Andon Health BP3L Wireless Blood Pressure Monitor User Manual

Andon Health Co., Ltd Wireless Blood Pressure Monitor

User Manual

Wireless Blood Pressure Monitor (BP3L)User GuideTable of ContentsINTRODUCTION..............................................................................................................................2PACKAGE CONTENTS.................................................................................................................. 2INTENDED USE...............................................................................................................................2CONTRAINDICATION.....................................................................................................................2PARTS AND DISPLAY INDICATORS........................................................................................... 2SET UP REQUIREMENTS.............................................................................................................2SET UP PROCEDURES.................................................................................................................2SPECIFICATIONS............................................................................................................................4GENERAL SAFETY AND PRECAUTIONS................................................................................. 4BATTERY HANDLING AND USAGE............................................................................................ 4TROUBLESHOOTING.................................................................................................................... 4CARE AND MAINTENANCE..........................................................................................................4WARRANTY INFORMATION.........................................................................................................4EXPLANATION OF SYMBOLS......................................................................................................4CONTACT AND CUSTOMER SERVICE..................................................................................... 4IMPORTANT INFORMATION REQUIRED BY THE FCC......................................................... 4OTHER STANDARDS AND COMPLIANCES............................................................................. 4ELECTROMAGNETIC COMPATIBILITY INFORMATION........................................................ 4
INTRODUCTIONThank you for selecting the iHealth Wireless Blood Pressure Monitor. The iHealth Wireless Blood Pressure Monitor is a fullyautomatic arm cuff Wireless Blood Pressure Monitor that uses the oscillometric principle to measure your blood pressure andpulse rate. The monitor works with your mobile device to test, track and share vital blood pressure data.PACKAGE CONTENTS* 1 iHealth Wireless Blood Pressure Monitor*1UserGuide* 1 Quick Start Guide* 1 Charging CableINTENDED USEThe iHealth Wireless Blood Pressure Monitor (Electronic Sphygmomanometer) is intended for use in a professionalsetting or at home and is a non-invasive blood pressure measurement system. It is designed to measure the systolicand diastolic blood pressures and pulse rate of an adult individual by using a technique in which an inflatable cuff iswrapped around the upper arm. The measurement range of the standard cuff circumference is 8-21/32” to14-3/16”(22cm-36cm).Note: Consult your physician for proper interpretation of blood pressure results.CONTRAINDICATIONIt is not recommended for people with serious arrhythmia to use this Wireless Blood Pressure Monitor.PARTS AND DISPLAY INDICATORSSETUP REQUIREMENTSThe iHealth View Wireless Blood Pressure Wrist Monitor is designed to be used with the following iPod touch,iPhone and iPad models:iPhone4s+iPad Air+iPad mini+iPad 3+iPod Touch5Please note that the compatible devices are subject to change. For the latest compatibility list（include Androiddevices), visit www.ihealthlabs.com/supportSETUP PROCEDURESConnect the cuff to BP3LInsert the cuff tubing connector into the air port in the left side of the monitor. Makesure that the connector is completely inserted to avoid air leakage during bloodpressure measurements.
Avoid compression or restriction of the connection tubing during measurement，which may cause inflation error, orharmful injury due to continuous cuff pressure.Download the Free iHealth MyVitals AppPrior to first use, download and install “iHealth MyVitals”from the App Store or Google Play StoreFollow the on-screen instructions to register and set up your personal account.Access the iHealth Cloud AccountYour iHealth account also gives you access to the free and secure iHealth cloud service. Go to www.ihealthlabs.comand sign in with the same account.Charge Battery Before First UseConnect the monitor to a USB port using the charging cable provided until the green indicator light stabilizes.Connect to iOS Device or Android Devivce via Bluetooth•TurnBluetooth"On" under the "Settings" menu on the iOS device or Android device.• Launch the “iHealth MyVitals” app .• Place your iOS device or Android device on the dock.• Wait for 3~6 seconds until the monitor connects with IOS device, when the green light on the dock is lit.Monitor Status Bluetooth IndicatorWaiting to connect No lightConnected and measuring Steady green lightMeasurement completed and Device far away from the monitor Extinguishing green lightMEASUREMENT PROCEDURESBlood pressure can be affected by the position of the cuff and your physiologic condition. It is very important that the cuffshould be placed at the same level as your heart.Body PostureSitting Comfortably During Measurementa. Sit with your feet flat on the floor without crossing your legs. Stay still during measurement. Do not move your arm, body, orthe monitor.b. Place your hand palm-side up in front of you on a flat surface such as a desk or a tablec. The center of the cuff should be at your heart level.Lying Down During Measurementa. Lie on your back.b. Place your left arm straight along your side with your hand palm-side up.c. The cuff should be level with your heart.Note: Blood pressure can be affected by the position of the cuff and your physiologic condition, so it is important that youalways measure your blood pressure in the same position.Apply the Cuffa. Pull the cuff end through the metal loop, positioning itoutward (away from your body).b. Place a bare left arm through the cuff with the red arrow
facing up and position the cuff 1/2"(1-2cm)above the elbow joint.c. Tighten the cuff by pulling it towards your body, securing it closed with theVelcro fastener.d. While seated, place your hand, palm-side up, in front of you on a flatsurface such as a desk or table. Position the monitor in the middle of yourarm so that it is aligned with your middle finger.e. The cuff should fit comfortably, yet snugly around your left arm. Youshould be able to insert one finger between your arm and the cuff.Remember to:1. Make sure that the appropriate cuff size is used; refer to the cuff circumference range in the Specifications section of thismanual.2. Stay still during measurement. Do not move your arm, body or the monitor.3. Stay still and calm for one to one and half minutes before taking a blood pressure measurement. Prolonged over-inflation ofthe bladder may cause bruises of your arm.4. Keep the cuff clean. Cleaning the cuff after every 200 measurements is recommended. If the cuff becomes dirty, remove itfrom the monitor and clean it with a moistened cloth. Do not rinse the monitor or cuff with running water.Press the “ ” button at any time to interrupt a measurement.Note: Physical activity, eating, drinking, smoking, excitement, stress, and many other factors influence blood pressure results.For answers to frequently asked questions, please visit www.ihealthlabs.comOPERATION INSTRUCTIONS• Tap “Start” in your app to start measurement. For detailed operating instructions, please visiting : http://www.iHealthLabs.comNote: Please consult a health care professional for interpretation of blood pressuremeasurements.SPECIFICATIONS1. Product name: Wireless Blood Pressure Monitor2. Model: BP3L3. Classification: Internally powered; Type BF applied part; IPX0, No AP or APG; Continuous operation4. Machine size: approx. 4.53”×4.53”×2.62”(115mm×115mm×66.5mm)5. Cuff circumference: 8-21/32” to 14-3/16”(22cm-36cm)6. Weight: approx. 8.47oz (240g) (exclusive cuff);7. Power: DC:5.0V 1A, Battery: 1*3.7V Li-ion 2200mAh8. Measurement range:Cuff pressure: 0-300 mmHgSystolic: 60-260 mmHgDiastolic: 40-199 mmHgPulse rate: 40-180 beats/minute9. Accuracy:Pressure: ±3 mmHgPulse rate: ±5%10. Wireless communication:Bluetooth Low Energy
Frequency Band: 2.402-2.480 GHz11.Environmental temperature for operation: 10°C-40°C(50°F -104°F)12. Environmental humidity for operation: ≤85%RH13. Environmental temperature for storage and transport:-20°C-55°C(-4°F-131°F)14. Environmental humidity for storage and transport: ≤85%RH15. Environmental pressure: 80kPa-105kPa16. Battery life: more than 500 measurements on a full charge, the battery can maintain the performance characteristics for aminimum of 300 charge cycles17.The blood pressure measurement system includes accessories: pump, valve, cuff, and sensor.Note: These specifications are subject to change without notice.GENERAL SAFETY AND PRECAUTIONS1. Read all of the information in the User Guide and other provided instructions before operating the unit.2. Consult your physician for any of the following situations:a)The application of the cuff over a wound or inflamed area.b)The application of the cuff on any limb with intravascular access or therapy, or an arteriovenous (A-V) shunt.c)The application of the cuff on the arm on the side of a mastectomy.d)Simultaneous use with other medical monitoring equipment on the same limb.e)The blood circulation of the user needs to be checked.3. Do not use this product in a moving vehicle as this may result in inaccurate measurements.4. Blood pressure measurements determined by this product are equivalent to those obtained by professional healthcarepractitioners using the cuff/stethoscope auscultation method within the limits prescribed by the American National Standard,Electronic or Automated Sphygmomanometer.5. If you are using a smart phone to operate the device and a phone call comes in during the measurement, the measurementprocess will be terminated automatically. It is thus recommended that the phone be set in Airplane mode during measurementto avoid interrupting the measurement.6. If an Irregular Heartbeat (IHB) is detected during the measurement procedure, the IHB symbol will be displayed. Under thiscondition, the Wireless Blood Pressure Monitor can keep functioning, but the results may be inaccurate. Please consult yourphysician for accurate assessment.The IHB symbol will be displayed under 2 sets of circumstances:1)The coefficient of variation (CV) of pulse period >25%.2)The difference of adjacent pulse period is ≥0.14s and more than 53 percent of the total number of pulses readings fallswithin this definition.7. Please do not use any cuff other than that supplied by the manufacturer as this may result in inaccurate measurements.8. For information regarding potential electromagnetic or other interference between the Wireless Blood Pressure Monitor andother devices together with advice regarding avoidance of such interference, please see ELECTROMAGNETICCOMPATIBILITY INFORMATION. It is suggested that the Wireless Blood Pressure Monitor should be operated at least 10metres away from electric or wireless devices (e.g. routers, microwave oven, etc.)9. If the blood pressure measurement (systolic or diastolic) is outside the rated range specified in part SPECIFICATIONS, theapp will immediately display a technical alarm on the screen. In this case, repeat the measurement ensuring that the propermeasurement procedures are followed and/or consult with your medical professional.The technical alarm is preset in thefactory and cannot be adjusted or inactivated. This technical alarm is assigned as low priority according to IEC 60601-1-8. Thetechnical alarm does not need to be reset.
10. This device requires a medical AC adapter with an output of DC 5.0V that complies with IEC 60601-1/UL 60601-1 and IEC60601-1-2 such as OH-1048A0501000U2(input: 100-240V, 50/60Hz; output: DC 5V, 1.0A). Please note that the monitor jacksize is USB Micro B. The USB jack should be used for charging only.This Monitor is designed for adults and should never be used on infants, young children, pregnant or pre-eclampticpatients. Consult your physician before use on children.This product might not meet its performance specifications if stored or used outside the specified temperature andhumidity ranges.Please do not share the cuff with any infectious person to avoid cross-infection.Please do not share the cuff with any infectious person to avoid cross-infection.BATTERY HANDLING AND USAGE• When the monitor is connected to the mobile device, the battery charge will be displayed on the mobile device. If the power isless than 25%, please charge the battery. The monitor will not work until the battery has enough power.• When the monitor needs charging, please connect the monitor to a power source. The monitor can work normally whilecharging.• You should charge the battery when the battery is less than 25% charged. Overcharging the battery may reduce its lifetime.• When in charging mode, the LED on the device will be displayed with different colous indicating the charging status. See thetable below for details.Monitor Status Status IndicatorCharging Flashing green lightFully charged Steady green lightLow battery Flashing red light (for a few seconds)Abnormal state Steady red lightDo not change the battery. If the battery can no longer be charged, please contact Customer Service.Overcharging the battery may reduce its lifetime.Lithium battery replacement by inadequately trained personnel could result in a hazard such as a fire or explosion.Do not plug or unplug the power cord into the electrical outlet with wet hands. If the AC adapter is abnormal, pleasechange the adapter.Do not pull out the adapter when you are using the monitor.Do not use when charging.The monitor, cable, battery and cuff must be disposed of according to local regulations at the end of their usage.Note: Battery life and charge cycles vary by use and settings.TROUBLESHOOTINGPROBLEM POSSIBLE CAUSE SOLUTIONLow Battery Battery is less than 25% Charge the batteryDisplay reads“ERROR”Blood pressure is outside of measurementrangeRetest and contact your health professional if bloodpressure measurement is still outside of normal rangeArm or monitor was moved during test Retest, make sure not to move your arm or the monitorThe cuff does not inflate properly orpressure falls quickly during testReview the cuff application instructions and retestThe cuff was not properly applied Review the cuff application instructions and retestDisplay readsan abnormalresultThe cuff position was not correct or it wasnot properly tightenedReview the cuff application instructions and retestBody posture was not correct during testing Review body posture instructions and retest
Speaking, moving arm or body, beingangry, excited or nervous during testRetest when calm; avoid speaking or movement duringthe testBluetoothconnectionunstableBluetooth connection unsuccessful,monitor is abnormal, or strongelectromagnetic interference is presentReset iOS/Android device. Reset monitor by pressingthe button . Make sure the monitor andiOS/Android device are away from other electricalequipment. Please see GENERAL SAFETY ANDPRECAUTIONSNo responseIncorrect operation or strongelectromagnetic interferencePress the button to reset the device and reconnectthe iOS/Android device to the monitor, relaunch app.CARE AND MAINTENANCE1. If this monitor is stored near freezing temperatures, allow it to return to room temperature before use.2. If the monitor is not used for a long time, please be sure to fully charge it every month.3. It is recommended that product performance be checked every 2 years or after each repair. Please contact the iHealthCustomer Service Center to do so.4. No monitor component needs to be maintained by the user. The circuit diagrams, component part lists, descriptions,calibration instructions, or other information which will assist the user’s appropriately qualified technical personnel to repairthose parts of the equipment which are designated for repair can be supplied by the iHealth technical department.5. Clean the monitor with a dry, soft cloth or a moistened and well wrung soft cloth using water, diluted disinfectant alcohol, ordiluted detergent.6. The monitor can maintain the safety and performance characteristics for a minimum of 10,000 measurements or threeyears of usage, and the cuff integrity is maintained after 1,000 open close cycles.7. The battery can maintain the performance characteristics for a minimum of 300 charge cycles.8. It is recommended that if the cuff is used in a hospital or a clinic, it be disinfected twice a week. Wipe the inner side (the sidethat contacts skin) of the cuff with a soft cloth lightly moistened with Ethyl alcohol (75-90%). Then air dry the cuff.Do not drop this monitor or subject it to strong impact.Avoid high temperature and direct sunlight. Do not immerse the monitor in water as this will result in damage to themonitor.Do not attempt to disassemble this monitor.Battery replacement should only be performed by a qualified iHealth technician. To do otherwise will void your warrantyand possibly damage your unit.Cuff replacement should only be performed by a qualified iHealth technician. To do otherwise will possibly damage yourunit.WARRANTY INFORMATIONThe iHealth Wireless Blood Pressure Monitor is warranted to be free from defects in materials and workmanship within oneyear from the date of purchase when used in accordance with the provided instructions. The warranty extends only to the enduser. We will, at our option, repair or replace without charge the iHealth Wireless Blood Pressure Monitor covered by thewarranty. Repair or replacement is our only responsibility and your only remedy under the warranty.EXPLANATION OF SYMBOLSSymbol for "TYPE BF APPLIED PARTS" (cuff only)Symbol for "THE OPERATION GUIDE MUST BE READ"The sign background color: blue The sign graphical symbol: white
Symbol for "ENVIRONMENT PROTECTION – Waste electrical products should not bedisposed of with household waste. Please recycle where facilities exist. Check with your local authority or retailerforrecycling advice".Symbol for "KEEP DRY"Symbol for "WARNING"Symbol for "MANUFACTURER"Symbol for "SERIAL NUMBER"Symbol for “DATE OF MANUFACTURE”Symbol for "EUROPEAN REPRESENTATIVE"Symbol for "COMPILES WITH MDD93/42/EEC REQUIREMENTS"iHealth is a trademark of iHealth Lab Inc."Made for iPod", "Made for iPhone", and "Made for iPad" mean that an electronic accessory has been designed to connectspecifically to iPod, iPhone, or iPad, respectively, and has been certified by the developer to meet Apple performancestandards. Apple is not responsible for the operation of this device or its compliance with safety and regulatory standards.Please note that the use of this accessory with iPod, iPhone, or iPad may affect wireless performance. iPad, iPhone, and iPodtouch are trademarks of Apple Inc., registered in the U.S. and other countries.The Bluetooth® word mark and logos are registered trademarks owned by Bluetooth SIG, Inc. and any use of such marks byiHealth Lab Inc. is under license.Other trademarks and trade names are those of their respective owners.CONTACT AND CUSTOMER SERVICEManufactured for iHealth Lab Inc.719N . Shoreline Blvd.,Mountain View, CA 94043, USATel:+1-855-816-7705 www.ihealthlabs.comiHealthlabs Europe3 Rue Tronchet,75008,Paris,Francesupport@ihealthlabs.eu www.ihealthlabs.euANDON HEALTH CO., LTD.No. 3 Jinping Street, YaAn Road, Nankai District, Tianjin 300190, China.Tel: 86-22-60526161
IMPORTANT INFORMATION REQUIRED BY THE FCCThis device complies with Part 15 of the FCC Rules. Its 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.Changes or modifications not expressly approved by iHealth Lab Inc. would void the user’s authority to operate the product.Note: This product has been tested and found to comply with the limits for a Class B digital device, pursuant to Part 15 of theFCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation.This product generates, uses, and can radiate radio frequency energy and, if not installed and used in accordance with theinstructions, may cause harmful interference to radio communications. However, there is no guarantee that interference willnot occur in a particular installation. If this product does cause harmful interference to radio or television reception, which canbe determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more ofthe 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.This product complies with Industry Canada. IC: RSS-210IC NOTICEThis device complies with Industry Canada licence-exempt RSS standard(s). Operation is subject to the following two conditions:(1) this device may not cause interference, and(2) this device must accept any interference, including interference that may cause undesired operation of the device.This product is approved in accordance to R&TTE directive transmitter.Hereby, [iHealth Lab Inc.], declares that this [BP3L CORE] is in compliance with the essentialrequirements and other relevant provisions of Directive 1999/5/EC. Directive 1999/5/ECdeclaration of conformity can be downloaded on the following link :https://www.ihealthlabs.eu/support/certicationsOTHER STANDARDS AND COMPLIANCESThe Wireless Blood Pressure Monitor corresponds to the following standards:IEC 60601-1:2005 corr.1(2006)+corr.2(2007)/EN 60601-1：2006/A11: 2011(Medical electrical equipment – Part 1: Generalrequirements for safety);IEC 60601-1-2:2007 /EN 60601-1-2:2007 /AC:2010 (Medical electrical equipment – Part 1: General requirements for safety;Collateral Standard-Electromagnetic compatibility - Requirements and tests);EN 1060-1: 1995 + A1: 2002 + A2: 2009 (Non-invasive sphygmomanometers - Part 1: General requirements);EN 1060-3: 1997 + A1: 2005 + A2: 2009 (Non-invasive sphygmomanometers - Part 3: Supplementary requirements forelectro-mechanical blood pressure measuring systems);AAMI/ANSI 80601-2-30：2009/IEC 80601-2-30：2009+Cor.2010(Medical electrical equipment –Part 2-30: Particularrequirements for the basic safety and essential performance of automated non-invasive sphygmomanometers).Le présent appareil est conforme aux CNR d'Industrie Canada applicables aux appareils radioexempts de licence. L'exploitation est autorisée aux deux conditions suivantes :(1) l'appareil ne doit pas produire de brouillage, et(2) l'utilisateur de l'appareil doit accepter tout brouillage radioélectrique subi, même si le brouillage est susceptible d'en compromettre le fonctionnement.The USB port for charging for charging only and can’t be used to transfer data.
ELECTROMAGNETIC COMPATIBILITY INFORMATIONTable 1For all ME EQUIPMENT and ME SYSTEMSGuidance and manufacture’s declaration - electromagnetic emissionsThe BP3L is intended for use in the electromagnetic environment specified below.The customer or the user of the BP3L should assure that it is used in such an environment.Emissions test Compliance Electromagnetic environment - guidanceRF emissionsCISPR 11Group 1The BP3L uses RF energy only for its internal function. Therefore, its RFemissions are very low and are not likely to cause any interference innearby electronic equipment.RF emissionsCISPR 11Class BThe BP3L is suitable for use in all establishments, including domesticestablishments and those directly connected to the public low-voltagepower supply network that supplies buildings used for domesticpurposes.Harmonic emissionsIEC 61000-3-2Class AVoltage fluctuations/flicker emissionsIEC 61000-3-3CompliesTable 2For all ME EQUIPMENT and ME SYSTEMSGuidance and manufacturer’s declaration - electromagnetic immunityThe BP3L is intended for use in the electromagnetic environment specified below. The customer or the user of the BP3Lshould assure that it is used in such an environment.IMMUNITY test IEC 60601test level Compliance level Electromagnetic environment - guidanceElectrostatic discharge(ESD)IEC 61000-4-2± 6 kV contact±8kVair± 6 kV contact±8kVairFloors should be wood, concrete or ceramictile. If floors are covered with syntheticmaterial, the relative humidity should be atleast 30 %.Electrical fasttransient/burstIEC 61000-4-4±2kVforpowersupplylines± 1 kV for input/outputlines±2kVforpowersupply linesMains power quality should be that of atypical commercial or hospital environment.SurgeIEC 61000-4-5±1kVline(s)toline(s)± 2 kV line(s) to earth±1kVline(s)toline(s)±2kVline(s)toearthMains power quality should be that of atypical commercial or hospital environment.Voltage dips, shortinterruptions andvoltage variationson power supplyinput linesIEC 61000-4-11<5 % UT(>95 % dip in UT)for 0.5 cycle40 % UT(60%dipinUT)for 5 cycles70 % UT(30%dipinUT)<5 % UT(>95 % dip in UT)for 0.5 cycle40 % UT(60 % dip in UT)for 5 cycles70 % UT(30 % dip in UT)Mains power quality should be that of atypical commercial or hospital environment. Ifthe user of the BP3L requires continuedoperation during power mains interruptions, itis recommended that the BP3L be poweredfrom an uninterruptible power supply or abattery.
for 25 cycles<5 % UT(>95 % dip in UT)for 5 sfor 25 cycles<5 % UT(>95 % dip in UT)for 5 sPower frequency(50/60 Hz)magnetic fieldIEC 61000-4-83 A/m 3 A/m Power frequency magnetic fields should be atlevels characteristic of a typical location in atypical commercial or hospital environment.NOTE: UTis the a.c. mains voltage prior to application of the test level.Table 3For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTINGGuidance and manufacturer’s declaration - electromagnetic immunityThe BP3L is intended for use in the electromagnetic environment specified below. The customer or the user of the BP3Lshould assure that it is used in such an environment.IMMUNITY test IEC 60601testlevelCompliancelevel Electromagnetic environment - guidanceConducted RFIEC 61000-4-6Radiated RFIEC 61000-4-33 Vrms 150 kHz to80 MHz3V/m80MHzto2,5 GHz3Vrms3V/mPortable and mobile RF communications equipment should beused no closer to any part of the BP3L, including cables, than therecommended separation distance calculated from the equationapplicable to the frequency of the transmitter.Recommended separation distance：80 MHz to 800 MHz800 MHz to 2,5 GHzWhere P is the maximum output power rating of the transmitter inwatts (W) according to the transmitter manufacturer and d is therecommended separation distance in meters (m).Field strengths from fixed RF transmitters, as determined by anelectromagnetic site survey,ashould be less than the compliancelevel in each frequency range.bInterference may occur in the vicinity of equipmentmarked with the following symbol:Pd 2.1=Pd 2.1=Pd 3.2=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 reflectionfrom 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 themeasured field strength in the location in which the BP3L is used exceeds the applicable RF compliance level above, theBP3L should be observed to verify normal operation. If abnormal performance is observed, additional measures may benecessary, such as re-orienting or relocating the BP3L.b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3V/m.Table 4For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTINGRecommended separation distances between portable and mobile RF communications equipment and the BP3LThe BP3L is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. Thecustomer or the user of the BP3L can help prevent electromagnetic interference by maintaining a minimum distance betweenportable and mobile RF communications equipment (transmitters) and the BP3L as recommended below, according to themaximum output power of the communications equipment.Rated maximum outputpower of transmitterWSeparation distance according to frequency of transmitterm150 kHz to 80 MHzPd 2.1=80 MHz to 800 MHzPd 2.1=800 MHz to 2,5 GHzPd 3.2=0,01 0,12 0,12 0,230,1 0,38 0,38 0,7311,2 1,22,310 3,8 3,8 7,3100 12 12 23For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m)can be determined using the equation applicable to the frequency of the transmitter, where P is the maximum output powerrating 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 reflectionfrom structures, objects and people.BP3L-SMSY01 V1.0

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