2A7JQTELEBGM2283-ABlood Glucose Meter

i Blood Glucose Monitoring System Dear MIO System User, Thank you for choosing the MIO Blood Glucose Monitoring System! MIO Blood Glucose Monitoring System is designed for easy test of blood glucose and helps you keep blood glucose under control. Read this User Manual carefully before you use your meter system. This manual will help you to get comfortable using the MIO Blood Glucose Monitoring System and get reliable test results. Please keep your User Manual in a safe place, you may want to refer it in the future. Thank you again for choosing the MIO System. Intended Use MIO Blood Glucose Monitoring System is comprised of the MIO Blood Glucose Meter and the MIO Blood Glucose Test Strips. MIO Blood Glucose Monitoring System is intended to quantitatively measure the glucose concentration in fresh capillary whole blood samples drawn from the fingertips. It is intended for use by persons with diabetes at home as an aid to monitor the effectiveness of diabetes control. It is not intended for neonatal use or for the diagnosis of or screening for diabetes. This system is intended for self-testing outside the body (in vitro diagnostic use), and should only be used by a single person and should not be shared. Principle of Operation MIO Blood Glucose Monitoring System is designed to quantitatively measure the glucose concentration in fresh capillary whole blood. The glucose measurement is achieved by using the amperometric detection method. The test is based on measurement of electrical current caused by the reaction of the glucose with the reagents on the electrode of the test strip. The blood sample is pulled into the tip of the test strip through capillary action. Glucose in the sample reacts with glucose oxidase and the mediator. Electrons are generated, producing a current that is positive correlation to the glucose concentration in the sample. After the reaction time, the glucose concentration in the sample is displayed . ii TABLE OF CONTENTS 1. Understanding Your Testing Tools............................................ 1 Your System Overview...................................................... 1 Your Meter Display................................................................... 2 Meter Use and Precautions........................................................ 3 Important Safety Information...................................................... 4 Limitations.............................................................................. 5 2. Setting Up Your System........................................................... 6 Set the Date and Time............................................................... 6 Set the Audio Feature................................................................ 8 Set the Meal Marker.................................................................. 8 Set the Hypoglycemia (Hypo) Warning......................................... 8 Set the Ketone Warning............................................................. 9 3. Performing a Test.................................................................... 10 Preparing the Test Strip............................................................. 10 Preparing the Lancing Device..................................................... 11 Getting a Blood Drop for Testing.................................................. 12 Discarding the Used Test Strip.............................................................. 14 Removing the Used Lancet ....................................................... 14 Expected Diabetes Control Goal.................................................. 15 Questionable or lnconsistent Results............................................ 16 Symptoms of High ro Low Blood Glucose...................................... 16 Precision and Accuracy............................................................. 17 Comparing Meter and Laboratory Results..................................... 19 Testing with Control Solution ................................................... 19 Understand Control Test Result.................................................. 21 Using the Meter Memory........................................................... 22 Viewing your Test Results.......................................................... 22 4. Maintenance and Troubleshooting............................................. 24 Charging the Battery............................................................. 24 Caring for Your Glucose Monitoring System.................................. 25 Cleaning and Disinfection.......................................................... 25 Troubleshooting Guide.............................................................. 28 5. Technical Information............................................................. 30 System Specifications............................................................... 30 4G Specifications..................................................................... 31 Warranty................................................................................ 31 iii EMC Guidance........................................................................ 32 FCC Requirement.................................................................... 35 1 CHAPTER 1: UNDERSTANDING YOUR TESTING TOOLS Your System Overview Note: The MIO Blood Glucose Test Strips, MIO Control Solution, MIO Lancing Device and MIO Lancets are not included in the meter box but are necessary for use, please contact 24/7 MIO Customer Support at (833) 445-5666 for purchase. 2 Your Meter Display The picture below shows all the symbols that appear on your meter display. Please make sure the display is working properly before testing. When the meter is off, press and hold to see the complete display. All display segments will appear. If you need more time to check the display, repeat the above operation. All display segments should be clear and exactly like the picture below. If not, contact 24/7 MIO Customer Support at (833) 4…

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i Blood Glucose Monitoring System Dear MIO System User, Thank you for choosing the MIO Blood Glucose Monitoring System! MIO Blood Glucose Monitoring System is designed for easy test of blood glucose and helps you keep blood glucose under control. Read this User Manual carefully before you use your meter system. This manual will help you to get comfortable using the MIO Blood Glucose Monitoring System and get reliable test results. Please keep your User Manual in a safe place, you may want to refer it in the future. Thank you again for choosing the MIO System. Intended Use MIO Blood Glucose Monitoring System is comprised of the MIO Blood Glucose Meter and the MIO Blood Glucose Test Strips. MIO Blood Glucose Monitoring System is intended to quantitatively measure the glucose concentration in fresh capillary whole blood samples drawn from the fingertips. It is intended for use by persons with diabetes at home as an aid to monitor the effectiveness of diabetes control. It is not intended for neonatal use or for the diagnosis of or screening for diabetes. This system is intended for self-testing outside the body (in vitro diagnostic use), and should only be used by a single person and should not be shared. Principle of Operation MIO Blood Glucose Monitoring System is designed to quantitatively measure the glucose concentration in fresh capillary whole blood. The glucose measurement is achieved by using the amperometric detection method. The test is based on measurement of electrical current caused by the reaction of the glucose with the reagents on the electrode of the test strip. The blood sample is pulled into the tip of the test strip through capillary action. Glucose in the sample reacts with glucose oxidase and the mediator. Electrons are generated, producing a current that is positive correlation to the glucose concentration in the sample. After the reaction time, the glucose concentration in the sample is displayed . ii TABLE OF CONTENTS 1. Understanding Your Testing Tools............................................ 1 Your System Overview...................................................... 1 Your Meter Display................................................................... 2 Meter Use and Precautions........................................................ 3 Important Safety Information...................................................... 4 Limitations.............................................................................. 5 2. Setting Up Your System........................................................... 6 Set the Date and Time............................................................... 6 Set the Audio Feature................................................................ 8 Set the Meal Marker.................................................................. 8 Set the Hypoglycemia (Hypo) Warning......................................... 8 Set the Ketone Warning............................................................. 9 3. Performing a Test.................................................................... 10 Preparing the Test Strip............................................................. 10 Preparing the Lancing Device..................................................... 11 Getting a Blood Drop for Testing.................................................. 12 Discarding the Used Test Strip.............................................................. 14 Removing the Used Lancet ....................................................... 14 Expected Diabetes Control Goal.................................................. 15 Questionable or lnconsistent Results............................................ 16 Symptoms of High ro Low Blood Glucose...................................... 16 Precision and Accuracy............................................................. 17 Comparing Meter and Laboratory Results..................................... 19 Testing with Control Solution ................................................... 19 Understand Control Test Result.................................................. 21 Using the Meter Memory........................................................... 22 Viewing your Test Results.......................................................... 22 4. Maintenance and Troubleshooting............................................. 24 Charging the Battery............................................................. 24 Caring for Your Glucose Monitoring System.................................. 25 Cleaning and Disinfection.......................................................... 25 Troubleshooting Guide.............................................................. 28 5. Technical Information............................................................. 30 System Specifications............................................................... 30 4G Specifications..................................................................... 31 Warranty................................................................................ 31 iii EMC Guidance........................................................................ 32 FCC Requirement.................................................................... 35 1 CHAPTER 1: UNDERSTANDING YOUR TESTING TOOLS Your System Overview Note: The MIO Blood Glucose Test Strips, MIO Control Solution, MIO Lancing Device and MIO Lancets are not included in the meter box but are necessary for use, please contact 24/7 MIO Customer Support at (833)445-5666 for purchase. 2 Your Meter Display The picture below shows all the symbols that appear on your meter display. Please make sure the display is working properly before testing. When the meter is off, press and hold to see the complete display. All display segments will appear. If you need more time to check the display, repeat the above operation. All display segments should be clear and exactly like the picture below. If not, contact 24/7 MIO Customer Support at (833)445…

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

Applicant Declaration QSF27-14-04 Rev 1.0 Rev. Feb 6, 2023 Page 1 of 1 Original Issue: Jan. 4, 2021 SGS North America Inc. 620 Old Peachtree Road SUITE 100 Suwanee, Georgia 30024 United States Applicant Legal Business Name MIO LABS INC. Address #1023, ZGC Innovation Center 4500 Great America Pkwy Santa Clara, CA 95054 United States Grantee Code 2A7JQ FCC ID 2A7JQTELEBGM2283-A Authorized Contact Name Jialong Fan Contact Email [email protected] Contact Phone +86 15728668528 I, the undersigned, certify that I am an authorized signatory for the Applicant and therefore declare; a)in ac cordance with 47CFR2.911(d), all of the statements herein and the exhibits attached hereto are true and correct to the best of my knowledge and beli ef. b)in ac cepting a Grant of Equipment Authorization issued by a TCB, under the authority of the FCC, as a result of the representations made i n thi s application, the Applicant is responsible for: (1)labeling the equipment with the exact FCC ID as specified in this application, (2)compliance statement labeling pursuant to the applicable rules , (3 )compliance of the equipment with the applicable technical rules , c)i f the Applicant is not the actual manufacturer of the equipment, appropriate arrangements have been made with the manufacturer to ensur e that pr oduction units of this equipment will continue to comply with the FCC’s technical requirements. d)in accordance with 47 CFR 2.909 and KDB394321, the Applicant has read, understood and agrees to accept that they are the responsibl e par ty and agree to abide by their responsibilities as specified under 47 CFR 2.909 and KDB394321. e)in accordance with ISO 17065, FCC KDB641163, FCC KDB610077, KDB394321 and RSP-100, the Applicant has read, understood, accepts and agrees to abide by the post market surveillance requirements. (1)the Applicant understands, accepts and agrees that a sample may be requested for surveillance testing. (2)the Applicant shall make provisions to always have a production sample available upon request by SGS, FCC and/or ISE D. (3 )the Applicant shall, upon request by SGS, at the Applicant’s expense, provide a production sample of the requested product to SGS , F CC and/or ISED as instructed. The sample shall include all support devices, cables, software, accessories or other hardware or software required for evaluation, review, certification and audit surveillance of products certified by SGS. f)neither the Applicant nor any party to the application is subject to a denial of Federal benefits, that includes FCC benefits, pursuant to Section 5301 of the A nti-Drug Abuse Act of 1988, 21 U.S.C. §862 because of a conviction for possession or distribution of a controlled substance. S ee 47CF R 1.2002(b) for the definition of a “party” for these purposes. g)the Applicant has read, understood, accepts and agrees to abide by the SGS North America, Inc.(TCB) terms and conditions . Li nk to CFRs: https://www.fcc.gov/wireless/bureau-divisions/technologies-systems-and-innovation-division/rules-regulations-title-47 Link to KDBs: https://apps.fcc.gov/oetcf/kdb/index.cfm Link to RSP-100: https://www.ic.gc.ca/eic/site/smt-gst.nsf/eng/sf01130.html Link to the Covered List: Covered List [MIO LABS INC.] (“the applicant”) certifies that the equipment for which authorization is sought is not “covered” equipment prohibited from receiving an equipment authorization pursuant to section 2.903 of the FCC rules. [MIO LABS INC.] (“the applicant”) certifies that, as of the date of the filing of the application, the applicant [is not] identified on the Covered list, established pursuant to §1.50002, as an entity producing “covered” equipment. Applicant Signature: Date: 2023/08/22 Print Name: Jialong Fan Title: RA Manager *NOTE: This declaration cannot be signed by an Agent, it shall be signed by an authorized person listed in the FCC database

UNI TED STATES DESIGNATED AGENT LETTER D ate: 2023/08/22 TO: F ederal Communication Commission Equipment Authorization Branch 7435 Oakland Mills Road Columbia, MID 21046 Applicant U.S. designated agent Company Name: MIO LABS INC. Company Name: MIO LABS INC. Grantee Code: 2A7JQ FRN: Contact Name: 0032569972 Jialong Fan Contact Name: Jialong Fan Address: #1023, ZGC Innovation Center 4500 Great America Pkwy Santa Clara, CA 95054 United States Address: #1023, ZGC Innovation Center 4500 Great America Pkwy Santa Clara, CA 95054 United States Telephone: Telephone: +86 15728668528 Email: (301) 910-0529 [email protected] Email: [email protected] Applicable Equipment: FCC ID: <2A7JQTELEBGM2283-A > AT TN: Director of Certification: We, < MIO LABS INC. > understand and acknowledge the applicants consent and th e designated agent’s obligation to accept service of process in the United States for matters related to the applicable equipment, and at the physical U.S. address and e-mail of the designated agent listed above. We, < MIO LABS INC. > acknowledge the applicant’s acceptance of its obligation to maintain an agent for service of process in the United States for no less than one year after either the grantee has permanently terminated all marketing and importation of the applicable equipment within the U.S., or the conclusion of any Commission-related administrative or judicial proceeding involving the equipment, whichever is later. Applicant U.S. designated agent Name (Printed): Jialong Fan Name (Printed): Jialong Fan Title: RA Manager Title: RA Manager Signature: Signature:

MIO LABS INC. Date: 2023/08/22 TO: Federal Communication Commission Equipment Authorization Branch 7435 Oakland Mills Road Columbia, MID 21046 Regarding: FCC ID: 2A7JQTELEBGM2283-A To whom it may concern: We, the undersigned, hereby authorize SGS-CSTC Standards Technical Services Co., Ltd. to act on our behalf in all manners relating to application for equipment authorization with respect to the FCC ID above, in cluding signing of all documents relating to these matters. Any and all acts carried out by the agent on our behalf shall have the same effect as acts of our own. We, the undersigned, hereby certify that we are not subject to a denial of federal benefit s, that includes FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. 853(a). Where our agent signs the application for certification on our behalf, I acknowledge that all responsibility for complying with the terms and conditions for Certification, as specified by SGS North America, Inc., still resides with MIO LABS INC. This authorization is valid until further written notice from the applicant. Sincerely, Print Name: Jialong Fan Title: RA Manager Signature: On behalf of Company: MIO LABS INC. Telephone: +86 15728668528 E-mail: [email protected]

MIO LABS INC. TO: F ederal Communication Commission Equipment Authorization Branch 7435 Oakland Mills Road Columbia, MID 21046 R egarding: Confidentiality Request regarding application for FCC ID: 2A7JQTELEBGM2283-A L ONG TERM CONFIDENTIALITY Pursuant to 47 CFR Section 0.459 and 0.457 of the commission’s rules, the applicant hereby request confidential treatment of the documents listed below, associated with the certification application referenced above. Schematic(s) Block Diagrams Operational Descriptions Tune up Th e documents above contain proprietary information not released to the public. Public disclosure of this information may prove harmful to the business of the applicant. S HORT TERM CONFIDENTIALITY Additionally, the applicant requests the following documents be held confidential until the device is marketed or 180 days from the grant date, whichever is less. If the device is marketed within aforementioned days of the Grant Date, the applicant will notify the TCB per FCC KDB 726920 D01 Confidentiality Request Procedures. E xternal Photos Internal Photos Test Setup Photos User manual(s) S incerely, Print Name: Jialong Fan Title: RA Manager Signature: On behalf of Company: MIO LABS INC. Telephone: +86 15728668528 E-mail: [email protected]

SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A02 Rev.A/0 Page: 1 of 7 Appendix External Photos for SZCR2308002639ME FCC ID:2A7JQTELEBGM2283-A SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A02 Rev.A/0 Page: 2 of 7 EUT Constructional Details (EUT Photos) Model No.: TeleBGM 2283-A Label Location SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A02 Rev.A/0 Page: 3 of 7 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A02 Rev.A/0 Page: 4 of 7 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A02 Rev.A/0 Page: 5 of 7 Model No.: TeleBGM 2284-A Label Location SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A02 Rev.A/0 Page: 6 of 7 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A02 Rev.A/0 Page: 7 of 7

技术要求： 1、黏合不可露胶； 2、保持印刷面板上的清洁； 3、注意套印的准确性； 4、表面处理不可爆开； 5、所用材料及工艺须满足RoHS、Reach的环保要求； 6、结构工艺以结构受控图为准； 7、通用要求：成型后制品以《不干胶类来料检验标准》验收； 8、测试要求：保证产品在60°C，48小时的恒温測试下不起边、脱胶、气泡，印刷内容必须通过蒸馏水、酒精、 异丙醇测试后能识别读出； 9、颜色参考： 产品型号TBG-2283A 28.98*41.51mm，两贴纸间增加虚刀线 零件名称 零件图号 80g铜版纸不干胶 TBG-2283A-GB-03-背贴-A4 单黑 可打印哑膜 郭健波 2023-08-24 徐紫燕 2023-08-24 徐紫燕 2023-08-24 TBG-2283A-GB-03 血糖仪 - 1:1 mm 产品名称 表面处理 共1张第1张 A/4版本 比例 材质 尺寸 印色 设计 审核 批准 单位 对应结构图纸 广东乐心医疗电子股份有限公司 测试项目测试要求验收标准 标签/贴纸酒精耐磨 用纯棉布(专用)蘸满无水酒精(浓度≥99.5% )，包在专用的测试头上(包上棉布后测试头的 面积约为1cm²)，施加500g的载荷，用专业仪器或手工以40次/分钟~ 50次/分钟的速 度，在样品表面来回擦拭。摩擦规定圈数：15圈。 印刷图文清晰，无断笔、缺划、模糊、掉油墨；允许图文有轻 微的磨损及褪色，但要求内容仍完整且清晰可认，条码能扫描 识别。 标签/贴纸橡皮耐磨 用专用的橡皮(橡皮型号：中华牌铅笔头部的圆形橡皮)，施加2kgf的载荷，以20~ 30次 /分钟的速度，以20 测试要求 实物要求符合Rohs、Reach、无卤、包装指令和环保标准 Blood Glucose Meter TeleBGM 2283-A Distributed by: Mio Labs lnc. #1023,ZGC lnnovation Center, 4500 Great America Pkwy, Santa Clara, CA 95054 24/7 MIO Customer support tel: (833) 445-5666 For in vitro diagnostic use. MODELTeleBGM 2283-A 3.7V 1080mAh mg/dL (XX)X X X X X X X X X X X SN G03BG00132100001 (XX)X X X X X X Blood Glucose Meter G03-BG Distributed by: Mio Labs lnc. #1023,ZGC lnnovation Center, 4500 Great America Pkwy, Santa Clara, CA 95054 24/7 MIO Customer support tel: 301-910-0529 For in vitro diagnostic use. MODELG03-BG3.7V 1080mAh mg/dL (XX)X X X X X X X X X X X SN G03BG00132100001 FCC IDxxxxxxxxxx (XX)X X X X X X 28.95 mm 41.51 mm 粘贴示意图 FCC ID: 2A7JQTELEBGM2283-A

产品型号TBG-2284A80g铜版纸不干胶零件名称 零件图号 28.98*41.51mmTBG-2284A-GB-03-背贴-A0-MIO版本 可打印哑膜 杨红红 2023-08-15 杨红红 2023-08-15 徐紫燕 2023-08-15 TBG-2284A-GB-03 血糖仪 - 1:1 mm 产品名称 表面处理 共1张第1张 A/1版本 比例 材质 尺寸 印色 设计 审核 批准 单位 对应结构图纸 广东乐心医疗电子股份有限公司 单黑 粘贴示意图： Blood Glucose Meter TeleBGM 2284-A Distributed by: Mio Labs lnc. #1023,ZGC lnnovation Center, 4500 Great America Pkwy, Santa Clara, CA 95054 24/7 MIO Customer support tel:(833)445-5666 For in vitro diagnostic use. MODELTeleBGM 2284-A 3.7V 1080mAh mg/dL (XX)XXXXXXXXXXX SN G04BG001XXXXXXXX (XX)XXXXXX 28.98mm 41.51 mm FCC ID: 2A7JQTELEBGM2283-A

SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 1 of 9 Appendix Internal Photos for SZCR2308002639ME FCC ID:2A7JQTELEBGM2283-A SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 2 of 9 EUT Constructional Details (EUT Photos) Model No.: TeleBGM 2283-A Antenna SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 3 of 9 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 4 of 9 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 5 of 9 Model No.: TeleBGM 2284-A Antenna SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 6 of 9 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 7 of 9 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 8 of 9 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 9 of 9 - End of the Appendix -

Doc No./Rev.: SGS-W-TRF-101 v00 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch Report No.: ZEWM2308001256RG01 Page : 1 of 44 Authorized Signature: Ervin Li Regulatory Manager FCC SAR TEST REPORT Application No.: ZEWM2308001256RG Applicant: MIO LABS INC. Manufacturer: MIO LABS INC. Product Name: Blood Glucose Meter Model No.(EUT): TeleBGM 2283-A, TeleBGM 2284-A FCC ID: 2A7JQTELEBGM2283-A Standards: FCC 47CFR §2.1093 Date of Receipt: 2023/08/25 Date of Test: 2023/08/27 to 2023/09/16 Date of Issue: 2023/09/19 Test conclusion: PASS * * In the configuration tested, the EUT detailed in this report complied with the standards specified above. Doc No./Rev.: SGS-W-TRF-101 v00 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch Report No.: ZEWM2308001256RG01 Page : 2 of 44 REVISION HISTORY Report Number Revision Description Issue Date ZEWM2308001256RG01 01 Original 2023/09/19 Prepared By Vito Wang Checked By Roman Pan Doc No./Rev.: SGS-W-TRF-101 v00 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch Report No.: ZEWM2308001256RG01 Page : 3 of 44 TEST SUMMARY Frequency Band Maximum Reported SAR1g(W/kg) CAT-M1 Extremity 0mm CatM1 LTE Band 2 0.70 CatM1 LTE Band 4 0.99 CatM1 LTE Band 12 0.37 CatM1 LTE Band 13 0.31 SAR Limited(W/kg) 4.0 Doc No./Rev.: SGS-W-TRF-101 v00 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch Report No.: ZEWM2308001256RG01 Page : 4 of 44 CONTENTS 1 GENERAL INFORMATION ................................................................................................................................. 6 1.1 DETAILS OF CLIENT ................................................................................................................................................. 6 1.2 TEST LOCATION ...................................................................................................................................................... 6 1.3 TEST FACILITY ......................................................................................................................................................... 7 1.4 GENERAL DESCRIPTION OF EUT ............................................................................................................................ 8 1.4.1 DUT Antenna Locations (Back View) ............................................................................................................ 9 1.4.2 Stand-alone SAR test evaluation ................................................................................................................... 9 1.5 TEST SPECIFICATION ............................................................................................................................................ 11 1.6 RF EXPOSURE LIMITS ............................................................................................................................................ 12 2 LABORATORY ENVIRONMENT ..................................................................................................................... 13 3 SAR MEASUREMENTS SYSTEM CONFIGURATION .................................................................................... 14 3.1 THE SAR MEASUREMENT SYSTEM ...................................................................................................................... 14 3.2 ISOTROPIC E-FIELD PROBE EX3DV4 .................................................................................................................. 15 3.3 DATA ACQUISITION ELECTRONICS (DAE) ........................................................................................................... 16 3.4 SAM TWIN PHANTOM ........................................................................................................................................... 16 3.5 ELI PHANTOM ....................................................................................................................................................... 17 3.6 DEVICE HOLDER FOR TRANSMITTERS .................................................................................................................. 18 3.7 MEASUREMENT PROCEDURE ................................................................................................................................ 19 3.7.1 Scanning procedure ....................................................................................................................................... 19 3.7.2 Data Storage ................................................................................................................................................... 21 3.7.3 Data Evaluation by SEMCAD ....................................................................................................................... 21 4 SAR MEASUREMENT VARIABILITY AND UNCERTAINTY .......................................................................... 23 4.1 SAR MEASUREMENT VARIABILITY ........................................................................................................................ 23 4.2 SAR MEASUREMENT UNCERTAINTY ..................................................................................................................... 23 5 DESCRIPTION OF TEST POSITION ................................................................................................................ 24 5.1 EXTREMITY EXPOSURE CONDITION ...................................................................................................................... 24 6 SAR SYSTEM VERIFICATION PROCEDURE ................................................................................................. 25 6.1 TISSUE SIMULATE LIQUID ..................................................................................................................................... 25 6.1.1 Recipes for Tissue Simulate Liquid ............................................................................................................. 25 6.1.2 Measurement for Tissue Simulate Liqui…

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Report No.: ZEWM2…

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