Sejoy DBP-6673B User manual

Safety NoticeModel DBP-6673B2Owner's ManualECG Blood Pressure Monitor Document No.:JDBP-7304- 154Contact InformationThe lay operator or lay responsible or ganization should contact the manufacturer or the representative of manufacturer.-for assistance,if needed,in setting up,using or maintaining the product,or-to report unexpected operation or events. Manufactured by JOYTECH Healthcare Co.,Ltd.Email: [e-mail]: [phone]Fax: [phone]No.365, Wuzhou Road,Yuhang Economic Development Zone,Hangzhou City,311100 Zhejiang,ChinaVersion：ZDate of Issue：2020.06Thank you for purchasing the DBP-6673B ECG Blood Pressure Monitor.Intended UseECG Blood Pressure Monitor is intended for non-invasive measuring an adults and adolecents over 12 years of ageindividual's systolic, diastolic blood pressure and heart rate using the oscillometric method. By switching to ECG measurement, ECG blood pressure monitor intend to display average heart rate and real-time heart rate, also can view real-time and historical ECG waveforms in App.ContraindicationsProduct is not intended for people under 12 years of age or individuals who cannot express their intentions.Precautions to Ensure Safe, Reliable Operation1. Do not drop the unit. Protect it from sudden jars or shocks.2. Do not insert foreign objects into any openings.3. Do not attempt to disassemble the unit.4. Do not crush the pressure cuff.5. If the unit has been stored at temperatures below 0 ℃, leave it in a warm place for about 15 minutes before using it. Otherwise, the cuff may not inflate properly.6. If the unit has been stored at temperatures above 40 ℃, leave it in a cool place for about 15 minutes before using it. Otherwise, the cuff may not inflate properly.7. Do not store the unit in direct sunlight, high humidity or dust.8. To avoid any possibility of accidental strangulation, keep this unit away from children and do not drape tubing around your neck.9. Ensure that children do not use the instrument unsupervised; some parts are small enough to be swallowed.10. Some may get a skin irritation from the cuff taking frequent readings over the course of the day, but this irritation typically goes away on its own after the monitor is removed. 11.Longest expected contact time between patient and cuff：Each blood pressure measurement should not exceed 3 minutes.Arm TypeArm TypeContentsSafety Notice .............................................................................................02Unit IllustrationImportant Testing Guidelines Quick Start .............................................................................................................10Memory Check and Last 3 Test AverageMemory CheckBlood Pressure InformationBlood Pressure Q&AMaintenanceSpecificationsElectromagnetic Compatibility Information .......................................................................................07 ...................................................................09Battery Installation ............................................................................12System Unit Operation .............................................................................................13 System Settings .............................................................................................13BP Unit Operation ...................................................................................................15 Applying the Arm Cuff ..............................................................................15 Blood pressure test .....................................................................................16 Power Off ......................................................................................................18 BP ......................................................19 BP Memory Deletion ........................................................................................19 Low Battery Indicator ...................................................................................20 Static Pressure Measurement ..........................................................................21ECG Unit Operation ...............................................................................................22 ........................................................................22 ........................................................................................................22 ECG .......................................................................................25 ECG Memory Deletion ...................................................................................25 Use Of App ....................................................................................................26Wireless Unit Operation ..........................................................................................27 Bluetooth requirement and connection .........................................................27 Wifi requirement and connection ..............................................................28Troubleshooting ......................................................................................................30 ....................................................................................31 ...............................................................................................34 ...........................................................................................................35 ..........................................................................................................36Warranty ................................................................................................................38 ............................................................39Gestures of ECG measurementsECG Test1

5Safety Notice3Important Instructions Before Use1. Do not confuse self-monitoring with self-diagnosis. Blood pressure measurements should only be interpreted by a health professional who is familiar with your medical history.2. Contact your physician if test results regularly indicate abnormal readings.3. If you are taking medication, consult with your physician to determine the most appropriate time to measure your blood pressure. NEVER change a prescribed medication without first consulting with your physician.4. Individuals with serious circulation problems may experience discomfort. Consult your physician prior to use.5. For persons with irregular or unstable circulation resulting from diabetes, liver disease, arteriosclerosis or other medical conditions, there may be variations in blood pressure values measured at the wrist versus at the upper arm. Monitoring the trends in your blood pressure taken at either the arm or the wrist is nevertheless useful and important.6. People suffering from vascular constriction, liver disorders or diabetes, people with cardiac pacemakers or a weak pulse, and women who are pregnant should consult their physician before measuring their blood pressure themselves. Different values may be obtained due to their condition.7. People suffering from arrhythmias such as atrial or ventricular premature beats or atrial fibrillation only use this ECG Blood Pressure Monitor in consultation with your doctor. In certain cases oscillometric measurement method can produce incorrect readings.8. Too frequent measurements can cause injury to the patient due to blood flow interference.9. The cuff should not be applied over a wound as this can cause further injury.10. DO NOT attach the cuff to a limb being used for IV infusions or any other intravascular access, therapy or an arterio-venous (A-V) shunt. The cuff inflation can temporarily block blood flow, potentially causing harm to the patient.11. The cuff should not be placed on the arm on the side of a mastectomy. In the case of a double mastectomy use the side of the least dominant arm.12. Pressurization of the cuff can temporarily cause loss of function of simultaneously used monitoring equipment on the same limb.13. A compressed or kinked connection hose may cause continuous cuff pressure resulting in blood flow interference and potentially harmful injury to the patient.14. Check that operation of the unit does not result in prolonged impairment of the circulation of the patient.15. Product is designed for its intended use only. Do not misuse in any way.16. Product is not intended for infants or individuals who cannot express their intentions.17. Prolonged over-inflation of the bladder may cause ecchymoma of your arm.18. Do not disassemble the unit or arm cuff. Do not attempt to repair.19. Use only the approved arm cuff for this unit. Use of other arm cuffs may result in incorrect measurement results.20. The system might produce incorrect readings if stored or used outside the manufacturer's specified temperature and humidity ranges. Make sure to store the ECG Blood Pressure Monitor ,children, pets and pests are outside of accessible range. 21. Do not use the device near strong electrical or electromagnetic fields generated by cell phones or other devices, they may cause incorrect readings and interference or become interference source to the device. 22. Do not mix new and old batteries simultaneously.Safety Notice
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Safety Notice
Reproducibility of theECG DETERMINATION
Refer 201.12.1.101.3.1 IEC 60601-2-47
Limits of the error ofthe manometerReproducibility of theBLOOD PRESSUREDETERMINATIONRefer 202.12.1.102 IEC 80601-2-30 Refer 201.12.1.107 IEC 80601-2-30 Electrosurgeryinterference recoveryRefer 202.6.2.101 IEC 80601-2-30 Federla Commulcation Commission (FCC) Interference Statement1.This device complies with part 15 of the FCC Rules. Operation is subject to the condition that this device does not cause harmful interference.2.This device is verified to comply with part 15 of the FCC Rules for use with cable television service.3.This device complies with part 15 of the FCC Rules. Operation is subject to the following two conditions:(1) This device may not cause harmful interference, and(2) this device must accept any interference received, including interference that may cause undesired operation. Please note that changes or modifications not expressly approved by the party responsible for compliance could void the user's authority to operate the equipment.4.This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:—Reorient or relocate the receiving antenna.—Increase the separation between the equipment and receiver.—Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.—Consult the dealer or an experienced radio/TV technician for help.5.This equipment complies with radio frequency exposure limits set forth by the FCC for an uncontrolled environment.6. This device must not be co-located or operating in conjunction with any other antenna ortransmitter.7.Essential performance:Discard the used product to the recycling collection point according to local regulations
The Bluetooth® Smart word mark and logos are registered trademarks owned by Bluetooth SIG, Inc. and any use of such marks by JOYTECH Healthcare Co.,Ltd.
Safety Notice423. Replace batteries when Low Battery Indicator“ ”appears on screen. Replace both batteries at the same time.24. Do not mix battery types. Long-life alkaline batteries are recommended.25. Remove batteries from device when not in operation for more than 3 months.26. Dispose batteries properly; observe local laws and regulations.27. Advising operator that Instruction manual/ Booklet must be consulted. 28. Do not use the device during transport vehicles for influencing measurement accuracy, such as patient transport in an ambulance or helicopter.29. Contains small parts that may cause a chocking hazard if swallowed by infants.30. Please align the polarities of each battery with the +ve and -ve signs imprinted on the battery housing when you replace the batteries .31. Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally.32. Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the unit, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.33. Do not touch the electrode of this product to other conductors (including grounding).34. During ECG measurement, if your skin or hands are too dry, please moisten it with a damp towel. Implement measurement.35.If the skin or finger is damaged and bleeding during electrocardiogram measurement, please replace the finger for measurement36. During ECG measurement, please do not use the product in reverse directions with your left and right hands.37.The performance of automatic ecg sphygmomanometer may be affected by extreme temperature, humidity and altitude.WARNING SIGNS AND SYMBOLS USED Keep off SunlightType BF EquipmentInstructions For Use MUST be ConsultedKeep Dry

Important Testing Guidelines 9101. 2. Sit in a calm environment for at least 5 minutes prior to testing. 3. Do not stand while testing. Sit in a relaxed position while keeping your arm level with your heart.4. Avoid speaking or moving body parts while testing.5. While testing, avoid strong electromagnetic interference such as microwave ovens and cell phones.6. Wait 3 minutes or longer before re-testing.7. Try to measure your blood pressure at the same time each day for consistency.8. Test comparisons should only be made when monitor is used on the same arm, in the same position, and at the same time of day.9. This ECG Blood Pressure Monitor is not recommended for people with severe arrhythmia.10. Do not use this ECG Blood Pressure Monitor if the device is damaged.Any blood pressure recording can be affected by the following factors:1. The position of the subject, his or her physiologic condition;2. The performance and accuracy of the device;3. Cuff size: too small cuff (bladder) will produce a higher blood pressure value than usual, too big cuff (bladder) will produce a lower blood pressure value;4. Measuring position does not keep level with your heart;5. Speaking or moving body parts while testing;6. Not relaxing for about 5 minutes before taking the measurement. Avoid eating, exercising, and bathing for 30 minutes prior to testing. Quick Start1. Install batteries2. Insert cuff air plug into the behind side of monitor unit. (See Figure B). (See Figure A )3. Remove thick clothing from the arm area.4. Rest for several minutes prior to testing. Sit down in a quietplace comfortably , back and arm support on a desk or table ,withyour legs uncrossed ,your arm resting on a firm and your feet flat on the floor. (See Figure C )5. Apply cuff to your left arm and middle of the cuff at the level of your heart. Bottom of cuff should be placed approximately 1-2cm (1/2'') above elbow joint. (See Figures D&E)
1-2cm ''(0.4-0.8)
Figure CFigure AFigure DFigure E6. Press " START/STOP " Button to start testing. Figure BUnit Illustration7Arm CuffMedium size cuff (fits arm circumference: 22.0 cm -36.0 cm). If air is leaking from the arm cuff, replace the arm cuff with a new one. It is generally recommended to have the cuff replaced timely to ensure correct functioning and accuracy. Please consult your local authorized Sejoy distributor or dealer. Monitor Unit MEM " " ButtonSTART/STOP " " ButtonLCDSET " " Button
1~2cm (0. 4~0.8 inch)
22~36cm（8.6~14.2 inch)
Mai n Art ery
LEFT ARM
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Arm Cuff Air TubeAir PlugUnit Illustration83.Arm Cuff2.Owner's Manual 1.Monitor UnitOwner's ManualArm-type Fully AutomaticECG Blood Pressure MonitorModel DBP-6673BArm Type4.Storage Bag
1~2cm (0.4~ 0.8 inch)
22~36cm（8.6 ~14.2 i nch)
Main Ar tery
LEFT ARM
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DisplayTime/DateOKAFSlowFast Group1 Group2SystolicBloodPressureDiastolicBloodPressure
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Irregular Heartbeat IndicatorBluetooth IndicatorBlood Pressure Indicator Heart Rate Indicator WHO Blood Pressure Classification IndicatorLast 3 Tests Average BatteryIndicatorArm Shake IndicatorCuff Loose Indicator
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BP Quick Start

14System Unit Operation 6. Saved Settings4. Voice SettingPress "SET" button to enter voice setting mode. Set voice format ON or OFF bypressing the "MEM" button.5. Volume SettingPress "SET" button to enter volume setting mode. Set the voice volume by adjustingthe "MEM" button . There are six volume levels. While in any setting mode, press " START/STOP " button to turn the unit off. All information will be saved. Note: If unit is left on and not in use for 3 minutes, it will automatically save all information and shut off.13System Unit Operation System Settings1. Select Memory Group While in the System Setting mode, you may accumulate test results into 2 different groups. This allows multiple users to save individual test results (up to 60 memories per group.) Press " MEM " button to choose a group setting. Test results will automatically store in each selected group.With power off, press "SET" button to activate System Settings. The Memory Group icon flashes.2. Time/Date setting Press“SET” button again to set the Time/Date mode. Set the year first by adjusting the “MEM” button. Press“SET” button again to confirm current month. Continue setting the dat, hour and minute in the same way. Every time the “SET” button is pressed, it will lock in your selection and continue in succession ( month,day,hour, minute,12/24 hours)3. Time Format setting Press “ SET ”button again to set the time fornat setting mode.Set the time format by adjusting the“MEM” button. EU means European Time US means U.S Time
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11Quick Start1. Install batteries. (See Figure A )2. Before measuring the device, rinse your hands with water or wipe them with a wet towel to keep the contact points moist.(See Figure B )Figure CFigure B4. Hold down the to bind the measurement device to the smart device, press to power off the device, and then press to start the test. " MEM"" START/STOP "" START/STOP "
ECG Quick Start
5.Press the palm of both hands on the electrode with moderate strength, not too tight (note: keep the palm of both hands on the electrode, sit still, relax, do not move or talk during the measurement)(See Figure D)3. Rest for several minutes prior to testing. Sit down in a quiet place, preferably at a desk or table, with your arm resting on a firm surface and your feet flat on the floor. (See Figure C )
ECG
LRFigure DFigure A12Battery Installation Battery Installation Slide battery cover off as indicated by arrow. Install 3 new AAA alkaline batteries according to polarity. Close battery cover.Battery level indicatorWhen the device is turned on, the icon of the current battery quantity is displayed. When the battery quantity is too low, the device indicates low battery quantity and the screen displays " ".When the battery is fully charged, the screen displays " ".

2. Testing for Blood After cuff inflation, air slowly rise as indicated by the corresponding cuff pressure value. A flashing " " will appear simultaneously on screen signaling heart beat detection. willNote: Keep relaxed during testing. Avoid speaking or moving body parts.3. Result Display The screen will display measurements for systolic and diastolic blood pressure with voice broadcast. An indicator representing the current measurement will appear next to the corresponding WHO Classification.Note: Refer to Page 32~33 for detail WHO Blood Pressure Classification Information.1716BP Unit Operation BP Unit Operation Blood pressure test1. Power On A voice tone will indicate when unit is ready for testing. Press and hold "START/STOP" button to turn the unit on. button to turn the unit on. The LCD screen will display for one second. Press and hold “START/STOP”Note: Make sure the switch is in BP mode before the measurement beginsUnit will not function if residual air from previous testing is present in cuff. The LCD will flash " " until pressure is stabilized.
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BP Unit Operation Irregular Heartbeat IndicatorIf the monitor detects an irregular heart rhythm two or more times during the measuring process, the Irregular Heartbeat Symbol " "appears on screen along with measurement results. Irregular heartbeat rhythm is defined as rhythm that is either 25% slower or faster than the average rhythm detected while measuring systolic blood pressure and diastolic blood pressure. Consult your physician if the Irregular Heartbeat Symbol " " frequently appears with your test results.Power Off turn off the power itself about 3 minutes no operation in any mode.The " START/STOP " button can be pressed to turn off the unit in any mode. The unit can Safety Precaution: If pressure in arm cuff becomes too extreme while testing, press the " START/STOP " button to turn power off. The cuff pressure will rapidly dissipate once the unit is off.
IHBIHB
If there is arm movement during the measurement, " " may be shown. Indicates thatit may lead to abnormal accurate measurement results.The measurement result shows " ". When viewing this memory, the memory result shows" ". Arm Shake IndicatorWhen starting the measurement, " "will be displayed when the cuff is properly wound.When the cuff is too loose, " "will be displayed. At this time, please wear the cuff correctlyand start measuring again. Cuff loose Indicator
OK
1815BP Unit Operation Applying the Arm Cuff1. Firmly insert air plug into opening located on behind side of monitor unit. 2. With sticky nylon section facing outward, insert end of cuff underneath metal ring of cuff 3. Fasten cuff about above the elbow joint. For best results apply cuff to bare arm and keep level with heart while testing.1-2cm (0.4-0.8'') .Note: Do not insert air plug into opening located on right side of monitor unit. This opening is designed for an optional power supply only.
1-2cm ''(0.4-0.8)

In the power down state, press and hold the " START/STOP" button, and theninstall the batteries. Until the LCD screen is full, release the " START/STOP" button. When the LCD screen displays the double zero, the ECG blood pressure meter is in static state. Static Pressure Measurement2120BP Unit Operation BP Unit Operation BP Memory Deletion Memory for a selected group may be deleted while in Memory Check mode. Press and hold the " SET " button for approximately 3 seconds to delete all memory records from the selected groupwith voice broadcast "Memory Clear" and then transfer into testing mode. Press the "START/STOP " button to turn the unit off. Note: Memory cannot be recovered once it has been deleted.Low Battery IndicatorThe unit will broadcast "Low Battery" when battery life is depleting and unable to inflate cuff for testing. The " " appears simultaneously for approximately 5 seconds prior to shutting off. No memory loss will occur throughout this process.Replace batteries at this time.Note: Only Service personnel permitted to access to this mode, the mode unavailable in normal use.
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11ECG Unit Operation 22Note:Before starting the measurement, make sure the switch is in ECG mode.Do not let your fingers go until the test results appear.Note:Wait for the signal to stabilize,and the 5S countdown starts to count.Gestures of ECG measurements1. Power On Press and hold “START/STOP” button to turn the unit on. The LCD screen will display for one second.ECG TestECGIHBOKAFSlowFast
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LR19BP Unit Operation Last 3 Tests AverageYou may check past test results by using the "MEM" button. The most recent test result and oldest test result in memory can be viewed by pressingand holding the "MEM" button. Upon activating test results. you can press the "MEM" button to scroll through all test results stored in memory. With power off，press the "MEM" button to activate screen display. After the unit performs a self-diagnosis ,the screen will display the average test results from the last 3 readings of the last group used. The "AVG" symbol will appear along with the corresponding WHO Blood Pressure Indicator. The Memory Check mode can be accessed bypressing "MEM" button. To check the average results from other groups, select the desired group first prior to activating "SET" button in the off position.(See "Select Memory Group" on Page 13)BP Memory Check
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25Unit Operation You may check past test results by using the "MEM" button. The most recent test result and oldest test result in memory can be viewed by pressingand holding the "MEM" button. Upon activating test results. you can press the "MEM" button to scroll through all test results stored in memory. ECG Memory Check
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25ECG Unit Operation ECG Memory Deletion Memory for a selected group may be deleted while in Memory Check mode. Press and hold the " SET " button for approximately 3 seconds to delete all memory records from the selected groupwith voice broadcast "Memory Clear" and then transfer into testing mode. Press the "START/STOP " button to turn the unit off. Note: Memory cannot be recovered once it has been deleted.
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(1) Search for "BP+ECG" in the Android App Store or Apple App Store to download, register, and log in. Use of APP() 2If you want to use Bluetooth connection, please turn on the Bluetooth function of your phone. If you want to use wifi connection, please turn it on Your phone's Bluetooth and wifi capabilities. And your phone needs to be connected to a routerECG Unit Operation
(3)See the App Operation guide for other operations
Unit Operation Atrial Fibrillation IndicatorIf the monitoring instrument detects the disappearance of P wave in electrocardiogram during the measurement process, it is replaced by F wave with different sizes, shapes, directions and uneven spacing (frequency is mostly 350-600bpm). The atrial fibrillation symbol " " is displayed on the screen along with the measurement results. If " " is a frequent sign of AF in your exam results, consult your doctor.Power Off turn off the power itself about 3 minutes no operation in any mode.The " START/STOP " button can be pressed to turn off the unit in any mode. The unit can 23If at the end of the measurement, when the 30s average heart rate is greater than 120beat/min, the tachy symbol and ecg results are displayed on the LCD, when the 30s average heart rate is less than 60beat/min, When the average heart rate is between 60 and 120beat/min for 30s, the normal heart rate symbol and ecg result will be displayed on the LCD screen together" .Heart Rate IndicatorAFAFAtrial Fibrillation IndicatorIf the ECG sphygmomanometer detects an abnormality in the RR interval during the measurement, it also detects different sizes, shapes, F waves with uneven orientation and spacing. The atrial fibrillation symbol " " is displayed on the screen along with the measurement results. If " " is a common sign in your test results, consult your doctor. 24If at the end of the measurement, when the 30s average heart rate is greater than 120beat/min, the tachy symbol and ecg results are displayed on the LCD, when the 30s average heart rate is less than 60beat/min, When the average heart rate is between 60 and 120beat/min for 30s, the normal heart rate symbol and ecg result will be displayed on the LCD screen together" .Heart Rate IndicatorAFAFECG Unit Operation 2. Testing for ECG Wait for the signal to stabilize,and the 5S countdown starts to count.Device side display (See Figure A), APP side page display (See Figure B). Note: Keep your fingers on the device.ECG Unit Operation 3. Result Display The screen will display measurements for heat rate. Suggest this measurement heart rate is normal or too fast or too slow. Device side display (See Figure A), APP give suggested symptoms of atrial fibrillation and abnormal heart rhythms(See Figure B). A flashing " " will appear simultaneously on screen signaling heart beat detection andThe buzzer buzzes.Displays heart rate values and saves 30 seconds of ECG data to the device.Device side display (See Figure A), APP side page display (See Figure B).
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28Wireless Unit Operation Wifi requirements The monitor requires a device with: . Android 5.0 or later . IOS 9.0 or later And works with: . iphone , iPod, iPad . Android Phones and Tablets1. Open the App on your phone or tablet. If requested, you should enable Bluetooth and wifi on your device. You can enable Bluetooth and wifi from the Settings menu on your smartphone or desk, and your phone is connected to a router.Wifi connection-Using for the first time-Pairing your monitor with a Smart Device1. Open the “ECG Blood Pressure Monitor” and follow the pairing instructions shown on your smart phone.The date and time on your monitor will automatically be set when you pair it with your smart device.27Wireless Unit Operation 1. Open the “” and follow the pairing instructions shown on your smart phone.The date and time on your monitor will automatically be set when you pair it with your smart device.2. Confirm that your monitor is connected successfully.When your monitor is connected successfully to your smart phone, it will be display like below.ECG Blood Pressure Monitor-Pairing your monitor with a Smart Device3. Create a new user login, or login with your existing user name and password. 4. Selection device “ECG Blood Pressure Monitor”.Bluetooth requirements The monitor requires a device with: . Bluetooth 4.0 or later . Android 5.0 or later . IOS 9.0 or later And works with: . iphone , iPod, iPad . Android Phones and TabletsBluetooth connection-Using for the first time1.Search for "BP+ECG" in the Android App Store or Apple App Store to download, register, and log in.2. Open the App on your phone or tablet. If requested, you should enable Bluetooth on your device. You can enable Bluetooth under the Settings menu on your smart phone or table.
BluetoothSMART
BluetoothSMARTBluetoothSMART
3. Press the BP [START/STOP] button to turn your monitor off.29Wireless Unit Operation 2. Confirm that your monitor is connected successfully.When your monitor is connectedsuccessfully to your smart phone, it will be display like below.4. Press the BP [START/STOP] button to turn your monitor off.
BluetoothSMART
3. When your monitor is connected successfully to your router, it will be display like below. Open the App on your phone or tablet, Click the network configuration button and input the router password currently connected to the intelligent device to connect the ECG sphygmomanometer to the router.-Using again1. Open the App on your phone or tablet. If requested, you should enable wifi on your device, which is connected to a router. You can enable wifi on your smartphone or desktop under the Settings menu-Pairing your monitor with a Smart Device1. Open the “ECG Blood Pressure Monitor” and follow the pairing instructions shown on your smart phone.The date and time on your monitor will automatically be set when you pair it with your smart device.2. Confirm that your monitor is connected successfully. When your monitor is connected successfully to your smart phone, it will be display like below.3. Press the BP [START/STOP] button to turn your monitor off.
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TroubleshootingTroubleshootingProblemSolution" "displayedCuff is too tight or not properly positioned on the armFirmly reposition cuff approximately () above the elbow joint( See Page 15) 1-2cm1/2"Inaccurate test results due to body movement or monitor movementSit in a relaxed position with arm placed near heart. Avoid speaking or moving body parts while testing. Make sure the monitor unit is placed in a stationary position throughout the testing period.( See Page 10)Blood pressure results are not within typical rangeCuff fails to inflate properlyMake sure hose is properly fastened to cuff and monitor unitPossible CausePressurization is over cuff rated pressure 300mmHg Read user manual carefully and re-test properly. Improper operationRead user manual carefully and re-test properly.Ecg waveform drift or clutter is large1.Skin too dry or greasy2.The electrode is not secure in contact with the human body3.Muscle tension1.Clean skin with soap or water to make it moist and grease-free2.Apply pressure to the electrode3.Relax the hand during measurement

31Blood Pressure InformationBlood Pressure Blood pressure is the force of blood pushing against the walls of arteries. It is typically measured in millimeters of mercury (mmHg.) Systolic blood pressure is the maximumforce exerted against blood vessel walls each time the heart beats. Diastolic blood pressure is the force exerted on blood vessels when the heart is resting between beats. An individual's blood pressure frequently changes throughout the course of a day. Excitement and tension can cause blood pressure to rise, while drinking alcohol and bathing can lower blood pressure. Certain hormones like adrenaline (which your body releases under stress) can cause blood vessels to constrict, leading to a rise in blood pressure.If these measuring numbers become too high, it means the heart is working harder than it should.Example: fluctuation within a day (male, 35 years old)
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200150100506121824Upper curve: systolic blood pressureLower curve: diastolic blood pressureTime of day32: Classification IndicatorBlood PressureBlood Pressure InformationWHO Blood Pressure Classification Indicator The DBP-6673B is equipped with a classification indicator based on established guidelines from the World Health Organization. The chart below (color coded on monitor unit) indicates test results.Severe HypertensionMild HypertensionHigh-nNormalOptimalModerate HypertensionormalNormal
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1Hypertension is a dangerous disease that can affect the quality of life. It can lead to a lot of problems including heart failure, kidney failure, and cerebral hemorrhaging. By maintaining a healthy lifestyle and visiting your physician on a regular basis, hypertension and relative diseases are much easier to control when diagnosed in theirearly stages.33Blood Pressure InformationHealth ReminderSevere HypertensionModerate HypertensionMild HypertensionHigh-normalNormal 18016014013012080 85 90 100 110Diastolic( mmHg )Systolic( mmHg )OptimalNote: Do not be alarmed if an abnormal reading occurs. each day over an extended period of time. Consult your physician if test results remain abnormal.A better indication of an individual's blood pressure occurs after 2-3 readings are taken at the same time34Blood Pressure Q&AQ: What is the difference between measuring blood pressure at home or at a professional healthcare clinic?A: Blood pressure readings taken at home are now seen to give a more accurate account as they better reflect your daily life. Readings can be elevated when taken in a clinical or medical environment. This is known as White Coat Hypertension and may be caused by feeling anxious or nervous. Note: Abnormal test results may be caused by: 1. Improper cuff placement Make sure cuff is snug-not too tight or too loose. Make sure bottom of the cuff is approximately 1-2cm (1/2'') above the elbow joint. 2. Improper body position Make sure to keep your body in an upright position. 3. Feeling anxious or nervous Take 2-3 deep breaths, wait a few minutes and resume testing. Q: What causes different readings?A: Blood pressure varies throughout the course of a day. Many factors including diet, stress, cuff placement, etc. may affect an individual's blood pressure.Q: Should I apply the cuff to the left or right arm? What is the difference?A: Either arm can be used when testing, however, when comparing results, the same arm should be used. Testing on your left arm may provide more accurate results as it is located closer to your heart.Q: What is the best time of day for testing?A: Morning time or any time you feel relaxed and stress free.

35Maintenance1. Avoid dropping, slamming, or throwing the unit.2. Avoid extreme temperatures. Do not expose unit directly under sunshine.3. When cleaning the unit, use a soft fabric and lightly wipe with mild detergent. Use a damp cloth to remove dirt and excess detergent.When the electrode surface is dirty, please wipe it with a damp cloth or alcohol cotton, at least once a month.36SpecificationsProduct DescriptionModelDisplayBP Measurement Method BP PressurizationMemoryECG FunctionOscillometric Method Arm-type Fully Automatic ECG Blood Pressure MonitorDBP-6673B LCD Digital Display Size:95.5mm×54.5mm (3.76" x 2.15")2x150 BP Memories in Two Groups with Date and TimeIrregular Heartbeat DetectionWHO Classification IndicatorLow Battery DetectionAutomatic Power-OffVoiceAutomatic Pressurization BP Measurement Range PulseSystolic Pressure
Pulse
60mmHg～260mmHg 30 ~ 180 Beats/Minute±5%Diastolic Pressure40mmHg～200mmHgPressure0mmHg～299mmHgPressure±3mmHgBacklightLast 3 Tests AverageAtrial Fibrillation IndicatorHeart Rate Indicator
bandwidth
0.67~40HZ2x20 ECG Memories in Two Groups with Date and TimeECG Measurement RangeHeart RateMeasuring Time30 SecondsECG Measurement Method 30 ~ 199 Beats/MinuteHeart Rate±5% Single-channel ECG37SpecificationsOperating Environment HumidityTemperature 10 ~ 45 (50~113)℃℃℉℉10% ~ 95%RHPressure 800hPa~1060hPaStorage Environment HumidityClassificationIngress Protection Rating Temperature-20℃~55℃ (-4℉~131℉)Internal Powered Equipment,Type BF ,Cuff is the Applied PartIp21, Indoor Use Only15% ~ 93%RHTransport Environment Humidity Temperature -20℃~55℃ (-4℉~131℉)15% ~ 93%RHBluetooth VersionV5.0 Speed1MbpsWIFI Communication Standard Frequency2.4GHz(2412-2462Mhz)802.11b BandwidthAbout 20 MHZ Type Of AntennaBuilt-in Onboard Antenna Antenna gainAbout 1.5dBiPower SourceBattery Life Unit WeightUnit DimensionsCuff Circumference3A AA batteries Approximately 2 m at 3 tests per dayonthsApprox.258g (9.1 oz.) (excluding battery)Approx.142.5 x 107.2 x 44mm (5.61" x 4.22" x 1.73" )(L x W x H)Approx.135 (W) x 485(L) mm (Medium cuff: Fits arm circumference 22-36 cm) Type Of AntennaBuilt-in Onboard Antenna
Transmission powerAbout 3dbm Transmission power
≤15dbm Frequency2.4GHz(2402-2480Mhz)BP FunctionOther Function38WarrantyThis complies with the European regulations and bears theCE mark“CE 0123”.This ECG Blood Pressure Monitor also complies with mainlyfollowing standards(included but not limited):Safety standard:EN 60601-1 Medical electrical equipment part 1: General requirements for safetyEMC standard:EN 60601-1-2 Medical Electrical Equipment -- Part 1-2: General Requirements For Basic Safety And Essential Performance -- Collateral Standard: Electromagnetic Disturbances – Requirements And Tests. Performance standards:IEC80601-2-30, Medical electrical equipment – Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers. EN 1060-3 Non-invasive sphygmomanometers - Supplementary requirements forelectromechanical blood pressure measuring systems.ISO 81060-2, non-invasive sphygmomanometers - part 2: clinical validation of automated measurement type.ECG Blood Pressure MonitorSpecifications are subject to change without notice.Please note that changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment.This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:—Reorient or relocate the receiving antenna.—Increase the separation between the equipment and receiver.—Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.—Consult the dealer or an experienced radio/TV technician for help.This device contains licence-exempt transmitter(s)/receiver(s) that comply with Innovation, Science and Economic Development Canada’s licence-exempt RSS(s). Operation is subject to the following two conditions:(1) This device may not cause interference; and(2) This device must accept any interference, including interference that may cause undesired operation of the device.L’émetteur/récepteur exempt de licence contenu dans le présent appareil est conforme aux CNR d’Innovation, Sciences et Développement économique Canada applicables aux appareils radio exempts de licence. L’exploitation est autorisée aux deux conditions suivantes :(1)L’appareil ne doit pas produire de brouillage;(2)L’appareil doit accepter tout brouillage radioélectrique subi, même si le brouillage est susceptible d’en compromettre le fonctionnement. The ECG Blood Pressure Monitor is calculated from the date of purchase, and its service life is 2 years. If the ECG Blood Pressure Monitor does not function properly due to defective components or poor workmanship, we will repair or replace it freely. The warranty does not cover damages to your Blood Pressue Monitor due to improper handling. Please contact local retailer for details.

Electromagnetic Compatibility Information
The device satisfies the EMC requirements of the international standard IEC 60601-1-2. The requirements are satisfied under the conditions described in the table below. The device is an electrical medical product and is subject to special precautionary measures with regard to EMC which must be published in the instructions for use. Portable and mobile HF communications equipment can affect the device. Use of the unit in conjunction with non-approved accessories can affect the device negatively and alter the electromagnetic compatibility. The device should not be used directly adjacent to or between other electrical equipment.Table 1Guidance and declaration of manufacturer-electromagnetic emissionsThe device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that it is used in such an environm-ent.Electromagnetic environment -guidanceComplianceEmissions testThe device uses RF energy only forits internal function. Therefore, itsemissions are very low and are notlikely to cause any interference innearby electronic equipment.Group 1,class B.Radiated emission CISPR 11The device is suitable for use in allestablishments, including domesticestablishments and those directlyconnected to the public low-voltagepower supply network that supplies buildings used for domestic purposes.Conducted emission CISPR 1139Group 1,class B.Table 2
Guidance and declaration of manufacturer-electromagnetic immunityThe device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that it is used in such an environm-ent.Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30 %.Electromagnetic environment -guidanceCompliancelevelIEC 60601test levelIMMUNITY test± 8 kV contact±2 kV,±4 kV, ±8 kV, ±15 kV airElectrostaticdischarge (ESD)IEC 61000-4-2Power frequency(50/60 Hz)magnetic fieldIEC 61000-4-8 30 A/m; 50Hz or 60Hz Power frequency magnetic fields should be at levels charactertic of a typical location in a typical comme-rcial or hospital environment.30 A/m; 50Hz or 60Hz± 8 kV contact±2 kV,±4 kV, ±8 kV, ±15 kV air
Electromagnetic Compatibility Information
40Radiated RF EM fieldsIEC 61000-4-3 3V/m or 10 V/m80MHz-2.7Ghz 80%AM at 1kHz3V/m or 10 V/m80MHz-2.7Ghz 80%AM at 1kHz
Portable and mobile RF communications equipment should be used no closer to any part of the device, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.Recommended seperation distance 80 MHz to 800 MHz 800 MHz to 2.7 Ghz where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in metres (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, a should be less than the compliance level in each frequency range. Interference may occur in the vicinity of equipment marked with the following symbol:
Table 3
Electromagnetic Compatibility Information
41
Guidance and declaration of manufacturer-electromagnetic immunity
Nowadays, many RF wireless equipments have being used in various healthcarelocations where medical equipment and/or systems are used. When they are used in close proximity to medical equipment and/or systems, the medical equipment and/or systems’ basic safety and essential performance may be affected. Arm-type Fully Automatic Digital ECG Blood Pressure Monitor has been tested with the immunity test level in the below table and meet the related requirements of IEC 60601-1-2:2014. The customer and/or user should help keep a minimum distance between RF wireless communications equipment and this medical equipment and/or systems as recommended below.
Service1970 Immunity test level (V/m) Distance (m)
Band(MHz)
0.3 Test frequency (MHz) Modulation Maximum power (W) TETRA 400 0.2 95785550052402400-2570 2450 800-960 280.3 2704-7870.27100.3 27 0.3 1.8 4509280.3 2745780810870 GMRS 460 FRS 460 FM± 5 kHz deviation1 kHz sine228 430-470 Pulse modulation 18Hz 380-390 38593017201700-1990218450.3 280.3 GSM 1800; CDMA 1900; GSM 1900; DECT; LTE Band 1, 3, 4, 25; UMTS Pulse modulation 18HzGSM 800/900, TETRA 800, iDEN 820, CDMA 850, LTE Band 5 Pulse modulation 217Hz LTE Band 13, 17Pulse modulation 217Hz WLAN 802.11 a/n Pulse modulation 217Hz Bluetooth,WLAN,802.11 b/g/n,RFID 2450,LTE Band 7 Pulse modulation 217Hz 5100-5800
Recommended separation distances between portable and mobile RF communications equipment and the deviceThe device is intended for use in an electromagnetic environment in which radiated therefore disturbances are controlled. The customer or the user of the device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the device as recommended below, according tothe maximum output power of the communications equipment.Rated maximumoutput power oftransmitter WTable 4Separation distance according to frequency of transmitter m80 MHz to 800 MHz800 MHz to 2.7 GHz 0.010.11
10
1000.120.381.23.8120.230.732.37.323For transmitters rated at a maximum output power not listed above, therecommended separation distance d in metres (m) can be estimated using theequation applicable to the frequency of the transmitter, where P is the maximumoutput power rating of the transmitter in watts (W) according to the transmittermanufacturer.NOTE1 At 80 MHz and 800 MHz, the separation distance for thfrequency range applies.NOTE2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.e higher
Electromagnetic Compatibility Information
42

43Important Instructions Before Use1. WARNING: Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally.2.WARNING: PORTABLE RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of Arm-type Fully Automatic Digital ECG Blood Pressure Monitor , including cables specified by the MANUFACTURER. Otherwise, degradation of the performance of this equipment could result.3.The software identifier refer to the software evaluation report , and the file code isJDBP-7304- 154.4.verify manometer pressure accuracy:In the power down state, press and hold the " START/STOP" button, and theninstall the batteries. Until the LCD screen is full, release the " START/STOP" button. When the LCD screen displays the double zero, the bloodpressure meter is in static state.At this point, 500ml gas capacity, calibrated standard pressure gauge and manual pressure device can be connected to the sphygmomanometer through the sleeve interface of the sphygmomanometer, and manual pressure can be applied to the effective display range of the sphygmomanometer, and then the difference between the reading of the sphygmomanometer and that of the standard pressure gauge can be compared.This mode can be used to verify manometer pressure accuracy.5.The patient is the operator:the PATIENT is an intended OPERATOR.the PATIENT Do not carry out other maintenance operations except to replace the battery.6.WARNING: Do not modify this equipment without authorization of the manufacturer.7. ESSENTIAL PERFORMANCE Maintenance advice:Pressure calibration will be carried out when this product leaves the factory. Patients can use the method described in the section "Verify Manometer Pressure Accuracy" to verify the accuracy. If the accuracy deviation is large, please contact the manufacturer to recalibration.8.Mechanical strength and resistance to heatThe resistance to heat will be retained by device during the EXPECTED SERVICE LIFE of the ME EQUIPMENT.
Additional Notes
449.Do not place the and cuff at will. It will cause asphyxiation if thechild swallows or twine around his neck.10.The cuff and the case of the ECG Blood Pressure Monitor have been tested for biocompatibilityand do not contain allergenic or harmful materials.Please stop using it if allergy occurs during use.11.Warning:Non-professionals do not modify the equipment, otherwise it will make the equipment measurement is not accurate.12.Warning:Do not expose the equipment for a long time, otherwise it will reduce the performance of the equipment.13.Warning:This device is not used for children and pets14.Clean:The equipment can be cleaned by lay operator according to rule 3 of maintenance in the instructions15.Warning:Do not use a damaged cuff for blood pressure measurement.16.Warning:When measuring with the cuff, if the tester feels seriously uncomfortable, press the button of the ECG Blood Pressure Monitor to deflate the cuff, or remove the cuff directly from the arm.17.Warning:If an unexpected reading occurs, the operator can take several more measurements and consult a doctor.18.Warning:This equipment is used outside the specified environment, may damage the equipment, and may be inaccurate measurement.19.ME equipment not intended for use in conjunction with flammable agents “ME equipment not intended for use in oxygen rich environment”ECG Blood Pressure Monitor Correct Disposal of This Product(Waste Electrical & Electronic Equipment) This marking shown on the product indicates that it should not be disposed with other household waste at the end of its life. To prevent potential harm to the environment or to human health, please separate this product from other types of wastes and recycle it responsibly. When disposing this type of product, contact the retailer where product was purchased or contact your local government office for details regarding how this item can be disposed in an environmentally safe recycling center.Business users should contact their supplier and check the terms and conditions of the purchasing agreement. This product should not be mixed with other commercial wastes for disposal. This product is free of hazardous materials.
Additional Notes