Joytech Healthcare DBP-6677B ECG Blood Pressure Monitor Owner’s Manual
- June 3, 2024
- Joytech Healthcare
Table of Contents
DBP-6677B ECG Blood Pressure Monitor
Owner’s Manual
ECG Blood Pressure Monitor Model DBP-6677B
Arm Type
Document No.:JDBP-7704-154 VersionZ Date of Issue2020.06
Contact Information
The 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. No.365,
Wuzhou Road,Yuhang Economic Development Zone, Hangzhou City,311100
Zhejiang,China Email: info@sejoy.com Telephone: +86-571-81957767 Fax:
+86-571-81957750
Contents
1
Safety Notice …………………………………………………………………………………02 Unit Illustration
……………………………………………………………………………07 Important Testing Guidelines
………………………………………………………….09 Quick Start ……………………………………………………………………………………………….10
Battery Installation ………………………………………………………………….12 System Unit Operation
…………………………………………………………………………………13
System Settings …………………………………………………………………………………13 BP Unit Operation
………………………………………………………………………………………15
Applying the Arm Cuff ……………………………………………………………………15 Blood pressure test
………………………………………………………………………….16 Power Off …………………………………………………………………………………………18
BP Memory Check and Last 3 Test Average………………………………………………19 BP Memory Deletion
…………………………………………………………………………….19 Low Battery Indicator
………………………………………………………………………..20 Static Pressure Measurement
………………………………………………………………..21 ECG Unit Operation
…………………………………………………………………………………..22 Gestures of ECG measurements
………………………………………………………………22 ECG Test …………………………………………………………………………………………..22
ECG Memory Check ……………………………………………………………………………25 ECG Memory Deletion
………………………………………………………………………..25 Use Of App
……………………………………………………………………………………….26 Wireless Unit Operation
………………………………………………………………………………27 Bluetooth requirement and connection
…………………………………………………27 Wifi requirement and connection ……………………………………………………..28
Troubleshooting …………………………………………………………………………………………30 Blood Pressure
Information …………………………………………………………………………31 Blood Pressure Q&A
…………………………………………………………………………………..34 Maintenance
……………………………………………………………………………………………..35 Specifications
…………………………………………………………………………………………….36 Warranty
………………………………………………………………………………………………….38 Electromagnetic Compatibility
Information ……………………………………………………39
Safety Notice
2
Thank you for purchasing the DBP-6673B ECG Blood Pressure Monitor. Intended
Use ECG 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. Contraindications Product is not intended for people under
12 years of age or individuals who cannot express their intentions.
Precautions to Ensure Safe, Reliable Operation 1. 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
cuffEach blood pressure
measurement should not exceed 3 minutes.
Safety Notice
3
Important Instructions Before Use 1. 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
5
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.
Federla Commulcation Commission (FCC) Interference Statement
1.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 or transmitter. 7.Essential
performance:
Safety Notice
4
23. 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.
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 measurement
36. 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 Dry
Keep off Sunlight
Type BF Equipment
Instructions For Use MUST be Consulted
Safety Notice
6
Electrosurgery interference recovery
Limits of the error of the manometer
Reproducibility of the BLOOD PRESSURE DETERMINATION
Reproducibility of the ECG DETERMINATION
Refer 202.6.2.101 IEC 80601-2-30 Refer 202.12.1.102 IEC 80601-2-30 Refer 201.12.1.107 IEC 80601-2-30 Refer 201.12.1.101.3.1 IEC 60601-2-47
Unit Illustration
7
Monitor Unit
LCD
” SET ” Button
“MEM” Button
” START/STOP ” Button
Arm Cuff Medium size cuff (fits arm circumference: 22.0 cm -36.0 cm).
LEFT ARM
82.62~~1346.c12~m2incmch(0).4~0.8 inch)
Main
Arte
ry
IN
D
E
X
Arm Cuff
Air Plug
Air Tube
If air is leaking from the arm cuff, replace the arm cuff with a new one. It is generally recomm ended to have the cuff replaced timely to ensure correct functioning and accuracy. Please consult your local authorized Sejoy distributor or dealer.
Unit Illustration
8
Display
Group2
Group1
Low Battery Indicator
Arm Shake Indicator WHO Blood Pressure Classification Indicator
Last 3 Tests Average
Blood Pressure
Indicator
Ecg Indicator
BP ECG
Time/Date
Bluetooth Indicator
OK Fast Slow AF IHB
Wifi
Slow Heartbeat
Indicator Indicator
Contents
Systolic Blood Pressure
Cuff Loose Indicator
Diastolic Blood Pressure
Heart Rate Indicator
Pulse Rate
Normal Heartbeat Indicator Fast Heartbeat Indicator Atrial Fibrillation
Indicator
Irregular Heartbeat Indicator
Owner’s Manual
Arm-type Fully Automatic ECG Blood Pressure Monitor
Model DBP-6677B
Arm Type
1.Monitor Unit
LEFT ARM
82.62~~1346.c12~m2incmc
h) (0.4~0.8
inch)
Main
Ar
tery IN
D
E
X
3.Arm Cuff
2.Owner’s Manual
4.Storage Bag
Important Testing Guidelines
99
1. Avoid eating, exercising, and bathing for 30 minutes prior to testing. 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.
Quick Start
BP Quick Start
1. Install batteries. (See Figure A ) 2. Insert cuff air plug into the left
side of monitor unit. (See Figure B)
10
Figure A
Figure B
3. Remove thick clothing from the arm area. 4. 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 )
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.
Figure C
5. Apply cuff to your left arm and keep level with your heart. Bottom of cuff
should be placed approximately 1-2cm (0.4-0.8”) above elbow joint. (See
Figures D&E)
1-2cm (0.4-0.8”)
Figure D 6. Press ” START/STOP ” Button to start testing.
Figure E
Quick Start
ECG Quick Start
1. Install batteries. (See Figure A )
11 BUantitteOrypIenrsattaiollnation
Battery Installation
Slide battery cover off as indicated by arrow. Install 3 new AAA alkaline
batteries according to polarity. Close battery cover.
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 B
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 )
12
Figure C
4. Hold down the” MEM” to bind the measurement device to the smart device,
press ” START/STOP ” to power off the device, and then press ” START/STOP ” to
start the test.
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)
ECG AM P/mUinL
Bluetooth SMART
Figure D
L
R
System Unit Operation
13
System Settings
With power off, press “SET” button to activate System Settings. The Memory
Group icon flashes. 1. 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.
System Unit Operation
4. Voice Setting Press “SET” button to enter voice setting mode. Set voice
format ON or OFF by pressing the “MEM” button.
5. Volume Setting Press “SET” button to enter volume setting mode. Set the voice volume by adjusting the “MEM” button . There are six volume levels.
14
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)
AM
AM
6. Saved Settings 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.
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
BP Unit Operation
Applying the Arm Cuff
1. Firmly insert air plug into opening located on behind side of monitor
unit.
15
BP Unit Operation
16
Blood pressure test
1. Power On Press and hold “START/STOP” button to turn the unit on. Press and
hold “START/STOP”
button to turn the unit on. The LCD screen will display for one second. A
voice tone will indicate when unit is ready for testing.
2. With sticky nylon section facing outward, insert end of cuff underneath
metal ring of cuff.
3. Fasten cuff about 1-2cm (0.4-0.8”) above the elbow joint. For best results
apply cuff to bare arm and keep level with heart while testing.
BP ECG
OK Fast Slow AF IHB
Note: Make sure the switch is in BP mode before the measurement begins Unit
will not function if residual air from previous testing is present in cuff.
The LCD will flash ” ” until pressure is stabilized.
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.
BP Unit Operation
17
2. Testing for Blood After cuff inflation, air will slowly rise as indicated by the corresponding cuff pressure value. A flashing ” ” will appear simultaneously on screen signaling heart beat detection.
OK mmHg
BP AM
Note: 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.
BP Unit Operation
18
Irregular Heartbeat Indicator If the monitor detects an irregular heart rhythm two or more times during the measuring process, the Irregular Heartbeat Symbol ” IHB “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 ” IHB ” frequently appears with your test results.
Power Off
The ” START/STOP ” button can be pressed to turn off the unit in any mode. The
unit can turn off the power itself about 3 minutes no operation in any mode.
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.
OK mmHg
BP Bluetooth
SMART
AM P/mUinL
Note: Refer to Page 32~33 for detail WHO Blood Pressure Classification Information.
Arm Shake Indicator
If there is arm movement during the measurement, ” ” may be shown. Indicates that
it may lead to abnormal accurate measurement results.The measurement result shows ” “.
When viewing this memory, the memory result shows” “.
Cuff loose Indicator
When starting the measurement, ” OK “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 correctly
and start measuring again.
BP Unit Operation
19
Last 3 Tests Average
With power offpress 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 by pressing “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 Unit Operation
20
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.
OK mmHg
BP Bluetooth
SMART
AM P/mUinL
BP Memory Check
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 pressing and
holding the “MEM” button. Upon activating test results. you can press the
“MEM” button to scroll through all test results stored in memory.
OK mmHg
BP AM
Note: Memory cannot be recovered once it has been deleted.
Low Battery Indicator
The 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. Replace batteries at this time.
No memory loss will occur throughout this process.
BBPP AM
BP Bluetooth
SMART
AM P/mUinL
BP Unit Operation
21
Static Pressure Measurement
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.
ECG Unit Operation
Gestures of ECG measurements
22
ECG AM P/mUinL
Bluetooth SMART
mmHg
BP AM
Note: Only Service personnel permitted to access to this mode, the mode
unavailable in normal use.
L
R
Note:Before starting the measurement, make sure the switch is in ECG mode. Do
not let your fingers go until the test results appear.
ECG Test
1. Power On Press and hold “START/STOP” button to turn the unit on. The LCD
screen will display for
one second.
BP ECG
OK Fast Slow AF IHB
Note:Wait for the signal to stabilize,and the 5S countdown starts to count.
ECG Unit Operation
23
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).
AM
1 ECG
UECniGt OUpneirt aOtpioenration
234
Atrial Fibrillation Indicator If the mEConGitsoprhinygminosmtruanmoemntetdeertedcetsecthtseadnisaabpnpoeramraanlictey oinf Pthwe aRvRe inteelrevcatlrodcuarrindgiotghream dmuerainsugrtehmeemnet,aistuarlesmo ednet epcrtoscdeisfsf,eirteinstrseipzleasc,esdhabpyeFs,wFavweawveitshwdiitfhfeurneenvtesnizoersi,esnhtaptieosn, and sdpiraeccitnigo.nTs haendaturniaelvfeibnrsipllaactionng s(fyrmeqbuoeln”cyAAFiFs”miossdtliysp3l5a0y-e6d0o0nbpthme)s.creen along with the mTheeasautrieaml feinbtrrilelsautilotsn. sIyfm” bAoFFl ” is a” cisodmimspolanyseidgnoninthyeousrcrteestnraelsounlgtsw, ciothnsthueltmyoeuasrudroecmtoern.t results. If ” ” is a frequent sign of AF in your exam results, consult your doctor.
A flashing ”
Figure A
Figure B
” will appear simultaneously on screen signaling heart beat detection and
The 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).
AM
1 ECG
Heart Rate Indicator If 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” .
Figure A
Figure B
Note: Keep your fingers on the device. 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).
AM
1 ECG
OK
Power Off
The ” START/STOP ” button can be pressed to turn off the unit in any mode. The
unit can turn off the power itself about 3 minutes no operation in any mode.
Figure A
Figure B
UECniGt OUpneirt aOtpioenration
25
ECG Memory Check
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 pressing and
holding the “MEM” button. Upon activating test results. you can press the
“MEM” button to scroll through all test results stored in memory.
ECG Unit Operation
26
Use of APP
(1) Search for “BP+ECG” in the Android App Store or Apple App Store to
download, register, and log in.
(2) If 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 router
(3)See the App Operation guide for other operations
BP ECG AM
BP ECG
AM P/mUinL
Bluetooth SMART
OK
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.
ECG AM
Note: Memory cannot be recovered once it has been deleted.
Wireless Unit Operation
27
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 Tablets
Bluetooth connection
-Using for the first time
1. 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. 3. Create a
new user login, or login with your existing user name and password. 4.
Selection device “ECG Blood Pressure Monitor”.
-Pairing your monitor with a Smart Device
1. 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.
Wireless Unit Operation
28
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 Tablets
Wifi connection -Using for the first time
1. 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.
-Pairing your monitor with a Smart Device
1. 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.
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.
Wireless Unit Operation
29
3. 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.When your monitor is connected successfully to your router, it will be display like below.
-Using again
1. 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 Device
1. 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.
Troubleshooting
30
Troubleshooting
Problem
Possible Cause
Solution
Cuff is too tight or not properly positioned on the arm
Firmly reposition cuff approximately1-2cm (1/2″) above the elbow joint ( See Page 15)
Blood pressure results are not within typical range
Inaccurate test results due to body movement or monitor movement
Sit 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)
Ecg waveform drift or clutter is large
1.Skin too dry or greasy 2.The electrode is not secure in contact with the human body 3.Muscle tension
1.Clean skin with soap or water to make it moist and grease-free 2.Apply pressure to the electrode 3.Relax the hand during measurement
2. Confirm that your monitor is connected successfully. When your monitor is connected successfully to your smart phone, it will be display like below.
” “displayed
Cuff fails to inflate properly
Make sure hose is properly fastened to cuff and monitor unit
Improper operation
Read user manual carefully and re-test properly.
3. Press the BP [START/STOP] button to turn your monitor off.
Pressurization is over cuff rated pressure 300mmHg
Read user manual carefully and re-test properly.
Blood Pressure Information
31 Blood Pressure Information
32
Blood 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 maximum force 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.
200
Upper curve : systolic blood pressure
Lower curve: diastolic blood pressure
150
mmHg
100
50
6
12
18
24
Time of day
Example: fluctuation within a day (male, 35 years old)
WHO 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 Hypertension Moderate Hypertension Mild Hypertension High-normal Normal
Optimal
AM Bluetooth SMART
1 BP
SYS
mmHg
Normal
: Blood Pressure Classification Indicator
Blood Pressure Information
33
Health Reminder
Hypertension 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 their early stages.
Systolic ( mmHg )
180 160 140 130 120
Severe Hypertension Moderate Hypertension Mild Hypertension High-normal Normal Optimal
80 85 90 100 110
Diastolic ( mmHg )
Note: Do not be alarmed if an abnormal reading occurs. A better indication of an individual’s blood pressure occurs after 2-3 readings are taken at the same time each day over an extended period of time. Consult your physician if test results remain abnormal.
Blood Pressure Q&A
34
Q: 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.
Maintenance
35
1. 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.
Specifications
36
Product Description
Arm-type Fully Automatic ECG Blood Pressure Monitor
Model
DBP-6677B
Display
LCD Digital Display Size:95.5mm×54.5mm (3.76″ x 2.15″)
BP Measurement Method Oscillometric Method
BP Pressurization
Automatic Pressurization Systolic Pressure 60mmHg260mmHg
Diastolic Pressure Pressure BP Measurement Range Pressure
40mmHg200mmHg 0mmHg299mmHg ±3mmHg
ECG Measurement Method
Pulse Pulse
30 ~ 180 Beats/Minute ±5%
Single-channel ECG
bandwidth
0.67~40HZ
Heart Rate
30 ~ 199 Beats/Minute
ECG Measurement Range Heart Rate Measuring Time
±5% 30 Seconds
Memory
2×150 BP Memories in Two Groups with Date and Time 2×20 ECG Memories in Two Groups with Date and Time
Irregular Heartbeat Detection
BP Function
WHO Classification Indicator
Last 3 Tests Average
ECG Function
Atrial Fibrillation Indicator Heart Rate Indicator
Automatic Power-Off
Other Function
Low Battery Detection Voice
Backlight
Power Source Battery Life
3A AA batteries Approximately 2 months at 3 tests per day
Specifications
37 Warranty
38
Unit Weight
Approx.219g (7.7 oz.) (excluding battery)
Unit Dimensions
Approx.149.8 x 80.4 x 45.7mm (5.90″ x 3.17″ x 1.80″ )(L x W x H)
Cuff Circumference Operating Environment Storage Environment
Approx.135 (W) x 485(L) mm (Medium cuff: Fits arm circumference 22-36 cm)
Temperature Humidity
10 ~ 45 (50~113) 10% ~ 95%RH
Pressure
800hPa~1060hPa
Temperature
-20~55 (-4~131)
Humidity
15% ~ 93%RH
Transport Environment
Temperature Humidity
-20~55 (-4~131) 15% ~ 93%RH
Bluetooth WIFI
Frequency
2.4GHz(2402-2480Mhz)
Type Of Antenna Built-in Onboard Antenna
Version
V5.0
Speed
1Mbps
Transmission power About 3dbm
Frequency
Communication Standard
Bandwidth
2.4GHz(2412-2462Mhz) 802. 11b About 20 MHZ
Type Of Antenna Built-in Onboard Antenna
Antenna gain
About 1.5dBi
Transmission power 15dbm
Classification
Internal Powered Equipment,Type BF ,Cuff is the Applied Part
Ingress Protection Rating
Ip21, Indoor Use Only
Specifications are subject to change without notice. This ECG Blood Pressure
Monitor complies with the European regulations and bears the CE mark”CE
0123″.This ECG Blood Pressure Monitor also complies with mainly following
standards (included but not limited): Safety standard: EN 60601-1 Medical
electrical equipment part 1: General requirements for safety EMC 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 for electromechanical blood pressure measuring systems. ISO
81060-2, non-invasive sphygmomanometers – part 2: clinical validation of
automated measurement type. 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 39
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 1
Guidance and declaration of manufacturer-electromagnetic emissions
The 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 environment.
Emissions test
Compliance
Electromagnetic environment -guidance
Radiated emission CISPR 11 Group 1, class B.
The device uses RF energy only for its internal function. Therefore, its emissions are very low and are not likely to cause any interference in nearby electronic equipment.
Conducted emission CISPR 11
Group 1, class B.
The device is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.
Electromagnetic Compatibility Information 40
Table 2
Guidance and declaration of manufacturer-electromagnetic immunity
The 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 environment.
IMMUNITY test
IEC 60601 test level
Compliance Electromagnetic environment
level
-guidance
Electrostatic discharge (ESD) IEC 61000-4-2
± 8 kV
± 8 kV
Floors should be wood, concrete
contact
contact
or ceramic tile. If floors are
±2 kV,±4 kV, ±2 kV,±4 kV, covered with synthetic material,
±8 kV,
±8 kV,
the relative humidity should be
±15 kV air ±15 kV air at least 30 %.
Power frequency (50/60 Hz) magnetic field 30 A/m; 50Hz
or 60Hz
IEC 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 commercial or hospital environment.
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.
Radiated RF EM 3V/m or 10 V/m 3V/m or 10 V/mRecommended seperation distance 80 MHz
fields IEC 61000-4-3
80MHz-2.7 Ghz 80%AM at 1kHz
80MHz-2.7 Ghz 80%AM 1kHz
at
to 800 MHz 800 MHz to 2.7 Ghz where P the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the
is
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:
Electromagnetic Compatibility Information 41
Table 3
Guidance and declaration of manufacturer-electromagnetic immunity
Nowadays, many RF wireless equipments have being used in various healthcare
locations 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.
Test frequency
(MHz)
385
450 710 745 780 810 870 930
Band (MHz)
380-390 430-470
Service Modulation
TETRA 400
GMRS 460 FRS 460
Pulse modulation
18Hz
FM ± 5 kHz deviation 1 kHz sine
Maximum power (W)
1.8
2
704-787
LTE Band
Pulse modulation
0.2
13, 17
217Hz
Distance (m)
0.3 0.3
0.3
GSM 800/900,
TETRA 800,
Pulse
800-960
iDEN 820, modulation
2
0.3
CDMA 850, LTE Band 5
18Hz
Immunity test level
(V/m) 27 28
9
28
1720
GSM 1800;
CDMA 1900;
Pulse
1845
1700-1990
GSM 1900; DECT;
LTE Band 1, 3,
modulation 217Hz
2
0.3
28
4, 25; UMTS
1970
2450
2400-2570
Bluetooth,WLAN, 802.11 b/g/n,RFID
Pulse modulation
2
0.3
28
2450,LTE Band 7
217Hz
5240
WLAN
Pulse
5500
5100-5800
802.11 modulation
0.2
0.3
9
a/n
217Hz
5785
Electromagnetic Compatibility Information 42
Table 4
Recommended separation distances between portable and mobile RF communications
equipment and the device
The 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 to the maximum
output power of the communications equipment.
Rated maximum Separation distance according to frequency of transmitter
output power of
m
transmitter
80 MHz to 800 MHz
800 MHz to 2.7 GHz
W
0.01
0.12
0.23
0.1
0.38
0.73
1
1.2
2.3
10
3.8
7.3
100
12
23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
Additional Notes
43 Additional Notes
44
Important Instructions Before Use 1. 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 Armtype 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 is JDBP-7704- 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.
9.Do not place the ECG Blood Pressure Monitor and cuff at will. It will cause asphyxiation if the child swallows or twine around his neck. 10.The cuff and the case of the ECG Blood Pressure Monitor have been tested for biocompatibility and 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 pets 14.Clean: The equipment can be cleaned by lay operator according to rule 3 of maintenance in the instructions 15.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”
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.
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