Home in vitro diagnostic products, blood glucose meter, Lipid Panel Meter
User Manual for JOYTECH models including: DBP-6285L Fully Automatic Digital Blood Pressure Monitor, DBP-6285L, Fully Automatic Digital Blood Pressure Monitor, Digital Blood Pressure Monitor, Blood Pressure Monitor, Pressure Monitor
JOYTECH HEALTHCARE CO., LTD. 0028 Amy-type Fully Automatic Digital Blood Pressure Monitor 2AQVU0028 2AQVU0028 0028
File Info : application/pdf, 11 Pages, 4.76MB
DocumentDocumentOwner's Manual Arm-type Fully Automatic Digital Blood Pressure Monitor Model DBP-6285L Arm Type Document No. : JDBP-8504-076 Version: A Date of Issue: 2020.09.26 Contact Information The lay operator or lay responsible or ganization should contact the manufacturer or the representative of manufacturer. -for assistance,if needed,in setting up,using or maintaining the product,or -to report unexpected operation or events. Manufactured by JOYTECH Healthcare Co.,Ltd. No.365, Wuzhou Road,Yuhang Economic Development Zone, Hangzhou City,311100 Zhejiang,China Email: info@sejoy.com Telephone: +86-571-81957767 Fax: +86-571-81957750 Contents 1 Safety Notice 2 Safety Notice ............................................................... 02 Unit Illustration ......................................................... 06 Important Testing Guidelines ..................................... 09 Quick Start ................................................................. 10 Unit Operation ........................................................... 11 Battery Installation ........................................... 11 System Settings .................................................. 12 Applying the Arm Cuff ....................................... 14 Testing ................................................................ 15 Power Off .............................................................17 Memory Check and Last 3 Test Average .............18 Memory Deletion ..................................................19 Low Battery Indicator ...........................................19 Bluetooth requirement and connection ...............20 Troubleshooting .....................................................22 Blood Pressure Information ........................................ 23 Blood Pressure Q&A ................................................... 26 Maintenance ............................................................... 27 Specifications ............................................................. 29 Warranty .................................................................... 31 Electromagnetic Compatibility Information .............. 32 Additional Notes ................................................... 37 Thank you for purchasing the DBP-6275B Blood Pressure Monitor. The unit has been constructed using reliable circuitry and durable materials. Used properly, this unit will provide years of satisfactory use. Indications for use: The Arm-type Fully Automatic Digital Blood Pressure monitors are intended to measure blood pressure(systolic and diastolic) and pulse rate of adults and adolescents over 12 years of age. All functions can be used safely and values can be read out in one LCD DISPLAY. Measurement position is on adult upper arm only. The PATIENT is an intended OPERATOR Blood pressure measurement determined with this device are equivalent to those obtained by a trained observer using the cuff/ stethoscope auscultation method, within the limits prescribed by the Recognized Consensus Standard (IEC 80601-2-30) for electronic sphygmomanometers. Precautions to Ensure Safe, Reliable Operation 1. Do not drop the unit. Protect it from sudden jars or shocks. 2. Do not insert foreign objects into any openings. 3. Do not attempt to disassemble the unit. 4. Do not crush the pressure cuff. 5. If the unit has been stored at temperatures below 0 , leave it in a warm place for about 15 minutes before using it. Otherwise, the cuff may not inflate properly. 6. If the unit has been stored at temperatures above 40 , leave it in a cool place for about 15 minutes before using it. Otherwise, the cuff may not inflate properly. 7. Do not store the unit in direct sunlight, high humidity or dust. 8.To avoid any possibility of accidental strangulation, keep this unit away from children and do not drape tubing around your neck. 9.Ensure that children do not use the instrument unsupervised; some parts are small enough to be swallowed. 10.Some may get a skin irritation from the cuff taking frequent readings over the course of the day, but this irritation typically goes away on its own after the monitor is removed. Safety Notice 3 Important Instructions Before Use 1. Do not confuse self-monitoring with self-diagnosis. Blood pressure measurements should only be interpreted by a health professional who is familiar with your medical history. 2. Contact your physician if test results regularly indicate abnormal readings. 3. If you are taking medication, consult with your physician to determine the most appropriate time to measure your blood pressure. NEVER change a prescribed medication without first consulting with your physician. 4. Individuals with serious circulation problems may experience discomfort. Consult your physician prior to use. 5. For persons with irregular or unstable circulation resulting from diabetes, liver disease, arteriosclerosis or other medical conditions, there may be variations in blood pressure values measured at the wrist versus at the upper arm. Monitoring the trends in your blood pressure taken at either the arm or the wrist is nevertheless useful and important. 6. People suffering from vascular constriction, liver disorders or diabetes, people with cardiac pacemakers or a weak pulse, and women who are pregnant should consult their physician before measuring their blood pressure themselves. Different values may be obtained due to their condition. 7. People suffering from arrhythmias such as atrial or ventricular premature beats or atrial fibrillation only use this blood pressure monitor in consultation with your doctor. In certain cases oscillometric measurement method can produce incorrect readings. 8.Too frequent measurements can cause injury to the patient due to blood flow interference. 9.The cuff should not be applied over a wound as this can cause further injury. 10.DO NOT attach the cuff to a limb being used for IV infusions or any other intravascular access, therapy or an arterio-venous (A-V) shunt. The cuff inflation can temporarily block blood flow, potentially causing harm to the patient. 11.The cuff should not be placed on the arm on the side of a mastectomy. In the case of a double mastectomy use the side of the least dominant arm. 12.Pressurization of the cuff can temporarily cause loss of function of simultaneously used monitoring equipment on the same limb. 13.A compressed or kinked connection hose may cause continuous cuff pressure resulting in blood flow interference and potentially harmful injury to the patient. 14.Check that operation of the unit does not result in prolonged impairment of the circulation of the patient. 15. Product is designed for its intended use only. Do not misuse in any way. 16. Product is not intended for infants or individuals who cannot express their intentions. 17. Prolonged over-inflation of the bladder may cause ecchymoma of your arm. 18. Do not disassemble the unit or arm cuff. Do not attempt to repair. 19. Use only the approved arm cuff for this unit. Use of other arm cuffs may result in incorrect measurement results. 20. The system might produce incorrect readings if stored or used outside the manufacturer's specified temperature and humidity ranges. Make sure to store the blood pressure monitor, children, pets and pests are outside of accessible range. 21. Do not use the device near strong electrical or electromagnetic fields generated by cell phones or other devices, they may cause incorrect readings and interference or become interference source to the device. 22. Do not mix new and old batteries simultaneously. Safety Notice 5 Federla Commulcation Commission (FCC) Interference Statement 1.This device complies with part 15 of the FCC Rules. Operation is subject to the condition that this device does not cause harmful interference. 2.This device is verified to comply with part 15 of the FCC Rules for use with cable television service. 3.This device complies with part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) This device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. Please note that changes or modifications not expressly approved by the party responsible for compliance could void the user's authority to operate the equipment. 4.This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures: --Reorient or relocate the receiving antenna. --Increase the separation between the equipment and receiver. --Connect the equipment into an outlet on a circuit different from that to which the receiver is connected. --Consult the dealer or an experienced radio/TV technician for help. 5.This equipment complies with radio frequency exposure limits set forth by the FCC for an uncontrolled environment. 6. This device must not be co-located or operating in conjunction with any other antenna or transmitter. 7.Essential performance: Electrosurgery interference recovery Refer 202.6.2.101 IEC 80601-2-30 Limits of the error of the manometer Reproducibility of the BLOOD PRESSURE DETERMINATION Refer 202.12.1.102 IEC 80601-2-30 Refer 201.12.1.107 IEC 80601-2-30 Safety Notice 4 23. Replace batteries when Low Battery Indicator" "appears on screen. Replace both batteries at the same time. 24. Do not mix battery types. Long-life alkaline batteries are recommended. 25. Remove batteries from device when not in operation for more than 3 months. 26. Dispose batteries properly; observe local laws and regulations. 27. Only use a recommended class II AC Medical approved adaptor which comply with 2MOPP, and pass IEC 60601-1, IEC 60601-1-2 (or FCC) standard . An unauthorized adapter may cause fire and electric shock. 28. Advising operator that Instruction manual/ Booklet must be consulted. 29. Do not use the device during transport vehicles for influencing measurement accuracy, such as patient transport in an ambulance or helicopter. 30. Contains small parts that may cause a chocking hazard if swallowed by infants. 31. Please align the polarities of each battery with the +ve and -ve signs imprinted on the battery housing when you replace the batteries . 32.Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally. 33.Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the unit, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result. 34.the blood pressure monitors equipped with bluetooth(BT) module is only transmit historical blood pressure (BP) from the subject device to a user-supplied digital device, and is not intended for active patient monitoring. WARNING SIGNS AND SYMBOLS USED Keep Dry Keep off Sunlight Type BF Equipment IP21 MR Instructions For Use MUST be Consulted Discard the used product to the recycling collection point according to local regulations The Bluetooth® Smart word mark and logos are registered trademarks owned by Bluetooth SIG, Inc. and any use of such marks by JOYTECH Healthcare Co.,Ltd. IP21 indicate dust proof and waterproof grade. Number 2 indicate that Protected against solid foreign objects of 12.5 mm and greater; Number 1 indicate that Protection against vertically falling water drops . Magnetic Resonance unsafe Unit Illustration 6 Monitor Unit LCD "GROUP2 "Button " GROUP1 "Button "START/STOP " Button "MEM" Button USB Adapter Jack Arm Cuff Medium size cuff (fits arm circumference: 22.0 cm -36.0 cm). 1~2 cm0. 4 ~0.8 inch MC atahuiatnitosAnu:rptSpeulribyesdt imt uitgihotnroefs ut hl te icnumf fedaisfuf erreemnet nf rt oemr ro r. Arm Cuff Air Plug Air Tube If air is leaking from the arm cuff, replace the arm cuff with a new one. It is generally recomm ended to have the cuff replaced timely to ensure correct functioning and accuracy. Please consult your local authorized Sejoy distributor or dealer. Unit Illustration 7 Important Testing Guidelines 8 Contents 1.Monitor Unit 1~2 cm 0.4~0.8 inch Main Artery Cathuatitosnu:pSpulibesdtimtuitgiohnt roefstuhlet icnufmf edaifsfuerreemntefnrtoemrror. 3.Arm Cuff Battery Indicator Irregular Heartbeat Indicator Owner's Manual Arm-type Fully Automatic Digital Blood Pressure Monitor Model DBP-6285L Arm Type 2.Owner's Manual 4.Storage Case 1. Avoid eating, exercising, and bathing for 30 minutes prior to testing. 2. Sit in a calm environment for at least 5 minutes prior to testing. 3. Do not stand while testing. Sit in a relaxed position while keeping your arm level with your heart. 4. Avoid speaking or moving body parts while testing. 5. While testing, avoid strong electromagnetic interference such as microwave ovens and cell phones. 6. Wait 3 minutes or longer before re-testing. 7. Try to measure your blood pressure at the same time each day for consistency. 8. Test comparisons should only be made when monitor is used on the same arm, in the same position, and at the same time of day. 9. This blood pressure monitor is not recommended for people with severe arrhythmia. 10. Do not use this blood pressure monitor if the device is damaged. Any blood pressure recording can be affected by the following factors: 1. The position of the subject, his or her physiologic condition; 2. The performance and accuracy of the device; 3. Cuff size: too small cuff (bladder) will produce a higher blood pressure value than usual, too big cuff (bladder) will produce a lower blood pressure value; 4. Measuring position does not keep level with your heart; 5. Speaking or moving body parts while testing; 6. Not relaxing for about 5 minutes before taking the measurement. 5.2MOPPMedical AC Adapter(DC5.0 V,1000mA) (recommended, not provided) Quick Start 9 1. Install batteries. (See Figure A ) 2. Insert cuff air plug into the left side of monitor unit. (See Figure B) Figure A Figure B 3. Remove thick clothing from the arm area. 4. Rest for several minutes prior to testing. Sit down in a quiet place, preferably at a desk or table, with your arm resting on a firm surface and your feet flat on the floor. (See Figure C ) Unit Operation 10 Lithium Battery Charging The device has a built-in lithium battery that must be recharged using a specific power adapter. When low battery indicator icon " "appears on the screen Please connect the power adapter to charge. When charging, the screen will be displayed in a cycle from " " to" ". Insert the adapter connector into the adapter interface, then insert the adapter into the socket, and then connect the adapter to the cable endInsert the adapter interface on the device and press the on/off button to measure normally. (if this model has been packed)When you plug in the adapter, the screen power display changes, indicating that you are using the adapter for power. Adapter interface The adapter connects to the cable head Figure C 5. Apply cuff to your left arm and keep level with your heart. Bottom of cuff should be placed approximately 1-2cm (0.4-0.8'') above elbow joint. (See Figures D&E) Adapter connector end AC Adapter jack is on the back side of the monitor. Medical AC adapter(DC 5.0 V,1000mA) can be used with the device (recommended, not provided). The adapter connect pin should be positive inside and negative outside with a 2.1mm coaxial joint. Do not use any other type of AC adapter as it may harm the unit. 1-2cm (0.4-0.8'') Figure D 6. Press " START/STOP " Button to start testing. Figure E USB Adapter Jack Note:Power supply is specified as part of ME EQUIPMENT. Unit Operation 11 System Settings With power off, press "GROUP1" button or "GROUP2" button to activate System Settings. The Memory Group icon flashes. 1. Select Memory Group While in the System Setting mode, you may accumulate test results into 2 different groups. This allows 2 different users to save individual test results Press " MEM " button to choose a group setting. Test results will automatically store in each selected group. Unit Operation 12 4.Voice Setting Press "GROUP1" button or "GROUP2" button to enter voice setting mode. Set voice format ON or OFF by pressing the "MEM" button. 2. Time/Date setting Press"GROUP1" button or "GROUP2" button again to set the Time/Date mode. Set the year first by adjusting the "MEM" button. Press"GROUP1" button or "GROUP2" button again to confirm current month. Continue setting the dat, hour and minute in the same way. Every time the "GROUP1" button or "GROUP2" button is pressed, it will lock in your selection and continue in succession ( month,day,hour, minute,12/24 hours) 5.Volume Setting Press "GROUP1" button or "GROUP2" button to enter volume setting mode. Set the voice volume by adjusting the "MEM" button . There are six volume levels. 3. Time Format setting Press "GROUP1" button or "GROUP2" button again to set the time format setting mode. Set the time format by adjusting the"MEM" button. EU means European Time US means U.S Time. 6. Saved Settings While in any setting mode, press " START/STOP " button to turn the unit off. All information will be saved. Note: If unit is left on and not in use for 3 minutes, it will automatically save all information and shut off. Unit Operation Applying the Arm Cuff 1. Firmly insert air plug into opening located on left side of monitor unit. 13 Unit Operation 14 Testing 1. Power On Press and hold "START/STOP" button to turn the unit on. The LCD screen will appear full for one second as unit performs a quick diagnosis. A voice tone will indicate when unit is ready for testing. 2. With sticky nylon section facing outward, insert end of cuff underneath metal ring of cuff. 3. Fasten cuff about 1-2cm (0.4-0.8'') above the elbow joint. For best results apply cuff to bare arm and keep level with heart while testing. Note: Unit will not function if residual air from previous testing is present in cuff. The LCD will flash " " until pressure is stabilized. 1-2cm (0.4-0.8'') Note: Do not insert air plug into opening located on back side of monitor unit. This opening is designed for an optional power supply only. Unit Operation 15 2. Testing After cuff inflation, air will slowly rise as indicated by the corresponding cuff pressure value. A flashing " " will appear simultaneously on screen signaling heart beat detection. Unit Operation 16 Irregular Heartbeat Indicator If the monitor detects an irregular heart rhythm two or more times during the measuring process, the Irregular Heartbeat Symbol " "appears on screen along with measurement results. Irregular heartbeat rhythm is defined as rhythm that is either 25% slower or faster than the average rhythm detected while measuring systolic blood pressure and diastolic blood pressure. Consult your physician if the Irregular Heartbeat Symbol " " frequently appears with your test results. Note: Keep relaxed during testing. Avoid speaking or moving body parts. 3. Result Display The screen will display measurements for systolic and diastolic blood pressure with voice broadcast. An indicator representing the current measurement will appear next to the corresponding WHO Classification. Note: Refer to Page 24~25 for detail WHO Blood Pressure Classification Information. Power Off The " START/STOP " button can be pressed to turn off the unit in any mode. The unit can turn off the power itself about 3 minutes no operation in any mode. Safety Precaution: If pressure in arm cuff becomes too extreme while testing, press the " START/STOP " button to turn power off. The cuff pressure will rapidly dissipate once the unit is off. Arm Shake Indicator If there is arm movement during the measurement, the " " icon may flash. Indicates that the measurement results may be inaccurate, and the situation will be recorded at the end of the measurement as a reminder. Cuff loose Indicator When starting the measurement, " OK "will be displayed when the cuff is properly wound. When the cuff is too loose, " "will be displayed. At this time, please wear the cuff correctly and start measuring again. Unit Operation 17 Last 3 Tests Average With power off, press the "MEM" button to activate screen display. After the unit performs a self-diagnosis ,The LCD screen will display the average of the last three measurements of the current memory group. The " AVG " symbol will appear along with the corresponding WHO Blood Pressure Indicator. The Memory Check mode can be accessed by pressing "MEM" button. If looking at the average of other memory groups, set the memory group you want to view before entering the mean view state. (See "Select Memory Group" on Page 12) Unit Operation 18 Memory Deletion Memory for a selected group may be deleted while in Memory Check mode. Press and hold the " GROUP1 " button or " GROUP2 " button for approximately 3 seconds to delete all memory records from the selected group with voice broadcast "Memory Clear" and then transfer into testing mode. Press the "START/STOP " button to turn the unit off. Note: Memory cannot be recovered once it has been deleted. Memory Check You may check past test results by using the "MEM" button. The most recent test result and oldest test result in memory can be viewed by pressing and holding the "MEM" button. Upon activating test results. you can press the "MEM" button to scroll through all test results stored in memory. To check the average results from other groups, please press corresponding "GROUP1" button or "GROUP2" button. Low Battery Indicator The unit will broadcast "Low Battery" when battery life is depleting and unable to inflate cuff for testing. The " " appears simultaneously for approximately 5 seconds prior to shutting off. Replace batteries at this time. No memory loss will occur throughout this process. Unit Operation 19 Static Pressure Measurement In the power down state, press and hold the " START/STOP" button, and then install the batteries. Until the LCD screen is full, release the " START/STOP" button. When the LCD screen displays the double zero, the bloodpressure meter is in static state. Software version is displayed:10 is a software version in the figure. Note: Only Service personnel permitted to access to this mode, the mode unavailable in normal use. Unit Operation 20 Bluetooth requirements Wireless communication The monitor requires a device with: Frequency range : 2.4 Ghz (2400-2483.5 MHz) . Bluetooth 4.0 or later Modulation : GFSK . Android 5.0 or later Antenna gain:0.5dBi . IOS 9.0 or later And works with: . iphone , iPod, iPad . Android Phones and Tablets Bluetooth connection -Using for the first time 1. Download the free "JoyHealth" App: On your mobile phone or table go to www.sejoy.com. 2.Open the App on your phone or tablet. If requested, you should enable Bluetooth on your device. You can enable Bluetooth under the Settings menu on your smart phone or table. 3. Create a new user login, or login with your existing user name and password. 4. Selection device "Blood pressure monitor". -Pairing your monitor with a Smart Device 1. Long press the "memory" button (or the "M" key) on your monitor until the word "boo" flashes on your monitor . Unit Operation 21 Unit Operation 2. Open the APP and click "pair device" button, a popup window will appear. Click "Search device" button to display all sphygmomanometer devices(The display information includes the device model and MAC address), then you can find the sphygmomanometer through the "device Name", click the pictureA film or text can be used to pair the device. Troubleshooting Abnormal phenomenon Cause analysis The armband is tied too tight or too loose, Or the arm strap is tied incorrectly; Processing method Roll the armband correctly 22 The MAC address 3. After the pairing is complete, the device interface switches from boo interface, indicating that the pairing is successful. Move the arm during measurement or Electronic sphygmomanometer Abnormal sphygmomanometer Speaking, nervous or emotional during measurement Incorrect measurement posture Stay quiet, keep your arm steady, and do not move the monitor Instead of talking, take deep breaths to calm your mood and relax your body Adjust posture, see "Blood pressure gauge Wearing" There is interference in charging process or improper operation in measuring process See operation Instructions. The following table shows the error signs that may occur during measurement, possible causes and handling methods. Please measure again using the correct method Error display Er1 Er2 Er3 The cause of the problem The solution Can't detect high and low pressure Please fasten the cuff before measuring Cuff too loose or loose Please fasten the cuff before measuring Improper compression caused Hold the arm or body still and by arm or body movement measure again -Transfer your readings 1. As soon as your measurement is complete, open the app on your smart phone to transfer your reedings. Notr: On the paired smartphone, Bluetooth must be enabled. 2. You can view your blood pressure readings on the app. Er4 Er5 Er6 The pressure exceeds 300mmHg Please fasten the cuff before measuring Check whether the cuff is knotted or the The pressure exceeds 15mmHg vent valve is blocked. If the problem for 3 minutes persists, contact the manufacturer Out of measurement range If the user can not resolve, please contact the manufacturer Battery dead Replace the battery or connect the power adapter (if any). Note: If you cannot solve the abnormal situation by yourself, you can consult the manufacturer or the manufacturer's designated unit by phone. It is forbidden to disassemble and repair without permission. If necessary, professional maintenance personnel can ask the manufacturer for the list of components and circuit schematic diagram. Blood Pressure Information 23 Blood Pressure Information 24 Blood Pressure Blood pressure is the force of blood pushing against the walls of arteries. It is typically measured in millimeters of mercury (mmHg.) Systolic blood pressure is the maximum force exerted against blood vessel walls each time the heart beats. Diastolic blood pressure is the force exerted on blood vessels when the heart is resting between beats. An individual's blood pressure frequently changes throughout the course of a day. Excitement and tension can cause blood pressure to rise, while drinking alcohol and bathing can lower blood pressure. Certain hormones like adrenaline (which your body releases under stress) can cause blood vessels to constrict, leading to a rise in blood pressure. If these measuring numbers become too high, it means the heart is working harder than it should. 200 Upper curve : systolic blood pressure Lower curve: diastolic blood pressure 150 mmHg 100 50 6 12 18 24 Time of day Example: fluctuation within a day (male, 35 years old) WHO Blood Pressure Classification Indicator The DBP-6285L is equipped with a classification indicator based on established guidelines from the World Health Organization. The chart below (color coded on monitor unit) indicates test results. Severe Hypertension Moderate Hypertension Mild Hypertension High-normal Normal Optimal Optimal : Blood Pressure Classification Indicator Blood Pressure Information 25 Health Reminder Hypertension is a dangerous disease that can affect the quality of life. It can lead to a lot of problems including heart failure, kidney failure, and cerebral hemorrhaging. By maintaining a healthy lifestyle and visiting your physician on a regular basis, hypertension and relative diseases are much easier to control when diagnosed in their early stages. Systolic ( mmHg ) 180 160 140 130 120 Severe Hypertension Moderate Hypertension Mild Hypertension High-normal Normal Optimal 80 85 90 100 110 Diastolic ( mmHg ) Note: Do not be alarmed if an abnormal reading occurs. A better indication of an individual's blood pressure occurs after 2-3 readings are taken at the same time each day over an extended period of time. Consult your physician if test results remain abnormal. Blood Pressure Q&A 26 Q: What is the difference between measuring blood pressure at home or at a professional healthcare clinic? A: Blood pressure readings taken at home are now seen to give a more accurate account as they better reflect your daily life. Readings can be elevated when taken in a clinical or medical environment. This is known as White Coat Hypertension and may be caused by feeling anxious or nervous. Note: Abnormal test results may be caused by: 1. Improper cuff placement Make sure cuff is snug-not too tight or too loose. Make sure bottom of the cuff is approximately 1-2cm (1/2'') above the elbow joint. 2. Improper body position Make sure to keep your body in an upright position. 3. Feeling anxious or nervous Take 2-3 deep breaths, wait a few minutes and resume testing. Q: What causes different readings? A: Blood pressure varies throughout the course of a day. Many factors including diet, stress, cuff placement, etc. may affect an individual's blood pressure. Q: Should I apply the cuff to the left or right arm? What is the difference? A: Either arm can be used when testing, however, when comparing results, the same arm should be used. Testing on your left arm may provide more accurate results as it is located closer to your heart. Q: What is the best time of day for testing? A: Morning time or any time you feel relaxed and stress free. Maintenance 1. Avoid dropping, slamming, or throwing the unit. 27 Maintenance 28 4. Cuff Cleaning: Do not soak cuff in water! Apply a small amount of rubbing alcohol to a soft cloth to clean cuff's surface. Use a damp cloth (water-based) to wipe clean. Allow cuff to dry naturally at room temperature. The cuff must be cleaned and disinfected before use between different users. 5. Do not use petrol, thinners or similar solvents. 2. Avoid extreme temperatures. Do not expose unit directly under sunshine. 6. Remove batteries when not in operation for an extended period of time. 3. When cleaning the unit, use a soft fabric and lightly wipe with mild detergent. Use a damp cloth to remove dirt and excess detergent. 7. Do not disassemble product. 8. It is recommended the performance should be checked every 2 years. 9. Expected service life: Approximately three years at 10 tests per day. 10.No service and maintenance while it is in use and maintenance only be performed by service personnel. Service and maintenance require parts, repair, technical support will be provided. Specifications 29 Specifications 30 Product Description Arm-type Fully Automatic Blood Pressure Monitor Model DBP-6285L Display LCD Digital Display Size:94mm x 90.6mm3.7" x 3.57" Measurement Method Oscillometric Method Systolic Pressure 60mmHg260mmHg Measurement Range Diastolic Pressure Pressure Pressure 4 0mmH g200 mmH g 0mmHg299mmHg ±3mmHg Pressurization Memory Pulse Pulse 30 ~ 180 Beats/Minute ±5% Automatic Pressurization 2x150 Memories in Two Groups with Date and Time Irregular Heartbeat Detection Function WHO Classification Indicator Last 3 Tests Average Low Battery Detection Automatic Power-Off Voice Backlight Power Source Battery Life Unit Weight Unit Dimensions Cuff Circumference Bluetooth Lithium battery 3.7 V or DC5.0v 1000mA medical external power supply (DC5.0V, 1000mA)(Optional,If users want to purchase other adapters, they need to meet the requirements of IEC 60601-1 ) Approximately 2 months at 3 tests per day Approx.319g (11.25 oz) (excluding battery) Approx.150mm X 108mm X 65mm5.90" x 4.25" x 2.56" Approx.135 (W) x 485(L) mm (Medium cuff: Fits arm circumference 22-36 cm) Operating Environment Storage Environment Temperature Humidity Pressure Temperature: Humidity 10 ~ 40 (50~104) 15% ~ 93%RH 800hPa~1060hPa -25~55 (-13~131) 93% RH Classification: Internal Powered Equipment,Type BF ,Cuff is the Applied Part Ingress Protection Rating: Bluetooth IP21, Indoor Use Only Modulation Type GFSK Version 5.0.1 BT Signal mode Operation frequency 2.4GHz(2400~2483.5MHz) Antenna gain 0 dBi Bandwidth 2.0 MHz Specifications are subject to change without notice. Safety Standard(included but not limited): 1. IEC 80601-2-30, medical electrical equipment - part 2-30: particular requirements for the basic safety and essential performance of automated noninvasive sphygmomanometers. (Cardiovascular) 2. ISO 81060-2, non-invasive sphygmomanometers - part 2: clinical validation of automated measurement type. (Cardiovascular) 3. AAMI / ANSI ES 60601-1:2005/(R)2012 and C1:2009/(R)2012 and, a2:2010/(r)2012 (consolidated text) medical electrical equipment -- part 1: general requirements for basic safety and essential performance 4. AAMI/ANSI/IEC 60601-1-2, Medical Electrical Equipment -- Part 1-2: General Requirements For Basic Safety And Essential Performance -- Collateral Standard: Electromagnetic Disturbances -- Requirements And Tests (General II (ES/EMC)). 5. IEC 60601-1-11, medical electrical equipment - part 1-11: general requirements for basic safety and essential performance - collateral standard: requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment. Warranty 31 The Blood Pressure Monitor is guaranteed for 2-year from the date of purchase. If the Blood Pressure Monitor does not function properly due to defective components or poor workmanship, we will repair or replace it freely. The warranty does not cover damages to your Blood Pressue Monitor due to improper handling. Please contact local retailer for details. Electromagnetic Compatibility Information 32 The device satisfies the EMC requirements of the international standard IEC 60601-1-2. The requirements are satisfied under the conditions described in the table below. The device is an electrical medical product and is subject to special precautionary measures with regard to EMC which must be published in the instructions for use. Portable and mobile HF communications equipment can affect the device. Use of the unit in conjunction with non-approved accessories can affect the device negatively and alter the electromagnetic compatibility. The device should not be used directly adjacent to or between other electrical equipment. Table 1 Guidance and declaration of manufacturer-electromagnetic emissions The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that it is used in such an environment. Emissions test Compliance Radiated emission CISPR 11 Group 1, class B. Electromagnetic environment -guidance The device uses RF energy only for its internal function. Therefore, its emissions are very low and are not likely to cause any interference in nearby electronic equipment. Conducted emission CISPR 11 Group 1, class B. The device is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes. Harmonic emissions IEC 61000-3-2 Voltage fluctuations/ flicker emissions IEC 61000-3-3 Class A Complies Electromagnetic Compatibility Information 33 Table 2 Guidance and declaration of manufacturer-electromagnetic immunity The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that it is used in such an environment. IMMUNITY test IEC 60601 test level Compliance Electromagnetic environment level -guidance ± 8 kV ± 8 kV Floors should be wood, concrete Electrostatic contact contact or ceramic tile. If floors are discharge (ESD) ±2 kV,±4 kV, ±2 kV,±4 kV, covered with synthetic material, IEC 61000-4-2 ±8 kV, ±8 kV, the relative humidity should be ±15 kV air ±15 kV air at least 30 %. Electrostatic transient/burst IEC 61000-4-4 ± 2 kV , ± 2 kV , Mains power quality should be that 100kHz, for 100kHz, for of a typical commercial or hospital AC power port AC power port environment. Surge IEC 61000-4-5 ±0.5kV, ±1kV ±0.5kV, ±1kV Mains power quality should be that (differential (differential of a typical commercial or hospital mode) mode) environment. Voltage dips, short interruptions and voltage variations on power supply input lines 0 % UT; 0 % UT; 0,5 cycle 0,5 cycle At 0°, 45°, 90°, At 0°, 45°, 90°, 135°, 180°, 225° , 270° and 315° 135°, 180°, 225° , 270° and 315° Mains power quality should be that of a typical commercial or hospital 0 % UT; 1 cycle 0 % UT; 1 cycle environment. and and 70 % UT; 70 % UT; 25/30 cycles 25/30 cycles Single phase: Single phase: at 0° at 0° IEC 61000-4-11 0 % UT; 0 % UT; 250/300 cycle 250/300 cycle Electromagnetic Compatibility Information 34 Table 2(continued) Guidance and declaration of manufacturer-electromagnetic immunity The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that it is used in such an environment. IMMUNITY test IEC 60601 test level Compliance Electromagnetic environment level -guidance Portable and mobile RF communications equipment should be used no closer to any part of the device, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Radiated RF EM 3V/m or 10 V/m 3V/m or 10 V/mRecommended seperation distance 80 MHz fields IEC 61000-4-3 80MHz-2.7 Ghz 80%AM at 1kHz 80MHz-2.7 Ghz 80%AM 1kHz at to 800 MHz 800 MHz to 2.7 Ghz where P the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the is recommended separation distance in metres (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, a should be less than the compliance level in each frequency range. Interference may occur in the vicinity of equipment marked with the following symbol: Conducted disturbances Induced by RF fields IEC 61000-4-6 3 V in 0.15 MHz- 80 MHz 6 V in ISM and/or amateur radio bands between 0.15 MHz and 80 MHz 80 % AM at 1kHz Portable and mobile RF communications equipment should be used no closer to any part of the device, including cables, than the recommended separation distance 3 V in 0.15 MHz- 80 MHz calculated from the equation applicable to the frequency of the transmitter. Recommended seperation distance 80 MHz 6 V in ISM to 800 MHz 800 MHz to 2.7 Ghz where P is and/or amateur the maximum output power rating of the radio bands between 0.15 MHz and 80 MHz 80 % transmitter in watts (W) according to the transm- itter manufacturer and d is the recommended separation distance in metres (m). Field strengths from fixed RF transmitters, as determined by an AM at 1kHz electromagnetic site survey, a should be less than the compliance level in each frequency range. Interference may occur in the vicinity of equipment marked with the following symbol: Power frequency (50/60 Hz) magnetic field 30 A/m; 50Hz or 60Hz IEC 61000-4-8 30 A/m; 50Hz or 60Hz Power frequency magnetic fields should be at levels charactertic of a typical location in a typical commercial or hospital environment. Electromagnetic Compatibility Information 35 Table 3 Guidance and declaration of manufacturer-electromagnetic immunity Nowadays, many RF wireless equipments have being used in various healthcare locations where medical equipment and/or systems are used. When they are used in close proximity to medical equipment and/or systems, the medical equipment and/or systems' basic safety and essential performance may be affected. Arm-type Fully Automatic Digital Blood Pressure Monitor has been tested with the immunity test level in the below table and meet the related requirements of IEC 60601-1-2:2014. The customer and/or user should help keep a minimum distance between RF wireless communications equipment and this medical equipment and/or systems as recommended below. Test frequency (MHz) 385 450 710 745 780 810 870 930 Band (MHz) 380-390 430-470 Service Modulation TETRA 400 GMRS 460 FRS 460 Pulse modulation 18Hz FM ± 5 kHz deviation 1 kHz sine Maximum power (W) 1.8 2 704-787 LTE Band Pulse modulation 0.2 13, 17 217Hz Distance (m) 0.3 0.3 0.3 GSM 800/900, TETRA 800, Pulse 800-960 iDEN 820, modulation 2 0.3 CDMA 850, LTE Band 5 18Hz Immunity test level (V/m) 27 28 9 28 1720 GSM 1800; CDMA 1900; Pulse 1845 1700-1990 GSM 1900; DECT; LTE Band 1, 3, modulation 217Hz 2 0.3 28 4, 25; UMTS 1970 2450 2400-2570 Bluetooth,WLAN, 802.11 b/g/n,RFID Pulse modulation 2 0.3 28 2450,LTE Band 7 217Hz 5240 WLAN Pulse 5500 5100-5800 802.11 modulation 0.2 0.3 9 a/n 217Hz 5785 Electromagnetic Compatibility Information 36 Table 4 Recommended separation distances between portable and mobile RF communications equipment and the device The device is intended for use in an electromagnetic environment in which radiated therefore disturbances are controlled. The customer or the user of the device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the device as recommended below, according to the maximum output power of the communications equipment. Rated maximum Separation distance according to frequency of transmitter output power of m transmitter 80 MHz to 800 MHz 800 MHz to 2.7 GHz W 0.01 0.12 0.23 0.1 0.38 0.73 1 1.2 2.3 10 3.8 7.3 100 12 23 For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. NOTE1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. NOTE2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. Additional Notes 37 Additional Notes 38 Important Instructions Before Use 1. WARNING: Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally. 2.WARNING: PORTABLE RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of Fully Automatic Digital Blood Pressure Monitor, including cables specified by the MANUFACTURER. Otherwise, degradation of the performance of this equipment could result. 3.The software identifier refer to the software evaluation report , and the file code is NYRJ211220005. 4.verify manometer pressure accuracy: In the power down state, press and hold the " START/STOP" button, and theninstall the batteries. Until the LCD screen is full, release the " START/STOP" button. When the LCD screen displays the double zero, the bloodpressure meter is in static state. At this point, 500ml gas capacity, calibrated standard pressure gauge and manual pressure device can be connected to the sphygmomanometer through the sleeve interface of the sphygmomanometer, and manual pressure can be applied to the effective display range of the sphygmomanometer, and then the difference between the reading of the sphygmomanometer and that of the standard pressure gauge can be compared.This mode can be used to verify manometer pressure accuracy. 5.Contraindications: Product is not intended for infants or individuals who cannot express their intentions. 6.Indications for use: The digital blood pressure monitor is used to measure blood pressure and pulse rate from upper-arm. 7.The patient is the operator: the PATIENT is an intended OPERATOR. the PATIENT Do not carry out other maintenance operations except to replace the battery. 8.WARNING: Do not modify this equipment without authorization of the manufacturer. 9. ESSENTIAL PERFORMANCE Maintenance advice: Pressure calibration will be carried out when this product leaves the factory. Patients can use the method described in the section "Verify Manometer Pressure Accuracy" to verify the accuracy. If the accuracy deviation is large, please contact the manufacturer to recalibration. 10.Mechanical strength and resistance to heatThe resistance to heat will be retained by device during the EXPECTED SERVICE LIFE of the ME EQUIPMENT. 11.Do not place the blood pressure monitor and cuff at will. It will cause asphyxiation if the child swallows or twine around his neck. 12.The cuff and the case of the blood pressure monitor have been tested for biocompatibility and do not contain allergenic or harmful materials.Please stop using it if allergy occurs during use. 13.Warning: Non-professionals do not modify the equipment, otherwise it will make the equipment measurement is not accurate. 14.Warning: Do not expose the equipment for a long time, otherwise it will reduce the performance of the equipment. 15.Warning: This device is not used for children and pets 16.Clean: The equipment can be cleaned by lay operator according to the cleaning procedures in the instructions 17.Warning: Do not use a damaged cuff for blood pressure measurement. 18.Warning: When measuring with the cuff, if the tester feels seriously uncomfortable, press the button of the blood pressure monitor to deflate the cuff, or remove the cuff directly from the arm. 19.Warning: If an unexpected reading occurs, the operator can take several more measurements and consult a doctor. 20.Warning: This equipment is used outside the specified environment, may damage the equipment, and may be inaccurate measurement. 21.Warning: The Operator should not use the system and should inform the customer service, if the ESSENTIAL PERFORMANCE is lost or degraded due to EM DISTURBANCES. 22.Warning: Use of accessories, transducers and cables other than those specified or provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation. 23.Warning: Failure to use this equipment in the specified type of shielded location could result in degradation of the performance of this equipment, interference with other equipment or interference with radio services 24.ME equipment not intended for use in conjunction with flammable agents "ME equipment not intended for use in oxygen rich environment" Additional Notes 39 Correct Disposal of This Product (Waste Electrical & Electronic Equipment) This marking shown on the product indicates that it should not be disposed with other household waste at the end of its life. To prevent potential harm to the environment or to human health, please separate this product from other types of wastes and recycle it responsibly. When disposing this type of product, contact the retailer where product was purchased or contact your local government office for details regarding how this item can be disposed in an environmentally safe recycling center. Business users should contact their supplier and check the terms and conditions of the purchasing agreement. This product should not be mixed with other commercial wastes for disposal. This product is free of hazardous materials.