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Monitor
Instruction Manual
C
Engli
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spañol
7 series Blood Pressure Monitor
Model BP760N
Instruction Manual
English
.
o, Kyoto, 617-0002 JAPAN
est, IL 60045 U.S.A.
Made in Vietnam
Español
2298836-5C
.
o, Kyoto, 617-0002 JAPÓN
est, IL 60045 U.S.A.
Hecho en Vietnam
El producto incluye:
Monitor
Manual de Instrucciones
Quick S
Guía re
Product includes:
7 series Blood Pressure Monitor
Model BP760N
Instruction Manual
ii
Monitor
Battery Set
Instruction Manual
ComFit™ Cuff
Engli
s
h
E
spañol
7 series Blood Pressure Monitor
Model BP760N
Instruction Manual
English
Español
2298836-5C
El producto incluye:
Monitor
Juego de Pilas
Manual de Instrucciones
Quick Start Guide
Guía resumida
Brazalete ComFit™
Product includes:
or
Contents
Thank you for purchasing the OMRON
®
BP760N 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 who can understand this instruction manual with the arm
circumference range printed on the arm cuff. The device detects the appearance of irregular
heartbeats during measurement and gives a warning signal with the measurement result.
Important Safety Information........................1
1. Know Your Device....................................4
1.1 Display Symbols.....................................5
1.2 Before Taking a Measurement...............6
2. Preparation ...............................................7
2.1 Battery Installation..................................7
2.2 Setting the Date and Time .....................8
3. Using the Device ......................................9
3.1 Applying the Arm Cuff ............................9
3.2 How to Sit Correctly .............................10
3.3 Taking a Measurement ........................11
3.4 Using the Memory Function .................14
4. Error Messages and Troubleshooting..17
4.1 Error Messages ................................... 17
4.2 Troubleshooting................................... 19
5. Maintenance and Storage......................20
5.1 Maintenance ........................................ 20
5.2 Storage ................................................ 21
5.3 Optional Medical Accessories ............. 22
6. Specifications.........................................24
7. FCC Statement........................................25
8. Limited Warranty....................................26
9.
Guidance and Manufacturer’s Declaration.. 27
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.
1
EN
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.
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 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 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 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.
(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.
2
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" (page11) 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 cuff is applied.
(AC Adapter (optional) Usage)
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.
3
Important Safety Information
EN
When handling the power cord, take care not to do the following:
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.
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.
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.
4
1.Know Your Device
Monitor
Air jack
Blood pressure color indicator
Date/Time setting button
USER ID selection switch
Display
Memory button
START/STOP button
Up/Down buttons
Battery compartment
AC adapter jack (for optional AC adapter)
Arm cuff
Arm cuff (Arm circumference
9” - 17” (22 - 42 cm))
Air plug
Air tube
Display
Memory symbol
USER ID symbol
Average value symbol
Systolic blood pressure
Diastolic blood pressure
Heartbeat symbol
(Flashes during measurement)
Date/Time display
Movement error symbol
Irregular heartbeat symbol
Blood pressure level indicator
Low battery symbol
Deflation symbol
Pulse display / Memory number
Open the rear cover page to read the following:
The letter identifiers on the rear cover page correspond to those in the body of this page.
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
5
1. Know Your Device
EN
1.1
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.
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.
Normal Heartbeat
Irregular Heartbeat
Pulse
Blood pressure
Blood pressure
Short
Long
Pulse
6
1. Know Your Device
Blood Pressure Color Indicator
If your Systolic Blood Pressure is 135 mmHg or above and/or the Diastolic Blood Pressure
is 85 mmHg or above, the blood pressure color indicator will light in “orange” when the
measurement result is displayed. If the results are within the standard range, the blood
pressure color indicator will light in “green”.
2013 ESH/ESC Guidelines for the management of arterial hypertension
Definitions of hypertension by office and home blood pressure levels
These are from statistical values for blood pressure
.
1.2
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.
Office Home
Systolic Blood Pressure ≥ 140 mmHg ≥ 135 mmHg
Diastolic Blood Pressure ≥ 90 mmHg ≥ 85 mmHg
7
EN
2.Preparation
2.1
Battery Installation
1. Remove the battery cover.
2. Insert 4 “AA” batteries as
indicated in the battery
compartment.
3. Replace the battery cover.
Notes:
• When the low battery symbol ( ) appears on the display, turn the monitor 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.
• Dispose of the device, components and optional accessories according to applicable local regulations.
Unlawful disposal may cause environmental pollution.
8
2. Preparation
2.2
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 Date/Time setting ( ) button.
The year flashes on the Date/Time display.
2. Push or button 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.
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.
Open the rear cover page to read the following:
The letter identifiers on the rear cover page correspond to those in the body of this page.
C
T
Year
Month
Day
Hour
Minute
Change Confirm
Change Confirm
Change Confirm
Change Confirm
Change Confirm
: Forward
: Back
9
EN
3.Using the Device
3.1
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. Apply the arm cuff to 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.
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.
Open both the front and rear covers to read the following:
The letter identifiers on the cover page correspond to those in the body of this page.
L
A
a
M
b
10
3. Using the Device
3.2
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. ---
c
d
11
3. Using the Device
EN
3.3
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).
2. Press the START/STOP button.
The arm cuff starts to inflate automatically.
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.
START
INFLATE
DEFLATE
COMPLETE
12
3. 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.
13
3. Using the Device
EN
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.
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.
14
3. Using the Device
3.4
Using the Memory Function
The monitor automatically stores the results up to 60 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”.
15
3. Using the Device
EN
3. Press the or button to view the values stored in the
memory.
: To view the older values
: To view the more recent values
Note: The value with the TruRead
TM
symbol is the average for the consecutive 3 measurements. To
display the individual measurement values, press
the button
while the average is displayed.
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 measurement values stored in the memory, the screen to
the right is displayed.
16
3. 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 Memory 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.
17
EN
4.
Error Messages and Troubleshooting
4.1
Error Messages
Display Cause Solution
Irregular heartbeats are detected.
Remove the arm cuff. Wait 2-3 minutes and
then take another measurement.
Repeat the steps in section 3.3. If this error
continues to appear, contact your physician.
Movement during measurement.
Carefully read and repeat the steps in section
3.3.
The batteries are low.
You should replace the batteries with new
ones ahead of time.
Refer to section 2.1.
The batteries are exhausted.
You should replace the batteries with new
ones at once.
Refer to section 2.1.
18
4. Error Messages and Troubleshooting
Air plug disconnected.
Insert the air plug securely.
Refer to section 3.1.
Arm cuff is applied too loosely.
Apply the arm cuff tighter.
Refer to section 3.1.
Air is leaking from the arm cuff.
Replace the arm cuff with a new one.
Refer to section 5.3.
Movement during measurement and the arm
cuff has not been inflated sufficiently.
Repeat measurement. Remain still and do not
talk during measurement.
Refer to section 3.3.
If “E2” appears repeatedly, inflate the arm cuff
manually until it is 30 to 40 mmHg above your
previous measurement result.
Refer to section 3.3.
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 section 3.3.
Movement during measurement.
Repeat measurement. Remain still and do not
talk during measurement.
Refer to section 3.3.
Clothing is interfering with the arm cuff.
Remove any clothing interfering with the arm
cuff.
Refer to section 3.1.
Device error. Contact Customer Service.
Display Cause Solution
19
4. Error Messages and Troubleshooting
EN
4.2
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 section 2.1.
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
section 1.2 and section 3.3.
20
5.
Maintenance and Storage
5.1
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.
21
5. Maintenance and Storage
EN
5.2
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.
22
5. Maintenance and Storage
5.3
Optional Medical Accessories
Arm Cuff
Arm circumference
9” - 17” (22 - 42 cm)
AC Adapter
CFX-WR17
(Model: HEM-FL31)
HEM-ADPTW5
23
5. Maintenance and Storage
EN
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.
24
6.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 in pregnancy.
Model
BP760N HEM-7320-Z
Display LCD digital display
Measurement range Pressure: 0 to 299 mmHg
Pulse: 40 to 180 beats / min.
Accuracy Pressure: ±3 mmHg or 2% of reading
Pulse: ± 5% of display reading
Inflation Fuzzy-logic controlled by electric pump
Deflation Automatic pressure release valve
Measurement method Oscillometric method
IP classification IP 20
Power source
4 “AA” batteries 1.5V or optional AC adapter (INPUT AC100-240V 50/60Hz 0.12A)
Battery life Approximately 1000 measurements (using new alkaline batteries)
Operating temperature / humidity 50°F to 104°F (10°C to 40°C) / 15 to 90% RH
Storage temperature / humidity / air pressure
-4°F to 140°F (-20°C to 60°C) / 10 to 95% RH / 700 to 1060 hPa
Weight Monitor : Approximately 13 5/8 oz. (385 g) not including batteries
Arm cuff : Approximately 5 3/4 oz. (163 g)
Dimensions Monitor : Approximately 4 7/8” (w) × 3 1/2” (h) × 6 3/8” (l)
(124 mm × 90 mm × 161 mm)
Arm cuff : Approximately 5 3/4” × 21” (air tube: 29 1/2”)
(145 mm × 532 mm (air tube: 750 mm))
Cuff circumference 9” to 17” (220 to 420 mm)
Memory Up to 60 per user
Contents
Monitor, arm cuff, battery set, instruction manual, quick start guide
Applied part
Protection against electric shock Internally powered ME equipment (When using only the batteries)
= Type BF
= Class II ME equipment (Optional AC adapter)
25
EN
7.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.
26
8.Limited Warranty
Your BP760N Automatic Blood Pressure Monitor, excluding the arm cuff and 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 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
27
EN
9.
Guidance and Manufacturer’s Declaration
OMRON Automatic Blood Pressure Monitor
Information for accompanying documents in the scope of IEC60601-1-2:2007
Model: BP760N 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 BP760N 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 BP760N including AC-adapter is to measure a blood pressure and a pulse rate and using the memory
function.
The BP760N including AC-adapter may be interfered with by other equipment, even if that other equipment complies with CISPR EMISSION
requirements.
Guidance and manufacturer’s declaration - electromagnetic immunity
OMRON BP760N including AC-adapter is intended for use in the electromagnetic environment specified below. The customer or the user of
this OMRON BP760N including AC-adapter should assure that it is used in such environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions CISPR 11 Group 1
The OMRON BP760N 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.
RF emissions CISPR 11 Class B
The OMRON BP760N 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.
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations/
flicker emissions
IEC61000-3-3
Complies
28
9. Guidance and Manufacturer’s Declaration
Guidance and manufacturer’s declaration - electromagnetic immunity
OMRON BP760N including AC-adapter is intended for use in the electromagnetic environment specified below. The customer or the user of
this OMRON BP760N 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 line(s)
±2 kV line(s) to earth
±1 kV line(s) to line(s)
±2 kV line(s) to earth
Mains power quality should be that of a typical
commercial and/or hospital environment.
Voltage dips, short interruptions
and voltage variations on power
supply inputlines
IEC 61000-4-11
<5 % UT (>95 % dip in UT)
for 0.5 cycle
<5 % UT (>95 % dip in UT)
for 0.5 cycle
Mains power quality should be that of a typical
commercial and/or hospital environment. If the
user of the OMRON BP760N including AC-
adapter requires continued operation during
power mains interruption, it is recommended
that the OMRON BP760N including AC-adapter
be powered from an uninterruptible power
supply.
40 % UT (60 % dip in UT)
for 5 cycles
40 % UT (60 % dip in UT)
for 5 cycles
70 % UT (30 % dip in UT)
for 25 cycles
70 % UT (30 % dip in UT)
for 25 cycles
<5 % UT (95 % dip in UT)
for 5 sec.
<5 % UT (95 % dip in UT)
for 5 sec.
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.
29
9. Guidance and Manufacturer’s Declaration
EN
Guidance and manufacturer’s declaration - electromagnetic immunity
OMRON BP760N including AC-adapter is intended for use in the electromagnetic environment specified below. The customer or the user of
this OMRON BP760N including AC-adapter should assure that it is used in such environment.
Immunity test IEC 60601 test level
Compliance
level
Electromagnetic environment - guidance
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
3 V rms
150 kHz to 80 MHz
3 V/m
80 MHz to 2.5 GHz
3 V rms
3 V/m
Portable and mobile RF communications equipment should be used no closer to
any part of the OMRON BP760N including AC-adapter including cables, than the
recommended separation distance calculated from the equation appropriate to the
frequency of the transmitter.
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
BP760N including AC-adapter is used exceeds the applicable RF compliance level above, the OMRON BP760N 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 BP760N including AC-adapter.
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
30
9. Guidance and Manufacturer’s Declaration
Recommended separation distance between portable and mobile RF communications equipment
and the OMRON BP760N including AC-adapter
OMRON BP760N 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 BP760N including AC-adapter can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the OMRON BP760N
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
d = 1.2 √P
800 MHz to 2.5GHz
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.
31
32
9. Guidance and Manufacturer’s Declaration
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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
Fabricado para : OMRON HEALTHCARE Co., Ltd.
53, Kunotsubo, Terado-cho, Muko, Kyoto, 617-0002 JAPÓN
Distribuido por : OMRON HEALTHCARE, INC.
1925 West Field Court Lake Forest, IL 60045 U.S.A.
www.omronhealthcare.com
© 2014 OMRON HEALTHCARE, INC.
Hecho en Vietnam
7 series Blo
Mo
Instr
