Coachcare BEAT User manual

User manual
BEAT Blood Pressure Monitor
Model: B02T
Distributed by CoachCare
97 3rd Avenue, New York, NY 10003 USA
Made in China
Model Number: B02T

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 cannot be used together with hf surgical equipment.
1.1 Remember…
• Only a healthcare professional is qualified to interpret blood pressure
measurements.
• This device is NOT intended to replace regular medical checkups.
• It is recommended that your physician review your procedure for using this
device.
• Blood pressure readings obtained by this device should be verified 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.
• This monitor is intended for use by adults only. Consult with a physician
before using this instrument on a child.
• In cases of irregular heartbeat, measurements made with this instrument
should only be evaluated after consultation with your doctor.
• Familiarize yourself with the section titled "Important Information on Blood
Pressure and its Measurement". It contains important information on the
dynamics of blood pressure readings and will help you to obtain the best
results.
• Host products, including accessories, shall be processed in accordance
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
21
22
22
22
23
28
CONTENTS

54
NOTE!
Warning:
• This device contains sensitive electronic components. Avoid strong electrical or
electromagnetic fields in the direct vicinity of the device (e.g. mobile telephones,
microwave ovens) during use. These can lead to erratic results.
• Do not attempt to service or repair this device yourself. Should a malfunction
occur, refer to a local distributor or the manufacturer.
1. Too frequent measurements can cause injury to the PATIENT due to blood
flow interference.
2. Do not place the cuff over a wound.
3. Pressurization of the CUFF can temporarily cause loss of function if you
are simultaneously 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 its power supply is 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 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 position the device to make it difficult to disconnect the
device while using adapter.
3. Do not allow the device to be prone to water leakage, high
temperature, moisture, direct sunlight or a corrosive gas
environment. 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

76
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.
• If your values are mostly normal under resting conditions but exceptionally
high under conditions of physical or psychological stress, it is possible that
you are suffering from so-called “labile hypertension.” Consult your doctor.
• Correctly measured diastolic blood pressure values above 120mmHg
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)

98
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 malfunc-
tions. 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.
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. 3 means the
device will automatically show the average result of 3 measurements.)
Music On/Off
1/3 Average
Tests Switch

1110
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 the batteries if the monitor will be unused for 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. Batteries can be dangerous. Do not mix batteries with any other trash.
Battery replacement
Configure the system settings after either afterloadaingthebatteryor
connecting themonitor.
4.2. System Settings
A. Setting theUser:
PresstheSETbuttonandthenyoucansettheA/Buserbyshiftingthe
A/Buserbutton.
B.Setting the Year/Month&Date/Time/Volume:
Long press the SET button for more than 3 seconds, and then you can
configure the settings.
Setting the Year:
Initial year is 2019. When the year display is flashing, press the MEM
button. The year will increase by 1 year each time. 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 it 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 it 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 are checking the memory data, long press the MEM button
for more than 3 seconds to delete existing user measurement data.
Note:
You can’t delete all measurement records from the monitor storage at one
times. If you decide to delete all the records, please store the record in
another way, in case you need them at a later date. Taking the battery out
will not delete record.

1312
5. Measurement Procedure
You should always be seated and calm before and during measurement.
Note:
• Avoid eating and smoking as well as all forms of exertion directly before
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.
• Remove any garment that fits closely to your upper arm.
• Always measure on the same arm (normally left).
• Always compare measurements taken at the same time of day, since blood
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 pre-formed 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 towards your hand. Make certain
the cuff lies approximately 0.8 to 1.2 in (2.0 to 3.0 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 circumfer-
ence 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!
•Conditions should always be quiet.
•All efforts by the user to support the arm can increase blood pressure. Make
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.
• If the arm artery lies considerably lower or higher than the heart, an
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!
• Cuffs that are too narrow or too short result in false measurement values.
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!
• A loose cuff or a sideways protruding air pocket causes false measurement
values.
• With repeated measurements, blood accumulates in the arm, which can
lead 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

1514
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 your arm is in correct position. 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:
a) Download your clinic’s app to your mobile device and follow in-app
instructions to set up your blood pressure monitor.
b) Open the app, press START on the device and start measuring!
1 ) Operate via the App on smart phone with Bluetooth
5.4. Measurement Procedure 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 are 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 the cuff
again 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:

1716
1. It is recommended that the PATIENT relax as much as possible and not talk
during the measurement PROCEDURE
2. It is recommended 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

1918
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
With the unit off, press the Memory button. The display first shows "A", then
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 BEAT Blood
Pressure Monitor B02T, or on its accessories. Some of the symbols represent
standards and compliances associated with the BEAT 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
Keepdry
Avoid the sun
Handlegently
Temperaturerange
No Sterilize requirement
Not category AP / APG equipment
Mode of operation: continuous
Troubleshooting

2120
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.
•Only use "NiMH" reusable batteries!
• If the battery symbol the batteries must be removed and recharged!
They 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!
• Recharge these batteries using an external charger and follow manufactur-
er’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 an AC adapter (output 5V DC/1A
with Micro USB plug).
Use only an 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

2322
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 are 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:
EN1060-1 • EN1060-3 • IEC 80601-2-30 • ISO81060-1 • IEC60601-1-11 •
IEC60601-1
Electromagnetic compatibility:
Device fulfills the stipulations of the International standard
IEC60601-1-2
9. Technical Specifications
10. EMC Declaration
Model: B02T
Weight: 267g (AC adapter not included)
Display: 58*85mm【3.35”x2.28”】LCD Digital Display
Size: 118 (W) x 110 (L) x 52(H) mm【4.65"(W)x4.33"(L)x2.05"(H)】
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℃;
Humidity:≤ 93% RH;
Atmospheric pressure range:70kPa~106kPa
Measuring method: Oscillometric
Pressure sensor: Resistive
Measuring range: 60-230mmHg (SYS) / 40-130mmHg (DIA)
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

2524
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
d=0.35√p
d=1.2√p
80MHz to 800MHz:
d=1.2√p
800MHzto 2.7GHz:
d=2.3√p
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
2726
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)

28
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
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