2BGGE-MR8000Massage Chair

Category: machinery and appliances general designation: household electric massage chair Purpose of use, effect-efficacy Substitution of massage for home-use •Thank you very much for purchasing Fujiiryoki massage chair. • Carefully read this operation manual before use and only use as directed. • Please read the safety precautions on pages 2-8 before use. • Keep this operation manual where it will be readily available for future referral. • Please recycle the outer packaging material where possible. Objectif de l'utilisation, effet-efficacité Substitution au massage pour un usage privé • Nousvousremercions d'avoir acheté lefauteuil de massage Fujiiryoki. •Veuillez lireattentivement ce manuel d'utilisationavanttoute utilisationetrespectez impérativement lesconsignes. •Veuillez lire les précautions de sécurité figurant dans les pages 26 à 32avanttoute utilisation. • Conservez ce manuel d'utilisation à portée de main. •Veuillezrecycler le matériel d'emballageextérieur dans la mesure du possible. home use Destiné à un usage privé MR6000 Massage Chair : Fauteuil de Massage : Manuel de l'utilisateur User manual Catégorie: machineset appareils. Désignationgénérale:fauteuil de massage électrique à usage personnel MR8000 • Read these "Important Safety Instructions" before use and use this product properly •These important safety instructions are prescribed to ensure correct usage of the product, and to prevent injury and damage to the user and other persons. • Followings are the display and contents. • Please keep to the regulations as these are important instructions for your safety. Prohibited actions The prohibited action is illustrated inside the illustration •Always keep this operation manual where it will be readily available for referral. •Attention: When disposing of this product and/or its accessories, do so in accordance with local laws and regulations. For details, please refer to your local authority. •elderly, ailing person, those who cannot operate by themselves •persons who took medicine that cause drowsiness(sleeping pills, cold medicine) •persons with heavy drinking, heavy tiredness •persons with hematogenous disorder (diabetes, etc.) •persons who recieve a note from the doctor •people with weak temperature sense. There is a risk of low temperature burns, dehydration. The following persons must consult a medical physician before using this product. •Persons using a medical electronic device embedded in the body such as a pacemaker susceptible to the electromagnetic disturbances. •persons with malignant tumors. •persons with heart diseases. •persons who are pregnancy or those immediately after childbirth. •persons who suffer from paresthesia related to peripheral circulatory disturbance due to diabetes etc. •persons with wounds on their skin. •persons in need of repose. •persons withTemperature sensory loss. •persons with body temperatures exceeding 38°C. (when strong acute inflammation symptoms, malaise, hills, blood pressure fluctuations are observed, when debilitated) •persons with herniated discs. •a person with tendovaginitis. •persons who suffer from osteoporosis, spinal column fractures, or acute pains. •persons with abnormalities in the spine, or those whose spines are bent. •persons who feel an abnormality on the body not prescribed above, persons in treatment by a doctor. Directives, actions which are compulsory The prohibited action is illustated inside the illustration Improper usage may result in serious injury of death. Improper usage may result in injury or damage to property.* IMPORTANT SAFETY INSTRUCTIONS TheBecausethisequipmenthasabuilt-inheaterandthesurfacebecomeshot,personwho arenotsensitivetoheatshouldpayattentiontouse. Payfullattentionwhenitfallsunderthefollowing. Useweakstimulationmassagewhenyoustarttouse.Injurymayoccur. Neverusepinsorothermetallicfastenerswiththisappliance. Carefullyexaminethe coveringbeforeeachuse.Discardtheapplianceifthe coveringshows anysignofdeterioration,suchaschecking,blistering,orcracking. IMPORTANT SAFETY INSTRUCTIONS Neveroperatetheappliancewiththeairopeningsblocked. Keeptheairopeningsfreeoflint,hair,andthelike. Neverdroporinsertanyobjectintoanyopening. Todisconnect,turnall controlstotheoffposition,thanremoveplugfromoutlet. Theapplianceisintendedforhouseholduse. DoNotCrush -Avoidsharpfolds. Temperaturessufficientlyhightocauseburnsmayoccuregardlessofthe controlsetting.Do notuseonaninfantorinvalidoronasleepingorunconsciousperson.Donotuseoninsensi- tiveskinoronapersonwithpoorbloodcirculation.Checktheskinin contactwiththeheated areaoftheappliancefrequentlytoreducethe riskofblistering. IMPORTANT SAFETY INSTRUCTIONS Thisapplianceisnotintendedforusebypersons(includingchildren)withreducedphysical, sensoryormentalcapabilities,orlackofexperienceandknowledge,unlesstheyhavebeen givensupervisionorinstruction concerninguseoftheappliancebyapersonresponsiblefor theirsafety. Children should be supervised to ensure that they do not play with the appliance. Thisappliancecanbeusedbychildrenagedfrom8yearsandaboveandpersonswith reducedphysical,sensoryormentalcapabilitiesorlackofexperienceandknowledgeifthey havebeengivensupervisionorinstruction concerninguseoftheapplianceinasafewayand understandthehazardsinvolved. Cleaning and user maintenance shall not be made by children without supervision Please do not listen at high volume. Listening at a high volume for a long time may damage your hearing. IMPORTANT SAFETY INSTRUCTIONS CirC3 AC110-240V 20 min 100W ClassI Made in China MR380 Product name Model name Power supply Rated time Power consumption Safety structure Country of origin 100kg Maximum user weight Product Specifications NOTE: This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and…

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FUJIMEDICALINSTRUMENTSMFG.CO.,LTD. 14F,OeBuilding,1-1-22,NoninbashiChuo-ku,Osakashi,540-0011Japan Date:2024-6-14 FederalCommunicationsCommission AuthorizationandEvaluationDivision 7435OaklandMillsRoad Columbia,MD21046 FCCID:2BGGE-MR8000 FRN:0035434059 USAgent–AttestationStatement/Part2.911(d)(7) FUJIMEDICALINSTRUMENTSMFG.CO.,LTD.,certifies,thatasof2023-11-14,wehavedesignated FCCUSAgent,LLCtoacceptserviceofprocessonourbehalfforFCCID:2BGGE-MR8000. FUJIMEDICALINSTRUMENTSMFG.CO.,LTD.,acceptstomaintainanagentofserviceofprocessinthe UnitedStatesfornolessthanoneyearaftereitherthegranteehaspermanentlyterminatedall marketingandimportationoftheapplicableequipmentwithintheU.S.,ortheconclusionofany Commission-relatedadministrativeorjudicialproceedinginvolvingtheequipment,whicheverislater. FCCUSAgent,LLC,acceptsasofthedateofthefilingofthisapplication,theobligationofbeing thedesignatedagentforthepurposeofacceptingserviceofprocessonbehalfof FUJIMEDICAL INSTRUMENTSMFG.CO.,LTD., forFCCID:2BGGE-MR8000 DesignatedAgentInformation: CompanyName:FCCUSAgent,LLC FRN:0033402884 Address:3722IllinoisAvenue,SaintCharles,IL,60174,USA ContactPerson:TimPayne Phone:708-571-3148 Email:[email protected] Sincerely, Company:FUJIMEDICALINSTRUMENTS MFG.CO.,LTD DesignatedAgent:FCCUSAgent,LLC CompanyRepresentative: DesignatedAgentRepresentative:TimPayne Signature: Signature: YUMURAJUMPEI

FUJIMEDICALINSTRUMENTSMFG.CO.,LTD. 06-14-2024 EurofinsElectricalandElectronicTestingNA,Inc. 914WestPatapscoAvenue Baltimore,MD21230 RE:AttestationStatementsPart2.911(d)(5)(i)requestfor(FCCID:2BGGE-MR8000) [FUJIMEDICALINSTRUMENTSMFG.CO.,LTD.](“theapplicant”)certifiesthatthe equipmentforwhichauthorizationissoughtisnot“covered”equipmentprohibited fromreceivinganequipmentauthorizationpursuanttosection2.903oftheFCCrules. Sincerely, MrYUMURAJUMPEI FUJIMEDICALINSTRUMENTSMFG.CO.,LTD. 06-14-2024 EurofinsElectricalandElectronicTestingNA,Inc. 914WestPatapscoAvenue Baltimore,MD21230 RE:AttestationStatementsPart2.911(d)(5)(ii)requestfor(FCCID:2BGGE-MR8000) [FUJIMEDICALINSTRUMENTSMFG.CO.,LTD.](“theapplicant”)certifiesthat,asofthe dateofthefilingoftheapplication,theapplicantisnotidentifiedontheCoveredListas anentityproducing“covered”equipment. Sincerely, MrYUMURAJUMPEI

FUJIMEDICALINSTRUMENTSMFG.CO.,LTD. AgentAuthorizationLetter 2024.06.14 EurofinsElectricalandElectronicTestingNA,Inc. 914WestPatapscoAvenue Baltimore,MD21230 USA RE:LETTEROFAGENTAUTHORIZATION ToWhomItMayConcern: We,theundersigned,herebyauthorizeShenzhenMostTechnologyServiceCo.,Ltd.toact onourbehalfinallmattersrelatingtoapplicationforequipmentauthorization,includingthe signingofalldocumentsrelatingtothesematters. Wealsoherebycertifythatnopartytotheapplicationauthorizedhereunderissubjecttothe denialofbenefits,includingFCCbenefits,pursuanttoSection5301oftheAnti-DrugAbuse Actof1988,21U.S.C.853(a). Thisagreementexpiresoneyearfromthecurrentdate. Sincerely, Name:MrYUMURAJUMPEI Position:Manager CompanyName:FUJIMEDICALINSTRUMENTSMFG.CO.,LTD. Address:14FOeBuilding1-1-22Noninbashi,Chuo-ku,Osakashi,540-0011 Japan Tel/Fax81647930611 E-Mail:[email protected]

FUJIMEDICALINSTRUMENTSMFG.CO.,LTD. LongTermConfidentialityRequestLetter 2024.06.14 EurofinsElectricalandElectronicTestingNA,Inc. 914WestPatapscoAvenue Baltimore,MD21230 USA RE:CONFIDENTIALITYREQUESTFOR(FCCID:2BGGE-MR8000) ToWhomItMayConcern: Thisletterservesasanofficialrequestforconfidentialityundersections0.457and0.459of CFR47.Wehaverequestedthatthe -e.g.Blockdiagram -e.g.SCH -e.g.OperationalDescription requiredtobesubmittedwiththisapplicationbepermanentlywithheldfrompublicreview. Theabovedocumentsarecompanyproprietaryinformationthatcouldnevergetinto thepossessionofyourcompetition. Pleasecontactmeifthereisanyinformationyoumayneed. Sincerely, Name:MrYUMURAJUMPEI Position:Manager CompanyName:FUJIMEDICALINSTRUMENTSMFG.CO.,LTD. Address:14FOeBuilding1-1-22Noninbashi,Chuo-ku,Osakashi,540-0011 Japan Tel/Fax81647930611 E-Mail:[email protected]

Modeldifferenceletter 2024.06.21 DearEurofinsReviewer, ThisisanewApplicationfromFUJIMEDICALINSTRUMENTSMFG.CO.,LTD. ModelNo.:MR8000,A669S UseMR8000foralltests . sincetheelectricalcircuitdesign,layout, componentsusedandinternalwiringwereidenticalfortheabovemodels,with differencebeingmodelname. Thankyouforyourcooperation! Yourssincerely, Signatory:

Model No.: MR8000 FRONT VIEW OF SAMPLE BACK VIEW OF SAMPLE Model No.: MR8000 LEFT VIEW OF SAMPLE RIGHT VIEW OF SAMPLE Model No.: MR8000 TOP VIEW OF SAMPLE BOTTOM VIEW OF SAMPLE Model No.: MR8000 Model No.: MR8000

MR8000 北米向 FCC認証用 Massage chair Model : MR8000 Rated Input : AC110-120V 60Hz Rated Time : 30min. FCC ID : 2BGGE-MR8000 Contains module : FCC ID : 2AOC9-ZENBDM10A This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.

ModelNo.:MR8000 Page1of9 INTERNALPHOTOOFSAMPLE INTERNALPHOTOOFSAMPLE ModelNo.:MR8000 Page2of9 INTERNALPHOTOOFSAMPLE INTERNALPHOTOOFSAMPLEPCB ModelNo.:MR8000 Page3of9 INTERNALPHOTOOFSAMPLEPCB INTERNALPHOTOOFSAMPLEPCB ModelNo.:MR8000 Page4of9 ModelNo.:MR8000 Page5of9

ModelNo.:MR8000 Page6of9 Antenna ModelNo.:MR8000 Page7of9

ModelNo.:MR8000 Page8of9 Model No.: MR8000 Page 9 of 9

ALPHA's reports is using a digital certificate that is trusted on Adobe's official server. If there is no digital certificate or the digital certificate shows damaged in your report. Please do not accept the report. E-mail: [email protected] Tel: 4008-3008-95 Website: http://www.a-lab.cn FCC TEST REPORT FCC ID: 2BGGE-MR8000 On Behalf of FUJI MEDICAL INSTRUMENTS MFG.CO., LTD. Massage Chair Model No.: MR8000, A669S Prepared for : FUJI MEDICAL INSTRUMENTS MFG.CO., LTD. Address : 14F Oe Building 1-1-22 Noninbashi, Chuo-ku, Osaka shi, 540-0011 Japan Prepared By : Shenzhen Alpha Product Testing Co., Ltd. Address : Building i, No.2, Lixin Road, Fuyong Street, Bao'an District, 518103, Shenzhen, Guangdong, China Report Number : A2405152-C01-R01 Date of Receipt : May 21, 2024 Date of Test : May 21, 2024 – May 23, 2024 Date of Report : May 23, 2024 Version Number : V0 Test Result : Pass Page 2 of 20 Report No.: A2405152-C01-R01 TABLE OF CONTENTS Description Page 1. Test Result Summary ................................................................................................................................ 5 2. EUT Description ......................................................................................................................................... 6 2.1. Description of Device (EUT) ................................................................................................................ 6 2.2. Accessories of Device (EUT) .............................................................................................................. 7 2.3. Tested Supporting System Details ...................................................................................................... 7 2.4. Block Diagram of Connection between EUT and Simulators.............................................................. 7 2.5. Description of Test Modes................................................................................................................... 7 2.6. Test Conditions ................................................................................................................................... 7 2.7. Test Facility ......................................................................................................................................... 8 2.8. Measurement Uncertainty ................................................................................................................... 8 3. Test Results and Measurement Data ....................................................................................................... 9 3.1. RF Exposure Test ............................................................................................................................... 9 3.1.1. Test Specification ....................................................................................................................... 9 3.1.2. Test Instruments ....................................................................................................................... 10 3.1.3. Test data ................................................................................................................................... 10 4. Photos of test setup ................................................................................................................................ 12 5. Photographs of EUT ................................................................................................................................ 20 Page 3 of 20 Report No.: A2405152-C01-R01 TEST REPORT DECLARATION Applicant : FUJI MEDICAL INSTRUMENTS MFG.CO., LTD. Address : 14F Oe Building 1-1-22 Noninbashi, Chuo-ku, Osaka shi, 540-0011 Japan Manufacturer : FUJI MEDICAL INSTRUMENTS MFG.CO., LTD. Address : 14F Oe Building 1-1-22 Noninbashi, Chuo-ku, Osaka shi, 540-0011 Japan EUT Description : Massage Chair (A) Model No. : MR8000, A669S (B) Trademark : N/A Measurement Standard Used: FCC CFR Title 47 Part 15 Subpart C FCC KDB 680106 D01 Wireless Transfer v04 The device described above is tested by Shenzhen Alpha Product Testing Co., Ltd. to determine the maximum emission levels emanating from the device and the severe levels of the device can endure and its performance criterion. The test results are contained in this test report and Shenzhen Alpha Product Testing Co., Ltd. is assumed full responsibility for the accuracy and completeness test. Also, this report shows that the EUT is technically compliant with the KDB 680106 D01 requirements. This report applies to above tested sample only. This report shall not be reproduced in parts without written approval of Shenzhen Alpha Product Testing Co., Ltd. Tested by (name + signature).............: Yannis Wen Project Engineer Approved by (name + signature).......: Reak Yang Project Manager Date of issue...... .......................: May 23, 2024 Page 4 of 20 Report No.: A2405152-C01-R01 Revision History Revision Issue Date Revisions Revised By V0 May 23, 2024 Initial released Issue Yannis Wen Page 5 of 20 Report No.: A2405152-C01-R01 1. Test Result Summary Requirement CFR 47 Section Result RF EXPOSURE §1.1307(b)(1) & KDB680106 PASS Note: 1. PASS: Test item meets the requirement. 2. Fail: Test item does not meet the requirement. 3. N/A: Test case does not apply to the test object. 4. The test result judgment is decided by the limit of test standard. Page 6 of 20 Report No.: A2405152-C01-R01 2. EUT Description 2.1. Description of Device (EUT) EUT Name : Massage Chair Model No. : MR8000, A669S DIFF : There is no difference except the name of the model. All tests are made with the MR8000 model. Trademark : N/A Power supply : AC 110-120V~ EUT information : Wireless Output: 5W, 7.5W, 10W, 15W Operation frequency : 115~148KHz Modulation : ASK Antenna Type : Coil Antenna, Maximum Gain is 0dBi (This value is supplied by applicant). Software version : 1.0~80.0 Hardware version : 1.0~80.0 Connector cable loss : 0.5dB (This value is supplied by applicant). Intend use en…

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ShenzhenMostTechnologyServiceCo.,Ltd. No.5,2ndLangshanRoad,NorthDistrict,Hi-techIndustrialPark,Nanshan, Shenzhen,Guangdong,China. TESTREPORT FCCPART15.209 ReportReferenceNo. ....................... : FCCID.. ............................................... : MTEB24050289-R 2BGGE-MR8000 Compiledby (position+printedname+signature)..:FileadministratorsAlisaLuo Supervisedby (position+printedname+signature)..:TestEngineerSunnyDeng Approvedby (position+printedname+signature) .. : ManagerYvetteZhou Dateofissue ......................................... :May29,2024 RepresentativeLaboratoryName . :ShenzhenMostTechnologyServiceCo.,Ltd. Address.................................................: No.5,2ndLangshanRoad,NorthDistrict,Hi-techIndustrialPark, Nanshan,Shenzhen,Guangdong,China. Applicant’sname...............................:FUJIMEDICALINSTRUMENTSMFG.CO.,LTD. Address ................................................. : 14FOeBuilding1-1-22Noninbashi,Chuo-ku, Osakashi,540-0011Japan Testspecification/Standard............: FCCRulesandRegulationsPart15SubpartC(Section15.209), ANSIC63.10:2013 TRFOriginator ...................................... :ShenzhenMostTechnologyServiceCo.,Ltd. ShenzhenMostTechnologyServiceCo.,Ltd.Allrightsreserved. Thispublicationmaybereproducedinwholeorinpartfornon-commercialpurposesaslongasthe ShenzhenMostTechnologyServiceCo.,Ltd.isacknowledgedascopyrightownerandsourceofthe material.ShenzhenMostTechnologyServiceCo.,Ltd.takesnoresponsibilityforandwillnotassume liabilityfordamagesresultingfromthereader'sinterpretationofthereproducedmaterialduetoits placementandcontext. Testitemdescription ........................ : MassageChair TradeMark ............................................ : N/A Model/Typereference.........................: MR8000 ListedModels ...................................... :A669S ModulationType .................................. : ASK OperationFrequency..........................: 115K-148KHz Rating.....................................................: 110-120V~,60Hz,210W HardwareVersion ............................... : 1.0~80.0 SoftwareVersion...............................: 1.0~80.0 Result.....................................................:PASS ReportNo.:MTEB24050289-RPage 2 of 24 TESTREPORT EquipmentunderTest:MassageChair Model/Type:MR8000 ListedModels:A669S RemarkIt'sjustadifferentmodel.Everythingelseisthesame Applicant: FUJIMEDICALINSTRUMENTSMFG.CO.,LTD. Address: 14FOeBuilding1-1-22Noninbashi,Chuo-ku,Osakashi,540-0011 Japan Manufacturer: FUJIMEDICALINSTRUMENTSMFG.CO.,LTD. Address: 14FOeBuilding1-1-22Noninbashi,Chuo-ku,Osakashi,540-0011 Japan TestResult : PASS Thetestreportmerelycorrespondstothetestsample. Itisnotpermittedtocopyextractsofthesetestresultwithoutthewrittenpermissionofthetest laboratory. ReportNo.:MTEB24050289-RPage 3 of 24 Contents 1.REVISIONHISTORY.........................................................................................................................4 2.TESTSTANDARDS............................................................................................................................5 3.SUMMARY...............................................................................................................................................6 3.1.GeneralRemarks.........................................................................................................................................6 3.2.ProductDescription....................................................................................................................................6 3.3.EquipmentUnderTest................................................................................................................................6 3.4.ShortdescriptionoftheEquipmentunderTest(EUT)............................................................................6 3.5.EUToperationmode....................................................................................................................................6 3.6.BlockDiagramofTestSetup......................................................................................................................7 3.7.TestItem(EquipmentUnderTest)Description*.......................................................................................7 3.8.AuxiliaryEquipment(AE)Description.......................................................................................................7 3.9.AntennaInformation*..................................................................................................................................7 3.10.EUTconfiguration......................................................................................................................................7 3.11.Modifications..............................................................................................................................................7 4.TESTENVIRONMENT.......................................................................................................................8 4.1.Addressofthetestlaboratory...................................................................................................................8 4.2.Environmentalconditions...........................................................................................................................8 4.3.TestDescription...........................................................................................................................................9 4.4.Statementofthemeasurementuncertainty.............................................................................................9 4.5.EquipmentsUsedduringtheTest...........................................................................................................10 5.TESTCONDITIONSANDRESULTS.....................................................................................11 5.1.ACPowerConductedEmission.................................................................................…

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Fine Page 1 of 3 承 認 書 SPECIFICATION FOR APPROVAL 客 戶： CUSTOMER: 豪中豪健康科技有限公司 客 戶 料 號： CUST P/N: 料 號： FINE P/N: MPA2-10UH 单线圈0.08*105P*12TS 産 品 型 號： DESC: MPA2-10UH-HZH 日 期： DATE: 2023/12/15 版 本： Version: A.0 擬制 PREPARED BY 審核 CHECKED BY 批准 APPROVED BY 客戶承認 CUSTOMER APPROVE 黄燕铭 黄燕铭 黄锦华 东莞市西联干城科技有限公司 工廠地址：东莞市东坑镇峻发路123号三甲高新技术产业园2栋8楼 TEL：0769-82989159 FAX：0755-82989159 E-mail：[email protected] Fine Page 2 of 3 版本變更履歷 Version Change History 版本 Rev. 變 更 前 Before Change 變 更 後 After Change 更 改 日 期 Change Date 批 准 Approved By A.0 新发行 ---- 2023/12/15 黄燕铭 Fine Page 3 of 3 SPECIFICATION 産 品 型 號： DESC MPA2-10UH-HZH 版本 Rev：A.0 客戶CUST: XXX 客户料号CUST P/N: 一、尺寸DIMENSION:(mm) 二、原理图SCHEMATIC DIAGRAM: A 49.5±0.5 B 19±1 D 45±2 E 30±2 F 3±2 H 3±0.2 注： 1.交叉出线; 2.出线位置缠9mm(ref)宽度高 温胶纸1-2Ts; 3.线圈贴圆形硬磁片带槽，磁 片尺寸49.5±0.5mm,内孔 5.3mm,厚度为1.0±0.2mm。 4.线圈背面贴2.0MMEVA胶 三、绕线参数Winding Specification: 序号 NO. 端子 TERMINAL 线径 WIRE 圈数 Turns 绕线方向 Winding Direction 1 S F 丝包线0.08*105P 12Ts CCW 四、电气特性ELECTRICAL CHARACTERISTICS: 温度TEMPERATURE:25±10°C, 湿度RELATIVE HUMIDITY:65±20% 序号 NO. 项目 ITEM 端子 TERMINAL 标准 SPECIFICATION 测试条件 TEST FREQUENCY 测试仪器 TEST EQUIPMENTS 1 IND. S-F 3.8uH ±20%单独线圈 100KHz/1.0V LCZ METER 1062B 2 IND. S-F 10uH ±10%加磁片 100KHz/1.0V LCZ METER 1062B 3 DCR S-F ≤55mΩ 100KHz/1.0V LCZ METER 502B 4 Q值 S-F ≤95 100KHz/1.0V LCZ METER 502B 擬制/日期PREPARED BY/DATE 審核/日期CHECKED BY/DATE 黄燕铭2023/12/15 黄锦华2023/12/15

ModelNo.:MR8000 CETESTSETUP RETESTSETUP ModelNo.:MR8000 RETESTSETUP