2ABTAHNL85CG1Automatic Upper Arm Blood Pressure Monitor

1 Instruction Manual Automatic Upper Arm Blood Pressure Monitor Model No. HL858CG 2 Table of Contents Medical Disclaimer.......................................................................................03 Intended Use...............................................................................................03 About Blood Pressure.................................................................................04 Measurement Method............................................................................06 Accuracy.......................................................................................................07 Precautions.................................................................................................... 08 Device Overview...........................................................................................10 Symbol Definitions.....................................................................................13 Features.......................................................................................................14 Installing Batteries.....................................................................................20 Using the AC/DC adapter...........................................................................21 Applying the Cuff........................................................................................22 Measurement Procedure..........................................................................23 Bluetooth Transmission.................................................................................30 Memory Function........................................................................................32 Storage and Maintenance.........................................................................35 Troubleshooting...........................................................................................36 Warranty & Recalibration..........................................................................37 Specifications..............................................................................................38 Note..............................................................................................................40 Appendix........................................................................................................42 Blood Pressure Diary.................................................................................44 3 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 HL858CG automatically measures human’s Systolic, Diastolic blood pressure and heart rate by using the oscillometric method during inflation. All values can be read out in one LCD panel. Measurement position is at human being’s upper arm. The intended use of this over- the-counter device is for adults aged 18 years and older with arm circumference ranging from 9 inches to 17 inches (approx.23 cm to 43 cm) and for home use. HL858CG detects the appearance of irregular heartbeats during measurement; an indicated symbol will appear with measuring reading. And the Risk Category Indicator will show the information with the readings on the screen for the user tracking their blood pressure level. Besides, the device features a built-in "Bluetooth Data 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 About Blood Pressure 1. 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. 2. 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 an event 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 physician 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 physicians 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 you can average all the results and this will give you an accurate idea of what your blood pressure really is. 5 About Blood Pressure A. Standards for assessment of high or low blood pressure without regard to age, have been established by the WHO, and classifications adapted from JNC7: WHO: World Health Organization JNC 7: The Seventh Report of the Joint National Committee on Prevention, Dete…

Text truncated - open the document above for the full version.

FCC ID: 2ABTAHNL85CG1 Date: March 02, 2021 Federal Communications Commission Authorization and Evaluation Division Confidentiality Request Pursuant to Sections 0.457 and 0.459 of the Commission’s Rules, the Applicant Hereby requests confidential treatment of information accompanying this Application As outlined below: Type of Confidentiality Requested Exhibit ☒ Permanent Block Diagrams ☐ Short Term External Photos ☐ Short Term Internal Photos ☒ Permanent Operation Description/Theory of Operation ☐ Permanent Parts List & Placement/BOM ☐ Permanent Tune-Up Procedure ☒ Permanent Schematics ☐ Short Term Test Setup Photos ☐ Short Term User’s Manual The above materials contain trade secrets and proprietary information not customarily Released to the public. The public disclosure of these matters might be harmful to the Applicant and provide unjustified benefits to its competitors. The Applicant understands that pursuant to Rule 0.457, disclosure of this Application and all accompanying documentation will not be made before the date of the Grant for this application. Permanent Confidentiality: The applicant requests the exhibits listed above as permanently confidential be permanently withheld from public review due to materials that contain trade secrets and proprietary information not customarily released to the public Short-Term Confidentiality: The applicant requests the exhibits selected above as short term confidential be withheld from public view for a period of 180 days from the date of the Grant of Equipment Authorization and prior to marketing. This is to avoid premature release of sensitive information prior to marketing or release of the product to the public. Sincerely, ------------------------------------------------------------ Vincent Lin, DEKRA Testing and Certification Co., Ltd.

Report No.: 20C0714R-E3032110108 Page: 1 of 4 Attachment 2 : EUT Detailed Photographs (1) EUT Photo (2) EUT Photo Report No.: 20C0714R-E3032110108 Page: 2 of 4 (3) EUT Photo (4) EUT Photo Report No.: 20C0714R-E3032110108 Page: 3 of 4 (5) EUT Photo (6) EUT Photo Report No.: 20C0714R-E3032110108 Page: 4 of 4 (7) EUT Photo

Health & Life Co. Ltd. FCC ID: 2ABTAHNL85CG1 9F., No. 186, Jian Yi Road, Zhonghe District, New Taipei City, Taiwan TEL: +886-2-8227-1300 FCC ID Label

Health & Life Co. Ltd. FCC ID: 2ABTAHNL85CG1 9F., No. 186, Jian Yi Road, Zhonghe District, New Taipei City, Taiwan TEL: +886-2-8227-1300 The FCC ID will be placed on the equipment as shown in the photograph below.

Report No.: 20C0714R-E3032110108 Page: 1 of 11 Attachment 2 : EUT Detailed Photographs (1) EUT Photo (2) EUT Photo Report No.: 20C0714R-E3032110108 Page: 2 of 11 (3) EUT Photo (4) EUT Photo Report No.: 20C0714R-E3032110108 Page: 3 of 11 (5) EUT Photo (6) EUT Photo Report No.: 20C0714R-E3032110108 Page: 4 of 11 (7) EUT Photo (8) EUT Photo Report No.: 20C0714R-E3032110108 Page: 5 of 11 (9) EUT Photo (10) EUT Photo RF Module Antenna Report No.: 20C0714R-E3032110108 Page: 6 of 11 (11) EUT Photo (12) EUT Photo Report No.: 20C0714R-E3032110108 Page: 7 of 11 (13) EUT Photo (14) EUT Photo Report No.: 20C0714R-E3032110108 Page: 8 of 11 (15) EUT Photo (16) EUT Photo Report No.: 20C0714R-E3032110108 Page: 9 of 11 (17) EUT Photo (18) EUT Photo Report No.: 20C0714R-E3032110108 Page: 10 of 11 (19) EUT Photo (20) EUT Photo Report No.: 20C0714R-E3032110108 Page: 11 of 11 (21) EUT Photo

Report No.: 20C0714R-E3082100014 Page: 1 of 5 RF Exposure Evaluation Report Product Name : Automatic Upper Arm Blood Pressure Monitor Model No. : HL858CG FCC ID : 2ABTAHNL85CG1 Applicant : Health & Life Co. Ltd. Address : 9F., No. 186, Jian Yi Road, Zhonghe District, New Taipei City, Taiwan Date of Receipt : Dec. 18, 2020 Date of Declaration : Jan. 25, 2021 Report No. : 20C0714R-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.: 20C0714R-E3082100014 Page: 2 of 5 Issued Date: Jan. 25, 2021 Report No.: 20C0714R-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. Model No. HL858CG FCC ID. 2ABTAHNL85CG1 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 / Joanne Lin ) Tested By : ( Senior Engineer / Wen Lee ) Approved By : ( Director / Vincent Lin ) Report No.: 20C0714R-E3082100014 Page: 3 of 5 Revision History Report No. Ve r s i o n Description Issued Date 20C0714R-E3082100014 V1.0 Initial issue of report. Jan. 25, 2021 Report No.: 20C0714R-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. HL858CG FCC ID. 2ABTAHNL85CG1 Frequency Range 2402-2480MHz Channel Number V4.2: 40CH Type of Modulation V4.2: GFSK(1Mbps) Antenna Type PCB Antenna Antenna Gain Refer to the table “Antenna List” Antenna List No. Manufacturer Part No. Antenna Type Peak Gain 1 atl LB-BLE-005 PCB Antenna 2.23dBi for 2.4GHz Report No.: 20C0714R-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 Peak Gain: 2.23dBi SAR Test Exclusion Threshold Calculated Threshold Value (≦3.0 SAR is not required) conducted (dBm) EIRP (dBm) EIRP (mW) (mW) 2402 2.92 5.15 3.27 10 1.015 Note1: The SAR/MPE measurement is not necessary. Note2: The maximum peak output power is refer to report No.: 20C0714R-E3032110108 from the DEKRA.

Report No.: 20C0714R-E3032110108 Page : 1 of 52 FCC Test Report Product Name Automatic Upper Arm Blood Pressure Monitor Model No. HL858CG FCC ID. 2ABTAHNL85CG1 Applicant Health & Life Co. Ltd. Address 9F., No. 186, Jian Yi Road, Zhonghe District, New Taipei City, Taiwan Date of Receipt Dec. 18, 2020 Issued Date Jan. 25, 2021 Report No. 20C0714R-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.: 20C0714R-E3032110108 Page : 2 of 52 Test Report Issued Date: Jan. 25, 2021 Report No.: 20C0714R-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. Model No. HL858CG FCC ID. 2ABTAHNL85CG1 EUT Rated Voltage AC 100-240V, 50-60Hz EUT Test Voltage AC 120V/60Hz(by Adapter), DC 6V (by Battery) 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 / Joanne Lin ) Tested By : ( Senior Engineer / Ivan Chuang ) Approved By : ( Director / Vincent Lin ) Report No.: 20C0714R-E3032110108 Page : 3 of 52 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 ................................................................................................ 31 5.1. Test Setup .............................................................................................................................................. 31 5.2. Limits ..................................................................................................................................................... 31 5.3. Test Procedure .…

Text truncated - open the document above for the full version.

Report No.: 20C0714R-E3032110108 Page : 1 of 3 Attachment 1: EUT Test Setup Photographs Front View of Conducted Test Back View of Conducted Test Report No.: 20C0714R-E3032110108 Page : 2 of 3 Front View of Spurious Emission Test Back View of Spurious Emission Test Report No.: 20C0714R-E3032110108 Page : 3 of 3 Front View of Spurious Emission Test (Horn) Back View of Spurious Emission Test (Horn)