Joytech Healthcare BM 92 Arm Type Fully Automatic Digital Blood Pressure Monitor Owner’s Manual

Owner's Manual

Arm-type Fully Automatic

Digital Blood Pressure Monitor

Model

BM 92

Document No.:

XXXXXXXXXX

Version

：

Z

Date of Issue

：

XXXXXX

Contact Information

The lay operator or lay responsible or ganization should contact

the manufacturer or the representative of manufacturer.

-for assistance,if needed,in setting up,using or maintaining the product,or

-to report unexpected operation or events.

Manufactured by JOYTECH Healthcare Co.,Ltd.

No.365, Wuzhou Road,Yuhang Economic Development Zone,

Hangzhou City,311100 Zhejiang,China

Email: [email protected]

Telephone: +86-571-81957767

Fax: +86-571-81957750

Contents

Safety Notice ............................................................................ 02

Unit Illustration ....................................................................... 06

Important Testing Guidelines ................................................. 08

Quick Start ................................................................................ 09

Unit Operation ......................................................................... 10

Battery Installation ........................................................................

System Settings .................................................................................

1 Safety Notice

Thank you for purchasing the BM 92 Blood Pressure Monitor. The unit has been constructed using reliable circuitry and durable materials. Used properly, this unit will provide years of satisfactory use.

Indications for use : The Arm type Fully Automatic Digital Blood Pressure monitors are intended to measure blood pressure ( systolic and diastolic ) and pulse rate of adults and adolescents over 12 years of age .

All functions can be used safely and values can be read out in one

LCD DISPLAY. Measurement position is on adult upper arm only.

The PATIENT is an intended OPERATOR.

Blood pressure measurement determined with this device are equivalent to those obtained by a trained observer using the cuff/ stethoscope auscultation method, within the limits prescribed by the Recognized Consensus Standard (IEC 80601-2-30) for electronic sphygmomanometers.

2

Cuff loose Indicator

Memory view and average view

Memory Deletion

......................................................... 18

.................................................................................. 18

Low Battery Indicator............................................................................ 19

Bluetooth connection..................................................................................... 20

Troubleshooting ......................................................................................... 22

Blood Pressure Information .................................................... 23

Blood Pressure Q&A ................................................................ 26

Maintenance .............................................................................. 27

Specifications ............................................................................. 29

Warranty .................................................................................... 31

Electromagnetic Compatibility Information ......................... 32

Precautions to Ensure Safe, Reliable Operation

1. Do not drop the unit. Protect it from sudden jars or shocks.

2. Do not insert foreign objects into any openings.

3. Do not attempt to disassemble the unit.

4. Do not crush the pressure cuff.

5. If the unit has been stored at temperatures below 0 ℃ , leave it in a warm place for

about 15 minutes before using it. Otherwise, the cuff may not inflate properly.

6. If the unit has been stored at temperatures above 40 ℃ , leave it in a cool place for about

15 minutes before using it. Otherwise, the cuff may not inflate properly.

7. Do not store the unit in direct sunlight, high humidity or dust.

8.To avoid any possibility of accidental strangulation, keep this unit away from children

and do not drape tubing around your neck.

9.Ensure that children do not use the instrument unsupervised; some parts are small

enough to be swallowed.

10.Some may get a skin irritation from the cuff taking frequent readings over the course

of the day, but this irritation typically goes away on its own after the monitor is removed.

Safety Notice

Important Instructions Before Use

1. Do not confuse self-monitoring with self-diagnosis. Blood pressure measurements should

only be interpreted by a health professional who is familiar with your medical history.

2. Contact your physician if test results regularly indicate abnormal readings.

3. If you are taking medication, consult with your physician to determine the most appropriate

time to measure your blood pressure. NEVER change a prescribed medication without first

consulting with your physician.

4. Individuals with serious circulation problems may experience discomfort. Consult your

physician prior to use.

5. For persons with irregular or unstable circulation resulting from diabetes, liver disease,

arteriosclerosis or other medical conditions, there may be variations in blood pressure

values measured at the wrist versus at the upper arm. Monitoring the trends in your blood

pressure taken at either the arm or the wrist is nevertheless useful and important.

6. People suffering from vascular constriction, liver disorders or diabetes, people with

cardiac pacemakers or a weak pulse, and women who are pregnant should consult their

physician before measuring their blood pressure themselves. Different values may be

obtained due to their condition.

7. People suffering from arrhythmias such as atrial or ventricular premature beats or atrial

fibrillation only use this blood pressure monitor in consultation with your doctor. In

certain cases oscillometric measurement method can produce incorrect readings.

8.Too frequent measurements can cause injury to the patient due to blood flow interference.

9.The cuff should not be applied over a wound as this can cause further injury.

10.

DO NOT attach the cuff to a limb being used for IV infusions or any other intravascular

access, therapy or an arterio-venous (A-V) shunt. The cuff inflation can temporarily

block blood flow, potentially causing harm to the patient.

11.The cuff should not be placed on the arm on the side of a mastectomy. In the case of a

double mastectomy use the side of the least dominant arm.

12.Pressurization of the cuff can temporarily cause loss of function of simultaneously used

monitoring equipment on the same limb.

13.A compressed or kinked connection hose may cause continuous cuff pressure resulting

in blood flow interference and potentially harmful injury to the patient.

14.Check that operation of the unit does not result in prolonged impairment of the circulation

of the patient.

15. Product is designed for its intended use only. Do not misuse in any way.

16. Product is not intended for infants or individuals who cannot express their intentions.

17. Prolonged over-inflation of the bladder may cause ecchymoma of your arm.

18. Do not disassemble the unit or arm cuff. Do not attempt to repair.

19. Use only the approved arm cuff for this unit. Use of other arm cuffs may result in

incorrect measurement results.

20. The system might produce incorrect readings if stored or used outside the manufacturer's

specified temperature and humidity ranges. Make sure to store the blood pressure monitor,

children, pets and pests are outside of accessible range.

21. Do not use the device near strong electrical or electromagnetic fields generated by cell

phones or other devices, they may cause incorrect readings and interference or become

interference source to the device.

22. Do not mix new and old batteries simultaneously.

3 Safety Notice 4

23. Replace batteries when Low Battery Indicator “ ” appears on screen. Replace both batteries at the same time.

24. Do not mix battery types. Long-life alkaline batteries are recommended.

25. Remove batteries from device when not in operation for more than 3 months.

26. Dispose batteries properly; observe local laws and regulations.

27. Only use a recommended class II AC Medical approved adaptor which comply with 2MOPP, and pass

IEC 60601-1, IEC 60601-1-2(or FCC ) standard . An unauthorized adapter may cause fire and electric shock.

28. Advising operator that Instruction manual/ Booklet must be consulted.

29. Do not use the device during transport vehicles for influencing measurement accuracy such as patient transport in an ambulance or helicopter.

30. Contains small parts that may cause a chocking hazard if swallowed by infants.

31. Please align the polarities of each battery with the +ve and -ve signs imprinted on the battery housing when you replace the batteries .

32.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.

33.Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer

than 30 cm (12 inches) to any part of the unit, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.

34.the blood pressure monitors equipped with bluetooth(BT) module is only transmit historical blood pressure (BP) from the subject device to a user-supplied digital device, and is not intended for active patient monitoring.

35. It cannot be maintained or repaired during normal use

.

36. The service life of the product is about 5 years, the service life of the cuff is about 2 years, and the battery is about 3 months.

WARNING SIGNS AND SYMBOLS USED

Keep Dry

IP21

MR

Keep off Sunlight

Type BF Equipment

Instructions For Use MUST be Consulted

Discard the used product to the recycling collection point according to local regulations

The Bluetooth® Smart word mark and logos are registered trademarks owned by Bluetooth SIG,

Inc. and any use of such marks by JOYTECH

Healthcare Co.,Ltd.

indicate that Protected against solid foreign objects of 12.5 mm and greater; Number 1 indicate that Protection against vertically falling water drops .

Magnetic Resonance unsafe

Safety Notice

Federla Commulcation Commission (FCC) Interference Statement

1.This device complies with part 15 of the FCC Rules. Operation is subject to the condition that this device does not cause harmful interference.

2.This device is verified to comply with part 15 of the FCC Rules for use with cable television service.

3.This device complies with part 15 of the FCC Rules. Operation is subject to the following two

conditions:

(1) This device may not cause harmful interference, and

(2) this device must accept any interference received, including interference that may cause undesired operation. Please note that changes or modifications not expressly approved by the party responsible for compliance could void the user's authority to operate the equipment.

4.This equipment has been tested and found to comply with the limits for a Class B digital

device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:

— Reorient or relocate the receiving antenna.

— Increase the separation between the equipment and receiver.

— Connect the equipment into an outlet on a circuit different from that to which the receiver

is connected.

— Consult the dealer or an experienced radio/TV technician for help.

5.This equipment complies with radio frequency exposure limits set forth by the FCC for an uncontrolled environment.

6.This device must not be co-located or operating in conjunction with any other antenna or transmitter.

7.Essential performance:

Electrosurgery interference recovery

Limits of the error of the manometer

Reproducibility of the

BLOOD PRESSURE

DETERMINATION

Refer 202.6.2.101 IEC 80601-2-30

Refer 202.12.1.102 IEC 80601-2-30

Refer 201.12.1.107 IEC 80601-2-30

5 Unit Illustration

Monitor Unit

CUFF " Button

- Button

Arm Cuff

Medium size cuff (fits arm circumference: 22.0 cm -36.0 cm).

LE

FT

AR

M

（

22

8.

~3

6~

6c

14

.2 i

1~

2c m

(0

.4

.8 i nc h)

M ain

Ar te ry

IN

D

E

X

LCD

" " Button

+ Button

MEM Button

" START/STOP " Button

Arm Cuff

Air Plug

Air Tube

If air is leaking from the arm cuff, replace the arm cuff with a new one. It is generally recomm ended to have the cuff replaced timely to ensure correct functioning and accuracy. Please consult your local authorized Sejoy distributor or dealer.

6

Unit Illustration

Display

HSD

Battery Indicator

7 Important Testing Guidelines

1. Avoid eating, exercising, and bathing for 30 minutes prior to testing.

2. Sit in a calm environment for at least 5 minutes prior to testing.

3. Do not stand while testing. Sit in a relaxed position while keeping your arm level with

your heart.

4. Avoid speaking or moving body parts while testing.

5. While testing, avoid strong electromagnetic interference such as microwave ovens and

cell phones.

6. Wait 3 minutes or longer before re-testing.

7. Try to measure your blood pressure at the same time each day for consistency.

8. Test comparisons should only be made when monitor is used on the same arm, in the

same position, and at the same time of day.

9. This blood pressure monitor is not recommended for people with severe arrhythmia.

10. Do not use this blood pressure monitor if the device is damaged.

8

Contents

Owner's Manual

Arm-type Fully Automatic

Digital Blood Pressure Monitor

Model

BM 92

Arm Type

1.Monitor Unit

LE

FT

AR

M

22

~3

6c m nc h

（

8.

6~

14

1~

2c m

)

.4

~0

.8 i nc h)

Ar

M ain

IN

D

E

X

2.Owner's Manual

4.Storage Bag

Any blood pressure recording can be affected by the following factors :

1. The position of the subject, his or her physiologic condition;

2. The performance and accuracy of the device;

3. Cuff size: too small cuff (bladder) will produce a higher blood pressure value than usual,

too big cuff (bladder) will produce a lower blood pressure value;

4. Measuring position does not keep level with your heart;

5. Speaking or moving body parts while testing;

6. Not relaxing for about 5 minutes before taking the measurement.

3.Arm Cuff

5 .

Battery

Quick Start

1. Before first use, please carefully check the packaging is complete, if not complete please contact the seller for replacement. Every time before use, please check the equipment for obvious damage, if there is equipment has been damaged, please use caution. In turn open the color box, asylum package (or receive bag), remove the blood pressure monitor, check whether the parts is complete, and install the batteries (as shown in figure A) battery installed, normal blood pressure monitor for power self-checking, if the battery power is insufficient, the screen shows "LO" error code, if the battery is normal, the device automatically after about 3 seconds time date set into the interface. After the setting, can enter the blood pressure measurement mode.

(See Figure A )

9 Unit Operation

Battery Installation

Slide battery cover off as indicated by arrow.

Install 4 new AAA alkaline batteries according to polarity.

Close battery cover.

10

Figure A Figure B

2. Insert cuff air plug into the behind side of monitor unit. (See Figure B)

3. Remove thick clothing from the arm area.

4. Rest for several minutes prior to testing. Sit down in a quietplace comfortably ,

back and arm support on a desk or table ,withyour legs uncrossed ,your arm

resting on a firm and your feet flat on the floor. (See Figure C )

Figure C

5. Apply cuff to your left arm and middle of the cuff at the level of your heart. Bottom

of cuff should be placed approximately 1-2cm (1/2'') above elbow joint. (See Figures D&E)

1-

2cm

(0.

4-

0.8

''

)

Figure D

6. Press " START/STOP " Button to start testing.

Figure E

Unit Operation

System Settings

1. Time/Date setting

First to electricity, battery installed, normal blood pressure monitor for power self-checking,

if the battery power is insufficient, the screen shows "LO" error code and flashing.


EU US

After the month of determining, into the day set patterns, in the meantime, display, 0.5 seconds icon will flash once, press the keys into the Λ plus the number of days, press the button V reduce the number of days, long press key into or V can quickly adjust the number of days. Press the open key to determine the date of the current setting, the system default date for no. 1.

12

If battery power is normal, the device automatically after about 3 seconds time date set into the interface. Not for the first time on electricity, under the main interface , long press "on/off" button for 3 seconds can be time date set into the interface. The first is for 24 h and 12 h mode

Settings. Can through the key Λ and V mode conversion, press the key to determine the time pattern, the system default for 24 h mode.

EU US

After determine the date, time set into the interface, in the meantime, according to time of 0.5 seconds icon will flash smelting time, first set the hours, according to the first step in setting model

to determine the time, if the first set is 12 h mode, the default time is 12: 00 am, if the first step is

24 h mode, set the default time for 0:00, more than two kinds of mode, press the Λ button in the add hours, press the button V reduced hours, long press the key into the or V can quickly adjust hour, press the key to determine the current setting hours.

EU US

Mode after a certain time period, into the year set pattern, in the meantime, a flashing icon of the

year is 0.5 seconds, press the button eight year of increase, press the button V decreased year, long

press the key into the Λ or V can be adjusted quickly. Press the open key to determine the current

Settings year, the system default for year 2022.

EU US

Determine the hours, minutes set into the interface, in the meantime, according to minutes 0.5 seconds icon will flash once, press the button add minutes, press the button V reduced minutes,

long press the key into the or V can quickly adjust minutes, press the key to determine the current set of minutes.

Determine the year after, enter in setting mode, in the meantime, icon will display month scintillation a 0.5 seconds, press the keys into the Λ increase in plus, V decrease in press buttons, long press buttons or keys in V can be adjusted quickly. Press the open key to determine the current

Settings in the system default for 1 month in September.

Unit Operation

EU US

2.Voice Setting

Time date set up is completed, enter the language setting interface, the system default is L1 language, press the keys into the into the next L2 language, press the button V into L0, L0 closed for language.


User memory group Settings

This device has two memory group, each group has 120 memory value respectively. In sleep mode, press the memory button, the device into the main screen display, 2 seconds, the screen shows the current time, date and user memory block. At the same time open the blood pressure monitor screen backlight.By pressing the buttons on the blood pressure cuff body 1 and 2 keys to select the corresponding memory block, press the button 1 on behalf of the current group 1 sphygmomanometer measurement data is stored in the user memory, memory speech group 1 at thesame time; Press the button 2 represent the current blood pressure measurement data is stored in theuser memory in group

2, speech user memory group 2 at the same time. Memory group selection iscompleted, presses the button, switch machine, the measurement of blood pressure. When blood pressure within 30 seconds without operation, backlit closed, no operation within 60 seconds, enter a dormant state.

14

V Λ

3.Volume Setting

After the completion of the language Settings, enter the sound Settings interface, the system default for V1 volume, press the button enter into the next volume L2, press the button V into

V0, V0 for voice closed, with a total of four standard and increasing the volume of successive

sound.

V

Λ

4. Saved Settings

While in any setting mode, press " START/STOP " button to turn the unit off. All

information will be saved.

Note: If unit is left on and not in use for 1 minutes, it will automatically save all information

and shut off.

Unit Operation

Applying the Arm Cuff

1. Firmly insert air plug into opening located on behind side of monitor unit.

15 Unit Operation 16 a b

2. With sticky nylon section facing outward, insert end of cuff underneath metal ring

of cuff .

3. Fasten cuff about 1-2cm (0.4-0.8'') above the elbow joint. For best results apply cuff to

bare arm and keep level with heart while testing

1-2c m

(0

.4

-0.8

''

)

.

Testing

1. Power On

Under the main interface display, press the switch machine buttons, backlight automatically open, 3 seconds after the show the most recent measurement values, continuous press switch machine button can be skipped if the above two delay directly into the measurement.

2. Testing

Blood pressure cuff pressure automatically, automatic stop, please keep quiet when measuring.

If the cuff is not connected or cuff loose connection causes such as cuff pressure rise is unusual, the blood pressure cuff at start-up pump inflatable after a certain period of time, will stop the pump work, turn to wait for pressure, the screen shown above Err3. Please test cuff pneumatic connection state, can press "memory" button to enter to view memory or press the "start/stop" button to turn it off.

Note: in the process of the pressure must not be arbitrary shaking body, otherwise, the

system will also to determine this for high blood pressure, and pressure again;

Blood pressure cuff pressure in the process of blood pressure measurement can be made.

Armband internal pressure increases gradually, LCD real-time display the current pressure.

When detected pulse, LCD screen flashing symbols, and display the current pressure corresponding to the heartbeat of cuff pressure value

Note: Do not speak, in the process of measuring twist arm, shaking body, etc., please keep

quiet state.

4. Result Display

The screen will display measurements for systolic and diastolic blood pressure with voice

broadcast. A indicator representing the current measurement will appear next to the

corresponding WHO Classification.

Note: Refer to Page 23~24 for detail WHO Blood Pressure Classification Information.

Unit Operation

Irregular Heartbeat Indicator

If the monitor detects an irregular heart rhythm two or more times during the measuring process, the Irregular Heartbeat Symbol " "appears on screen along with measurement results. Irregular heartbeat rhythm is defined as rhythm that is either 25% slower or faster than the average rhythm detected while measuring systolic blood pressure and diastolic blood pressure. Consult your physician if the Irregular Heartbeat Symbol

" " frequently appears with your test results.


Memory view and average view

In the main interface LCD screen all show self-checking, memory according to [memory] key value view, see the first is the average of the last seven days, and then the seven days before the measurement of mean and average in the afternoon in the morning, the last is the latest measurement data, and blood pressure by pressing enter key memory value view. According to the average switching, press V return on a liquid crystal display interface. On average, LCD shows average prompt "AVG", and display the corresponding average blood pressure classification information and classification identification on the morning of the afternoon.

18

Power Off

The " START/STOP " button can be pressed to turn off the unit in any mode. The unit can

turn off the power itself about 1 minutes no operation in any mode.

Safety Precaution: If pressure in arm cuff becomes too extreme while testing, press the " START/STOP " button to turn power off. The cuff pressure will rapidly dissipate once the unit is off.

HSD

HSD: A detection algorithm of human are strained, when measuring blood pressure, it can be through the human bodyMeasure blood flow rate to determine whether the body is in nervous condition, suitability for blood pressure measurement. If the body is in nervous condition, sphygmomanometer can remind and terminate the blood pressure measurement, the user should be measured again after at least 5 minutes. If the normal leisure of the human body, blood pressure will also remind and normal work and measured the blood pressure.

Cuff loose Indicator

At the beginning of the measurement, when the cuff is properly worn, the " " icon will be displayed, and when thecuff is loose, " " The icon will be displayed. When this happens, please turn off the machine, adjust the cuff and measure again. If the " " icon is still displayed, please check the cuff plugconnect with device correctly and measure again.

If it still cannot be resolved, please contact the seller or manufacturer.

If you want to see other memory within the group, please user memory group set up in front of the boot, specific operation as shown in the "system Settings" in " User memory group Settings ".

Memory Deletion

In the condition of main interface, press the [memory] key, enter the average interface. Through user button to select the user, long press A button and V 15 seconds for user delete memory value.

Press A button to enter the average interface in the morning, in the morning the average interface, can be long press A button Λ and V 15 seconds to delete all data.

Unit Operation

Note: Memory cannot be recovered once it has been deleted.

If you want to delete the other set of memories, please user memory group set up in front of the boot, specific operation as shown in the "system Settings" in " User memory group Settings ";

Power Off

In any state, the boot can be fixed by press the "start/stop" button for 2 seconds to turn it off. If the device idle for 30 seconds, backlit closed, 60 seconds after the device has reached the "sleep" mode.

Press any button except/key can be reactivated backlit.In the condition of error and low electricity, according to the key, open/equipment into "sleep" state immediately.

Low Battery Indicator

When measuring screen does not appear when the battery symbol, said the battery voltage is normal, sphygmomanometer can work normally.

When the screen appear when measuring marks, said the battery voltage is low, please replace the battery, prevent blood pressure monitor can not work normally.

Screen appears when measuring the flashing, and LCD screen will appear low voltage symbol

“LO”, sphygmomanometer automatic shutdown after about 5 s please immediately replace the battery, ensure the sphygmomanometer can normal use.


Bluetooth requirements

The monitor requires a device with:

. Bluetooth 4.0 or later

. Android 5.0 or later

. IOS 9.0 or later

And works with:

. iphone , iPod, iPad

. Android Phones and Tablets

Bluetooth connection

Wireless communication

Frequency range : 2.4 Ghz (2400-2483.5 MHz)

Modulation : GFSK

Antenna gain:0.5dBi

-Using for the first time

1. Download the free “JoyHealth” App: On your mobile phone or table go to www.sejoy.com.

2.Open the App on your phone or tablet. If requested, you should enable Bluetooth on your

device. You can enable Bluetooth under the Settings menu on your smart phone or table.

3. Create a new user login, or login with your existing user name and password.

4. Selection device “Blood pressure monitor”.

-Pairing

your monitor with a

S

mart Device

1. Long press the " " button on your monitor until the word "bE" flashes on your monitor .

20

Static Pressure Measurement

I n the press key insert battery into the test mode at the same time, according to an inferior version available algorithm and software version number, alternating press Λ and V may continue to see test.

Note: Only Service personnel permitted to access to this mode, the mode unavailable in

normal use.

2. Open the APP and click "pair device" button, a popup window will appear. Click "Search device"

button to display all sphygmomanometer devices(The display information includes the device model and MAC address), then you can find the sphygmomanometer through the "device Name", click the pictureA film or text can be used to pair the device.

Unit Operation

The MAC address

3. After the pairing is complete, the device interface switches from boo interface, indicating that

the pairing is successful.

-Transfer your readings

1. As soon as your measurement is complete, open the app on your smart phone to transfer

your reedings.

Notr: On the paired smartphone, Bluetooth must be enabled.

2. You can view your blood pressure readings on the app.


Troubleshooting

Abnormal phenomenon

Cause analysis

The armband is tied too tight or too loose,

Or the arm strap is tied incorrectly;

Processing method

Roll the armband correctly

Move the arm during measurement or

Electronic sphygmomanometer

Stay quiet, keep your arm steady, and do not move the monitor

Abnormal sphygmomanometer

Speaking, nervous or emotional

during measurement

Incorrect measurement posture

Instead of talking, take deep

breaths to calm your mood and relax your body

Adjust posture, see

"Blood pressure gauge Wearing”

There is interference in charging process or improper operation in measuring process

See operation Instructions.

The following table shows the error signs that may occur during measurement, possible causes and handling methods. Please measure again using the correct method

Error display

Er1

Er2

Er3

Er4

Er5

LO

The cause of the problem

Can't detect high and low pressure

Cuff too loose or loose

The pressure exceeds 15mmHg for 3 minutes

Improper compression caused by arm or body movement

The solution

Please fasten the cuff before measuring


Check whether the cuff is knotted or the vent valve is blocked. If the problem

persists, contact the manufacturer

Hold the arm or body still and

measure again

The pressure exceeds 300mmHg

Battery dead


Replace the battery or connect the

power adapter (if any).

Note: If you cannot solve the abnormal situation by yourself, you can consult the manufacturer or the manufacturer's designated unit by phone. It is forbidden to disassemble and repair without permission. If necessary, professional maintenance personnel can ask the manufacturer for the list of components and circuit schematic diagram.

22

Blood Pressure Information

Blood Pressure

Blood pressure is the force of blood pushing against the walls of arteries. It is typically measured in millimeters of mercury (mmHg.) Systolic blood pressure is the maximum force exerted against blood vessel walls each time the heart beats. Diastolic blood pressure is the force exerted on blood vessels when the heart is resting between beats.

An individual's blood pressure frequently changes throughout the course of a day.

Excitement and tension can cause blood pressure to rise, while drinking alcohol and bathing can lower blood pressure. Certain hormones like adrenaline (which your body releases under stress) can cause blood vessels to constrict, leading to a rise in blood pressure.

If these measuring numbers become too high, it means the heart is working harder than it should.

200 Upper curve : systolic blood pressure

Lower curve: diastolic blood pressure

150

100

50

6 1 2 1 8

Time of day

Example: fluctuation within a day (male, 35 years old)

2 4

23 Blood Pressure Information

WHO Blood Pressure Classification Indicator

The BM 92 is equipped with a classification indicator based on established guidelines from the World Health Organization. The chart below (color coded on monitor unit) indicates test results.

Mild Hypertension

Severe Hypertension

Moderate Hypertension

Mild Hypertension

High-n ormal

Normal

Optimal

: Blood Pressure Classification Indicator

24

Blood Pressure Information

Health Reminder

Hypertension is a dangerous disease that can affect the quality of life. It can lead to a lot of problems including heart failure, kidney failure, and cerebral hemorrhaging.

By maintaining a healthy lifestyle and visiting your physician on a regular basis, hypertension and relative diseases are much easier to control when diagnosed in their early stages.

Systolic

( mmHg )

Severe Hypertension

180

160

140

130

120

Optimal

Moderate Hypertension

Mild Hypertension

High-normal

Normal

80 85 90 100 110 Diastolic

( mmHg )

Note: Do not be alarmed if an abnormal reading occurs. A better indication of an individual's

blood pressure occurs after 2-3 readings are taken at the same time each day over an

extended period of time. Consult your physician if test results remain abnormal.

25 Blood Pressure Q&A

Q:

What is the difference between measuring blood pressure at home or at a professional

healthcare clinic?

A:

Blood pressure readings taken at home are now seen to give a more accurate account as

they better reflect your daily life. Readings can be elevated when taken in a clinical or

medical environment. This is known as White Coat Hypertension and may be caused by

feeling anxious or nervous.

Note: Abnormal test results may be caused by:

1. Improper cuff placement

Make sure cuff is snug-not too tight or too loose.

Make sure bottom of the cuff is approximately 1-2cm (1/2'') above the elbow

joint.

2. Improper body position

Make sure to keep your body in an upright position.

3. Feeling anxious or nervous

Take 2-3 deep breaths, wait a few minutes and resume testing.

26

Q:

What causes different readings?

A:

Blood pressure varies throughout the course of a day. Many factors including diet,

stress, cuff placement, etc. may affect an individual's blood pressure.

Q:

Should I apply the cuff to the left or right arm? What is the difference?

A:

Either arm can be used when testing, however, when comparing results, the same arm

should be used. Testing on your left arm may provide more accurate results as it is

located closer to your heart.

Q:

What is the best time of day for testing?

A:

Morning time or any time you feel relaxed and stress free.

Maintenance

1. Avoid dropping, slamming, or throwing the unit.

2. Avoid extreme temperatures. Do not expose unit directly under sunshine.

27 Maintenance

4. Cuff Cleaning and Disinfection:

A) Spread the cuff (skin-contact surface) upwards onto a clean table. Use a damp clean cloth

(water-based) to wipe the skin-contact surface with a force.

B) Soak the cloth clean with drinking water and wring it dry. Repeat A) with the damp cloth

(water-based) for 3 times.

C) Apply 70%-80% alcohol to a new cloth (or 75% alcohol cotton-ball), use it to

wipe the skin-contact surface with a force. Then soak the cloth with the alcohol again

(or change a new 75% alcohol cotton-ball), repeat the disinfection procedure for 3 times.

D ) When the disinfection towards the skin contactsurface is finished , wipe thenon skin

contact surface with a cloth (alcohol-based) or alcohol cotton-ball thoroughly for

3 times.

E ) Leave the cuff naturally dry , then it is ready for reuse .

Notice: Do not soak in water or splash water on it.

28

5. Do not use petrol, thinners or similar solvents.

3. When cleaning the unit, use a soft fabric and lightly wipe with mild detergent.

Use a damp cloth to remove dirt and excess detergent. If the previous cleaning instructions are not successful, repeat several times until the visible dirt is removed.

6. Remove batteries when not in operation for an extended period of time.

7. Do not disassemble product.

Specifications

Product Description

Model

Display

Arm-type Fully Automatic Blood Pressure Monitor

BM 92

LCD Digital Display Size:71mm x 76mm(

2.80" x 2.99")

Measurement Method

Measurement Range

Oscillometric Method

Systolic Pressure

Diastolic Pressure

Pressure

Pressure

60mmHg ～ 2 60 mmHg

40mmHg ～ 20 0 mmHg

0mmHg

～

299mmHg

± 3mmHg

Pressurization

Pulse 30 ~ 180 Beats/Minute

± 5%

Pulse

Automatic Pressurization

Memory

Function

2x120 Memories in Two Groups with Date and Time

Irregular Heartbeat Detection

WHO Classification Indicator

Last 7 days average

Average for the last 7 days

Afternoon average for the last 7 days

Low Battery Detection

Automatic Power-Off

Voice

Backlighting

Bluetooth

HSD

Power Source 4 AAA batteries

Battery Life

Unit Weight

Unit Dimensions

Cuff Circumference

Approximately 2 months at 3 tests per day

Approx.180g (6.35 oz.) (excluding battery)

Approx.125mm X 95mm X 44mm(4.92" x 3.74" x 1.73" ）

Medium cuff: Fits arm circumference 22-36 cm

Temperature

Operating Environment

Humidity

10 ℃ ~ 40 ℃ (50

15% ~ 93% RH

℉ ~104 ℉ )

8. It is recommended the performance should be checked every 2 years.

9. Expected service life: Approximately three years at 10 tests per day.

10.No service and maintenance while it is in use and maintenance only be performed by service

personnel. Service and maintenance require parts, repair, technical support will be provided.

29 Specifications

800hPa~1060hPa

Temperature:

Storage Environment

Humidity

Ingress Protection rating:

IP 21,Indoor Used Only

-25 ℃ ~55 ℃ (-13 ℉ ~131 ℉ )

≤ 93% RH

Battery Shelf life: 60 months

Battery Storage

Temperature:

-25

℃

~55

℃

(-13

℉

~131

℉

)

30

Specifications are subject to change without notice.

Safety Standard

( included but not limited

):

1

.

IEC 80601

-

2

-

30

, medical electrical equipment

- part 2

-

30

: particular requirements for the basic safety and essential performance of automated noninvasive sphygmomanometers . ( Cardiovascular )

2

.

ISO 81060

-

2

, non

invasive sphygmomanometers

- part 2

: clinical validation of automated measurement type

. (

Cardiovascular

)

3

.

AAMI

/

ANSI ES 60601

-

1

:

2005

/(

R

)

2012 and C1

:

2009

/(

R

)

2012 and

, a2

:

2010

/( r

)

2012

( consolidated text

) medical electrical equipment

-- part 1

: general requirements for basic safety and essential performance

4 . AAMI / ANSI / IEC 60601 1 2 , Medical Electrical Equipment -- Part 1 2 : General

Requirements For Basic Safety And Essential Performance -- Collateral Standard :

Electromagnetic Disturbances

--

Requirements And Tests

(

General II

(

ES

/

EMC

)).

5

.

IEC 60601

-

1

-

11

, medical electrical equipment

- part 1

-

11

: general requirements for basic safety and essential performance

- collateral standard

: requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment .

Correct Disposal of This Product

(Waste Electrical & Electronic Equipment)

This marking shown on the product indicates that it should not be disposed with other household waste at the end of its life. To prevent potential harm to the environment or to human health, please separate this product from other types of wastes and recycle it responsibly. When disposing this type of product, contact the retailer where product was purchased or contact your local government office for details regarding how this item can be disposed in an environmentally safe recycling center.

Business users should contact their supplier and check the terms and conditions of the purchasing agreement. This product should not be mixed with other commercial wastes for disposal. This product is free of hazardous materials.

Warranty

The Blood Pressure Monitor is guaranteed for 2-year from the date of purchase. If the

Blood Pressure Monitor does not function properly due to defective components or poor workmanship, we will repair or replace it freely. The warranty does not cover damages to your Blood Pressure Monitor due to improper handling. Please contact local retailer for details.

31

Electromagnetic Compatibility Information

The device satisfies the EMC requirements of the international standard IEC

60601-1-2. The requirements are satisfied under the conditions described in the table below. The device is an electrical medical product and is subject to special precautionary measures with regard to EMC which must be published in the instructions for use. Portable and mobile HF communications equipment can affect

the device. Use of the unit in conjunction with non-approved accessories can affect the device negatively and alter the electromagnetic compatibility. The device should not be used directly adjacent to or between other electrical equipment.

Table 1

Guidance and declaration of manufacturer-electromagnetic emissions

The device is intended for use in the electromagnetic environment specified below.

The customer or the user of the device should assure that it is used in such an environment.

32

Emissions test

Radiated emission CISPR 11

Conducted emission CISPR 11

Compliance

Group 1, class B.

Group 1, class B.

Electromagnetic environment

-guidance

The device uses RF energy only for its internal function. Therefore, its emissions are very low and are not likely to cause any interference in nearby electronic equipment.

The device is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.

Harmonic emissions

IEC 61000-3-2

Voltage fluctuations/

flicker emissions

IEC 61000-3-3

Class A

Complies


Table 2

Guidance and declaration of manufacturer-electromagnetic immunity



IMMUNITY test

IEC 60601 test level

Compliance level


-guidance

Electrostatic discharge (ESD)

IEC 61000-4-2

± 8 kV contact

±

2 kV,

±

4 kV,

±

8 kV,

± 15 kV air

± 8 kV contact

±

2 kV,

±

4 kV,

±

8 kV,

±

15 kV air

Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30 %.

Electrostatic transient/burst

IEC 61000-4-4

± 2 kV ,

100kHz, for

AC power port

±

2 kV ,

100kHz, for

AC power port

Mains power quality should be that of a typical commercial or hospital environment.

33

Surge

IEC 61000-4-5

±0.5kV, ±1kV

(differential mode)

±0.5kV, ±1kV

(differential mode)


Voltage dips, short interruptions and voltage variations on power supply input lines

IEC 61000-4-11

0 % UT;

0,5 cycle

At 0°, 45°, 90°,

135°, 180°, 225°

, 270° and 315°

0 % UT;

0,5 cycle

At 0°, 45°, 90°,

135°, 180°, 225°

, 270° and 315°


0 % UT; 1 cycle and

70 % UT;

25/30 cycles

Single phase:

at 0°

0 % UT; 1 cycle and

70 % UT;

25/30 cycles

Single phase:

at 0°

0 % UT;

250/300 cycle

0 % UT;

250/300 cycle


Table 2(continued)




IMMUNITY test

IEC 60601 test level

Compliance level


-guidance

Radiated RF EM

fields

IEC 61000-4-3

10 V/m80MHz-

2.7Ghz 80%AM

at 1kHz

Portable and mobile RF communications equipment should be used no closer to any part of the device, including cables, than

10 V/m80MHz-

2.7Ghz 80%AM at 1kHz the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.

Recommended seperation distance 80 MHz to 800 MHz 800 MHz to 2.7 Ghz where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in metres (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, a should be less than the compliance level in each frequency range. Interference may occur in the vicinity of equipment marked with the following symbol:

Conducted disturbances

Induced by RF fields

IEC 61000-4-6

3 V in 0.15

MHz- 80 MHz

6 V in ISM and/or amateur radio bands between 0.15

MHz and 80

MHz 80 %

AM at 1kHz

3 V in 0.15

MHz- 80 MHz

6 V in ISM and/or amateur radio bands between 0.15

MHz and 80

MHz 80 %

AM at 1kHz

Portable and mobile RF communications equipment should be used no closer to any part of the device, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.

Recommended seperation distance 80 MHz to 800 MHz 800 MHz to 2.7 Ghz where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in metres (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, a should be less than the compliance level in each frequency range. Interference may occur in the vicinity of equipment marked with the following symbol:

34

Power frequency

(50/60 Hz) magnetic field

IEC 61000-4-8

30 A/m; 50Hz or 60Hz

30 A/m; 50Hz or 60Hz

Power frequency magnetic fields should be at levels charactertic of a typical location in a typical commercial or hospital environment.

450

710

745

780

810

870

930

1720

1845


Table 3


Nowadays, many RF wireless equipments have being used in various healthcare locations where medical equipment and/or systems are used. When they are used in close proximity to medical equipment and/or systems, the medical equipment and/or systems’ basic safety and essential performance may be affected. Arm-type Fully Automatic Digital Blood Pressure Monitorhas been tested with the immunity test level in the below table and meet the related requirements of IEC 60601-1-2:2014. The customer and/or user should help keep a minimum distance between RF wireless communications equipment and this medical equipment and/or systems as recommended below.

Test frequency

(MHz)

385

Band

(MHz)

Service Modulation

Maximum

power

(W)

380-390

430-470

Pulse

TETRA 400 modulation

GMRS 460

FRS 460

18Hz

FM

± ٥ kHz deviation

1 kHz sine

1.8

2

Distance

(m)

0.3

0.3

Immunity

test level

(V/m)

27

28

704-787

800-960

LTE

Band

13, 17

Pulse

modulation

217Hz

GSM 800/900,

TETRA 800,

iDEN 820,

CDMA 850,

LTE Band 5

Pulse

modulation

18Hz

1700-1990

GSM 1800;

CDMA 1900;

GSM 1900;

DECT;

LTE Band 1, 3,

4, 25; UMTS

Pulse

modulation

217Hz

0.2

2

2

0.3

0.3

0.3

9

28

28

35

1970

2 0.3

28 2450

5240

5500

5785

2400-2570

Bluetooth,WLAN,

802.11 b/g/n,RFID

2450,LTE Band 7

5100-5800

WLAN

802.11

a/n

Pulse modulation

217Hz

Pulse modulation

217Hz

0.2

0.3

9


Table 4

Recommended separation distances between portable and mobile RF communications equipment and the device

The device is intended for use in an electromagnetic environment in which radiated therefore disturbances are controlled. The customer or the user of the device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the device as recommended below, according to the maximum output power of the communications equipment.

Rated maximum output power of transmitter

W

Separation distance according to frequency of transmitter

m

80 MHz to 800 MHz 800 MHz to 2.7 GHz

0.01

0.1

1

10

100

0.12

0.38

1.2

3.8

12

0.23

0.73

2.3

7.3

23

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.

NOTE1 At 80 MHz and 800 MHz, the separation distance for th frequency range applies.

e higher

NOTE2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

36

Additional Notes

Important Instructions Before Use

1. 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.

2.WARNING: 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 Armtype Fully Automatic Digital Blood Pressure Monitor, including cables specified by the

MANUFACTURER. Otherwise, degradation of the performance of this equipment could result.

3.The software identifier refer to the software verification and validation report , and the file code is JYRJ201009001.

4.

verify manometer pressure accuracy:

In the power down state, press and hold the " START/STOP" button, and theninstall the batteries. Until the LCD screen is full, release the " START/STOP" button.

When the LCD screen displays the double zero, the bloodpressure meter is in static state.

At this point, 500ml gas capacity, calibrated standard pressure gauge and manual pressure device can be connected to the sphygmomanometer through the sleeve interface of the sphygmomanometer, and manual pressure can be applied to the effective display range of the sphygmomanometer, and then the difference between the reading of the sphygmomanometer and that of the standard pressure gauge can be compared.This mode can be used to verify manometer pressure accuracy.

5.Contraindications:

Product is not intended for infants or individuals who cannot express their intentions.

6.Intended Use

The digital blood pressure monitor are reusable for clinical and home use and are non-invasive blood pressure measurement systems designed to measure the systolic and diastolic blood pressure and pulse rate of adolescents and adults individual by using a non-invasive technique, which is a well-known technique in the market called the “oscillometric method”.

it can measure the systolic blood pressure, diastolic blood pressure and pulse rated on up-arm,and the device is reusable for clinical or home use.

7.The patient is the operator: the PATIENT is an intended OPERATOR.

the PATIENT Do not carry out other maintenance operations except to replace the battery.

8.WARNING:

Do not modify this equipment without authorization of the manufacturer.

9. ESSENTIAL PERFORMANCE Maintenance advice:

Pressure calibration will be carried out when this product leaves the factory. Patients can use the method described in the section "Verify Manometer Pressure Accuracy" to verify the accuracy.

If the accuracy deviation is large, please contact the manufacturer to recalibration.

10.Mechanical strength and resistance to heatThe resistance to heat will be retained by device during the EXPECTED SERVICE LIFE of the ME EQUIPMENT.

37

Additional Notes

11.Do not place the blood pressure monitor and cuff at will. It will cause asphyxiation if the child swallows or twine around his neck.

12.The cuff and the case of the blood pressure monitor have been tested for biocompatibility and do not contain allergenic or harmful materials.Please stop using it if allergy occurs during use.

13.Warning:

Non-professionals do not modify the equipment, otherwise it will make the equipment measurement is not accurate.

14.Warning:

Do not expose the equipment for a long time, otherwise it will reduce the performance of the equipment.

15.Warning:

This device is not used for children and pets

16.Clean:

The equipment can be cleaned by lay operator according to the cleaning procedures in the instructions

17.Warning:

Do not use a damaged cuff for blood pressure measurement.

18.Warning:

When measuring with the cuff, if the tester feels seriously uncomfortable, press the button of the blood pressure monitor to deflate the cuff, or remove the cuff directly from the arm.

19.Warning:

If an unexpected reading occurs, the operator can take several more measurements and consult a doctor.

20.Warning:

This equipment is used outside the specified environment, may damage the equipment, and may be inaccurate measurement.

21.ME equipment not intended for use in conjunction with flammable agents “ ME equipment not intended for use in oxygen rich environment ”

2.Materials, accessories and detachable parts other than those specified in the manual may pose unacceptable risks.

23.Do not modify. Do not connect to other devices .

Correct Disposal of This Product

(Waste Electrical & Electronic Equipment)

This marking shown on the product indicates that it should not be disposed with other household waste at the end of its life. To prevent potential harm to the environment or to human health, please separate this product from other types of wastes and recycle it responsibly. When disposing this type of product, contact the retailer where product was purchased or contact your local government office for details regarding how this item can be disposed in an environmentally safe recycling center.

Business users should contact their supplier and check the terms and conditions of the purchasing agreement. This product should not be mixed with other commercial wastes for disposal. This product is free of hazardous materials.

38

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