OMRON M6 Comfort Automatic Blood Pressure Monitor
Instruction Manual
Important Safety Information
Warning: Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury.
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 device or other property.
General Use:
- Consult your doctor before using the device if you are pregnant, have been diagnosed with pre-eclampsia, or have an arrhythmia or arteriosclerosis.
- Do not use the device on an injured arm or an arm under medical treatment.
- Do not use the cuff on an arm where an IV drip or blood transfusion is in progress.
- Consult your doctor before using the device on an arm with an arteriovenous (A-V) shunt.
- Do not use the device simultaneously with other ME equipment.
- Do not use the device near electrosurgical equipment, MRI, CT scanners, or in an oxygen-rich environment.
- Do not leave the device unattended. The air tube or AC adapter cord poses a strangulation risk to newborns or infants.
- Do not leave the inflation jack, battery cover, or batteries unattended. Accidental ingestion by young children can cause suffocation.
Use of AC Adapter (Optional):
- Do not use the AC adapter if the device or power cord is damaged. Turn off the device and unplug the power cord immediately.
- Connect the AC adapter to the appropriate power outlet. Do not use a multi-plug adapter.
- Never plug in or unplug the power cord with wet hands.
General Precautions:
- Always consult a doctor. Self-diagnosis and treatment based on measurement results can be dangerous.
- Individuals with severe arterial circulation problems or arterial disorders should consult a doctor before using the device, as cuff inflation may cause minor internal bleeding leading to bruising.
- If any abnormalities occur during measurement, remove the cuff.
- Do not use the device on newborns, infants, or persons unable to express themselves.
- Do not inflate the cuff more than necessary.
- Do not use the device for purposes other than measuring blood pressure.
- Use only the cuff approved for this device. Using other cuffs may lead to inaccurate results.
- Do not use a mobile phone or other devices emitting electromagnetic waves near the device, as this may interfere with its operation.
- Do not disassemble the device or the cuff.
- Do not use the blood pressure monitor in a humid environment or where it may be splashed with water, as this may damage it.
- Do not use the device in a moving vehicle (car, airplane).
- Do not take more measurements than necessary, as this may cause internal bleeding due to interference with blood flow.
- Patients who have undergone a mastectomy should consult their doctor.
Battery Usage:
- Do not insert batteries with reversed polarity.
- Use only 4 "AA" alkaline or manganese batteries with this device. Do not use other types of batteries. Do not mix new and used batteries.
- Remove batteries if the device will not be used for three months or more.
General Precautions (continued):
- Do not force the cuff or excessively bend the air tube.
- Do not crush the air tube.
- To disconnect the inflation plug, pull it at the connection to the main unit, not the tube itself.
- Do not subject the device to strong shocks or vibrations, and do not drop the device or cuff.
- Do not inflate the cuff until it is wrapped around your arm.
- Do not use the device in an environment other than the one specified, as this may compromise measurement accuracy.
- Follow the EMC (Electromagnetic Compatibility) information in the "6. Specifications" section.
- Follow the disposal guidelines in the "How to Dispose of This Product Correctly" section of "6. Specifications" when discarding the device and accessories.
1. Device Description
Open the rear cover page to read the following:
The letter on the rear cover page corresponds to the letter in the body text.
Blood Pressure Monitor
A Display: Shows all readings and symbols.
B Cuff Wrapping Guide Indicator: Indicates if the cuff is wrapped correctly.
C Memory Button: Accesses stored measurements.
D Weekly Average Button: Displays weekly average readings.
E START/STOP Button: Starts and stops measurement.
F Up/Down Buttons: Navigate through settings or memory.
G USER ID Select Button: Selects user profile (1 or 2).
H Date and Time Setting Button: Sets the device's date and time.
I Blood Pressure Level Indicator: Color-coded indicator for blood pressure range.
J Air Jack: Port for connecting the cuff's air tube.
K Battery Compartment: Holds the batteries.
L AC Adapter Jack (Optional): Port for the AC adapter.
Display Symbols
P Memory Symbol: Indicates memory access.
Q USER ID Symbol: Shows the selected user.
R Average Value Symbol: Indicates average readings.
S Systolic Blood Pressure: Top number of the reading.
T Diastolic Blood Pressure: Bottom number of the reading.
U Pulse Symbol: Flashes during measurement, shows pulse rate.
V Date and Time Display: Shows current date and time.
W Morning Average Symbol: Indicates average morning reading.
X Evening Average Symbol: Indicates average evening reading.
Y Morning Hypertension Symbol: Appears if morning average exceeds 135/85 mmHg.
Z Motion Error Symbol: Appears if movement is detected during measurement.
AA Irregular Heartbeat Symbol: Appears if an irregular heartbeat is detected.
AB Blood Pressure Level Indicator: Similar to 'I', shows pressure range.
AC Cuff Wrapping Guide: Visual guide for cuff placement.
AD Low Battery Symbol: Indicates low battery power.
AE Deflation Symbol: Shows cuff is deflating.
AF Pulse / Memory Number Display: Shows pulse rate or memory entry number.
Display Symbols Explained
Irregular Heartbeat Symbol ( ): Detected when the heart rhythm is irregular at least twice during a measurement. This may indicate a pulse rate that is 25% higher or lower than the detected average. Consult your doctor if this symbol appears.
Motion Error Symbol ( ): Appears if you move during measurement. Remove the cuff and wait 2-3 minutes before re-measuring while remaining still.
Average Value Symbol ( ): Appears when the Memory button is held for over 3 seconds, displaying the most recent average value.
Cuff Wrapping Guide Indicator ( / ): The indicator turns orange if the cuff is too loose, and green if it is wrapped correctly. This helps ensure accurate readings.
Blood Pressure Level Indicator
If systolic or diastolic pressure is above the standard range (135 mmHg systolic / 85 mmHg diastolic), the indicator lights up orange. If values are within the standard range, it lights up green.
JNC7 Recommendations:
| General Guidelines for Blood Pressure | Prehypertension (Office) | Hypertension (Home) | |
| Systolic Blood Pressure | 120-139 mmHg | 135 mmHg | |
| Diastolic Blood Pressure | 80-89 mmHg | 85 mmHg |
* JNC7: Seventh report of the National High Blood Pressure Education Program Working Group on Management of High Blood Pressure in Adults (USA, December 2003).
2. Preparation
2.1 Battery Installation
- Remove the battery cover.
- Insert 4 "AA" batteries as indicated in the battery compartment.
- Replace the battery cover.
Notes:
- If the low battery symbol ( ) appears, stop the device and replace all batteries simultaneously. Long-lasting alkaline batteries are recommended.
- Measurement values are always stored in memory, even after replacing batteries.
- The supplied batteries may have a shorter lifespan.
Disposal of used batteries must comply with national regulations.
2.2 Setting the Date and Time
Set the correct date and time before taking the first measurement.
- Press the Date and Time Setting Button ( ). The year will flash on the date and time display.
- Press the or buttons to change the year. Press the button to confirm the year. The month will flash. Repeat the same steps to change the month, day, hour, and minutes.
Date/Time Setting Interface:
- Year: [Display shows '2014']
- Month: [Display shows month]
- Day: [Display shows day]
- Hour: [Display shows hour]
- Minute: [Display shows minute]
- Buttons: Change, Confirm
- Navigation: Advance ( ), Recede ( )
- Press the START/STOP button to turn off the device.
Notes:
- If batteries are replaced, the date and time settings must be reset.
- If the date and time are not set, "-/--:--" will appear during or after measurement.
3. Using the Device
3.1 Applying the Cuff
Remove tight clothing from your arm and roll up sleeves. Do not place the cuff over thick clothing.
- Firmly insert the inflation plug (N) into the air jack (J).
- Place and tighten the cuff on your left arm. The lower edge of the cuff should be positioned 1 to 2 cm (approx. 0.4 to 0.8 inches) above the elbow. The cuff should be positioned on the upper arm with the air tube pointing towards your hand.
- Firmly close the fabric band.
Notes:
- When measuring on the right arm, the air tube is located next to your elbow. Ensure your arm does not rest on the air tube (b).
- Blood pressure may differ between the right and left arms. OMRON recommends using the same arm for measurement. If readings differ significantly between arms, consult your doctor to determine which arm to use.
3.2 How to Sit Correctly
It is important to be relaxed and comfortably seated in a pleasant ambient temperature for measurement. Do not eat, drink alcohol or caffeine, smoke, or exercise for 30 minutes before measurement.
- Sit on a chair with your feet flat on the floor.
- Sit upright with your back straight (c).
- Ensure your back and arm are well supported.
- The cuff should be at heart level (d).
3.3 Taking a Measurement
Notes:
- To cancel a measurement, press the START/STOP button to deflate the cuff.
- Remain still during measurement.
The monitor is designed to take measurements and store them for two users (USER ID 1 and 2).
- Select your USER ID (1 or 2).
- Press the START/STOP button. The cuff inflates automatically.
Measurement Stages: START -> INFLATING -> DEFLATING -> FINISHED
If your systolic pressure is above 210 mmHg: While the cuff inflates, press and hold the START/STOP button until the monitor reaches a pressure 30 to 40 mmHg higher than your expected systolic pressure.
Notes:
- The monitor does not inflate above 299 mmHg.
- Do not inflate more than necessary.
- Remove the cuff.
- Press the START/STOP button to turn off the monitor. The monitor automatically stores the measurement in memory and turns off after 2 minutes.
Note: Wait 2-3 minutes before taking another measurement. This waiting period allows your arteries to return to their normal function.
Guest Mode Usage
The monitor stores measurement values for 2 users. Guest Mode allows a single measurement for another person. No measurement is stored when Guest Mode is selected.
- Press and hold the START/STOP button for more than 3 seconds. The USER ID symbol and date/time display will disappear.
- When the date and time display disappears, release the START/STOP button. The cuff will inflate automatically.
Always consult a doctor. Self-diagnosis and treatment based on measurement results can be dangerous.
3.4 Using the Memory Function
The monitor automatically stores up to 100 measurement sets for each user (1 and 2). It also calculates an average from the last 3 measurements taken within 10 minutes.
Notes:
- If only 2 measurements are stored for this period, the average will be calculated from these 2 measurements.
- If only 1 measurement is stored for this period, it will be displayed as the average value.
- If the memory is full, the monitor deletes the oldest measurements.
- When viewing measurements taken without setting the date and time, "-/--:--" will be displayed instead of the date and time.
To display stored measurements:
- Select your USER ID (1 or 2).
- Press the button. The memory number appears for one second before the pulse rate is displayed. The most recent reading is numbered "1".
Note: The cuff wrapping guide result is displayed on the screen with the measurement values. The cuff wrapping indicator light does not illuminate.
- Press the or buttons to display stored measurements.
- : To display older measurements
- : To display recent measurements
To display the average value:
- Select your USER ID (1 or 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 cannot be calculated.
- If no measurement results are stored in memory, the screen on the right will be displayed.
To display the weekly average value:
The device calculates and displays weekly averages of morning and evening measurements over 8 weeks for each user. Note: The week starts on Sunday at 2:00 AM.
- Select your USER ID (1 or 2).
- Press the button. The morning average for the current week ("THIS WEEK") appears on the screen.
Note: The morning hypertension symbol ( ) appears if the weekly average of morning measurements exceeds 135/85 mmHg.
Press the button again to display the evening average for the current week ("THIS WEEK").
Press the or buttons to display data from previous weeks.
- Current Week Morning Average
- Previous Week Morning Average
- 2 Weeks Ago Morning Average
- 7 Weeks Ago Morning Average
- Current Week Evening Average
- Previous Week Evening Average
- 2 Weeks Ago Evening Average
- 7 Weeks Ago Evening Average
Morning Weekly Average: This is the average of measurements taken in the morning (4:00 AM - 11:59 AM) from Sunday to Saturday. A daily average is calculated from a maximum of three measurements taken within 10 minutes following the first morning measurement.
Evening Weekly Average: This is the average of measurements taken in the evening (7:00 PM - 1:59 AM) from Sunday to Saturday. A daily average is calculated from a maximum of three measurements taken within 10 minutes following the last evening measurement.
To delete all stored memory values:
Stored memory values are deleted by USER ID.
- Select your USER ID (1 or 2).
- Press the Memory button when the memory symbol ( ) is displayed.
- While holding the Memory button down, press the START/STOP button for more than 3 seconds.
Note: It is impossible to delete only a portion of the stored values. All values for the selected user will be deleted.
4. Error Messages and Troubleshooting
4.1 Error Messages
| Display | Cause | Solution |
| Irregular heartbeat detected. | Remove the cuff. Wait 2-3 minutes, then take another measurement. Repeat steps in Section 3.3. If the error persists, contact your doctor. | |
| Movement during measurement. | Read carefully and repeat steps in Section 3.3. | |
| Cuff is not sufficiently tight. | Apply and tighten the cuff. Refer to Section 3.1. | |
| Batteries are low. | Replace with new batteries sooner than expected. Refer to Section 2.1. | |
| Batteries are depleted. | Replace immediately with new batteries. Refer to Section 2.1. |
Error Codes
| Display | Cause | Solution |
| E1 | Inflation plug is disconnected. | Firmly connect the inflation plug. Refer to Section 3.1. |
| E1 | Cuff is not sufficiently tight. | Apply and tighten the cuff. Refer to Section 3.1. |
| E1 | Cuff is leaking air. | Replace the cuff with a new one. Refer to Section 5.3. |
| E2 | Movement during measurement and insufficient cuff inflation. | Repeat the measurement. Remain still and do not speak during measurement. Refer to Section 3.3. If "E2" appears repeatedly, inflate the cuff manually until it is 30 to 40 mmHg above your previous measurement result. Refer to Section 3.3. |
| E3 | Cuff was inflated above 299 mmHg during manual inflation. | Do not inflate the cuff above 299 mmHg. Refer to Section 3.3. |
| E4 | Movement during measurement. | Repeat the measurement. Remain still and do not speak during measurement. Refer to Section 3.3. |
| E5 | Clothing is obstructing the cuff. | Remove any clothing that obstructs the cuff. Refer to Section 3.1. |
| Er | Device error. | Contact your retailer or OMRON dealer. |
4.2 Troubleshooting
| Problem | Cause | Solution |
| Measurement is extremely high (or low). | Cuff is not sufficiently tight. | Apply and tighten the cuff. Refer to Section 3.1. |
| Measurement is extremely high (or low). | Patient moved or spoke during measurement. | Remain still and do not speak during measurement. Refer to Section 3.3. |
| Measurement is extremely high (or low). | Clothing is obstructing the cuff. | Remove any clothing that obstructs the cuff. Refer to Section 3.1. |
| Cuff pressure does not increase. | Connector is not firmly connected to the air jack. | Verify that the air tube is correctly connected. Refer to Section 3.1. |
| Cuff pressure does not increase. | Cuff is leaking air. | Replace the cuff with a new one. Refer to Section 5.3. |
| Cuff deflates too soon. | Cuff is loose. | Apply the cuff correctly so it is firmly wrapped around the arm. Refer to Section 3.1. |
| Measurement impossible or values too low or too high. | Cuff did not inflate sufficiently. | Inflate the cuff to be 30 to 40 mmHg above your previous measurement result. Refer to Section 3.3. |
| Nothing happens when buttons are pressed. | Batteries are depleted. | Replace used batteries with new ones. Refer to Section 2.1. |
| Nothing happens when buttons are pressed. | Batteries were inserted incorrectly into the casing. | Insert batteries respecting polarity (+/-). Refer to Section 2.1. |
| Other problems. | • Press the START/STOP button and repeat the measurement. • Replace used batteries with new ones. If the problem persists, contact your retailer or OMRON dealer. |
5. Maintenance and Storage
5.1 Maintenance
To protect your device from potential damage, proceed as follows:
- Store the device and its components in a clean and safe place.
- Do not use abrasive or volatile cleaning agents.
- Do not wash the device or any of its components, nor immerse them in water.
- Do not use gasoline, thinner, or other solvents to clean the device.
- The blood pressure monitor and cuff should be cleaned with a soft, dry cloth, or a soft, damp cloth with mild soap.
- Any modification not authorized by the manufacturer will void the user's warranty. Do not disassemble or attempt to repair the device or its components. Consult a retailer or OMRON dealer.
Calibration and Maintenance
- Rigorous tests have been conducted to ensure the accuracy of this blood pressure monitor and to ensure a long service life.
- It is generally recommended to have the device inspected every 2 years to ensure proper function and accuracy. Consult a retailer or OMRON dealer.
5.2 Storage
Store the device in its storage case when not in use.
- Disconnect the inflation plug from the air jack.
- Gently fold the air tube into the cuff. Note: Do not excessively bend the air tube.
- Place the blood pressure monitor and cuff in the storage case.
Do not store the device under the following conditions:
- If the device is wet.
- In locations subject to extreme temperatures, humidity, direct sunlight, dust, or corrosive vapors.
- In locations subject to vibrations, shocks, or that require the device to be tilted.
5.3 Optional Medical Accessories
(According to CE Directive on Medical Devices 93/42/EEC)
Cuff
Arm circumference from 22 to 42 cm (approx. 8.7 to 16.5 inches)
Intelli™ Cuff Model: HEM-FL31
AC Adapter
Adapter S-9515336-9
Adapter UK 9983666-5
Using the Optional AC Adapter
- Insert the AC adapter plug into the AC adapter jack located on the rear of the device.
- Plug the AC adapter into an electrical outlet.
To disconnect the AC adapter, first disconnect it from the electrical outlet, then remove the AC adapter plug from the main unit.
6. Specifications
| Description | Specifications |
| Product Description | Automatic Blood Pressure Monitor |
| Model | OMRON M6 Comfort (HEM-7321-E) |
| Display | Digital LCD |
| Measurement Method | Oscillometric Method |
| Measurement Range | Pressure: 0 to 299 mmHg Pulse: 40 to 180 beats/min. |
| Accuracy | Pressure: ± 3 mmHg Pulse: ± 5% of displayed reading |
| Inflation | Fuzzy Logic controlled by electric pump |
| Deflation | Automatic pressure release valve |
| Memory | 100 measurements with date and time for each user (1 and 2) |
| Rated Value | 6 V DC 4 W |
| Power Source | 4 x 1.5 V "AA" batteries or optional AC adapter (Adapter S-9515336-9, AC INPUT 100-240 V 50/60 Hz 0.12 A) (UK Adapter 9983666-5, AC INPUT 100-240 V 50/60 Hz 15 VA) |
| Battery Life | Approx. 1000 measurements (with new alkaline batteries) |
| Applied Part | = Type BF |
| Protection Against Electric Shock | Internally powered ME equipment (when using batteries only) = Class II ME equipment (with optional AC adapter) |
| Operating Temperature/Humidity | +10 °C to +40 °C / 30% to 85% RH |
| Storage Temperature/Humidity/Atmospheric Pressure | -20 °C to +60 °C / 10% to 95% RH / 700-1060 hPa |
| IP Classification | IP 20 |
| Weight | Monitor: Approx. 380 g (without batteries) Cuff: Approx. 163 g |
| External Dimensions | Main Unit: Approx. 124 (W) mm × 90 (H) mm × 161 (L) mm Cuff: Approx. 145 mm × 532 mm (Air tube: 750 mm) |
| Cuff Circumference | 22 to 42 cm (approx. 8.7 to 16.5 inches) |
| Cuff/Tube Material | Nylon, Polyester, Polyvinyl Chloride |
| Package Contents | Blood pressure monitor, cuff, instruction manual, storage case, battery set, blood pressure log card |
Notes:
- Specifications are subject to change without notice.
- During clinical validation studies, the 5th phase was used on 85 subjects to determine diastolic blood pressure.
- This device has not been validated for use by pregnant women.
- This device complies with the provisions of the EC Directive 93/42/EEC concerning medical devices.
- This device is designed in accordance with European standard EN 1060, Non-invasive sphygmomanometers Part 1: General requirements and Part 3: Supplementary requirements concerning electromechanical measuring systems.
- This OMRON device is manufactured under the strict quality system of OMRON HEALTHCARE Co. Ltd., Japan. The key component, the pressure sensor, is manufactured in Japan.
Important Information Regarding Electromagnetic Compatibility (EMC)
With the increasing number of electronic devices such as PCs and mobile phones, medical devices may be subject to electromagnetic interference from other devices. Electromagnetic interference can disrupt the operation of the medical device and create a potentially hazardous situation. Medical devices should not interfere with other devices.
To regulate EMC requirements and prevent hazardous situations, standard EN60601-1-2:2007 has been implemented. This standard defines immunity levels to electromagnetic interference and maximum emission levels for medical devices.
This OMRON HEALTHCARE medical device complies with EN60601-1-2:2007 for both immunity and emissions.
Special precautions should be observed:
- Do not use mobile phones or other devices generating strong electric or electromagnetic fields near the device. This could disrupt the device's operation and create a potentially hazardous situation. A minimum distance of 7 m (approx. 23 ft) is recommended. Verify the device's proper operation if the distance is less.
Additional documentation conforming to EN60601-1-2:2007 is available from OMRON HEALTHCARE EUROPE at the address provided in this manual. Documentation is also available on the website www.omron-healthcare.com.
How to Dispose of This Product Correctly (Waste Electrical and Electronic Equipment)
This marking on the product or its documentation indicates that it should not be disposed of with other household waste at the end of its useful life. To prevent possible harm to the environment or human health from uncontrolled waste disposal, please separate it from other types of waste and recycle it responsibly. This will promote the sustainable reuse of material resources.
Private users should contact the retailer where they purchased the product or their local government office for information on 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 waste.
7. Warranty
Thank you for purchasing an OMRON product. This product is manufactured with high-quality materials and great care. It is designed to provide complete satisfaction when used and maintained correctly according to the instruction manual.
This product is guaranteed by OMRON for a period of 3 years from the date of purchase. The quality of manufacturing, workmanship, and materials is guaranteed by OMRON. During this warranty period, OMRON will repair or replace any defective product or part free of charge for labor or parts.
The warranty does not cover the following:
- a. Costs and risks associated with transportation.
- b. Costs of repairs and/or defects resulting from repairs performed by unauthorized persons.
- c. Periodic checks and maintenance.
- d. Failure or wear of optional parts or accessories other than the main unit itself, unless expressly warranted.
- e. Costs resulting from the non-acceptance of a claim (these costs will be charged).
- f. Any damages, including personal injury from accidents or improper use.
- g. Calibration service is not included in the warranty.
- h. Optional parts have a warranty of one (1) year from the date of purchase. Optional parts include, but are not limited to: cuff and cuff tube, AC adapter.
If warranty service is required, contact the retailer where the product was purchased or an authorized OMRON dealer. For addresses, refer to the packaging/product documentation or your specialized retailer.
If you have difficulty finding OMRON customer service, please contact us for information.
www.omron-healthcare.com
Repair or replacement under warranty does not extend or renew the warranty period. The warranty applies only if the complete product is returned, accompanied by the original invoice/receipt issued in the consumer's name by the retailer.
8. Useful Information on Blood Pressure
What is Blood Pressure?
Blood pressure is a measure of the pressure exerted by blood on the walls of the arteries. Blood pressure constantly changes throughout the cardiac cycle. The highest pressure during the cycle is called systolic blood pressure; the lowest is diastolic blood pressure. Both pressure measurements (systolic and diastolic) allow a doctor to evaluate a patient's blood pressure.
What is Arrhythmia?
Arrhythmia is a condition in which the heart rhythm is abnormal due to failures in the bio-electrical system that controls heartbeats. Classic symptoms include skipped heartbeats, premature contractions, abnormally fast pulse (tachycardia), or abnormally slow pulse (bradycardia).
Why is it Desirable 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 measurement may not be sufficient for an accurate diagnosis. Therefore, it is preferable to measure your blood pressure at the same time each day to get a precise indication of any changes in your blood pressure. Blood pressure is generally lower in the morning and increases in the afternoon and evening. It is lower in summer than in winter.
Graph: Fluctuation in blood pressure over a day (man, 35 years old)
Upper curve: Systolic blood pressure
Lower curve: Diastolic blood pressure
Device and Components Overview
Measurement Setup: The diagram shows a person sitting correctly at a table, with the blood pressure monitor and cuff ready for use. The person is seated upright with feet flat on the floor, back supported, and arm resting at heart level (indicated by 'c' and 'd'). The monitor (1) is placed on the table, connected to the cuff (M) via the air tube (O) and inflation plug (N) inserted into the air jack (J).
Cuff Application: The diagram illustrates the correct way to apply the cuff to the arm. The cuff is wrapped around the upper arm, positioned 1-2 cm above the elbow, with the air tube directed towards the hand (indicated by 'b'). The diagram also shows a 'no' symbol (cross) over a person speaking, emphasizing the need to remain silent during measurement.
Components Check
The illustration shows the main components of the OMRON M6 Comfort blood pressure monitor kit:
- The blood pressure monitor unit.
- The cuff with its air tube.
- Four AA batteries.
- A storage case.
- The instruction manual.
The image also depicts a person reading the instruction manual, suggesting a review of components before use.
Manufacturer and Distributor Information
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 HEALTHCARE MANUFACTURING VIETNAM CO., LTD., No.28 VSIP II, Street 2, Vietnam-Singapore Industrial Park II, Binh Duong Industry-Services-Urban Complex, Hoa Phu Ward, Thu Dau Mot City, Binh Duong Province, Vietnam
Subsidiaries:
- OMRON HEALTHCARE UK LTD., Opal Drive, Fox Milne, Milton Keynes, MK15 0DG, UK
- OMRON MEDIZINTECHNIK HANDELSGESELLSCHAFT mbH, Gottlieb-Daimler-Strasse 10, 68165 Mannheim, GERMANY
- OMRON SANTÉ FRANCE SAS, 14, rue de Lisbonne, 93561 Rosny-sous-Bois Cedex, FRANCE
Made in Vietnam
