Jamr Technology B02T User manual

薉俒䧭ⱃ勞餘㼓⯕HꜤ晜紺ⰻ곜兜鸑H⛼ⱗ 紺㽯㼄NN
CONTACT INFORMATION:
Digital Blood Pressure Monitor B02T is legal manufactured by:
Company name:
Address:
Website:
Telephone:
Shenzhen Jamr Technology Co., Ltd.
2nd Floor, A-building, No.2 Guiyuan Road, Guihua
community, Guanlan town, Longhua new district,
518100 Shenzhen, PEOPLE’S REPUBLIC OF CHINA
www.jiemeirui.com
0086 755 85292057
Authorized European Representative:
Company Name:
Contact person:
Address:
E-mail:
Shanghai International Holding Corp. GmbH (Europe)
Mr JIN LIANG
Eiffestrasse 80, 20537 Hamburg, Germany.
Fully Automatic Upper Arm
Model Number: B02T
USER’S MANUAL
Blood Pressure Monitor

Thank you for choosing a B02T blood pressure instrument. We're proud
of the care and quality that goes into the manufacture of each and every
item that bears our name. Only the finest materials are used to assure
you of a timeless instrument designed for optimum performance. You'll
quickly appreciate the results, for you now own one of the finest digital
blood pressure instruments that money can buy. With proper care and
maintenance, your B02T automatic blood pressure monitor is sure to
provide you with many years of dependable service. Please read the
following instructions and general information which will prove helpful in
allowing you to enjoy your B02T of Digital In hospitals and physician's
offices throughout the world, where accuracy and dependability are
critical,B02T professional diagnostic products are the instruments of
choice.
Now you too can enjoy the benefits of B02T engineering and quality in
the home. This feature rich instrument was designed to simplify the
measurement of blood pressure and pulse rate at home and deliver
consistent, dependable results.Your B02T digital blood pressure monitor
is a fully automatic digital blood pressure measuring device for use on
the upper arm. It enables very fast and reliable measurement of the
systolic and diastolic blood pressure as well as the pulse by way of the
oscillometric method. This device offers clinically proven accuracy and
has been designed to be user friendly. Read this booklet thoroughly
before attempting to use your new B02T Digital Blood Pressure Monitor.
Thank you for your patronage. It is indeed our pleasure to serve you.
Sincerely,
Shenzhen Jamr Technology Co., Ltd.
A Special Thank You...

1.Introduction and Intended Use
This manual is for B02T models. It is a fully automatic digital blood
pressure measuring device for use by adults on the upper arm at home or
in your doctor’s/nurse’s office. It enables very fast and reliable
measurement of systolic and diastolic blood pressure as well as pulse
through the oscillometric method. This device offers clinically proven
accuracy and has been designed to be user friendly.
Before using, please read this instruction manual carefully and then keep it
in a safe place. Please contact your doctor for further questions on the
subject of blood pressure and its measurement.
Warning:Not suitable for neonatal and infants.
Warning:Not suitable for people who cannot express their ideas correctly.
This device can not be used together with hf surgical equipment.
1.1 Remember…
measurements.
this device.
before prescribing or making adjustments to any medications used to
control hypertension. Under no circumstances should YOU alter the
dosages of any drugs prescribed by your doctor.
before using this instrument on a child.
instrument should only be evaluated after consultation with your doctor.
on the dynamics of blood pressure readings and will help you to obtain
the best results.
with local regulations after reaching the life cycle.
1.Introduction and Intended Use...........................................................
2.Important Information on Blood Pressure and its Measurement.......
3. Components of Your Blood Pressure Monitor..................................
4. Using Your Monitor for the First Time..............................................
5.Measurement Procedure..................................................................
6.Care and Maintenance.....................................................................
7. Warranty..........................................................................................
8. Certifications....................................................................................
9. Technical Specifications..................................................................
10. EMC Declaration...........................................................................
11. Warranty Card...............................................................................
3
6
8
10
12
23
24
24
24
25
30
CONTENTS

NOTE!
Warning:
or electromagnetic fields in the direct vicinity of the device (e.g. mobile
telephones, microwave ovens) during use. These can lead to erratic results.
occur, refer to local distributor or the manufacturer.
1.Too frequent measurements can cause injury to the PATIENT due to
blood flow interference.
2.Don’t place the cuff over wound part.
3.Pressurization of the CUFF can temporarily cause loss of function of
simultaneously used monitoring ME EQUIPMENT on the same limb.
Warning: The device contains sensitive electronic components. Avoid
strong electrical or electromagnetic fields in the direct vicinity of
the device (e.g. mobile telephones, microwave ovens).These
can lead to temporary impairment of the measuring accuracy.
Warning: Do not use cuffs, AC adapters or batteries other than those
included with this product or replacement parts supplied by the
manufacturer.
Warning: Do not use the batteries and the AC adapter to provide power
at the same time.
Warning: This system may fail to yield specified measurement accuracy if
operated or stored in temperature or humidity conditions outside
the limits stated in the specifications section of this manual.
Warning: The separate ac adapter which is intended to connect USB
interface of Blood Pressure Monitor has not been evaluated
according to IEC 60601-1. The safety of the product shall be
reappraised when it power supply by a separate ac adapter.
Note: To obtain the greatest accuracy from your blood pressure
instrument, it is recommended that the instrument be used within
the specified temperature and the relative humidity, please see
the Technical Specifications.
Note: The cuff is treated as the applied part.The user should contact
the manufacturer for assistance, if needed, in setting up, using
or maintaining the device.
Warning: Remove the battery if the ME EQUIPMENT is not likely to be
used for some time.
Warning: The user must check that the equipment functions safely and
see that it is in proper working condition before being used.
Warning: No modification of this equipment is allowed.
Warning: Use of power adapters
1.Adapter: input 100-240v, 50/60hz output DC 5V 1A
2.Do not to position the device to make it difficult to operate the
disconnection device while using adaptor.
3.Do not be prone to water leakage, high temperature, moisture,
direct sunlight and more or more corrosive gas environment. And
Do not use this product in the above environment.
Warning: The device is not suitable for use in the presence of flammable
anesthetic mixtures with air or with oxygen or nitrous oxide.
Warning: This equipment shall not be serviced or maintained while in use
with the patient.
Warning: The patient is an intended operator, the functions of monitoring
blood pressure and pulse rate can be safely used by patient. The
routine clean and changing batteries can be performed by the
patient.
Caution: To avoid any possibility of accidental strangulation, keep this unit
away from children and do not drape tubing around your neck.
Caution: To avoid damaging the device, keep this unit away from children
and pets.
Caution: The standard material used for the bladder and tubing is latex-free.
Attention: Self-measurement means control, not diagnosis or treatment.
Unusual values must always be discussed with your doctor. Under
no circumstances should you alter the dosages of any drugs
prescribed by your doctor.
Attention: The pulse display is not suitable for checking the frequency of
heart pacemakers!
Attention: In cases of irregular heartbeat, measurements made with this
instrument should only be evaluated after consultation with your
doctor.
Contraindication
Use of this instrument on patients under dialysis therapy or on anticoagulant,
antiplatelets, or steroids could cause internal bleeding.
1.2 Warnings and Precautions

2.Important Information on Blood Pressure
and its Measurement
2.1. How does high or low blood pressure arise?
Your level of blood pressure is determined in the circulatory center of the brain
and adjusts to a variety of situations through feedback from the nervous
system. To adjust blood pressure, the strength and speed of the heart (Pulse),
as well as the width of circulatory blood vessels is altered.Blood vessel width
is controlled by fine muscles in the blood vessel walls.
Your level of arterial blood pressure changes periodically during heart activity:
During the “blood ejection” (Systole) the value is highest (systolic blood
pressure value). At the end of the heart’s “rest period” (Diastole) pressure is
lowest (diastolic blood pressure value).
Blood pressure values must lie within certain normal ranges in order to prevent
particular diseases.
Blood pressure is very high if your diastolic pressure is above 90 mmHg
and/or your systolic blood pressure is over 160 mmHg, while at rest. In this
case, please consult your physician immediately. Long-term values at this
level endanger your health due to continual damage to the blood vessels in
your body. If your systolic blood pressure values are between 140 mmHg and
159 mmHg and/or the diastolic blood pressure values between 90 mmHg and
99 mmHg, consult your physician. Regular self-checks are necessary. If you
have blood pressure values that are too low, (i.e., systolic values under 105
mmHg and/or diastolic values under 60 mmHg), consult your physician. Even
with normal blood pressure values, a regular self-check with your blood
pressure monitor is recommended. You can detect possible changes in your
values early and react appropriately. If you are undergoing medical treatment
to control your blood pressure, keep a record of values along with time of day
and date. Show these values to your physician. Never use the results of your
measurements to independently alter the drug doses prescribed by your
physician.
high under conditions of physical or psychological stress, it is possible that
you are suffering from so-called “labile hypertension.” Consult your doctor.
require immediate medical treatment.
There are six grids in the display of device. Please refer to the picture-01-01.
Different grids represent different interval scales of WHO.
2.2. Which values are normal?
Further information
Please refer to the diagram below(Picture-01)

3. Components of your blood pressure monitor
1) Consult your doctor.
2)Increased blood pressure values (various forms of hypertension) are
associated with considerable health risks over time. Arterial blood vessels in
your body are endangered due to constriction caused by deposits in the
vessel walls (Arteriosclerosis). A deficient supply of blood to important
organs (heart, brain, muscles) can result from arteriosclerosis. Furthermore,
the heart will become structurally damaged with increased blood pressure
values.
3)There are many different causes of high blood pressure. We differentiate
between the common primary (essential) hypertension, and secondary
hypertension. The latter group can be ascribed to specific organ
malfunctions. Please consult your doctor for information about the possible
origins of your own increased blood pressure values.
4) There are measures which you can take to reduce and even prevent high
blood pressure.
2. Double users: 2 x 120 sets memory
4. Irregular heartbeat checking
6. Low battery display
8. Auto power-off
10.Volume adjustment
12.Bluetooth function
1.Talking function
3.Cuff self-checking function
5. Average value function
7. WHO function
9. External power adapter support
11. Date/time display
1.Systolic blood pressure
3.Irregular heartbeat symbol
5.Memory symbol
7.USER A
9.Movement error symbol
11.Average value symbol
13.Cuff self-checking function
15.Heartbeat symbol (Flashes during measurement)
16.WHO symbol
2.Diastolic blood pressure
4.Pulse unit symbol
6.Date/Time display
8.USER B
10.Mute symbol
12.Battery low symbol
14. Pulse display
17.Bluetooth symbol
Note: Arm circumference should be measured with a measuring tape in the
middle of the relaxed upper arm. Do not force cuff connection into the
opening. Make sure the cuff connection is not pushed into the AC adapter
port.
2.3. What can be done if regular high or low values are obtained?
Picture-04 Picture-05
3.3 Features of Model B02T
3.2 The symbols on the LCD display
1
2
3
4
5
6
7 8 9 1110 17 12
13
14
15
16
Picture-02 Picture-03
13.1/3 Average Measurements(choose the switch between 1 and 3 on the
right side of the device, 1 means the measurement of one time. And 3 means
device will automatically shows the average result of 3 times measurements )
Music On/Off
1/3 Average
Tests Switch

4. Using your Monitor for the First Time
Use only 1.5V “AAA” alkaline batteries with this device.
1. Press the hook on the bottom of the battery cover and lift the cover off in
the direction of the arrow.
2. Install 4 “AAA” size batteries so the + (positive) and (negative) polarities
match the polarities of the battery compartment, replace the battery
cover.Make sure that the battery cover is securely in position.
4.1 Activating the pre-installed batteries
Insert the cuff tube into the opening on the left side of the monitor indicated
by the drawing of a cuff.
4.3. Cuff tube connection
Battery Installation
Low Battery Indicator
1.When the Low Battery Indicator appears on the display, turn the monitor off
and remove all the batteries. Replace with 4 new batteries at the same time.
Long-life alkaline batteries are recommended.
2.To prevent the damage of monitor from leaked battery fluid, please take out
of battery if the monitor unused in a long time(generally more than 3 months).
If battery fluid should get in your eyes, immediately rinse with plenty of clean
water. Contact a physician immediately.
3. Attached battery is only for testing the function of the monitor, Long-life
alkaline batteries are recommended.
4. Dispose of the device, components and optional accessories according to
applicable local regulations. Unlawful disposal may cause environmental
pollution
5.Battery is dangerous stuff, do not mix it with other rubbish.
Battery replacement
After you load the battery or connect power for the monitor.
4.2. System Settings
A. Setting the User:
Press the SET button and then you can set the A/B user by shifting the A/B
user button.
B.Setting the Year/Month&Date/Time/Volume:
Long press the SET button for more than 3s, and then you can start to set.
Setting the Year:
Initial year is 2019, when the year display is flashing, press the MEM button,
the year will increase by I year each, hold the MEM button and it will increase
continuously 1 by 1, until 2049, and then rollover to 2019, once the year SET
is OK, press SET button to confirm.
Setting Month/Date:
Initial Month/Date is 1/01, when the Month display is flashing, press the MEM
button, the month will increase by 1, press SET button to confirm, and do in the
same way to set the date. Press SET button to confirm.
Setting Time :
When the hour display is flashing, press the MEM button, the hour will
increase by 1, press SET button to confirm, and do in the same way to set
the minute. Press SET button to confirm.
Setting Volume:
When display with SP is flashing, press MEM button to switch volume 1,
volume 2, volume 3 or OFF. Press SET button to confirm.
C.Record Delete:
When you checking the memory data, long press MEM button to delete
existing user measurement data.
Note:
You can’t delete all measurement record from the monitor storage at one
time, if you decide to delete the all record, please keep the record in another
way, in case you need it some days later. Take the battery out won’t lead to a
record missing.

5. Measurement Procedure
You should always be seated and calm before and during measurement.
Note:
measurement. These factors influence the measurement result. Find time to
relax by sitting in an armchair in a quiet atmosphere for about ten minutes
before taking a measurement.
pressure changes during the course of the day, as much as 20-40 mmHg.
5.1. Before measurement:
Please refer to picture-06
a) The cuff is preformed for easier use. Remove tight or bulky clothing from
your upper arm.
b) Wrap the cuff around your upper left arm. The rubber tube should be on
the inside of your arm extending downward to your hand. Make certain the
cuff lies approximately 1/2” to 3/4” (2 to 3 cm) above the elbow. Important!
The on the edge of the cuff (Artery Mark) must lie over the artery which
runs down the inner side of the arm.
c) To secure the cuff, wrap it around your arm and press the hook and loop
closure together.
d) There should be little free space between your arm and the cuff. You
should be able to fit 2 fingers between your arm and the cuff. Cuffs that don’t
fit properly result in false measurement values. Measure your arm
circumference if you are not sure of proper fit.
e) Lay your arm on a table (palm upward) so the cuff is at the same height as
your heart. Make sure the tube is not kinked.
f)Remain seated quietly for at least two minutes before you begin the
measurement.
5.3. Fitting the Cuff
Note: Comparable blood pressure measurements always require the same
conditions!
sure you are in a comfortable, relaxed position and do not flex any of the
muscles in the measurement arm during the measurement. Use a cushion for
support if necessary.
erroneously high or low blood pressure will be measured! Each 25-30cm
difference in height between your heart and the cuff results in a measurement
error of 10 mmHg!
Selecting the correct cuff is extremely important. Cuff size is dependent upon
the circumference of the arm (measured in the center). The permissible range
is printed on the cuff.
Cuff works Under the pressure range 0-300MMHG
The wide range rigid cuff is : 8.7” – 15.7” (22 - 40 cm)
Note: Only use approved cuffs!
values.
to false results. Consecutive blood pressure measurements should be
repeated after a 1 minute pause or after your arm has been held up in order to
allow the accumulated blood to flow away. If you decide to take your Averaging
Mode measurement again, be sure to wait at least one minute beforehand.
5.2. Common sources of error:
Picture-06

Refer to picture-07
The monitor is designed to take measurements and store the measurement
values in memory for two people using User ID A and User ID B.
1. Sit comfortably in a chair with your feet flat on the floor.
2. Select your User ID (A or B).
Stretch your arm forward on the desk and keep relaxing, make sure the palm
of hand is upturned. Make sure arm is in correct position, to avoid body
movement. Sit still and do not talk or move during the measurement.
After the cuff has been appropriately positioned on the arm and connected
to the blood pressure monitor, the measurement can begin:
Install the App from Google play store or Apple app store. Open Bluetooth on
smart phone, and then Turn on the App, the home interface will show up as
picture App 01. Please refer the below steps tell how to remote control on the
App:
1 ) Operate via the App on smart phone with Bluetooth
Click the SET button on the top left corner as picture App 02, then select My
Profile button to edit and save user information (male/female, name, age,
height and weight) as picture App 03.
a)Complete My Profile
After setting My Profile, back to select and save the BM monitor Language as
picture App 04.
b)Setting Language
5.4. Measure Procedure
After the setting is finished, click the HOME button on the top right corner as
picture App 01, then select Bluetooth Device button. A moment later, the
device will be connected as picture App 05 and App 06.
c)Connect Bluetooth
Once the Bluetooth is connected, click the “START” button on the App to start
the testing as picture App 06. When measuring is done, the assessment will
be voiced out and a interface about checking the result will show up as
picture App 07 and App 08.
d)Start the measurement
App01 App02 App03
App04 App05 App06
App07 App08

In the frame of home interface, it will show the last measurement as picture
App 09. You can
check the measurements with detail by clicking the History button as picture
App 10 and app 11 .
e)Checking the measurement 2 ) Operate on the device
a) Press the START/STOP button. The pump begins to inflate the cuff. In the
display, the increasing cuff pressure is continually displayed.
b) After automatically reaching an individual pressure, the pump stops and
the pressure slowly falls. The cuff pressure is displayed during the
measurement.
c) When the device has detected your pulse, the heart symbol in the display
begins to blink.
d) When the measurement has been concluded, the measured systolic and
diastolic blood pressure values, as well as the pulse will be displayed.
e) The appearance of this symbol signifies that an irregular heartbeat was
detected.This indicator is only a caution. It is important that you be relaxed,
remain still and do not talk during measurements.
f) The measurement results are displayed until you switch the device off. If no
button is pressed for 60 seconds, the device switches off automatically.
g) Cuff self-checking symbol ( )
The cuff correct symbol( ) will be displayed if the cuff position is correct,
otherwise the wrong symbol( ) will be displayed. Please check again the
cuff if the wrong symbol( ) is displayed.
h) Movement error symbol ( )
The Movement Error Symbol ( ) is displayed if you move your body during
the measurement. Please remove the cuff, and wait 2-3 minutes. Reapply the
cuff and take another measurement.
Patient Position:
1) Comfortably seated
2) Legs uncrossed
3) Feet flat on the floor
4) Back and arm supported
5) Middle of the CUFF at the level of the right atrium of the heart
NOTE:
App09 App10 App11

1.Recommendation that the PATIENT relax as much as possible and not talk
during the measurement PROCEDURE
2.Recommendation that 5 min should elapse before the first reading is taken
3.Any reading can be affected by the measurement site, the position of the
PATIENT, exercise, or the PATIENT’S physiologic condition
4.Performance of the AUTOMATED SPHYGMOMANOMETER can be
affected by extremes of temperature, humidity and altitude
5.To stop the inflation or measurement, push the START/STOP button. The
monitor will stop inflating, start deflating, and will turn off.
6.After the monitor has detected your blood pressure and pulse rate, the cuff
automatically deflates. Your blood pressure and pulse rate are displayed.
7.The monitor will automatically turn off after one minute.
Recommended Use Methods
This symbol - indicates that certain pulse irregularities were detected during
the measurement.
In this case, the result may deviate from your normal basal blood pressure –
repeat the measurement.
Information for the doctor on frequent appearance of the Irregular Heartbeat
Symbol.
This instrument is an oscillometric blood pressure monitor device that also
analyzes pulse frequency during measurement. The instrument is clinically
tested.
5.5. Irregular Heartbeat Detector
Picture-07
If pulse irregularities occur during measurement, the irregular heartbeat
symbol is displayed after the measurement. If the symbol appears more
frequently (e.g. several times per week on measurements performed daily) or
if it suddenly appears more often than usual, we recommend the patient to
seek medical advice. The instrument does not replace a cardiac examination,
but serves to detect pulse irregularities at an early stage.
5.6. Error Indicates
The following symbol will appear on the display when measuring abnormal
Er 1
SYMBOL
No display
appears
Weak battery or improper
placement
Sensor abnormal
Replace both batteries with new ones.
Check the battery installation for proper
placement of the battery polarities.
CAUSE CORRECTION
Er 2
Er 3
Er 4
Er 5
Er 6
Er 7
Er 8
Check if the pump is working or not. If it
is working, then the problem is sensor
abnormal. Please send it to the local
distributor.
Check if the air releasing is too slow or not.
If it is too slow, please check if there is any
dust in the tube plug of the cuff and the cuff
port in the device. If yes, please clean and
start the measurement again. If no, please
send the device back to the local distributor.
Occasionally-measure for one more time/
Always - send it to local distributor
Tie the cuff correctly and make sure the air
plug is properly inserted in the unit
Correct it and make the measurement again
Please keep quiet and don’t move
Please send back to the local distributor
Please send back to the local distributor
Monitor could not detect pulse
wave or cannot calculate the
blood pressure data
Measurement result is abnormal
(SYS≦45mmHg, DIA≦24mmHg)
Too loose cuff or air leakage
(Cannot inflate to 30mmHg within
15s)
The air tube is crimped
The sensor is sensing great
fluctuation in the pressure
The pressure that the sensor
sensing is over the limit
The demarcation is incorrect or the
device has not been demarcated

At the end of a measurement, this monitor automatically stores each result
with date and time. Each unit stores 120 sets measurements for 2 users,
totally 240 sets(User A and B).
5.7. Memory
shows an average of all measurements stored in the unit. Please note:
Measurements for each user are averaged and stored separately. Be certain
that you are viewing the measurements for the correct user. Pressing the
Memory button again displays the previous value. To view a particular stored
memory, press and hold the Memory button to scroll to that stored reading.
Viewing the stored values
If it is necessary to interrupt a blood pressure measurement for any reason
(e.g the patient feels unwell), the Start/Stop button can be pressed at any
time. The device then immediately lowers the cuff pressure automatically.
5.8. Discontinuing a Measurement
Batteries discharged– replacements required
When the batteries are discharged, the battery symbol will flash as soon as
the instrument is switched on. You cannot take any further measurements
and must replace the batteries.
5.9. Battery Change Indicator
The following symbols may appear in this manual, on the Digital Blood
Pressure Monitor B02T, or on it's accessories. Some of the symbols represent
standards and compliances associated with the Digital Blood Pressure Monitor
B02T and its use.
SYMBOL DESCRIPTIONS
Authorized Representative in the European Community
CE Mark: conforms to essential requirements of the Medical
Device Directive 93/42/EEC.
Date of manufacture.
Manufacturer
Specifies serial number
Type BF applied part
Direct current
DISPOSAL: Do not dispose this product as unsorted municipal
waste. Collection of such waste separately for special treatment
is necessary.
Follow instructions for use
Put up
Fragile
Keep dry
Avoid the sun
Handle gently
Temperature range
No Sterilize requirement
Not category AP / APG equipment
Mode of operation: continuous

6.Care and Maintenance
5.10. Using the AC Adapter
The battery compartment is located on the back side of the unit.
a) Remove cover from the bottom plate, as illustrated below picture-08
b) Insert the batteries (4 x size AAA ). Always use AAA long life batteries or
alkaline 1.5v batteries.
c) The memory retains all values although date and time must be reset - the
year number therefore flashes automatically after the batteries are replaced.
d) To set date and time, follow the procedure described in Section 4.2.
Which batteries and which procedure?
Use four new, longlife 1.5V AAA batteries. Do not use batteries beyond their
expiration date. If the monitor is not going to be used for a prolonged period
the batteries should be removed.
Using rechargeable batteries
You can also operate this instrument using rechargeable batteries.
must not remain inside the instrument, as they may become damaged
through total discharge even when switched off. The batteries must NOT be
discharged in the blood pressure monitor! If you do not intend to use the
instrument for a week or more, always remove the rechargeable batteries!
manufacturer’s instructions carefully.
Note: No power is taken from the batteries while the AC adapter is connected
to the monitor. If electrical power is interrupted,(e.g., by accidental removal of
the AC adapter from the outlet) the monitor must be reset by removing the
plug from the socket and reinserting the AC adapter connection.
Wash hands after each time measurement.
If one device is used by different patients, wash hands before and after each
use.
a) Do not expose the device to either extreme temperatures, humidity, dust or
direct sunlight.
b) The cuff contains a sensitive air-tight bubble. Handle this cuff carefully and
avoid all types of stress through twisting or buckling.
c) Clean the device with a soft, dry cloth. Do not use gas, thinners or similar
solvents. Spots on the cuff can be removed carefully with a damp cloth and
soapsuds. The cuff with bladder must not be washed in a dishwasher, clothes
washer, or submerged in water.
d) Handle the tube carefully. Do not pull on it. Do not allow the tubing to kink
and keep it away from sharp edges.
e) Do not drop the monitor or treat it roughly in any way. Avoid strong
vibrations.
f) Never open the monitor! This invalidates the manufacturer’s warranty.
g) Batteries and electronic instruments must be disposed of in accordance
with the locally applicable regulations, not with domestic waste.
You may also operate this monitor using the AC adapter (output 5V DC/1A
with Micro USB plug).
Use only the approved AC adapter to avoid damaging the unit.
a) Ensure that the AC adapter and cable are not damaged.
b) Plug the adapter cable into the AC adapter port on the right side of the
blood pressure monitor.
c) Plug the adapter into your electrical outlet. When the AC adapter is
connected, no battery current is consumed.
6.1. Accuracy test
Sensitive measuring devices must be checked for accuracy from time to time.
We recommend a periodical inspection of your unit by an authorized dealer
every 1 year. Please turn to local distributor or the manufacturer.
Picture-08

7. Warranty
Your blood pressure monitor is guaranteed for 1 year against manufacturers’
defects for the original purchaser only, from date of purchase. The warranty
does not apply to damage caused by improper handling, accidents,
professional use, not following the operating instructions or alterations made
to the instrument by third parties.
Warranty only applies to the instrument. All accessories including the cuff are
guaranteed for one year, USB charging cable is not included.
There are no user serviceable parts inside. Batteries or damage from old
batteries is not covered by the warranty.
Note: According to international standards, your monitor should be checked
for accuracy every year.
8. Certifications
Device standard:
This device is manufactured to meet the European blood pressure monitors:
IEC60601-1
Electromagnetic compatibility:
Device fulfills the stipulations of the International standard
IEC60601-1-2
9. Technical Specifications
10. EMC Declaration
Model: B02T
Wight: 267g (Batteries and AC adapter are not included)
Display: 58*85mm【3.35”x2.28”】LCD Digital Display
Size: 118 (W) x 110 (L) x 52(H) mm【】
Accessories: 1×Main Device, 1×Cuff, 1×Users manual, 1×Warranty card
Operating Conditions: Temperature: 5℃to 40℃;Humidity: 15% to 93% RH;
Storage And Shipping Conditions:Temperature: -25℃to 70℃;
Atmospheric pressure range:70kPa~106kPa
Measuring method: Oscillometric
Pressure sensor: Resistive
Measuring range: 0-280mmHg
Pulse: 40 to 199 per minute
Cuff pressure display range:<300mmHg
Memory: Automatically stores the last 120 measurements for 2 users (total
240)
Measuring resolution: 1 mmHg
Accuracy: Pressure within ± 3 mmHg / pulse ± 5 % of the reading
Power source: a) 4*AAA batteries, 1.5 V
b) AC adapter INPUT:100-240VAC 50/60HZ OUTPUT:5V DC 1A
Accessories: Wide range rigid cuff 8.7” – 15.7” (22 - 40 cm)
Automatically power off : 60 seconds
Users: Adult
Expected service life of the device and accessories: 5 years
Technical alterations reserved!
1) *This product needs special precautions regarding EMC and needs to be
installed and put into service according to the EMC information provided, and
this unit can be affected by portable and mobile RF communications
equipment.
2) * Do not use a mobile phone or other devices that emit electromagnetic
fields, near the unit. This may result in incorrect operation of the unit.
3) * Caution: This unit has been thoroughly tested and inspected to assure
proper performance and operation!
4) * Caution: this machine should not be used adjacent to or stacked with
other equipment and that if adjacent or stacked use is necessary, this
machine should be observed to verify normal operation in the configuration in
which it will be used

Guidance and manufacture’s declaration – electromagnetic immunity
The device is intended for use in the electromagnetic environment specified below. The customer or
the user of device should assure that it is used in such an environment. 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 level Electromagnetic environment -
guidance Immunity test IEC 60601 test level Compliance
level Electromagnetic environment - guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
Electrical fast
transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
Power frequency
(50Hz/60Hz)
magnetic field IEC
61000-4-8
30 A/m
50/60Hz 30 A/m
50/60Hz Power frequency magnetic
fields should be at levels
characteristic of a typical
location in a typical commercial
or hospital environment.
0 % UT; 0.5 cycle
at 0°,45°,90°, 135°,
180°, 225°, 270°,
315°
0 % UT ; 1 cycle
70 % UT; 25/30
cycle
0% UT; 250/300
cycle
Not applicable Mains power quality should be
that of a typical commercial or
hospital environment. If the user
of the device requires continued
operation during power mains
interruptions, it is recommended
that the device be powered from
an uninterruptible power supply
or a battery.
±8 kV contact
±2 kV, ±4 kV, ±8
kV, ±15 kV air
±2 kV for power
supply lines
±1 kV for input/output
lines
± 1 kV line(s) to
line(s)
± 2 kV line(s) to earth
±8 kV contact
±2 kV, ±4 kV, ±8
kV, ±15 kV air
Not applicable
Not applicable
Floors should be wood, concrete or
ceramic tile. If floor are covered with
synthetic material, the relative
humidity should be at least 30%.
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.
NOTE UT is the a.c. mains voltage prior to application of the test level.
Guidance and manufacture’s declaration – electromagnetic immunity
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
10 V/m
80 MHz to 2.7 GHz
80% AM at 1kHz
3 Vrms
150 kHz to 80 MHz
3 V RMS outside the
ISM band, 6 V RMS
in the ISM and
amateur bands
80% AM at 1kHz Not
applicable
10 V/m
80 MHz to
2.7 GHz
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 separation distance
80MHz to 800MHz:
800MHzto 2.7GHz:
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.
Field strengths from fixed RF transmitters, as determined
by an electromagnetic site survey, should be less than
the compliance level in each frequency range.
Interference may occur in the vicinity of equipment
marked with the following symbol:
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land
mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically
with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic
site survey should be considered. If the measured field strength in the location in which the device is used
exceeds the applicable RF compliance level above, the device should be observed to verify normal operation.
If abnormal performance is observed, additional measures may be necessary, such as re-orienting or
relocating the device.
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
A
B

Guidance and manufacture’s declaration – electromagnetic emission
The device is intended for use in the electromagnetic environment specified below. The customer of the
user of the device should assure that it is used in such an environment.
Guidance and manufacturer’s declaration - 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.
Emission test
RF emissions
CISPR 11
Compliance Electromagnetic environment – guidance
Group 1
The device use RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
The device is suitable for use in all establishments, including
domestic establishments other than domestic and those directly
connected to the public low-voltage power supply network that
supplies buildings used for domestic purposes.
RF emission
CISPR 11 Class B
Harmonic emissions
IEC 61000-3-2 Not applicable
Not applicable
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
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 RF 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)
Separation distance according to frequency of transmitter (m)
150 KHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.7 GHz
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.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
The MANUFACTURER should consider reducing the minimum separation distance, based on RISK
MANAGEMENT, and using higher IMMUNITY TEST LEVELS that are appropriate for the reduced
minimum separation distance. Minimum separation distances for higher IMMUNITY TEST LEVELS
shall be
calculated using the following equation:
NOTE If necessary to achieve the IMMUNITY TEST LEVEL, the distance between the transmitting
antenna and the ME EQUIPMENT or ME SYSTEM may be reduced to 1 m. The 1 m test distance is
permitted by IEC 61000-4-3.
a ) For some services, only the uplink frequencies are included.
b ) The carrier shall be modulated using a 50% duty cycle square wave signal.
c ) As an alternative to FM modulation. 50% pulse modulation at 18 Hz may be used because while it
does not represent actual modulation, it would be worst case.
Where P is the maximum power in W, d is the minimum separation distance in m, and E is the
IMMUNITY
TEST LEVEL in V/m.
Test
frequency
(MHz)
Band
(MHz) Service Modulation
Maximum
power
(w)
Distance
(m)
IMMUNITY
TEST LEVEL
(V/m)
385
450
710
745
780
810
870
930
430-470 GMRS 460,
FRS 460
FM
±5 kHz deviation
1 kHz sine
2
380-390 TETRA 400 Pulse Modulation
18 Hz
1.8 0.3 27
0.3 28
2 0.3 28
2 0.3 28
2 0.3 28
0.2 0.3 9
0.3 9
704-787
800-960
1700-1990
LTE Band 13,
17
GSM 800/900,
TETRA 800,
iDEN 820,
CDMA 850,
LTE Band 5
GSM 1800;
CDMA 1900;
GSM 1900;
DECT;
LTE Band 1,3
4,25;UMTS
Pulse
Modulation
18 Hz
Pulse
Modulation
217 Hz
Pulse
Modulation
217 Hz 0.2
1720
1845
1970
2450 2400-2570
5100-5800
Bluetooth,
WLAN
802.11 b/g/n,
RFID 2450,
LTE Band 7
WLAN 802.11
a/n
Pulse
Modulation
217 Hz
Pulse
Modulation
217 Hz
5240
5500
5785
a)
b)
b)
b)
b)
b)
b)
c)
a)
a)

11. Warranty Card
The First
Repair
The Second
Repair
Faults
Date: Repaired by:
Reasons What is Repaired
Faults
Date: Repaired by:
Reasons What is Repaired
FCC Statement
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.
Caution: Changes or modifications not expressly approved by the party
responsible for compliance could void the user’s authority to operate
the equipment.
NOTE: 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 important
announcement
Radiation Exposure Statement
The device has been evaluated to meet general RF exposure requirement. The
device can be used in portable exposure condition without restriction.
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