Omron M6 Comfort IT
Contents
1. 1 1 Know Your Device ee 4 2 Preparation eene 7 2 1 Battery Installation 7 2 2 Setting the Date and Time 8 3 Using the Device 9 3 1 Applying the Arm Cuf 9 3 2 How to Sit Correctly 10 3 3 Taking a Measurement 11 3 4 Using the Memory Function 13 9 N 9 Error Messages and Troubleshooting 19 4 1 Error Messages n 19 4 2 Troubleshooting 21 Maintenance and Storage 23 5 1 Maintenatice o eet 23 5 2 5900 096 wayan m l eya e EE ER 24 5 3 Optional Medical Accessories 25 5 4 Other Optional Replacement Parts 25 Specifications 27 Warranty cina nnn 30 Some Useful Information about Blood Pressure esse ee Re RR EER ER RR RE EE ER nnns 31 Please read this instruction manual thoroughly before using the device Be Please keep for future reference For specific information about your own blood pressure CONSULT YOUR PHYSICIAN Important Safety Information Warning Indicates a potentially hazardous situation which if not avoided could result in death or serious injury General Usage AA Consult your physician before using the2. Nederlands Automatic Blood Pressure Monitor Model M6 Comfort IT Instruction Manual sense 4a jali All for Healthcare IM HEM 7322U E 01 08 2013 2298871 3A __ p Al MJ L LI F Check following components V rifier les composants suivants Controleer de volgende onderdelen Pr fen Sie folgende Teile des Lieferumfangs MpoBepbte cnenyroujue KOMNOHEHTBI Controllare i componenti indicati di seguito A a daki bile enleri kontrol edin iCompruebe los siguientes componentes jii ci stal a giai Thank you for purchasing the OMRON M6 Comfort IT Automatic Blood Pressure Monitor The OMRON M6 Comfort IT is a compact fully automatic blood pressure monitor operating on the oscillometric principle It measures your blood pressure and pulse rate simply and quickly For comfortable controlled inflation without the need of pressure pre setting or re inflation the device uses its advanced IntelliSense technology Intended Use This device is a digital monitor intended for use in measuring blood pressure and pulse rate in adult patient population who can understand this instruction manual with the arm circumference range printed on the arm cuff The device detects the appearance of irregular heartbeats during measurement and gives a warning signal with the measurement result Important Safety Information
3. 4 1 Know Your Device N Open the rear cover page to read the following The letter identifiers on the rear cover page correspond to those in the body of this page Monitor Display Cuff wrap guide lamp OMemory button D Weekly average button START STOP button Up Down buttons USER ID selection switch Date Time setting button DBlood pressure colour indicator Air jack Battery compartment DAC adapter jack for optional AC adapter MUSB port Arm cuff N Arm cuff Arm circumference 22 42cm Air plug PAir tube Display Memory symbol USER ID symbol S Average value symbol DSystolic blood pressure U Diastolic blood pressure Transfer indicator WDATA FULL symbol OOK symbol Heartbeat symbol Flashes during measurement Date Time display Morning average symbol 3 Evening average symbol Morning hypertension symbol Movement error symbol Irregular heartbeat symbol Blood pressure level indicator amp G Cuff wrap guide amp BLow battery symbol b Deflation symbol Pulse display Memory number 1 Know Your Device Display Symbols Irregular Heartbeat Symbol J Normal Heartbeat When the monitor detects an irregular rhythm two or more times during the Pulse A measurement the irregular heartbeat symbol E will appear on the display with the measurement values Blood pressure NNS An irregular heartbeat rhythm is defined as a rhythm that is 25 less or 2
4. Morning Weekly Average p Measurements of the morning This is the average for the Sunday Monday Tuesday Wednesday Thursday Friday Saturday measurements taken during the morning a T First measurement of Q EETITIm 4 00 11 59 between Sunday and the moming b 5 3 measurements Saturday An average for each day is H calculated for up to three measurements Within 10 minutes Morning Blood Pressure taken within 10 minutes of the first measurement of the morning H e 11 59 Evening Weekly Average ER Measurements of the evening TT T This is the average for the Sunday Monday Tuesday Wednesday Thursday Friday Saturday measurements taken during the evening 100 19 00 1 59 between Sunday and s Saturday An average for each day is hd y 9 y calculated for up to three measurements e taken within 10 minutes of the last Within 10 minutes measurement of the evening Up to 3 measurements Last measurement of Measurement n the evening Evening Blood Pressure 16 1 59 a 3 Using the Device To Transfer the Measurement Values To begin using the Bi LINK software for the first time please visit www omron healthcare com for the initial set up instructions 1 Open the USB port cover 2 Connect the USB cable to a PC 3 Connect the USB cable to the monitor 17 3 Using the Device To Delete All the Values Stored in Memory The values stor
5. USB cable 9517499 4 25 5 Maintenance and Storage Using the Optional AC Adapter 1 Insert the AC adapter plug into the AC adapter jack on the rear side of the monitor 2 Plug the AC adapter into an electrical outlet To disconnect the AC adapter unplug the AC adapter from the electrical outlet first and then remove the AC adapter plug from the monitor 26 6 Specifications Product description Model Display Measurement method Measurement range Accuracy Inflation Deflation Memory Rating Power source Battery life Applied part Protection against electric shock Operating temperature humidity Storage temperature humidity air pressure IP classification Weight Outer dimensions Cuff circumference Cuff Tube material Package contents Automatic Blood Pressure Monitor OMRON M6 Comfort IT HEM 7322U E LCD digital display Oscillometric method Pressure 0 to 299 mmHg Pulse 40 to 180 beats min Pressure 43 mmHg Pulse 45 of display reading Fuzzy logic controlled by electric pump Automatic pressure release valve 100 measurements with date and time for each user 1 and 2 DC6V 4W 4 AA batteries 1 5V or optional AC adapter Adapter S 9515336 9 INPUT AC100 240V 50 60Hz 0 12A Adapter UK 9983666 5 INPUT AC100 240V 50 60Hz 15VA Approximately 1000 measurements using new alkaline batteries Type BF Internally powered ME equipment When using only the bat
6. Waste Electrical amp 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 from other types of wastes and recycle it HEE 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 take 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 29 30 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 to give you every satisfaction provided that it is properly operated and maintained as described in the instruction manual This product is guaranteed by OMRON for a period of 3 years after the date of purchase The proper construction workmanship and materials of this product is guaranteed by OMRON During this period of guarantee OMRON will without charge for labour or parts repair or replace the defect product or any defective parts The guarantee does no
7. Kyoto uid 617 0002 JAPAN EU representative OMRON HEALTHCARE EUROPE B V Scorpius 33 2132 LR Hoofddorp THE NETHERLANDS REP www omron healthcare com Production facility Planta de producci n OMRON DALIAN CO LTD Site de production Productiefaciliteit Dalian CHINA Produktionsstatte lipou3BoncrBeHHoe nogpazgenenne Stabilimento di produzione retim Tesisi WAA SALA Subsidiary Empresa filial OMRON HEALTHCARE UK LTD Succursale Dochteronderneming Opal Drive Fox Milne Milton Keynes MK15 0DG U K Niederlassung unuan Consociata Yan Kurulus OMRON MEDIZINTECHNIK HANDELSGESELLSCHAFT mbH Hata CAS EN Gottlieb Daimler Strasse 10 68165 Mannheim GERMANY www omron healthcare de OMRON SANT FRANCE SAS 14 rue de Lisbonne 93561 Rosny sous Bois Cedex FRANCE Uniquement pour le march fran ais OMRON Service Apr s Vente N Vert 0 800 91 43 14 consommateurs omron sante fr www omron healthcare fr Made in China Fabricado en China Fabriqu en Chine Geproduceerd in China Hergestellt in China CnenaHo B Kutae Prodotto in Cina Cin de retilmistir Dos aka
8. measurement on the right arm the air tube will be at the side of your elbow Be careful not to rest your arm on the air tube D The blood pressure can differ between the right arm and the left arm and therefore also the measured blood pressure values can be different OMRON recommends to always use the same arm for measurement If the values between both arms differ substantially please check with your physician which arm to use for your measurement 3 Using the Device 3 2 How to Sit Correctly To take a measurement you need to be relaxed and comfortably seated under comfortable room temperature Avoid bathing drinking alcohol or caffeine smoking exercising or eating 30 minutes before taking a measurement Sit on a chair with your feet flat on the floor Sit upright with your back straight c Sit with your back and arm being supported The arm cuff should be placed on your arm at the same level as your heart d 10 3 Using the Device 3 3 Taking a Measurement Notes To cancel a measurement press the START STOP button to release the air in the arm cuff Remain still while taking a measurement The monitor is designed to take measurements and store the measurement values in the memory for 2 people using USER ID 1 and USER ID 2 1 Select your USER ID 1 or 2 j GI ED n z2 2 Press the START STOP button The arm cuff starts to inflate au
9. treatment are dangerous 12 3 Using the Device 3 4 Using the Memory Function The monitor automatically stores the results up to 100 sets for each user 1 and 2 It can also calculate an average value based on the last 3 measurement values taken within 10 minutes Notes If there are only 2 measurement values in the memory for that period the average will be based on these LJ 2 values If there is 1 measurement value in the memory for that period this is displayed as the average If the memory is full the monitor will delete the oldest value When viewing the measurement value taken without setting the date and time is displayed instead of the date and time To View the Measurement Values Stored in Memory 1 Select your USER ID 1 or 2 2 Press the EP button Ey S2011 8 00 amp so m The Memory number appears for a second before the p ie pulse rate is displayed The newest set is numbered 1 67i Note The cuff wrap guide result appears on the display with the gi measurement values The cuff wrap guide lamp will not light 3 Press the 4 or gt button to view the values stored in the memory 4 To the older values To the more recent values 13 3 Using the Device To View the Average Value 1 Select your USER ID 1 or 2 2 Press and hold the amp button for more than 3 seconds Be ES i ru 3 3 3 ru L E Notes If th
10. 5 Irregular Heartbeat LJ more than the average rhythm detected while the monitor is measuring the Short Long Systolic and diastolic blood pressure Pulse If the irregular heartbeat symbol E displays with your measurement Blood pressure DUNN UP results we recommend you consult your physician Follow the directions of your physician Movement Error Symbol iJ The movement error symbol is displayed if you move your body during the measurement Please remove the arm cuff and wait 2 3 minutes Take another measurement remain still during measurement Average Value Symbol jig The average value symbol is displayed when you press and hold the memory button for more than 3 seconds The most recent average value appears on the display screen Cuff Wrap Guide Lamp 63 O If the cuff was wrapped too loosely it may cause unreliable results If the wrapping of cuff is too loose the cuff wrap guide Lamp lights in orange Otherwise ES lights in green This is the function which is used as an aid in determining if the cuff is wrapped snugly enough 1 Know Your Device Blood Pressure Colour Indicator If your systolic or diastolic pressure is above the standard range 135 mmHg for the systolic blood pressure and or 85 mmHg for the diastolic blood pressure the blood pressure colour indicator will light in orange when the measurement result is displayed If they are within the standard range the blood pressure colou
11. 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 device 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
12. consult a physician before using the device as the arm cuff inflation can cause bruising 2 Important Safety Information AN If there are any abnormalities during the measurement remove the arm cuff A Do not use this device on infants or persons who cannot express their intentions A Do not inflate the arm cuff more than necessary A Do not use the device for any purpose other than measuring blood pressure A Use only the approved arm cuff for this device Use of other arm cuffs may result in incorrect measurement results A Do not use a mobile phone or other devices that emit electromagnetic fields near the device This may result in incorrect operation of the device A Do not disassemble the monitor or arm cuff A Do not use in a location with moisture or a location where water may splash on the device This may damage the device A Do not use the device in a moving vehicle car airplane A Do not take measurements more than necessary It may cause bruising due to blood flow interference A Consult your physician before using the device if you had a mastectomy AC Adapter optional Usage AFully insert the power plug into the outlet A When disconnecting the power plug from the outlet do not pull the power cord Be sure to pull from the power plug safely AN When handling the power cord take care not to do the following Do not damage Do not break it Do not tamper with it Do not forcibly bend or pull Do not t
13. device in pregnancy including pre eclampsia or if diagnosed with arrhythmia or arteriosclerosis Do not use the device on the injured arm or the arm under medical treatment ADo not apply the arm cuff on the arm while being on an intravenous drip or blood transfusion LJ Consult your physician before using the device on the arm with an arterio venous A V shunt A Do not use the device with other medical electrical ME equipment simultaneously ADo not use the device in the area the HF surgical equipment MRI or CT scanner exists or in the oxygen rich environment A The air tube or the AC adapter cable may cause accidental strangulation in infants AA Contained small parts that may cause a choking hazard if swallowed by infants AC Adapter optional Usage ADo not use the AC adapter if the device or the power cord is damaged Turn off the power and unplug the power cord immediately A Plug the AC adapter into the appropriate voltage outlet Do not use in a multi outlet plug A Never plug in or unplug the power cord from the electric outlet with wet hands N 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 equipment or other property General Usage N Always consult your physician Self diagnosis of measurement results and self treatment are dangerous N People with severe blood flow problems or blood disorders should
14. e Press the HDate Time setting button The year flashes on the Date Time display 2 Push or button to change the year Push button to confirm the year and then the month flashes Repeat the same steps to change the month day hour and minutes Years ED M Month cath ERE Bay Change Confirm T rn Hour Mira p Forward Change Confirm Cs gt mc nio UT i Back Change Confirm CT Una Change Confirm lt BE Change Confirm 3 Press the STARTISTOP button to turn the monitor off Notes If the batteries have been replaced the date and time setting will need to be reset If the date and time are not set appears during or after measurement 3 Using the Device Open both the front and rear covers to read the following The letter identifiers on the cover pages correspond to those in the body of this page 3 1 Applying the Arm Cuff Remove tight fitting clothing or tight rolled up sleeve from your left upper arm Do not place the arm cuff over thick clothes LJ 1 Insert the air plug into the air jack securely 2 Apply the arm cuff to your left upper arm The bottom edge of the arm cuff should be a 1 to 2 cm above the elbow P Air tube is on the inside of your arm and aligned with your middle finger 3 Secure closed with the fabric fastener Notes When you take a
15. e previous measurement was taken without setting the date and time the average value is not calculated If there are no measurement values stored in the memory the screen to the he right is displayed 14 3 Using the Device To View the Weekly Average Value The monitor calculates and displays weekly averages for the measurements taken in the morning and evening within 8 weeks for each user Note The week begins Sunday at 2 00 1 Select your USER ID 1 or 2 EJ Press the x 2 button The morning average for THIS WEEK appears on the display Note The morning hypertension symbol E3 appears if the morning weekly average is above 135 85 mmHg E d B s cnc m D E3 N Press the 3x 7 button again and the evening average for THIS WEEK appears on the display J 5 Naum nk uu Press the or button to display the previous weeks This week Last week 2 weeks ago Continue to 7 weeks ago Morning average Morning average Morning average press Morning average C 7 s iC jan XU RD CH 2 B D D o VO Pe En This week Last week 2 weeks ago 7 weeks ago Evening average Evening average Evening average Evening average 15 3 Using the Device Note If there are no measurement values stored in the memory the screen to the right is displayed
16. ed in the memory are deleted by USER ID 1 Select your USER ID 1 or 2 2 Press the Memory button while the memory symbol E appears 3 While holding the amp button down press the START STOP button for more than 3 seconds Note You cannot partially delete the values stored in the memory All values for the user you select will be deleted 18 4 Error Messages and Troubleshooting 4 1 Error Messages Display Solution Remove the arm cuff Wait 2 3 minutes and then take another measurement Repeat the steps in section 3 3 If this error continues to appear contact your physician Irregular heartbeats are detected Movement during measurement Carefully read and repeat the steps in section 3 3 Apply the arm cuff tighter Refer to section 3 1 Arm cuff is applied too loosely You should replace the batteries with new The batteries are low ones ahead of time Refer to section 2 1 You should replace the batteries with new The batteries are exhausted ones at once Refer to section 2 1 19 4 Error Messages and Troubleshooting Display Air plug is disconnected Solution Insert the air plug securely Refer to section 3 1 Arm cuff is applied too loosely Apply the arm cuff tighter Refer to section 3 1 Air is leaking from the arm cuff Replace the arm cuff with a new one Refer to section 5 3 Movement during measurement and the a
17. 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 LJ 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 Why is it a Good Thing to measure Blood Pressure at Home Many factors such as physical activity 200 Upper curve systolic blood pressure anxiety or the time of day can influence EE ARA PEE EA your blood pressure A single 150 measurement may not be sufficient for an ge accurate diagnosis Thus it is best to try 100 mr E M CREME ol and measure your blood pressure at the same time each day to get an accurate BO indication of any changes in blood 6 12 18 24 pressure Blood pressure is typically low in the morning and increases from afternoon to evening It is lower in the summer and higher in the winter mmHg Example fluctuation within a day male 35 years old 31 Manufacturer OMRON HEALTHCARE Co Ltd 53 Kunotsubo Terado cho Muko
18. m the arm cuff Replace the arm cuff with a new one Refer to section 5 3 Arm cuff deflates too soon The arm cuff is loose Apply the arm cuff correctly so that it is firmly wrapped around the arm Refer to section 3 1 Cannot measure or the results are too low or too high The arm cuff has not been inflated sufficiently Inflate the arm cuff so that it is 30 to 40 mmHg above your previous measurement result Refer to section 3 3 21 4 Error Messages and Troubleshooting Problem Nothing happens when you press the buttons The batteries are empty Solution Replace the batteries with new ones Refer to section 2 1 The batteries have been inserted incorrectly Insert the batteries with the correct polarity Refer to section 2 1 Other problems 22 Press the START STOP button and repeat measurement Replace the batteries with new ones If the problem continues contact your OMRON retail outlet or distributor 5 Maintenance and Storage 5 1 Maintenance To protect your device from damage please observe the following Store the device and the components in a clean safe location Do not use any abrasive or volatile cleaners Do not wash the device and any components or immerse them in water Do not use petrol thinners or similar solvents to clean the device LJ Use a soft and dry cloth or a oa and moistened cloth and ne
19. r indicator will light in green The JNC7 Guideline recommends the following guideline General Guidelines for Blood Pressure Prehypertension at Office Hypertension at Home Systolic Blood Pressure 120 139 mmHg 135 mmHg Diastolic Blood Pressure 80 89 mmHg 85 mmHg These are from statistical values for blood pressure JNC7 The Seventh Report 2003 Dec of the Joint National Committee on Prevention Detection Evaluation and Treatment of High Blood Pressure 2 Preparation 2 1 Battery Installation 1 Remove the battery cover 2 Insert 4 AA batteries as indicated in the battery compartment 3 Replace the battery cover Notes When the low battery symbol 1 appears on the display turn the monitor off then replace all batteries at the same time Long life alkaline batteries are recommended The measurement values continue to be stored in memory even after the batteries are replaced The supplied batteries may have a shorter life A Disposal of used batteries should be carried out in accordance with the national local regulations for the disposal of batteries 2 Preparation N Open the rear cover page to read the following The letter identifiers on the rear cover page correspond to those in the body of this page 2 2 Setting the Date and Time Set the monitor to the correct date and time before taking a measurement for the first tim
20. rm cuff has not been inflated sufficiently Repeat measurement Remain still and do not talk during measurement Refer to section 3 3 If E2 appears repeatedly inflate the arm cuff manually until it is 30 to 40 mmHg above your previous measurement result Refer to section 3 3 The arm cuff was inflated above 299 mmHg when inflating the arm cuff manually Do not inflate the arm cuff above 299 mmHg Refer to section 3 3 Movement during measurement Repeat measurement Remain still and do not talk during measurement Refer to section 3 3 Clothing is interfering with the arm cuff Remove any clothing interfering with the arm cuff Refer to section 3 1 Device error Contact your OMRON retail outlet or distributor 4 Error Messages and Troubleshooting 4 2 Troubleshooting Problem The measurement result is extremely high or low Arm cuff is applied too loosely Solution Apply the arm cuff tighter Refer to section 3 1 Movement or talking during measurement Remain still and do not talk during measurement Refer to section 3 3 Clothing is interfering with the arm cuff Remove any clothing interfering with the arm cuff Refer to section 3 1 Arm cuff pressure does not rise The air connector is not securely connected into the air jack Make sure that the air tube is connected securely Refer to section 3 1 Air is leaking fro
21. t 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 guaranteed 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 guarantee 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 AC Adapter USB Cable Should guarantee 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 guarantee does not give rise to any extension or renewal of the guarantee period The guarantee will be granted only if the complete product is returned together with the original invoice cash ticket issued to the consumer by the retailer 8 Some Useful Information about Blood Pressure What is Blood Pressure Blood pressure is a measure of the
22. teries m Class II ME equipment Optional AC adapter 10 C to 40 C 30 to 85 RH 20 C to 60 C 10 to 95 RH 700 1060hPa IP 20 Monitor Approximately 380g without batteries Arm cuff Approximately 163g Monitor Approximately 124 w mm x 90 h mm x 161 I mm Arm cuff Approximately 145 mm x 532 mm air tube 750 mm 22 to 42 cm Nylon polyester polyvinyl chloride Monitor arm cuff instruction manual storage case battery set USB cable blood pressure pass 27 6 Specifications Notes These specifications are subject to change without notice In the clinical validation study the 5th phase was used on 85 subjects for determination of diastolic blood pressure This device has not been validated for use on pregnant patients C 0197 This device fulfils the provisions of EC directive 93 42 EEC Medical Device Directive This device 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 device is produced under the strict quality system of OMRON HEALTHCARE Co Ltd Japan The core component for OMRON devices which is the Pressure Sensor is produced in Japan 28 6 Specifications Important information regarding Electro Magnetic Compatibility EMC With the increased number of electronic devices such
23. tomatically WSTART WINFLATE WDEFLATE WCOMPLETE amp unm unm amp unm unm If your systolic pressure Is NBT a Se IB more than 210 mmHg ji n H After the arm cuff starts to inflate press and hold the START STOP button until the D _ monitor inflates 30 to 40 mmHg higher than l your expected systolic pressure 1 mmm OOI Notes The monitor will not inflate above 299 mmHg Do not apply more pressure than necessary 11 3 Using the Device 3 Remove the arm cuff 4 Press the START STOP button to turn the monitor off The monitor automatically stores the measurement result in its memory It will automatically turn off after 2 minutes Note Wait 2 3 minutes before taking another measurement Waiting between measurements allows the arteries to return to the condition prior to taking a measurement Using the Guest Mode The monitor stores measurement values for 2 users in the memory The guest mode can be used to take a single measurement for another user No measurement values are stored in the memory when the guest mode is selected 1 Press and hold the START STOP button for more than 3 seconds UT SS The USER ID symbol and the Date Time display will disappear 2 Release the START STOP button when the Date Time display turns off The arm cuff will start to inflate automatically N Always consult your physician Self diagnosis of measurement results and self
24. utral soap to clean on the monitor and the arm cuff Changes or modification not approved by the manufacturer will void the user warranty Do not disassemble or attempt to repair the device or components Consult your OMRON retail outlet or distributor Calibration and Service The accuracy of this device has been carefully tested and is designed for a long service life lt is generally recommended to have the device inspected every 2 years to ensure correct functioning and accuracy Please consult your OMRON retail outlet or distributor 23 5 Maintenance and Storage 5 2 Storage Keep the device in its storage case when not in use 1 Unplug the air plug from the air jack 2 Gently fold the air tube into the arm cuff Note Do not bend or crease the air tube excessively 3 Place the monitor and the arm cuff in the storage case Do not store the device in the following situations If the device 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 24 5 Maintenance and Storage 5 3 Optional Medical Accessories within the scope of EC Medical Device Directive 93 42 EEC Arm cuff AC adapter Arm circumference 22 42 cm LJ Intelli Cuff L 9911730 8 Adapter S 9515336 9 Adapter UK 9983666 5 Model HEM FL31 5 4 Other Optional Replacement Parts USB cable 2
25. wist Do not bundle during use Do not pinch Do not place under heavy objects A Wipe the dust off from the power plug A Unplug monitor when not in use A Disconnect the power plug before cleaning NUse only the original AC adapter designed for this device Use of unsupported adapters may damage and or may be hazardous to the device Important Safety Information Battery Usage Do not insert the batteries with their polarities incorrectly aligned A Use only 4 AA alkaline or manganese batteries with this device Do not use other types of batteries Do not use new and used batteries together A Remove the batteries if the device will not be used for three months or more General Precautions LJ Do not forcibly crease the arm cuff or the air tube excessively Do not press the air tube while taking a measurement To unplug the air plug pull on the air plug at the connection with the monitor not the tube itself Do not drop the monitor or subject device to strong shocks or vibrations Do not inflate the arm cuff when it is not wrapped around your arm Do not use the device outside the specified environment It may cause an inaccurate reading Read and follow the Important information regarding Electro Magnetic Compatibility EMC in the 6 Specifications Read and follow the Correct Disposal of This Product in 6 Specifications when disposing of the device and any used accessories or optional parts
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