2ABTAHNL85DMAutomatic Upper Arm Blood Pressure Monitor

1 VER: A001 202101 I I n n s s t t r r u u c c t t i i o o n n M M a a n n u u a a l l Automatic Upper Arm Blood Pressure Monitor Model No. HL858DM 2 VER: A001 202101 Table of Contents Medical Disclaimer.......................................................................................03 Intended Use...............................................................................................03 About Blood Pressure.................................................................................04 Measurement Method..............................................................................06 Accuracy..............................................................................................07 Precautions.....................................................................................08 Device Overview...........................................................................................11 Symbol Definitions.....................................................................................13 Features.........................................................................................................14 Installing Batteries.....................................................................................17 Using the AC/DC Adapter.....................................................................18 Applying the Cuff........................................................................................19 Measurement Procedure..........................................................................20 Memory Function........................................................................................23 Storage and Maintenance.........................................................................24 Bluetooth Communication.........................................................................25 Troubleshooting...........................................................................................27 Limited Warranty........................................................................................28 Specifications..............................................................................................29 Note..............................................................................................................30 Appendix........................................................................................................32 Blood Pressure Diary.................................................................................35 3 VER: A001 202101 Medical Disclaimer This manual and product are not meant as a substitute for advice provided by your doctor. You are not to use the information contained herein, or this product for diagnosing or treating a health problem or prescribing any medication. If you have or suspect that you have a medical problem, promptly consult your healthcare provider. Intended Use This device uses the oscillometric method to automatically measure systolic and diastolic blood pressure as well as heart rate.The measurement position is at human being’s arm. All values can be read out in the LCD panel. Measurement position is at human being’s upper arm. The intended user of this over-the-counter device is adults aged 18 years and older with arm circumference ranging from 9 inches to 17 inches (approx.23 cm to 43 cm) for home use. HL858DM features BP Category Indicator that will show the inf ormation with the readings on the screen for the user tracking their blood pressure level. HL858DM is equipped with an Advanced IHB detection feature to collect and analyze pulses. If the specific irregular heartbeats are detected and it may affect blood pressure reading with deviation, the device will give the user a warning signal. The feature can inform the user that the measured blood pressure reading may be inaccurate once the specific irregular heartbeats are detected. Besides, the device features a built-in "Bluetooth Transmission" function, which enables the device automatically transmit measuring results to paired Bluetooth-enabled device. Also, users could simply synchronize the current date and time, and check the battery status of blood pressure monitor by means of DailyChek ® application software with the paired Bluetooth-enabled device. 4 VER: A001 202101 About Blood Pressure A. What is blood pressure? Blood pressure is the measurement of the force of blood pushing against the walls of the arteries. Arterial blood pressure is constantly fluctuating during the course of the cardiac cycle. The highest pressure in the cycle is called the systolic blood pressure, and represents the pressure in the artery when the heart is beating. The lowest pressure is the diastolic blood pressure, and represents the pressure in the artery when the heart is at rest. Both the systolic and the diastolic pressure are necessary for a physician to evaluate the status of a patient's blood pressure. Many factors such as physical activity, anxiety or the time of day, can influence your blood pressure. Blood pressure is typically low in the mornings and increases from the afternoon to the evening. It is on average lower in the summer and higher in the winter. B. Why is it useful to measure blood pressure at home? Having one's blood pressure measured by a doctor in a hospital or a clinic, is often associated with a phenomenon called “White Coat Hypertension” where the patient becomes nervous or anxious, thus raising his blood pressure. There are also numerous other factors that might cause your blood pressure to be raised at a specific time of day. This is why medical practitioners recommend home monitoring as it is important to get readings of blood pressure during different times of the day to really get an idea of your real blood pressure. Medical practitioners generally recommend the “Rule of 3”, where you are encouraged to take your blood pressure three times in a row (at 3 ~ 5 minute interval), three times a day for three days. After three days yo…

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Report No.: 2130580R-E3032110108 Page: 1 of 17 Attachment 2 : EUT Detailed Photographs (1) EUT Photo (2) EUT Photo Report No.: 2130580R-E3032110108 Page: 2 of 17 (3) EUT Photo (4) EUT Photo Report No.: 2130580R-E3032110108 Page: 3 of 17 (5) EUT Photo (6) EUT Photo Report No.: 2130580R-E3032110108 Page: 4 of 17 (7) EUT Photo (8) EUT Photo

Health & Life Co. Ltd. FCC ID.: 2ABTAHNL85DM 9F., No. 186, Jian Yi Road, Zhonghe District, New Taipei City, Taiwan Tel：+88602-8227-1300 FCC ID Label

Health & Life Co. Ltd. FCC ID.: 2ABTAHNL85DM 9F., No. 186, Jian Yi Road, Zhonghe District, New Taipei City, Taiwan Tel：+88602-8227-1300 The FCC ID will be placed on the equipment as shown in the photograph below.

Report No.: 2130580R-E3032110108 Page: 5 of 17 (9) EUT Photo (10) EUT Photo Report No.: 2130580R-E3032110108 Page: 6 of 17 (11) EUT Photo (12) EUT Photo Report No.: 2130580R-E3032110108 Page: 7 of 17 (13) EUT Photo (14) EUT Photo Report No.: 2130580R-E3032110108 Page: 8 of 17 (15) EUT Photo (16) EUT Photo Report No.: 2130580R-E3032110108 Page: 9 of 17 (17) EUT Photo (18) EUT Photo Report No.: 2130580R-E3032110108 Page: 10 of 17 (19) EUT Photo (20) EUT Photo Report No.: 2130580R-E3032110108 Page: 11 of 17 (21) EUT Photo (22) EUT Photo Report No.: 2130580R-E3032110108 Page: 12 of 17 (23) EUT Photo (24) EUT Photo RF Module Antenna Report No.: 2130580R-E3032110108 Page: 13 of 17 (25) EUT Photo (26) EUT Photo Report No.: 2130580R-E3032110108 Page: 14 of 17 (27) EUT Photo (28) EUT Photo Report No.: 2130580R-E3032110108 Page: 15 of 17 (29) EUT Photo (30) EUT Photo Report No.: 2130580R-E3032110108 Page: 16 of 17 (31) EUT Photo (32) EUT Photo Report No.: 2130580R-E3032110108 Page: 17 of 17 (33) EUT Photo (34) EUT Photo

Report No.: 2130580R-E3082100014 Page: 1 of 5 RF Exposure Evaluation Report Product Name : Automatic Upper Arm Blood Pressure Monitor Model No. : HL858DM FCC ID : 2ABTAHNL85DM Applicant : Health & Life Co. Ltd. Address : 9F., No. 186, Jian Yi Road, Zhonghe District, New Taipei City, Taiwan Date of Receipt : Mar. 13, 2021 Date of Declaration : Apr. 09, 2021 Report No. : 2130580R-E3082100014 Report Version : V1.0 The test results relate only to the samples tested. The test results shown in the test report are traceable to the national/international standard through the calibration report of the equipment and evaluated measurement uncertainty herein. This report must not be used to claim product endorsement by TAF or any agency of the government. The test report shall not be reproduced without the written approval of DEKRA Testing and Certification Co., Ltd. Measurement uncertainties evaluated for each testing system and associated connections are given here to provide the system information for reference. Compliance determinations do not take into account measurement uncertainties for each testing system, but are based on the results of the compliance measurement. Report No.: 2130580R-E3082100014 Page: 2 of 5 Issued Date: Apr. 09, 2021 Report No.: 2130580R-E3082100014 Product Name Automatic Upper Arm Blood Pressure Monitor Applicant Health & Life Co. Ltd. Address 9F., No. 186, Jian Yi Road, Zhonghe District, New Taipei City, Taiwan Manufacturer Health & Life Co. Ltd. factory (ies) 1. Living Science Co., Ltd. 2. Health & Life Medical Technology Company Limited Model No. HL858DM FCC ID. 2ABTAHNL85DM Trade Name Health & Life Applicable Standard KDB 447498 D01 v06 Minimum test separation distance ≥ 20 cm For low power devices Test Result Complied Documented By : (Senior Adm. Specialist / Rita Huang ) Tested By : ( Supervisor / Wen Lee ) Approved By : ( Director / Vincent Lin ) Report No.: 2130580R-E3082100014 Page: 3 of 5 Revision History Report No. Version Description Issued Date 2130580R-E3082100014 V1.0 Initial issue of report. 2021-04-09 Report No.: 2130580R-E3082100014 Page: 4 of 5 1. GENERAL INFORMATION 1.1. EUT Description Product Name Automatic Upper Arm Blood Pressure Monitor Trade Name Health & Life Model No. HL858DM FCC ID. 2ABTAHNL85DM Frequency Range 2402 – 2480MHz Channel Separation 2MHz Channel Number Bluetooth V4.2: 40CH Type of Modulation Bluetooth V4.2: GFSK (1Mbps) Antenna Type PCB Antenna Channel Control Auto Antenna Gain Refer to the table “Antenna List” Antenna List No. Manufacturer Part No. Antenna Type Peak Gain 1 Raytac MDBT42Q-P Series PCB Antenna -1.61dBi for 2.4 GHz Report No.: 2130580R-E3082100014 Page: 5 of 5 2. RF Exposure Evaluation 2.1. Standard Applicable According to 1.1307 (b)(1), systems operating under the provisions of this section shall be operated in a manner that ensure that the public is not exposed to radio frequency energy level in excess of the Commission’s guideline. 2.2. Measurement Result: According to KDB Publication 447498 D01, section 4.3.1, per the calculations of item 1 (Power(mW)/separation (mm)*sqrt(f(GHz)≤3.0), SAR is required as shown in the table below where calculated values are greater than 3.0: Operation frequency = 2450MHz and antenna separation distance = 5mm Body SAR Test Exclusion Threshold = 10mW Frequency Band (MHz) Maximum peak output power SAR Test Exclusion Threshold Calculated Threshold Value (≦3.0 SAR is not required) conducted conducted (mW) (dBm) (mW) 2480.00 -1.14 0.770 10 0.242 Note1: The SAR/MPE measurement is not necessary. Note2: The maximum peak output power is refer to report No.: 2130580R-E3032110108 from the DEKRA.

Report No.: 2130580R-E3032110108 Page: 1 of 50 FCC Test Report Product Name Automatic Upper Arm Blood Pressure Monitor Model No. HL858DM FCC ID. 2ABTAHNL85DM Applicant Health & Life Co. Ltd. Address 9F., No. 186, Jian Yi Road, Zhonghe District, New Taipei City, Taiwan Date of Receipt Mar. 13, 2021 Issued Date Apr. 09, 2021 Report No. 2130580R-E3032110108 Report Version V1.0 The test results relate only to the samples tested. The test results shown in the test report are traceable to the national/international standard through the calibration report of the equipment and evaluated measurement uncertainty herein. This report must not be used to claim product endorsement by TAF or any agency of the government. The test report shall not be reproduced without the written approval of DEKRA Testing and Certification Co., Ltd. Measurement uncertainties evaluated for each testing system and associated connections are given here to provide the system information for reference. Compliance determinations do not take into account measurement uncertainties for each testing system, but are based on the results of the compliance measurement. Report No.: 2130580R-E3032110108 Page: 2 of 50 Test Report Issued Date: Apr. 09, 2021 Report No.: 2130580R-E3032110108 Product Name Automatic Upper Arm Blood Pressure Monitor Applicant Health & Life Co. Ltd. Address 9F., No. 186, Jian Yi Road, Zhonghe District, New Taipei City, Taiwan Manufacturer Health & Life Co. Ltd. factory (ies) 1. Living Science Co., Ltd. 2. Health & Life Medical Technology Company Limited Model No. HL858DM FCC ID. 2ABTAHNL85DM EUT Rated Voltage AC 100-240V, 47-63Hz EUT Test Voltage AC 120V / 60Hz Trade Name Health & Life Applicable Standard FCC CFR Title 47 Part 15 Subpart C ANSI C63.4: 2014, ANSI C63.10: 2013 Test Result Complied Documented By : ( Senior Adm. Specialist / Rita Huang ) Tested By : ( Senior Engineer / Ivan Chuang ) Approved By : ( Director / Vincent Lin ) Report No.: 2130580R-E3032110108 Page: 3 of 50 TABLE OF CONTENTS Description Page 1. GENERAL INFORMATION ............................................................................................................... 5 1.1. EUT Description ...................................................................................................................................... 5 1.2. Tested System Details .............................................................................................................................. 7 1.3. Configuration of Tested System .............................................................................................................. 7 1.4. EUT Exercise Software ........................................................................................................................... 7 1.5. Test Facility ............................................................................................................................................. 8 1.6. List of Test Equipment ............................................................................................................................. 9 1.7. Uncertainty ............................................................................................................................................ 10 2. CONDUCTED EMISSION ................................................................................................................ 11 2.1. Test Setup .............................................................................................................................................. 11 2.2. Limits ..................................................................................................................................................... 11 2.3. Test Procedure ....................................................................................................................................... 12 2.4. Test Result of Conducted Emission ....................................................................................................... 13 3. PEAK POWER OUTPUT .................................................................................................................. 15 3.1. Test Setup ............................................................................................................................................ 15 3.2. Limit ...................................................................................................................................................... 15 3.3. Test Procedure ....................................................................................................................................... 15 3.4. Test Result of Peak Power Output ......................................................................................................... 16 4. RADIATED EMISSION ..................................................................................................................... 17 4.1. Test Setup .............................................................................................................................................. 17 4.2. Limits ..................................................................................................................................................... 18 4.3. Test Procedure ....................................................................................................................................... 19 4.4. Test Result of Radiated Emission .......................................................................................................... 21 5. RF ANTENNA CONDUCTED TEST ................................................................................................ 29 5.1. Test Setup .............................................................................................................................................. 29 5.2. Limits .....................................................................................................................…

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Report No.: 2130580R-E3032110108 Page : 1 of 3 Attachment 1: EUT Test Setup Photographs Front View of Conducted Test Back View of Conducted Test Report No.: 2130580R-E3032110108 Page : 2 of 3 Front View of Radiated Test Back View of Radiated Test Report No.: 2130580R-E3032110108 Page : 3 of 3 Front View of Radiated Test (Horn) Back View of Radiated Test (Horn)