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Automatic Blood Pressure Monitor
Model M6 AC
Instruction Manual
IM-HEM-7322-E-01-08/2013
2298870-5A
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Check following components!
Vérifier les composants suivants !
Controleer de volgende onderdelen!
Prüfen Sie folgende Teile des Lieferumfangs! Uꢏꢐꢑꢒꢏꢓꢔꢒꢈꢕꢖꢒꢗꢘ ꢙꢚꢒ ꢛꢐꢜꢝꢐꢞꢒꢞꢔꢟ!
Controllare i componenti indicati di seguito!
ꢀꢁꢂꢃꢄꢅꢂꢆꢇꢈꢉꢇꢊꢋꢁꢋꢌꢊꢋꢍꢇꢈꢆꢎꢌ!ꢍꢎꢊꢈꢋꢅꢇꢌ"
¡Compruebe los siguientes componentes!
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Important Safety Information
Warning: Indicates a potentially hazardous situation which, if not avoided, could result in death or
serious injury.
(General Usage)
Consult your physician before using the device in pregnancy including pre-eclampsia, or if diagnosed with
arrhythmia or arteriosclerosis.
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.
EN
The air tube or the AC adapter cable may cause accidental strangulation in infants.
Contained 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.
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.
People with severe blood flow problems, or blood disorders, should consult a physician before using the device,
as the arm cuff inflation can cause bruising.
1
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Important Safety Information
If there are any abnormalities during the measurement, remove the arm cuff.
Do not use this device on infants or persons who cannot express their intentions.
Do not inflate the arm cuff more than necessary.
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.
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).
Do not take measurements more than necessary. It may cause bruising due to blood flow interference.
Consult your physician before using the device if you had a mastectomy.
(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.
When handling the power cord, take care not to do the following:
Do not damage.
Do not tamper with it.
Do not twist.
Do not break it.
Do not forcibly bend or pull.
Do not bundle during use.
Do not place under heavy objects.
Do not pinch.
Wipe the dust off from the power plug.
Unplug monitor when not in use.
Disconnect the power plug before cleaning.
Use only the original AC adapter designed for this device. Use of unsupported adapters may damage and/or may
be hazardous to the device.
2
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Important Safety Information
(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.
EN
• 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.
• Read and follow the "Important information regarding Electro Magnetic Compatibility (EMC)" in the
"6. Specifications".
• Read and follow the "Correct Disposal of This Product" in "6. Specifications" when disposing of the device and any
used accessories or optional parts.
3
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1. Know Your Device
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.
Monitor
Display
A
P
Display
Memory symbol
B
C
D
E
F
G
H
I
Q
R
S
T
Cuff wrap guide lamp
USER ID symbol
Memory button
Average value symbol
Systolic blood pressure
Diastolic blood pressure
Weekly average button
START/STOP button
U
Up/Down buttons
Heartbeat symbol
(Flashes during measurement)
USER ID selection switch
V
W
X
Y
Z
Date/Time setting button
Date/Time display
Blood pressure colour indicator
Morning average symbol
Evening average symbol
Morning hypertension symbol
Movement error symbol
Irregular heartbeat symbol
Blood pressure level indicator
Cuff wrap guide
J
K
L
Air jack
Battery compartment
AC adapter jack
Arm cuff
M
Arm cuff (Arm circumference 22-42cm)
N
Air plug
Low battery symbol
O
Air tube
Deflation symbol
Pulse display / Memory number
4
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1. Know Your Device
Display Symbols
Irregular Heartbeat Symbol (
)
Normal Heartbeat
When the monitor detects an irregular rhythm two or more times during the
measurement, the irregular heartbeat symbol (
display with the measurement values.
Pulse
) will appear on the
Blood pressure
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.
Irregular Heartbeat EN
Long
Short
Pulse
If the irregular heartbeat symbol (
results, we recommend you consult your physician. Follow the directions
of your physician.
) displays with your measurement
Blood pressure
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.
Cuff Wrap Guide Lamp (
/
)
If the cuff was wrapped too loosely, it may cause unreliable results. If the wrapping of cuff is too loose, the cuff wrap
guide Lamp lights in “orange”. Otherwise lights in “green”. This is the function which is used as an aid in
determining if the cuff is wrapped snugly enough.
5
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1. Know Your Device
Blood Pressure Colour Indicator
If your systolic or diastolic pressure is above the standard range (135 mmHg for the
systolic blood pressure and/or 85 mmHg for the diastolic blood pressure), the blood
pressure colour indicator will light in “orange” when the measurement result is displayed. If
they are within the standard range, the blood pressure colour indicator will light in “green”.
The JNC7* Guideline recommends the following guideline.
General Guidelines for Blood Pressure
Prehypertension at Office
120-139 mmHg
Hypertension at Home
135 mmHg
Systolic Blood Pressure
Diastolic Blood Pressure
80-89 mmHg
85 mmHg
These are from statistical values for blood pressure.
* JNC7: The Seventh Report, 2003 Dec, of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High
Blood Pressure.
6
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2. Preparation
2.1 Battery Installation
1. Remove the battery cover.
2. Insert 4 “AA” batteries as
indicated in the battery
compartment.
EN
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.
• The supplied batteries may have a shorter life.
Disposal of used batteries should be carried out in accordance with the national/local regulations for the
disposal of batteries.
7
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2. Preparation
2.2 Using the 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.
8
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2. Preparation
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.
2.3 Setting the Date and Time
Set the monitor to the correct date and time before taking a measurement for the first time.
EN
H
1. Press the Date/Time setting ( ) button.
V
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 minutes.
Year
Month
Day
Hour
Change
: Forward
: Back
Confirm
Minute
Change
Confirm
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.
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3. Using the Device
Open both the front and rear covers to read the following:
The letter identifiers on the cover pages correspond to those in the body of this page.
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.
N
J
1. Insert
the air plug into
the air jack securely.
2. Wrap the arm cuff firmly in place around your left upper
arm.
a
The bottom edge of the arm cuff should be
1 to 2 cm above the elbow.
O
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
b
not to rest your arm on the air tube. ---
• The blood pressure can differ between the right arm and the left arm, and therefore also 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 measurement.
10
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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.
EN
c
• 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. ---
d
11
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3. Using the Device
3.3 Taking a Measurement
Notes:
• To cancel a measurement, press the START/STOP button to release the air in the arm cuff.
• Remain still 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.
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.
Cuff Wrap Guide Lamp
Notes:
• The monitor will not inflate above 299 mmHg.
• Do not apply more pressure than necessary.
12
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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.
EN
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.
Always consult your physician. Self-diagnosis of measurement results and self-treatment are dangerous. 13
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3. Using the Device
3.4 Using the Memory Function
The monitor automatically stores the results up to 100 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”.
Note: The cuff wrap guide result appears on the display with the
measurement values. The cuff wrap guide lamp will not light.
3. Press the or button to view the values stored in the
memory.
: To the older values
: To the more recent values
14
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3. Using the Device
To View the Average Value
1. Select your USER ID (1 or 2).
2. Press and hold the button for more
than 3 seconds.
EN
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.
15
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3. Using the Device
To View the Weekly Average Value
The monitor calculates and displays weekly averages for the measurements taken in
the morning and evening within 8 weeks for each user.
1. SNoetel:eTchte wyeoekubergiUnsSSuEndRay aItD2:0(0.1 or 2).
2. Press the
button.
The morning average for “THIS WEEK” appears on the display.
Note: The morning hypertension symbol (
) appears if the morning weekly average is
above 135/85 mmHg.
Press the
button again, and the evening average for “THIS WEEK”
appears on the display.
Press the
or
button to display the previous weeks.
This week
Last week
2 weeks ago
7 weeks ago
Continue to
press...
Morning average
Morning average
Morning average
Morning average
Last week
This week
2 weeks ago
7 weeks ago
Evening average
Evening average
Evening average
Evening average
16
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3. Using the Device
Note: If there are no measurement values stored in the memory, the
screen to the right is displayed.
Morning Weekly Average
Measurements of the morning
Tuesday Wednesday Thursday
EN
Sunday
Monday
Friday
Saturday
This is the average for the
4:00
measurements taken during the morning
(4:00 - 11:59) between Sunday and
Saturday. An average for each day is
calculated for up to three measurements
taken within 10 minutes of the first
measurement of the morning.
First measurement of
the morning
Measurement
Measurement
Measurement
Measurement
Up to 3 measurements
Within 10 minutes
Morning Blood Pressure
Measurement
Measurement
11:59
Evening Weekly Average
Measurements of the evening
Tuesday Wednesday Thursday
Sunday
Monday
Friday
Saturday
This is the average for the
19:00
measurements taken during the evening
(19:00 - 1:59) between Sunday and
Saturday. An average for each day is
calculated for up to three measurements
taken within 10 minutes of the last
measurement of the evening.
Measurement
Measurement
Within 10 minutes
Measurement
Measurement
Measurement
Measurement
Up to 3 measurements
Last measurement of
the evening
Evening Blood Pressure
1:59
17
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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.
18
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4. Error Messages and Troubleshooting
4.1 Error Messages
Display
Cause
Solution
Remove the arm cuff. Wait 2-3 minutes and
then take another measurement.
Irregular heartbeats are detected.
Repeat the steps in section 3.3. If this error
EN
continues to appear, contact your physician.
Carefully read and repeat the steps in section
3.3.
Movement during measurement.
Apply the arm cuff tighter.
Refer to section 3.1.
Arm cuff is applied too loosely.
The batteries are low.
You should replace the batteries with new
ones ahead of time.
Refer to section 2.1.
You should replace the batteries with new
ones at once.
Refer to section 2.1.
The batteries are exhausted.
19
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4. Error Messages and Troubleshooting
Display
Cause
Air plug is disconnected.
Solution
Insert the air plug securely.
Refer to section 3.1.
Apply the arm cuff tighter.
Refer to section 3.1.
Arm cuff is applied too loosely.
Air is leaking from the arm cuff.
Replace the arm cuff with a new one.
Refer to section 5.3.
Repeat measurement. Remain still and do not
talk during measurement.
Refer to section 3.3.
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 section 3.3.
The arm cuff was inflated above 299 mmHg
when inflating the arm cuff manually.
Do not inflate the arm cuff above 299 mmHg.
Refer to section 3.3.
Repeat measurement. Remain still and do not
talk during measurement.
Refer to section 3.3.
Movement during measurement.
Remove any clothing interfering with the arm
cuff.
Clothing is interfering with the arm cuff.
Device error.
Refer to section 3.1.
Contact your OMRON retail outlet or
distributor.
20
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4. Error Messages and Troubleshooting
4.2 Troubleshooting
Problem
Cause
Solution
Apply the arm cuff tighter.
Refer to section 3.1.
Arm cuff is applied too loosely.
Remain still and do not talk during
measurement.
Refer to section 3.3.
EN
Movement or talking during
measurement.
The measurement result is extremely
high (or low).
Remove any clothing interfering
with the arm cuff.
Refer to section 3.1.
Clothing is interfering with the arm
cuff.
Make sure that the air tube is
connected securely.
Refer to section 3.1.
The air connector is not securely
connected into the air jack.
Arm cuff pressure does not rise.
Arm cuff deflates too soon.
Replace the arm cuff with a new
one.
Air is leaking from the arm cuff.
The arm cuff is loose.
Refer to section 5.3.
Apply the arm cuff correctly so that
it is firmly wrapped around the arm.
Refer to section 3.1.
Inflate the arm cuff so that it is 30 to
40 mmHg above your previous
measurement result.
Cannot measure or the results are
too low or too high.
The arm cuff has not been inflated
sufficiently.
Refer to section 3.3.
21
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4. Error Messages and Troubleshooting
Problem
Cause
Solution
Replace the batteries with new
ones.
Refer to section 2.1.
The batteries are empty.
Nothing happens when you press the
buttons.
Insert the batteries with the correct
(+/-) polarity.
Refer to section 2.1.
The batteries have been inserted
incorrectly.
• Press the START/STOP button and repeat measurement.
• Replace the batteries with new ones.
Other problems.
If the problem continues, contact your OMRON retail outlet or distributor.
22
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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 petrol, thinners or similar solvents to clean the device.
EN
• 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 your OMRON retail outlet or
distributor.
Calibration and Service
• The accuracy of this device has been carefully tested and is designed for a long service life.
• It is generally recommended to have the device inspected every 2 years to ensure correct functioning and
accuracy. Please consult your OMRON retail outlet or distributor.
23
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5. Maintenance and Storage
5.2 Storage
Keep the device in its storage case when not in use.
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.
3. Place the monitor and the arm cuff in the
storage case.
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 vapours.
• Locations exposed to vibrations, shocks or where it will be at an angle.
24
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5. Maintenance and Storage
5.3 Optional Medical Accessories
(within the scope of EC Medical Device Directive 93/42/EEC)
Arm cuff
AC adapter
Arm circumference 22-42 cm
EN
Adapter S-9515336-9
Easy Cuff L-9911729-4
(Model: HEM-RML31)
Adapter UK-9983666-5
25
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6. Specifications
Product description
Model
Display
Automatic Blood Pressure Monitor
OMRON M6 AC (HEM-7322-E)
LCD digital display
Measurement method
Measurement range
Oscillometric method
Pressure: 0 to 299 mmHg
Pulse: 40 to 180 beats / min.
Pressure: 3 mmHg
Accuracy
Pulse: 5% of display reading
Fuzzy-logic controlled by electric pump
Automatic pressure release valve
100 measurements with date and time for each user (1 and 2)
DC6V 4W
Inflation
Deflation
Memory
Rating
Power source
4 “AA” batteries 1.5V or optional AC adapter
(Adapter S-9515336-9, INPUT AC100-240V 50/60Hz 0.12A)
(Adapter UK-9983666-5, INPUT AC100-240V 50/60Hz 15VA)
Battery life
Applied part
Approximately 1000 measurements (using new alkaline batteries)
= Type BF
Protection against electric shock
Internally powered ME equipment (When using only the batteries)
= Class II ME equipment (AC adapter)
Operating temperature/ humidity
Storage temperature/ humidity/ air pressure
IP classification
+10°C to +40°C / 30 to 85% RH
-20°C to +60°C / 10 to 95% RH / 700-1060hPa
IP 20
Monitor: Approximately 380g without batteries
Arm cuff: Approximately 170g
Weight
Outer dimensions
Monitor: Approximately 124 (w) mm × 90 (h) mm × 161 (l) mm
Arm cuff: Approximately 145 mm × 594 mm (air tube: 750 mm)
22 to 42 cm
Cuff circumference
Cuff / Tube material
Package contents
Nylon, polyester, polyvinyl chloride
Monitor, arm cuff, instruction manual, storage case, battery set, AC adapter,
blood pressure pass
26
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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 on pregnant patients.
EN
• This device fulfils the provisions of EC directive 93/42/EEC (Medical Device Directive).
• This device is designed according to the European Standard EN1060, Non-invasive
sphygmomanometers Part 1: General Requirements and Part 3: Supplementary
requirements for electromechanical blood pressure measuring systems.
• This OMRON device is produced under the strict quality system of OMRON HEALTHCARE
Co. Ltd., Japan. The core component for OMRON devices, which is the Pressure Sensor, is
produced in Japan.
27
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6. Specifications
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 EN60601-1-2:2007 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.
This medical device manufactured by OMRON HEALTHCARE conforms to this EN60601-1-2:2007 standard for
both immunity and emissions.
Nevertheless, special precautions need to be observed:
• Do not use mobile (cellular) telephones and other devices, which generate strong electrical or electromagnetic
fields, near the medical device. This may result in incorrect operation of the device and create a potentially unsafe
situation. Recommendation is to keep a minimum distance of 7 m. Verify correct operation of the device in case
the distance is shorter.
Further documentation in accordance with EN60601-1-2:2007 is available at OMRON HEALTHCARE EUROPE at
the address mentioned in this instruction manual.
Correct Disposal of This Product
(Waste Electrical & Electronic Equipment)
This marking shown on the product or its literature, indicates that it should not be disposed of, with other
household wastes at the end of its working life. To prevent possible harm to the environment or human
health from uncontrolled waste disposal, please separate this from other types of wastes and recycle it
responsibly to promote the sustainable reuse of material resources.
Household users should contact either the retailer where they purchased this product, or their local government
office, for details of where and how they can take this item for environmentally safe recycling.
Business users should contact their supplier and check the terms and conditions of the purchase contract. This
product should not be mixed with other commercial wastes for disposal.
28
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7. Warranty
Thank you for buying an OMRON product. This product is constructed of high quality materials and great care has
been taken in its manufacturing. It is designed to give you every satisfaction, provided that it is properly operated and
maintained as described in the instruction manual.
This product is guaranteed by OMRON for a period of 3 years after the date of purchase. The proper construction,
workmanship and materials of this product is guaranteed by OMRON. During this period of guarantee OMRON will,
without charge for labour or parts, repair or replace the defect product or any defective parts.
The guarantee does not cover any of the following:
a. Transport costs and risks of transport.
EN
b. Costs for repairs and / or defects resulting from repairs done by unauthorised persons.
c. Periodic check-ups and maintenance.
d. Failure or wear of optional parts or other attachments other than the main device itself, unless explicitly guaranteed
above.
e. Costs arising due to non-acceptance of a claim (those will be charged for).
f. Damages of any kind including personal caused accidentally or from misuse.
g. Calibration service is not included within the guarantee.
h. Optional parts have a one (1) year warranty from date of purchase. Optional parts include, but are not limited to the
following items: Cuff and Cuff Tube, AC Adapter.
Should guarantee service be required please apply to the dealer whom the product was purchased from or an
authorised OMRON distributor. For the address refer to the product packaging / literature or to your specialised
retailer.
If you have difficulties in finding OMRON customer services, contact us for information.
Repair or replacement under the guarantee does not give rise to any extension or renewal of the guarantee period.
The guarantee will be granted only if the complete product is returned together with the original invoice / cash ticket
issued to the consumer by the retailer.
29
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8. Some Useful Information about Blood Pressure
What is Blood Pressure?
Blood pressure is a measure of the force of blood flowing against the walls of the arteries.
Arterial blood pressure is constantly changing during the course of the heart’s cycle.
The highest pressure in the cycle is called the Systolic Blood Pressure; the lowest is the
Diastolic Blood Pressure. Both pressures, the Systolic and Diastolic, are necessary to enable
a physician to evaluate the status of a patient’s blood pressure.
What is Arrhythmia?
Arrhythmia is a condition where the heartbeat rhythm is abnormal due to flaws in the bio-
electrical system that drives the heartbeat. Typical symptoms are skipped heartbeats,
premature contraction, an abnormally rapid (tachycardia) or slow (bradycardia) pulse.
Why is it a Good Thing to measure Blood Pressure at Home?
Many factors such as physical activity,
anxiety, or the time of day, can influence
your blood pressure. A single
Upper curve: systolic blood pressure
Lower curve: diastolic blood pressure
200
150
measurement may not be sufficient for an
accurate diagnosis. Thus it is best to try
and measure your blood pressure at the
same time each day, to get an accurate
indication of any changes in blood
pressure. Blood pressure is typically low in
the morning and increases from afternoon
100
50
6
12
18
24
Time of day
Example: fluctuation within a day (male, 35 years old)
30to evening. It is lower in the summer and higher in the winter.
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OMRON HEALTHCARE Co., Ltd.
Manufacturer
53, Kunotsubo, Terado-cho, Muko, Kyoto,
617-0002 JAPAN
OMRON HEALTHCARE EUROPE B.V.
Scorpius 33, 2132 LR Hoofddorp, THE NETHERLANDS
EU-representative
Production facility
Site de production
Produktionsstätte
Stabilimento di produzione
Planta de producción
Productiefaciliteit
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Üretim Tesisi
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OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD.
Binh Duong Province, VIETNAM
Subsidiary
Empresa filial
Dochteronderneming
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OMRON HEALTHCARE UK LTD.
Opal Drive, Fox Milne, Milton Keynes, MK15 0DG, U.K.
Succursale
Niederlassung
Consociata
OMRON MEDIZINTECHNIK HANDELSGESELLSCHAFT mbH
Gottlieb-Daimler-Strasse 10, 68165 Mannheim, GERMANY
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OMRON SANTÉ FRANCE SAS
14, rue de Lisbonne, 93561 Rosny-sous-Bois Cedex, FRANCE
Uniquement pour le marché français: OMRON Service Après Vente
Nº Vert 0 800 91 43 14
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