Omron M3 Manual
Omron M3 Manual
Omron M3 Manual
* JNC7: The Seventh Report, 2003 Dec, of the Joint National Committee on
Prevention, Detection, Evaluation, and Treatment of Hi Blood Pressure.
4. Error Messages and Troubleshooting 5. Maintenance and Storage 6. Specifications 7. Warranty
4.1 Error Messages 5.1 Maintenance Product description Automatic Blood Pressure Monitor
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
Model OMRON M3 (HEM-7131-E)
Error Display Cause Solution To protect your device from damage, please observe the following: to give you every satisfaction, provided that it is properly operated and maintained
Display LCD Digital Display as described in the instruction manual.
Remove the arm cuff. Wait 2 - 3 • Store the device and the components in a clean, safe Measurement Oscillometric method This product is guaranteed by OMRON for a period of 3 years after the date of
minutes and then take another location. method purchase. The proper construction, workmanship and materials of this product is
Irregular heartbeats are measurement. Repeat the steps
detected. in section 3.3. If this error • Do not use any abrasive or volatile cleaners. Measurement range Pressure: 0 to 299 mmHg guaranteed by OMRON. During this period of guarantee OMRON will, without
continues to appear, contact • Do not wash the device and any components or immerse Pulse: 40 to 180 beats/min. charge for labour or parts, repair or replace the defect product or any defective
your physician. them in water. Accuracy Pressure: ±3 mmHg parts.
• Do not use petrol, thinners or similar solvents to clean the Pulse: ±5% of display reading The guarantee does not cover any of the following:
Carefully read and repeat the a. Transport costs and risks of transport.
Movement during measurement. device. Inflation Fuzzy-logic controlled by electric pump
steps in section 3.3. b. Costs for repairs and / or defects resulting from repairs done by unauthorised
Deflation Automatic pressure release valve
persons.
You should replace the batteries Memory 60 measurements with date and time for each user (1 and 2)
c. Periodic check-ups and maintenance.
The batteries are low. with new ones ahead of time. Rating DC6V 4W d. Failure or wear of optional parts or other attachments other than the main device
Refer to section 2.1.
Power source 4 “AA” batteries 1.5V or optional AC adapter itself, unless explicitly guaranteed above.
You should replace the batteries (Adapter S-9515336-9, INPUT AC100-240V 50/60Hz 0.12A) e. Costs arising due to non-acceptance of a claim (those will be charged for).
The batteries are exhausted. with new ones at once. (Adapter UK-9983666-5, INPUT AC100-240V 50/60Hz 15VA) f. Damages of any kind including personal caused accidentally or from misuse.
Refer to section 2.1. Battery life Approx. 1000 measurements (using new alkaline batteries) g. Calibration service is not included within the guarantee.
h. Optional parts have a one (1) year warranty from date of purchase. Optional parts
Insert the plug securely. Applied part = Type BF include, but are not limited to the following items: Cuff and Cuff Tube, AC Adapter.
Air plug disconnected.
Refer to section 3.1. Should guarantee service be required please apply to the dealer whom the product
Protection against Internally powered ME equipment (When using only the was purchased from or an authorised OMRON distributor. For the address refer to
Apply the arm cuff tighter. electric shock batteries) the product packaging / literature or to your specialised retailer.
Arm cuff is applied too loosely.
Refer to section 3.1. • Use a soft and dry cloth, or a soft and moistened cloth and = Class II ME equipment (Optional AC adapter)
If you have difficulties in finding OMRON customer services, contact us for
neutral soap to clean on the monitor and the arm cuff. information.
Operating +10 to +40°C / 30 to 85% RH www.omron-healthcare.com
Air is leaking from the arm cuff.
Replace the cuff with a new one. • Changes or modification not approved by the manufacturer temperature/
Refer to section 5.3. will void the user warranty. Do not disassemble or attempt to humidity Repair or replacement under the guarantee does not give rise to any extension or
repair the device or components. Consult your authorised Storage -20 to +60°C / 10 to 95% RH / 700 to 1060 hPa renewal of the guarantee period.
Repeat measurement. Remain
still and do not talk during OMRON retail outlet or distributor. temperature/ The guarantee will be granted only if the complete product is returned together with
measurement. humidity/ the original invoice / cash ticket issued to the consumer by the retailer.
Movement during measurement Refer to section 3.3. Calibration and Service air pressure
and the arm cuff has not been • The accuracy of this blood pressure monitor has been IP classification IP 20
If “E2” appears repeatedly, Manufacturer OMRON HEALTHCARE Co., Ltd.
inflated sufficiently. Weight Monitor: Approx. 280 g without batteries
inflate the cuff manually until it is carefully tested and is designed for a long service life. 53, Kunotsubo, Terado-cho, Muko, Kyoto,
30 to 40 mmHg above your • It is generally recommended to have the device inspected Arm cuff: Approx. 170 g 617-0002 JAPAN
previous measurement result. Outer dimensions Monitor: Approx. 107 (w) mm x 79 (h) mm x 141 (l) mm
Refer to section 3.3. every 2 years to ensure correct functioning and accuracy.
Arm cuff: Approx. 145 mm x 594 mm EU-representative OMRON HEALTHCARE EUROPE B.V.
Please consult your authorised OMRON retail outlet or
The arm cuff was inflated above Do not inflate the cuff above 299 Cuff circumference 22 to 42 cm Scorpius 33, 2132 LR Hoofddorp, THE NETHERLANDS
299 mmHg when inflating the mmHg. distributor. www.omron-healthcare.com
Cuff/ Tube material Nylon, polyester, polyvinyl chloride
cuff manually. Refer to section 3.3.
Package contents Monitor, arm cuff, instruction manual, storage case,
Production facility OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD.
Repeat measurement. Remain battery set, blood pressure pass
Binh Duong Province, VIETNAM
still and do not talk during
Movement during measurement. 5.2 Storage Notes: Subsidiary OMRON HEALTHCARE UK LTD.
measurement.
Refer to section 3.3. Keep the device in its storage case when not in use. • These specifications are subject to change without notice. Opal Drive, Fox Milne, Milton Keynes, MK15 0DG, U.K.
• In the clinical validation study, the 5th phase was used on 85 subjects for OMRON MEDIZINTECHNIK HANDELSGESELLSCHAFT mbH
Remove any clothing interfering 1. Unplug the air plug from the air jack. determination of diastolic blood pressure. Gottlieb-Daimler-Strasse 10, 68165 Mannheim, GERMANY
Clothing is interfering with the
with the arm cuff. • This device has not been validated for use on pregnant patients. www.omron-healthcare.de
arm cuff.
Refer to section 3.1. 2. Gently fold the air tube into the arm cuff.
OMRON SANTÉ FRANCE SAS
14, rue de Lisbonne, 93561 Rosny-sous-Bois Cedex, FRANCE
Note: Do not bend or crease the air tube excessively.
Contact your OMRON retail
Device error. Made in Vietnam
outlet or distributor.
• This device fulfils the provisions of EC directive 93/42/EEC (Medical Device
Directive).
3. Place the monitor and the arm cuff in the
• This blood pressure monitor is designed according to the European Standard
storage case. EN1060, Non-invasive sphygmomanometers Part 1: General Requirements and
4.2 Troubleshooting Part 3: Supplementary requirements for electromechanical blood pressure
Problem Cause Solution measuring systems.
Do not store the device in the following situations:
• This OMRON product is produced under the strict quality system of OMRON
•If the device is wet.
HEALTHCARE Co. Ltd., Japan. The Core component for OMRON blood pressure
•Locations exposed to extreme temperatures,
Arm cuff is applied too Apply the arm cuff tighter. monitors, which is the Pressure Sensor, is produced in Japan.
humidity, direct sunlight, dust or corrosive
loosely. Refer to section 3.1.
vapours.
•Locations exposed to vibrations, shocks or Important information regarding Electro Magnetic Compatibility (EMC)
where it will be at an angle. With the increased number of electronic devices such as PC’s and mobile (cellular)
The measurement Remain still and do not talk telephones, medical devices in use may be susceptible to electromagnetic
Movement or talking during interference from other devices. Electromagnetic interference may result in
result is extremely during measurement.
measurement. incorrect operation of the medical device and create a potentially unsafe situation.
high (or low). Refer to section 3.3.
5.3 Optional Medical Accessories Medical devices should also not interfere with other devices.
(within the scope of EC Medical Device Directive 93/42/EEC) 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
Remove any clothing Arm cuff AC adapter been implemented. This standard defines the levels of immunity to
Clothing is interfering with
interfering with the arm cuff. Arm circumference electromagnetic interferences as well as maximum levels of electromagnetic
the arm cuff.
Refer to section 3.1. emissions for medical devices.
22 - 42 cm
This medical device manufactured by OMRON HEALTHCARE conforms to this
EN60601-1-2:2007 standard for both immunity and emissions.
The air connector is not Make sure that the air tube Nevertheless, special precautions need to be observed:
securely connected into the is connected securely. • Do not use mobile (cellular) telephones and other devices, which generate strong
air jack. Refer to section 3.1. electrical or electromagnetic fields, near the medical device. This may result in
Arm cuff pressure incorrect operation of the device and create a potentially unsafe situation.
does not rise. Recommendation is to keep a minimum distance of 7 m. Verify correct operation
Replace the arm cuff with a Easy Cuff L Adapter S Adapter UK of the device in case the distance is shorter.
Air is leaking from the arm
new one. 9911729-4 9515336-9 9983666-5 Further documentation in accordance with EN60601-1-2:2007 is available at
cuff.
Refer to section 5.3. (Model: HEM-RML31) OMRON HEALTHCARE EUROPE at the address mentioned in this instruction
manual.
Documentation is also available at www.omron-healthcare.com.
The cuff wrapping
Apply the cuff correctly so
guide lamp does not
that it is firmly wrapped Correct Disposal of This Product
light. The arm cuff is loose.
Arm cuff deflates too
around the arm. Using the Optional AC Adapter (Waste Electrical & Electronic Equipment)
Refer to section 3.1.
soon.
1. Insert the AC adapter plug This marking shown on the product or its literature, indicates that it
Inflate the cuff so that it is 30 into the AC adapter jack on should not be disposed of, with other household wastes at the end
Cannot measure or to 40 mmHg above your of its working life. To prevent possible harm to the environment or
The arm cuff has not been the rear side of the monitor. human health from uncontrolled waste disposal, please separate
the results are too low previous measurement this product from other types of wastes and recycle it responsibly to
inflated sufficiently. 2. Plug the AC adapter into an
or too high. result. promote the sustainable reuse of material resources.
Refer to section 3.3. electrical outlet. 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
Replace the batteries with return this item for environmentally safe recycling.
The batteries are empty. new ones. To disconnect the AC adapter, unplug the AC adapter from the electrical outlet Business users should contact their supplier and check the terms and conditions of
Refer to section 2.1. first and then remove the AC adapter plug from the monitor. the purchase contract. This product should not be mixed with other commercial
Nothing happens
wastes for disposal.
when you press the
buttons.
Insert the batteries with the
The batteries have been
correct (+/-) polarity.
inserted incorrectly.
Refer to section 2.1.