2ATOV-P-G7Personal Diabetes Assistant

AiDEX TM Continuous Glucose Monitoring System User Guide 0344 MicroTech Medical (Hangzhou) Co., Ltd. Index Important safety information 1 Indications for use .................................................... 2 Patients .................................................................... 2 Contraindications ...................................................... 3 Precautions .............................................................. 3 Product components 6 Component description ...........................................10 Accessories.............................................................15 Using a New Glucose Sensor 17 Applying a sensor .................................................. 17 Setting the Personal Diabetes Assistant (PDA) for the first time ...................................................... 22 Sensor start-up ...................................................... 24 Sensor calibration .................................................. 28 Removing a sensor 31 PDA settings 33 Target glucose range ............................................ 33 Date and time settings .......................................... 35 Using the PDA 36 Pairing with a new transmitter .............................. 36 PDA cautions .................................................... 40 Charing the Personal Diabetes Assistant (PDA) .. 41 Caring for your Continuous Glucose Monitoring System (CGMS) .................................. 42 Electromagnetic compatibility 50 Appendix 59 1 Important safety information Indications for use The Continuous Glucose Monitoring System (CGMS) is indicated for continuous or regular monitoring of glucose levels in subcutaneous tissue, and is used for daily detection and self-management of blood glucose levels in people 2 years and older. It is intended for use by patients at home and in healthcare facilities. Interpretation of the CGMS results should be based on the glucose trends and several sequential readings over time . The CGMS also aids in the detection of episodes of hyperglycemia and hypoglycemia, and facilitating therapy adjustments . The System is designed to replace fingerstick blood glucose (BG) testing. 2 Patients This Continuous Glucose Monitoring System is suit- able for patients with diabetes requiring regular blood glucose monitoring. Contraindications Patients who: 1. Suffer from alcoholism, drug abuse, severe mental disorders (such as depression, schizophrenia). 2. Are unconscious. 3. Are unable to understand or master the usage of the device. 4. Have severe hearing or vision impairment. 5. User below the age of 2 or are not capable of admin- istering diabetes therapy themselves or who always 3 need to use Continuous Glucose Monitor under strict supervision of parents or qualified healthcare professionals. Precautions • CGMS readings should only be used as a reference for the supplemental monitoring of diabetes mellitus and should not be used as a basis for clinical diagno- sis. • The CGMS should be completely removed before Magnetic Resonance Imaging (MRI). • The CGMS contains many small parts that can be dangerous if swallowed. • During rapid changes in blood glucose (more than 0. 1mmol/L per minute), glucose levels measured in interstitial fluid by the CGMS may not be the same as blood glucose levels. When blood glucose lev- els drop rapidly, the sensor may produce a higher reading than the blood glucose level; Conversely, 4 when blood glucose levels rise rapidly, the sensor may produce a lower reading than the blood glucose level. When experiencing symptoms of hypoglycemic or hyperglycemic, the sensor readings are checked by using a blood glucose meter for a fingertip blood glucose test. • Severe dehydration or excessive loss of water may result in inaccurate results. When you suspect you are dehydrated, consult a heathcare professional immediately. • If you think the CGMS sensor reading is inaccurate or inconsistent, use a blood glucose meter to test your blood glucose level or calibrate the glucose sensor. If the problem persists, remove and replace the sensor. • While extensive user testing was done on AiDEX TM CGMS in Type I and Type II diabetic patients, the study groups did not include women with gestational diabetes. • The performance of the CGMS has not been eval- uated when used with another implantable medical device, such as a pacemaker. 5 • Only MicroTech Medical consumables should be used with the CGMS. • If the product is not working properly or has been damaged, stop using the product. • When used in a medical facility, the operator should wear gloves while using. • The CGMS can not be used in oxygen rich enviro- ment. • Operator or the responsible organization shall read this instructions for use as the training or the knowledge required for using this equipment. • Any serious injury or death that has occurred in relation to the device should be reported to the man- ufacturer and the competent authority of the Member State in which the user and/or patient is established. 6 Product components Name: AiDEX™ continuous glucose monitoring sys- tem System configuration: This product includes a Per- sonal Diabetes Assistant, a Transmitter and a Glucose Sensor. Personal Diabetes Assistant will be referred as PDA in the text below. System Sensor Transmitter PDA G7 G7-S01 G7-T01 G7-P02、 MTM-2 G7-A G7-S01A G7-T01A G7-B G7-S01B G7-T01B 7 The PDA & Transmitter system consists of the fol- lowing components: • Personal Diabetes Assistant (Li-ion battery included) •Transmitter 8 Warning :No modification of this equipment is allowed. Unauthorized modification of the equipment may cause the product to malfunction and become unusable.Replacement of a component could result in an unacceptable risk. Warning :Remove the battery if not used for a long time ！ If the PDA battery charger does not work, do not try to repair it. Please contact your local supplier for a replacement. Note:The device is intended to be transported and stored in waterp…

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MicroTech Medical (Hangzhou) Co., Ltd. No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China DATE : 06/06/2023 MicroTech Medical (Hangzhou) Co., Ltd. No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China Attn: Director of Certification Authority to Act as Agent On our behalf, I appoint below company and person: Name Damon Hu Position Manager Company Name Dongguan Dongdian Testing Service Co.,Ltd. Address 17, Zongbu Road 2, Songshan Lake Sci&Tech, Industry Park, Dongguan City, Guangdong Province, China, 523808 Tel / Fax Tel: +86-0769-38826678-850 E-Mail [email protected] to act as our agent in the preparation of this application for equipment certification. I certify that submitted documents properly describe the device or system for which equipment certification is sought. I also certify that each unit manufactured, imported or marketed, as defined in the Federal Communications Commission’s regulations will have affixed to it a label identical to that submitted for approval with this application. Applicant name MicroTech Medical (Hangzhou) Co., Ltd. Address No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China Yours sincerely, Signatory Name Leo wang Position Registration Specialist Company Name MicroTech Medical (Hangzhou) Co., Ltd. Address No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China Tel +86 18621889766 E-Mail [email protected] MicroTech Medical (Hangzhou) Co., Ltd. No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China

1/1 Declaration of difference Date: 2023/06/06 To Whom It May Concern: The Product: Personal Diabetes Assistant Model No.: G7-P02, MTM-2 The appearance, color and internal circuitry of all models are consistent, the only difference is their built-in software. There is no influence on the test results. Yours sincerely, Signatory Name Leo wang Position Registration Specialist Company Name MicroTech Medical (Hangzhou) Co., Ltd. Address No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China Tel +86 18621889766 E-Mail [email protected]

C5266091_X8_Ed.1 1/1 Letter of Authorization MicroTech Medical (Hangzhou) Co., Ltd. Company: MicroTech Medical (Hangzhou) Co., Ltd. Address: No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China Product Name: Personal Diabetes Assistant Model Number: G7-P02, MTM-2 FCC Identifier: 2ATOV-P-G7 We authorize LGAI Technological Center S.A., Ronda de la Font del Carme, s/n, 08193 Bellaterra, Spain, to act on our behalf on all matters concerning the above named equipment. Any individual within LGAI Technological Center S.A. is authorized to act on our behalf and take action on the application. We declare that authorize LGAI Technological Center S.A., Ronda de la Font del Carme, s/n, 08193 Bellaterra, Spain, is allowed to forward all information related to the approval project to the Federal Communication Commission and to discuss any issues concerning the approval application. Any and all acts carried out by LGAI Technological Center S.A. on our behalf shall have the same effect as acts of our own. Name: Leo wang Date: 2023/06/06 Title: Registration Specialist Signature of applicant:

C5266091_X10_Ed.1 1/1 MicroTech Medical (Hangzhou) Co., Ltd. Office of Engineering Technology Federal Communications Commission 7435 Oakland Mills Road Columbia, MD 21046 Date: 2023/06/06 Subject: Request for Confidentiality FCC ID: 2ATOV-P-G7 To Whom It May Concern, Pursuant to the provisions of Sections 0.457 and 0.459 of Commission's rules (47CFR0.457, 0.459), we are requesting the Commission to withhold the following attachment(s) as confidential document from public disclosure. Exhibits Long-Term Confidentiality Short-Term Confidentiality ID Label/Location No No Attestation Statement No No External Photos No Block Diagram Schematics Test Report No No Test Setup Photos No User’s Manual Internal Photos Parts List / Tune Up RF Exposure Info Operational Description Cover Letter(s) No No SDR Software / Security Info No In case of short-term Confidentiality, the applicant requests the exhibits selected above are withheld from public view for a period of _180_ days from the date of the Grant of Equipment Authorization and prior to marketing. Above mentioned document contains detailed system and equipment description are considered as proprietary information in operation of the equipment. The public disclosure of above documents might be harmful to our company and would give competitor an unfair advantage in the market. It is our understanding that all measurement test reports, FCC ID label format and correspondent during certification review process cannot be granted as confidential documents and those information will be available for public review once the grant of equipment authorization is issued. Sincerely, Signature: C5266091_X10_Ed.1 1/1 Name: Leo wang Title: Registration Specialist

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Dongguan Dongdian Testing Service Co., Ltd. Report No.:DDT-R22081519-2E03 Page 1 of 6 RF EXPOSURE REPORT FOR Issued By: Dongguan Dongdian Testing Service Co., Ltd. Add.: No. 17, Zongbu Road 2, Songshan Lake Sci&Tech, Industry Park, Dongguan City, Guangdong Province, China, 523808 Tel.: +86-0769-38826678, E-mail: [email protected], http://www.dgddt.com Applicant : MicroTech Medical (Hangzhou) Co., Ltd. Address : No.108 Liuze St., Cangqian, Yuhang District, Hangzhou 311121 Zhejiang P.R.China Equipment under Test : Personal Diabetes Assistant Model No. : G7-P02, MTM-2 Trade Mark : FCC ID : 2ATOV-P-G7 Manufacturer : MicroTech Medical (Hangzhou) Co., Ltd. Address : No.108 Liuze St., Cangqian, Yuhang District, Hangzhou 311121 Zhejiang P.R.China Report No.: DDT-R22081519-2E03 Issued Date: Sep. 15, 2022 Dongguan Dongdian Testing Service Co., Ltd. Report No.:DDT-R22081519-2E03 Page 2 of 6 Table of Contents Test report declares........................................................................................................3 1. General Information ....................................................................................................... 5 1.1. Description of equipment ............................................................................................... 5 1.2. Assess laboratory ........................................................................................................... 5 2. RF Exposure evaluation for FCC ................................................................................... 5 Dongguan Dongdian Testing Service Co., Ltd. Report No.:DDT-R22081519-2E03 Page 3 of 6 Test Report Declare Standard Used: KDB447498 D01 General RF Exposure Guidance v06 We Declare: The equipment described above is assessed by Dongguan Dongdian Testing Service Co., Ltd. and in the configuration assessed the equipment complied with the standards specified above. The assessed results are contained in this report and Dongguan Dongdian Testing Service Co., Ltd. is assumed of full responsibility for the accuracy and completeness of these assess. After evaluation, our opinion is that the equipment In Accordance with above standard. Report No: DDT-R22081519-2E03 Date of Receipt: Aug. 26, 2022 Date of Test: Aug. 26, 2022 ~ Sep. 15, 2022 Prepared By: Approved By: _____________________ _____________________ Sanvin Zheng/Engineer Damon Hu/EMC Manager Note: This report applies to above tested sample only. This report shall not be reproduced in parts without written approval of Dongguan Dongdian Testing Service Co., Ltd. Applicant : MicroTech Medical (Hangzhou) Co., Ltd. Address : No.108 Liuze St., Cangqian, Yuhang District, Hangzhou 311121 Zhejiang P.R.China Equipment under Test : Personal Diabetes Assistant Model No. : G7-P02, MTM-2 Trade mark : Manufacturer : MicroTech Medical (Hangzhou) Co., Ltd. Address : No.108 Liuze St., Cangqian, Yuhang District, Hangzhou 311121 Zhejiang P.R.China E S T T I N N A I G D S G E N R O V D I C E N A C U O G . , G L N T O D D . Dongguan Dongdian Testing Service Co., Ltd. Report No.:DDT-R22081519-2E03 Page 4 of 6 Revision History Rev. Revisions Issue Date Revised By --- Initial issue Sep. 15, 2022 Dongguan Dongdian Testing Service Co., Ltd. Report No.:DDT-R22081519-2E03 Page 5 of 6 1. General Information 1.1. Description of equipment 1.2. Assess laboratory Dongguan Dongdian Testing Service Co., Ltd. Add.: No. 17, Zongbu Road 2, Songshan Lake Sci&Tech, Industry Park, Dongguan City, Guangdong Province, China, 523808. Tel.: +86-0769-38826678, http://www.dgddt.com, Email: [email protected]. CNAS Accreditation No. L6451; A2LA Accreditation Number: 3870.01 FCC Designation Number: CN1182, Test Firm Registration Number: 540522 Innovation, Science and Economic Development Canada Site Registration Number: 10288A Conformity Assessment Body identifier: CN0048 VCCI facility registration number: C-20087, T-20088, R-20123, R-20155, G-20118 2. RF Exposure evaluation for FCC According to 447498 D01 General RF Exposure Guidance v06 The 1-g and 10-g SAR test exclusion thresholds for 100 MHz to 6 GHz at test separation distances ≤ 50 mm are determined by: [(max. power of channel, including tune-up tolerance, mW)/(min. test separation distance, mm)] ·[√f(GHz)] ≤ 3.0 for 1-g SAR and ≤ 7.5 for 10-g extremity SAR, where: f(GHz) is the RF channel transmit frequency in GHz Power and distance are rounded to the nearest mW and mm before calculation The result is rounded to one decimal place for comparison EUT* Name : Personal Diabetes Assistant Model Number : G7-P02, MTM-2 Model difference : The appearance, color and internal circuitry of all models are consistent, the only difference is their built-in software. Therefore, G7-P02 was tested EUT function description : Please reference user manual of this device Power Supply : DC 5V from external USB or DC 3.7V built-in lithium battery Radio Specification : Bluetooth V5.0 Operation Frequency : 2402 MHz - 2480 MHz Modulation : GFSK Data Rate : 1 Mbps Antenna Gain : FPC antenna, maximum PK gain: 0.59 dBi Sample Number : S22081519-05 for conductive S22081519-06 for radiation Dongguan Dongdian Testing Service Co., Ltd. Report No.:DDT-R22081519-2E03 Page 6 of 6 Manufacturing Tolerance BLE GFSK (Peak) 1M Channel Channel 0 Channel 39 Channel 78 Target (dBm) -3.26 -3.81 -5.46 Tolerance ±(dB) 1 1 1 Estimtion Result Worse case is as below: [2402 MHz, -2.26 dBm, (0.59 mW) output power] (0.59/5) ·[√2.402(GHz)] = 0.18 < 3.0 for 1-g SAR Then SAR evaluation is not required. END OF REPORT

左蓝牙天线：P-A01-39A-B-1-1A 编制/变更日期变更理由变更内容版本 2022/9/14新版本发行 V1.0 品质结构射频核准 品质结构电子核准 客户料号： 1 2 3 编号：AFT—QR-066 深圳市安弗特电子有限公司 深圳市无限智联科技有限公司 客户:无锡创宇物联日期:2022-09-14 物料型号:H1581QA-1003P物料结构：FPC 物料编码:P-A01-39A-B-1-1A物料颜色：黑 天线结构：天线料号： 左蓝牙天线 样品承认书 变更记录栏 客户确认栏 客户要求： 深圳市安弗特电子有限公司 地址：深圳市龙华区大浪街道华宁路40号港深创新园B栋302室 电话：0755-27888203 传真：0755-27888450 网址：www.anfutesz.com 一、封面 二、目录 三、产品图 四、RF测试数据报告 五、QC工程图 六、包装信息 电话：0755-27888203 传真：0755-27888450 网址：www.anfutesz.com 编号：AFT—QR-066 深圳市安弗特电子有限公司 深圳市无限智联科技有限公司 目录 深圳市安弗特电子有限公司 地址：深圳市龙华区大浪街道华宁路40号港深创新园B栋3楼302室 深圳市安弗特电子有限公司 AFT tech Electronic Co., Ltd. (Shenzhen) 地址：深圳市龙华区大浪街道华宁路40号港深创新园B栋3楼 302室 电话：0755-27888203 传真：0755-27888450 无源驻波、回损、史密斯图和效率： 平台蓝牙(左) 深圳市安弗特电子有限公司 AFT tech Electronic Co., Ltd. (Shenzhen) 地址：深圳市龙华区大浪街道华宁路40号港深创新园B栋3楼 302室 电话：0755-27888203 传真：0755-27888450 效率增益 平台蓝牙(左) 频点（M/HZ) 效率 增益（dBi） 2400 46% 0.53 2405 46% 0.48 2410 46% 0.46 2415 46% 0.51 2421 47% 0.56 2426 48% 0.58 2431 48% 0.58 2436 48% 0.58 2442 47% 0.59 2447 46% 0.51 2452 47% 0.52 2457 47% 0.50 2463 46% 0.44 2468 46% 0.34 2473 46% 0.22 2478 45% 0.10 2484 44% -0.06 2489 44% -0.24 2494 43% -0.49 2500 42% -0.72 深圳市安弗特电子有限公司 AFT tech Electronic Co., Ltd. (Shenzhen) 地址：深圳市龙华区大浪街道华宁路40号港深创新园B栋3楼 302室 电话：0755-27888203 传真：0755-27888450 平台蓝牙(左) (unit: dBi) 深圳市安弗特电子有限公司 AFT tech Electronic Co., Ltd. (Shenzhen) 地址：深圳市龙华区大浪街道华宁路40号港深创新园B栋3楼 302室 电话：0755-27888203 传真：0755-27888450 OTA数据： Band Channal TRP(dBm) TIS(dBm) 平台BT L 3.61 -91.07 M 4.43 -90.63 H 4.81 -91.67 深圳市安弗特电子有限公司 AFT tech Electronic Co., Ltd. (Shenzhen) 地址：深圳市龙华区大浪街道华宁路40号港深创新园B栋3楼 302室 电话：0755-27888203 传真：0755-27888450 深圳市安弗特电子有限公司 AFT tech Electronic Co., Ltd. (Shenzhen) 地址：深圳市龙华区大浪街道华宁路40号港深创新园B栋3楼 302室 电话：0755-27888203 传真：0755-27888450 环境处理 屏两侧贴导电泡棉接锌合金中框 锌合金四处贴导电泡棉接地 主板贴导电泡棉使喇叭接 地 客户版本 无锡创宇物联A版 流程图工序名称仪器设备管制项目参考标准/指导书检验方法表单/记录担当 进料电子称 数量、品名 、规格标识 进料检验基准书、采 购订单 抽检（数量） 验收单 仓管员 /IQC 进料检验 卡尺、万 用表、二 外观、尺寸 、性能 进料检验基准书 抽 检 IQC进料检验 报告 IQC 入库单 IQC进料检验 报告 领料 卡尺数量、品名 、规格标识 领料审核单全检领料记录表开料部主 管 晒网记录表 定期保养表 生产部审核单开料记录表 开料机作业指导书定期保养表 电镀外发 油墨搅拌 机 生产部审核单生产记录表 丝印机丝印作业指导书定期保养表 烤箱精密烤箱工艺区分标 识 烤箱作业指导书工艺温度确认定期保养表丝印部主 管 覆盖膜 生产部审核单开料记录表 开料机作业指导书定期保养表 生产部审核单打孔记录表 打孔机作业指导书定期保养表 生产部审核单生产记录表 冲床机作业指导书定期保养表 安全规范 生产记录表 检验基准书出货单 数量检查品质检验工作站作业保 存 符 号 说 明 深圳电话：0755-27888203 传真：0755-27888450 网址：www.anfutesz.com 编号：AFT—QR-066 深圳市安弗特电子有限公司 地址：深圳市龙华区大浪街道华宁路40号港深创新园B栋3楼302室 包装包装 机.QC台 数量、品名 、规格标识 全检 品质主管 冲外型冲床机数量、工艺 、外形规格 标识 全检冲床主管 开料部主 管 打孔自动打孔 机 数量、品名 、规格标识 全检 装配主管 丝印/油墨数量、工艺 、规格标识 抽 检丝印部主 管 开离型纸自动开料 机 数量、工艺 、规格标识 全检 晒网员 开料 自动开料 机 数量、工艺 、规格标识 全检 开料部主 管 晒网/菲林晒版机流程标识生产指示单 全检 深圳市安弗特电子有限公司 深圳市无限智联科技有限公司 FPC天线 QC工程图 入库 卡尺 数量、品名 、规格标识 入库检验基准书 抽检（数量）仓管员 /IQC 项目名 H1581QA-1003P 客 户产品型号 FPC 产品名称文件编号 每箱数量每箱层数每层数量版 本 No. 1 2 3 4 5 6 7 审核:制作: 杜强苟贵琼 1. 客户、品名、料号、数量、生产日期不能写错。 2.不能漏贴RoHS标签. 3. 在包装过程中不可碰伤产品。 版次修订日期修订内容 注意事项： 包装方法及要求: 1、产品自检OK每张都用离心纸隔开，整齐放入PE袋，将PE袋空余的部分折叠后用胶纸贴 紧 按实际数量填写票品并在指定位置，将RoHS标签贴到制定位置。 2，将用PE袋包装好的FPC天线放入纸箱，空余的位置用气泡袋填充。 3、按实际装箱数量填写现品票并粘贴在指定位置，然后将产品放置,在指定区域待检。 包装图示： 包 装 材 料 清 单 材料名称材料规格用量 PE袋 纸箱 深圳市安弗特电子有限公司 深圳市无限智联科技有限公司 无锡创宇物联 H1581QA-1003P AFTCRSDM51901 A/0

Dongguan Dongdian Testing Service Co., Ltd. Report No.: DDT-R22081519-2E01 Page 1 of 59 FCC CERTIFICATION TEST REPORT FOR Issued By: Dongguan Dongdian Testing Service Co., Ltd. Add.: No. 17, Zongbu Road 2, Songshan Lake Sci&Tech, Industry Park, Dongguan City, Guangdong Province, China, 523808 Tel.: +86-0769-38826678, E-mail: [email protected], http://www.dgddt.com Applicant : MicroTech Medical (Hangzhou) Co., Ltd. Address : No.108 Liuze St., Cangqian, Yuhang District, Hangzhou 311121 Zhejiang P.R.China Equipment under Test : Personal Diabetes Assistant Model No. : G7-P02, MTM-2 Trade Mark : FCC ID : 2ATOV-P-G7 Manufacturer : MicroTech Medical (Hangzhou) Co., Ltd. Address : No.108 Liuze St., Cangqian, Yuhang District, Hangzhou 311121 Zhejiang P.R.China Report No.: DDT-R22081519-2E01 Issued Date: Sep. 15, 2022 Dongguan Dongdian Testing Service Co., Ltd. Report No.: DDT-R22081519-2E01 Page 2 of 59 Table of Contents Test report declares.......................................................................................................4 1. Summary of Test Results ............................................................................................... 6 2. General Test Information ............................................................................................... 7 2.1. Description of EUT ......................................................................................................... 7 2.2. Accessories of EUT ........................................................................................................ 8 2.3. Assistant equipment used for test .................................................................................. 8 2.4. Block diagram of EUT configuration for test .................................................................. 8 2.5. Test environment conditions .......................................................................................... 8 2.6. Deviations of test standard............................................................................................. 9 2.7. Test laboratory ............................................................................................................... 9 2.8. Measurement uncertainty ............................................................................................... 9 3. Equipment Used During Test ....................................................................................... 10 4. 6 dB Bandwidth and 99% Bandwidth ........................................................................... 11 4.1. Block diagram of test setup .......................................................................................... 11 4.2. Limits ............................................................................................................................ 11 4.3. Test procedure ............................................................................................................. 11 4.4. Test result ..................................................................................................................... 12 4.5. Original test data .......................................................................................................... 12 5. Maximum Peak Output Power ..................................................................................... 15 5.1. Block diagram of test setup .......................................................................................... 15 5.2. Limits ............................................................................................................................ 15 5.3. Test procedure ............................................................................................................. 15 5.4. Test result ..................................................................................................................... 15 5.5. Original test data .......................................................................................................... 16 6. Power Spectral Density ................................................................................................ 18 6.1. Block diagram of test setup .......................................................................................... 18 6.2. Limits ............................................................................................................................ 18 6.3. Test procedure ............................................................................................................. 18 6.4. Test result ..................................................................................................................... 18 6.5. Original test data .......................................................................................................... 19 7. Band Edge Compliance (Conducted Method) ............................................................. 21 7.1. Block diagram of test setup .......................................................................................... 21 7.2. Limits ............................................................................................................................ 21 7.3. Test procedure ............................................................................................................. 21 7.4. Test result ..................................................................................................................... 21 7.5. Original test data .......................................................................................................... 22 8. Radiated Emission ....................................................................................................... 23 Dongguan Dongdian Testing Service Co., Ltd. Report No.: DDT-R22081519-2E01 Page 3 of 59 8.1. Block diagram of test setup .......................................................................................... 23 8.2. Limit ...................................................…

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Dongguan Dongdian Testing Service Co., Ltd. Report No.: DDT-R22081519-2E01 Page 57 of 59 13. Test Setup Photograph Dongguan Dongdian Testing Service Co., Ltd. Report No.: DDT-R22081519-2E01 Page 58 of 59