2ATOV-1059UBlood glucose meter

For all GoChek Max series meters. MicroTech Medical (Hangzhou) Co., Ltd. Address: No.108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R.China Website: http://www.microtechmd.com CMC Medical Devices & Drugs S.L C/Horacio Lengo Nº 18 CP 29006, Málaga-Spain Name: XXXXXXX Address: XXXXXXXXX Document: 1059-PMTL-012 Revision: V02 Issued: 2026-05-13 2797 INSTRUCTION MANUAL BLOOD GLUCOSE METER 血糖仪使用说明书（英文CE版) ����-PMTL-��� V�� �.品牌修改为GoChek Max �.CExxxx改为CE���� �.内容修改 封面：封面封底200g铜版纸 内页：70g轻涂纸 黑白印刷 105*155mm For all GoChek Max series meters. MicroTech Medical (Hangzhou) Co., Ltd. Address: No.108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R.China Website: http://www.microtechmd.com CMC Medical Devices & Drugs S.L C/Horacio Lengo Nº 18 CP 29006, Málaga-Spain Name: XXXXXXX Address: XXXXXXXXX Document: 1059-PMTL-012 Revision: V02 Issued: 2026-05-13 2797 INSTRUCTION MANUAL BLOOD GLUCOSE METER Dear User: Thank you for choosing the GoChek Max Series blood glucose meter. Monitoring your blood glucose level is an integral partof treating diabetes. MicroTech Medical is committed to helping you ccontrol your condition so you can live a healthy and active life. Please read this user manual to help master the simple fiunctions of your GoChek Max Series meter. If used properly, the blood glucose meter will give you accurate results. The GoChek Max Series blood glucose monitoring system will give yoou accurate readings from fresh capillary or venous whole blood. This product is for professional use in medical institutes or for self-testing by diabetics. Test results serve only as helpful information, not as proof for clinical diagnoses. Thank you for choosing the GoChek Max Series blood glucose meter,This instruction manual contains all the information you need to know, including the blood glucose testing procedures and precautions for use. Please be sure to read it carefully and in full. Important safety instructions before use Only use the meter as directed by this instruction manual. Do not use accessories that are not provided or recommended by our company. Only our company or its authorized agencies are permitted to inspect or supply any parts and components. Do not use this product if it malfunctions or is damaged. Do not expose this product to surfaces that are too hot to touch. Do not place any objects on top of this product. Unless specifically required by the Instructions for Use, do not allow any objects to fall into or be inserted into the openings, tubing, or joints of this product. Do not use this product in areas where aerosol sprays are in use or oxygen is administered. Failure to use the device in accordance with the manufacturer’s specified method may impair the protection provided by the device. This blood glucose meter is for in vitro diagnostic use only. This blood glucose meter is suitable for both self-testing and professional monitoring. The blood glucose meter is intended for use with blood glucose test strips to quantitatively measure the blood glucose concentration in human body. Consult your doctor or diabetes care specialist before adjusting your medication, diet, or daily activities. Keep this blood glucose meter out of the reach of children and pets. Do not use the device outdoors. i ▼ Specification▼ Index Product Name: MCM-4 / MCM-6 / MCM-7 Connect Blood Glucose Meter Size: 87 mm (L) x 54 mm (W) x 25 mm (Thickness) Glucose Test Range: 0.6-33.3 mmol/L (10-600 mg/dL) Minimum Sample Volume: 0.6μL Test Time: 5 seconds Battery: 2×AAA(LR03) Battery Life: >1,000 readings(bluetooth functions disabled) Glucose Concentration Units: mmol/L or mg/dL depending on the standard of your country Memory Storage: 700(MCM-4) and 1100 (MCM-6, MCM-7) test results with date and time stamp Auto Shutdown: Automatic shutdown after 2 minutes Display Size: 40mm × 42mm Weight: about 75 grams (including battery) Operating Temperature: 5-45°C (41-113°F) Operating Altitude: 0-3048 m above sea level Operating Humidity: 10-90% (non-condensing) Hematocrit Range: 10-70% Valid Period: 5 years Storage and Transportation Temperature: -40-55°C Storage and Transportation Humidity: 10-90% (non-condensing) Model No. Data Storage Capacity Voice Prompt Function Wireless Transmission Function Backlit Display MCM-4 700 NO NO NO MCM-6 1100 YES NO YES MCM-7 1100 YES YES YES Note: The data storage capacity refers to the total number of stored blood sample data and control solution data. Among them, the MCM-4 blood glucose meter can store 200 sets of control solution data, while both the MCM-6 and MCM-7 models can store 100 sets of control solution data each. Note: Blood containing high levels of vitamin C or other reducing agents can lead to inaccurate test results. Triglycerides above 3,000 mg/dL and cholesterol above 500 mg/dL will lead to inaccurate test results. Specification ................................................................................................. Intended Use ................................................................................................. Product components.................................................................................... Component Descriptions............................................................................. Blood Glucose Meter.............................................................................................. Display................................................................................................................. Test Strips............................................................................................................. Control Solution..................................................................................................... Meter Setup Before Use ............................................................................... Battery Installation................................................................................................. Meter Setup.......…

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

UNITEDSTATESDESIGNATEDAGENTLETTER Date:2026.5.8 TO:FederalCommunicationCommission EquipmentAuthorizationBranch 7435OaklandMillsRoad Columbia,MID21046 ApplicantU.S.designatedagent Company Name: MicroTechMedical(Hangzhou) Co.,Ltd. Company Name: MicroTechMedical,Inc. FRN:0028573830FRN:0033955881 GranteeCode:2ATOV ContactName:XiaojingZhaoContactName DoreMark Address:No.108Liuze St.,Cangqian,YuhangDistrict Hangzhou,Zhejiang,P.R.China Address:1999S.BascomAve,Suite 700,Campbell,CALIFORNIA 95008,UnitedStates City/Province/Zi p: Hangzhou,Zhejiang,P.R.ChinaCity/Province/Zi p: Campbell,CALIFORNIA95008, UnitedStates Telephone:+86-18989848417Telephone:4085440744 Fax: 9571-88520092 Fax:46-4481055 Email:[email protected] om Email: [email protected] ApplicableEquipment:FCCID:<2ATOV-1059U> ATTN:DirectorofCertification: We,MicroTechMedical(Hangzhou)Co.,Ltd.andMicroTechMedical,Inc.understandandacknowledge theapplicantsconsentandthedesignatedagent’sobligationtoacceptserviceofprocessintheUnited Statesformattersrelatedtotheapplicableequipment,andatthephysicalU.S.addressande-mailofthe designatedagentlistedabove. We,MicroTechMedical(Hangzhou)Co.,Ltd.andMicroTechMedical,Inc.acknowledgetheapplicant’s acceptanceofitsobligationtomaintainanagentforserviceofprocessintheUnitedStatesfornoless thanoneyearaftereitherthegranteehaspermanentlyterminatedallmarketingandimportationofthe applicableequipmentwithintheU.S.,ortheconclusionofanyCommission-relatedadministrativeor judicialproceedinginvolvingtheequipment,whicheverislater. ApplicantU.S.designatedagent Name (Printed) :XiaojingZhaoName (Printed) :Doremark Title:R&DQualityManagementTitle:VicePresident Signature: Signature:

Applicant Declaration QSF27-14-04 Rev 1.4 April 25, 2025 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 MicroTech Medical (Hangzhou) Co., Ltd. Address No. 108 Liuze St., Cangqian, Yuhang District, Hangzhou, 311121 Zhejiang, P.R. China FRN 0028573830 Grantee Code 2ATOV FCC ID: 2ATOV-1059U Authorized Contact Name Xiaojing Zhao Contact Phone +86-18989848417 Contact Email [email protected] I, the undersigned, certify that I am an authorized signatory for the Applicant and therefore declare; a) in accordance 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 belief. b) in accepting a Grant of Equipment Authorization issued by a TCB, under the authority of the FCC, as a result of the representations made in this 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) if the Applicant is not the actual manufacturer of the equipment, appropriate arrangements have been made with the manufacturer to ensure that production 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 responsible party 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 ISED. (3) the Applicant shall, upon request by SGS, at the Applicant’s expense, provide a production sample of the requested product to SGS, FCC 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 Anti-Drug Abuse Act of 1988, 21 U.S.C. §862 because of a conviction for possession or distribution of a controlled substance. See 47CFR 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. terms and conditions as specified in the TCB Application Form 731 (QSF27-14-01). Link 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 Applicant Signature: Date: 2026-04-24 Print Name: Xiaojing Zhao Title: Regulatory Affairs *NOTE: This declaration cannot be signed by an Agent, it shall be signed by an authorized person listed in the FCC database

Microtech Medical (Hangzhou) Co.,Ltd Current Date 2026-06-29 To : SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. No. 588 West Jindu Road, Songjiang District, Shanghai, China. 201612 Dear Sir/Madam, Subject: Declaration Letter about Identity of Products *WE Microtech Medical (Hangzhou) Co.,Ltd, HEREBY DECLARED THAT Product Description: Blood glucose meter Model No.: MCM-6, MCM-7 Manufacturer’s Name: Microtech Medical (Hangzhou) Co.,Ltd. Manufacturer’s Address: No.108 Liuze St.,Cangqian,Yuhang District,Hangzhou,311121 Zhejiang, P.R.China *Except that the model number and appearance deviation, are identical with the original product as follows: Note: The definition of identical should be “electrically identical”. A device will be considered to be electrically identical if no changes are made to the devices’ schematics, board layouts, component layouts, chip sets, resistors and all other electrical aspects of the device are identical with the model which has been tested by SGS. Model No.: MCM-4 Manufacturer’s Name: Microtech Medical (Hangzhou) Co.,Ltd. Manufacturer’s Address: No.108 Liuze St.,Cangqian,Yuhang District,Hangzhou,311121 Zhejiang, P.R.China Sincerely, Signature: Printed Name : Xiaojing Zhao Position/Title : Regulatory Affairs Contact Number: +86-18989848417

Compliance Certification Services (Kunshan) Inc. Page: 1 of 5 External Photos for KSCR2606001294HS Compliance Certification Services (Kunshan) Inc. Page: 2 of 5 EUT Constructional Details (EUT Photos) Compliance Certification Services (Kunshan) Inc. Page: 3 of 5 Compliance Certification Services (Kunshan) Inc. Page: 4 of 5 Compliance Certification Services (Kunshan) Inc. Page: 5 of 5 - End of the Appendix -

Page 1 of 1

Compliance Certification Services (Kunshan) Inc. Page: 1 of 3 Internal Photos for KSCR2606001294HS Compliance Certification Services (Kunshan) Inc. Page: 2 of 3 EUT Constructional Details (EUT Photos) Compliance Certification Services (Kunshan) Inc. Page: 3 of 3 - End of the Appendix -

Report No.: KSCR260600129402 Page: 1 of 10 TRF No. CONN_001 A_Jun 1st ,2026 1 Cover Page RF Exposure Evaluation Report Application No.: KSCR2606001294HS FCC ID: 2ATOV-1059U Applicant: Microtech Medical (Hangzhou) Co.,Ltd. Address of Applicant: No.108 Liuze St.,Cangqian,Yuhang District,Hangzhou,311121 Zhejiang, P.R.China Manufacturer: Microtech Medical (Hangzhou) Co.,Ltd. Address of Manufacturer: No.108 Liuze St.,Cangqian,Yuhang District,Hangzhou,311121 Zhejiang, P.R.China Factory: Microtech Medical (Hangzhou) Co.,Ltd. Address of Factory: No.108 Liuze St.,Cangqian,Yuhang District,Hangzhou,311121 Zhejiang, P.R.China Equipment Under Test (EUT): EUT Name: Blood glucose meter Model No.: MCM-7 Standard(s) : FCC Rules 47 CFR §2.1093 KDB 447498 D04 interim General RF Exposure Guidance v01 Date of Receipt: 2026-06-03 Date of Test: 2026-06-04 to 2026-06-09 Date of Issue: 2026-06-09 Test Result: Pass* * In the configuration tested, the EUT complied with the standards specified above. Report No.: KSCR260600129402 Page: 2 of 10 TRF No. CONN_001 A_Jun 1st ,2026 Revision Record Version Description Date Remark 00 Original 2026-06-09 / Authorized for issue by: Tested By Damon_Zhou/Project Engineer Approved By Terry Hou /Reviewer Report No.: KSCR260600129402 Page: 3 of 10 TRF No. CONN_001 A_Jun 1st ,2026 2 Contents Page 1 Cover Page ........................................................................................................................................ 1 2 Contents ............................................................................................................................................ 3 3 General Information .......................................................................................................................... 4 3.1 General Description of E.U.T. .................................................................................................... 4 3.2 Details of E.U.T. ......................................................................................................................... 4 3.3 Separation Distance ................................................................................................................... 4 3.4 Test Location .............................................................................................................................. 5 3.5 Test Facility ................................................................................................................................ 5 4 Test Standards and Limits ............................................................................................................... 6 5 FCC Radiofrequency radiation exposure limits ............................................................................ 6 5.1 RF Exposure Test Exemptions for single RF sources ............................................................... 6 5.1.1 Blanket 1 mW Blanket Exemption ...................................................................................... 6 5.1.2 MPE-based Exemption ........................................................................................................ 6 5.1.3 SAR-based Exemption ........................................................................................................ 7 5.2 RF Exposure Test Exemptions for Simultaneous Transmission ................................................ 8 6 Measurement and Calculation ....................................................................................................... 10 6.1 Maximum transmit power ......................................................................................................... 10 6.2 RF Exposure Calculation ......................................................................................................... 10 Report No.: KSCR260600129402 Page: 4 of 10 TRF No. CONN_001 A_Jun 1st ,2026 3 General Information 3.1 General Description of E.U.T. Power supply: DC 3V (2*AAA Battery) Product Type: Portable device Mobile device Fixed device 3.2 Details of E.U.T. Operation Frequency: 2402MHz to 2480MHz Modulation Type: GFSK Number of Channels: 40 Channel Spacing: 2MHz Antenna Type: PCB Antenna Antenna Gain: -3.94dBi (Provided by manufacturer) Antenna Number: 1 3.3 Separation Distance Separation distance between the antenna to person (R): ＜5mm Remark: This minimum test separation distance is determined by the smallest distance from the antenna and radiating structures or outer surface of the device, according to the host form factor, exposure conditions and platform requirements, to any part of the body or extremity of a user or bystander. Report No.: KSCR260600129402 Page: 5 of 10 TRF No. CONN_001 A_Jun 1st ,2026 3.4 Test Location All tests were performed at: Compliance Certification Services (Kunshan) Inc. No.10 Weiye Rd, Innovation park, Eco&Tec, Development Zone, Kunshan City, Jiangsu, China. Tel: +86 512 5735 5888 Fax: +86 512 5737 0818 No tests were sub-contracted. Note: 1. SGS is not responsible for wrong test results due to incorrect information (e.g. max. clock frequency, highest internal frequency, antenna gain, cable loss, etc ) is provided by the applicant. (if applicable). 2. SGS is not responsible for the authenticity, integrity and the validity of the conclusion based on results of the data provided by applicant. (if applicable). 3. Sample source: sent by customer. 3.5 Test Facility The test facility is recognized, certified, or accredited by the following organizations: • A2LA (Certificate No. 2541.01) Compliance Certification Services (Kunshan) Inc. is accredited by the American Association for Laboratory Accreditation (A2LA). • FCC (Designation Number: CN1172) Compliance Certification Services (Kunshan) Inc. has been recognized as an accredited testing laboratory. • ISED (CAB Identifier: CN0072) Compliance Certification Services (Kunshan) Inc. has been recognized by Innovation, Science and Economic Development Canada (ISED) as an accredited testing laboratory. …

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

ANTENNASPECIFICATION Specifications ITEMSPEC. Modem Name1059 PCB ANTENNA FrequenceRange2400-2500MHZ Max Gain-3.94dB PolarizationHorizontaland Vertical Azimuth Beam PattemOmni-directional Impedance Antenna Length31.78mm Manufacture ShenzhenOushengbillion technologyCo.,LTD Antenna Photo &Length (mm) Room 720, Building C, No. 30 Hangkong Road, Sanwei Community, Xixiang Street, Bao'an District, Shenzhen, Guangdong 518100, China. Typicalfreespaceefficiencyandgain Frequency （ MHz ） 240024052415242524352445245524652475248524952500 Gain （ dBi ） -4.72-4.52-4.02-3.94-4.43-4.33-4.61-4.89-4.70-4.85-5.17-5.03 Efficiency （ dB ） -10.90-10.69-10.27-10.23-10.74-10.69-11.18-11.50-11.36-11.54-11.74-11.56 Typicalfreespaceradiationpattern TypicalFreeSpace3DRadiationPatternat2.45GHz:

Report No.: KSCR260600129401 Page: 1 of 76 TRF No. CONN_001 A_Jun 1st ,2026 TEST REPORT Application No.: KSCR2606001294HS FCC ID: 2ATOV-1059U Applicant: Microtech Medical (Hangzhou) Co.,Ltd. Address of Applicant: No.108 Liuze St.,Cangqian,Yuhang District,Hangzhou,311121 Zhejiang, P.R.China Manufacturer: Microtech Medical (Hangzhou) Co.,Ltd. Address of Manufacturer: No.108 Liuze St.,Cangqian,Yuhang District,Hangzhou,311121 Zhejiang, P.R.China Factory: Microtech Medical (Hangzhou) Co.,Ltd. Address of Factory: No.108 Liuze St.,Cangqian,Yuhang District,Hangzhou,311121 Zhejiang, P.R.China Equipment Under Test (EUT): EUT Name: Blood glucose meter Model No.: MCM-7 Standard(s) : 47 CFR Part 15, Subpart C 15.247 Date of Receipt: 2026-06-03 Date of Test: 2026-06-04 to 2026-06-09 Date of Issue: 2026-06-09 Test Result: Pass* * In the configuration tested, the EUT complied with the standards specified above. Report No.: KSCR260600129401 Page: 2 of 76 TRF No. CONN_001 A_Jun 1st ,2026 Revision Record Version Description Date Remark 00 Original 2026-06-09 / Authorized for issue by: Tested By Damon_Zhou/Project Engineer · Approved By Terry Hou /Reviewer Report No.: KSCR260600129401 Page: 3 of 76 TRF No. CONN_001 A_Jun 1st ,2026 2 Test Summary Radio Spectrum Technical Requirement Item Standard Method Requirement Result Antenna Requirement 47 CFR Part 15, Subpart C 15.247 N/A 47 CFR Part 15, Subpart C 15.203 & 15.247(b)(4) Pass Radio Spectrum Matter Part Item Standard Method Requirement Result Maximum Conducted Output Power 47 CFR Part 15, Subpart C 15.247 ANSI C63.10 (2020) Section 11.9.1 47 CFR Part 15, Subpart C 15.247(b)(3) Pass Minimum 6dB Bandwidth ANSI C63.10 (2020) Section 11.8.1 47 CFR Part 15, Subpart C 15.247a(2) Pass Power Spectral Density ANSI C63.10 (2020) Section 11.10.3 47 CFR Part 15, Subpart C 15.247(e) Pass Conducted Band Edges Measurement ANSI C63.10 (2020) Section 6.10.4 47 CFR Part 15, Subpart C 15.247(d) Pass Conducted Spurious Emissions ANSI C63.10 (2020) Section 11.11 47 CFR Part 15, Subpart C 15.247(d) Pass Radiated Emissions which fall in the restricted bands ANSI C63.10 (2020) Section 6.10.5 & 11.12 47 CFR Part 15, Subpart C 15.205 & 15.209 Pass Radiated Spurious Emissions Below 1GHz ANSI C63.10 (2020) Section 6.4,6.5 47 CFR Part 15, Subpart C 15.205 & 15.209 Pass Radiated Spurious Emissions Above 1GHz ANSI C63.10 (2020) Section 6.6 & 11.12 47 CFR Part 15, Subpart C 15.205 & 15.209 Pass Report No.: KSCR260600129401 Page: 4 of 76 TRF No. CONN_001 A_Jun 1st ,2026 3 Contents Page 1 COVER PAGE ........................................................................................................................................... 1 2 Test Summary ......................................................................................................................................... 3 3 Contents ................................................................................................................................................... 4 4 General Information ................................................................................................................................ 5 4.1 Details of E.U.T. ............................................................................................................................... 5 4.2 Description of Support Units ............................................................................................................ 5 4.3 Power level setting using in test ....................................................................................................... 5 4.4 Measurement Uncertainty ................................................................................................................ 6 4.5 Test Location .................................................................................................................................... 7 4.6 Test Facility ...................................................................................................................................... 7 4.7 Deviation from Standards ................................................................................................................. 7 4.8 Abnormalities from Standard Conditions .......................................................................................... 7 5 Equipment List ........................................................................................................................................ 8 6 Radio Spectrum Technical Requirement .............................................................................................. 9 6.1 Antenna Requirement ...................................................................................................................... 9 7 Radio Spectrum Matter Test Results .................................................................................................. 10 7.1 Maximum Conducted Output Power .............................................................................................. 10 7.2 Minimum 6dB Bandwidth................................................................................................................ 12 7.3 Power Spectral Density .................................................................................................................. 13 7.4 Conducted Band Edges Measurement .......................................................................................... 14 7.5 Conducted Spurious Emissions ..................................................................................................... 15 7.6 Radiated Emissions which fall in the restricted bands ................................................................... 16 7.7 Radiated Spurious Emissions Below 1GHz ................................................................................... 34 7.8 Radiated Spurious Emissions Above 1GHz ................................................................................... 39 8 Test Setup Photo .…

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

Compliance Certification Services (Kunshan) Inc. Page: 1 of 3 Appendix Photographs of Test Setup for KSCR2606001294HS Test Model No.: MCM-7 Compliance Certification Services (Kunshan) Inc. Page: 2 of 3 Test Setup Photo RF Conducted Radiated Spurious Emissions Below 1GHz Compliance Certification Services (Kunshan) Inc. Page: 3 of 3 Radiated Spurious Emissions Above 1GHz - End of the Appendix -