尺⼨：81*140mm
材质：128g铜版纸正反双折⻚4C印刷
⼯艺：折⻚
⽇期：2026-4-28
1. Safety Instructions
Thank you for purchasing Runstar Arm-type Electronic Blood Pressure Monitor.
Please read this instruction manual carefully before use.
This device is not a direct diagnostic device. It is only suitable for monitoring
the blood pressure and pulse rate of adults. The measurement results should
not be used for self-diagnosis or treatment. Please follow your doctor's advice.
Blood pressure is an important indicator of the human circulatory system. The
home blood pressure monitor is easy to use regularly. It is crucial for preventing
cardiovascular disease, encouraging hypertension patients to seek treatment,
and managing high blood pressure.
Blood pressure fluctuates continuously throughout the day and night. The
highest values typically occur during the day and the lowest at midnight. It is
recommended that you measure your blood pressure at roughly the same time
each day.
Various activities such as physical exercise, excitement, stress, eating, drinking,
smoking, body posture, and other factors (including taking a blood pressure
measurement) can influence blood pressure readings. Due to these factors, it is
uncommon to obtain identical blood pressure readings in multiple
measurements.
Definition and Classification of Blood Pressure Levels from WHO-ISH
Classification
Ideal Blood Pressure
Normal Blood Pressure
High Normal
Hypertension GradeⅠ(Slight)
Hypertension GradeⅡ(Medium)
Hypertension GradeⅢ(Serious)
Isolated Systolic Hypertension
<120
<130
130~139
140~159
160~179
≥180
≥140
Systolic Pressure
(mmHg)
<80
<85
85~89
90~99
100~109
≥110
<90
Diastolic Pressure
(mmHg)
2
The information above is for reference only.
3
4
13 1411
1.1 Warning:
This product is intended for daily blood pressure monitoring only and should not
be used for diagnosing hypertension.
● Use this product only for blood pressure measurements. Using it for other
purposes may lead to accidents.
● This device is suitable for use by adults only. Do not use it on infants, toddlers,
children or individuals who cannot express themselves.
2. Working Principle
The Electronic Blood Pressure Monitor adopts the principle of oscillometric
method, receives the blood pressure signal in the armband (cuff) through the
pressure sensor, and measures the systolic blood pressure and diastolic blood
pressure of the human body after processing by the chip. During the process of
measuring blood pressure, the blood pressure sensor detects the number of
pulsations of arterial blood vessels, and then converts them into the number of
pulsations within a minute to achieve pulse rate measurement.
3. Intended Purpose
4. Product Introduction
Product Name: Electronic Blood Pressure Monitor
Model: BP-206
This equipment is composed of a main body and a cuff. The main body is
composed of a central processing unit, a pressure sensor, an air pump, a
solenoid valve, a uniform speed vent valve, a PCB board, and an LED display.
5. Product Structures
6
7
8
7. Product Specification
Item
Operating
Environment
Storage and
Transportation
Environment
Measuring Method
Specification
Temperature: 5℃~40℃
Humidity: 15%~85% RH
Atmospheric pressure range: 70kPa~106kPa
Temperature: -20℃~50℃
Humidity: 15%~85% RH
Atmospheric pressure range: 70kPa~106kPa
Oscillometric method
Pressure Sensor
Resistance type pressure sensor
CONTENTS
1
● Self-diagnosis and treatment based on blood pressure readings are not
recommended. Consult healthcare professionals for proper evaluation and
guidance.
● Patients with severe blood pressure or circulation disorders, as well as blood
diseases, should use this device under medical supervision.
● The displayed pulse reading should not be used as medical heart rate
monitoring.
● Patients with arrhythmia or arteriosclerosis should have their blood pressure
readings confirmed by medical professionals.
● Do not apply the cuff on limbs with intravascular access, therapy, or arterio-
venous shunts to prevent blood flow interference and patient injury.
● Do not use the cuff on an injured or operated arm to prevent further harm.
● In the presence of common arrhythmias, such as premature beats or atrial
fibrillation, the accuracy of the readings may be affected.
● Keep the device away from any great power appliances (e.g. high-voltage
equipment, X-ray machine, and ultrasound equipment, etc.) to prevent
interference during use.
● Keep the device away from active HF surgical equipment, MRI system and RF
shielded rooms which generate strong electromagnetic interference.
● Keep the device away from strong electromagnetic fields (e.g. near the mobile
power supply, microwave oven, etc.), as it may affect accuracy.
● Do not submerge the device in water or any liquids.
● Do not use the device near flammable anesthetic mixtures.
● Do not stack this device with other equipment to prevent operational issues.
● Keep batteries away from fire and out of reach of children and pets.
1.2 Caution
- For best results, practice multiple times to become familiar with the
measurement technique.
- Make sure the batteries are installed correctly before use.
- Inspect the device for any damage before use, especially the cuff. Do not use if
damaged to avoid skin injury.
- Verify the device is in proper working condition before use.
- Do not inflate the cuff when not properly wrapped around the arm.
- If cuff pressure causes discomfort, stop the measurement immediately by
pressing the " " button or pulling out the air tube plug to release the pressure.
- Inaccurate measurement values may occur due to unconscious mis-operation.
- Please follow the provided cleaning instructions in section 11 of this manual to
minimize Cross-infection risks for the intended reuse of the product.
- Do not clean the device with volatile solvents.
- Avoid dropping the device or subjecting it to strong impacts.
- Use only specified accessories provided by the manufacturer to maintain
proper functionality.
- Do not modify this device. Only replace the battery when needed. Other
modifications may create safety risks.
- Follow local laws when disposing of parts or the device at the end of its life
cycle.
Instruction Manual
Electronic Blood Pressure Monitor
Model: BP-206
12
- Various factors such as measurement site, patient position (standing, sitting,
lying down), cuff placement, exercise, and physiological condition can affect
blood pressure readings.
- Extreme temperature, humidity, and altitude can impact the blood pressure
monitor's performance. Use the device in the environment in accordance with
the Instruction Manual.
- Avoid compressing or restricting the air tube.
- Proper cuff tightness is crucial for accurate readings.
- Maintain consistency in measurement timing, body position, posture, and
device usage.
- Please measure both arms for first-time use.
- If cuff pressure causes discomfort, stop the measurement immediately by
pressing the " " button or pulling out the air tube plug to release the pressure.
- Wait at least 2-3 minutes between measurements to allow the artery to return
to its normal state.
- Avoid frequent measurements to prevent blood flow interference and potential
injury.
- Kinking of the air tube can lead to continuous cuff inflation, causing harm to
the patient.
- Cuff pressurization may temporarily affect the function of other monitoring
devices on the same arm.
- Make sure that the blood pressure monitor operation does not excessively
impede blood circulation.
Notice:
15
WARNINGS!
This device should not be used in the vicinity or on the top of other electronic
equipment such as cell phone, transceiver or radio control products. If you
have to do so, the device should be observed to verify normal operation.
● The use of accessories and power cord other than those specified, with the
exception of cables sold by the manufacturer of the equipment or system as
replacement parts for internal components, may result in increased emissions
or decreased immunity of the equipment or system.
Table 3: Not Applicable
Harmonic Emissions (IEC 61000-3-2), Voltage Flicker Emissions (IEC
61000-3-3), Electrical Fast Transients (IEC 61000-4-4), Surge (IEC 61000-
4-5), Voltage dips (IEC 61000-4-11), Conducted Immunity (IEC 61000-4-6)
Note: These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures, objects,
and people.
Radiated RF
IEC 61000-4-3
80MHz- 2.7GHz 10 V/m
380MHz- 390MHz
430MHz- 470MHz
704MHz- 787MHz
800MHz- 960MHz
1.7GHz- 1.99GHz
2.4GHz- 2.57GHz
5.1GHz- 5.8GHz
27 V/m
28 V/m
9 V/m
28 V/m
28 V/m
28 V/m
9 V/m
Table 2: Electromagnetic Immunity
Guidance and Declaration - Electromagnetic Emissions
Electrostatic Discharge (ESD)
IEC 61000-4-2
Power Frequency (50/60 Hz)
Magnetic Field IEC 61000-4-8
30 A/m
Immunity Test
Compliance
±8 kV contact
±15 kV air
Table 1: Electromagnetic Emissions
Guidance and Declaration - Electromagnetic Emissions
The product is intended for use in the electromagnetic environment specified
below. The customer or the user of the product should assure that it is used
in such an environment.
Emission Test
RF emissions CISPR 11
Compliance
Group 1, Group B
ER4
The cuff is too loose or
leaks air.
ER5
The cuff is too tight or
the airway is blocked.
10. Error and Fault Troubleshooting
ER1
ER2
Symbol
Cause
Abnormal sensor signal
Solution
Check whether the cuff is normal and
whether it is worn correctly, re-measure.
No measurement results
Check whether the cuff is normal,
whether it is worn correctly, whether
the blood pressure monitor
communicates with heart. Using
correct sitting posture, keep relaxed
and quiet, re-measure.
ER3
Abnormal
measurement results
Please check if the cuff is normal and
properly worn, and ensure the blood
pressure monitor is aligned with the level
of the heart. Adopt the correct sitting
posture, maintain a relaxed and quiet
state, and take the measurement again.
Check whether the cuff is tight
enough to fit one or two fingers into
your arm; check whether the air
tube joint is inserted into the device;
check whether there is obvious air
leakage between the air tube and the
cuff, re-measure.
Check whether the cuff is tight enough
to fit one or two fingers into your arm;
check whether the air tube connected
to the cuff is bent or pressed by heavy
objects, re-measure.
ER6
ER7
Severe pressure
interference during
measurement.
Pressure exceeds upper
limit
Do not speak during measurement
and keep relaxed.
Do not use force or move the arm
suddenly during measurement,
re-measure.
Check whether there are strong
interference devices in the
measurement environment, such as
mobile phones, motors, and
microwave ovens.
Do not speak during measurement
and keep relaxed.
Do not use force or move the arm
suddenly during measurement,
re-measure.
9.3 Start Blood Pressure Measurement
1) Press the " " button while the device is in shutdown or standby mode to
initiate the measurement process. The cuff will automatically inflate.
Note: During inflation, please keep your arm still to ensure accurate readings.
Any movement may affect the measurement. Feeling the cuff pressure is
normal during inflation. Refer to the "Error and Fault Troubleshooting" section
for error indications.
2) The device will stop automatically after full inflation and proceed to detect
your pulse rate.
1. Safety Instructions .................................................................2
2. Working Principle...................................................................4
3. Intended Purpose ..................................................................4
4. Product Introduction ..............................................................4
5. Product Structures.................................................................4
6. Symbol Explanation...............................................................5
7. Product Specification.............................................................6
8. Settings..................................................................................8
9. Blood Pressure Measurement Method ..................................9
10. Error and Fault Troubleshooting ..........................................11
11. Maintenance and Cleaning ..................................................12
12. Product Charging.................................................................13
13. After-sale Service ................................................................13
14. EMC Information and Statement .........................................13
15. Manufacturer Information ....................................................15
15. Manufacturer Information
8. Settings
9 10
11.1 Maintenance
1) Do not disassemble, repair, replace parts, or modify the device. Contact the
seller or manufacturer for any necessary assistance.
2) Avoid exposing the equipment to high temperatures, moisture, excessive
humidity, or direct sunlight. Follow the instructions in this manual for proper
usage and storage under specified environmental conditions.
3) Avoid folding, pulling, or twisting the cuff containing an airbag.
4) Store the device in a secure location out of children's reach.
11.2 Cleaning:
1) Clean the device with a soft, dry cloth or a slightly damp cloth. It is advised
11. Maintenance and Cleaning
Made in China
Measuring Range
Measuring
Accuracy
Blood Pressure/Indication Range: 0-299mmHg (0-39.9kPa)
Pulse Rate: 40-199 beats/minute
Blood Pressure: ±3mmHg (±0.4kPa)
Pulse Rate: ±5 %
Reproducibility of
Blood Pressure
Determination
Resolution
Power Supply
Memory Capacity
Measure Time
Auto off
Dimension
Weight
Package List
Lifetime
1mmHg (0.1kPa)
Rechargeable Lithium-ion (1000mAh/3.7V/3.7Wh)
2 users with 99 memories each
<60s
Auto power off after 60 seconds of inactivity
Approx. 150mm (l) × 114mm (w) × 65mm (h)
(5.91" × 4.49" × 2.44")
Approx. 310g (not included cuff )
Cuff, USB-C cable, Instruction manual
5 years
Stability of Blood
Pressure
Determination
Cuff Specification
Display LED display
Maximum allowed
pressure
299mmHg
Cuff deflation
pressure
＜10s deflate 260mmHg to less than 15mmHg
Static leakage
≤±6mmHg for 6min
Manometer
test mode
Dynamic pressure mode, Static pressure mode
Approx. 22 to 42cm (8.6" to 16.5")
Statement
The electronic blood pressure monitor has been performed clinical
investigation according to ISO 81060-2: 2018 Non-invasive
sphygmomanometers - Part 2: Clinical investigation of intermittent
automated measurement type. The mean error and the maximum
permissible standard deviation met the requirements of ISO 81060-2:
2018.
±3mmHg (Root mean square between 10
measurements and their average)
≤±3mmHg (Maximum deviation between the
maximum value of 10 measurements and its average)
DC 5.0VCharging Voltage
- This monitor is clinically investigated in accordance with the
requirements of IEC 80601-2-30:2018.
- This monitor’s biocompatibility has been verified by test according to ISO
10993 series standards.
- This monitor has been designed and tested in accordance with EN
60601-1:2006+A1:2013 to ensure safety and essential performance.
- Any serious incidents should be reported to the EU representative,
manufacturer, and competent authority.
9. Blood Pressure Measurement Method
9.1 Check and Prepare Before Measurement
1) Avoid exercising, bathing, drinking stimulating drinks (such as coffee or
alcohol), and smoking within 30 minutes before the measurement.
2) Rest in a comfortable and stable environment for at least 5 minutes before
the measurement.
3) Remove tight-fitting or thick clothing from your arm, bare the upper arm or
wear thin shirts for the measurement.
4) Sit in a chair with your feet flat on the floor and arms on the table.
5) Make sure the batteries are correctly installed.
9.2 Apply the Cuff on the Arm
1) Take out the cuff and open it into a tubular shape, ensuring it is suitable for
the arm to fit in.
2) Wrap the cuff around the upper arm. Make sure the air tube is positioned
along the forearm and on the inside of your arm.
Warnings:
- This product should not be used close to or stacked with other devices. If it
must be used close to or stacked with other devices, it should be observed to
verify that it can operate normally under the configuration used.
14. EMC Information and Statement
Precautions:
- This product conforms to the electromagnetic compatibility requirements of
IEC 60601-1-2:2014 standard.
- The user shall use the device according to EMC information provided in this
manual.
- Portable and mobile RF communication equipment may affect the
performance of the product. Avoid strong electromagnetic interference, such as
12. Product Charging
12.1 How to Charge
This monitor is powered by a built-in lithium-ion battery. Please ensure the
device is sufficiently charged before use. When the battery is low, please
charge the device using the steps below:
1) Insert the charging cable into the power port on the monitor.
2) Plug the USB end of the cable into a DC 5V/1A USB power adapter, then
plug the adapter into a standard 110V-240V AC outlet. The battery indicator
will flash sequentially during charging.
3) Once fully charged, the battery indicator will stop flashing and remain solid.
Unplug the adapter and disconnect the cable.
Important Safety Notes:
When used with a power adapter, this device is classified as a Medical
Electrical System. Please ensure the adapter complies with the requirements
of GB9706.1-2020.
12.2 Battery Life
A full charge provides approximately 150 measurements under normal usage
conditions.
13. After-sale Service
Visit official website or scan QR code to
activate lifetime warranty：
www.runstar.com
5
LED Display Explanation
The WEEE mark for electronic product recovery indicates
that when the end user intends to discard the product, it must
be taken to the appropriate facility for recovery and
recycling.
Manufacture date
Manufacturer
Production batch number
6. Symbol Explanation
Graphic Symbol
Content
WARNING Indicates a potentially hazardous situation, which
if not avoided, could result in death or serious injury.
CAUTION Indicates a potentially hazardous situation, which
if not avoided, may result in minor or moderate injury to the
user or patient or damage to the equipment or other property.
Please read the instructions before use.
Cover Protection Class IP22:2 Protected against solid
foreign objects of 12,5 mm ∅ and greater; 2 Protected
against vertically falling water drops when enclosure tilted
up to 15°.
It belongs to the electric shock protection BF application
part.
UN38.3
Lithium battery certification
UDI
Unique device identifier
1 2
mmHgmmHgmmHg
kPakPakPa
SYS
DIA
PULPULPUL
/min/min/min
M
AVG
MO.
OK
OKOK
OK
!
PM
1
2
3
4
5 6 7 8 9
10
11
12
13
14
15
16
17
18
User Icon
Systolic Blood Pressure
Diastolic Blood Pressure
Pulse Rate Icon
Battery Indicator
① ② ③ ④ ⑤
⑥ ⑨
10
AM/PM Icon
Average of Last 3
Measurements
Movement Error
12
Irregular Pulse
13
Cuff Wrap Guide: Loose
14
Cuff Wrap Guide: Correct
Normal Blood Pressure
15
Blood Pressure Out of Range
⑦
Sound Icon
Wireless Connection Icon
Month Icon
⑧
Memory Icon
11
Day Icon
16
17
18
mmHg
1
mmHg
1
Start Measuring Inflating
mmHg
1
mmHg
1
SYS
DIA
PUL
/mi n
Once the measurement is complete, your blood pressure and pulse values will
be displayed.
Note: Maintain a correct posture and a quiet environment during measurement.
To end the measurement, press the " " button to stop the pressure and
deflate the cuff.
3) After the measurement, remove the cuff, press the " " button to manually
turn off the device. If no action is taken, the device will turn off automatically
after 60 seconds.
to clean the device before each use.
2) Disinfect the device with a soft cloth dampened with 75% medical alcohol
after cleaning. Daily disinfection is recommended. Allow the device to air dry
in a cool place after disinfection.
3) Avoid using strong volatile or corrosive solvents or abrasive cleaners.
This device is a digital monitor intended for use in measuring blood pressure
and pulse rate in adult patient population who can understand this instruction
manual with the arm circumference range printed on the arm cuff.
Population: Adult, not including pregnant patients.
Contraindications: No known contradictions.
Side effects: Not applicable.
Cuff
Memory Button
ON/OFF Button
Set Button
Power Port
LED display
Air Tube Port
① ② ③ ④ ⑤ ⑥ ⑦
①
②
③
④
⑤
⑥
⑦
close to mobile phones and microwave ovens.
- The guidance and manufacturer's statement are detailed in the table below.
3) The bottom edge of the cuff should be
2cm to 3cm (about 1 inch) above the
elbow joint.
4) Wrap the cuff securely with the Velcro
fastener. Leave enough space to fit one
finger between the cuff and your arm.
5) Plug the arm cuff into the monitor by
fully inserting the air tube plug into the air
tube port (located on the left side of the
monitor).
Correct measurement posture:
A. Rest your elbows on the table.
B. Align the cuff with your heart height.
C. Relax your body with palms facing up.
8.4 Read the Memory
While the device is turned off, press the " " button to view the stored
memory values.
8.3 Date/Time Setting
1) While the device is turned off, press the " " button three times to
enter year adjustment. Then press the " " button to adjust the year.
2) Press the " " button to make the month flash, entering the month
setting mode. Then press the " " button to adjust the month.
3) Press the " " button to make the date flash, entering the date setting
mode. Then press the " " button to adjust the date.
4) Press the " " button to make the time flash, entering the hour format
setting mode. Then press the " " button to adjust the 12/24-hour format,
5) Press the " " button to make the hour flash, entering the hour setting
mode. Then press the " " button to adjust the hour,
6) Press the " " button to make the minute flash, entering the minute
setting mode. Then press the " " button to adjust the minute.
7) Press the " " button to save the setting and turn off the device.
Note: New settings will not be saved after a power outage.
8.1 Unit Switching
1) While the device is turned off, press the " " button to switch units.
2) If the unit is mmHg, press " " button to switch to kPa. When the
0.0kPa displayed, the setting is successful.
3) Press the " " button to save the setting and turn off the device.
8.2 User Switching
1) While the device is turned off, press the " " button twice to enter the
user setting mode.
2) Press the " " button to switch between "User 1" and "User 2".
3) Press the " " button to save the setting and turn off the device.
Note: The device will automatically power off and the settings will be
saved after 60 seconds of inactivity.
8.6 Clear Memory Data
1) While the device is turned off, press the " " button 10 times until "CL"
is displayed.
2) Press the " " button and " " button at the same time for about 2
seconds. When the screen displays "--", all memory data will be deleted.
Note: All measurement data for all users will be deleted at once.
8.5 Voice Settings
1) While the device is turned off, press the " " button 9 times, the sign
"SP" will be displayed.
2) Press the " " button to switch between “ON” (voice enable) and
"OFF" (voice disable). Then press the " " button to save the setting and
turn off the device.
Version: 1.0
Revise date: 2023-02
MR unsafe
MR
MEDICAL DEVICE SINGLE AUDIT PROGRAM
Manufacturer: Shenzhen HBcare Technology Co.,Ltd
Manufacturer Address: 4-5/F, Building 11, Tongfuyu Industrial Park,
Lezhujiao, Huangmabu Community, Hangcheng Street, Bao’an
District, Shenzhen, China
DAY
