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3.4 Using the Memory Function
The unit automatically stores up to 30 sets of measurement values (blood pressure and pulse rate). If the memory is full, the monitor will delete the oldest readings.
To View the Readings Stored in Memory
1.Press the
button.
The Memory number appears for a second before the pulse rate is displayed. The newest set is numbered “1”.
Note: If there are no measurements results stored in the memory, the screen to the right is displayed.
2.Press the button repeatedly to view the readings stored in memory.
To Delete All the Values Stored in Memory
When the memory symbol ( ) appears, first press the
button. Then while holding it down, press the START/STOP button simultaneously for about 2 - 3 seconds.
First Second
Note: You cannot partially delete the stored readings.
4.Troubleshooting and Maintenance
4.1The Icons and Error Messages
Error Display | Cause | Remedy | |
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| Remove the wrist cuff. Wait | |
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| 2 - 3 minutes and then take | |
| Irregular heartbeats | another measurement. | |
| are detected. | Repeat the steps in section | |
|
| 3.3. If this error continues to | |
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| appear, contact your doctor. | |
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| |
| The batteries are | You should replace them with | |
Blink | new ones ahead of time. | ||
low. | |||
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| Refer to section 2.1. | |
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| |
| The batteries are | You should replace them with | |
Lit | new ones at once. | ||
exhausted. | |||
Refer to section 2.1. | |||
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| ||
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| |
| Wrist cuff not | Apply the wrist cuff correctly. | |
| applied correctly. | Refer to section 3.1. | |
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| |
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| Repeat Measurement while | |
| Movement during | remaining still and refraining | |
| from talking during the | ||
| measurement. | ||
| measurement. | ||
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| ||
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| Refer to section 3.3. | |
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| |
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| Apply the wrist cuff correctly | |
| Wrist cuff not | and repeat measurement | |
| applied correctly, or | while remaining still and | |
| movement during | refraining from talking during | |
| measurement. | the measurement. | |
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| Refer to section 3.1 and 3.3. | |
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| |
| Device error. | Contact your OMRON retail | |
| outlet or distributor. | ||
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| ||
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Note: The irregular heartbeat symbol ( ) may also be displayed with error messages.
4.2 Troubleshooting
Problem | Cause | Remedy | |
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| |
| The wrist cuff is not | Measure while in the | |
| at heart level. | correct posture. | |
| Refer to section 3.2. | ||
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| ||
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| |
| The cuff is not | Wrap the cuff correctly. | |
| wrapped snugly | ||
The reading is | Refer to section 3.1. | ||
around the wrist. | |||
| |||
extremely low |
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| |
The arms and | Relax and try taking the | ||
(or high). | |||
| shoulders are | measurement again. | |
| tense. | Refer to section 3.3. | |
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| |
| Movement or | Remain still and do not | |
| talking during | talk during Measurement. | |
| measurement. | Refer to section 3.3. | |
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| |
Wrist cuff pressure | Air is leaking from | Consult your OMRON | |
does not rise. | the wrist cuff. | retail outlet or distributor. | |
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| |
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| Apply the cuff correctly so | |
Wrist cuff deflates | The wrist cuff is | that it is firmly wrapped | |
too soon. | loose. | around the wrist. Refer to | |
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| section 3.1. | |
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| |
|
| 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. | |
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|
| |
The unit loses |
| Replace the batteries with | |
power during | The batteries are | ||
measurement. | new ones. | ||
exhausted. | |||
| Refer to section 2.1. | ||
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| ||
Nothing happens |
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| |
when you press | The batteries have | Insert the batteries with | |
the buttons. | been inserted | the correct | |
| incorrectly. | Refer to section 2.1. | |
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|
| |
| • Press the START/STOP button and repeat | ||
| measurement. |
| |
Other problems. | • If the problem continues, try replacing the | ||
batteries with new ones. | |||
| |||
| If this still does not solve the problem, contact | ||
| your OMRON retail outlet or distributor. | ||
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|
|
4.3 Maintenance
To protect your unit from damage, please observe the following:
•Do not subject the main unit and the cuff to extreme temperatures, humidity, moisture or direct sunlight.
•Do not disassemble the unit.
•Do not subject the unit to strong shocks or vibrations (for example, dropping the unit on the floor).
•Do not use volatile liquids to clean the main unit. •Do not wash the cuff or immerse it in water. •Do not use petrol, thinners or similar solvents to clean the cuff.
•Do not carry out repairs of any kind yourself. If a defect occurs, consult your OMRON retail outlet or distributor as mentioned on the packaging.
•The unit should be cleaned with a soft, dry cloth. •Use a soft, moistened cloth and soap to clean the cuff.
•Keep the unit in its storage case when not in use.
•Fold the cuff into the storage case.
Do not store the unit in the following situations:
•If the unit 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.
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 RS2 |
Display | LCD Digital Display |
Measurement Method | Oscillometric method |
Measurement Range | Pressure: 0 to 299 mmHg |
| Pulse: 40 to 180/min. |
Accuracy | Pressure: ±3 mmHg |
| Pulse: ±5% of display reading |
Inflation | Automatic inflation by pump |
Deflation | Automatic rapid deflation |
Memory | 30 Measurements |
Power Source | 2 “AAA” alkaline (LR03) batteries 1.5V |
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/ | |
Humidity | 700 to 1060hPa |
Console Weight | Approximately 101g without batteries |
Outer Dimensions | Approximately 78 (w) mm x 60 (h) mm x |
| 21 (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 |
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,
•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
This medical device manufactured by OMRON HEALTHCARE conforms to this
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
Documentation is also available at
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, |
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OMRON HEALTHCARE EUROPE B.V. | |
| Scorpius 33, 2132 LR Hoofddorp |
| THE NETHERLANDS |
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Production facility | OMRON (DALIAN) CO., LTD. |
| Dalian, CHINA |
Subsidiary | OMRON HEALTHCARE UK LTD. |
| Opal Drive, Fox Milne, Milton Keynes, MK15 0DG |
| U.K. |
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| OMRON MEDIZINTECHNIK |
| HANDELSGESELLSCHAFT mbH |
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| OMRON SANTÉ FRANCE SAS |
| 14, rue de Lisbonne, 93561 |
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| Made in China |