weight (not including the battery) DS-7141 : 5.3kg DS-7101L : 5.1kg DS-7101LT : 5.2kg Environmental Condition Operating Temperature Operating Humidity Transport / Storage Temperature : Transport / Storage Temperature : Safety General Standard 10∼40?C 30∼85% (without condensation) −10∼60?C 10∼95% (at 60?C) : EN60601-1:1990 (Medical electrical equipment – Part 1: General requirements for safety) Amendment A1 to EN 60601-1:1993 Amendment A2 to EN 60601-1:1995 EMC Standard : IEC 60601-1-2:1993 (Medical electrical equipment−Part 1: General requirements for safety −2.Collateral standard: Electromagnetic compatibility −requirements and tests. IEC 601-1-2:1993 ) Withstand Voltage : Class I, Type CF Power Requirements Voltage Frequency Power Consumption 11−2 AC100∼240V ? 10% DC14V ? 10% 50/60Hz 82VA 60W Performance Display Device Control Waveform Trace Waveform Speed Parameter 8.4 inch TFT Color LCD Touch Screen Type Stationary Trace ECG / SpO2 / BP (6.25mm/s, 12.5mm/s, 25mm/s) RESP / CO2 (6.25mm/s, 12.5mm/s, 25mm/ s) : ECG, RESP, TEMP, SpO2 (Arterial Oxygen Saturation), BP1, BP2, NIBP, CO2 concentration Recording Recording Method Recording Speed Recording Waveform Recording Width Operation Touch Screen : Eight-Wire Resistive Analog Touch Screen ECG Lead Type Frequency Characteristic Input Impedance Max. Input Voltage Polarization Voltage Common Mode Rejection Ratio HR Measurement Range Thermal Array Type 25mm/s Max. 3 waveforms 50mm Wired 3-electrode, 4-electrode, 5-electrode 40Hz / 15Hz 5M? or above ±10mV ±825mV or above : 80 dB or above : Adult 0, 12∼300bpm±3% or ±5bpm Neonate 0, 30∼300bpm±3% or ±5bpm Waveform Size Selection : 1/4, 1/2, 1, 2, 4 Defibrillation Proof : Provided Temperature Method Probe Measurement Range No. of Channel : Thermistor Method : only YSI-400 series : 0∼50?C±0.2?C : 1 channel Specification / Performance Respiration Method Frequency Characteristic Current Measurement Range 11 Impedance Method 1.5Hz (adult, child) / 2.5Hz (neonate) 100μA or lower 0, 4∼150Bpm±5Bpm SpO2 (Arterial Oxygen Saturation) Method : 2 Wavelength Pulse Wave Method Measurement Range : 0%∼100% Resolution : 1% Accuracy : Adult at 70∼100% ±2% at 0∼69% not specified Neonate at 70∼100% ±3% at 0∼69% not specified Measurement Range : 20∼250bpm±3bpm 11−3 Blood Pressure Transducer Sensitivity Measurement Range Frequency Characteristic Accuracy Zero Balance Range Measurement Range Channel 5μV / V / mmHg −50∼300mmHg DC∼6Hz / 8Hz / 12Hz / 40Hz ±2% of full scale or within ±1mmHg within ±150mmHg Adult 20∼300bpm±3% Neonate 30∼300bpm±3% : 2 channels Non-Invasive Blood Pressure Method : Oscillometric Method Measurement Range : 10∼280mmHg Resolution : 1mmHg Accuracy : ±4mmHg Measurement Range : 40∼240bpm±5% CO2 Concentration (DS-7141) Method : Infra-Red Solid-State Method, Microstream Method Measurement Range : 0∼99mmHg 0-20min 0∼38mmHg:±4mmHg 39∼99mmHg:±12% 20min. and up 0∼38mmHg:±2mmHg 39∼99mmHg:±5% RR Measurement Range : 0∼150bpm 0∼40bpm:±1bpm 41∼70bpm:±2bpm 71∼100bpm:±3% 101∼150bpm:±5% Flow Rate : 50±7.5 ml/min System 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 MHz Exact frequency depends on the destination. RF Output Power : -15dBm Standard, 0dBm MAX Channel Spacing : 12.5 kHz Modulation Mode : Digital, Frequency Shift Keying (FSK) 11−4 − Setup Item − Default and Backup This 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 discharging procedure 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 / Discharge Item Patient Name Sex Age Birth Date ID Patient Type Pacemaker Impedance Measurement Filter Mode Bed ID Room/Bed ID Room ID Selection Numeric, Alphabet, Symbol (16 characters) Male, Female 0∼150 years or 0∼999 days Birth Date (Year, Month, Day) Numeric, Alphabet, Symbol (10 characters) Adult, Child, Neonate Used, Not used ON, OFF Monitor, ST Display, ESIS 0∼999 Numeric, Alphabet, Symbol (4 characters) Default Backup Blank △ Undetermined 0 year Blank △ △ △ Blank △ Adult Not used ON Monitor ○ △ △ ○ ○ BED− ○ Alarm Setup ST Selection Suspend, ON ON, OFF 20−300bpm ON, OFF 3−10 sec. ON, OFF ON, OFF ON, OFF ON, OFF 2−8 beats ON, OFF ON, OFF 1.5−5 sec. ON, OFF ON, OFF ON, OFF 1−50 beats / min. ON, OFF 20−300 ON, OFF 20−300 ON, OFF ST1 ±2.0mV / ±20mm ST2 ±2.0mV / ±20mm BP1 (mmHg) ON, OFF 0−300mmHg BP1 (kPa) ON, OFF 0−40.0kPa Default Suspend ON 40−120 ON 5 sec. ON ON ON ON 3 beats OFF OFF 2 sec. OFF OFF OFF, 10 beats ON ON Backup 11 Setup Item Item System Alarm HR AYSTOLE VF VT SLOW_VT RUN COUPLET PAUSE BIGEMINY TRIGEMINY FREQUENT TACHY BRADY ○/△ OFF ON SYS DIA MEAN ON SYS DIA MEAN 80−180 OFF−OFF OFF−OFF 10.0−24.0 OFF−OFF OFF−OFF 11−5 Item Selection BP2（mmHg） ON, OFF 0−300mmHg BP2（kPa） ON, OFF 0−40.0kPa RR APNEA SpO2 ON, OFF ON, OFF ON, OFF 5−150Bpm 5−20sec. 50−100% NIBP (mmHg) ON, OFF 10−300mmHg NIBP (kPa) ON, OFF 1.5−40.0kPa TEMP EtCO2 (mmHg) EtCO2 (kPa) EtCO2 (%) InspCO2 (mmHg) InspCO2 (kPa) InspCO2 (%) ON, OFF ON, OFF ON, OFF ON, OFF ON, OFF ON, OFF ON, OFF 30−50?C 1−100mmHg 0.1−13.3kPa 0.1−13.3% 1−4mmHg 0.1−0.4kPa 0.1−0.4% Default ON SYS OFF−OFF DIA OFF−OFF MEAN OFF−OFF ON SYS OFF−OFF DIA OFF−OFF MEAN OFF−OFF ON 5−30 ON 15sec. ON 90−OFF ON SYS 80−180 DIA OFF−OFF MEAN OFF−OFF ON SYS 10.0−24.0 DIA OFF−OFF MEAN OFF−OFF OFF OFF−OFF ON 30−45mmHg ON 4.0−6.0kPa ON 4.0−6.0% ON 3mmHg ON 0.4kPa ON 0.4% Backup ○/△ 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 the selected alarm mode. NOTE Parameter Setup Item ECG RESP 11−6 Selection Ⅰ, Ⅱ, Ⅲ, aVR, aVL, aVF, Default ECG1 Lead Ⅱ Lead ECG2 Lead V ECG1 ×1 Waveform Size ×1/4, ×1/2, ×1, ×2, ×4 ECG2 ×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 Auto, 10ms, 20ms, 40ms, Pace Pulse Mask Time Auto OFF ECG 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, CO2 Auto Impedance Meas. ON, OFF ON Backup ○/△ △ ○ ○ ○ ○ ○ ○ ○ ○ △ ○ △ ○ ○ SpO2 NIBP Item Waveform Size SpO2 SEC Alarm Ignore NIBP Auto Mode End Tone Quick SYS List PR Quick SYS 1-Min. Auto Mean Selection ×1/4, ×1/2, ×1, ×2, ×4 OFF, 10, 25, 50, 100 ON, OFF ON, OFF ON, OFF ON, OFF ON, OFF 3, 5, 10 min. 10, 20 min. ON, OFF 20, 50, 75, 100, 150, 200, 250, 300mmHg 4, 8, 12, 16, 20, 24, 32, 40kPa 6, 8, 12, 40Hz Default ×1 OFF ON OFF ON ON OFF 10 min. 20 min. OFF 12Hz ○ OFF ○ Filter ON, OFF 20, 50, 75, 100, 150, 200, 250, 300mmHg 4, 8, 12, 16, 20, 24, 32, 40kPa 6, 8, 12, 40Hz 12Hz ○ Mean ON, OFF OFF ○ Meas. Unit mmHg, kPa, % mmHg EtCO2 Average 10, 20, 30 sec., OFF 50, 100mmHg 4, 8, 10kPa 4, 8, 10% 10 sec. 50mmHg 4kPa 4% Scale BP1 Filter Mean Scale BP2 CO2 Scale Backup △ ○ ○ △ ○ ○ ○ ○ ○ ○ 150mmHg ○/△ 20kPa 50mmHg ○/△ 8kPa ○ ○／△ ○／△ 11 Review Function Setup Parameter Duration Graphic Trend Scale Selection HR, PR, VPC, ST1/ST2, RR, APNEA, SpO2, BP, NIBP, TEMP, EtCO2 / InspCO2, EVENT1, EVENT2 1, 2, 4, 8, 12, 24 hours HR : 100, 200, 300bpm ST : ±0.2, ±0.5, ±1.0, ±2.0mV ±2, ±5, ±10, ±20mm VPC : 20, 50, 100 beats BP1 : 20, 50, 100, 150, 200, 300mmHg 4, 8, 16, 20, 24, 40kPa BP2 : 20, 50, 100, 150, 200, 300mmHg 4, 8, 16, 20, 24, 40kPa NIBP : 100, 150, 200, 300mmHg 16, 20, 24, 40kPa TEMP : 20-45, 30-40?C SpO2 : 0-100, 50-100, 80-100% RR : 100, 200, 300bpm APNEA : 15, 30 sec. CO2 : 50, 100mmHg 4, 8, 10kPa 4, 8, 10% Default Backup HR ○ 4 hours ○ HR ST : 100bpm : ±0.5mV ±5mm VPC : 20 beats BP1 : 150mmHg 20kPa BP2 : 50mmHg 8kPa NIBP : 150mmHg 20kPa TEMP : 30-40?C SpO2 : 80-100% RR : 50bpm APNEA : 15 sec. CO2 : 50mmHg 4.0kPa 4.0% ○ 11−7 Setup Item Item Item Tabular Trend OCRG Selection Backup Duration 1, 5, 10, 15, 30, 60 min. 60 min. ○ Display Time 4, 8 min. 8 min. ○ Waveform Impedance Resp., CO2 Impedance Resp. ○ Parameter ECG1, ECG2 HR/PR/BPR : ST RR APNEA SpO2 BP1 BP2 NIBP TEMP CO2 ASYSTOLE : VF VT SLOW_VT : RUN COUPLET : PAUSE BIGEMINY : TRIGEMINY : FREQUENT : TACHY BRADY 120ms ○ Meas. Point ECG1, ECG2, BP, SpO2, RESP, CO2 HR/PR/BPR : ON, OFF ST : ON, OFF RR : ON, OFF APNEA : ON, OFF SpO2 : ON, OFF BP1 : ON, OFF BP2 : ON, OFF NIBP : ON, OFF TEMP : ON, OFF CO2 : ON, OFF ASYSTOLE : ON, OFF VF : ON, OFF VT : ON, OFF SLOW_VT : ON, OFF RUN : ON, OFF COUPLET : ON, OFF PAUSE : ON, OFF BIGEMINY : ON, OFF TRIGEMINY : ON, OFF FREQUENT : ON, OFF TACHY : ON, OFF BRADY : ON, OFF 0∼560ms Ref. Point 0∼−240ms −80ms Alarm Factor Recall Arrhythmia Factor ST Meas. Default NOTE ON ON ON ON ON ON ON ON ON ON ON ON ON ON ON ON ON ON ON ON ON ON ○ ○ ○ ○ ? The graphic trend data, tabular trend data will be retained even after the power is turned OFF. ? The ST data, OCRG data, recall data will be retained until 5 minutes after the power is turned OFF. System Configuration Setup ●Volume Setup Volume 11−8 Item Pulse Selection 16 levels Default Level 8 from left Backup ○ Key 16 levels Level 10 from left ○ Alarm 16 levels Level 10 from left ○ Other Bed 16 levels Level 10 from left ○ Others 16 levels Level 8 from left ○ ●Display Configuration Item No. of waveforms No. of numeric data Displayed Display waveform Configuration Displayed numeric data Enlarged Display Short Trend NOTE Selection 0∼6 waveforms Default 3 waveforms 0∼7 numeric data 4 numeric data ECG1, ECG2, BP, SpO2 RESP, CO2 HR, BP, NIBP, SpO2 RESP, RR, CO2, VPC/ST ON, OFF ON, OFF, Overlap ECG1, SpO2, RESP Backup ○／△ HR, NIBP, SpO2, RR OFF OFF By selecting ON for backup at discharge, the setup item will be stored even after discharge. Selecting OFF will initialize the display configuration to the initial setting of the selected display mode. ●System Configuration Menu Item ECG1, BP, RESP ○ Rec. Duration Selection ECG1, ECG2, BP, SpO2 RESP, CO2 24 sec., Continuous 24 sec. ○ Delay Time None, 8sec., 16 sec. 8 sec. ○ ON, OFF, Center ECG1, ECG2, BP, SpO2 Wave Select RESP, CO2, Alarm Factor Rec. Duration 12, 24 sec. HR (HR / PR / BPR) Alarm Factor Numeric Data, Arrhythmia ASYSTOLE, VF, VT, SLOW_VT, RUN, COUPLET, PAUSE, Arrhythmia Record BIGEMINY, TRIGEMINY, FREQUENT, TACHY, BRADY Periodic Record ON, OFF, Center ECG1, ECG2, BP, SpO2, Wave Select RESP, CO2 Rec. Duration 6, 12, 24 sec. OFF ○ ECG1, Alarm Factor ○ 12 sec. HR (HR / PR / BPR) Arrhythmia ○ Periodic Interval Wave Select Manual Recording Alarm Record Alarm Recording Rec. Operation Sweep Speed Night Mode Backup ○ 11 ASYSTOLE, VF, VT, SLOW_VT, RUN, TACHY, BRADY ○ OFF ○ ECG1, BP, RESP ○ 12 sec. ○ 60 min. ○ Paper Feed to Top ON, OFF OFF ○ Paper Feed to End ON, OFF ON ○ 5, 10, 15, 30, 60 min. QRS Classification ON, OFF ON ○ ECG, BP, SpO2 25, 12.5, 6.25mm/s 25mm/s ○ RESP, CO2 25, 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 Time Disp. Only, Slightly Dark, Dark No change, Quiet, Very quiet, Silence ON, OFF 7:00 ○ Dark ○ Very quiet ○ OFF ○ Display Volume Alarm Pole Setup Item Periodic Recording Default 11−9 Item Selection Default Backup ECG Green ○ ST Green ○ VPC White ○ PACE White ○ BP1 Red ○ Cyan ○ Cyan ○ SpO2 Yellow ○ TEMP Orange ○ RESP White ○ CO2 ST2 (Trend) Alarm Suspend 1, 3, 5 min. Cyan Orange 3 min. Alarm Silence 1, 3, 5 min. 3 min. Item AC filter Selection 50, 60Hz Default According to Dip_SW Date 07/19, 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 mm, mV 0801~0879, 0900~0979, 1000~1079, 1100~1179, 1200~1279, 1300~1379 00∼63 ?C mV ○ 1100 ○ 00 ○ BP2 Color NIBP Alarm Setup 32 colors ○ Fixed ○ ○ ●Hospital Setup Unit ST Channel Telemeter Group Jul.19, 19.Jul Backup ○ ○ ●Ward Setup Item Trend Clip Selection 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 All Key (excluding system config.) All Key (excluding pre-set) All Key (excluding ward setup) Waveform ○ All Key ○ All Key ○ All Key ○ Menu Key Mask System Config. Pre-Set Menu 11−10 Default Backup ○ Item User Key Selection Alarm Pole Alarm Level Alarm Pole Selection Rec. START/STOP, Alarm Silence, Alarm, Key Lock, NIBP List, Graphic Trend, Tabular Trend, Recall, OCRG, Freeze, NIBP Auto Mode, Size/Lead, HR Source, BP Zero, Admit/Discharge, Night Mode, Display Config., Record, Tone/Volume, Other Bed, ST Display, Cease, Enlarged Display ON, OFF Level１, Level 1 and 2, Level 1, 2, and 3 Default Backup Alarm Silence, Rec. START/STOP, Size/Lead, Admit/Discharge (from left of display) ○ ON ○ Level１ ○ Level 1：Pattern 1 Pattern Setup Pattern 1∼10 Level 2：Pattern 10 ○ Level 3：Pattern 4 NIBP Data Erase Time 10, 30, 60min, 24hourr ○ 60min ●Monitor Setup Selection 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 Positive Logic, Negative Logic OFF, APNEA, Level 1, Level 1 and 2, Level 1, 2 and 3 Positive Logic, Negative Logic, Pulse HR ○ Positive Logic ○ Level 1 ○ Positive Logic ○ Sync. Sygnal Output Status Output Setup Alarm Output Default Backup ○ 11 Setup Item Item Battery Operation 11−11 Display Mode Setup Item Mode Selection Mode 1 Mode 2 Mode 3 Mode 4 Mode 5 11−12 Default Backup ○ 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 ○ Comment 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 ○ Comment 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 ○ Comment 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 ○ Comment CONFIG. 4 ○ No. of Waveforms 6 Waveforms ○ No. of Numeric Data 7 Numeric Data ○ Displayed Waveforms ○ Enlarged Display ECG1, BP1/2 (overlap),, SpO2, CO2 HR, BP1, BP2, NIBP, SpO2, TEMP/ RR, CO2 OFF Short Trend OFF ○ Comment CONFIG. 5 ○ Displayed Numeric Data ○ ○ Alarm Mode Setup Item Alarm Mode HR AYSTOLE VF VT SLOW_VT RUN COUPLET PAUSE BIGEMINY TRIGEMINY FREQUENT TACHY BRADY ST BP1 (mmHg) BP1 (kPa) Alarm Mode 1∼5 BP2 (mmHg) BP2 (kPa) NIBP (mmHg) NIBP (%) EtCO2 (mmHg) EtCO2 (kPa) EtCO2 (%) InspCO2 (mmHg) InspCO2 (kPa) InspCO2 (%) Backup ○ ○ ○ ○ ○ ○ ○ ○ ○ ○ ○ ○ ○ ○ ○ ○ ○ ○ 11 ○ Setup Item APNEA SpO2 Default ON 40−120 ON 5 sec. ON ON ON ON 3 beats OFF OFF 2 sec. OFF OFF OFF 10 beats ON ON OFF ON SYS 80−180 DIA OFF−OFF MEAN OFF−OFF ON SYS 10.0−24.0 DIA OFF−OFF MEAN OFF−OFF OFF SYS OFF−OFF DIA OFF−OFF MEAN OFF−OFF OFF SYS OFF−OFF DIA OFF−OFF MEAN OFF−OFF ON 15 sec. ON 90−OFF ON SYS 80−180 DIA OFF−OFF MEAN OFF−OFF ON SYS 10.0−24.0 DIA OFF−OFF MEAN OFF−OFF ON 30‐45 ON 4.0‐6.0 ON 4.0‐6.0 ON 3 ON 0.4 ON 0.4 ○ ○ ○ ○ ○ ○ ○ ○ ○ ○ 11−13 − External Connection − Pin Assignments This section explains the connector pin assignments. Serial Connector Output Signal No. Signal Type RESET RSV TxD SG RxD +5V Description Port Reset Reserved Serial Transmit Data Output Signal GND Serial Receive Data Input +5V Signal Level TTL Hi Level Reset ―― RS232C RSV Reserved ―― NC No Connection ―― Description QRS SYNC Output Alarm Output ＋ (Isolation） Signal Level Logic TTL RS232C ＋5V power supply (150mA) Status I/O Signal No. Signal Type QRS SYNC ALM_OUT+ RSV Reserved ―― RSV Reserved ―― RSV Reserved ―― RSV Reserved ―― ＋5V +5V ＋5V power supply (150mA) ALM_OUT- GND Alarm Output − (Isolation) Power Supply Digital GND Photo MOS Relay Contact Photo MOS Relay Contact ―― ※ As the serial connector and status I/O connector uses the same isolation power supply, the total power supply capacity for ＋5V should be up to 200mA. 11−14 Chapter 12 Accessories − Accessories − ･･･････････････････････････ 2 − Optional Accessories − ･･････････････････････ 3 ECG, Impedance Respiration Measurement･･････ 3 Invasive Blood Pressure Measurement ･･････････ 3 Non-Invasive Blood Pressure Measurement ･･････ 3 Temperature Measurement ････････････････････ 4 SpO2 Measurement ･･･････････････････････････ 4 CO2 Concentration Measurement ･･･････････････ 4 Others ･･････････････････････････････････････ 4 12 Accessories 12−1 − Accessories − This section lists the accessories for the DS-7100 system. ? Use only the accessories specified for this device. Otherwise, proper function cannot be executed. C A U T I O N ? For quality improvement, specifications are subject to change without prior notice. Power Cable : CS-34 (3m) ECG Lead Cable (5-lead) : #3380.0661.13 ECG Relay Cable (5-lead) : CI-700D-5 2ch BP Conversion Cable : CJ-7546 NIBP Air Hose : OA-7109B (3.5m) Adult Cuff (Medium) : CUF-7102A SpO2 Interface Cable : DOC-10 Recording Paper : OP-124TE This Operation Manual 12−2 − Optional Accessories − The following products are available as optional accessories for the DS-7100 system. Purchase them as required. ? Use only the accessories specified for this device. Otherwise, proper function cannot be executed. C A U T I O N ? For quality improvement, specifications are subject to change without prior notice. ECG, Impedance Respiration Measurement Item ECG Lead Cable ECG Lead Cable ECG Lead Cable ECG Relay Cable Model Type 3380.0648.13 3380.0661.13 500308800 CI-700D-3 ECG Relay Cable CI-700E-3 3-electrode (electrosurgery-proof) ※ ECG Relay Cable CI-700D-4 4-electrode (defibrillation-proof) ECG Relay Cable CI-700E-4 4-electrode (electrosurgery-proof) ※ ECG Relay Cable CI-700D-5 5-electrode (defibrillation-proof) ECG Relay Cable CI-700E-5 5-electrode (electrosurgery-proof) ※ CAUTION Q’ty Note 3-electrode (hook type) 5-electrode (hook type) 4-electrode (hook type) 3-electrode (defibrillation-proof) ※ When using the electrosurgery-proof type ECG relay cable, respiration measurement can not be performed. Invasive Blood Pressure Measurement Model Type CJ-369 CJ-410 CJ-7546 Q’ty Note Q’ty Note 12 Optional Accessories Item Interface Cable (for Gambro) Interface Cable (for Becton Dichinson) 2ch BP Conversion Cable Non-Invasive Blood Pressure Measurement Item Adult Cuff (Large) Adult Cuff (Medium) Adult Cuff (Small) Pediatric Cuff Infant Cuff NIBP Air Hose (1.5m) NIBP Air Hose (3.5m) NIBP Extension Hose (1.5m) NIBP Extension Hose (3.5m) Model Type CUF-7101 CUF-7102A CUF-7103 CUF-7104 CUF-7105 OA-7109A OA-7109B OA-7110A OA-7110B BP Conversion Socket CUFJ-MO1 for connection to neonate cuff 12−3 Temperature Measurement Item Rectal Temperature Probe (for adult) Rectal Temperature Probe (for pediatric) Body Surface Temperature Probe Probe Cover Model Type 401J 402J 409J 70 14 616 Q’ty 10 Note Q’ty Note SpO2 Measurement Item SpO2 DURASENSOR® Model Type DS-100A SpO2 OXISENSOR® Ⅲ D-25 24 per box SpO2 OXISENSOR Ⅲ D-20 24 per box SpO2 OXISENSOR Ⅲ I-20 24 per box SpO2 OXISENSOR Ⅲ N-25 24 per box SpO2 OXISENSOR Ⅲ R-15 24 per box SpO2 Relay Cable MAX-FAST DOC-10 MAX-FAST 24 per box ® ® ® ® CO2 Concentration Measurement Item Model Type Q’ty FilterLine H Set (Adult / Pediatric) XS04624 FilterLine H Set (Infant / Neonate) 006324 Capno Line H (Adult) 008177 Capno Line H (Pediatric) 008178 CapnoLine H (Baby / Neonate) 008179 CapnoLine H / O2 (Adult) 008180 CapnoLine H / O2 (Pediatric) 008181 Calibration Gas Kit (5% CO2) GR08081 Note with Nafion, adapter (25 per box) with Nafion, adapter (25 per box) for nasal, with Nafion (25 per box) for nasal, with Nafion (25 per box) for nasal, with Nafion (25 per box) for nasal, with Nafion, oxygen delivery (25 per box) for nasal, with Nafion, oxygen delivery (25 per box) Others Item Ground Cable Battery Pack DS-7100 Mount Kit Recording Paper Cleaning Cloth 12−4 Model Type CE-12 T4UR18650F-2-4644 OA-451 OP-124TE OA-57 Q’ty Note
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