U7I-BP3MX1-3TDigital Blood Pressure Monitor

Accumeawith Instru c EN rate home b surements the WatchB c tion Manual 3 b lood pressu r P Home T. r e 2 Federal Communications Commission (FCC) Statement changes or modifications not expressly appr oved by the party responsible for compliance could void the user’s authority to operate the equipment. This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interfer ence received, including interference that may cause undesired operation. Note: This equipment has been tested and found to comply with the li mits 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 installatio n. This equipment generates, uses, and can radiate radio frequency energy, and if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which c an be determined by turning the equipment off and on, the user is encour aged to try to correct the interference by one or more of the following measures: – – Reo rient or relocate the re ceiving antenna. – Inc rease the separation between the equipment and receiver. – Connect the equipment into an outlet on a circuit diff erent from that to which the receiver is connected . Consult the dealer or an experien ced radio/TV technician for help. This device complies with FCC radiatio n e xposure limits set fo rth for an uncontrolled environment. End users must follow the specific operating instructions for sati sfying RF exposure compliance .) 3 EN Microlife WatchBP Home T is the world’s first digital blood pressu re measurement device that stri ctly follows European Society of Hypertension (ESH) 1, 2 and American Heart Association (AHA) recommendation s for home blood pressure measurement. Using the WatchBP Home T device helps you collect accu rate home blood pressure measurements your doctor can trust. This WatchBP Home T device has been clinically valid ated according to the ESH protocol 3 . Indications For Use The Microlife Upper Arm Automatic Digital Blood Pressure Monitor, M o d e l W a t c h B P H o m e T ( B P 3 M X 1 - 3 T ) i s a d e v i c e i n t e n d e d t o measure the systolic and diastolic blood pressure and pulse rate of an adult individual with arm cuff circumference sizes rangi ng from 22 -42 cm by using a non-invasive oscillometric technique in on e inflatable cuff being wra pped around the upper arm. The memory data can be transferred to the PC (personal computer) running the WatchBP An alyzer Home software by connecting the monitor via cable. The device can also be used in connection with smart mobile devices runni ng the APP and via Bluetooth. The device detects the appearance of atrial fibrillation during measurement and gives a warning signal with the reading once atrial fibrillation is detected. It is in tended for use in individuals previously diagnosed with AFib. Th e feature has not been tested for and is not intended for use in people under 22 years of age. Table of Contents Before using WatchBP Home T for the first time Product description ................................. ...................... 5–6 Activating the device .. ............................ .......................... 7 Selecting the correct cuff ........................ .......................... 8 Taking measurements using WatchBP Home T «DIAG.» Mode ....................... ........................... ........... 9–10 «USUAL» Mode ..................... ........................... .............. 12 Eight steps for measure blood pressure properly Blood pressure measurement procedures .............. 13–14 Special Function Atrial Fibrillation Detectio n ......................... .................. 17 About Atrial Fibrillation ............................... .................. 18 Atrial Fibrillation Detector ........................... .................. 19 Atrial fibrillation detection instructions ........................ 20 Information for the doctor ............................. ................ 20 Viewing, deleting, and transferring measurements Viewing measurements ......... ............................ ..... 21–22 Deleting measurements .... ............................ .......... 23–24 Installation of the software program ............................ 25 Bluetooth connectivity .. ........................... ................ 26-27 Batteries and power adapto r ......................... .......... 29–30 Safety, care, accuracy test and disposal .................. 31–32 Error messages ................... ............................ .......... 33–34 Important facts ........................ ............................ ..... 35–36 Technical specifications . ................................ ................ 37 Appendix ........................... ............................ ................ 38 5 EN USUAL DIAG. NOCTURNAL Bluetooth symbol SYS mmHg DIA mmHg PUL /min Serial Port Mode Switch Power Socket Di splay ON/OFF Button M Button (Memory) Batt ery Compartment Cuff Socket 6 Atrial F Outsid e Mode Indicatio n Doctor Symb o F ibrillation Detecti o e Measurement Ti m Rel a Battery Displ a Delete Memory Da Stored Val u n o l o n m e a x a y ta u e Morning Data Evening Data Date/Time Systolic Value Diastolic Valu e Pulse Indicato r Pulse Rate Number of St o EN e r o red Data Before u Activating t Pull out the pro t compartment. 1) Set the year installing ne w the display. Uthe ON/OFF B sing Watch B t he Device t ective strip from the – Upon removing the w batteries, the Year n se the M Button to s e B utton to confirm yo u B P Home T f battery protective strip or n umber flashes in e lect the Year. Press u r …

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Report No.: EED32M00333301Page 53 of 60 PHOTOGRAPHS OF EUT Constructional Details Test model No.: WatchBP Home T(BP3MX1-3T) View of Product-1 View of Product-2 Report No.: EED32M00333301Page 54 of 60 View of Product-3 View of Product-4 Report No.: EED32M00333301Page 55 of 60 View of Product-5 View of Product-6 Report No.: EED32M00333301Page 56 of 60 View of Product-7 View of Product-8

BP3MX1-3TFCClabelandsize

Report No.: EED32M00333301Page 56 of 60 View of Product-7 View of Product-8 Report No.: EED32M00333301Page 57 of 60 View of Product-9 View of Product-10 Report No.: EED32M00333301Page 58 of 60 View of Product-11 View of Product-12 Report No.: EED32M00333301Page 59 of 60 View of Product-13 View of Product-14 Report No.: EED32M00333301Page 60 of 60 View of Product-15 View of Product-16 The test report is effective only with both signature and specialized stamp, The result(s) shown in this report refer only to the sample(s) tested. Without written approval of CTI, this report can’t be reproduced except in full. *** End of Report *** Antenna

Report No.: EED32M00333302Page 1 of 8 1 COVER PAGE RF Exposure Evaluation Report Product:Digital Blood Pressure Monitor Trade mark:microlife Model/Type reference :WatchBP Home T(BP3MX1-3T) Serial Number:N/A Report Number:EED32M00333302 FCC ID: U7I-BP3MX1-3T Date of Issue:Dec. 01, 2020 Test Standards: 47 CFR Part 1.1307 47 CFR Part 1.1310 KDB447498D01 General RF Exposure Guidance v06 Test result:PASS Prepared for: Microlife Corporation 9F, 431, RuiGuang Road, NeiHu Taipei 11492, Taiwan Prepared by : Centre Testing International Group Co., Ltd. Hongwei Industrial Zone, Bao’an 70 District, Shenzhen, Guangdong, China TEL: +86-755-3368 3668 FAX: +86-755-3368 3385 Compiled by:Reviewed by: Sunlight SunBill Lu Approved by:Date:Dec. 01, 2020 Aaron Ma CheckNo.:4538050193 Report No. : EED32M00333302Page 2 of 8 2 Version Version No.DateDescription 00Dec. 01, 2020Original Report No. : EED32M00333302Page 3 of 8 3 Contents Page 1 COVER PAGE ..................................................................................................................................................................... 1 2 VERSION .............................................................................................................................................................................. 2 3CONTENTS .......................................................................................................................................................................... 3 4 GENERAL INFORMATION ............................................................................................................................................... 4 4.1 C LIENT I NFORMATION .................................................................................................................................................... 4 4.2 G ENERAL D ESCRIPTION OF EUT .................................................................................................................................. 4 4.3 P RODUCT S PECIFICATION SUBJECTIVE TO THIS STANDARD ........................................................................................ 4 4.4 T EST L OCATION ............................................................................................................................................................. 5 4.5 D EVIATION FROM S TANDARDS ...................................................................................................................................... 5 4.6 A BNORMALITIES FROM S TANDARD C ONDITIONS .......................................................................................................... 5 4.7 O THER I NFORMATION R EQUESTED BY THE C USTOMER .............................................................................................. 5 5 SAR EVALUATION ............................................................................................................................................................. 6 5.1 RF E XPOSURE C OMPLIANCE R EQUIREMENT ............................................................................................................... 6 5.1.1 Standard Requirement ........................................................................................................................................ 6 5.1.2 EUT RF Exposure ............................................................................................................................................... 7 PHOTOGRAPHS OF EUT CONSTRUCTIONAL DETAILS ........................................................................................... 8 Report No. : EED32M00333302Page 4 of 8 4 General Information 4.1 Client Information Applicant: Microlife Corporation Address of Applicant: 9F, 431, RuiGuang Road, NeiHu Taipei 11492, Taiwan Manufacturer: ONBO Electronic (Shenzhen) Co., Ltd. Address of Manufacturer: No.138, Huasheng Road, Langkou Community, Dalang Street, Longhua District, Shenzhen, China Factory: ONBO Electronic (Shenzhen) Co., Ltd. Address of Factory: No.138, Huasheng Road, Langkou Community, Dalang Street, Longhua District, Shenzhen, China 4.2 General Description of EUT Product Name:Digital Blood Pressure Monitor Model No.(EUT): WatchBP Home T(BP3MX1-3T) Trade Mark: microlife EUT Supports Radios application: 4.2(BLE) 4.3 Product Specification subjective to this standard Frequency Range:2402MHz~2480MHz Modulation Type:GFSK Test Power Grade: Default Test Software of EUT: Default Antenna Type:CeramicAntenna Antenna Gain:3dBi Power Supply:DC 6.0V Max Conducted Peak Output Power: BT4.2: -4.132dBm The Max Conducted Peak Output Power data refer to the report EED32M00333301 Sample Received Date: Nov. 16, 2020 Sample tested Date: Nov. 16, 2020 to Nov. 20, 2020 Company Name and Address shown on Report, the sample(s) and sample Information was/ were provided by the applicant who should be responsible for the authenticity which CTI hasn’t verified. Model No.: WatchBP Home T(BP3MX1-3T) Only the model WatchBP Home T(BP3MX1-3T) was tested. Their electrical circuit design, layout, components used, internal wiring, software and outer decoration are identical, only the model name are different, the tested product has two model names, WatchBP Home T is the market model name; BP3MX1-3T is the factory internal model name. Report No. : EED32M00333302Page 5 of 8 4.4 Test Location All tests were performed at: Centre Testing International Group Co., Ltd Building C, Hongwei Industrial Park Block 70, Bao'an District, Shenzhen, China Telephone: +86 (0) 755 33683668 Fax:+86 (0) 755 33683385 No tests were sub-contracted. FCC Designation No.: CN1164 4.5 Deviation from Standards None. 4.6 Abnormalities from Standard Conditions None. 4.7 Other Information Requested by the Customer None. Report No. : EED32M00333302Page 6 of 8 5 SAR Evaluation 5.1 RF Exposure Compliance Requirement 5.1.1 Standard Requirement According to KDB447498D01 General RF Exposure Guidance v06 Standalone SAR test exclusion considerations Unless specifically req…

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Report No.: EED32M00333301Page 1 of 60 1 COVER PAGE TEST REPORT Product:Digital Blood Pressure Monitor Trade mark:microlife Model/Type reference :WatchBP Home T(BP3MX1-3T) Serial Number:N/A Report Number:EED32M00333301 FCC ID: U7I-BP3MX1-3T Date of Issue:Dec. 01, 2020 Test Standards: 47 CFR Part 15Subpart C Test result:PASS Prepared for: Microlife Corporation 9F, 431, RuiGuang Road, NeiHu Taipei 11492, Taiwan Prepared by : Centre Testing International Group Co., Ltd. Hongwei Industrial Zone, Bao’an 70 District, Shenzhen, Guangdong, China TEL: +86-755-3368 3668 FAX: +86-755-3368 3385 Compiled by:Reviewed by: Sunlight SunBill Lu Approved by:Date:Dec. 01, 2020 Aaron Ma Check No.:4538050193 Report No.: EED32M00333301Page 2 of 60 2Version Version No.DateDescription 00Dec. 01, 2020Original Report No.: EED32M00333301Page 3 of 60 3TestSummary Test ItemTest RequirementTest methodResult Antenna Requirement 47 CFR Part 15Subpart C Section 15.203/15.247 (c) ANSI C63.10-2013PASS AC Power Line Conducted Emission 47 CFR Part 15Subpart C Section 15.207 ANSI C63.10-2013PASS Conducted Peak Output Power 47 CFR Part 15Subpart C Section 15.247 (b)(3) ANSI C63.10-2013PASS 6dB Occupied Bandwidth 47 CFR Part 15Subpart C Section 15.247 (a)(2) ANSI C63.10-2013PASS Power Spectral Density 47 CFR Part 15Subpart C Section 15.247 (e) ANSI C63.10-2013PASS Band-edge for RF Conducted Emissions 47 CFR Part 15Subpart C Section 15.247(d) ANSI C63.10-2013PASS RF Conducted Spurious Emissions 47 CFR Part 15Subpart C Section 15.247(d) ANSI C63.10-2013PASS Radiated Spurious Emissions 47 CFR Part 15Subpart C Section 15.205/15.209 ANSI C63.10-2013PASS Restricted bands around fundamental frequency (Radiated Emission) 47 CFR Part 15Subpart C Section 15.205/15.209 ANSI C63.10-2013PASS Remark: Test according to ANSI C63.4-2014 & ANSI C63.10-2013. Company Name and Address shown on Report, the sample(s) and sample Information was/ were provided by the applicant who should be responsible for the authenticity which CTI hasn’t verified. Model No.: WatchBP Home T(BP3MX1-3T) Only the model WatchBP Home T(BP3MX1-3T) was tested. Their electrical circuit design, layout, components used, internal wiring, software and outer decoration are identical, only the model name are different, the tested product has two model names, WatchBP Home T is the market model name; BP3MX1-3T is the factory internal model name. Report No.: EED32M00333301Page 4 of 60 4 Content 1 COVER PAGE..................................................................................................................................................................... 1 2 VERSION..............................................................................................................................................................................2 3 TEST SUMMARY................................................................................................................................................................3 4CONTENT.............................................................................................................................................................................4 5 TEST REQUIREMENT.......................................................................................................................................................5 5.1 T EST SETUP ................................................................................................................................................................... 5 5.1.1 For Conducted test setup ................................................................................................................................... 5 5.1.2 For Radiated Emissions test setup ................................................................................................................... 5 5.1.3 For Conducted Emissions test setup ............................................................................................................... 6 5.2 T EST E NVIRONMENT ...................................................................................................................................................... 6 5.3 T EST C ONDITION ........................................................................................................................................................... 6 6 GENERAL INFORMATION...............................................................................................................................................7 6.1 C LIENT I NFORMATION ....................................................................................................................................................7 6.2 G ENERAL D ESCRIPTION OF EUT..................................................................................................................................7 6.3 D ESCRIPTION OF S UPPORT U NITS ...............................................................................................................................9 6.4 T EST L OCATION .............................................................................................................................................................9 6.5 A BNORMALITIES FROM S TANDARD C ONDITIONS ..........................................................................................................9 6.6 O THER I NFORMATION R EQUESTED BY THE C USTOMER ..............................................................................................9 6.7 M EASUREMENT U NCERTAINTY (95% CONFIDENCE LEVELS , K =2)..............................................................................9 7EQUIPMENTLIST............................................................................................................................................................ 10 8 RADIO TECHNICAL REQUIREMENTS SPECIFICATION........................................................................................12 Appendix A): 6dB Occupied Bandwidth .............…

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Report No.: EED32M00333301Page 50 of 60 PHOTOGRAPHS OF TEST SETUP Test model No.: WatchBP Home T(BP3MX1-3T) Radiated spurious emissionTest Setup-1(Below 30MHz) Radiated spurious emissionTest Setup-2(Below 1GHz) Report No.: EED32M00333301Page 51 of 60 Radiated spurious emission Test Setup-3( Above 1GHz) Radiated spurious emission Test Setup-3( Above 1GHz) There are absorbing materials under the ground. Report No.: EED32M00333301Page 52 of 60 Conducted Emissions Test Setup