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HEM-6310F-E.book Page 2 Monday, December 10, 2012 4:14 PM
To View the Readings Stored in Memory
The Blood Pressure Trend Graph
This unit also displays the Blood Pressure Trend Graph which
1.
Press the
button, while the average value is
shows the weekly averages for the Systolic Blood Pressure
displayed.
(SYS) taken in the morning and evening within 8 weeks for
each user. The graph is displayed 4 weeks averages so that
The Memory number
you can see the continuous blood pressure change.
appears for a second
before the pulse rate is
Systolic blood
displayed. The newest
pressure
Alternating
set is numbered "1".
above169 mmHg
date/time
152 - 168 mmHg
display
136 - 151 mmHg
2.
Press the
button repeatedly to view the
readings stored in memory.
119 - 135 mmHg
118 mmHg or less
To View the Weekly Averages
This unit calculates and displays weekly averages for the
measurements taken in the morning and evening within 8
3 weeks ago
2 weeks ago
weeks for each user.
7 weeks ago
6 weeks ago
Note: The week begins Sunday at 2:00.
This week - 3 weeks ago
1.
Select your User ID.
2.
Press the
button once.
The morning average for the current
week "THIS WEEK" appears on the
display.
This week
morning SYS average
118 mmHg
3.
Press the
button again.
4 weeks ago - 7 weeks ago
The evening average for the current
week "THIS WEEK" appears on the
display.
4.
Continue to press the
button to display the
previous weeks.
7 weeks ago
The unit displays "-1 WEEK" for the previous week to
morning SYS average
112 mmHg
"-7 WEEK" for the oldest set of averages.
Note: If there are not enough
To Delete All the Values Stored in Memory
measurements taken in a week
to calculate the average the
The values stored in the memory are deleted by
display will appear as
User ID.
illustrated.
When the memory symbol (
the
button. Then while holding it down, press the
This week
This week
Last week
START/STOP button simultaneously for about 2 - 3
Morning average
Evening average
Morning average
seconds.
Last week
Evening average
7 weeks ago
7 weeks ago
Evening average
Morning average
First
Second
Note: You cannot partially delete the stored readings.
5.
Press the START/STOP button to turn off the
All values for the user you select will be deleted.
monitor.
4. Troubleshooting and Maintenance
Morning Weekly Average
4.1 The Icons and Error Messages
This is the average for the measurements taken during the
morning (4:00 - 11:59) between Sunday and Saturday. An
Error Display
average for each day is calculated for up to three
measurements taken within 10 minutes of the first
measurement of the morning.
Irregular heartbeats
Measurements of the morning
are detected.
Sunday
Monday
Tuesday
Wednesday
Thursday
Friday
Saturday
4:00
First measurement of
Measurement
the morning
Measurement
Up to 3 measurements
Measurement
Within 10 minutes
Morning Blood Pressure
Measurement
Movement during
measurement.
Measurement
Measurement
The batteries are
11:59
Blink
low.
Evening Weekly Average
This is the average for the measurements taken during the
The batteries are
Lit
evening (19:00 - 1:59) between Sunday and Saturday. An
exhausted.
average for each day is calculated for up to three
measurements taken within 10 minutes of the last
Wrist cuff not
measurement of the evening.
applied correctly.
Measurements of the evening
Wednesday
Sunday
Monday
Tuesday
Thursday
Friday
Saturday
19:00
Measurement
Movement during
Measurement
measurement.
Within 10 minutes
Measurement
Measurement
Measurement
Up to 3 measurements
Last measurement of
Measurement
the evening
Evening Blood Pressure
1:59
Wrist cuff not
applied correctly, or
movement during
measurement.
Arm position
changed during
measurement.
Device error.
Note: The irregular heartbeat symbol (
symbol (
) may also be displayed with error messages.
4.2 Troubleshooting
Problem
Cause
Measure while in the
The wrist cuff is not
correct posture.
at heart level.
Refer to section 3.2.
Note:It flashes to show
which week
The cuff is not
Wrap the cuff correctly.
average value is
wrapped snugly
Refer to section 3.1.
displayed.
around the wrist.
The reading is
extremely low
(or high).
The arms and
Relax and try taking the
shoulders are
measurement again.
tense.
Refer to section 3.3.
Last week
This week
Movement or
Remain still and do not
5 weeks ago
4 weeks ago
talking during
talk during Measurement.
measurement.
Refer to section 3.3.
Wrist cuff pressure
Air is leaking from
Consult your OMRON
does not rise.
the wrist cuff.
retail outlet or distributor.
Apply the cuff correctly so
This week
Wrist cuff deflates
The wrist cuff is
that it is firmly wrapped
evening SYS average
too soon.
loose.
around the wrist. Refer to
140 mmHg
section 3.1.
Blood pressure readings
constantly vary with time
The blood pressure is different
of day and how relaxed
each time. The reading is
you are. Take several
extremely low (or high).
deep breaths and try to
remain relaxed before
taking a measurement.
7 weeks ago
evening SYS average
The unit loses
138 mmHg
power during
Replace the batteries with
The batteries are
measurement.
new ones.
exhausted.
Refer to section 2.1.
Nothing happens
when you press
The batteries have
Insert the batteries with
) appears, first press
the buttons.
been inserted
the correct (+/-) polarity.
incorrectly.
Refer to section 2.1.
• Press the START/STOP button and repeat
measurement.
• If the problem continues, try replacing the
Other problems.
batteries with new ones.
If this still does not solve the problem, contact
your OMRON retail outlet or distributor.
4.3 Transferring the Data to the Online
Solution
To begin using the software for the first time, please
visit www.omron-healthcare.com for the initial set-up
instructions.
Cause
Remedy
4.4 Maintenance
Remove the wrist cuff. Wait
To protect your unit from damage, please observe the
2 - 3 minutes and then take
following:
another measurement.
Repeat the steps in section
• Do not subject the main unit and the cuff to
3.3. If this error continues to
appear, contact your doctor.
extreme temperatures, humidity, moisture or
direct sunlight.
Carefully read and repeat the
• Do not disassemble the unit.
steps in section 3.3.
• Do not subject the unit to strong shocks or
vibrations (for example, dropping the unit on the
You should replace them with
floor).
new ones ahead of time.
Refer to section 2.1.
• Do not use volatile liquids to clean the main unit.
• Do not wash the cuff or immerse it in water.
You should replace them with
• Do not use petrol, thinners or similar solvents to
new ones at once.
Refer to section 2.1.
clean the cuff.
• Do not carry out repairs of any kind yourself. If a
Apply the wrist cuff correctly.
defect occurs, consult your OMRON retail outlet
Refer to section 3.1.
or distributor as mentioned on the packaging.
Repeat Measurement while
remaining still and refraining
from talking during the
measurement.
Refer to section 3.3.
Apply the wrist cuff correctly
and repeat measurement
while remaining still and
refraining from taking during
the measurement.
Refer to section 3.1 and 3.3.
Remain still until the
• The unit should be cleaned with a soft, dry cloth.
measurement is complete.
• Use a soft, moistened cloth and neutral soap to
Refer to section 3.3.
clean the cuff.
Contact your OMRON retail
• Keep the unit in its storage case when not in
outlet or distributor.
use.
• Fold the cuff into the storage case.
) and the movement error
Do not store the unit in the following situations:
• If the unit is wet.
Remedy
• 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.
Calibration and Service
• The accuracy of this blood pressure monitor has
been carefully tested and is designed for a long
service life.
• It is generally recommended to have the unit
inspected every two years to ensure correct
functioning and accuracy. Please consult your
authorised OMRON dealer or the OMRON
Customer Service at the address given on the
packaging or attached literature.
5. Technical Data
Product Description
Wrist Blood Pressure Monitor
Model
OMRON RS8 (HEM-6310F-E)
Display
LCD Digital Display
Measurement Method
Oscillometric method
Transmission Method
NFC-F (conforming to ISO/IEC)
Measurement Range
Pressure: 0 to 299 mmHg
Pulse: 40 to 180 beats/min.
Accuracy
Pressure: ±3 mmHg
Pulse: ±5% of display reading
Inflation
Automatic inflation by pump
Deflation
Automatic rapid deflation
Memory
100 Measurements with date and time for
each user (A and B)
Power Source
2 x 1.5V (LR03, AAA alkaline batteries)
Battery Life
Approx. 300 measurements with new
alkaline batteries at a room temperature of
23°C
Applied Part
= Type B
Protection Against
Internally powered ME equipment
Electric Shock
Operating temperature/
+10 to +40°C / Maximum: 30 to 85% RH
Humidity
Storage temperature/
-20 to +60°C / Maximum: 10 to 95% RH /
Humidity/Air pressure
700 to 1060 hPa
Console Weight
Approximately 80 g without batteries
Outer Dimensions
Approximately 89 (w) mm x 61 (h) mm x
13 (d) mm (without the wrist cuff)
Measurable
Approximately 13.5 to 21.5 cm
circumference
Cuff Material
Nylon and polyester
Package Content
Main unit, storage case, battery set,
instruction manual, guarantee card, blood
pressure pass
Note: Subject to technical modification without prior notice.
• This device fulfils the provisions of EC directive 93/42/EEC
(Medical Device Directive).
• This blood pressure monitor 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 product is produced under the strict quality system of
OMRON HEALTHCARE Co. Ltd., Japan. The Core component for
OMRON blood pressure monitors, which is the Pressure Sensor, is
produced in Japan.
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 unit
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.
Documentation is also available at www.omron-healthcare.com.
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 product 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 return 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.
Manufacturer
OMRON HEALTHCARE Co., Ltd.
53, Kunotsubo, Terado-cho, Muko, Kyoto,
617-0002 JAPAN
EU-representative
OMRON HEALTHCARE EUROPE B.V.
Scorpius 33, 2132 LR Hoofddorp
THE NETHERLANDS
www.omron-healthcare.com
Production Facility
OMRON (DALIAN) CO., LTD.
Dalian, CHINA
Subsidiary
OMRON HEALTHCARE UK LTD.
Opal Drive, Fox Milne, Milton Keynes, MK15 0DG
U.K.
OMRON MEDIZINTECHNIK
HANDELSGESELLSCHAFT mbH
John-Deere-Str. 81a 68163 Mannheim, GERMANY
www.omron-medizintechnik.de
OMRON SANTÉ FRANCE SAS
14, rue de Lisbonne, 93561 Rosny-sous-Bois
Cedex, FRANCE
Made in China
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