iHealth Labs BP7S Wireless Blood Pressure Wrist Monitor User Manual 15 BP7S UserMan
iHealth Lab Inc. Wireless Blood Pressure Wrist Monitor 15 BP7S UserMan
15_BP7S UserMan
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| Document ID | 2796733 |
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| Document Description | 15_BP7S UserMan |
| Short Term Confidential | No |
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| Document Type | User Manual |
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| Filesize | 21.88kB (273479 bits) |
| Date Submitted | 2015-10-29 00:00:00 |
| Date Available | 2015-10-29 00:00:00 |
| Creation Date | 2015-07-13 15:13:30 |
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| Document Title | 15_BP7S UserMan |
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| Document Author: | 00895 |
iHealth® View Wireless Blood Pressure Wrist Monitor (BP7S) USER GUIDE Table of Contents INTRODUCTION...............................................................................................................................2 PACKAGE CONTENTS.................................................................................................................... 2 INTENDED USE................................................................................................................................ 2 CONTRAINDICATION..................................................................................................................... 2 PARTS AND DISPLAY INDICATORS............................................................................................. 2 SET UP REQUIREMENTS................................................................................................................2 SET UP PROCEDURES.....................................................................................................................3 MEASUREMENT PROCEDURES................................................................................................ 3 SPECIFICATIONS............................................................................................................................. 4 GENERAL SAFETY AND PRECAUTIONS....................................................................................5 BATTERY HANDLING AND USAGE............................................................................................. 6 TROUBLESHOOTING......................................................................................................................6 CARE AND MAINTENANCE.......................................................................................................... 7 WARRANTY INFORMATION......................................................................................................... 8 EXPLANATION OF SYMBOLS.......................................................................................................8 CONTACT AND CUSTOMER SERVICE........................................................................................ 8 IMPORTANT INFORMATION REQUIRED BY THE FCC............................................................ 9 OTHER STANDARDS AND COMPLIANCES................................................................................9 ELECTROMAGNETIC COMPATIBILITY INFORMATION......................................................... 9 INTRODUCTION Thank you for selecting the iHealth View Wireless Blood Pressure Wrist Monitor. The iHealth Wireless Blood Pressure Wrist Monitor is a fully automatic wrist cuff blood pressure monitor that uses the oscillometric principle to measure your blood pressure and pulse rate. The monitor works with your mobile devices to track and share vital blood pressure data. PACKAGE CONTENTS * 1 iHealth View Wireless Blood Pressure Wrist Monitor * 1 User Guide * 1 Quick Start Guide * 1 Charging Cable * 1 Travel Case INTENDED USE The iHealth View Wireless Blood Pressure Wrist Monitor (Electronic Sphygmomanometer) is intended for use in a professional setting or at home and is a non-invasive blood pressure measurement system. It is designed to measure the systolic and diastolic blood pressures and pulse rate of an adult individual by using a technique in which an inflatable cuff is wrapped around the wrist. The measurement range of the standard cuff circumference is 5.3” to 8.7”(13.5cm-22cm). Note: Consult your physician for proper interpretation of blood pressure results. CONTRAINDICATION It is not recommended for people with serious arrhythmia to use this Wireless Blood Pressure Monitor. PARTS AND DISPLAY INDICATORS Bluetooth indicator Sync indicator Systolic Diastolic Pulse indicator Charging indicator Position detect indicator Pulse Battery SET UP REQUIREMENTS The 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 Touch5 Please note that the compatible devices are subject to change. For the latest compatibility list（include Android devices), visit www.ihealthlabs.com/support SET UP PROCEDURES Download the Free iHealth MyVitals App Prior to first use, download and install “iHealth MyVitals” from the App Store or Google Play Store. Follow the on-screen instructions to register and set up your personal account. Access the iHealth Cloud Account Your iHealth account also gives you access to the free and secure iHealth cloud service. Go to www.ihealthlabs.com and sign in with the same account. Charge Battery before First Use Connect the monitor to a USB port using the charging cable provided until indicator steady. BODY POSTURE DURING MEASUREMENT Blood pressure can be affected by the position of the cuff and your physiologic condition. It is very important that the cuff is positioned at your heart level during blood pressure measurements. 1. Sit comfortably with your feet flat on the floor without crossing your legs. Stay still during measurement. Do not move your wrist, body, or the monitor. 2. Place your hand palm-side up in front of you and leave 1-2cm between the monitor and the bottom of your palm. If the monitor is correctly placed, iHealth logo will be facing upright. 3. The center of the cuff should be at your heart level. 4. It is advised to place the monitor’s travel case under your arm for support and to keep your arm at optimal height for measurement. TAKING YOUR BLOOD PRESSURE READING 1. Apply the cuff or press the START/STOP button, the monitor will activate and begin to detect your wrist position. 2. Adjust the height of your wrist, the monitor will detect your wrist position and the measurement will start ONLY when the correct position is detected. When the position is correct, press "START/STOP" button again to start measurement. Wrist position too low Wrist position too high Wrist position good 3. Then the cuff will be slowly inflated. The blood pressure and pulse will be measured during inflation Inflation will stop as soon as the blood pressure and pulse rate have been calculated and displayed on the screen. The result will be automatically stored in the memory, and all results will be uploaded to the App automatically upon the next successful Bluetooth connection. SYNC TIME AND RESULTS VIA BLUETOOTH Connect to iOS Device via Bluetooth • Press the START/STOP button for 3 seconds, the Bluetooth indicator will begin flashing. • Enable the Bluetooth on your iOS device(Setting->General->Bluetooth->On) . • Launch the "iHealth MyVitals" app to initiate the connection, the Bluetooth indicator will light up and stop flashing when a successful connection is established. • When sync is processing, the sync indicator flash and , when sync is finished, the sync indicator lights up Connect to Android Device via Bluetooth • Press the START/STOP button for 3 seconds, the Bluetooth indicator will begin flashing. • Enable the Bluetooth on your Android Device. • When using the monitor for the first time, you should pair the monitor to the Android device. Go into your device’s setting to pair it with your Android device. Check the Bluetooth menu for the model name of your monitor (BP7SXXX) to appear, and then select it to pair. This may take up to 30 seconds and your monitor’s Bluetooth indicator will light up when a connection has been established. • Launch the “iHealth MyVitals” app to sync with your monitor. • When sync is processing, the sync indicator flash and , when sync is finished, the sync indicator lights up • Please repeat these steps when you switch to another Android device with the monitor. Remember to: 1. Make sure your wrist size is within cuff circumference; see the range in “SPECIFICATIONS” 2. Measure on the same wrist each time. 3. Stay still and calm for one to one and half minutes before taking a blood pressure measurement. Prolonged over-inflation of the bladder may cause bruises of your wrist. 4. Keep the cuff clean. Cleaning the cuff after every 200 times of usage is recommended. If the cuff becomes dirty, clean it with a moistened cloth. Do not rinse the monitor or cuff with running water. 5. Press the “START/STOP” button at any time to interrupt a measurement. Note: Physical activity, eating, drinking, smoking, excitement, stress, and many other factors influence blood pressure results. SPECIFICATIONS 1. Product name: iHealth View Wireless Blood Pressure Wrist Monitor 2. Model: BP7S 3. Classification: Internally powered; Type BF applied part; IP22, No AP or APG; Continuous operation 4. Machine size: approx. 2.8"×2.9"×0.7" (72mm×74mm×17.6mm) 5. Cuff circumference: 5.3"- 8.7" (13.5cm-22cm) 6. Weight: approx. 4.2oz(120g)(including cuff) 7. Power: DC:5.0V 1.0A, Battery: 1*3.7V Li-ion 400mAh 8. Measurement range: Cuff pressure: 0-300 mmHg Systolic: 60-260 mmHg Diastolic: 40-199 mmHg Pulse rate: 40-180 beats/minute 9. Accuracy: Pressure: ±3 mmHg Pulse rate: ±5% 10. Environmental temperature for operation: 10°C-40°C(50°F -104°F) 11. Environmental humidity for operation: ≤85%RH 12. Environmental temperature for storage and transport:-20°C-55°C(-4°F-131°F) 13. Environmental humidity for storage and transport: ≤85%RH 14. Environmental pressure: 80kPa-105kPa 15. Battery life: more than 80 measurements on a full charge 16. The blood pressure measurement system includes accessories: pump, valve, cuff, and sensor. Note: These specifications are subject to change without notice. GENERAL SAFETY AND PRECAUTIONS 1. 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 healthcare practitioners using the cuff/stethoscope auscultation method within the limits prescribed by the American National Standard, Electronic or Automated Sphygmomanometer. This device is also clinically validated according to the 2010 Protocol of the European Society of Hypertension (ESH 2010). 6. If an Irregular Heartbeat (IHB) is detected during the measurement procedure, the IHB symbol will be displayed in the “iHealth MyVitals” APP. Under this condition, the Wireless Blood Pressure Wrist Monitor can keep functioning, but the results may be inaccurate. Please consult your physician for accurate assessment. The IHB symbol will be displayed under 2 conditions: 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 falls within 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 blood pressure monitor and other devices together with advice regarding avoidance of such interference, please see ELECTROMAGNETIC COMPATIBILITY INFORMATION. It is suggested that the blood pressure monitor should be operated at least 10 meters 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, the monitor will immediately display a technical alarm on the screen. In this case, repeat the measurement ensuring that the proper measurement procedures are followed and/or consult with your medical professional. The technical alarm is preset in the factory and cannot be adjusted or inactivated. This technical alarm is assigned as low priority according to IEC 60601-1-8. The technical 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 IEC 60601-1-2/EN 60601-1-2 such as ASP5-05010002JU (input: 100-240V, 50/60Hz, 200mA; output: DC 5V, 1.0A). Please note that the monitor jack size is USB mini 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-eclamptic patients. Consult your physician before use on children. This product might not meet its performance specifications if stored or used outside the specified temperature and humidity ranges. Please do not share the cuff with any infectious person to avoid cross-infection. BATTERY HANDLING AND USAGE •The battery charge will be displayed on the LED screen when the monitor is active. And when the monitor is connected to the “iHealth MyVitals” APP, the battery charge will be displayed in the APP. If the power is less 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. • 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 charging status will be displayed on the LED screen. See the table below for details. Monitor Status Status Indicator Charging rolling Fully charged symbol steady Low battery symbol flashing (for a few seconds) Do 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, please change the adapter. Do not pull out the adapter when you are using the monitor. Do not use any other type of AC adapter as it may harm the monitor. 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. TROUBLESHOOTING PROBLEM POSSIBLE CAUSE SOLUTION Low Battery Battery do not have enough power Charge the battery LED display reads Pressure system is unstable before measurement “Er0” LED display reads Fail to detect systolic pressure Retest, make sure not to move your arm or the monitor “Er1” LED display reads Fail to detect diastolic pressure “Er2” LED display reads Pneumatic system blocked or cuff is too tight during inflation “Er3” Apply the cuff correctly and try again LED display reads Pneumatic system leakage or cuff is too loose during inflation “Er4” LED display reads Cuff pressure above 300mmHg “Er5” LED display reads More than 160 seconds with cuff pressure above 15 mmHg “Er6” LED display reads Measure again after five minutes. If the monitor is still abnormal, please memory accessing error “Er7” contact the local distributor or the factory. LED display reads Device parameter checking error “Er8” LED display reads Pressure sensor parameter error “ErA” LED display reads Connect the mobile device correctly and try again, If the monitor is still Bluetooth communicate error “ abnormal, please contact the local distributor or the factory. Er” The cuff position was not correct or it was not Review the cuff application instructions and retest LED display reads properly tightened an abnormal Body posture was not correct during testing result Speaking, moving arm or body, being angry, Review body posture instructions and retest Retest when calm; avoid speaking or movement during the test excited or nervous during test Reset iOS/Android device. Reset monitor by pressing the START/STOP Bluetooth Bluetooth connection unsuccessful, monitor is connection abnormal, or strong electromagnetic interference unstable is present button and holding for about 10 seconds. Make sure the monitor and iOS/Android device are away from other electrical equipment. Please see GENERAL SAFETY AND PRECAUTIONS No response when you Press the START/STOP button and hold for about 10 seconds to reset the Incorrect operation or strong electromagnetic interference press button device. CARE AND MAINTENANCE 1. 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. 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 repair those parts of the equipment which are designated for repair can be supplied by the iHealth technical department. 4. Clean the monitor with a dry, soft cloth or a moistened and well wrung soft cloth using water, diluted disinfectant alcohol, or diluted detergent. 5. The monitor can maintain the safety and performance characteristics for a minimum of 10,000 measurements or three years of usage, and the cuff integrity is maintained after 1,000 open close cycles. 6. The battery can maintain the performance characteristics for a minimum of 300 charge cycles. 7. 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 side that contacts skin) of the cuff with a soft cloth lightly moistened with Ethyl alcohol (75-90%). Then air dry the cuff. 8. It is recommended that product performance be checked every 2 years or after each repair. Please contact the iHealth Customer Service Center to do so. 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 the monitor. Do not attempt to disassemble this monitor. Battery replacement should only be performed by a qualified iHealth technician. To do otherwise will void your warranty and possibly damage your unit. Cuff replacement should only be performed by a qualified iHealth technician. To do otherwise will possibly damage your unit. WARRANTY INFORMATION The iHealth View Wireless Blood Pressure Wrist Monitor is warranted to be free from defects in materials and workmanship within one year from the date of purchase when used in accordance with the provided instructions. The warranty extends only to the end user. We will, at our option, repair or replace without charge the iHealth View Wireless Blood Pressure Wrist Monitor covered by the warranty. Repair or replacement is our only responsibility and your only remedy under the warranty. EXPLANATION OF SYMBOLS Symbol 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 be disposed of with household waste. Please recycle where facilities exist. Check with your local authority or retailer for recycling advice". Symbol for "KEEP DRY" Symbol for "WARNING" Symbol for "MANUFACTURER" Symbol for "SERIAL NUMBER" 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 connect specifically to iPod, iPhone, or iPad, respectively, and has been certified by the developer to meet Apple performance standards. 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 iPod touch are trademarks of Apple Inc., registered in the U.S. and other countries. CONTACT AND CUSTOMER SERVICE Manufactured for iHealth Lab Inc. 719N . Shoreline Blvd.,Mountain View, CA 94043, USA Tel:+1-855-816-7705 www.ihealthlabs.com iHealthlabs Europe 3 Rue Tronchet,75008,Paris,France support@ihealthlabs.eu www.ihealthlabs.eu ANDON HEALTH CO., LTD. No. 3 Jinping Street, YaAn Road, Nankai District, Tianjin 300190, China. Tel: 86-22-60526161 IMPORTANT INFORMATION REQUIRED BY THE FCC This 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 the FCC 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 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 product 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. This product complies with Industry Canada. IC: RSS-210 IC NOTICE This 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. OTHER STANDARDS AND COMPLIANCES The Wireless Blood Pressure Wrist 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: General requirements 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 for electro-mechanical blood pressure measuring systems); AAMI/ANSI 80601-2-30：2009/IEC 80601-2-30：2009+Cor.2010/EN 80601-2-30:2010(Medical electrical equipment –Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers). ELECTROMAGNETIC COMPATIBILITY INFORMATION Table 1 For all ME EQUIPMENT and ME SYSTEMS Guidance and manufacture’s declaration - electromagnetic emissions BP7S is intended for use in the electromagnetic environment specified below. The user of BP7S should ensure that it is used in such an environment. Emissions test Compliance Electromagnetic environment - guidance BP7S uses RF energy only for its internal function. Therefore, its RF RF emissions Group 1 CISPR 11 emissions are very low and are not likely to cause any interference in nearby electronic equipment. RF emissions Class B CISPR 11 Harmonic emissions Class A IEC 61000-3-2 BP7S 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. Voltage fluctuations/ flicker emissions Complies IEC 61000-3-3 Table 2 For all ME EQUIPMENT and ME SYSTEMS Guidance and manufacturer’s declaration - electromagnetic immunity BP7S is intended for use in the electromagnetic environment specified below. The user of BP7S should ensure that it is used in such an environment. IMMUNITY test Electrostatic discharge (ESD) IEC 60601test level Compliance level Electromagnetic environment - guidance ± 6 kV contact ± 6 kV contact Floors should be wood, concrete or ceramic tile. ± 8 kV air ± 8 kV air If floors are covered with synthetic material, the IEC 61000-4-2 relative humidity should be at least 30 %. Electrical fast ± 2 kV for power supply ± 2 kV for power supply Main power quality should be that of a typical transient/burst lines lines commercial or hospital environment. ± 1 kV line(s) to line(s) ± 1 kV line(s) to line(s) Main power quality should be that of a typical IEC 61000-4-5 ± 2 kV line(s) to earth ± 2 kV line(s) to earth commercial or hospital environment. Voltage dips, short <5 % UT <5 % UT Main power quality should be that of a typical IEC 61000-4-4 Surge interruptions and (>95 % dip in UT) (>95 % dip in UT) commercial or hospital environment. If the user of voltage variations for 0.5 cycle for 0.5 cycle BP7S requires continued operation during power on power supply 40 % UT 40 % UT main interruptions, it is recommended that BP7S input lines (60 % dip in UT) (60 % dip in UT) be powered from an uninterruptible power supply IEC 61000-4-11 for 5 cycles for 5 cycles or a battery. 70 % UT 70 % UT Power frequency (30 % dip in UT) (30 % dip in UT) for 25 cycles for 25 cycles <5 % UT <5 % UT (>95 % dip in UT) (>95 % dip in UT) for 5 s for 5 s 3 A/m 3 A/m Power frequency magnetic fields should be at (50/60 Hz) levels characteristic of a typical location in a magnetic field typical commercial or hospital environment. IEC 61000-4-8 NOTE: UT is the a.c. main voltage prior to application of the test level. Table 3 For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING Guidance and manufacturer’s declaration - electromagnetic immunity BP7S is intended for use in the electromagnetic environment specified below. The user of BP7S should ensure that it is used in such an environment. IMMUNITY test IEC 60601test level Complian Electromagnetic environment - guidance ce level Portable and mobile RF communications equipment should be used no closer to any part of BP7S, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distance： d = 1.2 P Conducted RF 3 Vrms 150 kHz to IEC 61000-4-6 80 MHz Radiated RF 3 V/m 80 MHz to 2.5 IEC 61000-4-3 GHz 3V d = 1 .2 P 3 V/m d = 2 .3 P 80 MHz to 800 MHz 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 meters (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.b Interference may occur in the vicinity of equipment marked with the following symbol: 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 BP7S is used exceeds the applicable RF compliance level above, BP7S should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating BP7S. b) Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m. Table 4 For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING Recommended separation distances between portable and mobile RF communications equipment and the Wireless Blood Pressure Wrist Monitor BP7S is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The user of BP7S can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and BP7S as recommended below, according to the maximum output power of the communication equipment. Rated maximum output Separation distance according to frequency of transmitter power of transmitter W 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2,5 GHz d = 1 .2 P d = 1 .2 P 0.01 0.12 0.12 0.23 0.1 0.38 0.38 0.73 1.2 1.2 2.3 10 3.8 3.8 7.3 100 12 12 23 d = 2 .3 P For 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 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. BP7S-SMSY01 V1.0
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