BLOOD PRESSURE MONITOR
Contents
1. This device is contraindicated for any female subject who may be suspected of or is pregnant Besides provided inaccurate readings the affects of this device on the fetus are unknown P 0 In DISPLAY GUIDE SYS DIA l mmHg n a kPa j WA LI LIJ Pul min Qo Ti EIC ULL LILI Ci A A Systolic Blood Pressure 85 8 High blood pressure DIA Diastolic Blood Pressure Low blood pressure Pulimin Pulse per minute Beats per minute BPM User 1 User 2 Start measurement for user 1 Start measurement for user 2 Shocking reminder Shocking will result in inaccurate LAM Low Battery Low battery and please replace the batteries Measurement unit of blood pressure mmHg mmHg ImmHg 0 133kPa kPa kPa oa of blood pressure 88 88 Memory Display the serial number of the measurement 92 88 Current Time Month Day Hour Minute wy Deflating Exhaust the air in the cuff QW Arrhythmia Irregular Heartbeat Q2 Heartbeat Heartbeat detection during the measurement INSTALLING AND REPLACING THE BATTERIES Battery powered mode 6VDC 4 AA alkaline batteries 1 Slide off the battery cover 2 Install the batteries by matching the correct polarity as shown 3 Close the battery door caution n order to get the best effect and protect you monitor please use the right battery which complies with CE2. supply input Hage eon 40 UT NIA IEC 61000 4 11 60 dip in UT or 5 cycles 70 UT NIA 30 dip in UT or 25 cycles lt 5 UT N A gt 95 dip in UT or 5 sec Power frequency 3A m 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 voltage prior to application of the test level Table 4 Guidance and manufacturer s declaration electromagnetic immunity for ME EQUIPMENT and ME SYSTEMS that are not LIFE SUPPORTING Guidance and manufacture s declaration electromagnetic emission The BPA 9300 is intended for use in the electromagnetic environment specified below The customer or user of the BPA 9300 should assure that it s used in such an environment NOTE 2 These guidelines may not app reflection from structures objects and people y IEC 60601 Compliance Electromagnetic Immunity test k test level level environment guidance Portable and mobile RF communications equipment should be used no closer to any part of the BPA 9300 including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance Conducted RF 3Vrms NIA d 1 167 JP IEC 61000 4 6 150 kHz to 80 MHz Radiated RF 3VIm 3VIm d 1 167 JP 80 MHz to 800 MHz IEC 61000 4 3 80MHzto 2 5 GHz d 2333 P 800 MHz
3. to 2 5 GHz where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacture and d is the recommended separation distance in metres m Field strengths from fixed RF transmitters as determined by an electromagnetic site survey should be less than the compliance level in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol tJ NOTE 1 At 80 MHz and 800 MHz the higher frequency range applies in all situations E ectromagnetic propagation is affected by absorption and mobile radios amateur radio AM and the electromagnetic environment due MHz field streng Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land FM radio broadcast cannot be predicted theoretically with accuracy To assess to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the BPA 9300 is used exceeds the applicable RF compliance level above the BPA 9300 should be observed to verify normal operation If abnormal performance is observed additional Measures may be necessary such as re orienting or relocating the BPA 9300 Over the frequency range 150 kHz to 8 ths should be less than 3V m Table 6 Recommended separation distances between portable and mobile RF communications equipment and the E
4. QUIPMENT or SYSTEM for ME EQUIPMENT or ME SYSTEM that are not LIFE SUPPORTING Recommended separation distances between portable and mobile RF communications equipment at the BPA 9300 The BPA 9300 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of the BPA 9300 can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmittters and the BPA 9300 as recommended below according to the maximum output power of the communications equipment Rated maximum output power of transmitter Separation distance according to frequency of transmitter m 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 01 NIA 0 117 0 233 0 1 NIA 0 369 0 738 1 NIA 1 167 2 333 10 NIA 3 690 7 377 100 NIA 11 67 23 33 Tequency of the transmitter w For transmitters rated at a maximum output power not listed above the recommended separation distance d in metres m can be determined using the equation applicable to the output power rating of the transmitter in watts W according to the transmitter manufacture NOTE 1 At 80MHz and 800MHz the separation distance for the higher frequency range appli NOTE 4 These guidelines may not apply in all situations Electromagnetic propagation is af reflection from structures objects and
5. SALTER BLOOD PRESSURE MONITOR Instructions and Guarantee BPA 9300 l SAFETY INFORMATION The below signs might be in the user manual labeling or other components They are the requirement of standard and using Symbol for THE OPERATION GUIDE z T e MUST BE READ 4 Symbol for TYPE BF APPLIED PARTS Symbol for ENVIRONMENT PROTECTION Wast electrical products Symbol for COMPLIES WITH i C Enz MDD 93 42 EEC REQUIREMENTS should not be disposed of with household waste Please follow local guidelines iud Symbol for MANUFACTURER E Symbol for DIRECT CURRENT S N Symbol for SERIAL NUMBER Sym ol for Authorised Representative in the European Community 3 For indoor use only Symbol for Class II Equipment F1 TIA 250V 3 6 10CCC Symbol for MANUFACTURE DATE WEEE EXPLANATION This marking indicates that this product should not be disposed with other household wastes 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 mam material resources To return 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 BATTERY DIRECTIVE This symbol indicates that batteries must not be disposed of in
6. e 86kPa to 106kPa Storage amp transportation condition Temperature 20 C to 60 C RH 10 to 93 Atmospheric pressure 50kPa to 106kPa Measurement perimeter of the wrist About 22cm 32cm Net Weight Approx 385g Excluding the dry cells External dimensions Approx 120 160 69mm Attachment 4 M alkaline batteries user manual Mode of operation Continuous operation Degree of protection Type BF applied part Protection against ingress of water IP22 Software version vol WARNING No modification of this equipment is allowed CONTACT INFORMATION m For more information about our products please visit www salterhousewares com For UK Sales and Service contact HoMedics Group Ltd HoMedics House Somerhill Business Park Five Oak Green Road Tonbridge Kent TN11 OGP UK Helpline Tel No 01732 360783 For Ireland please contact Petra Brand Masters Unit J4 Maynooth Business Campus Maynooth Co Kildare Ireland Tel 00 353 0 1 6510660 e mail sales petrabrandmasters ie www salterhousewares com servicecentres Table 1 Guidance and manufacturer s declaration electromagnetic emissions for all EQUIPMENT and SYSTEMS Guidance and manufacture s declaration electromagnetic emission The BPA 9300 is intended for use in the electromagnetic environment specified below The customer or the user of the BPA 9300 should assure that it is used in such an environment Emission
7. e on the same arm or as directed by a physician ADVICE FOR USE AND CARE To obtain the best performance please follow below instructions Put in a dry place and avoid the sunshine Avoid immersing it in the water Clean it with a dry cloth Avoid shaking and collision Avoid dusty environment and unstable temperature surrounding Use the slightly damp cloth to remove the dirt Avoid washing the cuff ABOUT BLOOD PRESSURE What are systolic pressure and diastolic pressure NEU j Diastolic blood entering vein Systolic blood discharging artery When ventricles contract and pump blood out of the heart the blood pressure reaches its maximum value in the cycle which is called systolic pressure When the ventricles relax the blood pressure reaches its minimum value in the cycle which is called diastolic pressure What is the standard blood pressure classification The blood pressure classification published by World Health Organization WHO and International Society of Hypertension ISH in 1999 is as follows caution Only a physician can tell your normal BP range Please contact a physician if your measuring result falls out of the range Kindly note that only a physician could tell whether your blood pressure value has reached a dangerous point Grade 3 hypertension severe Grade 2 hypertension moderate 0 5 High normal blood pressure Normal blood pressure Optima
8. l blood pressure Diastolic blood pressure mmHg gt 120 130 140 150 160 180 Systolic blood pressure mmHg Blood Level Optimal Normal High normal Mild Moderate Severe pressure mm Hg SYS lt 120 120 129 130 139 140 159 160 179 2180 DIA 80 80 84 85 89 90 99 100 109 2110 IRREGULAR HEARTBEAT DETECTOR This Blood Pressure Monitor is equipped with an intelligent function of Irregular Heartbeat IHB Detector During each measurement this equipment records the heartbeat intervals and works out the standard deviation If the calculated value is larger than or equal to 15 this equipment will light up the IHB symbol on the screen when displaying the measuring result caution The appearance of the IHB icon indicates that a pulse irregularity consistent with an irregular heartbeat was detected during measurement Usually this is NOT a cause for concern However if the symbol appears often we recommend you seek medical advice Please note that the device does not replace a cardiac examination but serves to detect pulse irregularities at an early stage QUESTIONS amp ANSWERS Why my blood pressure varies even in one day 1 Individual blood pressure varies during the day It also affected by the way you tie your cuff and your measurement position so please take the measurement under similar conditions 2 The variance of the pressure is greater if the pe
9. low Replace with new batteries the display Edishows The cuff is not secure Re asten the cuff and then measure again Readjust the cuff not too loose or EZ shows The cuff is very tight too tight and then measure again E3 shows The pressure of the cuff is excess Relax for a moment and then measure again E10 or The montor mE motion Relax for a moment and then talking or the pluse is too poor E11 shows measure again while measuring Error message The measurement process does not Loosen the clothing on the arm and E 20 shows Rh K detect the pulse signal then measure again The treatment of the measurement Relax for a moment and then E21 shows P s failed measure again Retake the measurement If the problem persists contact the EExx shows on the S retailer or our customer service A calibration error occurred f display department for further assistance Refer to the warranty for contact information and return instructions In SPECIFICATIONS Power supply 6VDC 4 AA alkaline batteries Display mode Digital LCD V A 78 92mm Measurement mode scillographic testing mode Rated cuff pressure kpa 40kpa OmmHg 300mmHg Measurement range Measurement pressure 4kPa 34kPa 40mmHg 230mmHg pulse value 40 199 beat minute Pressure Accuracy 5 C 40 c within 0 4kpa 3mmHg pulse value 5 Normal working condition Temperature 5 C to 40 C Relative humidity lt 85 Atmospheric pressur
10. people here P is the maximum ie ected by absorption and o Register your product today at www homedicsgroup com register C E SALTER HoMedics Group Ltd HoMedics House Somerhill Business Park Five Oak Green Road Tonbridge Kent TN11 0GP UK www salterhousewares co uk 18 BPA9300 68 0114 01
11. ptor The user must check that the equipment functions safely and see that it is in proper working condition before being used Please note that Luer lock connectors are not used on the product and please DO NOT change any provided connectors Do not wind the air tube round the neck ease use ACCESSORIES and detachable parts specified authorised by MANUFACTURER therwise it may cause damage to the unit or danger to the user patients Manufacturer will make available on request circuit diagrams component parts list etc After the cuff inflated long time the patient s arm and fingers will is insufficient anaesthesia destending pain and ecchymosis Please use the device under the environment which was provided in the user manual otherwise the performance and lifetime of the device will been impacted and reduced During use the patient will contact with the cuff The materials of the cuff have been tested and found to comply with requirements of ISO 10993 5 2009 and ISO 10993 10 2010 It will not cause any potential alergic reaction or contact injury Atleast two years of reliable service without need for calibration Please dispose of ACCESSORIES detachable parts and the EQUIPMENT according to the local guidelines When the device is used to measure patients who have common arrhythmias such as atrial or ventricular premature beats or artrial fibrillation results may vary Please consult your physician about the result
12. rson take medicine 3 Wait at least 3 minutes for another measurement Why are the blood pressure readings get from the hospital different from home The blood pressure readings are different even during 24 hour because of the weather emotion exercise etc especially the white coat effect in hospital which makes the results are higher than the ones at home The attention you need to pay when you measure your blood pressure at home Ifthe cuff is tied properly Ifthe cuff is too tight or too loose Ifthe cuff is tied on the upper arm f you feel anxious or under stress Take deep breaths 2 3 times before beginning Advice Relax for 5 minutes before measurement if necessary If the result is the same if measuring on the right arm It is ok to measure either arm but there will be some different results for different persons so it is suggested you measure the same arm every time TROUBLESHOOTING This section includes a list of error messages and frequently asked questions for problems you may encounter with your blood pressure monitor If the products is not operating as you think it should check here before arranging for servicing PROBLEM SYMPTOM CHECK THIS REMEDY Batteries are exhausted Replace with new batteries Display is dim or will No power not light up i Batteries are inserted incorrectly Insert the batteries correctly Low batteries Eo auw T Batteries are
13. safety standard Replace the batteries under following circumstances E Lo displays on the LCD The LCD display dims e When powering on the monitor the LCD doesn t light up caution Remove batteries if the device is not likely to be used for some time The old battery is harmful to the environment so please dispose of according to the guidlines on page 2 Remove the old battery from the device and follow your local recycling guidelines Do not dispose of batteries in fire Batteries may explode or leak SETTING DATE TIME AND MEASUREMENT UNIT When the monitor is OFF press and hold button to enter Time Setting Mode The YEAR numeral will start blinking Press button to change the numeral Each press will increase the numeral by one in a cycling manner Press button again to confirm YEAR Then the numeral representing MONTH blinks Repeat step 2 and 3 to confirm MONTH and DAY Repeat step 2 and 3 to confirm HOUR and MINUTE Hour Format 24 Hour Repeat step 2 and 3 to confirm the measurement unit After confirming the measurement unit the LCD will display dOnE and the monitor will shut off TIE THE CUFF Tie the cuff on your upper arm position the tube off center toward the inner side of arm in line with the little finger The cuff should be snug but not too tight You should be able to insert one finger between the cuff and your arm Sit comfortably with yo
14. test Compliance Electromagnetic environment guidance Ky The BPA 9300 must emit electro magnetic energy in order to RF emissions he ELLE Group 1 perform its intended function Nearby electronic equipment CISPR 1 may be affected RF emission CISPR 1 Class B Harmonic emissions IEC 61000 3 2 Not applicable Voltage fluctuations flicker emissions Not applicable IEC 61000 3 3 11 Table 2 Guidance and manufacturer s declaration electromagnetic immunity for all ME EQUIPMENT and ME SYSTEMS Guidance and manufacture s declaration electromagnetic emission BPA 9300 should assure t The BPA 9300 is intended for use in the electromagnetic environment specified be hat it is used in such an environment low The customer or the user of the 50Hz magnetic field IEC 61000 4 8 Immunity test IEC 60601 test level Compliance level Electromagnet s environment guidance Electrostatic 6 kV contact 6 kV contact Floors should be wood concrete or discharge ESD 8 kV air 8 kV air ceramic tile If floors are covered IEC 61000 4 2 with synthetic material the relative humidity should be at least 30 Electrical fast 2 kV for NIA transient burst power supply lines IEC 61000 4 4 Surge 1 kV line s to line s N A IEC 61000 4 5 2 kV line s to earth Voltage dips short lt 5 UT N A interruptions and gt 95 dip in UT voltage variations on or 0 5 cycle ower
15. the domestic waste as they contain substances which can be damaging to the environment and health Please dispose of batteries in designated collection points GUARANTEE Salter will repair or replace the product or any part of this product free of charge if within 2 years of the date of purchase it can be shown to have failed through defective workmanship or materials This guarantee covers working parts that affect the function of the blood pressure monitor It does not cover cosmetic deterioration caused by fair wear and tear or damage caused by accident or misuse Opening or taking apart the blood pressure monitor or its components will void the guarantee Claims under guarantee must be supported by proof of purchase and be returned carriage paid to Salter or local Salter appointed agent if outside the UK Care should be taken in packing the blood pressure monitor so that it is not damaged while in transit This undertaking is in addition to a consumer s statutory rights and does not affect those rights in any way For UK Sales and Service contact HoMedics Group Ltd HoMedics House Somerhill Business Park Five Oak Green Road Tonbridge Kent TN11 OGP UK Helpline Tel No 01732 360783 e mail support homedics co uk For Ireland please contact Petra Brand Masters Unit J4 Maynooth Business Campus Maynooth Co Kildare Ireland Tel 00 353 0 1 6510660 e mail sales petrabrandmasters ie www salterhousewares com servicecentres ca
16. ur tested arm resting on a flat surface Correct Posture for Patients with Hypertension especially for Hypertension patient Bare your arm before applying the cuff Sit comfortably with legs uncrossed feet flat on the floor back and arm supported The centre of the cuff should be maintained at the same level as the heart Rest for 5 minutes before measuring Wait at least 3 minutes between measurements This allows your blood circulation to recover For a meaningful comparison try to measure under similar conditions For example take daily measurements at approximately the same time on the same arm or as directed by a physician oe w nN sO Pwr START THE MEASUREMENT When the monitor is off press amp button to turn on the monitor and it will finish the whole measurement and then save the Measurement data for User 1 The same for User 2 1 Press the amp to power off otherwise it will turn off within one minute Tips a When the measurement has finished press another user button the blood pressure monitor will begin measuring again b Maximum 60 records are both for user 1 and user 2 RECALL THE RECORDS 1 When the monitor is OFF press button to access the memory 2 The LCD will display the latest measuring result of the selected user ID which completes the last measurement The record number measuring date and measuring time will be displayed alternatively Press amp button to rotate the histor
17. ution 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 or for functions other than obtaining a blood pressure measurement Do not confuse self monitoring with self diagnosis This unit allows you to monitor your blood pressure Do not begin or end medical treatment relay solely on a doctor for treatment advice If you are taking medication consult your physician to determine the most appropriate time to measure your blood pressure Never change a prescribed medication without consulting your physician This unit is not suitable for continuous monitoring during medical emergencies or operations 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 any 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 To avoid measurement errors please avoid strong electromagnetic field radiated interference signal or electrical fast transient burst signals when using the AC ada
18. y records When in the memory mode press button to recall the measurement history of User 1 or press button to recall the measurement history When no history stored for the specific user in the monitor press button and the LCD will display 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 e g 2 becomes 3 and so on and the last record 60 is dropped from the list p es en When under the query mode press and hold C button for 3 seconds to clear the memory When the LCD display dEL ALL press button to confirm The LCD will display dEL dOnE and then shut off If you wish to stop clearing the memory you may press the other button rather than button to turn off the monitor or wait until the monitor shuts off TIPS FOR MEASUREMENT It can cause inaccuracy if the measurement is taken in the following circumstances 1 Immediately after eating a meal or drinking Immediate measurement after tea coffee or smoking Immediately after taking a bath When talking or moving your fingers In a very cold environment When you need the lavatory Rest for 5 minutes before measuring Wait at least 3 minutes between measurements This allows your blood circulation to recover Try to measure under similar conditions for example take daily measurements at approximately the same tim
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