JOYTECH DBP-1359b User manual

Contents Safety Notice
1 2
Thank you for purchasing the DBP-1359b Blood Pressure Monitor. The unit has been constructed
using reliable circuitry and durable materials. Used properly, this unit will provide yeas of
satisfactory use.
Measure blood pressure(systolic and diastolic)and pulse rate of adults and adolecents age
12 through 21years of age. All functions can be used safely and values can be read out in one
LCD DISPLAY. Measurement position is on adult upper arm only.
Blood pressure measurement determined with this device are equivalent to those obtained
by a trained observer using the cuff/ stethoscope auscultation method, within the limits
prescribed by the Recognized Consensus Standard (IEC 81060-2-30) for electronic
sphygmomanometers.
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 oC, 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 oC, 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.
Model DBP-1359b
Arm Type
Owner's Manual
Arm-type Fully Automatic
Digital Blood Pressure Monitor
Document No.:JDBP-5504-050
Version: Z
Date of Issue: 2018.12
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.
Email: [e-mail]
Telephone: [phone]
Fax: [phone]
No.365, Wuzhou Road,Yuhang Economic Development Zone,
Hangzhou City,311100 Zhejiang,China
Safety Notice ............................................................... 02
Unit Illustration ......................................................... 06
Important Testing Guidelines ..................................... 09
Quick Start ................................................................. 10
Unit Operation ........................................................... 11
Blood Pressure Information ........................................ 25
Blood Pressure Q A ................................................... 28
Maintenance ............................................................... 29
Specifications ............................................................. 31
Warranty .................................................................... 33
＆
Battery Installation ..................................................
System Settings ........................................................ 12
Applying the Arm Cuff ............................................. 14
Testing ..................................................................... 15
Power Off ................................................................ 18
Memory Check ...................................................... . 19
Last3 Tests Average .......... ....................................... 20
Memory Deletion ..................................................... 21
Low Battery Indicator ............................................. 21
Troubleshooting ...................................................... 24
11
Bluetooth requirements ........................................... 22
Electromagnetic Compatibility Information .............. 34

Unit Illustration
Safety Notice Safety Notice
3 4
6
Safety Notice 5
Monitor Unit
Battery cover
AC Adapter Jack
Systolic Blood Pressure
M " " Button
" " Button
"SET" Button
Diastolic Blood Pressure
Pulse Rate
Air Jack
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 blood pressure monitor in consultation with your doctor. In
certain cases oscillometric measurement method can produce incorrect readings.
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.
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.
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.
27. Only use a recommended AC adaptor double-insulated complying with EN 60601-1 and
EN 60601-1-2. An unauthorized adapter may cause fire and electric shock.
28. Advising operator that Instruction manual/ Booklet must be consulted.
29. Do not use the device during transport vehicles for influencing measurement accuracy,
such as patient transport in an ambulance or helicopter.
30. Contains small parts that may cause a chocking hazard if swallowed by infants.
31. Please align the polarities of each battery with the +ve and -ve signs
imprinted on the battery housing when you replace the batteries .
32.This ME equipment or ME systems should be only used in shielded location.
33.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.
34.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.
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 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.
WARNING SIGNS AND SYMBOLS USED
Keep off Sunlight
Type BF Equipment
Discard the used product to the recycling
collection point according to local
regulations
Instructions For Use MUST be Consulted
Keep Dry
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.

Quick Start
Unit Illustration Unit Illustration
7 8
10
Important Testing Guidelines 9
Arm Cuff Air Tube
Air Plug
Arm Cuff
1~2cm (0.4~0.8 inch)
22~36cm
（8.6~14.2 inch)
Main Arter y
LEFT ARM
INDEX
Medium 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 distributor or dealer.
Groups
Systolic
Blood Pressure
Pulse Rate
Time and Data
Display
Diastolic
Blood Pressure
WHO Blood Pressure
Classification Indicator
Last 3 Results Average
Low Battery Indicator
Irregular Heartbeat Indicator
Contents
1~2cm (0.4~0.8 inch)
22~36cm
（8.6~14.2 inch)
Main Artery
LEFT ARM
INDEX
3.Arm Cuff
2.Owner's Manual
1.Monitor Unit
5.2MOPPMedical AC Adapter(DC6.0 V,600mA)
(recommended, not provided)
4.Storage Bag
Model DBP-135 9b
Arm Type
Owner's Manual
Arm-type Fully Automatic
Digital Bl ood Pres sure Mon itor
1.
Sit in a calm environment for at least 5 minutes prior to testing.
3
. Wait 3 minutes or longer before re-testing.
7
. 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 blood pressure monitor is not recommended for people with severe arrhythmia.
Avoid eating, exercising, and bathing for 30 minutes prior to testing.
2.
. 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
. Try to measure your blood pressure at the same time each day for consistency.
8
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.
10. Do not use this blood pressure monitor if the device is damaged.
1. Install batteries
2. Insert cuff air plug into the left 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 C
Figure A
Figure D Figure E
6. Press " " Button to start testing.
Figure B

12
1413 Unit Operation
Unit Operation 11
Battery Installation
Slide battery cover off as indicated by arrow.
Install 4 new AAA alkaline batteries according to polarity.
Close battery cover.
AC Adapter jack is on the back side of the monitor. Medical AC adapter(DC 6.0 V,600mA)
can be used with the device (recommended, not provided). The adapter connect pin should
be positive inside and negtive outside with a 2.1mm coaxial joint.
Do not use any other type of AC adapter as it may harm the unit.
Note:Power supply is specified as part of ME EQUIPMENT.
AC Adapter Jack
Unit Operation
System Settings
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 " M " 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 “M” button.
Press“SET” button again to confirm curret month. Continue setting the date, hour
and minute in the same method. Every time the “SET” button is pressed, it will lock
in your seletion and continue in succession ( month,date,hour, minute)
/
Unit Operation
5. Saved Settings
While in any setting mode, press " " 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.Voice Setting
Press "SET" button to enter voice setting mode. Set voice format ON or OFF by
pressing the "M" button.
4.Volume Setting
Press "SET" button to enter volume setting mode. Set the voice volume by adjusting
the "M" button . There are six volume levels.
Applying the Arm Cuff
1. Firmly insert air plug into opening located on left 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)

17
16
18
Unit Operation
Unit Operation
Unit Operation
Unit Operation 15
Testing
Note: Unit will not function if residual air from previous testing is present in cuff.
The LCD will flash " " until pressure is stabilized.
1. Power On
Press and hold " “ button to turn the unit on. The LCD screen will appear
for one second as unit performs a quick diagnosis. A voice tone will indicate when unit is
ready for testing.
2. Pressurization
The unit will automatically inflate to the proper shelf and stop inflating. During this time,
please keep quiet.
Note: Pressurization will gradually subside and ultimately stop when cuff is not
properly applied to the arm. If this occurs, press“ ”button
to turn the unit off.
mmHg
/
3. Testing
After cuff inflation, air will slowly subside as indicated by the corresponding cuff pressure
value. A flashing " " will appear simultaneously on screen signaling heart beat
detection.
Note: Keep relaxed during testing. Avoid speaking or moving body parts.
4. 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.
Indicator
Note: Refer to Page 23~24 for detail WHO Blood Pressure Classification Information.
mmHg
/
mmHg
/
Irregular Heartbeat Indicator
If 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.
5. Deleting/Storing Test Results
User may delete their current test result due to unfavorable testing conditions or for any
other reason. To delete the last test result, press the "SET" button after result is displayed.
If result is not deleted, it will automatically store by date within the previously configured
Memory Group.
Note: Be sure the appropriate Memory Group selection is made prior to testing.
If the number of tests surpasses the allotted 60 memories per group, the most recent tests
will appear first, thus eliminating the oldest readings.
Power Off
turn off the power itself about 3 minutes no operation in any mode.
The " " 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 " " button to turn power off. The cuff pressure will rapidly
dissipate once the unit is off.

21
20
22
Unit Operation
Unit Operation
Unit Operation
Unit Operation 19
Memory Check
With power off, you may check past test results by using the " M " button. The most
recent test result and oldest test result in memory can be viewed by pressing and holding
the " M " button upon activating test results you can press the “ M ”button to scroll
through all test results stored in memory.
No
/
mmHg
/
Note: Previous test results will only be displayed from the most recently used memory
group. To check previous test results in other memory groups, you must first select
the desired group and then turn monitor off.
(See "Select Memory Group" on Page 10.)
Last 3 Tests Average
With power off, press the " M " 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 with voice broadcast. The " " symbol will appear along
with the corresponding WHO Blood Pressure Indicator. The Memory Check mode can be
accessed by pressing the "M " buttons. To check the average results from other groups, select
the desired group first prior to activating the " M " button in the off position. (See "Select
Memory Group" on Page 11.)
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 " " button to turn the unit off.
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.
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
Wireless communication
Frequency range : 2.4 Ghz (2400-2483.5 MHz)
Modulation : GFSK
Antenna gain:0.5dBi

25
24
26
Unit Operation
Unit Operation 23
1. Download the free “JOYTECH healthcare” App: On your mobile phone or table
go to www.sejoy.com.
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 “Blood pressure monitor”.
Bluetooth connection
Using for the first time
The date and time on your monitor will automatically be set when you pair it with your
smart device.
1. Make sure the Bluetooth in your smart device is turned on.
2. Open the app on your smart device and follow the set-up and pairing instructions.
3. Confirm the monitor is connected successfully.
If the monitor is connected successfully to the smart device, “bLE on” will appear on the
monitor display.
Pairing your monitor with a Smart Device
mmHg
/
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.
Example: fluctuation within a day (male, 35 years old)
mmHg
200
150
100
50
6 1 2 1 8 2 4
Upper curve : systolic blood pre ssur e
Lower curve: diastolic blood pressure
Time of day
Blood Pressure Information Blood Pressure Information
: Classification IndicatorBlood Pressure
WHO Blood Pressure Classification Indicator
The DBP-1359b 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
Mild Hypertension
High-n
Normal
Optimal
Moderate Hypertension
ormal
Mild Hypertension
mmHg
/
Troubleshooting
Problem Solution
" "displayed
Connection failure./
Data is not being
transmitted
Cuff is too tight or not
properly positioned on
the arm
Firmly reposition cuff
approximately ( )
above the elbow joint
( See Page 12)
1-2cm 1/2"
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 7)
Blood pressure
results are not
within typical range
Cuff fails to inflate properly
The blood pressure monitor
might not be porperly placed
within the smart device’s
tranmission range and is too far
from the smart device.
Make sure hose is properly
fastened to cuff and monitor unit
If there are no causes of data
transmission interference found
near the blood pressure monitor,
move the blood pressure monitor
within 16ft.(5m) of the smart
device and try again
Possible Cause
Pressurization is over
cuff rated pressure
300mmHg
The blood pressure did not pair
successfully to the smart device
Read user manual carefully and
re-test properly.
Try to pair the devices once again.
Improper operation
The application on the smart
device is not ready.
Read user manual carefully and
re-test properly.
Check the application then try
sending the data again.

29
28
27
30
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.
Health Reminder
Severe Hypertension
Moderate Hypertension
Mild Hypertension
High-normal
Normal
180
160
140
130
120
80 85 90 100 110 Diastolic
( mmHg )
Systolic
( mmHg )
Optimal
Note: 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 time
Blood Pressure Information Blood Pressure Q＆A
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
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.
4.
5. Do not use petrol, thinners or similar solvents.
6. Remove batteries when not in operation for an extended period of time.
7. Do not disassemble product.
Cuff Cleaning: Do not soak cuff in water! Apply a small amount of rubbing alcohol to
a soft cloth to clean cuff's surface. Use a damp cloth (water-based) to wipe clean.
Allow cuff to dry naturally at room temperature. The cuff must be cleaned and disinfected
before use between different users.
8. It is recommended the performance should be checked every 2 years.
9. Expected service life: Approximately three years at 10 tests per day.
10.No service and maintenance while it is in use and maintenance only be performed by service
personnel. Service and maintenance require parts, repair, technical support will be provided.
Maintenance

32
31
33 34
Specifications
Warranty
Product Description
Model
Display
Measurement Method Oscillometric Method
Arm-type Fully Automatic Blood Pressure Monitor
DBP-1359b
Pressurization
Memory
Function
120 Memories in Two Groups with Date and Time
Irregular Heartbeat Detection
WHO Classification Indicator
Low Battery Detection
Automatic Power-Off
voice
Automatic Pressurization
LCD Digital Display Size: 69mm 67mm ×
Power Source
Battery Life
Unit Weight
Unit Dimensions
Cuff Circumference
4 AA Abatteries or Medical AC Adapter(DC6.0V, 600mA)
(recommended, not provided)
Approximately 2 months at 3 tests per day
Approx.480g (16.93 oz.) (excluding battery)
Approx.131.2 x 101.8 x 44.1mm (L x W x H)
Approx.135 (W)×485(L) mm
(Medium cuff: Fits arm circumference 22-36 cm)
Operating Environment
Humidity
Pressure
Temperature 10 ~ 40 (50 ~104 )℃ ℃ ℉ ℉
15% ~ 93% RH
700hPa~1060hPa
Last3 Tests Average
Measurement Range
Pulse
Systolic Pressure
Pulse
60mmHg～280mmHg
30 ~ 180 Beats/Minute
±5%
Diastolic Pressure 30mmHg～200mmHg
Pressure 0mmHg～300mmHg
Pressure
±3mmHg or ±2% of the reading above 200 mmHg
Backlight
Bluetooth
Specifications
International Standards:
1. IEC 80601-2-30, medical electrical equipment - part 2-30: particular requirements for
the basic safety and essential performance of automated noninvasive sphygmomanometers.
(Cardiovascular)
2. ANSI/AAMI ISO 81060-2, non-invasive sphygmomanometers - part 2: clinical validation
of automated measurement type. (Cardiovascular)
3. AAMI / ANSI ES60601-1:2005/(R)2012 and C1:2009/(R)2012 and, a2:2010/(r)2012
(consolidated text) medical electrical equipment -- part 1: general requirements for basic
safety and essential performance
4. AAMI/ANSI/IEC 60601-1-2, Medical Electrical Equipment -- Part 1-2: General
Requirements For Basic Safety And Essential Performance -- Collateral Standard:
Electromagnetic Disturbances -- Requirements And Tests (General II (ES/EMC)).
5. IEC 60601-1-11, medical electrical equipment - part 1-11: general requirements for basic
safety and essential performance - collateral standard: requirements for medical electrical
equipment and medical electrical systems used in the home healthcare 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.
Specifications are subject to change without notice.
Storage Environment
Humidity
Classification:
Temperature:
Internal Powered Equipment,Type BF . Cuff is the Applied Part
≤93% RH
-25 ~70 (-13 ~158 )℃ ℃ ℉ ℉
Ingress Protection Rating: IP20, Indoor Use Only
The Blood Pressure Monitor is guaranteed for 2-year from the date of purchase. If the
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 Pressure 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 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.
Electromagnetic environment
-guidance
ComplianceEmissions test
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.
Group 1,
class B.
Radiated emission CISPR 11
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.
Conducted emission CISPR 11
Harmonic emissions
IEC 61000-3-2 Class A
Voltage fluctuations/
flicker emissions
IEC 61000-3-3 Complies
Group 1,
class B.

36
35
37
Electromagnetic Compatibility Information
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 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
-guidance
Compliance
level
IEC 60601
test level
IMMUNITY test
± 8 kV
contact
±2 kV,±4 kV,
±8 kV,
±15 kV air
Electrostatic
discharge (ESD)
IEC 61000-4-2
Electrostatic
transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
±0.5kV, ±1kV
(differential
mode)
Voltage dips,
short interrupti-
ons and voltage
variations on p-
ower supply in-
put lines
IEC 61000-4-11
0 % UT;
0,5 cycle
At 0°, 45°, 90°,
135°, 180°, 225°
, 270° and 315°
0 % UT; 1 cycle
and
70 % UT;
25/30 cycles
Single phase:
at 0°
0 % UT;
250/300 cycle
Power frequency
(50/60 Hz)
magnetic field
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 comme-
rcial or hospital environment.
30 A/m; 50Hz
or 60Hz
± 8 kV
contact
±2 kV,±4 kV,
±8 kV,
±15 kV air
± 2 kV ,
100kHz, for
AC power port
0 % UT;
0,5 cycle
At 0°, 45°, 90°,
135°, 180°, 225°
, 270° and 315°
0 % UT; 1 cycle
and
70 % UT;
25/30 cycles
Single phase:
at 0°
0 % UT;
250/300 cycle
±0.5kV, ±1kV
(differential
mode)
± 2 kV ,
100kHz, for
AC power port
Mains power quality should be that
of a typical commercial or hospital
environment.
Mains power quality should be that
of a typical commercial or hospital
environment.
Mains power quality should be that
of a typical commercial or hospital
environment.
Electromagnetic Compatibility Information Electromagnetic Compatibility Information
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.
Electromagnetic environment
-guidance
Compliance
level
IEC 60601
test level
IMMUNITY test
Conducted
RF IEC
61000-4-6
Radiated RF
IEC 61000-
4-3
Table 3
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 transm-
itter 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:
3V for 0.15-
80MHz; 6V in
ISM and amate
-ur radio bands
between0.15-
80MHz
450MHz, 28V
/m
710MHz,745
MHZ,780MHz
9V/m
810MHz,870
MHZ,930MHz
28V/m
1720MHz,1845
MHZ,1970MHz
28V/m
2450MHz, 28V
/m
5240MHz,5500
MHZ,5785MHz
9V/m
385MHz, 27V
/m
3V for 0.15-
80MHz; 6V in
ISM and amate
-ur radio bands
between0.15-
80MHz
450MHz, 28V
/m
710MHz,745
MHZ,780MHz
9V/m
810MHz,870
MHZ,930MHz
28V/m
1720MHz,1845
MHZ,1970MHz
28V/m
2450MHz, 28V
/m
5240MHz,5500
MHZ,5785MHz
9V/m
385MHz, 27V
/m
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
output power of
transmitter
W
Table 4
Separation distance according to frequency of transmitter
m
80 MHz to 800 MHz 800 MHz to 2.7 GHz
0.01
0.1
1
10
100
0.12
0.38
1.2
3.8
12
0.23
0.73
2.3
7.3
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 th
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.
e higher