OMRON HEALTHCARE HEM6321T User Manual

1EN

2ES 3FR

INSTRUCTION MANUAL

Wrist Blood

Pressure Monitor

Model BP654

3200764-8A

INTRODUCTION

Thank you for purchasing the OMRON BP654 Wrist Blood Pressure Monitor.

Fill in for future reference.

DATE PURCHASED: __________________

SERIAL NUMBER: ____________________

• Staple your purchase receipt here

• Register your product on-line at
www.register-omron.com

The monitor is compact and easy-to-use at home, at work, and portable for travel.
Perfect for people who frequently monitor their own blood pressure.
Your new digital blood pressure monitor uses the oscillometric method of blood
pressure measurement. This means the monitor detects your blood’s movement
through your brachial artery and converts the movements into a digital reading. An
oscillometric monitor does not need a stethoscope so the monitor is simple to use.
Clinical research has proven a direct relationship between blood pressure in the
wrist and blood pressure in the arm. Changes in wrist blood pressure reflect changes
in arm blood pressure because the arteries in the wrist and the arm are close to each
other. Frequently measuring the blood pressure in your wrist will provide your
physician with an accurate indication of changes in your blood pressure.
The BP654 comes with the following components:

• Monitor • Storage Case • 2 “AAA” Alkaline Batteries

• Instruction Manual • Quick Start Guide

Please read this instruction manual thoroughly before using the unit. Please
keep for future reference. For specific information about your own blood
pressure, CONSULT YOUR DOCTOR.

SAVE THESE INSTRUCTIONS

SAFETY INFORMATION

INTENDED USE

The device is a digital monitor intended for use in measuring blood pressure and
pulse rate in adult patient population with wrist circumference ranging from 5 1/4
inches to 8 1/2 inches (13.5 cm to 21.5 cm). The device detects the appearance of
irregular heartbeats during measurement and gives a warning signal with readings.

To assure the correct use of the product, basic safety measures should always be
followed including the warnings and cautions listed in this instruction manual.

SAFETY SYMBOLS USED IN THIS INSTRUCTION MANUAL

WARNING

CAUTION

GENERAL USAGE

Contact your physician for specific information about your blood pressure.
Self-diagnosis and treatment using readings may be dangerous. Follow the
instructions of your physician or licensed healthcare provider.
DO NOT adjust medication based on readings from this blood pressure monitor.
Take medication as prescribed by your physician. Only a physician is qualified to
diagnose and treat High Blood Pressure.
The monitor is not intended to be a diagnostic device.
Consult your physician before using the device for any of the following conditions:
common arrhythmias such as atrial or ventricular premature beats or atrial fibrillation,
arterial sclerosis, poor perfusion, diabetes, age, pregnancy, pre-eclampsia, renal diseases.
Note that PATIENT motion, trembling, shivering may affect the reading
Do not use the device on the injured wrist or the wrist under medical treatment.
Do not apply the wrist cuff on the arm while being on an intravenous drip or blood
transfusion.
Contains small parts that may cause a choking hazard if swallowed by infants.
Consult your physician before using the device on the wrist with an arterio-venous
(A-V) shunt.
Do not use the device with other medical electrical (ME) equipment simultaneously.
Do not use the device in the area the high frequency (HF) surgical equipment,
magnetic resonance imaging (MRI), or computerized tomography (CT) scanner
exists, or in the oxygen rich environment.

BATTERY USAGE

Keep the batteries out of the reach of young children

DATA TRANSMISSION

Do not use this product on aircraft or in hospitals. Please remove the battery from
the unit. This product emits radio frequencies (RF) in the 2.4 GHz band, use of this
product in locations where RF is restricted is not recommended.
The use of RF in this product is licensed for use by the FCC/IC, for further
information on any potential restrictions refer to documentation on Bluetooth
by the FCC/IC.

GENERAL USAGE

Consult your physician before using the device for any of the following conditions:

• If you have had a mastectomy.

• If you have a condition that may compromise circulation, you may get an

inaccurate reading with this device.

• People with severe blood flow problems or blood disorders as cuff inflation can

cause bruising.
Do not take measurements more than necessary. It may cause bruising due to blood
flow interference.
Read all of the information in the instruction manual and any other literature in the
box before operating the unit.
Do not use this device on infants or persons who cannot express their intentions.
Operate the device only as intended. Do not use the device for any other purpose.
Do not use a mobile phone or other devices that emit electromagnetic fields near
the device except when in use for wireless communications. This may result in
incorrect operation of the device.
Do not use the device in a moving vehicle (car, airplane).
Use only Omron authorized parts and accessories. Parts and accessories not
approved for use with the device may damage the unit.
Although this device is waterproof (IP22), please be careful about the operating
environment.

BATTERY USAGE

Use only 1.5V Alkaline batteries with this device. Do not use other types of
batteries. This may damage the device.
Do not replace the batteries while the data is transferred.

Indicates a potentially hazardous situation which, if not
avoided, could result in death or serious injury.

Indicates a potentially hazardous situation which, if not
avoided, may result in minor or moderate injury to the user or
patient or damage to the equipment or other property.

.

.

®

usage

GENERAL PRECAUTIONS

Do not subject the monitor to strong shocks, such as dropping the unit on the floor.
Do not submerge the device or any of the components in water.
Store the device and the components in a clean, safe location.
Changes or modification not approved by the manufacturer will void the user
warranty. Do not disassemble or attempt to repair the unit or components. This
may cause an inaccurate reading as well.
Do not use the device outside the specified environment. It may cause an
inaccurate reading.
Dispose of the device, components and optional accessories according to applicable
local regulations. Unlawful disposal may cause environmental pollution.

BEFORE TAKING A MEASUREMENT

To ensure a reliable reading, follow these recommendations:

1. Avoid eating, drinking alcohol, smoking, exercising, and bathing for 30 minutes
before taking a measurement. Rest for at least 5 minutes before taking the
measurement.

2. Stress raises blood pressure. Avoid taking measurements during stressful times.

3. The cuff can be applied to your left or right wrist.

4. Measurements should be taken in a quiet place.

5. Position the unit at heart level throughout the measurement.

6. Remain still and do not talk during the measurement.

7. Keep a record of your blood pressure and pulse readings for your physician. A
single measurement does not provide an accurate indication of your true blood
pressure. You need to take and record several readings over a period of time.
Try to measure your blood pressure at the same time each day for consistency.

KNOW YOUR UNIT

Main Unit:

Battery
compartment

Components:

2 “AAA”
Alkaline Batteries

Wrist cuff

Display

Storage
Case

Memory button

Transfer button
(Date/Time setting button)

START/STOP button

1EN

2ES3FR

INSTRUCTION MANUAL

Wrist Blood

Pressure Monitor

Model BP654

3200764-8A

INTRODUCTION

Thank you for purchasing the OMRON BP653 Wrist Blood Pressure Monitor.

Fill in for future reference.

DATE PURCHASED:__________________

SERIAL NUMBER:____________________

• Staple your purchase receipt here

• Register your product on-line at

Instruction
Manual

3200765-6A

Quick Start
Guide

GETTING
STARTED

Wrist Blood Pressure Monitor

1EN

2ES 3FR

BP654

UNIT DISPLAY

Average reading symbol

Memory symbol

Systolic blood
pressure

Diastolic blood

Date/Time display

Blood pressure level
indicator (bar)

Positioning indicator

pressure

Battery symbol
(low/depleted)

Heartbeat symbol

(Flashes during

Positioning symbol

Movement error symbol
Irregular heartbeat symbol

measurement)

Pulse display /

Memory number

Memory full

Deflation symbol
OK symbol
Transfer symbol

symbol

DISPLAY SYMBOLS

HEARTBEAT SYMBOL ( )

The Heartbeat symbol flashes on the display at every heartbeat during the
measurement.

AVERAGE READING SYMBOL ( )

The Average Reading Symbol is displayed when you press and hold the button for
more than 2 seconds. The most recent average reading appears on the display screen.

IRREGULAR HEARTBEAT SYMBOL ( )

When the monitor detects an irregular rhythm two or more times during the
measurement, the Irregular Heartbeat Symbol will appear on the display with the
readings.

Pulse

Blood

pressure

Pulse

Blood

pressure

Normal Hear tbeat

Irregular Heartbeat

Short Long

≥ 135 mmHg

An irregular heartbeat rhythm is defined as a
rhythm that varies by 25% less or 25% more
than the average rhythm detected while the
monitor is measuring the systolic and diastolic
blood pressure.

If the irregular heartbeat symbol displays with
your readings, we recommend you consult your
physician. Follow the directions of your physician.

MOVEMENT ERROR SYMBOL ( )

The Movement Error Symbol ( ) is displayed if you move your body during the
measurement. Please remove the wrist cuff, and wait 2-3 minutes. Reapply the
wrist cuff and take another measurement.

BLOOD PRESSURE LEVEL INDICATOR (BAR)

Blood pressure level indicator (bar) will light up between
the systolic blood pressure and the diastolic blood
pressure.

2013 ESH/ESC Guidelines for the management of arterial hypertension

Definitions of hypertension by office and home blood pressure levels

Office Home

Systolic Blood Pressure

Diastolic Blood Pressure ≥ 85 mmHg

≥ 140 mmHg

≥ 90 mmHg

BATTERY INSTALLATION

1. Push down the hook of the battery cover and
pull downward.

2. Install 2 “AAA” size batteries so the +
(positive) and - (negative) polarities match the
polarities of the battery compartment as
indicated.

3. Replace the battery cover.

NOTE: Make sure that the battery cover is

securely in position.

WARNING

• If battery fluid should get in your eyes, immediately rinse with plenty of
clean water. Contact a physician immediately.

• Keep the batteries out of the reach of young children.

NOTES: • When the depleted battery symbol ( ) appears on the display, turn

the monitor off and remove all the batteries. Replace with 2 new
batteries at the same time.

• Turn the unit off before replacing the batteries. If the batteries are
removed while the unit is still on, the date and time will be reset to
that of the previous use. The readings are not deleted.

• When the batteries are replaced, you may need to reset the date and

time. Refer to “Setting the Date and Time”.

• The batteries included with the device may have a shorter life.

SETTING THE DATE AND TIME

Set the monitor to the correct date and time before taking a measurement for the
first time.

1. When the unit is off, press the / button repeatedly until the year flashes
on the display.

2. Set the monitor to the correct date and time .

1) Press the button to change.

• Hold down to advance the digit
rapidly.

2) Press the / button to confirm.

• Next setting appears.

Year

Month

Day

Hour

Minute

3. Press the START/STOP button to store the setting.

NOTES: • If the batteries have been removed, the date and time setting will

need to be reset.

• The date and time can be automatically set when you transfer your

readings to the Omron Wellness App. However, the date/time will
only be set for future measurements taken after the reading that was
transferred, it will not be saved to the reading that was just
transferred.

• If the date and time are not set, “-:--” appears during or after

measurement.

APPLYING THE WRIST CUFF

APPLYING THE CUFF ON THE LEFT WRIST

1. Roll up sleeve. Make sure your sleeve is not rolled up
too tightly on your arm. This may constrict the flow of
blood in your arm.

2. Put your arm through the cuff loop. Your palm
should face upward.

3. Position the cuff leaving a clearance of approximately
1/2 inch (1 cm to 2 cm) between the cuff and the bottom
of your palm.

4. Wrap the wrist cuff firmly around your wrist.
Do not apply over clothing.

NOTES: • Make sure the wrist cuff does not cover the

protruding part of the wrist bone on the
outside of the wrist.

• If the wrist cuff comes off, re-assemble as
shown in the figure.

APPLYING THE CUFF ON THE RIGHT WRIST

When taking a measurement using the right wrist position
the cuff as shown in the illustration.

TAKING A MEASUREMENT

1. Sit comfortably on a chair with your feet flat on the floor.
Keep your back straight. Place your elbow on a table and and
elevate cuff wrist to heart level.

NOTES: • The distance from the top of your seat measuring

to the top of the table you are sitting at, should be
12 ± 2 inches (30 ± 5 cm). If the distance
measured between the top of your seat and table
do not fall within this parameter, please correct
your seat or table height. If you are unable to
make any seat or table adjustments, please turn off the position
indicator and position your wrist at heart-level by yourself.

• The cuff must be approximately the same height as your heart. If
the cuff is too high above your heart, your blood pressure will read
artificially low. If the cuff is too low below your heart, your blood
pressure will be artificially high.

• Relax your wrist and hand. Do not bend your wrist back, clench
your fist, or bend your wrist forward.

2. Press the START/STOP button to start the measurement.
All symbols appear on the display before starting the measurement.

Positioning Indicator - The monitor has a built-in positioning indicator that is used
as an aid in determining if the monitor is at the correct height. It has been designed
to work with most people so that when your wrist is at the correct position relative
to your heart, the positioning indicator will be blue. If the positioning indicator
changes to orange, the device may not be at the correct height relative to your
heart. Due to difference in individual size and physique, this feature may not
helpful in all cases and you may wish to turn off this feature. If you feel the
position of the wrist according to positioning indicator's guidance does NOT match
your heart level, please turn off this feature and follow your judgement. It can be
disabled, see “Turn OFF (ON) the Positioning Indicator”.
NOTE: Even if the device is not positioned properly and the positioning indicator

is orange, after 5 seconds the monitor will start the measurement and the
wrist cuff will start to inflate.

blue
light

(Proper position)

orange
light

(Wrist is too high)

orange
light

(Wrist is too low) (Forward-bent posture)

As the cuff inflates, the monitor automatically determines your ideal inflation
level. This monitor detects your blood pressure and pulse rate during inflation.
The Heartbeat Symbol ( ) flashes at every heartbeat.

Remain still and do not move until the entire measurement process is
completed.

After the monitor has detected your blood pressure and pulse rate, the cuff
automatically deflates. Your blood pressure and pulse rate are displayed.

INFLATESTART DEFLATE COMPLETE

NOTE: To stop the inflation or measurement, push the START/STOP button.

The monitor will stop inflating, start deflating, and will turn off.

3. Press the START/STOP button to turn the monitor off.

NOTES: • The monitor will automatically turn off after 2 minutes.

• Wait 2-3 minutes between measurements. The wait time allows the

arteries to return to the condition prior to taking the blood pressure
measurement. You may need to increase the wait time depending
on your individual physiological characteristics.

TURN OFF (ON) THE POSITIONING INDICATOR

The positioning indicator is set “on” as default.

1. When the unit is off, press and hold the / and button for more than 5
seconds to set the positioning indicator.

2. Press the START/STOP button to store the positioning indicator setting.

USING THE MEMORY FUNCTION

The monitor automatically stores up to 100 readings.
It can also calculate an average reading based on the last 3 readings taken within
10 minutes.

TO VIEW THE READINGS STORED IN MEMORY

1. Press the button.

The Memory number appears for a second
before the pulse rate is displayed. The
most recent reading set is numbered “1”.

NOTES: • If the positioning indicator is set to

“on” before the measurement, the
positioning indicator is displayed
with the readings.

• When viewing the readings taken without setting
the date and time, “-:--” is displayed instead of the
date and time.

• If there are no readings stored in the memory, the

screen to the right is displayed.

2. Press the button repeatedly to view the readings stored in the memory.

TO VIEW THE AVERAGE READING

When the unit is off, press and hold the button for
more than 2 seconds.

NOTES: • If the previous measurement was taken

without setting the date and time, the
average reading is not calculated.

• If there are only 2 readings in the memory for that
period, the average will be based on these 2
readings.

• If there is 1 reading in the memory for that period, this is displayed as
the average.

TO PAIR THIS DEVICE WITH A SMARTPHONE

To begin using the OMRON Wellness software for the first time, please visit
www.omronwellness.com for the initial set-up instructions.

1. Download and install onto your smartphone, the free “Omron Wellness” App.

2. Open the App on your smartphone and follow set-up and pairing instructions.
NOTE: Please make sure that you do not currently have an

active reading screen on. If there is a reading on the
screen, press the START/STOP button to clear the
screen to allow you to begin to transfer your readings.

3. Press and hold the / button for more than 2 seconds.

The transfer symbol ( ) will appear on the display.

4. Open the App on your smartphone and follow the device
pairing instructions shown on your smartphone, while the
transfer symbol is flashing on the display.

5. The OK symbol and will flash when pairing is completed.

Any readings currently saved in the blood pressure monitor's
memory will automatically be transferred to the App after
successful completion of the pairing process.

NOTES: • If the pairing has failed, the screen to the right is

displayed.

• The monitor will automatically turn off after 10
seconds without any operations.

TO TRANSFER THE DATA

1. Open the App on your smartphone and log in.

2. Tap “Transfer Readings” on the App and follow the instructions.
NOTE: When the Memory full symbol ( ) blinks or is lit on the display,

transfer the data before the readings are deleted.

Blinking: 80 readings have been stored.
Lit: 100 readings have been stored.

If the memory is full, the monitor will delete the oldest reading. Please
transfer your readings to the Omron Wellness App to help ensure your
data is saved before old readings are deleted from the memory.

TO DELETE ALL THE READINGS STORED IN MEMORY

1. Press the button, the memory symbol ( ) appears.

2. While holding the button down, press the
START/STOP button for more than 2 seconds.

NOTE: You cannot partially delete the

readings stored in the memory.
All readings will be deleted.

TO DELETE ALL READINGS AND SETTINGS

You can delete all readings and settings when you want to dispose of the device or
present it to others.

1. While holding the / button down, press the
START/STOP button for more than 5 seconds.

2. When the CLr symbol appears, release the

/ button and START/STOP button.

3. Press the START/STOP button to turn the
monitor off.

NOTES: •

Unpairing your device will not delete the information in the mobile App.

• The monitor will automatically turn off after 2 minutes.

• If you re-pair your smartphone to your blood pressure monitor, all

prior reading history stored on the mobile App will be retained.

Alternating
date/time
display

CARE AND MAINTENANCE

To keep your digital blood pressure monitor in the best condition and protect the
unit from damage, follow the directions listed below:

CAUTION

• Do not forcefully bend the cuff. Do not fold tightly.

• Clean the monitor with a soft and dry cloth.

• Do not use any abrasive or volatile cleaners.

• Wipe clean on the surface of the cuff with a soft, moistened cloth with a

dilution of neutral detergent.

• Do not allow any liquids inside the cuff. If a liquid gets in the cuff, dry the

inside well.

CAUTION

Do not wash the device and any components or immerse them in water. Do
not subject the monitor to extreme hot or cold temperatures, humidity or
direct sunlight.

CAUTION

Store the device and the components in a clean, safe location.

CAUTION

Do not subject the monitor to strong shocks, such as dropping the unit on the floor.

CAUTION

Remove the batteries if the unit will not be used for three months or longer.
Always replace all the batteries with new ones at the same time.

CAUTION

Use only OMRON authorized parts and accessories. Parts and accessories
not approved for use with the device may damage the unit.

CAUTION

Changes or modification not approved by the manufacturer will void the user
warranty. Do not disassemble or attempt to repair the unit or components.

CAUTION

Do not store the device in the following situations:

• If the device is wet.

• Locations exposed to extreme temperatures, humidity, direct sunlight, dust

or corrosive vapors such as bleach.

• Locations exposed to vibrations, shocks or where it will be at an angle.

ERROR MESSAGES

SYMBOL CAUSE CORRECTION

Please remove the wrist cuff, and wait
2-3 minutes. Reapply the wrist cuff and

Irregular heartbeats are
detected.

Movement during
measurement.

Wrist cuff not applied
correctly.

Movement during
measurement.

Wrist cuff not applied
correctly or movement
during measurement.

Arm position changed
during measurement.

Device error.

Batteries are low.

Batteries are depleted.

take another measurement.
Repeat the steps in section “Taking a
Measurement
If this error continues to appear, contact
your physician.

Carefully read and repeat the steps in
section

Apply the wrist cuff correctly. Refer to
“Applying the Wrist Cuff ”.

Do not hold the wrist cuff. Remain still
and do not talk during measurement.
Refer to “Taking a Measurement”.

Apply the wrist cuff correctly. Refer to
“Applying the Wrist Cuff ”.
Remain still and do not talk during
measurement. Refer to “Taking a
Measurement”.

Remain still until the measurement is
complete. Refer to “Taking a
Measurement”.

Contact Customer Service.

Recommend to replace the batteries
with new ones ahead of time.
Refer to “Battery Installation”.

Replace the two batteries.
Refer to “Battery Installation”.

”

.

“

Taking a Measurement”.

TROUBLESHOOTING TIPS

PROBLEM

No power.
No display appears on the unit.

Readings appear too high or too
low.

Data cannot be sent.

Replace both batteries with new ones at the
same time. Check the battery installation for
proper placement of the battery polarities.
Review the section “Battery Installation”.

Blood pressure varies constantly. Many factors
including stress, time of day, how you wrap the
cuff, where you position your wrist, may affect
your blood pressure.
Review the sections “Before Taking a
Measurement” and “Taking a Measurement”.

The destination device is too far away from the
monitor. After checking that there are no sources
of interference nearby, move the device to a
distance within 16 ft. (5 m) of the monitor.

The
device is turned off. Turn on the
function and try sending the data again.

The Bluetooth function on the monitor is not
turned on. Press the
Bluetooth function and try sending the data again.

Pairing (registering) has not been completed.
Perform pairing (registration). Refer to
This Device With a Smartphone

The application on the destination device is not
ready. Check the application then try sending the
data again. Refer to “To Pair This Device With a
Smartphone”. If the Err symbol still lights after
checking the application, contact customer service.

CAUSES AND SOLUTIONS

Bluetooth

function on the destination

/

Bluetooth

button, turn on the

“

To Pair

”

.

FCC/IC STATEMENT AND TRADEMARKS

FCC CAUTION
Changes or modifications not expressly approved by the party responsible for
compliance could void the user's authority to operate the equipment.

Note:

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

• Reorient or relocate the receiving antenna.

• 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.

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

This equipment complies with FCC/IC radiation exposure limits set forth for an
uncontrolled environment and meets the FCC radio frequency (RF) Exposure
Guidelines and RSS 102 of the IC radio frequency (RF) Exposure rules. This
equipment has very low levels of RF energy that are deemed to comply without
testing of specific absorption ratio (SAR).

This device complies with Part 15 of FCC Rules and Industry Canada
license-exempt RSS standard(s). Operation is subject to the following two
conditions: (1) this device may not cause interference, and (2) this device must
accept any interference, including interference that may cause undesired operation
of this device.

This Product operates in the unlicensed ISM band at

2.4GHz. In case this Product is used around the other
wireless devices including microwave and wireless LAN,
which operate same frequency band of this Product, there
is a possibility that interference occurs between this
Product and such other devices. If such interference
occurs, please stop the operation of other devices or
relocate this Product before using this Product or do not
use this Product around the other wireless devices.

The Bluetooth
trademarks owned by Bluetooth SIG, Inc. and any use of
such marks by OMRON HEALTHCARE Co.,Ltd. is under
license. Other trademarks and trade names are those of
their respective owners.

Apple, the Apple logo, iPad, and iPhone are trademarks of Apple Inc., registered
in the U.S. and other countries.
App Store is a service mark of Apple Inc.

Android and Google Play are both trademarks of Google Inc.

Samsung and Galaxy S are both registered trademarks of Samsung Electronics
Co., Ltd.

®

Smart word mark and logos are registered

LIMITED WARRANTY

Your BP654 Wrist Blood Pressure Monitor, excluding the batteries, is warranted to
be free from defects in materials and workmanship appearing within 5 years from
the date of purchase, when used in accordance with the instructions provided with
the monitor. The above warranty extends only to the original retail purchaser.

We will, at our option, replace without charge any monitor covered by the above
warranty. Replacement is our only responsibility and your only remedy under the
above warranty.

To obtain warranty service contact Customer Service by calling 1-800-634-4350
for the address of the inspection center and the return shipping and handling fee.

Enclose the Proof of Purchase. Include a letter, with your name, address, phone
number, and description of the specific problem. Pack the product carefully to
prevent damage in transit. Because of possible loss in transit, we recommend
insuring the product with return receipt requested.

THE FOREGOING IS THE SOLE WARRANTY PROVIDED BY OMRON IN
CONNECTION WITH THIS PRODUCT, AND OMRON HEREBY
DISCLAIMS ANY OTHER WARRANTIES, EXPRESS OR IMPLIED,
INCLUDING IMPLIED WARRANTIES OF MERCHANTABILITY AND
FITNESS FOR A PARTICULAR PURPOSE. IMPLIED WARRANTIES AND
OTHER TERMS THAT MAY BE IMPOSED BY LAW, IF ANY, ARE
LIMITED IN DURATION TO THE PERIOD OF THE ABOVE EXPRESS
WARRANTY.

OMRON SHALL NOT BE LIABLE FOR LOSS OF USE OR ANY OTHER
SPECIAL, INCIDENTAL, CONSEQUENTIAL OR INDIRECT COSTS,
EXPENSES OR DAMAGES.

This warranty provides you with specific legal rights, and you may have other
rights which vary from state to state. Some states do not allow limitations on how
long an implied warranty lasts, so the above limitation may not apply to you. Some
states do not allow the exclusion or limitation of incidental or consequential
damages, so the above limitation or exclusion may not apply to you.

Visit our web site at: www.omronhealthcare.com /

www.omronhealthcare.ca

Call toll free: 1-800-634-4350

FOR CUSTOMER SERVICE

SPECIFICATIONS

Model:
Display:
Measurement Range:

Accuracy:

Inflation:
Deflation:
Measurement Method:
IP Classification :
Power Source:
Battery Life:
Operating Temperature

/Humidity:
Storage Temperature

/Humidity/Air Pressure:
Main Unit Weight:

Main Unit Dimensions:

Measurable
Circumference of Wrist:

Memory:
Contents:

Protection against
Electric Shock:

Applied Part:

NOTES: • These specifications are subject to change without notice.

• In the clinical validation study, the 5th phase was used on 85 subjects

for determination of diastolic blood pressure.

• This device has not been validated for use in pregnancy.

• IP classification is degrees of protection provided by IEC 60529.

BP654 HEM-6320T-Z
LCD Digital Display

Pressure: 0 mmHg to 299 mmHg

Pulse: 40 beats/min to 180 beats/min
Pressure: ±3 mmHg or 2% of reading

Pulse: ±5% of reading
Automatic by electric pump
Automatic rapid deflation
Oscillometric method
IP 22
2 “AAA” alkaline batteries 1.5V
Approximately 300 uses with 2 new alkaline batteries

50ºF to 104ºF (10ºC to 40ºC) /15% RH to 90% RH

-4ºF to 140ºF (-20ºC to 60ºC) /10% RH to 95% RH

700 hPa to 1060 hPa
Approximately 3 1/2 oz. (100 g)

not including batteries
Approximately 3 1/2''(w) × 2 3/8''(l) × 1''(d)

(89 mm × 61 mm × 25 mm) (not including the wrist cuff)

Approximately 5 1/4" to 8 1/2" (13.5 cm to 21.5 cm)

Up to 100 readings
Main Unit, Storage Case, 2

Instruction Manual, and Quick Start Guide

Internally powered ME equipment

“AAA”

Alkaline Batteries,

GUIDANCE AND MANUFACTURER’S DECLARATION

OMRON Wrist Blood Pressure Monitor (BPM)

Information for accompanying documents in the scope of IEC60601-1-2:2007

Important information regarding Electro Magnetic Compatibility (EMC)

With the increased number of electronic devices such as PC’s and mobile
(cellular) telephones, medical devices in use may be susceptible to
electromagnetic interference from other devices. Electromagnetic interference
may result in incorrect operation of the medical device and create a potentially
unsafe situation. Medical devices should also not interfere with other devices.

In order to regulate the requirements for EMC (Electro Magnetic Compatibil­ity) with the aim to prevent unsafe product situations, the IEC60601-1-2
standard has been implemented. This standard defines the levels of immunity
to electromagnetic interferences as well as maximum levels of electromagnetic
emissions for medical devices.

Medical devices manufactured by OMRON Healthcare conform to this
IEC60601-1-2:2007 standard for both immunity and emissions.
Nevertheless, special precautions need to be observed:

• The use of accessories and cables other than those specified by OMRON,
with the exception of cables sold by OMRON as replacement parts for
internal components, may result in increased emission or decreased
immunity of the device.

• The medical devices should not be used adjacent to or stacked with other
equipment.
In case adjacent or stacked use is necessary, the medical device should be
observed to verify normal operation in the configuration in which it will be
used.

• Refer to further guidance below regarding the EMC environment in which
the device should be used.

• The MEDICAL ELECTRICAL EQUIPMENT BPM needs special
precautions regarding EMC and needs to be installed and put into service
according to the EMC information provided in this documentations.

• The Essential Performance of the BPM is to measure a blood pressure and a
pulse rate and using the memory function.

The BPM may be interfered with by other equipment, even if that other
equipment complies with CISPR EMISSION requirements.

(Table 1)

Guidance and manufacturer’s declaration – electromagnetic emissions

OMRON BPM is intended for use in the electromagnetic environment
specified below. The customer or the user of this OMRON BPM should assure
that it is used in such environment.

Emissions test

RF emissions CISPR 11

RF emissions CISPR 11
Harmonic emissions

IEC 61000-3-2

Voltage fluctuations/
flicker emissions
IEC61000-3-3

(Table 2)

Guidance and manufacturer’s declaration – electromagnetic immunity

OMRON BPM is intended for use in the electromagnetic environment
specified below. The customer or the user of this OMRON BPM should assure
that it is used in such environment.

Immunity test

Electrostatic
discharge (ESD)
IEC 61000-4-2

Electrical fast
transient/burst
IEC 61000-4-4

Surge
IEC 61000-4-5

Voltage dips,
short
interruptions
and voltage
variations on
power supply
inputlines
IEC 61000-4-11

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

Note: UT is the A.C. mains voltage prior to application of the test level.

Compliance

Group 1

Class B
Not

Applicable.

Not
Applicable.

IEC 60601
Test level

±6 kV contact
±8 kV air

±2 kV for
power
supply lines

±1 kV for
input/output
lines

±1 kV
line(s) to
line(s)

±2 kV
line(s) to
earth

UT

<5 %

(>95 % dip

in

UT

)

for 0.5 cycle
40 %

UT

(60 % dip in

UT

)

for 5 cycles

70 %

UT

(30 % dip in

UT

)

for 25 cycles

UT

<5 %
(>95 % dip
in

UT

)

for 5 sec.

3 A/m

Compliance
level

±6 kV contact
±8 kV air

Not
Applicable.

Not
Applicable.

Not
Applicable.

3 A/m

Electromagnetic environment
– guidance

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

The OMRON BPM
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.

Electromagnetic environment
– guidance

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

Not Applicable.

Not Applicable.

Not Applicable.

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

(Table 4)

Guidance and manufacturer’s declaration – electromagnetic immunity

OMRON BPM is intended for use in the electromagnetic environment
specified below. The customer or the user of this OMRON BPM should assure
that it is used in such environment.

Immunity test

Conducted RF
IEC 61000-4-6

Radiated RF
IEC 61000-4-3

Note1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note2: 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 radio, AM and FM radio broadcast, and
TV broadcast cannot be predicted theoretically with accuracy. To assess the
electromagnetic environment due to fixed RF transmitters, an electromagnetic
site survey should be considered. If the measured field strength in the location
in which the OMRON BPM is used exceeds the applicable
RF compliance level above, the OMRON BPM should be observed to
verify normal operation. If abnormal performance is observed, additional
measures may be necessary, such as reorienting or relocating the OMRON
BPM.

b

Over the frequency range 150 kHz to 80 MHz, field strengths should be less
than 3 V/m.

(Table 6)

Recommended separation distance between portable and mobile RF
communications equipment and the OMRON BPM

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

Output Power of

Transmitter in

Watt

0.01

0.1
1

10

100

For transmitters rated at a maximum output power not listed above, the
recommended separation distance d in meters (m) can be estimated using the
equation applicable to the frequency of the transmitter, where P is the maximum
output power rating of the transmitter in watts (W) according to the transmitter
manufacturer.
Note: At 80 MHz and 800 MHz, the separation distance for the higher frequency
range applies
Note: These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures,
objects, and people.

Manufactured for :
OMRON HEALTHCARE Co., Ltd
53, Kunotsubo, Terado-cho
Muko, Kyoto, 617-0002 JAPAN

Distributed by :
OMRON HEALTHCARE, INC.

1925 West Field Court

Lake Forest, IL 60045 U.S.A.
www.omronhealthcare.com

© 2014 OMRON HEALTHCARE, INC.
Made in Vietnam

IEC 60601
Test level

3 V rms
150 kHz to
80 MHz

3 V/m
80 MHz to

2.5 GHz

Separation distance according to frequency of
transmitter in meter

150 kHz to 80 MHz

Compliance
level

Not
Applicable.

3 V/m

Not Applicable.

Not Applicable.
Not Applicable.
Not Applicable.
Not Applicable.
Not Applicable.

Electromagnetic environment
– guidance

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

Recommend
separation distance

Not Applicable.

d = 1.2 √P

80 MHz to 800 MHz

d = 2.3 √P

800 MHz to 2.5 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 meters (m).
Field strengths from fixed RF
transmitters as determined by an
electromagnetic site survey,
should be less than the compli­ance level in each frequency

b

range.
Interference may occur in the
vicinity of equipment marked
with the following symbol:

80 MHz to 800 MHz

d = 1.2 √P

0.12

0.38

1.2

3.8
12

800 MHz to 2.5GHz

d = 2.3 √P

a

0.23

0.73

2.3

7.3

23