HoMedics BPA-2000-EU blood pressure unit
Contents
1. NOTE 1 At 80 MHz and 800 MHz the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people a Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile radios amateur radio AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the ELE007839V1 is used exceeds the applicable RF compliance level above the ELE007839V1 should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as reorienting or relocating the ELE007839V1 b Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m Table 4 Recommended separation distances between portable and mobile RF communications equipment and the EQUIPMENT or SYSTEM for ME EQUIPMENT or ME SYSTEM that are not LIFE SUPPORTING Recommended separation distances between portable and mobile RF communications equipment and the ELE007839V1 Fitness Equipment The BPA 2000 EU is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The custom2. 120 130 140 150 160 180 Systolic blood pressure mmHg Optimal Norm Norm G1 G2 lt 120 120 129 130 139 140 159 160 179 lt 80 80 84 85 89 90 99 100 109 caution Only a physician GP can tell you your normal blood pressure range and the point at which you are at risk Consult your physician to obtain these values If the measurements taken with this product fall outside the range consult your physician GP SAFETY INFORMATION Caution consult accompanying documents Type B applied part Disposal do not dispose of this product as unsorted municipal waste Collection of such waste separately for special treatment is necessary CE mark conforms to essential C 0120 requirements of the Medical Device Directive 93 42 EEC Lt gt w Manufacturer Direct current SN Specifies serial number caution This device is intended for adult use only This device is intended for non invasive measuring and monitoring of arterial blood pressure It is not intended for use on extremities other than the arm Do not confuse self monitoring with self diagnosis This unit allows you to monitor your blood pressure Do not begin or end medical treatment based solely on the readings from this unit Always consult your physician first If you are taking medication consult your physician to determine the most appropriate time to measure your blood pressure Never
3. Pulse Pulse minute VW Deflating CUFF is deflating 10 Time hour minute Current time I Memor The displayed measurement values is from the If y memory kPa kPa Measurement Unit of the blood pressure mmHg mmHg Measurement Unit of the blood pressure L O co Lowbattery Batteries are low and need to be replaced D Arrhythmia Irregular heartbeat Grade The grade of the blood pressure MONITOR COMPONENTS CUFF AIR HOSE AIR CONNECTOR P MEM UP TOUCH KEY SET DOWN BUTTON START STOP BUTTON BATTERY LCD DISPLAY COMPARTMENT List 1 Blood Pressure Monitor 2 Cuff A 1 Slide off the battery cover 3 4 AA batteries 4 User manual 2 Install the batteries by matching the correct polarity as shown AT 3 Replace the cover Replace the batteries whenever the below happen Thel 0 Z shows The display dims The display does not light up AC adaptor Alternatively an AC adaptor powered mode CAUTION is available 100 240V 50 60HZ 400mA Remove batteries if the device is not likely to be used for You can purchase the AC adaptor some time PP ADPR2K3K EU from the HoMedics website This product uses the Oscillometric Measuring method to detect blood pressure Before every measurement the unit establishes a zero pressure eguivalent to the air pressure Then it starts inflating the arm cuff meanwhile the unit detects pressure oscillations generated by beat to beat pulsatile whi
4. If the cuff is not assembled at first use put the end of the cuff which is furthest away from the tube through the D ring to form a noose 2 Apply the tube to the left side of the device 3 Remove tight fitting clothing from your left upper arm and position the cuff at approximately 2 3 cm above the elbow so that the tube is centred at the middle of the arm The tube must face downward towards the hand 4 Pull gently at the end of the cuff so that it tightens easily and smoothly around the arm The cuff is secured by pulling the Velcro fastener towards the cuff y You should be able to fit two fingers between the cuff and your arm The cuff should not be fitted any tighter than this 6 Relax your body and rest your arm on a table with your palm up so that the cuff is positioned at the same height as the heart Make sure that the tube does not bend If it is not possible to fit the cuff on the left arm it can be placed on the right arm instead However it is important that all measurements are carried out on the same arm If the measurement is to be taken on the OP right arm the artery symbol on the cuff should be positioned above the main artery Press the arm s arteries with two fingers at approximately 2 gt cm above the elbow on the inside of the arm to find out where the pulse is strongest This is the main artery Worth knowing about blood pressure measurement Blood pressure measurements should be perfo
5. change a prescribed medication without consulting your physician This unit is not suitable for continuous monitoring during medical emergencies or operations e If the cuff pressure exceeds 40 kPa 300 mmHg the unit will automatically deflate Should the cuff not deflate when pressures exceeds 40 kPa 300 mmHg detach the cuff from the arm and press the 0 button to stop inflation To avoid measurement errors carefully read this manual before using the product The equipment is not AP APG equipment and not suitable for use in the presence of a flammable anesthetic mixture with air of with oxygen or nitrous oxide The operator shall not touch output of AC adapter and the patient simultaneously e To avoid measurement errors please avoid the condition of strong electromagnetic field radiated interference signal or electrical fast transient burst signal when using the AC adaptor The user must check that the equipment functions safely and see that it is in proper working condition before being used e Please note that Luer lock connectors are not used on the product and please DO NOT change any provided connectors LCD display signal Symbol SYS Description Systolic blood pressure lt 7 i lt a SEP gac gt at ant i vu Q 3 3 a Explanation High pressure result DIA Diastolic blood pressure Low pressure result Pulimin
6. the pressure when the heart is at ease and filling with blood before the next muscle contraction The connection between values mmHg is expressed as e g 130 over 85 which means that the systolic pressure is 130 and the diastolic pressure is 85 Why is it important to keep an eye on your blood pressure Many of today s most common diseases are connected to hypertension also referred to as high blood pressure Hypertension is closely connected to cardiovascular diseases and for people in the danger zone the blood pressure provides an important tool to keep an eye on the development Diastolic blood entering vein Systolic blood discharging artery What are systolic pressure and diastolic pressure When ventricles contract and pump blood out of the heart blood pressure reaches its maximum value the highest pressure in the cycle is known as systolic pressure When the heart relaxes between heartbeats the lowest blood pressure is diastolic pressure High normal Blood Pressure 4 What is the standard blood pressure E classification tio Grade 3 hypertension severe 7 v Grade 2 hypertension moderate Below illustrates the blood pressure classification mode by 5 100 EEEE w rade pertension mi World Health Organization WHO and International 95 we saaana Society of Hypertension Isa in 1999 3 90 E 2 85 5 50 Normal Blood Pressure 2 Optimal a Blood Pressure
7. HOMEDICS Automatic Arm Blood Pressure Monitor Instruction Manual year guarantee BPA 2000 EU HOMEDICS BLOOD PRESSURE MONITOR Before use Before the blood pressure monitor is taken into use a number of basic steps should be observed Please read this manual thoroughly before the blood pressure monitor is used for the first time and keep the manual for future use The blood pressure monitor is intended for home use only Any measurement is solely for your information and can under no circumstances replace a visit to the doctor The blood pressure measurements should always be assessed by a qualified person a doctor nurse or similar who is familiar with the user s general medical condition By regular use and by keeping a record of the results this person can be kept well informed about developments in the user s blood pressure Measurements must never be interpreted by the user with the aim of changing levels in the use of medicine as prescribed by a doctor The doctor s instructions must be followed AT ALL TIMES Use of appropriate cuff size is crucial to correct measurement Follow the instructions presented in this manual and printed on the cuff to ensure that the correct cuff size is used The blood pressure monitor is not suited for users who suffer from arrhythmia heart rhythm disturbances and errors may occur in the measurement results if the user has suffered a stroke suffers from cardiovascular diseases ha
8. ch is used to determine the systolic and diastolic pressure and also pulse rate The device also compares the longest and the shortest time intervals of detected pulse waves to mean time interval then calculates standard deviation The device will display a warning signal with the reading to indicate the detection of irregular heartbeat when the difference of the time intervals is over 25 SETTING DATE TIME AND MEASUREMENT UNIT It is important to set the clock before using your blood pressure monitor so that a time stamp can be assigned to each record that is stored in the memory year 2000 2050 time 24 H 1 When the unit is off hold pressing SET for 3 seconds to enter the mode for year setting SET 2 Press the MEM to change the YEAR 3 When you get the correct year press SET and it will turn to the next step automatically 4 Repeat step 2 and 3 to set 5 Repeat step 2 and 3 to set the MONTH and DAY the HOUR and MINUTE A A ME ME SE SE v 4 Aw 4D I 6 Repeat step 2 and 3 to set the UNIT Z M a A a MEM m f mmHg N sE SET x 7 After the unit is set done will show then turn off automatically HOW TO USE THE BLOOD PRESSURE DEVICE Fitting the cuff Correct cuff size is critical to accurate measurement This monitor comes with a standard size 22 32cm arm cuff A large size cuff 32 42cm is available from the HoMedics website www homedics co uk 1
9. concrete or ceramic tile If floor are covered with synthetic material the relative humidity should be at least 30 Electrical fast 2 kV for power 2kV for power Mains power quality should be that of a transient burst supply lines supply lines typical commercial or hospital environment IEC 61000 4 4 Surge IEC 1 kV line s to 1 kV differential Mains power quality should be that of a 61000 4 5 line s mode typical commercial or hospital environment 50Hz magnetic field IEC 61000 4 8 Voltage dips short lt 5 UT lt 5 UT Mains power quality should be that of a interruptions and gt 95 dip in UT gt 95 dip in UT typical commercial or hospital environment voltage variations for 0 5 cycle for 0 5 cycle If the user of the BPA 2000 EU requires on power supply continued operation during power mains input lines IEC 40 UT 40 UT interruptions it isrecommended that the 61000 4 11 60 dipin UT 60 dipin UT BPA 2000 EU be powered from an for 5 cycles for 5 cycles uninterruptible power supply or a battery 70 UT 70 UT 30 dipin UT 30 dip in UT for 25 cycles for 25 cycles lt 5 UT lt 5 UT gt 95 dip in Ut gt 95 dip in Ur for 5 sec for 5 sec Power frequency 3A m 3A m Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment NOTE UT is the a c mains volta
10. ded up tightly The device must not be activated if it is not appropriately fitted to the upper arm Avoid dropping the device and do not subject it to heavy pressure The device must not be exposed to extreme shocks such as being dropped on the floor The device is intended for use in private households only and is only suited for use with adults over 18 years of age If the highly unlikely incident should occur that the cuff continues to inflate and does not stop immediately remove the cuff from the upper arm Battery Directive This symbol indicates that batteries must not be disposed of in the domestic waste as they contain X substances which can be damaging to the environment and health Please dispose of batteries in designated collection points WEEE explanation This marking indicates that this product should not be disposed with other household wastes et throughout the EU To prevent possible harm to the environment or human health from uncontrolled waste disposal recycle it responsibly to promote the sustainable reuse of material resources To return MENEM your used device please use the return and collection systems or contact the retailer where the product was purchased They can take this product for environmental safe recycling 13 Table 1 Guidance and manufacture s declaration electromagnetic emissions for all EQUIPMENT and SYSTEMS Guidance and manufacture s declaration electromagnetic emission T
11. e g 2 becomes 3 and so on and the last record 60 is dropped from the list Deleting your records If you did not get the correct measurement you can delete all results using the ri following steps gt gt 1 When the device is off hold MEM for 3 seconds The flash display will show dEL ALL 2 Press SET to confirm deleting and the monitor will turn off automatically 3 If you do not want to delete the record press to cancel 4 If there is no record the right display will show Error search This section includes a list of error messages and frequently asked questions for problems you may encounter with your blood pressure monitor If irregularities occur during use please check the following items PROBLEM SYMPTOM CHECK THIS REMEDY Batteries are exhausted Replace with new batteries N Display is dim or will o power 3 not light up Batteries are inserted P Insert the batteries correctly incorrectly A Show on the Low batteries Lo o display Batteries are low Replace with new batteries E 1 shows The cuff is not secure Refasten the cuff and then measure again E 2 shows The cuff is very tight ina cuff and then measure again The pressure of the cuff is Refasten the cuff and then E 3 shows 3 excess measure again Movement can affect the The monitor detected measurement Relax for a E 10 or E 11 shows P 4 motion while measuring moment and then measure Erro
12. er or the user of the BPA 2000 EU can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the BPA 2000 EU as recommended below according to the maximum output power of the communications equipment Separation distance according to frequency of transmitter Rated maximum output m power of transmitter w 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz d 1 167 VP d 1 167 VP d 2 333 VP 0 01 0 167 0 167 0 233 0 1 0 369 0 369 0 738 1 1 167 1 167 2 333 10 3 690 3 690 7 338 100 11 67 11 67 23 330 For transmitters rated at a maximum output power not listed above the recommended separation distance din meters 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 NOTE 1 At 80 MHz and 800 MHz the separation distance for the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people HOMEDICS C Er HoMedics Group Ltd HoMedics House Somerhill Business Park Five Oak Green Road Tonbridge Kent TN11 OGP UK Register your product today at http www homedicsgroup com register IB BPA 2000EU 0912 01
13. ff Mode of operation Continuous operation Degree of protection Type B applied part Protection against ingress of water IPX O Cleaning and maintenance The blood pressure monitor and the cuff can be wiped with a soft cloth moistened with a mild detergent and wiped dry with a soft dry cloth or paper towel Never use strong caustic detergents as these may cause damage to the synthetic parts Also never use diluents alcohol or kerosene to clean the device Safety and electrical devices When the device is not used store it in a safe place Only use the device on the upper arm not on other body parts When the device is not used for extended periods of time it is recommended that you remove the batteries to avoid leakage which may cause damage to the device If the device has been stored at very low temperatures near the freezing point please allow it to obtain room temperature before using it again Neither device nor cuff must be dissembled as this may cause serious damage to the device If repair is necessary the device must be returned to the store where it was purchased Do not attempt to open the device or adjust the inner parts yourself Do not submerge the device in water or other liquids as this will cause damage to the device Do not expose the device nor the cuff to extreme temperatures moisture or direct sunlight Protect the device against dust The cuff and the tube should not be fol
14. ge prior to application of the test level Table 3 Guidance and manufacture s declaration electromagnetic immunity for ME EQUIPMENT and ME SYSTEMS that are not LIFE SUPPORTING Guidance and manufacture s declaration electromagnetic immunity The BPA 2000 EU is intended for use in the electromagnetic environment specified below The customer or the user should assure that it is used in such an environment Immunity test IEC 60601 test level Compliance level Electromagnetic environment guidance Conducted RF IEC 61000 4 6 Radiated RF IEC 61000 4 3 3 Vrms 150 kHz to 80 MHz 3 V m 80 MHz to 2 5 GHz 3 Vrms 3V m Portable and mobile RF communications equipment should be used no closer to any part of the YS 6100 including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance d 1 167 VP d 1 167 VP 80 MHz to 800 MHz d 2 333 VP 800 MHz to 2 5 GHz where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and d is the 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
15. he BPA 2000 EU is intended for use in the electromagnetic environment specified below The customer of the user of the BPA 2000 EU should assure that it is used in such and environment Harmonic emissions IEC 61000 3 2 Not applicable Voltage fluctuations flicker emissions IEC 61000 3 3 Not applicable Emission test Compliance Electromagnetic environment guidance The BPA 2000 EU uses RF energy only for its internal RF emissions Group 1 function Therefore its RF emissions are very low and are CISPR 11 P not likely to cause any interference in nearby electronic equipment RF emission CISPR 11 Class B The BPA 2000 EU is suitable for use in all establishments other than domestic and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes Table 2 Guidance and manufacture s declaration electromagnetic immunity for all ME EQUIPMENT and ME SYSTEMS Guidance and manufacture s declaration electromagnetic immunity The BPA 2000 EU is intended for use in the electromagnetic environment specified below The customer or the user of BPA 2000 EU should assure that it is used in such an environment Immunity test IEC 60601 test level Compliance level Electromagnetic environment guidance Electrostatic discharge ESD IEC 61000 4 2 6 kV contact 8 kV air 6 kV contact 8 kV air Floors should be wood
16. r Message again E 20 or E21 shows Measure incorrectly sees moment and then measure again Retake the measurement If the problem persists contact the retailer or our customer Eexx shows on the service department for further System error a display assistance Refer to the warranty for contact information and return instructions If the device still does not function please contact the store where the device was purchased Do not attempt to open the device or adjust any of the inner parts yourself Specifications Power supply Battery powered mode 6VDC 4 AA batteries AC adaptor powered mode 100 240V 50 60HZ 400mA You can purchase the AC adaptor PP ADPR2K3K EU from the HoMedics website Display mode Digital LCD V A 93 61mm Measurement mode Oscillographic testing mode Measurement range Pressure 0 40kpa 0 300mmHg pulse value 40 199 times minute Accuracy Pressure 15 25 C within 0 4kpa 3mmHg 10 C 40 C out of 15 C 25 C within 0 8kpa 6mmHg pulse value 5 Normal working condition Temperature 5 C 40 C Relative humidity lt 80 Storage amp transportation condition Temperature 20 C 60 C Relative humidity 10 93 Measurement perimeter of the upper arm About 22cm 32cm Weight Approx 353g Excluding the batteries External dimensions Approx 140 120 70mm Attachment 4 AA batteries user manual cu
17. rmed in quiet and comfortable surroundings as measurements can be affected by high or low temperatures The blood pressure should be measured at normal body temperatures Do not move or speak during measurement Keep your feet flat on the floor Do not touch the cuff or the blood pressure device during measurement To obtain the best possible measurement the blood pressure should be measured at approximately the same time every day and on the same arm If you are to perform several successive measurements please wait 5 minutes between each measurement The measurements are for guidance only If you have doubts about your blood pressure consult your doctor The blood pressure device automatically deflates when the pressure exceeds 300 mmHg The product is not suited for persons suffering from arrhythmia heart rhythm disturbances Measurement errors may occur if the user suffers from diabetes poor blood circulation kidney problems or has suffered a stroke The blood pressure changes with every heartbeat and is consequently changing constantly 24 hours a day The measurement of blood pressure can be influenced by the user s position condition or other factors To obtain the highest degree of accuracy it is recommended that the measurement is taken 1 hour after workout bathing finishing a meal consuming alcoholic or caffeine beverages or after smoking Before measurement it is recommended that you sit still and relax for 15 minutes The u
18. s a very low blood pressure or suffers from other symptoms such as circulatory diseases diabetes kidney diseases arterial sclerosis deposits in the arteries or poor peripheral blood circulation e g in hands and feet Electromagnetic disturbances The device contains sensitive electronic components Keep it clear of strong electric or electromagnetic fields in the immediate surroundings e g mobile telephones microwave ovens as these may temporarily reduce measurement accuracy Use the blood pressure monitor only for its original purpose The device is intended for measurement of blood pressure and pulse with adult persons Do not apply the monitor to infants nor to persons who cannot express their permission The device must not be operated by children The blood pressure monitor functions in accordance with the oscillometric measurement principle These blood pressure changes are measured in the cuff on the basis of the arm pulse and are converted into a numerical value of the current blood pressure Simultaneously the number of pulse beats are registered and calculated as number of pulse beats per minute There are two kinds of discernible blood pressures Both are expressed in mmHg millimetres on the mercury column The systolic and the diastolic The systolic the high blood pressure states the pressure when the heart chambers contract to send blood through your body and the diastolic the low blood pressure states
19. ser should not be physically tired or exhausted when the measurement is taken The user must not talk or move arm or hand during measurement How to measure blood pressure 1 Press the U to turn on the monitor and it will start and finish the whole measurement automatically 2 When the measurement is completed the cuff automatically deflates and the display will show the systolic pressure the diastolic pressure and the pulse The measurement is simultaneously stored in the monitor s memory 3 The device automatically switches off approximately 1 minute after use but can also be switched off manually by pressing the 0 button NOTE If necessary a measurement can be interrupted by pressing the 0 button The cuff will subsequently deflate immediately The cuff will automatically re inflate if the device determines that the body requires higher pressure to complete the measurement Recalling records A 1 Please press the MEM to show the recent record M 2 Press the MEM or SET to get the record you want UP A e a DOWN al SET al we LL The number of the record K PE DR date and time will be shown 0 A H b accordingly The current record is The month and day The in buaii time shown will show and alternate L with date J caution The most recent record 1 is shown first Each new measurement is assigned to the first 1 record All other records are pushed back one digit
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