Omron Healthcare Bp742N Owners Manual 7131

BP742N_IM BP742N_IM

BP742N_IM BP742N_IM

2014-08-26

: Omron-Healthcare Omron-Healthcare-Bp742N-Owners-Manual omron-healthcare-bp742n-owners-manual omron-healthcare pdf

Open the PDF directly: View PDF PDF.
Page Count: 38

DownloadOmron-Healthcare Omron-Healthcare-Bp742N-Owners-Manual 7131
Open PDF In BrowserView PDF
INSTRUCTION MANUAL

5 series
Blood Pressure Monitor

ENGLISH

ESPAÑOL

Model BP742N

TABLE OF CONTENTS
Before using the Monitor
Introduction ............................................................................................... 3
Important Safety Information..................................................................... 4
Operating Instructions
Know Your Device..................................................................................... 8
Display symbols ..................................................................... 10
Before Taking a Measurement ............................................... 12
Preparation ............................................................................................. 13
Battery Installation.................................................................. 13
Setting the Date and Time...................................................... 14
Using the Device..................................................................................... 15
Applying the Arm Cuff ............................................................ 15
How to Sit Correctly................................................................ 17
Taking a Measurement ........................................................... 17
Using the Memory Function ................................................... 20
Care and Maintenance
Error Messages and Troubleshooting..................................................... 23
Error Messages ...................................................................... 23
Troubleshooting...................................................................... 25
Maintenance and Storage....................................................................... 26
Maintenance........................................................................... 26
Storage ................................................................................... 27
Optional Medical Accessories ................................................ 27
Specifications .......................................................................................... 29
FCC Statement ....................................................................................... 31
Limited Warranty..................................................................................... 32
Guidance and Manufacturer’s Declaration ............................................. 33

2

INTRODUCTION
Thank you for purchasing the OMRON® BP742N Blood Pressure Monitor.
Your new blood pressure monitor uses the oscillometric method of blood
pressure measurement. This means the monitor detects your blood 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.
Intended Use
This device is a digital monitor intended for use in measuring blood pressure
and pulse rate in adult patient population. The device detects the appearance of
irregular heartbeats during measurement and gives a warning signal with the
measurement result.
Please read this instruction manual thoroughly before using the device.
Please keep for future reference. For specific information about your own
blood pressure, CONSULT YOUR PHYSICIAN.

3

IMPORTANT SAFETY INFORMATION
Warning: Indicates a potentially hazardous situation which, if not
avoided, could result in death or serious injury.
(General Usage)
DO NOT adjust medication based on measurement results from this blood
pressure monitor. Take medication as prescribed by your physician. Only a
physician is qualified to diagnose and treat High Blood Pressure.
This device 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 measurement
reading.
Do not use the device on the injured arm or the arm under medical
treatment.
Do not apply the arm cuff on the arm while being on an intravenous drip or
blood transfusion.
Consult your physician before using the device on the arm with an arteriovenous (A-V) shunt.
Do not use the device with other medical electrical (ME) equipment
simultaneously.
Do not use the device in the area the HF surgical equipment, MRI, or CT
scanner exists, or in the oxygen rich environment.
The air tube or the AC adapter cable may cause accidental strangulation in
infants.
Contains small parts that may cause a choking hazard if swallowed by
infants.

4

IMPORTANT SAFETY INFORMATION
Caution: 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.
(General Usage)
Always consult your physician. Self-diagnosis of measurement results and 
self-treatment are dangerous.
Consult your physician before using the device for any of the following
conditions:
• If you have had a mastectomy.
• Do not take measurements more than necessary. It may cause bruising
due to blood flow interference.
• People with severe blood flow problems or blood disorders as cuff inflation
can cause bruising.
Remove the arm cuff if it does not start deflating during the measurement.
Do not use this device on infants or persons who cannot express their
intentions.
Do not use the device for any purpose other than measuring blood pressure.
Use only the approved arm cuff for this device. Use of other arm cuffs may
result in incorrect measurement results.
Do not use a mobile phone or other devices that emit electromagnetic fields,
near the device. This may result in incorrect operation of the device.
Do not disassemble the monitor or arm cuff. This may cause an inaccurate
reading.
Do not use in a location with moisture, or a location where water may splash
on the device. This may damage the device.
Do not use the device in a moving vehicle (car, airplane).
Read “If your systolic pressure is more than 210 mmHg” of this instruction
manual, if your systolic pressure is known to be more than 210 mmHg.
Inflating to a higher pressure than necessary may result in bruising where
the arm cuff is applied.

5

IMPORTANT SAFETY INFORMATION
(AC Adapter (optional) Usage)
Do not use the AC adapter if the device or the power cord is damaged. Turn
off the power and unplug the power cord immediately.
Plug the AC adapter into the appropriate voltage outlet. Do not use in a
multi-outlet plug.
Never plug in or unplug the power cord from the electric outlet with wet
hands.
Fully insert the power plug into the outlet.
When disconnecting the power plug from the outlet, do not pull the power
cord. Be sure to pull from the power plug safely.
When handling the power cord, take care not to do the following:
Do not damage.
Do not break it.
Do not tamper with it. Do not forcibly bend or pull.
Do not twist.
Do not bundle during use.
Do not pinch.
Do not place under heavy objects.
Wipe the dust off from the power plug.
Unplug monitor when not in use.
Disconnect the power plug before cleaning.
Use only an OMRON AC adapter designed for this device. Use of
unsupported adapters may damage and/or may be hazardous to the device.
(Battery Usage)
Do not insert the batteries with their polarities incorrectly aligned.
Use only 4 “AA” alkaline or manganese batteries with this device. Do not use
other types of batteries. Do not use new and used batteries together.
Remove the batteries if the device will not be used for three months or more.

6

IMPORTANT SAFETY INFORMATION
General Precautions
• Do not forcibly crease the arm cuff or the air tube excessively.
• Do not press the air tube while taking a measurement.
• To unplug the air plug, pull on the air plug at the connection with the monitor,
not the tube itself.
• Do not drop the monitor or subject device to strong shocks or vibrations.
• Do not inflate the arm cuff when it is not wrapped around your arm.
• 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.

7

KNOW YOUR DEVICE
Contents:
Monitor, arm cuff, battery set, instruction manual, quick start guide

Monitor:
G

A

I

D
B
H
F
E

C

D
A.
B.
C.
D.
E.

Display
Up/Down buttons
USER ID selection switch
Date/Time setting button
START/STOP button

F.
G.
H.
I.

Memory button
Battery compartment
Air jack
AC adapter jack 
(for optional AC adapter)

Arm cuff:
J

K

Arm cuff 
(Arm circumference 9” - 17” (22 - 42 cm))
K. Air plug
L. Air tube
J.

L

8

KNOW YOUR DEVICE
Display:
R
S
T

M

U
N

V

O

W

P

X
Y

Q
M.
N.
O.
P.
Q.

USER ID symbol
Systolic blood pressure
Diastolic blood pressure
Low battery symbol
Heartbeat symbol
(Flashes during measurement.)
R. Memory symbol

S.
T.
U.
V.
W.
X.
Y.

9

Average value symbol
Date/Time display
Movement error symbol
Irregular heartbeat symbol
Blood pressure level indicator
Deflation symbol
Pulse display / Memory number

KNOW YOUR DEVICE
Display symbols
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
measurement values.
An irregular heartbeat rhythm is defined
as a rhythm that is 25% less or 25% more
than the average rhythm detected while
the monitor is measuring the systolic and
diastolic blood pressure.

Normal Heartbeat
Pulse
Blood pressure

Irregular Heartbeat
Short Long

Pulse
Blood pressure

If the irregular heartbeat symbol displays with your measurement results, 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 arm cuff, and wait 2 - 3 minutes. 
Take another measurement, remain still during measurement.

Average Value Symbol (

)

The average value symbol is displayed when you press and hold the memory
button for more than 3 seconds. The most recent average value appears on the
display screen.

10

KNOW YOUR DEVICE
Blood Pressure Level Indicator

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

 140 mmHg

 135 mmHg

Diastolic Blood Pressure

 90 mmHg

 85 mmHg

These are from statistical values for blood pressure.

11

KNOW YOUR DEVICE
Before Taking a Measurement
To help ensure an accurate reading, follow these directions:
1. Avoid bathing, drinking alcohol or caffeine, smoking, exercising and eating for
30 minutes before taking a measurement. Rest for at least 15 minutes before
taking the measurement.
2. Stress raises blood pressure. Avoid taking measurements during stressful
times.
3. Measurements should be taken in a quiet place.
4. Remove tight-fitting clothing from your arm.
5. Sit on a chair with your feet flat on the floor. Rest your arm on a table so that
the arm cuff is at the same level as your heart.
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.

12

PREPARATION
Battery Installation

1. Remove the battery cover.

2. Insert 4 “AA” batteries as
indicated in the battery
compartment.

3. Replace the battery cover.
Notes:
) appears on the display, turn the monitor
• When the low battery symbol (
off, then replace all batteries at the same time. Long life alkaline batteries
are recommended.
• The measurement values continue to be stored in memory even after the
batteries are replaced.
• The supplied batteries may have a shorter life.
• Dispose of the device, components and optional accessories according to
applicable local regulations. Unlawful disposal may cause environmental
pollution.

13

PREPARATION
Setting the Date and Time
Set the monitor to the correct date and time before taking a measurement for
the first time.

1. Press the button.
2. Push or
to change the year.
Push
button to confirm the year and then the month flashes. Repeat the
same steps to change the month, day, hour, and minute.
Year
Month
Day
Hour

Change Confirm

Minute
Change Confirm

: Forward
: Back

Change Confirm
Change Confirm
Change Confirm

3. Press the START/STOP button to turn the monitor off.
Notes:
• If the batteries have been replaced, the date and time setting will need to be
reset.
• If the date and time are not set, “-:--” appears during or after measurement.

14

USING THE DEVICE
Applying the Arm Cuff
Remove tight-fitting clothing or tight rolled up sleeve from your left upper arm. 
Do not place the arm cuff over thick clothes.

1. Insert the air plug into the air jack
securely.

2. Wrap the arm cuff firmly in
place around your left upper
arm.

The bottom edge of the arm cuff
should be 1/2 inch (1 to 2 cm) above
the elbow. Air tube is on the inside
of your arm and aligned with your
middle finger.

15

1/2 inch
(1 - 2 cm)

USING THE DEVICE
3. Secure closed with the
fabric fastener.

Notes:
• When you take a measurement on the right
arm, the air tube will be at the side of your
elbow. Be careful not to rest your arm on the
air tube.
• The blood pressure can differ between the right arm and the left arm, and
the measured blood pressure values can be different. OMRON
recommends to always use the same arm for measurement. If the values
between both arms differ substantially, please check with your physician
which arm to use for your measurements.

16

USING THE DEVICE
How to Sit Correctly
To take a measurement, you need to
be relaxed and comfortably seated,
under comfortable room temperature.
Avoid bathing, drinking alcohol or
caffeine, smoking, exercising or eating
30 minutes before taking a
measurement.
• Sit on a chair with your feet flat on the floor.
• Sit upright with your back straight.
• Sit with your back and arm being
supported.
• The arm cuff should be placed on your arm
at the same level as your heart.

Taking a Measurement
Notes:
• To stop the measurement, press the START/STOP button once to deflate the
arm cuff.
• Remain still and quiet while taking a measurement.
The monitor is designed to take measurements and store the measurement
values in the memory for 2 people using USER ID 1 and USER ID 2.

1. Select your User ID (1 or 2).

17

USING THE DEVICE
2. Press the START/STOP button.
The arm cuff will start to inflate automatically.

START

INFLATE

DEFLATE

COMPLETE

If your systolic pressure is more than 210 mmHg
After the arm cuff starts to inflate, press and hold the START/STOP
button until the monitor inflates 30 to 40 mmHg higher than your
expected systolic pressure.

Notes:
• The monitor will not inflate above 299 mmHg.
Inflating to a higher pressure than necessary may result in bruising
where the arm cuff is applied.

18

USING THE DEVICE
3. Remove the arm cuff.
4. Press the START/STOP button to turn the monitor off.
The monitor automatically stores the measurement result in its memory.
It will automatically turn off after 2 minutes.
Note: Wait 2-3 minutes before taking another measurement. Waiting
between measurements allows the arteries to return to the condition
prior to taking a measurement.

Using the Guest Mode

The monitor stores measurement values for 2 users in the memory. 
The guest mode can be used to take a single measurement for another user.
No measurement values are stored in the memory when the guest mode is selected.

1. Press and hold the START/STOP
button for more than 3 seconds.
The USER ID symbol and the Date/Time
display will disappear.

2. Release the START/STOP button when the Date/Time
display turns off.
The arm cuff will start to inflate automatically.

DO NOT adjust medication based on measurement results from this blood
pressure monitor. Take medication as prescribed by your physician. Only a
physician is qualified to diagnose and treat High Blood Pressure.
This device is not intended to be a diagnostic device.

19

USING THE DEVICE
Always consult your physician. Self-diagnosis of measurement results and 
self-treatment are dangerous.
Inflating to a higher pressure than necessary may result in bruising where
the arm cuff is applied.

Using the Memory Function
The monitor automatically stores the results up to 50 sets for each user (1 and 2).
It can also calculate an average value based on the last 3 measurement values
taken within 10 minutes.
Notes:
• If there are only 2 measurement values in the memory for that period, the
average will be based on these 2 values.
• If there is 1 measurement value in the memory for that period, this is displayed
as the average.
• If the memory is full, the monitor will delete the oldest value.
• When viewing the measurement value taken without setting the date and time,
“-:--” is displayed instead of the date and time.

To View the Measurement Values Stored in Memory

1. Select your User ID (1 or 2).
2. Press the button.
The Memory number appears for a second
before the pulse rate is displayed. 
The newest set is numbered “1”.

20

Alternating date/time 
display

USING THE DEVICE
3. Press the

or
button to view the values stored in
memory.
: To view the older values
: To view the more recent values

To View the Average Value

1. Select your User ID (1 or 2).
2. Press and hold the button for
more than 3 seconds.

Notes:
• If the previous measurement was taken without setting the date and time,
the average value is not calculated.
• If there are no measurements results stored in the memory,
the screen to the right is displayed.

21

USING THE DEVICE
To Delete All the Values Stored in Memory
The values stored in the memory are deleted by USER ID.

1. Select your User ID (1 or 2).
2. Press the button, while the memory symbol appears.
3. While holding the
button down, press the
START/STOP button for
more than 3 seconds.
Note: You cannot partially delete the values stored in the memory. 
All values for the user you select will be deleted.

22

ERROR MESSAGES AND TROUBLESHOOTING
Error Messages
Error Display

Cause

Solution

Irregular heartbeats
are detected.

Remove the arm cuff. Wait 2 - 3 minutes
and then take another measurement.
Repeat the steps in “Taking a
Measurement”. If this error continues to
appear, contact your physician.

Movement during
measurement.

Carefully read and repeat the steps in
“Taking a Measurement”.

You should replace the batteries with
The batteries are low. new ones ahead of time.
Refer to “Battery Installation”.
The batteries are
exhausted.

You should replace the batteries with
new ones at once.
Refer to “Battery Installation”.

Air plug
disconnected.

Insert the plug securely.
Refer to “Applying the Arm Cuff”.

Arm cuff is applied
too loosely.

Apply the arm cuff tighter.
Refer to “Applying the Arm Cuff”.

Air is leaking from
the arm cuff.

Replace the arm cuff with a new one.
Refer to “Optional Medical Accessories”.

23

ERROR MESSAGES AND TROUBLESHOOTING
Error Display

Cause

Solution
Repeat measurement. Remain still
and do not talk during measurement.
Refer to “Taking a Measurement”.

Movement during
measurement and
the arm cuff has not
been inflated
sufficiently.

If “E2” appears repeatedly, inflate 
the arm cuff manually until it is
30 to 40 mmHg above your previous
measurement result.
Refer to “Taking a Measurement”.

The arm cuff was
inflated exceeding the
maximum allowable
pressure, and then
deflated automatically
when inflating the arm
cuff manually.

Do not touch the arm cuff and/or bend
the air tube while taking a
measurement. Do not inflate the arm
cuff more than necessary.
Refer to “Taking a Measurement”.

Movement during
measurement.

Repeat measurement. Remain still
and do not talk during measurement.
Refer to “Taking a Measurement”.

Remove any clothing interfering with
Clothing is interfering
the arm cuff.
with the arm cuff.
Refer to “Applying the Arm Cuff”.
Device error.

Contact Customer Service.

24

ERROR MESSAGES AND TROUBLESHOOTING
Troubleshooting
Problem

Cause and Solution

No power.
No display appears on the monitor.

Replace all batteries with new ones.
Check the battery installation for
proper placement of the battery
polarities.
Refer to “Battery Installation”.

Measurement values appear too high
or too low.

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

25

MAINTENANCE AND STORAGE
Maintenance
To protect your device from damage, please observe the
following:
• Store the device and the components in a clean, safe location.
• Do not use any abrasive or volatile cleaners.
• Do not wash the device and any components or immerse them
in water.
• Do not use gasoline, thinners or similar solvents to clean the
device.

• Use a soft and dry cloth, or a soft and moistened cloth and
neutral soap to clean on the monitor and the arm cuff.
• Changes or modification not approved by the manufacturer
will void the user warranty. Do not disassemble or attempt to
repair the device or components. Consult Customer Service.
26

MAINTENANCE AND STORAGE
Storage

1. Unplug the air plug from the air jack.
2. Gently fold the air tube into the arm
cuff.
Note: Do not bend or crease the air tube
excessively.

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.

Optional Medical Accessories
Arm cuff
Arm circumference
9” - 17” (22 - 42 cm)

AC Adapter

CD-WR17
(Model: HEM-RML31)

HEM-ADPTW5

27

MAINTENANCE AND STORAGE
Using the Optional AC Adapter

1. Insert the AC adapter plug
into the AC adapter jack on
the rear side of the monitor.

2. Plug the AC adapter into an
electrical outlet.
To disconnect the AC adapter, unplug the AC adapter from the electrical
outlet first, and then remove the AC adapter plug from the monitor.

28

SPECIFICATIONS
Model

BP742N

Display

LCD digital display
Pressure: 0 to 299 mmHg
Pulse: 40 to 180 beats / min.
Pressure: r3 mmHg or 2% of reading
Pulse: r 5% of display reading
Fuzzy-logic controlled by electric pump
Automatic pressure release valve
Oscillometric method
IP 20
4 “AA” batteries 1.5V or optional AC adapter 
(INPUT AC100-240V 50/60Hz 0.12A)
Approximately 1000 measurements (using new alkaline batteries)

Measurement range
Accuracy
Inflation
Deflation
Measurement method
IP classification
Power source

HEM-7131-Z

Battery life
Operating temperature /
50°F to 104°F (10°C to 40°C) / 15 to 90% RH
humidity
Storage temperature / -4°F to 140°F (-20°C to 60°C) / 10 to 95% RH / 700 to 1060 hPa
humidity / air pressure
Monitor : Approximately 10 5/8 oz. (300 g) not including batteries
Weight
Arm cuff : Approximately 6 oz. (170 g)
Monitor : Approximately 4 1/4” (w) u 3 1/8” (h) u 5 1/2” (l)
(107 mm u 79 mm u 141 mm)
Dimensions
Arm cuff : Approximately 5 3/4” u 23 1/2” (air tube: 29 1/2”)
(145 mm u 594 mm (air tube: 750 mm))
Cuff circumference
9” to 17” (220 to 420 mm)
Memory
Up to 50 per user
Contents
Monitor, arm cuff, battery set, instruction manual, quick start guide
Applied part

= Type BF
Internally powered ME equipment (When using only the batteries)

Protection against
electric shock

= Class II ME equipment (Optional AC adapter)

29

SPECIFICATIONS
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 on pregnant patients.

30

FCC STATEMENT
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.

31

LIMITED WARRANTY
Your BP742N Automatic Blood Pressure Monitor, excluding the arm cuff and
batteries, is warranted to be free from defects in materials and workmanship
appearing within 2 years from the date of purchase, when used in accordance with
the instructions provided with the monitor. The arm cuff is warranted to be free
from defects in materials and workmanship appearing within 1 year from the date
of purchase when the monitor is 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 or arm cuff 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 original printed receipt. 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 that vary by jurisdiction. Because of special local requirements, some of
the above limitations and exclusions may not apply to you.
FOR CUSTOMER SERVICE
Visit our web site at:
www.omronhealthcare.com
Call toll free:
1-800-634-4350

32

GUIDANCE AND MANUFACTURER’S DECLARATION
OMRON Automatic Blood Pressure Monitor
Information for accompanying documents in the scope of IEC60601-1-2:2007
Model: BP742N including AC-adapter
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 BP742N including AC-adapter 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 BP742N including AC-adapter is to measure a blood
pressure and a pulse rate and using the memory function.
The BP742N including AC-adapter may be interfered with by other equipment, even if that
other equipment complies with CISPR EMISSION requirements.

33

GUIDANCE AND MANUFACTURER’S DECLARATION
Guidance and manufacturer’s declaration - electromagnetic immunity
OMRON BP742N including AC-adapter is intended for use in the electromagnetic environment
specified below. The customer or the user of this OMRON BP742N including AC-adapter should
assure that it is used in such environment.
Emissions test

Compliance

RF emissions 
CISPR 11

Group 1

RF emissions 
CISPR 11

Class B

Harmonic
emissions
IEC 61000-3-2

Class A

Voltage
fluctuations/flicker
emissions
IEC61000-3-3

Complies

Electromagnetic environment - guidance
The OMRON BP742N including AC-adapter 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 BP742N including AC-adapter 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.

34

GUIDANCE AND MANUFACTURER’S DECLARATION
Guidance and manufacturer’s declaration - electromagnetic immunity
OMRON BP742N including AC-adapter is intended for use in the electromagnetic environment
specified below. The customer or the user of this OMRON BP742N including AC-adapter should
assure that it is used in such environment.
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

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

Electrical fast 
transient/burst
IEC 61000-4-4

±2 kV for power
supply lines
±1 kV for 
input/output lines

±2 kV for power
supply lines
±1 kV for input/
output lines

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

Surge
IEC 61000-4-5

±1 kV line(s) to
±1 kV line(s) to
Mains power quality should be
line(s)
line(s)
that of a typical commercial
±2 kV line(s) to earth ±2 kV line(s) to earth and/or hospital environment.

<5 % UT (>95 % dip <5 % UT (>95 % dip Mains power quality should
in UT)
in UT)
be that of a typical
commercial and/or hospital
for 0.5 cycle
for 0.5 cycle
environment. If the user of
40 % UT (60 % dip  40 % UT (60 % dip 
the OMRON BP742N
in UT)
in UT)
Voltage dips, short
including AC-adapter
interruptions and
for 5 cycles
for 5 cycles
requires continued operation
voltage variations on
70 % UT (30 % dip  70 % UT (30 % dip  during power mains
power supply inputlines
interruption, it is
in UT)
in UT)
IEC 61000-4-11
recommended that the
for 25 cycles
for 25 cycles
OMRON BP742N including
<5 % UT (95 % dip  <5 % UT (95 % dip  AC-adapter be powered from
in UT)
in UT)
an uninterruptible power
for 5 sec.
for 5 sec.
supply.
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.

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

35

GUIDANCE AND MANUFACTURER’S DECLARATION
Guidance and manufacturer’s declaration - electromagnetic immunity
OMRON BP742N including AC-adapter is intended for use in the electromagnetic environment
specified below. The customer or the user of this OMRON BP742N including AC-adapter should assure
that it is used in such environment.
CompliIEC 60601
Electromagnetic environment - guidance
ance
Immunity test
test level
level
Portable and mobile RF communications equipment should be
used no closer to any part of the OMRON BP742N including 
AC-adapter including cables, than the recommended
separation distance calculated from the equation appropriate to
the frequency of the transmitter.
Conducted RF 3 V rms
IEC 61000-4-6 150 kHz to
80 MHz

3 V rms

Radiated RF
3 V/m
IEC 61000-4-3 80 MHz to
2.5 GHz

3 V/m

Recommend separation distance
d = 1.2 P
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,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:

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 BP742N including AC-adapter is used exceeds the applicable RF compliance
level above, the OMRON BP742N including AC-adapter should be observed to verify normal
operation. If abnormal performance is observed, additional measures may be necessary, such as
reorienting or relocating the OMRON BP742N including AC-adapter.
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

36

GUIDANCE AND MANUFACTURER’S DECLARATION
Recommended separation distance between portable and mobile RF communications
equipment and the OMRON BP742N including AC-adapter
OMRON BP742N including AC-adapter is intended for use in an electromagnetic environment in
which radiated RF disturbances are controlled. The customer or the user of this OMRON BP742N
including AC-adapter can help prevent electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications equipment (transmitters) and the
OMRON BP742N including AC-adapter as recommended below, according to the maximum
output power of the communications equipment.

Output Power of Transmitter
in Watt

Separation distance according to frequency of
transmitter in meter
150 kHz to 80
MHz
d = 1.2 P

80 MHz to 800 MHz 800 MHz to 2.5GHz
d = 1.2 P
d = 2.3 P

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 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.

37

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
© 2013 OMRON HEALTHCARE, INC.
Made in Vietnam

2298802-0D



Source Exif Data:
File Type                       : PDF
File Type Extension             : pdf
MIME Type                       : application/pdf
PDF Version                     : 1.5
Linearized                      : Yes
XMP Toolkit                     : Adobe XMP Core 4.0-c321 44.398116, Tue Aug 04 2009 14:24:39
Format                          : application/pdf
Title                           : 7131.book
Creator                         : W7 Blank 0
Create Date                     : 2014:06:02 18:50:02-05:00
Creator Tool                    : FrameMaker 10.0.2
Modify Date                     : 2014:06:02 18:50:02-05:00
Metadata Date                   : 2014:06:02 12:58:11-05:00
Producer                        : Acrobat Distiller 8.3.1 (Windows)
Document ID                     : uuid:8670a2e9-e92f-4603-bddc-fbd93fb81a37
Instance ID                     : uuid:c155a35c-7dea-436e-9f09-5375a211ad64
Page Count                      : 38
Author                          : W7 Blank 0
EXIF Metadata provided by EXIF.tools

Navigation menu