Homedics BPA-065 User Manual

WITH SMART MEASURE

™

TECHNOLOGY

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BPA-065

TABLE OF CONTENTS

INTRODUCTORY INFORMATION:
Important Product Notices and Safety

Instructions ..............................................................3

About Blood Pressure ............................................5

Blood Pressure Standard ....................................... 6

How This Blood Pressure Monitor Works ............. 7

USAGE INFORMATION:

Name/Function of Each Part ..................................8

Display Explanations ..............................................9

Installing Batteries ................................................ 11

Using the AC Adapter (not included)...................12

Date & Time Set Procedure .................................. 13

Using the Arm Cuff ...............................................14

Measurement Procedure ......................................17

Risk Category Index ..............................................19

Irregular Heartbeat Detector (IHB).......................20

Recalling Values from Memory ............................ 21

Clearing Values from Memory ..............................22

1

Important Notes Regarding Your

Blood Pressure Measurement ..............................23

Care, Maintenance, & Cleaning ............................24

Potential for Electromagnetic Interference .........26

Electromagnetic Compatibility (EMC) .................27

Troubleshooting .................................................... 29

Specifications ........................................................ 30

5-Year Limited Warranty ....................................... 31

2

IMPORTANT PRODUCT NOTICES
AND SAFETY INSTRUCTIONS

When using your blood pressure monitor, basic precautions
should always be followed. Please read and follow all instructions
and warnings before using this product. Save these instructions
for future reference.

• Please note that this is a home health care product only and
is not intended to serve as a substitute for the advice of a
physician or medical professional.

• This device uses oscillometric method to measure systolic and
diastolic blood pressure, as well as heart rate.

• DO NOT use this device for diagnosis or treatment of
any health problem or disease. Measurement results are
for reference only. Consult a health care professional for
interpretation of pressure measurements. Contact your
physician if you have or suspect any medical problem. Do not
change your medications without the advice of your physician
or health care professional.

• Proper cuff size is critical for accurate measurements. Follow
the instructions in this manual and printed on the arm cuff to
ensure the appropriate size of cuff is being used.

• This device may have difficulty determining the proper blood
pressure for pregnant women and for users with irregular
heartbeat, diabetes, poor circulation, kidney problems, or for
users who have suffered a stroke. This product is not suitable
for people with arrhythmias

• Not suitable for people undergoing intravenous injection on any
limb and for those with pre-eclampsia.

• Those who have had a mastectomy surgery (especially when
lymph nodes have been removed), it is recommended to take
measurements on the unaffected side.

3

• The pulse display is not suitable for checking the frequency of
heart pacemakers.

• When used along with other electronic medical equipment on
the same arm, pressurization of the cuff may cause the other
devices to temporarily malfunction.

• Electromagnetic interference: This device contains
sensitive electronic components. Avoid strong electrical or
electromagnetic fields in the direct vicinity of the device (e.g.
cell phones, microwave ovens). These may lead to temporary
impairment of measurement accuracy.

• Consider the electromagnetic compatibility of the device (ex.
power disturbance, radio frequency interference etc.) Please
use this device in a home health care environment only.

• Use blood pressure monitor only for its intended use.

• DO NOT wrap the cuff around body parts other than your arm.

• Not for use by or on persons under the age of 18.

• DO NOT use this device on infants, children, or those who
cannot express their own intention.

• DO NOT plug or unplug the adapter power cord with
wet hands.

• Excessive use may result in blood flow interference, which
is likely to cause uncomfortable sensations, such as partial
subcutaneous hemorrhage, or temporary numbness to
your arm. In general, these symptoms should not last long.
However, if you continue to experience these sensations,
please seek advice from a medical professional.

• Please use only a 6V AC adapter (as specified in this manual)
or 1.5V AA alkaline batteries.

Blood pressure measurements determined with this device are
equivalent to those obtained by a trained observer using the cuff/
stethoscope auscultatory method, within the limits prescribed by
the American National Standard, manual, electronic, or automated
sphygmomanometers.

4

ABOUT BLOOD PRESSURE

What is blood pressure?

Blood pressure is the pressure exerted on the artery walls while
blood flows through the arteries. The pressure measured when
the heart contracts and sends blood out of the heart is systolic
(highest) blood pressure. The pressure measured when the heart
dilates with blood flowing back into the heart is called diastolic
(lowest) blood pressure.

Why measure your blood pressure?

Among today’s various health problems, those associated with
high blood pressure are very common. High blood pressure
dangerously correlates with cardiovascular diseases. Therefore,
blood pressure monitoring is important for identifying those at risk.

Why do my readings vary?

Blood pressure is a body parameter that is subject to normal
variations throughout the day. A single reading that is different from
yours or your doctor's readings are not necessary inaccurate. The
average of several readings, taken under similar conditions, using
the same arm is preferred for accurate blood pressure readings.

Why are my readings different than those taken at my
doctor's office?

Many experience a phenomenon called “White Coat Hypertension”
when measured by a doctor. White Coat Hypertension refers to
blood pressure that rises above its usual level when measured in a
clinical setting, such as a doctor's office.

5

BLOOD PRESSURE STANDARD

The table below contains defined levels for hypertension that are
publicly available from the American Heart Association®
(AHA 2017).

Users can compare their own blood pressure readings against
these defined levels to determine if they may be potentially at
increased risk.

This table is applicable to most adults aged 18 and older.

Category Systolic (mmHg) Diastolic (mmHg)

Normal Less than 120 and Less than 80
Prehypertension 120-139 or 80-89

High blood pressure

Hypertension – Stage 1 140-159 or 90-99
Hypertension – Stage 2 160 or higher or 100 or higher
Hypertension Crisis –

Consult your doctor
immediately

Blood pressure tends to go up and down, even in people who
normally don’t have high readings. If your numbers stay above the
normal range most of the time, you may be at increased risk and
should consult your physician.

Although one can easily find where their own blood pressure
readings fall on this table, this monitor comes equipped with
a Risk Category Indicator that automatically compares each
reading to the defined levels and provides a helpful cue if your
reading falls into one of the stages that could potentially indicate
increased risk. See page 19 for more information on this feature.

Higher than 180 and/or Higher than 120

6

Please note that cues provided by this monitor are only intended
to assist you in using this table. The table and cues are only
provided for convenience in helping you to understand your
noninvasive blood pressure reading as it relates to the American
Heart Association (AHA 2017) information. They are not a
substitute for a medical examination by your physician. It is
important for you to consult with your physician regularly. Your
physician will tell you your normal blood pressure range as well
as the point at which you may actually be considered to be
at risk.

HOW THIS BLOOD PRESSURE MONITOR WORKS

This monitor uses Smart Measure™ Technology to detect
your blood pressure. This technology enables the monitor to
automatically inflate and deflate at the appropriate level for each
individual. With the touch of a button, the cuff will automatically
inflate to block the blood flow through your artery. Next, the
deflation process starts. Please note that any muscle movement
during inflation or deflation will cause measurement error. When
measurement is complete, the monitor will display your systolic
pressure, diastolic pressure, and pulse readings.

The monitor automatically finds where your measurement results
fall on the American Heart Association (AHA 2017) table and
provides a cue if your reading falls into one of the stages that
could potentially indicate increased risk. Please refer to page 19
for more information on this feature.

The appearance of the icon indicates that a pulse irregularly
consistent with an irregular heartbeat was detected during
measurement. Refer to page 20 for more information on the
Irregular Heartbeat Detector.

7

NAME/FUNCTION OF EACH PART

Arm Cuffs

Air Tube
and Connector

LCD Display

Battery Cover
(Located on
bottom of unit)

Date/Time Set
Buttons

Other Accessories:

MEMORY Recall
Button

1 6V DC Output AC Adapter (not included)
4 AA size, 1.5V alkaline batteries

Note: Please unload the batteries when operating
with the AC adapter for an extended period of time.

User Select
Button

START/STOP
Button

8

DISPLAY EXPLANATIONS

Date/Time
Indicator

Irregular
Heartbeat
Detector

PM

Systolic
Pressure

Diastolic
Pressure

Heart Rate

9

Display Symbols:

User 1: Appears when the monitor is operated by User 1.

User 2: Appears when the monitor is operated by User 2.

Weak Battery Symbol: Appears when batteries should

be replaced.

Pulse Symbol: Shows the heart rate per minute.

Risk Category Index: See page 19 for more information.

Irregular Heartbeat Detector: See page 20 for

more information.

Memory Average: Displays average of last 3 readings

If

and any of the following letters and numbers appear in the
area that systolic pressure should be displayed, an error has occurred
with your reading. See the Troubleshooting section of this manual for
more information.

Excessive Body Motion Detected/Measurement Error:
Wrap the cuff correctly and keep arm steady during
measurement. Measure again.

Air Circuit Abnormality: Check cuff connection.
Measure again.

Pressure Exceeding 300 mmHg: Turn the unit off to
clear, then measure again.

Error Determining Measurement Data: Measure again.

System Error: Measure again.

10

INSTALLING BATTERIES

1. Press down on latch and lift the battery cover to open the

battery compartment.

2. Install or replace 4 AA sized alkaline batteries in the

battery compartment according to the indications inside
the compartment.

3. Close the battery cover by pushing in the top end of the

battery door.

Battery
Cover

Replace the batteries if:

• The weak battery symbol appears on the display.

• Nothing appears on the display when the power is switched on.

Note:

• Date and time will need to be reset if batteries are removed

or replaced.

• Replace all batteries at one time (as simultaneous set). Use

only 1.5V AA alkaline batteries. Use only the size and type of
batteries specified.

• When installing batteries, observe proper +/- polarities. Incorrect

installation of batteries may cause damage to the unit.

• When the batteries are removed, the measurement values

stored in the memory are retained. However, the date and time
must be reset.

• Remove batteries when unit is not in use for extended periods of

time to prevent damage due to possible leakage.

• Clean contacts on battery and in battery compartment with a

soft, dry cloth each time you install batteries.

11

• Batteries are hazardous waste. DO NOT dispose of them

together with household garbage.

• DO NOT dispose of batteries in fire. Batteries may explode

or leak.

• Recycle or dispose of properly in accordance with local, state,

province, and country regulations.

USING THE AC ADAPTER (NOT INCLUDED)

This monitor is designed for operation with batteries or an optional
AC adapter. Please use only with compatible AC adapter with
required voltage and current as indicated in this manual. Contact
HoMedics Consumer Relations at 1-800-466-3342 to purchase a
compatible AC adapter.

Note:

• When the AC adapter is your main power supply, make sure the

adapter plug can be easily removed from the unit.

• Please unload the batteries when operating with an AC adapter

for an extended period of time. Leaving the batteries in the
compartment for a long time may cause leakage, which may
lead to damage to the unit.

• No batteries are needed when operating with an AC adapter.

• Date and time will need to be reset if AC adapter is unplugged

and unit is without batteries.

Connect the AC adapter with the AC adapter jack in the back of the
unit as shown below.

AC Adapter

Input: 100-240V~0.18A 50/60Hz
Output: 6V DC 1A 6W Max

Connect AC Adapter

12

DATE & TIME SET PROCEDURE

1. To adjust the date and time, press the Date/Time set button.

2. The display will show a blinking number showing the MONTH.

Change the MONTH by pressing the + button. Each press
will increase the number by one in a cycling manner. Press the
Date/Time set button again to confirm the entry, and the
screen will show a blinking number representing the DAY.

3. Change the DAY, HOUR AND MINUTE as described in Step

2 above, using the + button to change the numbers and the

Date/Time set button to confirm the entries.

Press the button

blinking MONTH

increasing MONTH

confirm the entry

repeat process to set

DAY, HOUR AND MINUTE

13

USING THE ARM CUFF

Very Important: Proper cuff size is critical to accurate
measurement.

This monitor comes with 2 sizes of arm cuffs:
Standard: Fits 9"–13" (23 cm – 33 cm)
Large: Fits 13"–17" (33 cm – 43 cm)

The appropriate cuff is suitable for your use if the colored
arrow falls within the solid color line as shown below.

Colored arrow

Position cuff
edge 0.6˝

–

1.0˝

(1.5

–

ARROW MUST FALL

WITHIN YELLOW BAND

ARROW MUST FALL

WITHIN YELLOW BAND

Center tube over
middle of arm.

Center tube over
middle of arm

2.5cm) above elbow.

Fit cuff securely. Allow room for
two fingers to fit between the cuff
and your arm.

Solid colored line

14

1. If the cuff is not assembled, pass the end of the cuff furthest

Position cuff edge

0.8

–

1.2 inches (2

–

3cm)

above elbow.

Fit cuff

Allow

to fi

and

Cen
mi

away from the tubing through the metal D-ring in order to form
a loop. The smooth side without the felt material should be on
the inside of the cuff loop.

ARROW MUST FALL

End of cuff

WITHIN YELLOW BAND

D-ring

2. Plug the cuff tube into the left side of the unit.

Insert plug

(0.8”~1.2”)

2~3 cm

3. Open the arm cuff so that your arm may be placed through it.

4. Remove tight fitting clothing from your upper left arm so that

the cuff can be wrapped around your exposed arm.

5. Position cuff edge 0.8-1.2

inches (2-3 cm) above elbow.

15

6. Center tube over middle of arm.

7. Pull the end of the cuff so that it tightens

evenly around your arm. Press the hook
and loop material together to secure.
Allow room for 2 fingers to fit between
the cuff and your arm.

8. Lay your arm on a table (palm upward)

so the cuff is at the same height as your
heart. Make sure the tube is not kinked.

Note:

• The device should not be used when your arm is wounded

or injured.

• If it is not possible to fit the cuff to your left arm, it can also be

placed on your right arm. However, all measurements should
be made using the same arm.

• To use on the right arm, you must

position the artery symbol over

Main Artery

the main artery. Locate the main
artery by pressing with 2 fingers
approximately 1" (2 cm) above the
bend of your elbow on the inside of
your right arm. Identify where the
pulse can be felt the strongest. This
is your main artery.

16

MEASUREMENT PROCEDURE

Note:

• Blood pressure changes with every heartbeat and is in

constant fluctuation throughout the day.

• Blood pressure measurement can be affected by the position

of the user, his or her physiologic condition, and other factors.

Before measurement:

To help ensure an accurate reading, follow these instructions
BEFORE taking a measurement:

• Wait 1 hour after exercising, bathing, eating, drinking

beverages with alcohol or caffeine, or smoking.

• Sit quietly and rest for 15 minutes.

• Stress raises blood pressure. Avoid taking measurements

during stressful times.

• Take your reading in a comfortable environment as

measurements can be affected by hot or cold temperatures.
Take your blood pressure at a normal body temperature.

During measurement:

• DO NOT talk or move your arm or hand muscles.

• DO NOT cross your legs. Sit with feet flat on the floor.

• DO NOT touch cuff or monitor during measurement.

If you are using this blood pressure monitor for the first
time, please remove the protective film from the screen.

17

1. Press the User Select button to choose User 1 or User 2.

OR

2. With the cuff wrapped around your arm, press the START/

STOP button. Do not inflate the cuff unless it is wrapped
around your arm. All digits will light up to check the display
functions. The checking procedure will be completed after
about 3 seconds.

3. After all symbols disappear, the display will show “00”. The

monitor is ready to measure and will automatically inflate the
cuff to begin measurement. The cuff will then start deflating as
measurement continues.

4. When the measurement is completed, the

cuff will deflate entirely. Systolic pressure,
diastolic pressure, and pulse will be shown
simultaneously on the LCD screen. The

measurement is then automatically stored
into memory.

18

PM

Note:

(No Symbol)

• If the monitor detects Excessive Body movement during the

measurement, EE “error” will display on the screen. Keep arm
steady and measure again.

• This monitor will reinflate automatically if the system detects

that your body requires more pressure for measurement.

• This monitor automatically turns off approximately 1 minute

after last operation. You may also press the START/STOP
button to turn the unit off.

• To interrupt the measurement, you may press the START/

STOP (recommended), MEMORY, User Select or Date/
Time SET button. The cuff will deflate immediately after a

button is pressed.

RISK CATEGORY INDEX

This monitor comes equipped with a Risk Category Index
that automatically compares each reading to defined levels
established by the American Heart Association (AHA 2017) as
described earlier in this manual, and provides a helpful cue if your
reading falls into one of the stages that could potentially indicate
increased risk. No cue is given if the reading falls in the normal
range as defined by AHA. Please note that cues provided by this
monitor are only intended to assist you in using this table. The
table and cues are only provided for convenience to help you
understand your noninvasive blood pressure reading as it relates
to the AHA information. They are not a substitute for a medical
examination by your physician. It is important for you to consult
with your physician regularly. Your physician will tell you your
normal blood pressure range as well as the point at which you
may actually be considered to be at risk.

Stage 2 Hypertension Elevated Normal (No Symbol)

Stage 1 Hypertension Hypertension Crisis

19

IRREGULAR HEARTBEAT DETECTOR (IHB)

The appearance of the icon
indicates that a pulse irregularity
consistent with an irregular heartbeat
was detected during measurement.
Usually this is not a cause for
concern. However, if the symbol

Irregular
Heartbeat
Detector

appears often, we recommend that
you seek medical advice. Please note
that the device does not replace a
cardiac examination, but serves to detect pulse irregularities at an
early stage.

Movement, shaking, or talking during the measurement can
result in pulse irregularities that may cause the appearance of this

icon. Therefore, it is of great importance to not move or talk

during measurement.

To determine the presence of an irregular heartbeat, the average
of the heartbeat intervals is calculated with the first 3 normal
effective heartbeat values. It is important to note that the average
is not a strict mathematical averaging of all recorded intervals.
At least 3 beats with 25% or greater difference from the average
heartbeat interval will generate the icon on the screen.

IMPORTANT INFORMATION:

This blood pressure monitor is not designed for use by people
with arrhythmias nor for diagnosing or treating an arrhythmia
problem. 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 blood pressure monitor.

PM

20

RECALLING VALUES FROM MEMORY

This monitor can be used by 2 individuals. Each user can store

up to 60 measurements.

1. Press the User Select button to select User 1 or User 2.

2. Press the MEMORY button to access the memory.

3. The monitor will first display the calculated average applied to

the last 3 memories.

21

4. Every new press of the MEMORY button will recall a previous

reading. The latest reading will be recalled first.

CLEARING VALUES FROM MEMORY

1. Press the User Select button to select User 1 or User 2.

2. Press and hold the DATE/TIME Set buttons + at the same

time while in memory recall mode, and the data for the selected
user will be erased automatically.

and

Note: Once deleted, your readings cannot be restored.

22

IMPORTANT NOTES REGARDING YOUR BLOOD
PRESSURE MEASUREMENT

• Take your reading in a comfortable environment as

measurements can be affected by hot or cold temperatures.
Take your blood pressure at normal body temperature.

• DO NOT move or talk during measurement as this can elevate

readings.

• DO NOT move or cross legs during measurement. Keep feet

flat on floor.

• DO NOT touch cuff or monitor during measurement procedure.

• It is suggested that you take your measurements at the same

time each day and use the same arm for consistency.

• Users should wait a minimum of 5 minutes before taking

additional measurements. More time may be necessary
depending upon your physiology.

• The measurement results that users receive are for

reference only. If users have any blood pressure concerns,
please consult a physician.

• Once inflation reaches 300 mmHg, the unit will deflate

automatically for safety reasons.

• This device may have difficulty determining the proper blood

pressure for pregnant women and for users with irregular
heartbeat, diabetes, poor circulation of blood, kidney
problems, or for users who have suffered a stroke.

23

CARE, MAINTENANCE, & CLEANING

• Clean the blood pressure monitor body and cuff carefully with

a slightly damp, soft cloth. Do not press. Do not wash cuff or
use chemical cleaner on it. Never use thinner, alcohol, or petrol
(gasoline) as cleaner.

• Leaky batteries can damage the unit. Remove the batteries

when the unit will not be used for a long time.

• Follow local ordinances and recycling instructions regarding

disposal or recycling of the device and device components,
including batteries.

• If the unit is stored near freezing, allow it to acclimate to room

temperature before use.

• This blood pressure monitor is not field serviceable. You should

not use any tool to open the device nor should you attempt to
adjust anything inside the device. If you have any problems
with this device, please contact HoMedics Consumer Relations
(contact information can be found in the Warranty section).

• DO NOT immerse the unit in water as this will result in damage

to the unit.

• DO NOT subject the monitor or cuff to extreme temperatures,

humidity, moisture, or direct sunlight. Protect from dust.

• DO NOT fold the cuff and tubing tightly.

• DO NOT disassemble the monitor or cuff. If in need of repair,

refer to the Warranty section of this manual.

• DO NOT subject the monitor to extreme shocks (do not drop

on floor).

• DO NOT inflate the cuff unless wrapped around arm.

• DO NOT wrap the cuff around body parts other than your arm.

• DO NOT drop or insert any object into any opening or hose.

24

• To avoid accidental strangulation, keep this product away

from children. Do not drape tube around neck.

• This monitor may not meet its performance specifications if

stored or used outside of these temperature and humidity
ranges:

• Storage/Transportation • Operating

Environment Environment

Temperature:

-13°F~158°F (-25°C~70°C)

Temperature:
41°F~104°F (5°C ~40°C)

Humidity:
less than 93% RH

Humidity:
15% ~ 93% RH

25

POTENTIAL FOR ELECTROMAGNETIC
INTERFERENCE

To avoid inaccurate results caused by electromagnetic interference
between electrical and electronic equipment, do not use the device near a
cell phone or microwave oven. For most wireless communication devices,
it is recommended to maintain a distance of 10.8 feet (3.3m) in order to
avoid electromagnetic interference.

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.

FEDERAL COMMUNICATIONS COMMISSION COMPLIANCE STATEMENT

Changes or modifications to this equipment not expressly approved by the
manufacturer could void the user’s authority to operate the equipment.

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.

26

ELECTROMAGNETIC COMPATIBILITY (EMC)

• Guidance and manufacturer’s declaration – electromagnetic emissions

The device is intended for use in the electromagnetic environments listed below, and should only be used in

such environments:

Emissions test Compliance Electromagnetic environment – guidance

RF emissions
CISPR 11

RF emissions
CISPR 11

Harmonic emissions IEC
61000-3-2

Voltage fluctuations/flicker
emissions IEC 61000-3-3

• Guidance and manufacturer’s declaration – electromagnetic immunity

The device is intended for use in the electromagnetic environments listed below, and should only be used in

such environments:

Immunity test IEC 60601 test level Compliance level Electromagnetic environment–

Electrostatic
discharge (ESD)
IEC 61000-4-2

Power frequency
(50 or 60 Hz)
magnetic field
IEC 61000-4-8

Electrical fast
transient/burst
IEC 61000-4-4

Surge
IEC 61000-4-5

Interruptions and
voltage variations
on power supply
input lines

IEC 61000-4-11

± 8 kV contact discharge

± 15 kV air discharge

30 A/m
50 or 60 Hz

± 2 kV for power supply

± 1 kV for input/output lines

± 2 kV Power lines ± 2 kV Power lines Mains power quality should be that

0% UT; 0.5 cycle
At 0°, 45°, 90°, 135°, 180°,
225°, 270°, and 315°

0% UT; 1 cycles
70% UT; 25/30 cycles
0% UT; 250/300 cycles

Group 1 RF energy is used only to maintain device’s operation. Therefore,

Class B

Class A

Complies

its RF emissions are so low that it’s 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.

guidance

lines

± 8 kV contact discharge

± 15 kV air discharge

3 A/m
50 or 60Hz

± 2 kV for power supply

lines

± 1 kV for input/output

lines

0% UT; 0.5 cycle
At 0°, 45°, 90°, 135°, 180°,
225°, 270°, and 315°

0% UT; 1 cycles
70% UT; 25 cycles
0% UT; 250 cycles

In air discharge testing, the climatic
conditions shall bw within the
following rages:
Temperature:15˚~35˚,
Humidity:30%~60%.

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

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

of a typical commercial or hospital
environment..

Mains power quality should be that
of a typical commercial or hospital
environment. If the user of the device
requires continued operation during
power mains interruptions, it is
recommended that the device be
powered from an uninterruptible power
supply or a battery.

27

• Recommended separation distances between portable and mobile RF communication equipment

and the device.

The device is intended for use in an electromagnetic environment where radiated RF disturbances are

under control. User can help prevent electromagnetic interference by keeping the device at a minimum
distance from portable and mobile RF communications equipment (transmitters). The table below details
the maximum output power of transmit ter:

Rated maximum
output power of

transmitter

W

0.01 0.12 0.12 0.23

0.1 0.38 0.38 0.73
1 1.2 1.2 2.3

10 3.8 3.8 7.3

100 12 12 23

For tran smitters ra ted at a maximu m output power n ot listed above , the recommen ded separati on distance d i n metres (m) can
be estim ated using the e quation appl icable to the fr equency of the t ransmitte r, where P is the max imum output po wer rating of th e
transm itter in wat ts (W) acc ording to the tra nsmitter ma nufacture r.
NOTE 1 At 80 M Hz and 800 MHz, t he separatio n distance fo r the higher fre quency range a pplies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from
structures, objects and people.

• Guidance and manufacturer’s declaration – electromagnetic immunity

The device is intended for use in the electromagnetic environments listed below, and should only be used
in such environments:

150 kHz to 80 MHz

Immunity test IEC 60601 test level Compliance

Conducted RF
IEC 61000-4-6

Radiat ed RF
IEC 61000-4-3
(Proxim ity fields
from RF wireless
communications
equipment
IEC 61000- 4-3)

NOTE 1 At 80 M Hz and 800 MHz, th e higher freque ncy range appl ies.
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 s trengths fro m fixed transmi tters, such a s base statio ns for radio (cellu lar/cordless) te lephones and la nd mobile
radios , amateur radio, A M and FM radio broa dcast and TV br oadcast can not be predicte d theoretica lly with accur acy. To
asses s the electrom agnetic envir onment due to fix ed RF transmit ters, an elec tromagnetic si te survey shou ld be considere d.
If the mea sured field st rength in the loc ation in which t he device is use d exceeds the appl icable RF comp liance level ab ove,
the 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 f requency ran ge 150 kHz to 80 MHz, fie ld strengths s hould be less tha n 3 V/m.

3V rms
At 0.15-80 MH z

6V rms
At ISM & Rad io Amateur
Freq.

10 V/m at 80-2 700 MHz
AM Modul ation And 9 -28V/
m at 385 -6000 MHz,Pulse
Mode and other Modula­tion. The system shall
be teste d as specifie d in
IEC60 601-1-2 Table 9 for
proximi ty fields fr om RF
wireless communications
equipm ent using the te st
methods specified in IEC
61000-4-3

Separation distance according to frequency of transmitter m

d = 1.2

3V rms
At 0.15-80 MH z

6V rms
At ISM & Rad io Amateur
Freq.

10 V/m at 80-2 700 MHz
AM Modul ation And 9 -28V/
m at 385 -6000 MHz,Pulse
Mode and other Modula­tion. The system shall
be teste d as specifie d in
IEC60 601-1-2 Table 9 for
proximi ty fields fr om RF
wireless communications
equipm ent using the te st
methods specified in IEC
61000-4-3

80 MHz to 800 MHz

d = 1.2

level

Electromagnetic environment –

Portable and mobile RF communications
equipm ent should be us ed no closer to any
part of the device, including cables, than the
recommended separation distance calculated
from the e quation appl icable to the fr equency of
the transmitter.

Recommended separation distance

d = 1.2
d = 1.2 8 0 MHz to 800 MHz
d = 2 .3 800 MHz t o 2.7 GHz

where P is t he maximum ou tput power rat ing
of the tra nsmitter in w atts (W) a ccording to
the tran smitter man ufacturer a nd d is the
recommended separation distance in metres (m).
Field st rengths fro m fixed RF trans mitters, a s
determ ined by an elect romagnetic s ite survey, a
should b e less than the co mpliance lev el in each
frequency range.b
Inter ference may oc cur in the vicin ity of
equipm ent marked wit h the following s ymbol:

800 MHz to 2.7 GHz

d = 2.3

guidance

28

TROUBLESHOOTING

If any abnormality arises during use, please check the following points:

SYMPTOMS

Unit does not turn on when
the START/STOP button
is pushed.

POSSIBLE

CAUSES

Batteries have run down. Replace them with

Battery polarities have been
positioned incorrectly.

CORRECTION

four new AA
alkaline batteries.

Reinsert the batteries in the
correct positions.

EE measurement error
symbol shown on display or
the blood pressure value is
displayed excessively low
(or high).

E1 error symbol shown
on display.

E2 error symbol shown
on display.

E3 error symbol shown
on display.

EP error symbol shown
on display.

Cuff has been
placed incorrectly.

Did you talk or move
during measurement?

Shaking of the arm with the
cuff on.

Air circuit abnormality. Cuff
tube may not be plugged into
monitor correctly.

Inflation pressure exceeding
300 mmHg.

Error determining
measurement data.

System error. Measure again.

Wrap the cuff properly so that
it is positioned correctly.

Keep arm steady during
measurement.
Measure again.

Check cuff connection.
Measure again.

Switch the unit off, then
measure again.

Rewrap the cuff properly so
that it is positioned correctly.
Take new measurement.

Note: If the unit still does not work, contact HoMedics Consumer Relations. Under
no circumstance should you disassemble or attempt to repair the unit by yourself.
Contact information for HoMedics Consumer Relations Department can be found in
the Warranty section.

29