OMRON HEM-7361T-EBK Automatic Upper Arm Blood Pressure Monitor Instruction Manual

OMRON HEM-7361T-EBK Automatic Upper Arm Blood Pressure Monitor

Introduction

Thank you for purchasing the OMRON Automatic Upper Arm Blood Pressure Monitor. This blood pressure monitor uses the oscillometric method of blood pressure measurement. This means this monitor detects your blood movement through your brachial artery and converts the movements into a digital reading.

Safety Instructions

This instruction manual provides you with important information about the OMRON Automatic Upper Arm Blood Pressure Monitor. To ensure the safe and proper use of this monitor, READ and UNDERSTAND all of the safety and operating instructions. If you do not understand these instructions or have any questions, contact your OMRON retail outlet or distributor before attempting to use this monitor. For specific information about your own blood pressure, consult with your physician.

 Intended Use

The device is a digital monitor intended for use in measuring blood pressure and pulse rate in adult patient population. The device detects the appearance of irregular heartbeats during measurement and gives a warning signal with readings. It is mainly designed for general household use.
The device can detect an irregular pulse suggestive of Atrial Fibrillation (Afib). Please note that the device is not intended to diagnose Afib. A diagnosis of Afib can only be confirmed by Electrocardiogram (ECG). If the Afib symbol appears, consult your physician.

Receiving and Inspection

Remove this monitor and other components from the packaging and inspect for damage. If this monitor or any other components is damaged, DO NOT USE and consult with your OMRON retail outlet or distributor.

Important Safety Information

Read the Important Safety Information in this instruction manual before using this monitor. Follow this instruction manual thoroughly for your safety. Keep for future reference. For specific information about your own blood pressure, CONSULT WITH YOUR PHYSICIAN

Warning| Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury.
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• DO NOT use this monitor on infants, toddlers, children or persons who cannot express themselves.
• DO NOT adjust medication based on readings from this blood pressure monitor. Take medication as prescribed by your physician. ONLY a physician is qualified to diagnose and treat high blood pressure and Afib.
• DO NOT use this monitor on an injured arm or an arm under medical treatment.
• DO NOT apply the arm cuff on your arm while on an intravenous drip or blood transfusion.
• DO NOT use this monitor in areas containing high frequency (HF) surgical equipment, magnetic resonance imaging (MRI) equipment, computerized tomography (CT) scanners. This may result in incorrect operation of the monitor and/or cause an inaccurate reading.
• DO NOT use this monitor in oxygen rich environments or near flammable gas.
• Consult with your physician before using this monitor if you have common arrhythmias such as atrial or ventricular premature beats or atrial fibrillation; arterial sclerosis; poor perfusion; diabetes; pregnancy; pre-eclampsia or renal disease. NOTE that any of these conditions in addition to patient motion, trembling, or shivering may affect the measurement reading.
• NEVER diagnose or treat yourself based on your readings. ALWAYS consult with your physician.
• To help avoid strangulation, keep the air tube and AC adapter cable away from infants, toddlers and children.
• This product contains small parts that may cause a choking hazard if swallowed by infants, toddlers and children.

 Data Transmission

• This product emits radio frequencies (RF) in the 2.4 GHz band. DO NOT use this product in locations where RF is restricted, such as on an aircraft or in hospitals. Turn off the Bluetooth® feature in this monitor, remove batteries and/or unplug the AC adapter when in RF restricted areas.

AC Adapter (optional accessory) Handling and Usage

• DO NOT use the AC adapter if this monitor or the AC adapter cable is damaged. If this monitor or the cable is damaged, turn off the power and unplug the AC adapter immediately.
• Plug the AC adapter into the appropriate voltage outlet. DO NOT use in a multi-outlet plug.
• NEVER plug in or unplug the AC adapter from the electric outlet with wet hands.
• DO NOT disassemble or attempt to repair the AC adapter.

Battery Handling and Usage

• Keep batteries out of the reach of infants, toddlers and children.

Caution| Indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate injury to the user or patient, or cause damage to the equipment or other property.
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•  Stop using this monitor and consult with your physician if you experience skin irritation or discomfort.

• Consult with your physician before using this monitor on an arm where intravascular access or therapy, or an arteriovenous (A-V) shunt, is present because of temporary interference to blood flow and could result in injury.

• Consult with your physician before using this monitor if you have had a mastectomy

• Consult with your physician before using this monitor if you have severe blood flow problems or blood disorders as cuff inflation can cause bruising.

• DO NOT take measurements more often than necessary because bruising, due to blood flow interference, may occur.

• ONLY inflate the arm cuff when it is applied on your upper arm.

• Remove the arm cuff if it does not start deflating during a measurement.

• DO NOT use this monitor for any purpose other than measuring blood pressure and/or detecting the possibility of Afib.

• During measurement, make sure that no mobile device or any other electrical device that emit electromagnetic fields is within 30 cm of this monitor. This may result in incorrect operation of the monitor and/or cause an inaccurate reading.

• DO NOT disassemble or attempt to repair this monitor or other components.
  This may cause an inaccurate reading.

• DO NOT use in a location where there is moisture or a risk of water splashing this monitor. This may damage this monitor.

• DO NOT use this monitor in a moving vehicle such as in a car or on an aircraft.

• DO NOT drop or subject this monitor to strong shocks or vibrations.

• DO NOT use this monitor in places with high or low humidity or high or low temperatures. Refer to section 6.

• During measurement, observe the arm to ensure that the monitor is not causing prolonged impairment to blood circulation.

• DO NOT use this monitor in high-use environments such as medical clinics or physician offices.

• DO NOT use this monitor with other medical electrical (ME) equipment simultaneously. This may result in incorrect operation and/or cause an inaccurate reading.

• Avoid bathing, drinking alcohol or caffeine, smoking, exercising and eating for at least 30 minutes before taking a measurement.

• Rest for at least 5 minutes before taking a measurement.

• Remove tight-fitting, thick clothing and any accessories from your arm while taking a measurement.

• Remain still and DO NOT talk while taking a measurement

• ONLY use the arm cuff on persons whose arm circumference is within the specified range of the cuff.

• Ensure that this monitor has acclimated to room temperature before taking a measurement. Taking a measurement after an extreme temperature change could lead to an inaccurate reading. OMRON recommends waiting for approximately 2 hours for the monitor to warm up or cool down when the monitor is used in an environment within the temperature specified as operating conditions after it is stored either at the maximum or at the minimum storage temperature. For additional information on operating and storage / transport temperature, refer to section 6.

• DO NOT use this monitor after the durable period has ended. Refer to section 6.

• DO NOT crease the arm cuff or the air tube excessively.

• DO NOT fold or kink the air tube while taking a measurement. This may cause an injury by interrupting blood flow

• To unplug the air plug, pull on the plastic air plug at the base of the tube, not the tube itself.

• ONLY use the AC adapter, arm cuff, batteries and accessories specified for this monitor. Use of unsupported AC adapters, arm cuffs and batteries may damage and/or may be hazardous to this monitor.

• ONLY use the approved arm cuff for this monitor. Use of other arm cuffs may result in incorrect readings.

• Inflating to a higher pressure than necessary may result in bruising of the arm where the cuff is applied. NOTE: refer to “If your systolic pressure is more than 210 mmHg” in section 13 of instruction manual for additional information.

• Read and follow the “Correct Disposal of This Product” in section 7 when disposing of the device and any used accessories or optional parts.

Data Transmission

• DO NOT replace batteries or unplug the AC adapter while your readings are being transferred to your smart device. This may result in incorrect operation of this monitor and failure to transfer your blood pressure data.

AC Adapter (optional accessory) Handling and Usage

• Fully insert the AC adapter into the outlet.

• When unplugging the AC adapter from the outlet, be sure to safely pull from the AC adapter. DO NOT pull from the AC adapter cable.

• When handling the AC adapter cable:
  Do not damage it. / Do not break it. / Do not tamper with it. / DO NOT pinch it. / Do not forcibly bend or pull it. / Do not twist it. / DO NOT use it if it is gathered in a bundle. / DO NOT place it under heavy objects.

• Wipe any dust off of the AC adapter.

• Unplug the AC adapter when not in use.

• Unplug the AC adapter before cleaning this monitor

Battery Handling and Usage

• DO NOT insert batteries with their polarities incorrectly aligned.
• ONLY use 4 “AA” alkaline or manganese batteries with this monitor. DO NOT use other types of batteries. DO NOT use new and used batteries together. DO NOT use different brands of batteries together.
• Remove batteries if this monitor will not be used for a long period of time.
• If battery fluid should get in your eyes, immediately rinse with plenty of clean water. Consult with your physician immediately.
• If battery fluid should get on your skin, wash your skin immediately with plenty of clean, lukewarm water. If irritation, injury or pain persists, consult with your physician.
• DO NOT use batteries after their expiration date.
• Periodically check batteries to ensure they are in good working condition.

General Precautions

• To stop a measurement, press the [START/STOP] button while taking a measurement.
• When you take a measurement on the right arm, the air tube should be at the side of your elbow. Be careful not to rest your arm on the air tube.
• Blood pressure may differ between the right and left arm, and may result in a different measurement value. Always use the same arm for measurements. If the values between both arms differ substantially, check with your physician on which arm to use for your measurements.
• When using an optional AC adapter, make sure not to place your monitor in a location where it is difficult to plug and unplug the AC adapter
  

Battery Handling and Usage

• Disposal of used batteries should be carried out in accordance with local regulations.
• The supplied batteries may have a shorter life span than new batteries.

Error Messages and Troubleshooting

If any of the below problems occur during measurement, check to make sure that no other electrical device is within 30 cm. If the problem persists, please refer to the table below.

turn the monitor off.
After inserting the air plug securely and applying the arm cuff correctly, [ress the [START/STOP] button.
Air plug is not completely plugged into the monitor.| Insert the air plug securely.
The arm cuff is not applied correctly.| Apply the arm cuff correctly, then take another measurement. Refer to section 7 of instruction manual .
Air is leaking from the arm cuff.| Replace the arm cuff to the new one. Refer to section 14 of instruction manual .
appears or a measurement cannot be completed after the arm cuff inflates.| You move or talk during a measurement and the arm cuff does not inflate sufficiently.| Remain still and do not talk during a measurement. lf”E2″ appears repeatedly, inflate the arm cuff manµally until the systolic pressure is 30 to 40 mmHg above your previous reading s. Refer to section 13 of instruction manualm.
Due to the systolic pressure is above

210 mmHg, a measurement cannot be taken.

appears| The arm cuff is inflated exceeding the maximum allowable pressure.| Do not touch the arm cuff and/or bend the air tube while taking a measurement. If inflating the arm cuff manually, refer to section 13 of instruction manual .
appears| You move or talk during a measurement. Vibrations disrupt a measurement.| Remain still and do not talk during a measurement.
appears| The pulse rate is not detected correctly.| Apply the arm cuff correctly, then take another measurement. Refer to section 7 of instruction manual . Remain still and sit correctly during a measurement.
If the” ” symbol continues to appear, we recommend you to consult with your physician.
appears
  does not flash during a measurement
**** appears| Blood pressure measurements were not taken correctly in an Afib mode measurement .| Apply the arm cuff correctly, then take another measurement. Refer to section 7 of instruction manual . Remain still and sit correctly during a measurement. Refer to section 8 of instruction manual .
appears| The monitor has malfunctioned.| Press the [START/STOP] button again. If “Er” still appears, contact your OMRON retail outlet or distributor.
appears| The monitor cannot connect to a smart device or transmit data correctly.| Follow the instructions shown in the “OMRON connect” app. If the “Err” symbol still appears after checking the app, contact your OMRON retail outlet or distributor.
flashes| The monitor is waiting for pairing with the smart device.| Refer to section 5 of instruction manual for pairing your monitor With your smart device, or press [START/STOP] button to cancel pairing and turn your monitor off.
flashes| The monitor is ready to transfer your readings to the smart device.| Open the “OMRON connect” app to transfer your readings.
 flashes| More than 80 readings are not transferred .| Pair or transfer your readings to the “OMRON connect” app so you can keep them in memory in the app, and this error symbol disappears.
The date and time is not set.
appears| 100 readings are not transferred.|
flashes| Batteries are low.| Replacing all 4 batteries with new ones is recommended. Refer to section 4 of instruction manual .
appears or the monitor is turned off unexpectedly during a measurement| Batteries are depleted.| Immediately replace all 4 batteries with new ones. Refer to section 4 of instruction manual .

Nothing appears on the display of the monitor.

| Battery polarities are not properly aligned.| Check the battery installation for proper placement. Ref er to section 4 of instruction manual .
Readings appear too high or too low.| Blood pressure varies constantly. Many factors including stress, time of day, and/or how you apply the arm cuff, may affect your blood pressure. Review section 2 of instruction manual .
Any other communication issue occurs.| Follow the instructions snow in the smart device, or visit the “Help” section in the “OMRON connect ” app for further help. If the problem still persists,contact your OMRON retail outlet or distributor.
Any other problem occurs.| Press the [START/S1OP] button to turn the monitor off, then press it again to take a measurement. If the problem continues, remove all batteries and wait for 30 seconds.Then re-in stall batteries. If the problem still persists, contact your OMRON retail outlet or distributor.
Troubleshooting for Afib indicator function:
What is different between the Afib indicator function and ECG?| The Afib indicator function and ECG use completely different technologies. An ECG measures the elect rical activity of the heart and can be used to diagnose Afib. The Afib indicator function detects irregular heartbeat and can suggest the possibility of Afib with a sensitivity of 95.5% and specificity of 93.8%. Refer to section 11 for details.
If the “ ” symbol does not appear, it means there is no possibility of Afib?| Even if the” ” symbol does not appear, there is still a possibility of Afib.
Should I consult with my physician if the “ ” symbol appears?| We recommend you to consult with your physician because there is a possibility of Afib. However, the “ ” symbol may be displayed for other reasons, such as other heart arrhythmias.
What is different between Afib indicator function and irregular heart beat function?| The irregular heartbeat function detects irregularities in the pulse waves in one measurement. The Afib indicator function suggests the possibility of Afib when blood pressure is measured 3 consecutive times.
What should I do if the” ” symbol sometimes appears?| Afib does not always have symptom s. We recommend you to consult with and follow the directions of your physician.
I have been diagnosed with Afib by the physician, but the “ “ symbol does not appear.| Afib may not occur at the time of specific blood pressure measurements. We recommend you to consult with your physician regularly.
Is the blood pressure reading reliable when the” ” symbol appears?| Afib or an irregular heartbeat can influence your blood pressure measurements and make it difficult to get an accurate reading. Repeated measurements may be required to overcome variabilities.*In Afib mode, the blood pressure measurement is taken 3 times, and the average is displayed. The monitor will indicate an error message (ES/E6) if the influence of the irregular heartbeat is too severe to give a measurement result. If this occurs repeatedly, we recommend that you consult with your physician .

Limited Warranty

Thank you for buying an OMRON product. This product is constructed of highquality 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 warranted by OMRON for a period of 3 years after the date of purchase. The proper construction, workmanship and materials of this product is warranted by OMRON. During this period of warranty OMRON will, without charge for labour or parts, repair or replace the defect product or any defective parts.

The warranty does not cover any of the following:
A. Transport costs and risks of transport.
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 warranted 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 warranty.
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.

Should warranty 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:

www.omron-healthcare.com

Repair or replacement under the warranty does not give rise to any extension or renewal of the warranty period.

The warranty will be granted only if the complete product is returned together with the original invoice / cash ticket issued to the consumer by the retailer.

Maintenance

Maintenance

To protect your monitor from damage, follow the directions below:
Changes or modifications not approved by the manufacturer will void the user warranty.

Caution

DO NOT disassemble or attempt to repair this monitor or other components. This may cause an inaccurate reading

Storage

• Keep your monitor in the storage case when not in use.
  1. Remove the arm cuff from the monitor.
  2. Gently fold the air tube into the arm cuff. Note: Do not bend or crease the air tube excessively.
  3. Place your monitor and other components in the storage cas

• Store your monitor and other components in a clean, safe location.

• Do not store your monitor and other components:

• If your monitor and other components are wet.

• In locations exposed to extreme temperatures, humidity, direct sunlight, dust or corrosive vapors such as bleach

• In locations exposed to vibrations or shocks.

• To protect your monitor during storage, an optional LCD cover is available as accessory. Refer to section 15 of Instruction Manual .

Cleaning

• Do not use any abrasive or volatile cleaners.
• Use a soft dry cloth or a soft cloth moistened with mild (neutral) detergent to clean your monitor and arm cuff, and then wipe them with a dry cloth.
• Do not wash or immerse your monitor and arm cuff or other components in water.
• Do not use gasoline, thinners or similar solvents to clean your monitor and arm cuff or other components.

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.

Specifications

DIA: 40 to 215 mmHg
Pulse measurement range| 40 to 180 beats / min.
Accuracy| Pressure: ±3 mmHg
Pulse: ±5% of display reading
Inflation| Automatic by electric pump
Deflation| Automatic pressure release valve
Measurement method| Oscillometric method
Transmission method| Bluetooth ® Low Energy
Wireless communication| Frequency range: 2.4 GHz (2400 – 2483.5 MHz) / Modulation: GFSK Effective radiated power: < 20 dBm
Operation mode| Continuous operation
IP classification| Monitor: IP20
Optional AC adapter: IP21 (HHP-CM01) or IP22 (HHP-BFH01)
Rating| DC6 V 4.0 W
Power source| 4 “AA” batteries 1.5 V or optional AC adapter (INPUT AC 100 – 240 V 50/60 Hz 0.12 – 0.065 A)
Battery life| Approximately 1000 measurements (using new alkaline batteries) The number of times may decrease when using Afib mode because one Afib indication consists of 3 regular measurements.
Durable period (Service life)| Monitor: 5 years / Cuff: 5 years / Optional AC adapter: 5 years
Operating conditions| +10 to +40°C / 15 to 90% RH (non-condensing) / 800 to 1060 hPa
Storage / Transport conditions| -20 to +60°C / 10 to 90% RH (non-condensing)
Weight| Monitor: approximately 460 g (not including batteries) Arm cuff: approximately 163 g
Dimensions (approximately value)| Monitor: 191 mm (W) × 85 mm (H) × 120 mm (L) / Arm cuff:145 mm × 532 mm (air tube: 750 mm)
Cuff circumference applicable to the monitor| 220 to 420 mm
Memory| Stores up to 100 readings per user
Contents| Monitor, arm cuff (HEM-FL31), 4 “AA” batteries, Instruction Manual and , setup instructions, storage case
Protection against electric shock| Internally powered ME equipment (When using only batteries) Class II ME equipment (Optional AC adapter)
Applied part| Type BF (arm cuff)

Note

• These specifications are subject to change without notice.
• This monitor is clinically investigated according to the requirements of ISO 81060-2:2013. In the clinical validation study, K5 was used on 85 subjects for determination of diastolic blood pressure.
• This device has been validated for use on pregnant and pre-eclampsia patients according to the Modified European Society of Hypertension Protocol*.
• This device has been validated for use on diabetic (Type II) population**.
• IP classification is degrees of protection provided by enclosures in accordance with IEC 60529. This monitor and optional AC adapter are protected against solid foreign objects of 12.5 mm diameter and greater such as a finger. The optional AC adapter HHP-CM01 is protected against vertically falling water drops which may cause issues during a normal operation. The optional AC adapter HHP-BFH01 is protected against oblique falling water drops which may cause issues during a normal operation.
• Topouchian J et al. Vascular Health and Risk Management 2018:14 189–197
  ** Chahine M.N. et al. Medical Devices: Evidence and Research 2018:11 11–20

About a wireless communication interference
This product operates in an unlicensed ISM band at 2.4 GHz. In the event this product is used near other wireless devices such as microwave and wireless LAN, which operate on the same frequency band as this product, there is a possibility that interference may occur. If interference occurs, stop the operation of the other devices or relocate this product away from other wireless devices before attempting to use it

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 waste for disposal.

Important Information regarding Electromagnetic Compatibility (EMC)

HEM-7361T-EBK/ESL conforms to the EN60601-1-2:2015 Electromagnetic Compatibility (EMC) standard.
Further documentation in accordance with this EMC standard is available at OMRON HEALTHCARE EUROPE at the address mentioned in this instruction manual or at: www.omron-healthcare.com.

Guidance and Manufacturer’s Declaration

• 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.
• Hereby, OMRON HEALTHCARE Co., Ltd., declares that the radio equipments type HEM-7361T-EBK/ESL is in compliance with Directive 2014/53/EU.
• The full text of the EU declaration of conformity is available at the following internet address: www.omron-healthcare.com
• 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.
• Please report to the manufacturer and the competent authority of the Member State in which you are established about any serious incident that has occurred in relation to this device

How to Calculate Weekly Averages

Morning Weekly Average Calculation

This is the average for the measurements taken during the morning (4:00 – 9:59) between Sunday and Saturday. The 2 or 3 readings taken within the first 10 minute timeframe in the morning between 4:00 – 9:59 will be used to calculate the morning average for each day.

Evening Weekly Average Calculation

This is the average for the measurements taken during the evening (19:00 – 1:59) between Sunday and Saturday. The 2 or 3 readings taken within the last 10 minute timeframe in the evening between 19:00 – 1:59 will be used to calculate the evening average for each day

Useful Information

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

What is Afib?

Atrial fibrillation (also called Afib or AF) is a quivering or irregular heartbeat
(arrhythmia) that can lead to blood clots, stroke, heart failure and other heart related complications. During atrial fibrillation, the heart’s two upper chambers (the atria) beat chaotically and irregularly — out of coordination with the two lower chambers (the ventricles) of the heart. Episodes of atrial fibrillation can come and go, or you may develop atrial fibrillation that doesn’t go away and may require  treatment.
A fib indicator function detects the possibility of A fib with an accuracy of 94.2% (with sensitivity of 95.5% and specificity of 93.8%) as demonstrated in the study* with Single-lead ECG as reference measurement.

*M. Ishizawa, T. Noma, T. Minamoto et al., Multiple measurements with automated blood pressure monitor can detect atrial fibrillation with high sensitivity and specificity in general cardiac patients, ESC Congress 2018

References

• Medical Devices and Healthcare Solutions - OMRON Healthcare EMEA
• Medical Devices and Healthcare Solutions - OMRON Healthcare EMEA

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