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Automatic
Wrist Blood Pressure Monitor
MMooddeell NNoo.. HHLL115588HHMM
1
Table of Contents
Medical Disclaimer……………………………………………………………………………03
Intended Use………………………………………………………………………………..…03
About Blood Pressure………………………………………………………………………04
Measurement Method………………………………………………………………06
Accuracy………………………………………………………………………………………….. 06
Precautions…………………….…………………………………………………………………07
Device Overview……………………………………………………………………………….09
Symbol Definitions………………………………………………………………………….11
Features………………………………………………………………………………………….12
Installing Batteries………………………………………………………………………….16
Applying the Cuff…………………………………………………………………………….17
Positioning Guide………….………………………………………………………………….18
Measurement Procedure………….…………………………………………………….19
Bluetooth Transmission……………………………………………………………………21
Memory Function…………………………………………………………………………….22
Storage and Maintenance……………………………………………………………….23
Troubleshooting……………………………………………………………………………….24
Warranty & Recalibration………………………………………………………………….25
Specifications………………………………………………………………………………….26
Note………………………………………………………………………………………….…….28
Appendix…………………………………………………………………………………….…….29
Blood Pressure Diary……………….……………………………………………….…….31
2
Medical Disclaimer
This manual and product are not meant as a substitute for advice
provided by your doctor.
You are not to use the informatio n cont ained here in, or this pr oduct
for diagnosing or treating a health problem or prescribing any
medication. If you have or suspect that you have a medical problem,
promptly consult your healthcare provider.
Intended Use
This device uses th e oscillometr ic method to au tomatically measure
systolic and diastolic blood pressure as well as heart rate.
The measurement position is at human being’s wrist.
All values can be read out in one LCD panel.
The device is desig ned for home use and recommende d for use by
adults aged 18 years and ol der with wrist circumference ranging 135
~ 195 mm (approx. 5.3 ~ 7.7 inch).
3
About Blood Pressure
1. What is blood pressure?
Blood pressure is the me asurement o f the force of blood pushing
against the walls of the arteries. Arterial blood pressure is
constantly fluctuati ng during the co urse of the cardiac cycle. T he
highest pressure in the cycle is called the systolic blood pressure,
and represents the pressure in the artery when the heart is beating.
The lowest pressure is the diastolic blood pressure, and represents
the pressure in the artery when the heart is at rest. Both the
systolic and the diastolic pressure are necessary for a physician to
evaluate the status of a patient's blood pressure.
Many factors such as phys ica l activity, anx ie ty o r the ti me o f day,
can influence your bloo d pr e ssur e . B lo o d pr e ssur e is typically low
in the mornings and increases from the afternoon to the evening.
It is on average lower in the summer and higher in the winter.
2. Why is it useful to measure blood pressure
at home?
Having one's blood pressure measured by a doctor in a hospital or
a clinic, is often associated with a phenomenon called “White Coat
Hypertension” where the patient becomes nervous or anxious,
thus raising his blood pressure. There are also numerous other
factors that might cause your blood pressure to be raised at a
specific time of day. This is why medical practitioners recommend
home monitoring as it is important to get readings of blood
pressure during differe nt times o f the day to re ally get an i dea of
your real blood pressure.
Medical practitioners generally recommend the “Rule of 3”, where
you are encouraged to take your blood pressure thre e times in a
row (at 3 ~ 5 minut e interval), three ti mes a d ay for thre e days.
After three days you can average al l th e r esults and t his wi ll give
you an accurate idea of what your blood pressure really is.
4
About Blood Pressure
A. WHO blood pressure classifications:
Standards for assessment
of high or low blood pressure
without regard to age, have
been established by the World
Health Organization (WHO),
as shown in the chart.
However this chart is not
exact for classification of blood pressure and it's intended to be
used as a guide in u nde rs tandi ng no n-in vasive b loo d pressu re
measurements. Please c onsult with your physician for pro per
diagnosis.
B. Variations in blood pressure:
Individual blood pre ssures vary greatly both on a daily and a
seasonal basis. These variations are eve n mor e pro nounced i n
hyper tense patients. Normally the blood pressure rises while at
work and is at its lowest during sleeping period.
(hyper tense: means a person who has high blood
pressure symptom.)
The graph below illustrated the
variations in blood pressure over a
whole day with measurement taken
every five minutes.
The thick line represents sleep. The
rise in blood pres sure at 4 PM (A in
the graph) and 12 PM (B in the graph) correspond to an attack
of pain.
5
Measurement Method
HL158HM Automatic Wrist Blood Pressure Monitor measures blood
pressure and heart rate by oscillometric method, meaning the
fluctuations in pressure are measured. Once the cuff is wrapped
around your wrist, just turn on the monitor and inflation
automatically starts. The inflation of the cuff creates pressure around
the arteries inside the wrist.
Within the cuff is a gauge which senses the fluctuations (oscillations)
in pressure. The fluctuation measured represents the degree of
intensity that your arteries contracting with each heart beat, and also
a res ult of the pressure that the cuff has placed on the wrist. The
monitor m easures these contractions and converts the information to
a digital value. This is the result displayed on the monitor screen.
Once the measurement is complete, the cuff will automatically
deflate.
Accuracy
HL158HM Automatic Wrist Blood Pressure Monitor has been clinically
tested against a scientific device called a mercury
sphygmomanometer, considered the gold standard in blood pressure
measurement.
All HL158HM Automatic Wrist Blood Pressure Monitors have
performed equivalent to measurements taken with this scientific
device and are within the accuracy limits prescribed by the American
National Standard for Electronic or Automated
Sphygmomanometers.
*We suggest our users
have their blood pressure monitor
checked every 2 years. T
his operation should only be
performed by Manufacturer or by authorized representatives.
6
Precautions
* Do not use this ma nual a nd pro duct a s a subs tit ute for ad vice,
diagnosing or treating a health problem or prescribing any
medication by your doctor. If you have a medical problem,
promptly consult your healthcare provider.
* Read the Instruction Manual thorough ly before measur ing and
keep it at han d for your reference at any tim e.
* This device uses th e oscillometric method to me asure systolic
and diastolic blood pressure as well as your heart rate. It’s
recommended for use by people over the age of 18 and not to be
used on infant or children.
* The device is designed for home use and not suitable for clinical
use.
Do not take a me asurement in a low (less than 41 ℉/5 ℃) and
high (more than 104 ℉/40 ℃) temperature, nor in a place outside
humidity ranges (15% ~ 93% R.H.), or you may get inaccurate
readings.
Wait 30 ~ 45 minutes before measurement if you’ve just
consumed caffeinated beverages or smoked cigarettes.
Rest at least 5 ~ 10 minutes befo re taking a measurement.
To allow your blood vessels to return to the condition prior to
taking the measure ment, please wait at least 3 ~ 5 minutes in
between measurements. You may need to adjust the wait time
according to your personal physiological situation.
We recommend you using the same wrist (preferably the left wrist)
and measuring around the same time each day.
Sit down comfortably and place your elbow on the table with your
feet flat on the floor. Please do not cross your legs during
measurements.
Keep the device at heart level. Relax your hand with the palm
facing up.
Perform measurements in a quiet and relaxed environment at
room temperature.
Do not move or sh ake the device dur ing a measurement. Please
keep quiet and do not talk during measurements.
7
Precautions
Keep in mind that blood pressure naturally varies from time to
time through out the day and is affected by lots of different factors
such as stress, eating, smoking, alcohol consumption, medication,
and physical activity, etc.
Normally the blood pressure rises while at work and is at its lowest
during sleeping period.
Blood pressure measurements should be interpreted by a
physician or a trained health professional who is familiar with your
medical history. Using the unit and recording the results regularly
for your physician to interpret, you will keep your physician
informed of the continuing changes in your blood pressure.
If you have one of the circulatory problems as arteriosclerosis,
diabetes, liver disease, kidney disease, severe hypertension,
peripheral circulation….., please consult your healthcare
professional before using the device.
This product is not suitable for people with arrhythmias and
pregnant women.
Blood pressure measurements taken with this device are
equivalent to those obtained by a trained observer using the cuff /
stethoscope auscultation method and are within the accuracy
limits prescribe d by the American National S tandard for Manual,
electronic, or Automated Sphygmomanometers.
*Attention
！
1. Do not use the device on infants, children, or those who cannot express their
own intention.
2. The device is equipped with sensitive electronic components. While
measuring, avoid strong electrical or electromagnetic fields, e.g. mobile
phones, microwave ovens, etc; or it m ay lead to temp orary rea din g error or
inaccuracy.
3. Consider the electromagnetic compatibility of the device (ex. power
disturbance, radio frequency interference etc.) Please use it indoor only.
4. Over high frequency measurements may result in blood flow interference,
which is likely to cause uncomfortable sensations, such as partial
subcutaneous hemorr hage, or tempor ary numbnes s to your wrist. In general,
these symptoms should not last long. However, if you do not recover in time,
please seek your medical practitioners for help.
8
Device Overview
Product components
LCD DISPLAY
START / STOP
BUTTON
AAA “LR03” (1.5V)
ALKALINE BATTERY X 2
STORAGE
CASE
*Caution！
Substitution of a component different from that supplied might result in measurement error.
MODE
BUTTON
MEMORY
BUTTON
RISK CATEGORY
INDICATOR
User Select
BUTTON
BLUETOOTH
Indicator
+
BUTTON
9
Device Overview
Unit display
Heart Rate
Low Battery Symbol
User 1
User 2
Hour : Minute
Month / Date/ Year
Pulse Symbol
Diastolic Ra te
Systolic Rate
Risk Category
Indicator
Irregular Heartbeat
Detector
Error Symbol
The last 3 Average
Symbol
10
Symbol Definitions
SYMBOLS Definitions
Low Battery Symbol
This symbol ap pears when the battery power
is excessively
low or the polarity reverses.
We suggest you replace all batteries with new ones
, and
make sure the +/- polarities are properly positioned.
Pulse Symbol
Once pulse is detected, the symbol flashes with each pulse
beat.
Our suggestion:
Please do not talk or move during measurements.
Error Symbol
This symbol appears when measurement error.
Irregular Heartbeat
Detector
This symbol appears for 1 minute when the user was talking,
moving, shaking, or an irregular heart beat was detected
during measurements.
Our suggestion:
Please do not talk or move during measurements.
Repeat the meas ure ment after resting for at
least 5 min ut es,
and restart your measurement while sitting down comfortably
and quietly.
User 1
Symbol for User 1.
User 2
Symbol for User 2.
Memory Average
This symbol appears when LCD displays average value of last
3 readings.
Risk Category Indicator
icon
Compares readings against blood pressure guidelines. See
next page for more information.
11
Features
Risk Category Indicator
This device is equipped w ith Risk C ateg or y Indicator which classifies
your blood pressure measurements into four stages (Normal,
Pre-hypertension, Stage 1 Hypertension to Stage 2 Hypertension)
based on the blood pressure standards established by the U.S.
Department of Health and Human Services and the National Institutes
of Health. Besides, for yours and your loved ones’ health, we further
classify the four stages into numeral ranges, which sorts out
hypertension symptom s more clearly. Moreov er, to your convenien ce
and readability, we use four corresponding colors to represent your
measuring result. Refer to below comparison chart for details:
After each measurement is completed, LCD displays the stages of
blood pressure symbols will depend on your readings and
corresponds to Risk Category Indicator.
Stages of Blood
Pressure Levels
Systolic
(mmHg)
Diastolic
(mmHg)
Important Notice
Stage 2
Hypertension
≧160 ≧ 100
You may use the function to
effectively track your blood
pressure. Yet the standard
s and
classifications a r e g e neral guidelin e s
for your refe rence a s an
individual’s
blood pressure varies among
different people, age groups, etc. It
is important that you consult with
your physician to know your normal
blood pressur e range a s well as th e
p
oint at which you will be considered
at risk.
Stage 1
Hypertension
140 ~ 159 90 ~ 99
Pre-hyperten
sion
120 ~ 139 80 ~ 89
Normal < 120 < 80
Normal
Pre-hypertension
Stage 1 Hypertension
Stage 2 Hypertension
12
Features
For adults 18 and older who are not on medicine for high blood
pressure, are not having a short-term serious illness, and do not have
other conditions, such as diabetes and kidney disease. To determine
category of risk when systolic and diastolic readings fall into two areas,
use the higher of the two numbers for classification. There is an
exception to the ab ove definition of high blood pressure for people
with diabetes and chronic kidney disease. A blood p ressure of 130/80
mmHg or higher is considered high blood pressure for those
individuals.
*Note !
The above table is not exact for classification of b lood pressure and it's
intended to be used as a guide in understanding non-invasive blood
pressure measurements.
Usually this is not a cause for concern; however we recommend you
consult with your physic ian for proper diagnosis or s eek medical advice.
Please note that the device does not appropriate to diagnose hypertension,
and it is only for user reference on blood pressure monitoring.
13
Features
Irregular Heartbeat Detector
The symbol will appear on screen indicating a certain
heartbeat irregularity was detected during measurement.
The heartbeat rhythm that is more than or less than 25% from the
average rhythm is usually defined as an irregular heartbeat rhythm.
Talking, moving, shaking or an irregular pulse during the
measurement can result in the appearance of this symbol.
Usually this is not a cause for concern, however if the symbol
appears often, we recommend you seek medical advice.
And please note that the device does not replace a cardiac
examination, but s erves to detect pulse irregularities at an early
stage.
*Note！
The pulse display is not suitable for checking the frequency of heart
pacemakers. If a certain pul se irregularity is det ected during measu rement
often, we recommend you seek medical advice
As a safeguard, we recommend that if you have arrhythmias such as atrial or
ventricular premature beats and atrial fibrillation or any other special
conditions you should check with your physician before using your device.
The IHB function is not designed for use by people with arrhythmias nor for
diagnosin g or treati ng an arrh ythmic p roblem. In orde r to fil ter the un stable
status of user and avoid affecting the detection of heart rate from any
movement, shaking o r talking in the beginning of me asurement, the method of
averaging heart beat intervals o f subject dev ice is calcu lated with the three
proper heart beat pulses detected in the beginning of measurement and that is
different from a strict mathematical averaging of all recorded intervals.
At least 3 beats w ith at least 25 % di fference from the averag e heart beat
interval will generate the IHB icon on the screen.
14
Features
Bluetooth Data Transmission
HL158HM features a built-in “Bluetooth Data Transmission” function,
which enables the device automatically transmit measuring results
to paired Bluetooth device.
Bluetooth compatibility with blood pressure monitor for
Bluetooth-enabled device is:
Bluetooth 3.0 or 4.0 for Android 2.3.3 or above,
Bluetooth 4.0 for iOS device
Note:
HL158HM is subject to and complies with electromagnetic
compatibility (EMC) standard of EN 60601-1-2 and U.S. federal
guidelines, Part 15 of the FCC (Federal Communications
Commission) rules for devices with RF capability. These
guidelines help ensure that your device will not affect the
operation of other nearby devices. Additionally, other devices
should not affect the use of your device.
Other wireless devices that are in use nearby, such as a cell or
mobile phone, or a wire less network, may prevent or de lay the
transmission of data from your device to paired Bluetooth device.
Moving away from the source of the interference or turning off
these devices to res olve the problem.
Make sure HL158HM and paired Bluetooth device are within
acceptable distance (no more than 10 meters) with each other . If
not, put them closer.
If you plan to transmit test results to paired Bluetooth device, be
sure to select User 1 or 2 before measurements, in case other
people’s results may be transmitted to your paired Bluetooth
device or included in your past results.
About Bluetooth Transmission Function
The Bluetooth transmission function might not be workable to some
Bluetooth devices because of the compatibility of Android system.
Some issues that the Bluetooth implementations on these devices
have unresolved errors. It is not because of the Bluetooth module in
blood pressure monitor is not supported.
15
Installing Batteries
When LOW BATTERY SYMBOL appe ars on the display, or no
reaction toward operation, please change batteries.
Replace all worn-out batteries with new ones and do not mix new and
used batteries. Do not mix alkaline, standard (carbon-zinc) or
rechargeable (cadmium) batteries either. Such action may shorten
the battery life or cause the device to malfunction.
Slide the battery cover and insert 2 AAA “LR03” alkaline batteries into
the battery compartme nt as shown on the f igure below. Make sure
the polarities “+” and “–” ends are properly positioned.
*Attention！
Batteries are hazardous w aste. Do not dispose of them together
with the household garbage . Ple a se discard worn-out batteries to
the recycling site according to local regulations.
Keep the battery away from children in case they choke on it.
If the device is not to be used for over 2 months, please remove
the batteries from its compartment for power-saving.
Please replace all worn-out batteries with new ones when you are
operating the Bluetooth transmission function, and the LOW
BATTERY SYMBOL appears on the display.
16
Applying the Cuff
Do not place the pressure cuff over a
jacket or sweater sleeve. Wrap the
pressure cuff around t he bare wrist with
the monitor facing you.
Wrap the cuff snugly. Do not make it too tight.
Fold the remaining part of the cuff back
out of the way.
Leave approximately 0.4 inch (10 mm)
between the cuff and the bottom o f your
hand palm.
*Note！
Do not use this device if your wrist has any wound or injury.
Do no t wrap the cuff around a ny body part othe r than your
wrist.
0.4 inch (10 mm)
5.3 ~ 7.7 inch (135 ~ 195 mm)
17
Positioning Guide
It is extremely imp ortant that the cuff be at the same he ight as the
heart.
Having the cuff higher or lower may cause inaccurate results.
1. Sit down comfortably with your
feet flat on the floor.
2. Position the blood pressure
monitor on your wrist.
3. Place your elbow on the table and
rest the back of your hand on the
device storage case or other
object.
4. Rest your wrist on the armrest
until it’s at the same height as
your heart.
5. Relax your hand and turn your
palm upwards.
18
Measurement Procedure
Switch on the Monitor
A. Press button to switch on the monitor.
B. All segments appear on the screen.
Setting Year, Date and Time
A. Press button ("YEAR" flashes). Press button to adjust
YEAR value.
B. Press button ("MONTH" flashes). Use button to adjust
MONTH (1, 2, 3,……, 12).
C. Adjust DATE (1, 2, 3,…, 31), HOUR (1, 2, 3,……..12PM,1
PM
,…, 12)
and MINUTE (00, 01,02,03,..... 59) as described i n Step A above.
When settings are done, press button to confirm the entries.
The device is ready to measure.
Taking a Measurement
A. Before measurement, press button to select User 1 or 2.
19
Measurement Procedure
B. With the cuff wrapped around your wrist, press button to
start measurement. All display units appear on the screen.
*Note！
Do not inflate the cuff until it is wrapped around your wrist.
After all symbols disappear, the display
will show “00”. The monitor is “Ready
to Measure” and will automatically inflate
to the level that is right for you.
C. After inflation of the cuff, the pressure will
slowly decrease. When pulse is detected,
PULSE SYMBOL flashes.
*Note！
If the cuff does not stop inflating, remove the cuff at once.
To stop measurement, press button.
D. LCD screen displays your systolic rate,
diastolic rate, pulse, Risk Category
Indicator icon and Irregular Heartbeat
Detector symbol (if any) with date and
time for 2 minutes.
E. Without any operation for 2 minutes, device automatically shuts
off.
20
Bluetooth Transmission
After measurements, user can transmit pas t results to your paired
Bluetooth device by following below steps:
1. Make sure to turn on Bluetooth funct ion of your Blueto oth device
beforehand (For example: mobile phone).
Under standby mode of blo od pressure monitor, the device
automatically activate the Bluetooth function
Under sleep mode of blood pressure monitor, press any
button to wake up the device and activate Bluetooth Function
2. Once connected and receive the data request from APP, paired
Bluetooth device automatically
starts downloading measuring
results from blood pressure monitor
if it’s in an acceptable range
(no more than 10 meters) with
each other.
(“ ” with LED backlight)
3. HL158HM can only pair up with one
Bluetooth device at a time. To
transmit measuring results to other
Bluetooth device, please redo Steps
1 ~ 2.
*Note！
Bluetooth in Standby/ Link/ Transmission：Bluetooth I n dic a to r
ON. (“ ” with LED backlight).
Without any operation in 2 minutes, the device shuts off
automatically and Bluetooth Indicator OFF.
21
Memory Function
Stori n g data
After each measurement, the systolic and diastolic pressure, heart
rate, Risk Category Indicator icon, and Irregular Heartbeat Detector
symbol (if any) with date and time will be automatically stored.
The monitor can store up to 120 memory sets for 2 users, and
automatically replace the oldest data with new one.
Recalling data
A. Press button to select User 1
or 2.
B. Press M button to enter Memory Mode.
LCD displays average of last 3 measuring
results first.
C. Press M button again, LCD displays the
latest measuring result. Use button
to scroll through all sto r e d measuring
results.
D. To stop reading memories, press
button, and switch to Standby Mode.
Erasing data
A. Press button to select User 1 or 2.
B. Press M button to enter Memory Mode.
C. Press and hold and buttons at the
same time, the data will be erased
automatically.
D. To confirm the data in the selected user
has been erased, press M button and no
data should appear.
Note: Once deleted, your data can NOT be restored.
22
Storage and Maintenance
General Use
Do not in any way twist the cuff.
Do not press button if the cuff is not wrapped around the
wrist.
Do not drop the product and avoid any strong impacts.
Maintenance
Use a piece of cloth with water or mild cleansing agent to wipe the
device and dry it immediately with a dry cloth.
Do not use detergent or any strong chemicals to clean the device.
Use only a dry cloth to wipe the cuff.
Do not attempt to disassemble or change any parts of the monitor,
including wrist cuff, due to substitution of a c omponent different
from that supplied might result in measurement error.
If any suggestion or service is requested, please consult your
service station.
Storage
If the device is not to be used for a lo ng time , ple ase r e move the
batteries from the device (leaking of battery acid can ca use the
device to malfunction).
Always store the unit in the storage case after use.
Do not place the device directly under sunlight, in high
temperature, or in humid or dusty places.
Do not store the device in extremely low (less than –13 °F/–25 °C)
and high (more than 158 °F/70 °C) temperature, nor in a place its
humidity exceeds 93% R.H.
23
Troubleshooting
SYMBOLS/SYMPTOMS CONDITIONS/CAUSES
INDICATION/CORR
ECTION
Unit does not turn on
when button is
pushed.
Worn-out batteries.
Replace them with 2
new AAA “LR03”
alkaline batteries.
Battery polarities have been
positioned incorrectly.
Re-insert the
batteries in the
correct positions.
Measuring Error Symbol
appears when blood
pressure value displayed
is
exce ss ive ly lo w o r h igh.
Cuff has been placed incorrectly. Wrap the cuff proper ly
so that it is positioned
correctly.
Did you talk or move during
measurement?
Measure again. Keep
arm steady during
measurement.
Shaking of the arm with the cuff on.
Measuring Error Symbol
Air circuit abnormality. Cuff tube may
not be plugged into monitor correctly.
Check cuff
connection. Measur e
again.
Measuring Error Symbol
Inflation pressure exceeding 300
mmHg.
Switch the unit off,
then measure
again.
Measuring Error Symbol
Error determining measurement data.
Measure again.
BPM cannot
communicate
with Bluetooth-enabled
device
Bluetooth-enabled device does not
pair with BPM or pair with a wrong
device.
Please re-pairing the
BPM and
Bluetooth-enabled
device with each other.
Bluetooth function is not turn on.
Please make sure the
device is in standby
mode.
The distance between BPM and
Bluetooth-enabled device is out of
transmitting range.
Please make sure the
acceptable distance
(
≦10 meters) with
each other.
Use an incompatible
Bluetooth-enabled device.
Please refer to
Page 15 “Bluetooth
compatibility” &
Page 27
"RF Specification”
Use non-Bluetooth-enabled device.
Unexpected loss of
electrical/mecha nical integrit y.
Re-insert the batteries
and try again.
Return the device to
your local distributor
or importer.
Note: If "EP" appears on the display, just retu r n th e dev ic e to your local distributor or impor ter.
24
Warranty & Recalibration
Warranty For One Year from the manufacturing date
Please note that this warranty does not cover damage caused by
misuse or abuse; accident; the attachment of any unauthorized
accessory; alteration to the product; improper installation;
unauthorized repairs or modifications; improper use of
electrical/power supply; loss of power; dropped product; malfunction
or damage of an operating part from failure to provide
manufacturer’s recommended maintenance; transportation damage;
theft; neglect; vandalism; or environmenta l conditions; loss o f use
during the period the product is at a repair facility or otherwise
awaiting parts or repa ir; or any oth er conditions whatsoev er that are
beyond the control of importers or distributors.
Recalibration Notice
To ensure continued measurement precision, all digital blood
pressure monitors requ ire recalibration regularly.
After 2 years from the manufacturing date, we recommend you have
your monitor recalibrate at the local distributor or importer. The
recalibration service plus the charge of shipping and handling fee
shall be charged accordingly.
25
Specifications
Model Number HL158HM
Measurement
Method
Oscillometric
Rated Range of Cuff
Pressure
Pressure: 0 ~ 300 mmHg
Rated Range of
Determination
40 ~ 280 mmHg
Measurement
Range of Heart
Rate
Pulse: 40 ~ 199 Beats / Minute
Accuracy
Pressure: ± 3 mmHg
Pulse: ± 5 % Max.
Inflation
Automatic Inflation (Air Pump)
Deflation
Automatic Air Release Control Valve
Display
Liquid Crystal Display
Memory
120 Memory Total for 2 Users
Unit Dimensions
72.85 X 78 X 32.8 mm (L X W X H)
2.87 X 3.07 X 1.29 inch (L X W X H)
Unit Weight
(Cuff & Batteries Excluded)
142.5 g ± 5 g （5.03 oz ± 0.18 oz）
Cuff Size
135 ~ 195 mm (5.3 ~ 7.7 inch)
Storage/
Transportation
Environment
Temperature: -25 °C ~ 70 °C (-13 °F ~ 158 °F)
Humidity: ≤ 93 % R.H.
Operation
Environment
Temperature: 5 °C ~ 40 °C (41 °F ~ 104 °F)
Humidity: 15 % ~ 93 % R.H.
Power Supply DC 3 V, AAA “LR03” (1.5V) Alkaline Battery x 2
Battery Life Approx. 150 Measurements
Power-saving Mode
Without any operation for 2 minutes, device
automatically shuts off.
Accessories
Instruction Manual, 2 AAA “LR03” Alkaline
Batteries, Storage Case
*The contents of this manual and the specifications of the device
covered by this manual are subject to change for improvement
without notice.
26
Specifications
RF Type Bluetooth 3.0+EDR & 4.0
RF Modulation
π/4-DQPSK/8DPSK/GFSK
Effective Radiated Power 2 dBm
Data Throughput
Deliver data rates: 115200 bps.
(3.0)Maximum application throughput: 3Mbps
(4.0)Maximum application throughput : 1Kbps
Expected Delay (Latency
Range) in Wireless (RF)
Communication
The
latency time is less than 0.1 second from
sender to receiver.
Integrity
Channel Quality-
Driven Data Rate (CQDDR)
technology increases the effective data rate
and integrity in noisy environments.
Security
By agreeing on passkey number in Bluetooth
Pairin
g Process, the two device can only
recognise each
other, thus makes
transmission
free from the risk of
eavesdropping.
Wireless Operation
Distance
Class 2 (Maximum: 10 meter)
RF Frequency / Need for
Spectrum Management
2402 - 2480 MHz
(allowing for guard bands)
Maximum Limitation 7
Maximum Permitted
Power
2.5 mW
Proximity of Oth er
In-band Transmitters
Used in Vicinity
up to 79 bands (1
MHz each; centered from
2402 to 2480 MHz)
Wireless Communication
Profile
SPP Profile
Wireless Coexistence Support for 802.11 Coexistence
System requirement of
the Bluetooth device
SPP requirement available
27
Note
Follow instructions for use.
BF Classifica tion:
- Internally powered equipment
- BF type applied part
- IPX0
- Not suitable for use in presence of flammable anesthetic mixture with air or with
Oxygen or nitrou s oxi d e
- Continuous operation with short-time loading
Keep dry.
To avoid inaccurate results caused by electromagnetic interference between
electrical and electronic equipments, do not use the device near a mobile phone or
microwave oven. At least keep a maximum output power of 2 W yields and a
distance 3.3m away from this equipment.
Discard the used product to the recycling collection point according to local
regulations.
Manufacturer: HEALTH & LIFE CO., LTD.
9F, No. 186, Jian Yi Road, Zhonghe District, New Taipei City, Taiwan.
www.healthandlife.com.tw
*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 installe d and us ed in
accordance with the instructions, may cause harmful interference to radio communications. However , there is no
guarantee that interference will not occur in a partic ular 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:
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 the receiver.
Connect the equipment into an outlet on a circuit different f ro m that to whic h the receiver is connected.
Consult the dealer or an experienced radio/TV technician for help.
CAUTION:
To assur e continued FC C complianc e :
1. Any changes or modi f ic a tio ns not expre s s ly approved by the grantee of this device co uld void the user's
authority to operate the equipment.
2. This equipment complies with FCC radiation exposure limits set forth for an uncontrolled environment. This
equipment should be installed and operated with minimum distance 20cm between the radiator & your body .
FCC Label Compliance Statement:
This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions:
(1) this device may not cause harmful interference , and
(2) this device must accept any interference rece ived, inc luding inte r ference that may cause undesired
operation.
*Note！
“Changes or modifications not expressly approved by the manufacturer could void the user’s authority to operate
the equipment”.
28
Appendix
Guidance and manufacturer’s de c laration – elect romagnetic emissions
The device is intended for use in the e
lectromagnetic envir onments lis ted bel ow, an d should on ly be
used in such environments:
Emissions test Compliance
Electromagnetic environment –
guidance
RF emissions
CISPR 11
Group 1
RF energy is used only to maintain device’s
operation. Therefore, its RF emissions are so
low that it’s not likely to cause any
interference in nearby electronic eq uip m e nt.
RF emissions
CISPR 11
Class B
The device is suitable for use in all
establishments, including domesti c
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
Not Applicable
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Not Applicable
Guidance and manufacturer’s de c laration – electromagnetic i mmu nity
The device is in tended for use in the elec tromagne tic env ironmen ts listed b elow, a nd shou ld only be
used in such environments:
Immunity test
IEC 60601
test level
Compliance level
Electromagnetic environment
–
guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
±6 kV contact
±8 kV air
±6 kV contact
±8 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 %.
Power frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
3 A/m
3 A/m
Power frequency magnetic fields
should be at levels characteristic of a
typical location in a typical
commercial or hospital
environment.
Recommended separation distances between portable and mobile RF communication
equipment and the dev ice.
The device is intended for use in an electromagnetic environment where radiated RF disturbances
are under control. User can help prevent electr oma gnetic interference by keeping the device at a
minimum distance from portable and mobile RF c ommunications equipment (transmitters). Below
table details the maximum output power of transmitte r :
Rated maximum output
power of transmitter
W
Separation distance according to frequency of transmitter
m
150 kHz to 80 MHz
Not applicable
80 MHz to 800 MHz
d = 1.2
800 MHz to 2.5 GHz
d = 2.3
0.01
NA
0.12
0.23
0.1
NA
0.38
0.73
1
NA
1.2
2.3
10
NA
3.8
7.3
100
NA
12
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 applicab le to the freq ue ncy of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to the transmitter manufac turer.
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, ob jects and peop le .
29
Appendix
Guidance and manufacturer’s de c laration – electromagnetic immu nity
The device is in tended for use in the elec tromagne tic env ironmen ts listed b elow, a nd shou ld only be
used in such environments:
Immunity test
IEC 60601 test
level
Compliance
level
Electromagnetic environment – guidance
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
3 Vrms
150 kHz to 80 MHz
3 V/m
80 MHz to 2.5 GHz
Not applicable
3 V/m
Portable and mobile RF communications
equipment should be used no closer to any part
of the device, including cables, than the
recommended separation distance calculated
from the equation applicable to the frequency
of the transmitter.
Recommended separation dis ta nce
d = 1.2 80 MHz to 800 MHz
d = 2.3 800 MHz to 2.5 GHz
where P is the maximum output powe r 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 elect romagnetic site surv ey ,
a
should be less than the compliance level in
each frequency range.
b
Interference may occur in the vicinity of
equipment marked with the following symbol:
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption
and reflection from structures, objects and people.
a 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 envi ronment due to fix ed RF transmitters, an elec tromagnetic sit e survey should be considered. If the measured
field strength in the location in which the device is used exceeds the applicable RF complianc e lev el abov e, th e device should be
observed to verify normal operation. If abnormal performance is observed , additional measures may be necessary, such as
reorienting or relocating the device.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
30
Blood Pressure Diary
Date：
Time：
□
Before
□After
Meal
Systolic / Diastolic：
Pulse：
Date：
Time：
□
Before
□After
Meal
Systolic / Diastolic：
Pulse：
Date：
Time：
□Before
□
After
Meal
Systolic / Diastolic：
Pulse：
Date：
Time：
□Before
□
After
Meal
Systolic / Diastolic：
Pulse：
Date：
Time：
□
Before
□After
Meal
Systolic / Diastolic：
Pulse：
Date：
Time：
□
Before
□After
Meal
Systolic / Diastolic：
Pulse：
Date：
Time：
□Before
□
After
Meal
Systolic / Diastolic：
Pulse：
Date：
Time：
□Before
□
After
Meal
Systolic / Diastolic：
Pulse：
Date：
Time：
□
Before
□After
Meal
Systolic / Diastolic：
Pulse：
Date：
Time：
□
Before
□After
Meal
Systolic / Diastolic：
Pulse：
P/N：XXXXXXXXX VER：A001 YYYYMMDD
31
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