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User Manual | Users Manual | 968.85 KiB | August 25 2022 | |||
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1 | User Manual | Users Manual | 968.85 KiB | August 25 2022 |
Upper Arm Blood
Pressure Monitor
Model :FDBP-A10BL
USER MANUAL
Subject to our actual product.
■ Thanks for using our product.
■ Take care of this instruction manual.
■ Please read this manual carefully before using.
Precaution:
Please read the instruction manual carefully before use it.
If you have any questions, please consult the salesperson
in the purchasing center or ask your doctor.
FCC ID:PONFDBP
CONTENT
1. Quick instructions ........................................................................1
2. Product Structure Description ...................................................1
3. Warnings and precautions ..........................................................2
4. Instruction ........................................................................................2
5. Product operation instructions ................................................3
6. Connect the cuff .............................................................................3
7. Correct measurement posture .................................................3
8. Measuring blood pressure .........................................................4
9. View measurement results .........................................................4
10. Set the function ..........................................................................5
11. WHO blood pressure definition function ............................6
12. Maintenance and storage ........................................................6
13. Blood pressure measurement Q&A ...........…........…............7
14. Blood pressure knowledge ......................................................7
15. Error warning/Troubleshooting ........................................8
16. Reference standard .....................................................................9
17. Place in ...........................................................................................9
18. Technical specifications ........................................................... 9
19. List of attachment .....................................................................10
20. Standardized symbolic description .................................10
21. Electromagnetic compatibility information ...............10
1.Quick instructions
2.Product Structure Description
2.1 Upper Arm Blood Pressure Monitor
2.2display
2.3cuff
3. Warnings and precautions
3.1 Warning
• This product is not suitable for newborns.
• This product is for home use only. When the measurement is complete, consult your doctor if you have any doubts
about the measurement results.Do not self-diagnosis and treatment according to measurement results.
• When common arrhythmia (such as atria premature beats, premature ventricular and atrial fibrillation) occurs, it will affect the
measurement accuracy of blood pressure. If it is only sporadic, please take a rest for two hours before measuring. If it is a frequent
nature, please go to the hospital for confirmation and treatment immediately.
• If the airbag is inflated for a long time, immediately press the [START/STOP] button to stop the measurement. Continued
inflation presses the hand arm, which can cause limb numbness.
• Do not allow children to use the instrument without authorization: Some small parts may cause ingestion.
• It is forbidden to measure blood pressure on the side where the breast is removed.
•Do not allow children to use instruments without permission:Small parts can cause the risk of ingestion.Hose may cause
choking hazard.
•Do not allow service and maintain the product while in use
•Do not allow use the product while in charging
•In order to avoid bacterial cross-infection, the product alone is recommended
•pressurization of the CUFF can temporarily cause loss of function of simultaneously used monitoring ME EQUIPMENT on the
same limb;
•do not used together with HF SURGICAL EQUIPMENT
3.2 Precautions
• Avoid high temperature, humidity, dust and direct sunlight.
• Avoid damage to the arm band and rubber tube due to folding
• Do not disassemble this unit yourself! Otherwise it will cause the manufacturer's school pressure calibration to fail!
• Avoid falling or violently vibrating the body.
• The normal measurement period is about 1 minute. If the measurement is not stopped for a long time, please press
the [START/STOP] button to stop the measurement. Avoid numbness of the limbs due to prolonged compression of the arm.
• Original or medically compliant power adapters (eg iec 60601-1 certified) must be used, and non-original
accessories may present unpredictable risks.
• For better reading of the display, please note the following visible conditions: - Ambient brightness: 100lx~1500lx
- Line of sight: less than 30cm - Viewing angle: normal display ± 30 °
• Extreme temperature, humidity, and altitude conditions can affect the performance of the measurement, and the
Upper Arm Blood Pressure Monitor may not meet the stated performance specifications.
• Do not put the cuff on the wound, which will cause further damage.
• Do not measure blood pressure if there is intravascular access or treatment, or arteriovenous (A-V) shunt.
3.3 Purpose/intended use of device
Upper Arm Blood Pressure Monitor is intended to measure the blood pressure and pulse rate of adults and children at least 12
years of age, at household or medical center. (Not suitable for neonate, pregnancy or pre-eclampsia). with the cuff around the
left upper arm according to the instruction in the user's guide manual.
the patient is an intended operator
Intended operator should receive at least 8 years of education so that can read and understand the user manual
4.Instruction
4.1 Product Features
The FDBP-A10BL is an Upper Arm Blood Pressure Monitor that simultaneously measure systolic, diastolic blood pressure and
pulse rate through the principle of pressure oscillation.Not only its accuracy reaches the medical grade, but also suitable for
home health care. In addition, the humanized design provides users with the greatest convenience.
4.2 Self -Measurement
• Please keep in mind :self-measurement is equal to self control, not diagnosis or treatment. If you have abnormal
blood pressure, should consult physician immediately and follow physician’s instructions to take medicine.
• The pulse displayed by this unit is not suitable to be a fixed frequency detector that identify heart rate! Those who have a history of
heavier arrhythmia, should consult a professional physician about measured blood pressure value and confirm.
4.3 Electromagnetic Interference
Due to the unit has sensitive electronic components, avoid using it directly in strong electromagnetic environment (such as:mobile
phone, microwave oven etc.), as it may lead to inaccurate results.
5.Product operation instructions
5.1unpacking
Unpack the box and lay the product flat on the table.
Note:If you bring the product from a storage environment, place it in a normal use
environment for 20 minutes
5.2 battery
If there is a signal of low power on the display, connect your charger.
Icon lit: Battery is low.
Lo icon lights up: battery is exhausted.
Please connect adapter to charge.
※ Do not use this product while charging. No measurement function during charging
Please pay attention!
Once the signal of low power is displayed, the product will not
be used unless you charge it.
Note:
• Consult the dealer at the place of purchase for any adapter problems.
5.3Use adapter
Except the battery, this unit can also use a adapter (USB 5V).Must use the original or medical power supplies that meet medical
standards.
(example: IEC 60601-1 certification). Transformer connects to power socket is shown on the following. Adaptor connects to the
power socket of the product and press the START/STOP/memory button to test if it is power.
If power failure suddenly during measurement (for example, adapter plug is disconnected to power outlet), adapter single-pin
plug should be unplugged and reinsert into the unit again.
Any problems about adapter, please consult purchased dealer locally.
6.Connect the cuff
The correct method of using the cuff:
a.Insert the air tube plug into the air tube connector
a. Make sure the arm strap connector is fully inserted into the
Upper Arm Blood Pressure Monitor vent.
b. Please take off your coat, sweater and
other thicker clothes, do not have any
accessories, bare upper arm or wear a
thin shirt for measurement.
c. Wrap the cuff around the left arm.
d. Do not wrap the cuff too tightly (It
is the best to easily insert a finger)
and the lower edge of the cuff should
be 2~3 cm from the hand bend (as shown).
e. After wrapping the cuff around the upper arm, place the air tube on
the inside of the arm and on the same line as the middle finger (as
shown).
f. When measuring, please sit in the chair, place your feet flat on the
floor, place your arms on the table, and put the arms and the heart
on the same level to relax and measure in a relaxed and natural
posture.
7.Correct measurement posture
Preparation before measurement
For wireless features, see the attachment
A v o i d e a t i n g , s m o k i n g o r any form of activity before
measuring, all of which will affect the measurement. Try to relax
in a quiet environment, rest for 10 minutes, and then take
measurements.
If you have heavy clothing, please detach from the upper arm.
Select the arm for blood pressure measurement (usually the left
arm) and take blood pressure measurements on the same arm
and in the same area.
Regularly take blood pressure measurements at the same time
every day, because blood pressure will change differently over
time.
Common factors that lead to erroneous
measurements
Note: Comparative blood pressure measurements should be performed in the same condition
(usually referred to quiet conditions)!
If the arm artery is low (high) relative to the heart , it will result in a high (low) blood pressure value. (Each 15cm height
difference will produce 1.3kPa/mmHg error value)!
This unit is not suitable for newborns.
Note: Please use the original arm cuff that meets the clinical test requirement!
The loose or air bag exposed cuff will lead to false blood pressure.
The arm will compress the blood vessels due to repeated measurements. This condition will also cause a biased blood
pressure value. Therefore, when making repeated measurements, be sure to rest for 3-5 minutes or raise your arm for 3 minutes
to reduce the congestion.
8.Measuring blood pressure
8.1 Start measuring
Press the [start/stop] key to start automatic measurement.
Stop measurement
If there is any discomfort or for some reason, such as when the airbag is in a persistent over-inflated state, there may be a risk.
At this time, the blood pressure measurement must be stopped. You can press the [START/STOP] button and the Upper Arm
Blood Pressure Monitor will immediately release the air pressure in the cuff to suit your need.
2 Confirm measurement results
Automatic storage of measurement results. SYS
1) irregular pulse: DIA
PULSE
The unit can detect the arrhythmia. When this symbol appears after the measurement is completed, it may differ from your
normal blood pressure. Please measure it a few more times. If this symbol is displayed frequently, it is recommended that you
tell the doctor about this situation, and ask the doctor for frequent information on the irregular heartbeat indicator.
2) Error action prompt function:
The display represents speaking or moving during the measurement,
The measurement may not be correct. Please measure again.
3)Cuff wearing self-test prompt icon:
When the cuff is wrapped correctly, the screen displays
When the cuff is wrapped too loosely, the screen displays
Please press the [START/STOP] button to turn off the power, rewind the cuff correctly, and measure again
8.3 Removing the Arm Strap.
8.4 Automatic Shutdown
The number is displayed until the power is turned off (if you forget to turn off the
power, the monitor will automatically turn off after 30 seconds to save power).
Note: depending on the location, this product is available in mmHg or kPa display
mode, and can be used according to the selected display mode according to this
operating instructions.
9.View measurement results
The Upper Arm Blood Pressure Monitor can automatically record 120 measurements.If the measurement result is
remembered more than 120 times, the earlier measurement record will be deleted and the new measurement result will be recorded.
9.1 Check the memory
Press the [MEM] button to display the latest measurement results
Query memory value
9.2 Delete memory
This Upper Arm Blood Pressure Monitor can only delete all records at one time. Cannot delete a
single record.
When the measurement result is displayed, press and hold the [MEM] key while pressing the
[start/stop] key for about 3 seconds.
※Please do not press the 【start/stop】key first, otherwise the power will be cut off.
10. Set the function
The system defaults to user
1. In shutdown mode, press the [SET] button to switch to user 2, which can be switched cyclically.
10.2Setting time, date and kPa/mmHg unit selection
The unit automatically records the date and time of each measurement, which is very important.Because the blood pressure
of the human body is constantly changing on the same day, it is recommended that you set the correct date and time
immediately after installing the battery.Please set the correct date and time as following,(Example: enter time and day -12:08
pm. on December. 08th )
1. In the shutdown mode, press the [SET] key for 3 seconds, the product enters the function setting mode (if not selected, the
system defaults to the manufacturing time).The last two digits of the year will flash on the screen. You can enter the year by
pressing the [MEM] button (for example, you can increase the year from 21 to 22 by pressing it one time).
2.Press the [SET] button, and there will be a jump of the month in the left corner of the screen. At this time, the first digit of the
month starts to flash. You can enter the month by pressing the [MEM] button (for example, you can increase the month from
January to 12 months by pressing 11 times).
3.Press the [SET] button again, the screen will switch to the date setting, at this time, the last two digits of the date will start to
flash. You can enter the date by pressing the [MEM] button (for example, you can change the date from 1st to 08th by pressing
the button 7 times)
4Press the [SET] button again, the screen will switch to the time setting. At this time, the first digit (indicating hour) starts to
flash. Please input the time by pressing the [MEM] button (for example, you can change the time from 0:00 to 12:00 by pressing
the [MEM] button 12 times).
5.Press the [SET] button again, and the last two digits (in minutes) will start to flash. You can enter the minute by pressing the
[MEM] button (for example, pressing the button 8 times will increase the time from 0 minutes to 8 minutes).
6.Press the [SET] button again to enter the kPa/mmHg unit selection. You can select kPa or mmHg by pressing the [MEM]
button, “0.0” will display on the screen when kPa is selected, and “0”will display when mmHg is selected.
8. In the last step, press the [SET] button, and the date will be displayed after the setting is completed (the date will be
displayed first, and it will automatically jump to the time after 3 seconds). When there is no operation, it will automatically shut
down after 30 seconds.
11.WHO blood pressure definition function
This unit comes with a SYS warning and a warning bar reminder function. we can read from the height of the World Health
Organization blood pressure indicators, blood pressure is distributed in DIA (no WHO voice prompts) and ideal blood
pressure, normal blood pressure (green), normal partial hypertension (yellow), mild hypertension, moderate hypertension, and
severe hypertension (red). After the measurement is completed, the black zebra crossing appears at the corresponding position
according to the SYS and DIA.
The correspondence between color and blood pressure values is shown in the following table:
The meaning of the indicator color:
Green, it represents normal blood pressure.
Red,please consult physician
12.Maintenance and storage
11 Remove the plug of the air pipe
2 Gently bend the air pipe of the arm band and put it into the arm band
Do not over bend the windpipe of the arm band.
Otherwise it may not be possible to make a correct measurement.
Clean
When the product is dirty due to prolonged use, it is necessary to
follow the requirements for cleaning:
When the outer shell is dirty, gently wipe it with a wet soft cotton
cloth. If the outer shell is seriously soiled, wipe it with a soft dry
cloth dipped in 75% medical alcohol. It is recommended to clean at
least once a month.
Please pay attention to keeping the cuffs clean. After repeated
use for a long time, 95% concentration of medical alcohol can
be sprayed on the inside of the measuring contact of the cuff for
disinfection. If it is heavily soiled, it is recommended to replace the
cuff. You can contact the dealer or manufacturer for disposal.
This product is intended for home use and is a personal product.
Please use medical alcohol to clean it before use it to others.
Note: This product is not waterproof. Please be careful not to be
too moist when cleaning. Also it is not suitable for splashing with
water.
Please do not use any other solutions to clean this unit except
those method recommended by manufacturer.Because it may
damage your Upper Arm Blood Pressure Monitor.
Avoid washing the cuff!
Maintenance
Our company does not authorize any organization and individuals
to carry out maintenance.Therefore, please do not disassemble
or adjust this unit if you feel the product has functional problems.
Electronic Upper Arm Blood Pressure Monitor is a very precise product, any improper
maintenance, disassembly and adjustment will lead to inaccurate
measurement.
Avoid the damage of cuff and rubber tube caused by folding
Avoid falling or shaking this unit violently.
Within warranty period,please contact the distributor or
manufacturer if you have any questions about the product.
■ Calibration
The electronic Upper Arm Blood Pressure Monitor has been calibrated at the
time of manufacture. We recommend a static pressure test for this
Upper Arm Blood Pressure Monitor every 2 years, with the option of an authorized
dealer to calibrate your device. At any time, if you question the
accuracy of the measurement, please feel free to contact your dealer or
manufacturer for disposal.
13.Blood pressure measurement Q&A (when the measurement
value is high/low)
Q: Why is the blood pressure value measured at home lower than the blood pressure value
measured in the hospital?
A: I often feel nervous when measuring blood pressure in the hospital, so the measured value will
be high. Because I feel calm when measuring in my own home, sometimes it is
20mmHg~30mmHg (2.7kPa~4.0kPa) lower than the hospital's measurement value. It is very
important to know the blood pressure measurement value when you are calm at home.
Answer: If the measurement position is higher than the heart, the measurement value will also be
low. If the table where the Upper Arm Blood Pressure Monitor is placed is too high, it will cause
the armband to be higher than the heart, and the blood pressure value measured at this time will
also be low.
Q: Why is blood pressure measured at home higher than at the hospital?
A: If you are taking blood pressure medication, it will cause your blood pressure to rise when it
loses its potency.After a few hours of taking blood pressure medication, the effect wears off and
blood pressure increases accordingly.Consult your doctor for details.
A: Incorrectly positioned armbands can sometimes lead to high measurements.When the
armband is in the wrong position, the blood pressure monitor has a hard time picking up arterial
signals, and the blood pressure readings are too high.Please confirm again that the binding
position of the armband is correct.
A: Wrapping the armband too loosely can sometimes lead to high measurements.If the band is
wrapped too loosely, the pressure does not reach the arteries, so the blood pressure is measured
higher than it actually is.Please be careful not to leave a gap between the cuff and the arm when
binding.
A: Incorrect posture during measurement can sometimes lead to a higher measurement
result.Measurement postures such as sitting cross-legged, sitting on a couch or at a low desk, or
bending forward, can result in high blood pressure readings because of abdominal pressure or
because the armband is lower than the heart.
Q: Why is the blood pressure value measured each time different?
A: The blood pressure will vary according to the measurement time period. Even within a day,
such a change will occur. In order to manage blood pressure correctly, please take measurements
at the same time every day.
Q: Why is there pain and numbness around the arm strap?
A: This is a temporary phenomenon. Please do not worry.Some pain and numbness may be felt in
the arm as blood flow in the artery is temporarily stopped by tightening the arm band to measure
blood pressure.When the armband is removed, a short rest can relieve the pain.
Q: What is the key to blood pressure management?
A: Please record your medication status and living conditions.Recording daily changes in blood
pressure can provide a clearer picture of blood pressure trends, which can be more helpful in
personal health management.In addition, this record is very important for the doctor's
diagnosis.Therefore, we recommend that you record your blood pressure measurements as well
as the relevant measurement environment (such as the use of antihypertensive drugs, life status,
etc.).
Q: When is the best time to measure blood pressure?
Answer: The best time to measure blood pressure is within 1 hour after getting up in the morning,
or before going to bed at night. It is also recommended to measure at the same time every day.
14.Blood pressure knowledge
14.1High and low pressure
The highest blood pressure when the heart contracts and sends blood to the arteries is called "high pressure", and the lowest
blood pressure when the heart expands to store the next blood is called "low pressure". They are called systolic blood pressure
and diastolic blood pressure.
The following is a standard taxonomy established by the World Health Organization (WHO) for blood pressure, showed in the
below table: Unit (mmHg)
At the same time, the United Nations Committee on the Investigation, Evaluation and Treatment of Hypertension in 1988
recommended that whether it is systolic (SYS) or diastolic (DIA), average person must undergo at least three
measurements ,further diagnosis is needed when blood pressure is found to be higher than the normal level.
14.2 What measure should be taken when blood
pressure is too high or low?
a) Please consult physician.b) Prolonged ascending blood pressure (different types of SYS) will endanger human health.
Deposits on the walls of the blood vessels limit the flow of blood (that can result in arteriosclerosis), which
is very dangerous. Because it will cause insufficient blood supply to body’s important part (heart, brain, muscles and etc.), even
severely destroy the structure of heart. c) There are many factors that cause high blood pressure. We
could divide them into common hypertension and secondary hypertension. Secondary hypertension will lead to organ
disorders.
If your blood pressure value continues to rise, ask physician about
possible causes.
d) Changing your lifestyle also can prevent or lower hypertension, but this habit must be a part of healthy life, including:
1)Dietary Habit
Maintain normal weight as guided by doctor. Do not eat too much salt, as many "packaged foods" contain more salt. Avoid
eating greasy food. (Packaged foods usually contain large amounts of fat).
2)Preventing Diseases
Adhere to medical guidelines for preventing certain diseases, such as diabetes, fat metabolic disorders and gout .
3) Living Habit
Don't smoke, avoid drinking too much or high concentration drinking; limit the intake of caffeine (coffee, tea, chocolate and
etc.)
4)Physical Exercise
After medical examination, carry out regularly physical exercise; choose the sports program that requires endurance rather than
strength. Please note that do not exercise reaching your physical limit. Patients over 40 years old who is with medical history,
consult physician before you start to exercise.
Precaution:Consult your physician before using the device for any of the following conditions: common irregular pulse such as
atrial or ventricular premature beats or atrial fibrillation, arterial sclerosis, poor perfusion, diabetes, old age, pregnancy,
pre-eclampsia, renal diseases. Note that PATIENT motion, trembling, shivering may affect the reading.
15.Error warning/Troubleshooting
15.1 False Alarm
The LCD will display an error warning If any of the following occurs,as
shown in figure marked:
Error code after
Description
Reason of error
Solutions
leaving the
factory
Er01
Error of
Too much noise to detect an
Please rest for 2 minutes, adjust the cuff, keep
measurement
effective pulse signal
quiet during measurement, do not move or
Error
measurement
Error
measurement
of
of
Static pressure
exceeds the set
protection point
No pulse was detected
talk.
Test results deviate from normal
range
Pressure exceeds design ceiling
protection
Measure blood pressure again
Zero overtime
1. During the process of returning to
zero, the air pressure in the cuff
continues to fluctuate;
1. Keep the cuff intact when returning
to zero;
2. Detecting the power supply of the
2. The sensor part of the circuit is
sensor;
abnormal;
3. Sensor damage.
3. Replace the sensor.
Er02
Abnormal cuff
wearing
1. The cuff is not worn;
2. Wearing too loose;
Adjust the cuff. It is advisable to insert
two fingers just after the tightness
3. Wearing too tight;
is tied. The cuff mouth of the cuff is kept 2cm
4.5s did not reach 10mmHg or 18s
on the elbow socket.
did not reach 25mmHg;
5. After the air pressure exceeds
30mmHg, the air pressure is lower
than 20mmHg due to the looseness
of the cuff;
The power is lower
than the minimum
operating voltage.
Replace the battery
Lo
Power is not
enough
Over range alarm
When the test blood pressure value is higher than 280mmhg (excluding 280mmhg), the blood pressure value will continue to
flash at a frequency of 2HZ. When the blood pressure value is lower than 280mmhg, the flicker is released.
Other Information
Even a healthy individual, the blood pressure is constantly changing (presenting a jagged line), so when you make comparative
measurements, you must be in a fixed state (quiet environment)! If the difference is greater than 2.0 kPa / 15 mmHg if the above
conditions are met, or in some cases, in case of irregular hear beat, please consult your doctor.
15.2Troubleshooting
If any faults (or abnormal conditions) occur during use, you can check and exclude according to the items listed in the following
table:
Malfunction
When the battery is installed
and the switch is turned on,
shows nothing.
Exclude
Check whether the product has power
The air pump has begun to inflate, but there is no rise in
* Check the hose connection for air leakage or whether it is fully
arm pressure.
inserted into the socket.
Upper Arm Blood Pressure Monitor s fail to measure blood
pressure
1. Re-set the correct cuff.
2. If the left upper arm of the belt is covered with sleeves or other
frequently, or the blood pressure is abnormally high or low.
clothing, please take off. Re-measure blood pressure.
self-measured value is different from the measured
consult your doctor. Record daily measurements and consult
value of the doctor.
your doctor.
After the Upper Arm Blood Pressure Monitor is pressurized,
*The air hole connection of the hose in the arm belt has the
the air pressure of the cuff is released. And the rate is slow
phenomenon of "plastic ring" falling off. Please put the plastic
even not released at all.
ring on and measure again.
Any technical problems related to blood pressure monitor, should consult experts or medical personnel, do not disassemble
repair without permission!Unauthorized disassembly, will lose the warranty right!
16Reference standard 参考标准
We Famidoc Technology Co., Ltd. solemnly declares that the FDBP-A10BL
Upper Arm Blood Pressure Monitor we produced and sold meets the
following standards:
Performance safety standard:YY 0670/ IEC 80601-2-30
Electromagnetic compatibility:IEC60601-1-2
Safety standard:GB 9706.1/ IEC60601-1
Claim: The blood pressure value tested by this device is equivalent
to that measured by auscultation, and the error is in accordance
with the requirements of the code IEC/EN 80601-2-30.
Please read this instruction carefully before use.The product is
part of BF application equipment of internal power supply.
17.Place in
If this unit is damaged and need to be discarded,please dispose of the
discarded electronic waste in accordance with the relevant national
laws and regulations , dispose of the battery or product should not be
directly placed in the garbage can.
Please consult the licensor who responsible for local waste disposal if
you have any questions,.
18.Technical specifications
Mode
display
FDBP-A10BL
LCD display
Measuring method
Oscillometric method
Memory
Resolution
Automatically store each 60 sets of measured values for two users
0.1kPa(1mmHg)
Measurement Range
stress: 0kPa~39.3kPa(0~295mmHg);
Accuracy
Power
Pulse: 40 to 199beats/min
Static pressure: ±0.4 kPa (±3 mmHg)
Pulse: within ±5% of the reading
3.7V rechargeable lithium battery
Special accessory
Cuff, instruction manual
Size
Weight
153mm*101 mm*50 mm
About 300g(including battery)
Withstand pressure for the cuff
360mmHg
Upper arm circumference
220~420mm
Software version
V1.0
Electric shock protection type
Class II device
Shock protection procedure
BF application part
Expected use lifetime
Body in 5 years, Cuff in 2 years
Application component
Cuff
Operating condition
Transportation and
storage condition
Temperature: 5° C~40° C
Humidity: 15% RH~90% RH, No condensation
Atmospheric pressure: 70kPa~106kPa
Temperature: -25° C~55° C
Humidity: 15% RH~95% RH, No condensation
Atmospheric pressure: 70kPa~106kPa
Please strictly observe the environmental
conditions of transportation and storage,
otherwise it will affect the accuracy of the
equipment.
19.List of attachment
Component
Upper Arm Blood
Pressure Monitor
Quantity
1 PCS
Instruction manual
1 PCS
Cuff
AAA battery
1 PCS(with trachea)
4pcs
20.Standardized symbolic description
21.Electromagnetic compatibility information
FCC STATEMENT
This device complies with part 15 of the FCC Rules. Operation is subject to thefollowing 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
FCC 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.
⚫
⚫ 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.
Increase the separation between the equipment and receiver.
This transmitter must not be co-located or operated in conjunction with any other antenna or transmitter.
This equipment complies with FCC radiation exposure limits set forth for an uncontrolled environment and meets
the FCC radio frequency (RF) Exposure Guidelines. This equipment has very low levels of RF energy that are
deemed to comply without testing of specific absorption ratio (SAR).
When using the device, it is recommended to keep the device at a 30cm distance from the human body
Note:
● The Upper Arm Blood Pressure Monitor FDBP-A10BL meets the electromagnetic compatibility requirements of YY0505,
YY0670, IEC60601-1-2;
●Users should install and use the electromagnetic compatibility information provided by the random files. Portable and mobile
RF communication devices may affect the performance of the Upper Arm Blood Pressure Monitor FDBP-A10BL. Avoiding strong
electromagnetic interference when used, such as Close to mobile phones, microwave
26
ovens, etc.
●The instructions for the guide and the manufacturer are detailed in the attachment.
Warning:
·Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper
operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are
operating normally.
·Use of accessories, transducers and cables other than those specified or provided by the manufacturer of this the FDBP-A10BL
could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in
improper operation
·Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be
used no closer than 30 cm (12 inches) to any part of the FDBP-A10BL, including cables specified by the manufacturer. Otherwise,
degradation of the performance of this equipment could result.
Attachment:
Guidance and manufacturer´s declaration – electromagnetic emission – for all EQUIPMENT AND SYSTEMS
Guidance and manufacturer´s declaration – electromagnetic emission
The FDBP-A10BL is intended for use in the electromagnetic environment specified below. The customer or the
user of FDBP-A10BL should assure that it is used in such an environment.
Emissions test
Compliance
Electromagnetic environment - guidance
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic
emissions
IEC 61000-3-2
Voltage
fluctuations/flicker
emissions
IEC 61000-3-3
The FDBP-A10BL uses RF energy only for its internal function. There
Group 1
for, its RF emissions are very low and are not likely to cause any
interference in nearby electronic equipment.
Class B
The FDBP-A10BL is suitable for use in all establishments,
N/A
including domestic establishments and those directly connected
to
the public low-voltage power supply network that supplies
N/A
buildings used for domestic purposes.
Guidance and manufacturer's declaration – electromagnetic immunity
– for all EQUIPMENT and SYSTEMS
Guidance and manufacturer´s declaration – electromagnetic immunity
The FDBP-A10BL is intended for use in the electromagnetic environment specified below. The customer or the
user of the FDBP-A10BL should assure that it is used in such an environment.
Immunity test
IEC 60601 test
level
Compliance level
Electromagnetic environment -guidance
Electrostatic
± 8 kV contact
± 8 kV contact
discharge (ESD)
± 2 kV, ± 4 kV, ±
± 2 kV, ± 4 kV, ±
IEC 61000-4-2
8 kV,± 15 kV air
8 kV,± 15 kV air
Electrostatic
transient / burst
IEC 61000-4-4
± 2 kV for power
supply lines
± 1 kV differential
Surge
mode
IEC 61000-4-5
± 2 kV common
N/A
N/A
mode
0 % UT (100 % dip in
UT) for 0,5 cycle
0 % UT (100 % dip in
UT) for 1 cycles
Floors should be wood, concrete or ceramic
tile. If floors are covered with synthetic
material, the relative humidity should be at
least 30 %. If ESD interfere with the operation
of equipment, counter measurements such
as wrist strap, grounding shall be considered.
Mains power quality should be that of a
typical commercial or hospital environment.
Mains power quality should be that of a
typical commercial or hospital environment.
Mains power quality should be that of a
typical commercial or hospital environment.
If the user of the FDBP-A10BL requires
70 % UT (30 % dip in
N/A
continued operation during power mains
UT) for 25/30cycles
0 % UT (100 % dip in
UT) for 250/300
cycles
30 A/m
30 A/m
interruptions, it is recommended that the
FDBP-A10BL be powered from an
uninterruptible power supply or a battery.
Power frequency magnetic fields should be
at levels characteristic of a typical location in
a typical commercial or hospital
environment.
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
Power frequency
(50/60Hz) magnetic
field
IEC 61000-4-8
NOTE:UT is the a. c. mains voltage prior to application of the test level.
Guidance and manufacturer´s declaration – electromagnetic immunity –
for EQUIPMENT and SYSTEM that are not LIFE-SUPPORTING
Guidance and manufacturer´s declaration – electromagnetic immunity
The FDBP-A10BL is intended for use in the electromagnetic environment specified below. The customer or the
user of the FDBP-A10BL should assure that it is used in such an environment.
Immunity test
IEC 60601 test
Compliance level
Electromagnetic environment - guidance
level
Portable and mobile RF communications
equipment should be used no closer to any
part of the FDBP-A10BL, including cables,
than the recommended separation distance
calculated from the equation applicable to
the frequency of the transmitter.
Recommended separation distance:
Conducted RF
3 Vrms
3V
IEC 61000-4-6
150 kHz to 80 MHz
150 kHz to 80 MHz
6 V in ISM and
6 V in ISM and
amateur radio
amateur radio
bands between 0,15
bands between 0,15
MHz and 80 MHz.a
MHz and 80 MHz.a
Radiated RF
10 V/m
10 V/m
IEC 61000-4-3
80 MHz to 2.7 GHz
80 MHz to 2.7 GHz
80 MHz to 800 MHz
800 MHz to 2.7 GHz
385MHz-5785MHz
385MHz-5785MHz
where p is the maximum output power rating
Test specifications
Test specifications
of the transmitter in watts (W) according to
for ENCLOSURE
for ENCLOSURE
the transmitter manufacturer and d is the
PORT IMMUNITY to
PORT IMMUNITY to
recommended separation distance in metres
RF wireless
RF wireless
(m).
communication
communication
Field strengths from fixed RF transmitters, as
equipment (Refer
equipment (Refer
determined by an electromagnetic site
to table 9 of IEC
to table 9 of IEC
survey,b should be less than the compliance
60601-1-2)
60601-1-2)
level in each frequency range.c
Interference may occur in the vicinity of
equipment marked with the following
symbol:
Proximity magnetic
30 kHz ,CW,8A/m
N/A
The FDBP-A10BL does not contain
fields
(This test is
IEC 61000-4-39
applicable only to
magnetically sensitive components.
ME EQUIPMENT
and ME SYSTEMS
intended for use in
the HOME
HEALTHCARE
ENVIRONMENT)
134,2 kHz ,Pulse
modulation 2,1
kHz
65 A/m
13,56 MHz Pulse
modulation 50 kHz
7,5 A/m
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic is affected by absorption and
reflection from structures, objects and people.
a The ISM (industrial, scientific and medical) bands between 150 kHz and 80 MHz are 6,765 MHz to 6,795 MHz;
13,553 MHz to 13,567 MHz; 26,957 MHz to 27,283 MHz; and 40,66 MHz to 40,70 MHz. The amateur radio bands
between 0,15 MHz and 80 MHz are 1,8 MHz to 2,0 MHz, 3,5 MHz to 4,0 MHz, 5,3 MHz to 5,4 MHz, 7 MHz to 7,3
MHz, 10,1 MHz to 10,15 MHz, 14 MHz to 14,2 MHz, 18,07 MHz to 18,17 MHz, 21,0 MHz to 21,4 MHz, 24,89 MHz
to 24,99 MHz, 28,0 MHz to 29,7 MHz and 50,0 MHz to 54,0 MHz.
b 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 theFDBP-A10BL is used
exceeds the applicable RF compliance level above, the FDBP-A10BL should be observed to verify normal
operation. If abnormal performance is observed, additional measures may be necessary, such as
re_x005f_x005f_x005f_x005f_x005f_x005f_x005f_x005f_x005f_x005f_x005forienting or relocating theFDBP-A10BL.
c Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3V/m.
Recommended separation distances between portable and mobile
RF communications equipment and the EQUIPMENT or SYSTEM -for EQUIPMENT and SYSTEMS
Recommended separation distances between
portable and mobile RF communications equipment and the FDBP-A10BL
The FDBP-A10BL is intended for use in an electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the FDBP-A10BL can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and
the FDBP-A10BL as recommended below, according to the maximum output power of the communications
equipment
Separation distance according to frequency of transmitter
Rated maximum
150 kHz to 80 MHz
output of
transmitter
(W)
outside ISM and
amateur radio
bands
(m)
150 kHz to 80 MHz
in ISM and amateur
80 MHz to 800 MHz
800 MHz to 2.7 GHz
radio bands
0.01
0.1
1
10
100
N/A
N/A
N/A
N/A
N/A
0.2
0.63
2
6.32
20
0.035
0.11
0.35
1.1
35
0.07
0.22
0.7
2.21
70
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.
Famidoc Technology Co., Ltd.
Add.: No. 212 Yilong Road, Hexi Industrial Zone,Jinxia, Changan Town, Dongguan 523853, Guangdong
Province, P.R. China.
Tel.: +86-769-89272488
Website: www.famidoc.com
Name: Shanghai International Holding Corp. GmbH (Europe)
Add: Eiffestrasse 80, 20537 Hamburg, Germany
PN:
Description Version: V1.0
Revision date: April 2022
1 | Label and Label Locations | ID Label/Location Info | 522.25 KiB | August 25 2022 |
背面镭雕
K 80
注:型号根据实际变化
Model:
共用的型号
FDBP-A8/FDBP-A8B/FDBP-A8T/FDBP-A8BT
FDBP-A10/FDBP-A10B/FDBP-A10T/FDBP-A10BT
注:以下信息根据实际变化
(cid:31)(cid:30)(cid:31)(cid:28)(cid:30)(cid:30)(cid:30)(cid:30)(cid:30)(cid:30)(cid:27)
流水号
根据型号变化
例如
FDBP-A8BT : (cid:31)(cid:30)(cid:31)(cid:25)(cid:24)(cid:28)(cid:30)(cid:30)(cid:30)(cid:30)(cid:30)(cid:30)(cid:27)
生产年月
(cid:26)(cid:30)(cid:26)(cid:26)(cid:28)(cid:30)(cid:29)
Upper Arm Blood
Pressure Monitor
Model: FDBP-A10BL
IP classification: IP21
Power source: 3.7V rechargeable lithium
battery
Manufacturer: FAMIDOC TECHNOLOGY CO.,LTD
Shelf Life: Five years
FCC ID:PONFDBP
10BL(cid:28)(cid:30)(cid:30)(cid:30)(cid:30)(cid:30)(cid:27)
(cid:26)(cid:30)(cid:26)(cid:26)(cid:28)(cid:30)(cid:29)
WARNING
DO NOT adjust medication
based on measurement
results from this blood
pressure monitor. Take
medication as prescribed
by your physician.
The monitor is not
intended to for newborns.
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
表单编号:QR-09-001 B/0
1 | Antenna Specification | Parts List/Tune Up Info | 737.36 KiB | August 25 2022 |
Antenna
describe
1.Antenna
describe:
Antenna
plate
Monoploe
antenna
Make name/model
name
FDAC4110
Antenna
gain
OdBi
Frequency
range
2.4GHZ-2.483GHZ
type
Connector
direct
Location
of
Famidoc Technology
Co., Ltd.
mearement(company
name)
2.External
view drawing:
Picture
of antenna
U
i
IE
8
飞
0"1
WlII
Q
co
·g
—
10.40mm 三
§L厂
$厂
ci
乓
:
0.50Illlll
|
y
J
O
:
5.50Illlll l
mI
mm
75
50
0
3.Antenna Radiation
Pattern
Radiation
pattern@2.402GHZ
k
Total Pea
Gain:-0.475dbi
Phi I。 I45 I go I 135 180 235 270 315
-o.1 I -o. 3 I -o. 8 I -o. 5 I -o. 2 I -o. 6 I -o. 8 I -o. 5
Radiation pattern@2.441GHZ
k
Total Pea
Gain:-0.275dbi
Phi I。 I45 I go I 135 180 I 235 270 315
。 -o.1 I -o. 3 I -o. 6 I -o. 1 I -o. 2 I -o. 6 I -o. 4
Radiation
pattern@2.480GHZ
k
Total Pea
Gain:-0.237dbi
Phi 。 45 90 135
。 -0. 1 -0.2 -0.5
180 235 270 315
。 -0.3 -0.6 -0.2
Gain
1 | FCC Agent Authorization | Cover Letter(s) | 11.24 KiB | August 25 2022 |
Famidoc Technology Co., Ltd. Agent Authorization Letter 2022-08-01 Eurofins Electrical and Electronic Testing NA, Inc. 914 W. Patapsco Avenue Baltimore, MD 21230 USA RE: LETTER OF AGENT AUTHORIZATION To Whom It May Concern:
We, the undersigned, hereby authorize (The Hong Kong Standards and Testing Centre Limited) to act on our behalf in all matters relating to application for equipment authorization, including the signing of all documents relating to these matters. We also hereby certify that no party to the application authorized hereunder is subject to the denial of benefits, including FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C.853(a). This agreement expires one year from the current date. Sincerely, Print name: Reanny wang Title: Vice General Manager Signature:
1 | FCC Long Term Confidentiality Letter | Cover Letter(s) | 11.24 KiB | August 25 2022 |
Famidoc Technology Co., Ltd. Long Term Confidentiality Request Letter Date: 2022-08-01 Eurofins Electrical and Electronic Testing NA, Inc. 914 W. Patapsco Avenue Baltimore, MD 21230 USA RE: CONFIDENTIALITY REQUEST FOR EUT NAME: Arm Blood Pressure Monitor/Automatic Wireless Smart Blood Pressure Monitor MODEL: FDBP-A10BL FCC ID: PONFDBP To Whom It May Concern:
This letter serves as an official request for confidentiality under sections 0.457 and 0.459 of CFR 47. We have requested that the (block diagram/schematics/PCB /operational description ) required to be submitted with this application be permanently withheld from public review. The above documents are company proprietary information that could never get into the possession of your competition. Please contact me if there is any information you may need. Sincerely, Print name: Reanny wang Title: Vice General Manager Signature:
1 | Model Declaration Letter | Attestation Statements | 845.91 KiB | August 25 2022 |
To : STC (Dongguan) company Limited DECLARATION OF IDENTITY Hereby we:
Famidoc Technology Co.,Ltd.
(Name of Manufacturer) Basic Model Number: FDBP-A7BL. FDBP-A10BL Basic Brand Name: FAMIDOC Basic Product Name: Am Blood Pressure Monitor
/Automatic Wireless Smart Blood Pressure Monitor Basic Test Report Application Number:
Declare the Circuit, PCB Layout, Electrical Parts and Outlook of the following product(s) are identical to the basic model:
Ei New /_] Additional Model Number(s): eppp-47, FDBP-A7L, FDBP-A7B. FDBP-A7T. FDBP-A7LT, FDBP-A7BT. FDBP-A7BLT. FDBP-A8. FDBP-A8L. FDBP-A8B. FDBP-A8BL. FDBP-A8T. FDBP-ASLT. FDBP-A8BT. FDBP-A8BLT. FDBP-A9, FDBP-A9L. FDBP-A9B. FDBP-A9BL. FDBP-A9T. FDBP-ASLT. FDBP-A9BT. FDBP-A9BLT. FDBP-A10. FDBP-A10L. FDBP-A10B, FDBP-A10BL. FDBP-A10T, FDBP-A10LT. FDBP-A10BT. FDBP-A10BLT 1 New /[] Additional Brand Name(s): Fayapoc
{2 New/(] Additional Product Name(s): Arm Blood Pressure Monitor
/Automatic Wireless Smart Blood Pressure Monitor Except the following(s) :
Remarks; FDBP-A7, FDBP-A7L. FDBP-A7B. FDBP-A7BL. FDBP-A7T. FDBP-A7LT. FDBP-
A7BT. FDBP-A7BLT. FDBP-A8. FDBP-A8L. FDBP-ASB. FDBP-A8BL. FDBP-AST. FDBP-A8SLT. FDBP-A8BT. FDBP-A8BLT. FDBP-A9, FDBP-ASL. FDBP-A9B. FDBP-
ASBL. FDBP-AST, FDBP-A9LT. FDBP-A9BT. FDBP-A9BLT. FDBP-A10. FDBP-
AI0L. FDBP-A10B. FDBP-A10BL. FDBP-A10T, FDBP-A10LT, FDBP-Al0BT. FDBP-
ALOBLT are consistent in key components, working principle, basic function, performance index, expected use, printed circuit diagram and ,power supply and function configuration. Thexefore, LED sigplay sP-A7BL and LCD display FDBP-A1OBL were selected as the main inspection models for the whole project inspection. Signature with
(AR RH) Printed Name DATE:
Updated on 2005/02007 by Kally Chan main inspection models Coverage model model FDBP-A7BL FDBP-A7 FDBP-A7L FDBP-A7B FDBP-A7T FDBP-A7LT FDBP-A7BT FDBP-A7BLT Power Rechargeable 3.7V lithium battery 4*AAA Same 4*AAA 4*AAA Same 4*AAA Same source /USB 5V battery battery battery battery
/USB 5V /USB 5V /USB 5V /USB 5V Number of keys Three Same Same Same Two Two Two Two Display module LED (No backlight) Same Same Same Same Same Same Same Display size 130*41 mm Same Same Same l Same Same Same Same
(length* width) Machine size 153*101*45 mm Same ij Same Same Same
(length * width *
height) circuit structure It is mainly composed of power supply Same Same Same Same circuit, control circuit, display circuit, L measurement circuit Key component Pressure sensor, cuff, CPU, air pump, air valve | Same Same Same Same Performance measuring range : Same Same Same Same difference systolic pressure: 8%33.3kPa (60~250mmHg ) diastolic pressure : 4~26kPa(30~195mmHg) Pulse: 40-199 times/min accuracy :
static pressure : + 3mmHg (+ 0.4kpa) Pulse: within +5% of the reading
| main inspection models Coverage model model FDBP-A7BL FDBP-A8& FDBP-A8L FDBP-A8B FDBP-A8BL FDBP-A8T FDBP-A8LT FDBP-A8BT FDBP-A8BLT Power Rechargeable 3.7V lithium battery 4* AAA Same 4*AAA Same A*AAA Same 4*AAA Same source /USB 5V battery battery battery battery
/USB 5V /USB 5V /USB 5V /USB 5V Number of keys Three Same Same Same Same Two Two Two Two Display module LED (No backlight) Same Same Same Same Same Same Same Same Display size 130*41 mm Same Same Same Same Same Same Same Same
(length* width) Machine size 153*101*45 mm Same Same Same Same Same Same Same Same
(length * width *
height) circuit structure It is mainly composed of power Same Same Same Same Same Same supply circuit, control circuit, display circuit, measurement circuit Key component Pressure sensor, cuff, CPU, air pump, Same Same Same Same Same Same air valve Performance measuring range : Same Same Same Same Same Same difference systolic pressure: 8~33.3kPa
(60~250mmHg) diastolic pressure :
(30~195mmbg ) Pulse: 40-199 times/min 4~26kPa accuracy :
static pressure : + 3mmHg
(+ 0.4kpa) Pulse: within +5% of the reading main inspection models Coverage model
model FDBP-A10BL FDBP-A9 FDBP-A9SL FDBP-A9B FDBP-A9BL FDBP-AST FDBP-A9LT FDBP-A9BT | FDBP-A9BLT Power Rechargeable 3.7V lithium battery 4*AAA Same 4*AAA Same | 4*AAA Same 4*AAA Same source /USB 5V battery battery battery battery
/USB 5V /USB 5V /USB 5V /USB 5V Number of keys Three Same Same Same Same Two Two Two Two Display module LCD (backlight) Same Same Same Same Same Same Same Same Display size 123*30 mm Same Same Same Same Same Same Same Same
(length* width) Machine size 153*101*50 mm Same Same Same Same Same Same Same Same
(length * width *
height) circuit structure It is mainly composed of power Same Same Same Same Same Same supply circuit, control circuit, display circuit, measurement circuit Key component Pressure sensor, cuff, CPU, air pump, Same Same | Same Same Same Same air valve Performance measuring range : Same Same Same Same Same Same difference systolic pressure: 8~33.3kPa
(60~250mmHg ) diastolic pressure : 4~26kPa
(30~195mmHg ) Pulse: 40-199 times/min accuracy :
static pressure : + 3mmHg
(+ 0.4kpa) Pulse: within +5% of the reading main inspection models Coverage model
(60~250mmHg) diastolic pressure :
(30195mmHg) Pulse: 40-199 times/min 4~26kPa accuracy :
static pressure : + 3mmHg
(+ 0.4kpa) Pulse: within +5% of the reading model FDBP-A10BL FDBP-A10 FDBP-A10L FDBP-A10B FDBP-A10T FDBP-A10LT FDBP-A10BT FDBP-A10BLT Power Rechargeable 3.7V lithium battery 4*AAA battery | Same 4*AAA battery | 4*AAA battery | Same 4*AAA battery | Same source /USB 5V /USB 5V /USB 5V /USB 5V /USB 5V Number of keys Three Same Same Same Two Two Two Two
| Display module LCD (backlight) Same Same Same Same Same Same Same Display size 123*30 mm Same Same Same Same Same | Same
(length* width) Machine size 153*101*50 mm Same Same Same Same Same Same
(length * width *
height) circuit structure It is mainly composed of power Same Same Same Same Same supply circuit, control circuit, display circuit, measurement circuit Key component Pressure sensor, cuff, CPU, air pump, Same Same Same Same Same air valve Performance measuring range : Same Same Same Same Same difference systolic pressure: 8%33.3kPa
1 | WIFI and BT Module | Parts List/Tune Up Info | 386.53 KiB | August 25 2022 |
Medical pulse WIFI
IC planning
Draftsman:Chen Jiale
version: V1.1.1
date : 2022-04-14
formula
te
Auditing
sanctio
n
Old file
processin
g
Revision experience
version
Revised content
V1.0.0
First planning
V1.0.1
Change some details after communicating
with Boxin
V1.0.2
Increase the WIFI AP functionality
V1.0.3
Fixed a MAC definition
V1.0.4
Add UUID recognition Bluetooth and AT command
acquisition status
V1.0.5
Invalid update requirement due to the IIC
V1.0.6
Update the schematic and add WIFI / BLE to enable
control
V1.0.7
Add a WIFI communication port description
V1.0.8
Correct current parameters, protocol AT + instruction
return format
V1.0.9
Add a data transfer description
V1.1.0
Add WIFI read MAC address and modify name
function
V1.1.1.
Adjust the schematic pin naming
V1.1.2
Modify product reference graphs and template
dimensions
Bluetooth specifications: Bluetooth 5.1
WIFI : 802.11n
IC: BL2028 QFN32
The WIFI module name:FDAC4110
Product reference circuit:
Footposition instructions ( See the lower right corner of
the circuit diagram):
order
numbe
foot position
IC foot
position
1
2
3
4
WIFI_ACTIVE
P7
BLE_ACTIVE
P8
AP_CEN
P9
BLE_TX
P11
mold
function declaration
other
O
O
I
O
WIFI connection status
0 - not connected
1 - connected
BLEconnection status
0 - not connected
1 - connected
WIFI mode selection
0 - STA
1 - AP
UART communication
TX
Compatible with
burning mouth
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
BLE_RX
RST
VCC
GND
IO_0
IO_1
IO_2
IO_3
IO_4
IO_5
IO_6
IO_7
BLE_CEN
P10
RST
/
/
P14
P15
P16
P17
P20
P21
P24
P26
P22
WIFI_CEN
P23
ANT
ANT
I
/
/
/
O
O
O
O
O
O
O
O
O
I
/
Compatible with
burning mouth
UART communication
RX
Reset the foot, and the
low level is effective
Power input pin
power ground
Controlled output port
The default low level
BLE Enable end
1 - BLE open
0 - BLE close
WIFI Enable end
1 - WIFI open
0 - WIFI close
Antenna mouth
The suspension is
high level
The suspension is
high level
Electrical parameter requirements:
order
numbe
1
2
3
project
supply voltage
Sleep current
work environment
demand
2.1~3.6
≤ 10
-20~70
unit
other
V
uA
℃
3.8uA
The WIFI block parameters:
order
numbe
1
2
3
4
5
6
project
demand
working
frequency
transmitting
power
working
current
receiving
sensitivity
Standby
current
peak current
2412~2484
13~15
≤100
≤-70
≤100
≤200
BLE, the block parameter:
unit
MHz
dBm
mA
dBm
mA
mA
other
non-tunable
(75 mA)
Bluetooth function
turned off(75mA)
order
numbe
1
2
3
2
3
4
5
6
7
project
demand
frequency
receiving
sensitivity
transmitting
power
Radio gap
Minimum
connection gap
Maximum
connection gap
Connection
timeout
Standby current
Receiving /
transmitting
current
2402~2480
≤ -94
0
100
10
10
5
≤35
≤45
Communication requirements:
UART communication:
order
number
1
2
3
project
Baud rate
check bit
stop bit
demand
57600
none
1
other
unit
Mhz
dBm
dBm
Automatic adjustable
ms
ms
ms
s
mA
mA
unit
Bit/S
bit
The WIFI
functionality is turned
off(25mA)
bluetooth connection
(31 mA)
other
Modifiable (by
default)
Bluetooth protocol description (APP interface):
Bluetooth Service UUID:0000feef-0000-1000-8000-
00805f9b34fb
UUID
Handle
attribute
0xFF01
0xFF02
notify
Write
Byte
number
The longest
single
package517
The longest
single
package517
remarks
Data entered from the serial port RX will
generate a notification to the mobile
device in this channel
Data written by the APP is output from
the serial port TX
0xFF03
0xFF04
0xFF05
0xFF07
0xFF08
0xFF09
0xFF0A
0xFF0B
0xFF0C
0xFF0D
0xFF0E
0xFF0F
Write
longest9 Module broadcast name
Read
6
0x01
Read
0x02
Write
0xFF06
Read
2
2
Write
Module MAC address
Address coding format see attachment
Set the serial port port rate:(default
57600)
0: 4800 bps
1: 9600 bps
2: 19200 bps
3: 38400 bps
4: 57600 bps
5: 115200 bps
Read the module software version(3 个
Byte:000000)
0xAA,0x55: factory data reset
other: invalid instruction
Restore content: Name, wifi memory
Write
longest32 Write to the WIFI SSID
Write
longest32 Write to the WIFI password
Read
1
Query distribution status
0 - Distribution network failure
1 - Distribution network success
2 - wrong password
HTTP Server IP
HTTP Server PORT
The HTTP Server URL
1
2
Gets the server connection status
0 - not connected
1 - Connection success
Specifies the IO port status
High byte-IO port serial number (Start
with 0x00)
Low byte-IO port status 0x00 - output
low level 0x01 -Output high level
Write
Write
Write
Write
\Read
0x01
Read
0x02
Write
The server does the user management , The WIFI module
uploads the MAC to the server for identification
WIFI protocol specification:
STA pattern:
WIFI distribution network : The BLE distribution network is
adopted for the first time, establish the connection with BLE, and
then input the SSID and password of the target AP, after the
configuration, the module automatically connects to the AP, after
each wifi boot automatically connected, with memory saving function,
only one set of WIFI information is saved.
Save the relevant information after the successful network connection,
and automatically connect the save network every time you boot on
WIFI configure:
When the product is connected to the wifi, the module can be
configured through the mobile phone. The configuration information is
as follows:
UDP protocol
Configure the port:6090
Configuring commands:
data head: fixed 0x18
instruct - To the objects to be read or sent
instruction
00
-
character
Representative write / send
Representative
read
01
-
record - When read, data bits are not, only sending instructions
and operators When written / sent, data bits are used to
indicate content to be given
data head instruct instruction
remarks
record
(byte)
Directive
exporter
0x18
0x18
0x18
0x18
0x18
0x18
0x03
0x04
0x05
character
0x01
0x00
0x01
0x00
0x01
0x06
0x00
longest9
APP
/
6
/
1
/
APP
module
APP
APP
APP
Change the module
broadcast name
Module MAC address
Address coding format
see attachment
Set the serial port port
rate:(default57600)
0: 4800 bps
1: 9600 bps
2: 19200 bps
3: 38400 bps
4: 57600 bps
5: 115200 bps
Read the module
software version
0x18
0x18
0x01
0x07
0x01
3
2
module
APP
(APPRead the data:
000000)
0xAA , 0x55: factory
data reset
Other:invalid instruction
Restore content:Name,
wifi memory
WIFI Penetrate:
When the product has data transmitted to the module via the UART
(non-AT command data), the wifi module proactively transmits the data
to the server
AP Penetrate mode:
In the AP mode, the APP is directly connected to the WIFI
module, and the product data is directly transmitted to the APP
through the wifi
Serial port of communication:35000
The WIFI gets the information from the server / APP:
1、Internet Time (only valid after the product time is issued by the product order)
2、User data (voice, control instructions, etc.)
3、OTA upgrade(Users upgrade the WIFI through the APP)(Specialized OTA software, which the APP does not need to
do)
functional
description
data head
(data[0])
port
OTA
function
6090
Inform the
device to
start the
OTA
Equipment
feedback on
the OTA
progress
directive
(data[1])
0x38 (Start
of OTA)
Content
(data[2])
For example, as
0x64 (100), the
data [3] ~data
[3 + 100-1] is
in the json
range
Like 0x05 (5),
indicates data
[3] ~data [3 +
5-1]
persist
(data[3]
)
persist
(data[4])
persist
(data[5])
Accumulation
and check
(data[6])
Content of json such as: {"url": "http: /
/ 192.168.1.1:8090 / ota_file"}
According to the
calculation
In
progress,
bit7:1 OTA
bit6~bit0:
OTA%
data[4]
persist
data[5]
persist
data[6]check
0x17
0x17|0x80
0x39 (ota
progress
report)
Query device
version
number
0x27
Report the
equipment
version
number
0x27|0x80
0x38
0x39
Like 0x05 (5),
indicates data
[3] ~data [3 +
5-1]
As in 0x64
(100), it
indicates that
data [3] ~data
[3 + 100-1]为
json 范围
data[3]pers
ist
data[4]
persist
data[4]
persist
According to the
calculation
The json content is something like:
{"version": "FW-20210125-V001"}
According to the
calculation
The data format of the communication is as follows: "Device MAC address" + "Device type" + "Command character" +
"Transtransmission data", in Json format"MAC":"XXXXXXXXXXXX",
"TYPE":"…",
"CMD":"…",
"VALUE":"…………",
}
protocol :HTTP
Module protocol description (product interface)
The string starting with "AT +" is resolved and executed as an AT
instruction and returned from the serial port, followed by additional
output execution results, "AT + OK" or "AT + ERR" or "AT + (return
information)", etc.Serial packets that do not start with "AT +" will
be treated as transmission data.
Content
bytes
9
2
0
0
0
0
0
3
instruction
character
REN=xxxxxxxx
x
PTY=xx
BSW
RSV
RBS
RWS
RIO=GPIOxx
SIO=GPIOxx,x
WLMAC
attribute
remarks
Write
Write
Module naming(This is the Bluetooth and WIFI
name)
product type(Need to be put in the broadcast to
the APP identification, or server data)
ET - electronic thermometer
IR - Infrared thermometer
BP - tonometer
ES - Physical therapy instrument
Other reserved
Read the module software version
Returns the data, AT + XXXXXX(Three-gear
module version)
Gets the server connection status(Effective only
for the WIFI)
bridging order:
AT+HOST OK
AT+HOST ERR
Gets the BLE connection status
bridging order:
AT+BLE OK --BLE linkage OK
AT+BLE ERR--The BLE connection was
unsuccessful
Gets the WIFI connection status
bridging order:
AT+WIFI OK --WIFI linkage OK
AT+WIFI ERR --WIFI connection unsuccessful
Gets the IO port output status
xx - IO mouth serial number
Return data:
AT+GPIOxx,x
Change the IO port status
xx - IO mouth serial number
x - IO port level 0-low level
1-High power level
Read the module MAC address
Return data:
Read
Read
Read
Read
Read
Write
Read
AT+WLMACxxxxxxxxxxxx
(xxxxxxxxxxxxFor hexadecimal numbers)
failure:AT+ERR
Send the data to the server(Return data)
Write
HTTP_POST=x
xxxxxxxxxxxxx
x
(The x table is
the data)
example:AT+REN=FDIR8001 Module naming:FDIR8001
The above settings require power-off storage
Other requirements:
Account management:
1 、 Each module has a separate MAC address for later server account
management discrimination
2、OTA upgrade
3 、 Information required in the broadcast: module name, device type,
service UUID (0xFEEF)
4 、 When both BLE and WIFI are connected, if BLE is APP connection,
transfer data from BLE is preferred, if BLE is other connection (such
as network connection), select transmission from WIFI
5、WIFI Default name FD_WIFI,Bluetooth default name FD_BLE
data transmission :
1、 Directive package length:
BLE:Short bag≤32 Byte,Long bag≤517 Byte;
WIFI:most 1460 Byte;
2、 Data transmission mechanism:
After the Bluetooth data transmission, more than 100ms did not
receive the data transmission to re-enter the low power
consumption state。
During the data transmission process, if the data is not received
within 20ms, no longer wait, and the data is sent directly, used
to judge each instruction node。
Burning configuration:
WIFI name, Bluetooth name, port rate。
Attached a: The MAC address information is as follows:
The MAC address should contain the content: XX XX XX XXXXXX
first XX:tatted code
the second XX:A high 4bit means year + 2015, for example a high four
digits of 6 represents 2021
Low 4bit indicates the month
The third XX: date
The last three XXXXXX:serial number
Module size:
thickness0.8MM
frequency | equipment class | purpose | ||
---|---|---|---|---|
1 | 2022-08-25 | 2412 ~ 2462 | DTS - Digital Transmission System | Original Equipment |
app s | Applicant Information | |||||
---|---|---|---|---|---|---|
1 | Effective |
2022-08-25
|
||||
1 | Applicant's complete, legal business name |
Famidoc Technology Co., Ltd.
|
||||
1 | FCC Registration Number (FRN) |
0022073563
|
||||
1 | Physical Address |
No. 212 Yilong Road, Hexi Industrial Zone, Jinxia, Changan Town
|
||||
1 |
No. 212 Yilong Road, Hexi Industrial Zone, Jinxia
|
|||||
1 |
Dongguan, N/A
|
|||||
1 |
China
|
|||||
app s | TCB Information | |||||
1 | TCB Application Email Address |
t******@metlabs.com
|
||||
1 | TCB Scope |
A4: UNII devices & low power transmitters using spread spectrum techniques
|
||||
app s | FCC ID | |||||
1 | Grantee Code |
PON
|
||||
1 | Equipment Product Code |
FDBP
|
||||
app s | Person at the applicant's address to receive grant or for contact | |||||
1 | Name |
R****** W****
|
||||
1 | Title |
Vice General Manager
|
||||
1 | Telephone Number |
0086 ******** Extension:
|
||||
1 | Fax Number |
0086 ********
|
||||
1 |
q******@famidoc.com
|
|||||
app s | Technical Contact | |||||
1 | Firm Name |
Famidoc Technology Co., Ltd.
|
||||
1 | Name |
R****** w********
|
||||
1 | Physical Address |
No 212 Yilong Road, Hexi Industrial Zone, Jinxia
|
||||
1 |
523853
|
|||||
1 |
China
|
|||||
1 | Telephone Number |
086 7********
|
||||
1 |
q******@famidoc.com
|
|||||
app s | Non Technical Contact | |||||
n/a | ||||||
app s | Confidentiality (long or short term) | |||||
1 | Does this application include a request for confidentiality for any portion(s) of the data contained in this application pursuant to 47 CFR § 0.459 of the Commission Rules?: | Yes | ||||
1 | Long-Term Confidentiality Does this application include a request for confidentiality for any portion(s) of the data contained in this application pursuant to 47 CFR § 0.459 of the Commission Rules?: | No | ||||
if no date is supplied, the release date will be set to 45 calendar days past the date of grant. | ||||||
app s | Cognitive Radio & Software Defined Radio, Class, etc | |||||
1 | Is this application for software defined/cognitive radio authorization? | No | ||||
1 | Equipment Class | DTS - Digital Transmission System | ||||
1 | Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant) | Arm Blood Pressure Monitor/Automatic Wireless Smart Blood Pressure Monitor | ||||
1 | Related OET KnowledgeDataBase Inquiry: Is there a KDB inquiry associated with this application? | No | ||||
1 | Modular Equipment Type | Does not apply | ||||
1 | Purpose / Application is for | Original Equipment | ||||
1 | Composite Equipment: Is the equipment in this application a composite device subject to an additional equipment authorization? | No | ||||
1 | Related Equipment: Is the equipment in this application part of a system that operates with, or is marketed with, another device that requires an equipment authorization? | No | ||||
1 | Grant Comments | Output Power listed is conducted. This device has 20 MHz and 40 MHz bandwidth modes. The antenna(s) used for this transmitter must be installed to provide a separation distance of at least 30 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi- transmitter product procedures. | ||||
1 | Is there an equipment authorization waiver associated with this application? | No | ||||
1 | If there is an equipment authorization waiver associated with this application, has the associated waiver been approved and all information uploaded? | No | ||||
app s | Test Firm Name and Contact Information | |||||
1 | Firm Name |
The Hong Kong Standards and Testing Centre Ltd.
|
||||
1 | Name |
B**** C******
|
||||
1 | Telephone Number |
852 2********
|
||||
1 |
b******@stc.group
|
|||||
Equipment Specifications | |||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Line | Rule Parts | Grant Notes | Lower Frequency | Upper Frequency | Power Output | Tolerance | Emission Designator | Microprocessor Number | |||||||||||||||||||||||||||||||||
1 | 1 | 15C | 2402 | 2480 | 0.001683 | ||||||||||||||||||||||||||||||||||||
1 | 2 | 15C | 2412 | 2462 | 0.00636 |
some individual PII (Personally Identifiable Information) available on the public forms may be redacted, original source may include additional details
This product uses the FCC Data API but is not endorsed or certified by the FCC