2BMCJGMIX-TRI-03Geri Mixer

i Geri Mixer GMIX-TRI-03 User Manual Genea Biomedx Pty Ltd ii GENERAL INFORMATION Copyright This user manual and all contents contained herein are subject to copyright. All rights reserved. No part of this user manual may be reproduced, copied, translated or transmitted in any form or by any means without the prior written approval of Genea Biomedx. Technical Support Manufacturer If any serious incident has occurred in relation to this device, it should be reported directly to the manufacturer and the competent authority of the Member State in which the user and/or patient is established. Genea Biomedx Pty Ltd Level 2, 321 Kent Street Sydney, New South Wales, 2000, Australia Country of origin: China Email: [email protected] Web: www.geneabiomedx.com iii List of accessories No. Content GMIX-TRI-03 1 Main Device 1 2 Power Cord 1 3 Gas Connecting Pipe 1 4 Fuse 2 5 Gas Pipe Connector 1 6 Supporting Documents 1 In case of any missing accessories, please promptly contact your local Genea Biomedx representative. This product does not contain any parts that are prone to wear and tear or loss. The accessories require replacement only in the event of damage. *Note: In some cases, the “User Manual” can be obtained digitally as an eIFU; please contact your local Genea Biomedx representative to get the latest version of the User Manual. Copyright description This manual contains proprietary information protected by copyright law. All rights reserved. Reproduction, photography, or translation of any part of the Manual into other languages is prohibited without the express written consent of the manufacturer. See the nameplate for the date of manufacture for the device. iv Table of contents 1. Safety &Precautions ................................................................................................... 1 1.1 Important Notice ................................................................................................ 1 1.2 Safety Tips ........................................................................................................... 1 1.2.1 General Security .................................................................................... 1 1.2.2 Electrical safety ..................................................................................... 2 1.2.3 Accessory safety .................................................................................... 2 1.3 Definition of icons, symbols and abbreviations ................................................ 2 2. Instrument Overview ................................................................................................. 4 2.1 Intended Use ...................................................................................................... 4 2.2 Working Principle ............................................................................................... 4 2.3 System composition ........................................................................................... 4 3. Instrument Installation ............................................................................................... 7 3.1 Normal operating conditions ............................................................................. 7 3.2 Check the instrument ......................................................................................... 8 3.2.1 Access Rights......................................................................................... 8 3.3 Prepare the power supply .................................................................................. 9 3.4 Instrument Installation ....................................................................................... 9 4. Instrument Operation .............................................................................................. 10 4.1 Equipment Installation ..................................................................................... 10 4.2 Power on and off .............................................................................................. 10 4.3 Start and stop ................................................................................................... 10 4.4 Operation mode switching ............................................................................... 10 4.5 Mute Alarm ....................................................................................................... 11 5. Maintenance and care ............................................................................................. 11 5.1 Main device maintenance ................................................................................ 11 5.2 Power supply maintenance .............................................................................. 11 5.3 Software Maintenance ..................................................................................... 11 5.4 Transportation and storage .............................................................................. 12 6. Warnings & Faults: Troubleshooting ........................................................................ 12 1 1. Safety &Precautions This chapter introduces the precautions for using the instrument. Before using, please read and understand the contents carefully to ensure correct use and operator safety. 1.1 Important Notice In this manual, some words are preceded by the following symbols for warnings and special reminders. The specific usage is as follows: Item Description Warning Prompts the operator to follow the instructions, otherwise personal injury may result. Caution The operator is reminded to follow the instructions, otherwise the instrument may malfunction or be damaged. 1.2 Safety Tips 1.2.1 General Security Warning  Do not perform any operation on the instrument before reading the user manual to avoid damage to the instrument or personal injury.  This instrument must be operated by trained doctors or laboratory technicians.  Do not place the instrument in a humid place or near water to …

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AOGES CO., LIMITED 2.911 (d)(7)USA Agent v1.5 Section 2.911(d)(7) USA Agent for Service of Process Company Name: Suzhou Basecare Medical Device Co., Ltd. Address: 77 Jingu Road, Industrial Park, Suzhou, Jiangsu Province, China 215000 Product Name: Geri Mixer FCC ID: 2BMCJGMIX-TRI-03 Model(s): GMIX-TRI-03 FRN: 0036309508 2.911(d)(7) USA Designated Agent for Service of Process We, [Suzhou Basecare Medical Device Co., Ltd.] (“the applicant”) designate [AOGES CO., LIMITED] NOTE1 for the purpose of accepting service of process on behalf of the applicant. Applicant consent: We acknowledge our consent to accept service of process in the United States for matters related to the applicable equipment, and at the physical U.S. address and email address of the designated agent and acknowledge our acceptance of our obligation to maintain an agent for service of process in the United States for no less than one year after either we the grantee have permanently terminated all marketing and importation of the applicable equipment within the U.S., or at the conclusion of any Commission-related administrative or judicial proceeding involving the equipment, whichever is later. Agent obligation: We acknowledge our obligation to accept service of process in the United States for matters related to the applicable equipment at our physical U.S. address and email address 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 at the conclusion of any Commission-related administrative or judicial proceeding involving the equipment, whichever is later. USA Agent Company name: AOGES CO., LIMITED USA Address: 1624 Market St, Ste 226, #30327 Denver CO, 80202 USA FRN Number：0033947847 Contact Name: XIAOYAN LAl Telephone No: +1 303 623 1940 Email: [email protected] Applicant Company name: Suzhou Basecare Medical Device Co., Ltd. Address: 77 Jingu Road, Industrial Park, Suzhou, Jiangsu Province, China 215000 Grantee FRN Number：0036309508 FCC Grantee Code: 2BMCJ Contact Name: Liuhao Telephone No: 18550818299 AOGES CO., LIMITED 2.911 (d)(7)USA Agent v1.5 Email: [email protected] Signature: Title: CEO Signature: Title: CEO Date: 2026.03.13 Date: 2026.03.13 NOTE 1: An applicant located in the United States may designate itself as the agent for service of process. Reference; Federal Register document 2022-28263 published on 02/06/23 https://www.federalregister.gov/documents/2023/02/06/2022-28263/protecting-against-nation al-security-threats-to-the-communications-supply-chain-through-the

Suzhou Basecare Medical Device Co., Ltd. 2.911 (d)(5)(i) Equipment Type Attestation v1.2 Section 2.911(d)(5)(i) Certification – Equipment Type Company Name: Suzhou Basecare Medical Device Co., Ltd. Address: 77 Jingu Road, Industrial Park, Suzhou, Jiangsu Province, China 215000 Product Name: Geri Mixer FCC ID: 2BMCJGMIX-TRI-03 Model(s): GMIX-TRI-03 FRN: 0036309508 2.911(d)(5)(i) Equipment Type We, [Suzhou Basecare Medical Device Co., Ltd.] (“the applicant”) certify that the equipment for which authorization is sought through certification is not:  Prohibited from receiving an equipment authorization pursuant to § 2.903; of the FCC rules.  Identified as an equipment type in the “Covered List” NOTE 1 Yours sincerely, Name: Liuhao Date: 2026.03.13 Title and Company name: Manager / Suzhou Basecare Medical Device Co., Ltd. NOTE 1 “Covered List”; is the List of Equipment and Services Covered By Section 2 of The Secure Networks Act, available at https://www.fcc.gov/supplychain/coveredlist References; 1) 986446 D01 Covered Equipment v01 https://apps.fcc.gov/oetcf/kdb/forms/FTSSearchResultPage.cfm?switch=P&id=325672 2) Federal Register document 2022-28263 published on 02/06/23 https://www.federalregister.gov/documents/2023/02/06/2022-28263/protecting-against-national-security-threats-to-the-com munications-supply-chain-through-the

Suzhou Basecare Medical Device Co., Ltd. 2.911 (d)(5)(ii) Applicant Attestation v1.3 Section 2.911(d)(5)(ii) Certification – Applicant (Covered List ) Company Name: Suzhou Basecare Medical Device Co., Ltd. Address: 77 Jingu Road, Industrial Park, Suzhou, Jiangsu Province, China 215000 Product Name: Geri Mixer FCC ID: 2BMCJGMIX-TRI-03 Model(s): GMIX-TRI-03 FRN: 0036309508 2.911(d)(5)(ii) Applicant filing We, [Suzhou Basecare Medical Device Co., Ltd.] (“the applicant”) certify that, as of the date of the filing of the application, the applicant is is not identified NOTE 1 on the “Covered List” NOTE 2 , established pursuant to § 1.50002 of this chapter, as an entity producing covered communications equipment. Yours sincerely, Name: Liuhao Date: 2026.03.13 Title and Company name: Manager / Suzhou Basecare Medical Device Co., Ltd. NOTE 1 Delete option not applicable to this application. NOTE 2 “Covered List”; is the List of Equipment and Services Covered By Section 2 of The Secure Networks Act, available at https://www.fcc.gov/supplychain/coveredlist References; 1) 986446 D01 Covered Equipment v01 https://apps.fcc.gov/oetcf/kdb/forms/FTSSearchResultPage.cfm?switch=P&id=325672 2) Federal Register document 2022-28263 published on 02/06/23 https://www.federalregister.gov/documents/2023/02/06/2022-28263/protecting-against-national-security-threats-to-the-com munications-supply-chain-through-the

Suzhou Basecare Medical Device Co., Ltd. Office of Engineering Technology Federal Communications Commission 7435 Oakland Mills Road Columbia, MD 21046 USA Date: 2026.03.13 Subject; Request for Confidentiality FCC ID: 2BMCJGMIX-TRI-03 To Whom It May Concern, Pursuant to the provisions of the Commission’s rules Title 47 Sections §0.457 and §0.459, we are requesting the Commission to withhold the following attachment(s) as confidential documents from public disclosure indefinitely. These documents contain detailed system and equipment descriptions and are considered as proprietary information in operation of the equipment. The public disclosure of these documents might be harmful to our company and would give competitors an unfair advantage in the market. Schematic Diagram Block Diagram Operational Description Tune-up Procedure SOFTWARE SECURITY REQUIREMENTS FOR U-NII DEVICES In additional to above mentioned documents, in order to comply with the marketing regulations in Title 47 CFR §2.803 and the importation rules in Title 47 CFR §2.1204, while ensuring that business sensitive information remains confidential until the actual marketing of newly authorized devices, we request Short Term Confidentiality of the following attachment(s); External Photos Test Setup Photos Internal Photos User Manual For 45 days, pursuant to Public Notice DA 04-1705. OR For 180 days pursuant to KDB 726920 D01. It is our understanding that all measurement test reports, FCC ID label format and correspondence during the certification review process cannot be granted as confidential documents and this information will be available for public review once the grant of equipment authorization is issued. Sincerely, Signature: Name: Jiankuai Li Title: PM

2025.12.05 Federal Communications Commission Authorization & Evaluation Division 7345 Oakland Mills Road Columbia, Maryland 21046 RE: LETTER OF AGENT AUTHORIZATION To Whom It May Concern: We, the undersigned, hereby authorize SHENZHEN STS TEST SERVICES CO.,LTD./ A 1/F, Building B, Zhuoke Science Park, No.190 Chongqing Road, HepingShequ, Fuyong Sub-District,Bao’an District, Shenzhen, Guang Dong, China/Jiankuai Li(Name of Agent company name and address, Name of Agent) to act on our behalf in all matters relating to application for equipment authorization, including the signing of all documents relating to these matters. This appointment is valid until further December 31, 2026. Name: Jiankuai Li Title: PM E-mail:[email protected] Name: Liuhao Title: Manager E-mail: [email protected] Company: Suzhou Basecare Medical Device Co., Ltd. Signature:

Suzhou Basecare Medical Device Co., Ltd. Letter of Authorization Company Name: Suzhou Basecare Medical Device Co., Ltd. Address: 77 Jingu Road, Industrial Park, Suzhou, Jiangsu Province, China 215000 Product Name: Geri Mixer FCC ID: 2BMCJGMIX-TRI-03 Model(s): GMIX-TRI-03 FRN: 0036309508 We authorize MiCOM Labs Inc., 575 Boulder Court, Pleasanton, California 94566, USA, to act on our behalf on all matters concerning the certification of above named equipment. We declare that MiCOM Labs Inc. is allowed to forward all information related to the approval and certification of equipment to the regulatory agencies as required and to discuss any issues concerning the approval application. Any and all acts carried out by MiCOM Labs on our behalf shall have the same effect as acts of our own. Signature: Date: 2026.03.13 Name: Jiankuai Li Title: PM Company: Shenzhen STS Test Services Co., Ltd.

Page 1 of 5 Report No.: STS2510145 APPENDIX-PHOTOGRAPHS OF EUT CONSTRUCTIONAL DETAILS Model: GMIX-TRI-03 Photo 1 Photo 2 WIFI Antenna Page 2 of 5 Report No.: STS2510145 Photo 3 Photo 4 Page 3 of 5 Report No.: STS2510145 Photo 5 Photo 6 Page 4 of 5 Report No.: STS2510145 Photo 7 Photo 8 Page 5 of 5 Report No.: STS2510145 Photo 9

Label 4*6cm

Page 1 of 10 Report No.: STS2510145 APPENDIX-PHOTOGRAPHS OF EUT CONSTRUCTIONAL DETAILS Model: GMIX-TRI-03 Photo 1 Photo 2 Page 2 of 10 Report No.: STS2510145 Photo 3 Photo 4 Page 3 of 10 Report No.: STS2510145 Photo 5 Photo 6 Page 4 of 10 Report No.: STS2510145 Photo 7 Photo 8 Page 5 of 10 Report No.: STS2510145 Photo 9 Photo 10 Page 6 of 10 Report No.: STS2510145 Photo 11 Photo 12 Page 7 of 10 Report No.: STS2510145 Photo 13 Photo 14 Page 8 of 10 Report No.: STS2510145 Photo 15 Photo 16 Page 9 of 10 Report No.: STS2510145 Photo 17 Photo 18 Page 10 of 10 Report No.: STS2510145 Photo 19 Photo 20

The test results presented in this report relate only to the object tested. This report shall not be reproduced, except in full, without the written approval of the Shenzhen STS Test Services Co., Ltd. MPE Report Report No.:STS2510145H01 Issued for Suzhou Basecare Medical Device Co., Ltd. 77 Jingu Road, Industrial Park, Suzhou, Jiangsu Province, China 215000 Product Name: Geri Mixer Brand Name: N/A Model Name: GMIX-TRI-03 Series Model(s): N/A FCC ID: 2BMCJGMIX-TRI-03 Test Standards: FCC 47CFR §2.1091 Page 2 of 10 Report No.: STS2510145H01 TEST REPORT Applicant’s Name ................. : Suzhou Basecare Medical Device Co., Ltd. Address ................................. : 77 Jingu Road, Industrial Park, Suzhou, Jiangsu Province, China 215000 Manufacturer's Name ........... : Suzhou Basecare Medical Device Co., Ltd. Address ................................. : 77 Jingu Road, Industrial Park, Suzhou, Jiangsu Province, China 215000 Product Description Product Name ........................ : Geri Mixer Brand ................................... : N/A Model Number ....................... : .. : GMIX-TRI-03 Series Model(s) ...................... : N/A Standards ............................. : FCC 47CFR §2.1091 447498 D04 Interim General RF Exposure Guidance v01 The test results presented in this report relate only to the object tested. This report shall not be reproduced, except in full, without the written approval of the Shenzhen STS Test Services Co., Ltd. Date of Test ........................................... : Date of receipt of test item ...................... : 23 Oct.. 2025 Date (s) of performance of tests ............. : 23 Oct.. 2025~04 Dec. 2025 Date of Issue .......................................... : 04 Dec. 2025 Test Result .............................................. : Pass Testing Engineer : (Aaron Bu) Technical Manager : (Skylar Li) Authorized Signatory : (Bovey Yang) Page 3 of 10 Report No.: STS2510145H01 TABLE OF CONTENTS 1. GENERAL INFORMATION 5 1.1 GENERAL DESCRIPTION OF THE EUT 5 1.2 TEST FACTORY 6 2. FCC 47CFR §2.1091 REQUIREMENT 7 2.1 TEST STANDARDS 7 2.2 LIMIT 7 2.3 TEST RESULT 10 Page 4 of 10 Report No.: STS2510145H01 Revision History Rev. Issue Date Report No. Effect Page Contents 00 04 Dec. 2025 STS2510145H01 ALL Initial Issue Page 5 of 10 Report No.: STS2510145H01 1. GENERAL INFORMATION 1.1 GENERAL DESCRIPTION OF THE EUT Product Name Geri Mixer Brand N/A Model Name GMIX-TRI-03 Series Model(s) N/A Model Difference N/A Product Description The EUT is Geri Mixer Operation Frequency: 2.4G WLAN: 802.11b/g/n 20: 2412~2462 MHz 5.2G WLAN: IEEE 802.11a/ n(HT20): 5.180GHz-5.240GHz IEEE 802.11n(HT40): 5.190GHz-5.230GHz 5.8 WLAN: IEEE 802.11a/ n(HT20):5.745GHz-5.825GHz IEEE 802.11a/ n(HT40):5.755GHz-5.795GHz Modulation Type: 2.4G WLAN: 802.11b(DSSS):CCK,DQPSK,DBPSK 802.11g(OFDM):BPSK,QPSK,16-QAM,64-QAM 802.11n(OFDM):BPSK,QPSK,16-QAM,64-QAM 5G WLAN: 802.11a(OFDM): BPSK,QPSK,16-QAM,64-QAM 802.11n(OFDM): BPSK,QPSK,16-QAM,64-QAM Antenna gain: 2.4G WLAN:2.88dBi 5.2G WLAN:3 dBi 5.8 WLAN:2.84 dBi Antenna Designation: external Antenna Power Rating Input: 100V-240V~,50/60Hz Adapter N/A Battery N/A Hardware Version N/A Software Version N/A Page 6 of 10 Report No.: STS2510145H01 1.2 TEST FACTORY SHENZHEN STS TEST SERVICES CO., LTD Add. : 101, Building B, Zhuoke Science Park, No.190 Chongqing Road, ZhanChengShequ, Fuhai Sub-District, Bao’an District, Shenzhen, Guang Dong, China FCC test Firm Registration Number: 625569 IC test Firm Registration Number: 12108A A2LA Certificate No.: 4338.01 Page 7 of 10 Report No.: STS2510145H01 2. FCC 47CFR §2.1091 REQUIREMENT 2.1 TEST STANDARDS Follow the maximum permissible exposure (MPE) limits specified in 447498 D04 Interim General Radio Frequency Exposure Guidelines v01. The gain of the antenna used in the product was extracted from the supplied antenna data sheet and the maximum total power input to the antenna was also measured. Calculate the distance from the product to the MPE limit by the formula. 2.2 LIMIT For single RF sources (i.e., any single fixed RF source, mobile device, or portable device, as defined in paragraph (b)(2) of this section): A single RF source is exempt if: (A) The available maximum time-averaged power is no more than 1 mW, regardless of separation distance. This exemption may not be used in conjunction with other exemption criteria other than those in paragraph (b)(3)(ii)(A) of Part 1.1307. Medical implant devices may only use this exemption and that in paragraph (b)(3)(ii)(A); (B) Or the available maximum time-averaged power or effective radiated power (ERP), whichever is greater, is less than or equal to the threshold Pth (mW) described in the following formula. This method shall only be used at separation distances (cm) from 0.5 centimeters to 40 centimeters and at frequencies from 0.3 GHz to 6 GHz (inclusive). Pth is given by: Page 8 of 10 Report No.: STS2510145H01 (C) Or using below table and the minimum separation distance (R in meters) from the body of a nearby person for the frequency (f in MHz) at which the source operates, the ERP (watts) is no more than the calculated value prescribed for that frequency. For the exemption in Table 1 to apply, R must be at least λ/2π, where λ is the free-space operating wavelength in meters. If the ERP of a single RF source is not easily obtained, then the available maximum time-averaged power may be used in lieu of ERP if the physical dimensions of the radiating structure(s) do not exceed the electrical length of λ/4 or if the antenna gain is less than that of a half-wave dipole (1.64 linear value). RF Source frequency (MHz) Threshold ERP(watts) 0.3-1.34 1,920 R 2 . 1.34-30 3,450 R 2 /f 2 . 30-300 3.83 R 2 . 300-1,500 0.0128 R 2 f. 1,500-100,000 19.2R 2 . Page 9 of 10 Report No.: STS2510145H01 For multiple RF sources: Multiple RF sources are exempt if: (A) The available maximum time-averaged power of each source is no more than 1 mW and there is a separation distance of two centi…

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Page 1 of 81 Report No.:STS2510145W01 The test results presented in this report relate only to the object tested. This report shall not be reproduced, except in full, without the written approval of the Shenzhen STS Test Services Co., Ltd. Radio Test Report Report No.:TS2510145W01 Issued for Suzhou Basecare Medical Device Co., Ltd. 77 Jingu Road, Industrial Park, Suzhou, Jiangsu Province, China 215000 Product Name: Geri Mixer Brand Name: N/A Model Name: GMIX-TRI-03 Series Model(s): N/A FCC ID: 2BMCJGMIX-TRI-03 Test Standards: FCC Part15.247 Page 2 of 81 Report No.:STS2510145W01 TEST REPORT Applicant’s Name ................. : Suzhou Basecare Medical Device Co., Ltd. Address ................................. : 77 Jingu Road, Industrial Park, Suzhou, Jiangsu Province, China 215000 Manufacturer's Name ........... : Suzhou Basecare Medical Device Co., Ltd. Address ................................. : 77 Jingu Road, Industrial Park, Suzhou, Jiangsu Province, China 215000 Product Description Product Name ........................ : Geri Mixer Brand Name ........................... : N/A Model Name .......................... : GMIX-TRI-03 Series Model(s) .................... : N/A Standards ............................. : FCC Part 15.247 Test Procedure........................: ANSI C63.10-2020 This device described above has been tested by STS, the test results show that the equipment under test (EUT) is in compliance with the FCC requirements. And it is applicable only to the tested sample identified in the report. The test results presented in this report relate only to the object tested. This report shall not be reproduced, except in full, without the written approval of the Shenzhen STS Test Services Co., Ltd. Date of Test ........................................... : Date of receipt of test item ...................... : 23 Oct. 2025 Date (s) of performance of tests ............. : 23 Oct. 2025~04 Dec. 2025 Date of Issue .......................................... : 04 Dec. 2025 Test Result .............................................. : Pass Testing Engineer : (Aaron Bu) Technical Manager : (Skylar Li) Authorized Signatory : (Bovey Yang) Page 3 of 81 Report No.:STS2510145W01 Table of Contents Page 1. SUMMARY OF TEST RESULTS 6 1.1 TEST FACTORY 7 1.2 MEASUREMENT UNCERTAINTY 7 2. GENERAL INFORMATION 8 2.1 GENERAL DESCRIPTION OF THE EUT 8 2.2 DESCRIPTION OF THE TEST MODES 10 2.3 TEST SOFTWARE AND POWER LEVEL 10 2.4 BLOCK DIAGRAM SHOWING THE CONFIGURATION OF SYSTEM TESTED 11 RF CONDUCTED TEST 11 2.5 DESCRIPTION OF NECESSARY ACCESSORIES AND SUPPORT UNITS 12 2.6 EQUIPMENTS LIST FOR ALL TEST ITEMS 13 3. EMC EMISSION TEST 14 3.1 CONDUCTED EMISSION MEASUREMENT 14 3.2 RADIATED EMISSION MEASUREMENT 18 4. CONDUCTED SPURIOUS & BAND EDGE EMISSION 40 4.1 LIMIT 40 4.2 TEST PROCEDURE 40 4.3 DEVIATION FROM STANDARD 40 4.4 TEST SETUP 40 4.5 EUT OPERATION CONDITIONS 40 4.6 TEST RESULTS 40 5. POWER SPECTRAL DENSITY TEST 41 5.1 LIMIT 41 5.2 TEST PROCEDURE 41 5.3 DEVIATION FROM STANDARD 41 5.4 TEST SETUP 41 5.5 EUT OPERATION CONDITIONS 41 5.6 TEST RESULTS 41 6. BANDWIDTH TEST 42 6.1 LIMIT 42 6.2 TEST PROCEDURE 42 6.3 DEVIATION FROM STANDARD 42 6.4 TEST SETUP 42 Page 4 of 81 Report No.:STS2510145W01 Table of Contents Page 6.5 EUT OPERATION CONDITIONS 42 6.6 TEST RESULTS 42 7. PEAK OUTPUT POWER TEST 43 7.1 LIMIT 43 7.2 TEST PROCEDURE 43 7.3 DEVIATION FROM STANDARD 43 7.4 TEST SETUP 43 7.5 EUT OPERATION CONDITIONS 43 7.6 TEST RESULTS 43 8. ANTENNA REQUIREMENT 44 8.1 STANDARD REQUIREMENT 44 8.2 EUT ANTENNA 44 APPENDIX 1-TEST DATA 45 DUTY CYCLE 45 MAXIMUM PEAK CONDUCTED OUTPUT POWER 51 -6DB BANDWIDTH 52 MAXIMUM POWER SPECTRAL DENSITY LEVEL 58 BAND EDGE 64 CONDUCTED RF SPURIOUS EMISSION 71 APPENDIX 2-PHOTOS OF TEST SETUP 81 Page 5 of 81 Report No.:STS2510145W01 Revision History Rev. Issue Date Report No. Effect Page Contents 00 04 Dec. 2025 STS2510145W01 ALL Initial Issue Page 6 of 81 Report No.:STS2510145W01 1. SUMMARY OF TEST RESULTS Test procedures according to the technical standards: KDB 558074 D01 15.247 Meas Guidance v05r02. FCC Part 15.247,Subpart C Standard Section Test Item Judgment Remark 15.207 Conducted Emission PASS -- 15.247 (a)(2) 6dB Bandwidth PASS -- 15.247 (b)(3) Output Power PASS -- 15.209 Radiated Spurious Emission PASS -- 15.247 (d) Conducted Spurious & Band Edge Emission PASS -- 15.247 (e) Power Spectral Density PASS -- 15.205 Restricted Band Edge Emission PASS -- Part 15.247(d)/ part 15.209(a) Band Edge Emission PASS -- 15.203 Antenna Requirement PASS -- NOTE: (1) ‘N/A’ denotes test is not applicable in this Test Report. (2) All tests are according to ANSI C63.10-2020. Page 7 of 81 Report No.:STS2510145W01 1.1 TEST FACTORY SHENZHEN STS TEST SERVICES CO., LTD Add. : 101, Building B, Zhuoke Science Park, No.190 Chongqing Road, ZhanChengShequ, Fuhai Sub-District, Bao’an District, Shenzhen, Guang Dong, China FCC test Firm Registration Number: 625569 IC test Firm Registration Number: 12108A A2LA Certificate No.: 4338.01 1.2 MEASUREMENT UNCERTAINTY The reported uncertainty of measurement y ±U, where expended uncertainty U is based on a standard uncertainty multiplied by a coverage factor of k=2, providing a level of confidence of approximately 95 %. No. Item Uncertainty 1 RF output power, conducted ±0.751dB 2 Unwanted Emissions, conducted ±2.888dB 3 All emissions, radiated 9K-30MHz ±2.48dB 4 All emissions, radiated 30M-1GHz ±2.52dB 5 All emissions, radiated 1G-18GHz ±3.48dB 6 All emissions, radiated>18GHz ±4.18dB 7 Conducted Emission (9KHz-150KHz) ±2.48dB 8 Conducted Emission (150KHz-30MHz) ±2.52dB 9 Occupied Channel Bandwidth ±3.6% 10 Power Spectral Density, conducted ±1.214dB 11 Duty Cycle ±3.2% Page 8 of 81 Report No.:STS2510145W01 2. GENERAL INFORMATION 2.1 GENERAL DESCRIPTION OF THE EUT Product Name Geri Mixer Brand Name N/A Model Name GMIX-TRI-03 Series Model(s) N/A Model Difference N/A Product Description The EUT is a Geri Mixer Operation Frequency: 802.11b/g/n 20: 2412~2462 MHz Modulation Type: …

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深圳市英佳创电子科技有限公司 http://www.szsyjc.com 电话：0755-27810060传真：0755-27810057网址：http://www.szsyjc.com CUSTOMERNAME 客户名称 CUSTOMERP/N 客户料号 PDANBZ01000037 PARTNAME 品名 P/N 料号 YJC-60201-W27 APPROVALREV. 版次 A2 DELIVERYDATE 送样日期 2024年12月11日 PREPAREDBY 承办 殷飞杰 CHECKEDBY 审核 方文锋 APPROVEDBY 核准 肖汉 CustomerApproved 客户承认 PreparedBy 承办 CheckedBy 审核 ApprovedBy 核准 2.4G/5G WIFI Antenna Suzhou Basecare Medical Device Co., Ltd. 深圳市英佳创电子科技有限公司 http://www.szsyjc.com 目录 1、封面。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。1 2、目录。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。2 3、履历表。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。。3 4、天线平面图。。。。。。。。。。。。。。。。。。。。。。。。。。。。。4 5、天线技术参数及环境性能测试。。。。。。。。。。。。。。。。。。。。。5 6、天线实物图。。。。。。。。。。。。。。。。。。。。。。。。。。。。。6 7、天线性能测试图。。。。。。。。。。。。。。。。。。。。。。。。。。。6 8、2D、3D(2.4G/5G)测试数据。。。。。。。。。。。。。。。。。。。。6-8 9、ROHS物料控制报告。。。。。。。。。。。。。。。。。。。。。。。。。9 深圳市英佳创电子科技有限公司 http://www.szsyjc.com 履历表： 版本变更内容及更改原因日期发行 A0 初版发行 2024 年 07 月 04 日 A1 增加包装方式 2024 年 09 月 11 日 A2 下固增加镭雕 Dual 丝印 2024 年 12 月 11 日 深圳市英佳创电子科技有限公司 http://www.szsyjc.com 天线平面图： 深圳市英佳创电子科技有限公司 http://www.szsyjc.com 天线技术参数及环境测试： 电气技术参数 电性能指标ElectricalSpecifications 频率范围2400-2500/5150-5850MHzFrequencyRange2400-2500/5150-5850MHz 电压驻波比＜2.5VSWR＜2.5 输入阻抗50ΩInputImpedance50Ω 方向全向DirectionAll 增益3.0±1dBiGain3.0±1dBi 机械指标MechanicalSpecifications 天线颜色白色AntennaColorWhite 接口形式SMAInputconnectorSMA 天线长度 108.00mm Cablelength 108.00mm 工作温度-30°C~+70°C Working Temperature -30°C~+70°C 工作湿度20%~80% Working Humidity 20%~80% 环境性能测试: 项目测试条件规格 储存环境 在没有指定的情况下测试温度、湿度、气压如下： 1.温度为-30°C～+70°C 2.相对湿度为45%-85% 3.气压为86kpa-106kpa 电气机械性能正常 高低温试验 在70°C与-30°C之间进行5次循环，然后在正常条件下 1-2H，检查外观质量。 尺寸应满足规定并应满足于机 械、电气性能 耐恒定 湿热试验 相对湿度95±3%，试验温度：40°C.持续2H作用后， 试品取出后5min之内测定电气性能，试品在正常条 件下1-2H，检查外观质量 尺寸应满足规定并应满足于机 械、电气性能 振动试验 振频范围10-55HZ，位移幅值：0.35MM，加速度幅值： 50.0M/S，扫频循环次数：30次 电气机械性能正常 跌落试验1M高空按照互相垂直的轴方向自由跌落3次电气机械性能正常 深圳市英佳创电子科技有限公司 http://www.szsyjc.com 天线实物图：天线性能测试图： 2D、3D测试数据(2.4G/5G)： FrequencyEfficiency(%)Gain.(dBi) 2400MHz 52.392.29 2410MHz 53.712.13 2420MHz 52.282.24 2430MHz 52.952.19 2440MHz 52.282.22 2450MHz 55.802.65 2460MHz 52.612.35 2470MHz 52.172.82 2480MHz 51.802.88 2490MHz 64.912.59 2500MHz 63.432.88 5150MHz 64.572.94 5250MHz 64.713.00 5350MHz 59.982.77 5450MHz 64.273.14 5550MHz 64.713.01 5650MHz 63.833.20 5750MHz 61…

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