2AQVU0029Arm-Type Fully Automatic Digital Blood Pressure Monitor

Contents Safety Notice ............................................................................ 02 Unit Illustration ....................................................................... 06 Important Testing Guidelines ................................................. 08 Quick Start ................................................................................ 09 Unit Operation ......................................................................... 10 Blood Pressure Information .................................................... 23 Blood Pressure Q&A ................................................................ 26 Maintenance .............................................................................. 27 Specifications ............................................................................. 29 Warranty .................................................................................... 31 Electromagnetic Compatibility Information ......................... 32 Battery Installation ........................................................................ 10 System Settings ................................................................................. 11 Applying the Arm Cuff .............................................................. 15 Testing ................................................................................................. 15 Power Off .......................................................................................... 17 HSD ........................................................................................................ 17 ........................................................................ 17 ......................................................... 18 .................................................................................. 18 Cuff loose Indicator Memory Deletion Low Battery Indicator............................................................................ 19 Troubleshooting ......................................................................................... 22 Memory view and average view Bluetooth connection..................................................................................... 20 Safety Notice Model BM 92 Arm Type 12 Owner's Manual Arm-type Fully Automatic Digital Blood Pressure Monitor Thank you for purchasing the BM 92 Blood Pressure Monitor. The unit has been constructed using reliable circuitry and durable materials. Used properly, this unit will provide years of satisfactory use. Indications for use: The Arm-type Fully Automatic Digital Blood Pressure monitors are intended to measure blood pressure(systolic and diastolic) and pulse rate of adults and adolescents over 12 years of age. All functions can be used safely and values can be read out in one LCD DISPLAY. Measurement position is on adult upper arm only. The PATIENT is an intended OPERATOR. Blood pressure measurement determined with this device are equivalent to those obtained by a trained observer using the cuff/ stethoscope auscultation method, within the limits prescribed by the Recognized Consensus Standard (IEC 80601-2-30) for electronic sphygmomanometers. Precautions to Ensure Safe, Reliable Operation 1. Do not drop the unit. Protect it from sudden jars or shocks. 2. Do not insert foreign objects into any openings. 3. Do not attempt to disassemble the unit. 4. Do not crush the pressure cuff. 5. If the unit has been stored at temperatures below 0 °C, leave it in a warm place for about 15 minutes before using it. Otherwise, the cuff may not inflate properly. 6. If the unit has been stored at temperatures above 40 °C, leave it in a cool place for about 15 minutes before using it. Otherwise, the cuff may not inflate properly. 7. Do not store the unit in direct sunlight, high humidity or dust. 8.To avoid any possibility of accidental strangulation, keep this unit away from children and do not drape tubing around your neck. 9.Ensure that children do not use the instrument unsupervised; some parts are small enough to be swallowed. 10.Some may get a skin irritation from the cuff taking frequent readings over the course of the day, but this irritation typically goes away on its own after the monitor is removed. Document No.:XXXXXXXXXX Contact Information The lay operator or lay responsible or ganization should contact the manufacturer or the representative of manufacturer. -for assistance,if needed,in setting up,using or maintaining the product,or -to report unexpected operation or events. Manufactured by JOYTECH Healthcare Co.,Ltd. Email: [email protected] Telephone: +86-571-81957767 Fax: +86-571-81957750 No.365, Wuzhou Road,Yuhang Economic Development Zone, Hangzhou City,311100 Zhejiang,China Version：Z Date of Issue：XXXXXX Arm Type Unit Illustration 6 Arm Cuff Medium size cuff (fits arm circumference: 22.0 cm -36.0 cm). If air is leaking from the arm cuff, replace the arm cuff with a new one. It is generally recomm ended to have the cuff replaced timely to ensure correct functioning and accuracy. Please consult your local authorized Sejoy distributor or dealer. 5 Safety Notice 3 Important Instructions Before Use 1. Do not confuse self-monitoring with self-diagnosis. Blood pressure measurements should only be interpreted by a health professional who is familiar with your medical history. 2. Contact your physician if test results regularly indicate abnormal readings. 3. If you are taking medication, consult with your physician to determine the most appropriate time to measure your blood pressure. NEVER change a prescribed medication without first consulting with your physician. 4. Individuals with serious circulation problems may experience discomfort. Consult your physician prior to use. 5. For persons with irregular or unstable circulation resulting from diabetes, liver disease, arteriosclerosis or other medical conditions, there may be variations in blood pressure values measured at the wrist versus at the upper arm. Monitoring the tre…

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Report No.: 2207RSU046-UE 1 of 3 External Photograph (1) EUT Photo (2) EUT Photo Report No.: 2207RSU046-UE 2 of 3 (3) EUT Photo (4) EUT Photo Report No.: 2207RSU046-UE 3 of 3 (5) EUT Photo (6) EUT Photo

Size: 35mm x16mm Arm-Type Fully Automatic Digital Blood Pressure Monitor Manufacturers by JOYTECH Healthcare Co., Ltd. No. 365, Wuzhou Road, Yuhang Economic Development Zone, Hangzhou City,311100 Zhejiang, China Power: Batteries 4×1.5V AAA Series number: Manufacturing Date: FCC ID :2AQVU0029 Model: BM 92 Made in China IP21

Report No.: 2207RSU046-UE 1 of 5 Internal Photograph (1) EUT Photo (2) EUT Photo Report No.: 2207RSU046-UE 2 of 5 (3) EUT Photo (4) EUT Photo Report No.: 2207RSU046-UE 3 of 5 (5) EUT Photo (6) EUT Photo Report No.: 2207RSU046-UE 4 of 5 (7) EUT Photo (8) EUT Photo Report No.: 2207RSU046-UE 5 of 5 (9) EUT Photo (10) EUT Photo

MRT Technology (Suzhou) Co., Ltd Report No.: 2207RSU046-U3 Phone: +86-512-66308358 Report Version: V01 Web: www.mrt-cert.com Issue Date: 2022-09-23 1 of 10 RF Exposure Evaluation Declaration FCC ID: 2AQVU0029 Applicant: JOYTECH HEALTHCARE CO., LTD. Product: Arm-Type Fully Automatic Digital Blood Pressure Monitor Model No.: BM 92 FCC Rule Part(s): FCC Part 2.1093 Result: Complies Reviewed By: Sunny Sun Approved By: Robin Wu The test results relate only to the samples tested. The test results shown in the test report are traceable to the national/international standards through the calibration of the equipment and evaluated measurement uncertainty herein. The test report shall not be reproduced except in full without the written approval of MRT Technology (Suzhou) Co., Ltd. Report No.: 2207RSU046-U3 2 of 10 Revision History Report No. Version Description Issue Date Note 2207RSU046-U3 Rev. 01 Initial Report 2022-09-23 Valid Report No.: 2207RSU046-U3 3 of 10 CONTENTS Description Page 1. General Information ................................................................................................................................ 4 1.1. Applicant ........................................................................................................................................ 4 1.2. Manufacturer ................................................................................................................................. 4 1.3. Testing Facility ............................................................................................................................... 4 1.4. Product Information ....................................................................................................................... 5 1.5. Applied Standards ......................................................................................................................... 5 1.6. Device Classification ..................................................................................................................... 5 2. RF Exposure Evaluation ......................................................................................................................... 6 2.1. Test Limits ..................................................................................................................................... 6 2.1. MPE Exemptions ........................................................................................................................... 7 2.2. Calculated Result ........................................................................................................................ 10 Report No.: 2207RSU046-U3 4 of 10 1. General Information 1.1. Applicant JOYTECH HEALTHCARE CO., LTD. No. 365. Wuzhou Road, Yuhang Economic Development Zone, Hangzhou City, Zhejiang, China 1.2. Manufacturer JOYTECH HEALTHCARE CO., LTD. No. 365. Wuzhou Road, Yuhang Economic Development Zone, Hangzhou City, Zhejiang, China 1.3. Testing Facility Test Site – MRT Suzhou Laboratory Laboratory Location (Suzhou - Wuzhong) D8 Building, No.2 Tian’edang Rd., Wuzhong Economic Development Zone, Suzhou, China Laboratory Location (Suzhou - SIP) 4b Building, Liando U Valley, No.200 Xingpu Rd., Shengpu Town, Suzhou Industrial Park, China Laboratory Accreditations A2LA: 3628.01 CNAS: L10551 FCC: CN1166 ISED: CN0001 VCCI: R-20025 G-20034 C-20020 T-20020 R-20141 G-20134 C-20103 T-20104 Test Site – MRT Shenzhen Laboratory Laboratory Location (Shenzhen) 1G, Building A, Junxiangda Building, Zhongshanyuan Road West, Nanshan District, Shenzhen, China Laboratory Accreditations A2LA: 3628.02 CNAS: L10551 FCC: CN1284 ISED: CN0105 Test Site – MRT Taiwan Laboratory Laboratory Location (Taiwan) No. 38, Fuxing 2nd Rd., Guishan Dist., Taoyuan City 333, Taiwan (R.O.C.) Laboratory Accreditations TAF: L3261-190725 FCC: 291082, TW3261 ISED: TW3261 Report No.: 2207RSU046-U3 5 of 10 1.4. Product Information Product Name Arm-Type Fully Automatic Digital Blood Pressure Monitor Model No. BM 92 Test Device Identification No. 20220721Sample#01 (Conducted Test) 20220721Sample#03 (Radiated Test) Bluetooth Version V5.0 (BLE only) Hardware Version v1.0 Software Version v1.0 Power Supply 4 x 1.5v AAA batteries Remark: The information of EUT was provided by the manufacturer, and the accuracy of the information shall be the responsibility of the manufacturer. 1.5. Applied Standards According to the specifications of the manufacturer, the EUT must comply with the requirements of the following standards: ⚫ FCC Part 2.1093 & KDB 447498 D04 Interim General RF Exposure Guidance v01 1.6. Device Classification According to the user manual, the device can be used in the portable exposure condition without restriction. This device is classified as a Portable Device. So, the RF exposure evaluation requirements of § 2.1093 for portable device exposure conditions subject to MPE limits. Report No.: 2207RSU046-U3 6 of 10 2. RF Exposure Evaluation 2.1. Test Limits According to FCC §1.1310: The criteria listed in the following table shall be used to evaluate the environment impact of human exposure to radio frequency (RF) radiation as specified in §1.1307(b) Limits For Maximum Permissible Exposure (MPE) Frequency Range (MHz) Electric Field Strength (V/m) Magnetic Field Strength (A/m) Power Density (mW/cm 2 ) Average Time (Minutes) (A) Limits for Occupational/ Control Exposures 0.3-3.0 614 1.63 *(100) ≤6 3.0-30 1842/f 4.89/f *(900/f 2 ) <6 30-300 61.4 0.163 1.0 <6 300-1,500 -- -- f/300 <6 1,500-100,000 -- -- 5 <6 (B) Limits for General Population/ Uncontrolled Exposures 0.3-1.34 614 1.63 *(100) <30 1.34-30 824/f 2.19/f *(180/f 2 ) <30 30-300 27.5 0.073 0.2 <30 300-1,500 -- -- f/1500 <30 1,500-100,000 -- -- 1.0 <30 f= frequency in MHz. * = Plane-wave equivalent power density. Report No.: 2207RSU046-U3 7 of 10 2.1. MPE Exemptions For single RF sources (i.e., any single fixed RF source, mobile device, or portable device, as defined in paragraph §1.1307(b)(2) of this s…

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MRT Technology (Suzhou) Co., Ltd Report No.: 2207RSU046-U2 Phone: +86-512-66308358 Report Version: V01 Web: www.mrt-cert.com Issue Date: 2022-09-23 1 of 46 RF MEASUREMENT REPORT FCC ID: 2AQVU0029 Applicant: JOYTECH HEALTHCARE CO., LTD. Product: Arm-Type Fully Automatic Digital Blood Pressure Monitor Model No.: BM 92 FCC Classification: Digital Transmission System (DTS) FCC Rule Part(s): Part 15 Subpart C (Section 15.247) Result: Complies Test Date: 2022-07-27 ~ 2022-09-06 Reviewed By: Sunny Sun Approved By: Robin Wu The test results relate only to the samples tested. This equipment has been shown to be capable of compliance with the applicable technical standards as indicated in the measurement report and was tested in accordance with the measurement procedures specified in ANSI C63.10-2013. Test results reported herein relate only to the item(s) tested. The test report shall not be reproduced except in full without the written approval of MRT Technology (Suzhou) Co., Ltd. Report No.: 2207RSU046-U2 2 of 46 Revision History Report No. Version Description Issue Date Note 2207RSU046-U2 Rev. 01 Initial Report 2022-09-23 Valid Report No.: 2207RSU046-U2 3 of 46 CONTENTS Description Page 1. General Information ................................................................................................................................ 5 1.1. Applicant ...................................................................................................................................... 5 1.2. Manufacturer ................................................................................................................................ 5 1.3. Testing Facility ............................................................................................................................. 5 1.4. Product Information ...................................................................................................................... 6 1.5. Radio Specification under Test .................................................................................................... 6 1.6. Working Frequencies ................................................................................................................... 7 2. Test Configuration ................................................................................................................................... 8 2.1. Test System Connection Diagram................................................................................................ 8 2.2. Test Software ............................................................................................................................... 8 2.3. Applied Standards ........................................................................................................................ 9 2.4. Test Environment Condition ......................................................................................................... 9 3. Antenna Requirements ......................................................................................................................... 10 4. Measuring Instrument ........................................................................................................................... 11 5. Decision Rules and Measurement Uncertainty .................................................................................. 12 5.1. Decision Rules ........................................................................................................................... 12 5.2. Measurement Uncertainty .......................................................................................................... 12 6. Test Result .............................................................................................................................................. 13 6.1. Summary .................................................................................................................................... 13 6.2. 6dB Bandwidth Measurement .................................................................................................... 14 6.2.1. Test Limit .................................................................................................................................... 14 6.2.2. Test Procedure ........................................................................................................................... 14 6.2.3. Test Setting ................................................................................................................................ 14 6.2.4. Test Setup .................................................................................................................................. 14 6.2.5. Test Result ................................................................................................................................. 14 6.3. Output Power Measurement ...................................................................................................... 15 6.3.1. Test Limit .................................................................................................................................... 15 6.3.2. Test Procedure ........................................................................................................................... 15 6.3.3. Test Setting ................................................................................................................................ 15 6.3.4. Test Setup .................................................................................................................................. 15 6.3.5. Test Result ................................................................................................................................. 15 6.4. Power Spectral Density Measurement ...................................................................................... 16 6.4.1. Test Limit .............................................................................…

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蓝牙天线规格 1：Antenna Description Antenna Type Microtrip Antenna Antenna peak gain 0dBi Frequency range 2.402GHz～2.480GHz Connect type Simulation 2：Antenna pictu re on the PCB borad 3：Antenna radiation of 3D polar Solution frequency at 2.453G 3：Antenne radiation pattern

Report No.: 2207RSU046-UT Test Setup Photo Description: Radiated Spurious Emission Test Setup for Below 1GHz Description: Radiated Spurious Emission Test Setup for Above 1GHz Report No.: 2207RSU046-UT Description: RF Conducted Test Setup