2A2R4V03DUpper Arm blood pressure monitor

Shenzhen Hingmed Medical Instrument Co., Ltd. Upper Arm Blood Pressure Monitor User manual (Apply to：V03、V03D) Edit：2022-12-20 Version: A/0 Shenzhen Hingmed Medical Instrument Co., Ltd. About this manual The manual mainly introduces the installation and application method of upper arm blood pressure monitor.Users should read carefully before application (include warnings, contraindications and notes). Manufacturer Shenzhen Hingmed Medical Instrument Co., Ltd. Manufacturing address: 4 th Floor, Zhonghangfeixiang Building, NO. 371, Guangshen Road, Baoan District, Shenzhen, People’s Republic of China Tel: +86 755 23730601 Fax: +86 755 23730602 Post code: 518102 After-sales service Company: Shenzhen Hingmed Instruments Co., Ltd. Address: 4 th Floor, Zhonghangfeixiang Building, NO. 371, Guangshen Road, Baoan District, Shenzhen, People’s Republic of China Tel: +86 755 23730601 Fax: +86 755 23730602 Post code: 518102 European Representative Company Name:Wellkang Ltd Company Address: The Black Church,St.Mary’s Place,Dublin 7,D07 P4AX,Ireland Te l : +353(1)2542900,+353(1)4433560 Fax: +353(1)6864856 Web:www.wellkang.ltd.uk & www.CE-marking.eu Email: [email protected] Version Information This manual may upgrade due to software upgrading. User will not be notified further. ■ Version: A/0 ■ Issue date: Dec 2022 Software version:V1 Shenzhen Hingmed Medical Instruments Co., Ltd. owns and reserves the copyright. Shenzhen Hingmed Medical Instrument Co., Ltd. Table of Content 1.Introduction ................................................................................................................................................ 4 1.1product feature ................................................................................................................................... 4 1.2Safety Instructions .............................................................................................................................. 4 1.3Intended Use ...................................................................................................................................... 4 1.4Important Information ....................................................................................................................... 4 1.5 Consist of blood pressure monitor .................................................................................................... 4 2 Important safety information ............................................................................................................... 5 2.1Warning .............................................................................................................................................. 5 10、Component replacement list ............................................................................................................... 15 Caution:Please use the component supply by the manufacture ,otherwise might cause the measurement error or injury ................................................................................................................................................ 16 NO. ................................................................................................................................................................ 16 Component .................................................................................................................................................... 16 Type .............................................................................................................................................................. 16 1 .................................................................................................................................................................... 16 11、 Warranty Card ..................................................................................................................................... 17 12 EMC information ...................................................................................................................................... 18 13.FCC Compliance Statements ................................................................................................................... 22 Shenzhen Hingmed Medical Instrument Co., Ltd. 1.Introduction 1.1product feature Thank you for purchasing the HINGMED upper arm blood pressure monitor. This monitor can be used by multiple users, This blood Pressure monitor use the oscillometric method of blood pressure measurement. It has some functions that measure the blood pressure and display the result. When measuring the blood pressure, the user need to wear the cuff on the upper arm. 1.2Safety Instructions This instruction manual provides you with important information about the HINGMED upper arm blood pressure monitor. To ensure the safe and proper use of this monitor, Read and UNDERSTAND all of these instructions, If you do not understand these instructions or have any questions, contact +86 755 23720600 before attempting to use this monitor, For specific information about your own blood pressure, consult with your physician. 1.3Intended Use This device is a digital monitor intended for use in measuring blood pressure(SYS and DIA) and pulse rate. Environments of use: home healthcare environment Patient population: Adult 1.4Important Information Read the Important safety Information in this instruction manual before using this monitor. Follow this Instruction manual thoroughly for your safety. Keep for future reference. For specifies information about your own blood pressure, consult with your physician. 1.5 Consist of blood pressure monitor V03 consist of Monitor, cuff, USB wire and APP V03D consist of Monitor, cuff , USB wire and displayer Note: t he cuff do not replace. 1.5.1 Difference of model model APP Displayer V03 √ × V03D × √ 1.5.2 Performance Shenzhen Hingmed Medical Instrument Co., Ltd. Item Type Model V03, V03D Measuring method Oscillometric method Range From 0 to 289mmH…

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ApplicantDeclaration QSF27-14-04Rev1.0Rev.Feb6,2023Page 1 of 1 OriginalIssue:Jan.4,2021 SGSNorthAmericaInc. 620OldPeachtreeRoad SUITE100 Suwanee,Georgia30024 UnitedStates ApplicantLegalBusinessName ShenzhenHingmedMedicalInstrumentCo.,Ltd. Address 4thFloor,ZhonghangfeixiangBuilding,NO.371,GuangshenRoad,BaoanDistrict, Shenzhen,China,518102 GranteeCode 2A2R4 FCCID 2A2R4V03D AuthorizedContactName HuangYongban ContactEmail [email protected] ContactPhone 86-755-234206946 I,theundersigned,certifythatIamanauthorizedsignatoryfortheApplicantandthereforedeclare; a)inaccordancewith47CFR2.911(d),allofthestatementshereinandtheexhibitsattachedheretoaretrueandcorrecttothebestofmy knowledgeandbelief. b)inacceptingaGrantofEquipmentAuthorizationissuedbyaTCB,undertheauthorityoftheFCC,asaresultoftherepresentationsmadein thisapplication,theApplicantisresponsiblefor: (1)labelingtheequipmentwiththeexactFCCIDasspecifiedinthisapplication, (2)compliancestatementlabelingpursuanttotheapplicablerules, (3)complianceoftheequipmentwiththeapplicabletechnicalrules, c)iftheApplicantisnottheactualmanufactureroftheequipment,appropriatearrangementshavebeenmadewiththemanufacturertoensure thatproductionunitsofthisequipmentwillcontinuetocomplywiththeFCC’stechnicalrequirements. d)inaccordancewith47CFR2.909andKDB394321,theApplicanthasread,understoodandagreestoacceptthattheyaretheresponsible partyandagreetoabidebytheirresponsibilitiesasspecifiedunder47CFR2.909andKDB394321. e)inaccordancewithISO17065,FCCKDB641163,FCCKDB610077,KDB394321andRSP-100,theApplicanthasread,understood,accepts andagreestoabidebythepostmarketsurveillancerequirements. (1)theApplicantunderstands,acceptsandagreesthatasamplemayberequestedforsurveillancetesting. (2)theApplicantshallmakeprovisionstoalwayshaveaproductionsampleavailableuponrequestbySGS,FCCand/orISED. (3)theApplicantshall,uponrequestbySGS,attheApplicant’sexpense,provideaproductionsampleoftherequestedproducttoSGS, FCCand/orISEDasinstructed.Thesampleshallincludeallsupportdevices,cables,software,accessoriesorotherhardwareor softwarerequiredforevaluation,review,certificationandauditsurveillanceofproductscertifiedbySGS. f)neithertheApplicantnoranypartytotheapplicationissubjecttoadenialofFederalbenefits,thatincludesFCCbenefits,pursuanttoSection 5301oftheAnti-DrugAbuseActof1988,21U.S.C.§862becauseofaconvictionforpossessionordistributionofacontrolledsubstance.See 47CFR1.2002(b)forthedefinitionofa“party”forthesepurposes. g)theApplicanthasread,understood,acceptsandagreestoabidebytheSGSNorthAmerica,Inc.(TCB)termsandconditions. LinktoCFRs:https://www.fcc.gov/wireless/bureau-divisions/technologies-systems-and-innovation-division/rules-regulations-title-47 LinktoKDBs:https://apps.fcc.gov/oetcf/kdb/index.cfm LinktoRSP-100:https://www.ic.gc.ca/eic/site/smt-gst.nsf/eng/sf01130.html LinktotheCoveredList:CoveredList [ShenzhenHingmedMedicalInstrumentCo.,Ltd.](“theapplicant”)certifiesthattheequipmentforwhichauthorizationissoughtisnot “covered”equipmentprohibitedfromreceivinganequipmentauthorizationpursuanttosection2.903oftheFCCrules. [ShenzhenHingmedMedicalInstrumentCo.,Ltd.](“theapplicant”)certifiesthat,asofthedateofthefilingoftheapplication,the applicant[isnot]identifiedontheCoveredlist,establishedpursuantto§1.50002,asanentityproducing“covered”equipment. ApplicantSignature: Date:2023/03/21 PrintName: HuangYongban Title: QA *NOTE:ThisdeclarationcannotbesignedbyanAgent,itshallbesignedbyanauthorizedpersonlistedintheFCCdatabase

UNITEDSTATESDESIGNATEDAGENTLETTER Date:2023-07-10 TO:FederalCommunicationCommission EquipmentAuthorizationBranch 7435 OaklandMills Road Columbia,MID 21046 ApplicantU.S. designatedagent CompanyName:ShenzhenHingmedMedical InstrumentCo., Ltd. CompanyName:UnitedConsultingTechnology ServicesCo., Ltd. GranteeCode:2A2R4FRN: ContactName: 0033495714 David Wu ContactName:HuangYongbanAddress:17800CASTLETONST STE 665 CITY OF INDUSTRYCA 91748UnitedStates Address:4th Floor, Zhonghangfeixiang Building,NO. 371, Guangshen Road,BaoanDistrict, Shenzhen,China,518102 Telephone:(626) 217-4022 Telephone:86-755-234206946 Email:[email protected] Email:[email protected] ApplicableEquipment:FCC ID: <2A2R4V03D> ATTN:Directorof Certification: We, <ShenzhenHingmedMedicalInstrumentCo., Ltd.> and < UnitedConsultingTechnologyServices Co., Ltd.> understandand acknowledgethe applicantsconsentand the designatedagent ’s obligationto acceptserviceof processin the UnitedStatesfor mattersrelatedto the applicableequipment,and at the physicalU.S. addressand e-mailof the designatedagent listed above. We, <ShenzhenHingmedMedicalInstrumentCo., Ltd.> and < UnitedConsultingTechnologyServices Co., Ltd.> acknowledgethe applicant’s acceptanceof its obligationto maintainan agent for serviceof processin the UnitedStatesfor no less than one year after either the granteehas permanently terminatedall marketingand importationof the applicableequipmentwithin the U.S., or the conclusionof any Commission-relatedadministrativeor judicialproceedinginvolvingthe equipment,whicheveris later. ApplicantU.S. designatedagent Name (Printed) :HuangYongbanName (Printed) : David Wu Title:QATitle: CEO Signature: Signature:

ShenzhenHingmedMedicalInstrumentCo.,Ltd. Date:2023/03/21 TO:FederalCommunicationCommission EquipmentAuthorizationBranch 7435OaklandMillsRoad Columbia,MID21046 Regarding:FCCID:2A2R4V03D Towhomitmayconcern: We,theundersigned,herebyauthorizeSGS-CSTCStandardsTechnicalServicesCo.,Ltd.toactonour behalfinallmannersrelatingtoapplicationforequipmentauthorizationwithrespecttotheFCCIDabove, includingsigningofalldocumentsrelatingtothesematters.Anyandallactscarriedoutbytheagenton ourbehalfshallhavethesameeffectasactsofourown. We,theundersigned,herebycertifythatwearenotsubjecttoadenialoffederalbenefits,thatincludes FCCbenefits,pursuanttoSection5301oftheAnti-DrugAbuseActof1988,21U.S.C.853(a). Whereouragentsignstheapplicationforcertificationonourbehalf,Iacknowledgethatallresponsibility forcomplyingwiththetermsandconditionsforCertification,asspecifiedbySGSNorthAmerica,Inc.,still resideswithShenzhenHingmedMedicalInstrumentCo.,Ltd. Thisauthorizationisvaliduntilfurtherwrittennoticefromtheapplicant. Sincerely, PrintName:HuangYongbanTitle:QA Signature: OnbehalfofCompany:ShenzhenHingmedMedicalInstrumentCo.,Ltd. Telephone:86-755-234206946 E-mail:[email protected]

ShenzhenHingmedMedicalInstrumentCo.,Ltd. TO:FederalCommunicationCommission EquipmentAuthorizationBranch 7435OaklandMillsRoad Columbia,MID21046 Regarding:ConfidentialityRequestregardingapplicationforFCCID:2A2R4V03D LONGTERMCONFIDENTIALITY Pursuantto47CFRSection0.459and0.457ofthecommission’srules,theapplicantherebyrequest confidentialtreatmentofthedocumentslistedbelow,associatedwiththecertificationapplication referencedabove. Schematic(s) BlockDiagrams OperationalDescriptions Thedocumentsabovecontainproprietaryinformationnotreleasedtothepublic.Publicdisclosureofthis informationmayproveharmfultothebusinessoftheapplicant. SHORTTERMCONFIDENTIALITY Additionally,theapplicantrequeststhefollowingdocumentsbeheldconfidentialuntilthedeviceis marketedor180daysfromthegrantdate,whicheverisless.Ifthedeviceismarketedwithin aforementioneddaysoftheGrantDate,theapplicantwillnotifytheTCBperFCCKDB726920D01 ConfidentialityRequestProcedures. ExternalPhotos InternalPhotos TestSetupPhotos Usermanual(s) Sincerely, PrintName:HuangYongbanTitle:QA Signature: OnbehalfofCompany:ShenzhenHingmedMedicalInstrumentCo.,Ltd. Telephone:86-755-234206946 E-mail:[email protected]

SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A02 Rev.A/0 Page: 1 of 4 Appendix External Photos for SZCR2303000533ME FCC ID: 2A2R4V03D SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A02 Rev.A/0 Page: 2 of 4 EUT Constructional Details (EUT Photos) SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A02 Rev.A/0 Page: 3 of 4 Sample Label, Label Location SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A02 Rev.A/0 Page: 4 of 4 - End of the Appendix -

标签（HINGMED） 不干胶，覆哑膜 A/0 1：1 Wellkang LtdWellkang Ltd YYYY-MM YYYY-MM 85.00 mm Model: V03D Shenzhen Hingmed Medical Instrument Co.,Ltd.Shenzhen Hingmed Medical Instrument Co.,Ltd. Shenzhen Hingmed Medical Instrument Co.,Ltd. 4F,Zhonghangfeixiang Building, NO.371,4F,Zhonghangfeixiang Building, NO.371, Guangshen Road, Baoan District,Shenzhen,China.Guangshen Road, Baoan District,Shenzhen,China. 41.00 mm Cuff Circumference: 22cm-41cm 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. xxxxxxxxxxxx Power: DC 3.7V Li-ion battery Upper Arm Blood Pressure Monitor FCC ID : 2A2R4V03D

SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 1 of 5 Appendix Internal Photos for SZCR2303000533ME FCC ID: 2A2R4V03D SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 2 of 5 EUT Constructional Details (EUT Photos) SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 3 of 5 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 4 of 5 Antenna SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-A03 Rev.A/0 Page: 5 of 5 - End of the Appendix -

SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-01 Rev. A/0 Aug01,2022 Report No.: SZCR230300053303 Page: 1 of 9 Keny Xu EMC Laboratory Manager 1 Cover page RF Exposure Report Application No.: SZCR2303000533ME Applicant: Shenzhen Hingmed Medical Instrument Co., Ltd. Address of Applicant: 4th Floor, Zhonghangfeixiang Building, NO. 371, Guangshen Road, Baoan District, Shenzhen 518102 China Manufacturer: Shenzhen Hingmed Medical Instrument Co., Ltd. Address of Manufacturer: 4th Floor, Zhonghangfeixiang Building, NO. 371, Guangshen Road, Baoan District, Shenzhen, Guangdong, China Factory: Shenzhen Hingmed Medical Instrument Co., Ltd. Address of Factory: 4th Floor, Zhonghangfeixiang Building, NO. 371, Guangshen Road, Baoan District, Shenzhen, Guangdong, China Equipment Under Test (EUT): EUT Name: Upper Arm blood pressure monitor Model No.: V03D Trade Mark: Hingmed FCC ID: 2A2R4V03D Standards: FCC Rules 47 CFR §2.1093 KDB 447498 D04 interim General RF Exposure Guidance v01 Date of Receipt: 2023-03-06 Date of Test: 2023-03-10 to 2023-03-20 Date of Issue: 2023-03-20 Test Result : Pass* * In the configuration tested, the EUT complied with the standards specified above. SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-01 Rev. A/0 Aug01,2022 Report No.: SZCR230300053303 Page: 2 of 9 2 Version Revision Record Version Chapter Date Modifier Remark 01 2023-03-20 Original Authorized for issue by: Edison Li/Project Engineer Eric Fu/Reviewer SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-01 Rev. A/0 Aug01,2022 Report No.: SZCR230300053303 Page: 3 of 9 3 Contents Page 1 COVER PAGE .............................................................................................................................................. 1 2 VERSION ...................................................................................................................................................... 2 3 CONTENTS .................................................................................................................................................. 3 4 GENERAL INFORMATION .......................................................................................................................... 4 4.1 GENERAL DESCRIPTION OF E.U.T. .......................................................................................................... 4 4.2 GENERAL DESCRIPTION OF EUT ............................................................................................................. 4 4.3 SEPARATION DISTANCE .......................................................................................................................... 4 4.4 TEST LOCATION ...................................................................................................................................... 5 4.5 TEST FACILITY ........................................................................................................................................ 5 4.6 DEVIATION FROM STANDARDS ................................................................................................................. 5 4.7 ABNORMALITIES FROM STANDARD CONDITIONS ....................................................................................... 5 4.8 OTHER INFORMATION REQUESTED BY THE CUSTOMER ............................................................................. 5 5 FCC RADIOFREQUENCY RADIATION EXPOSURE LIMITS .................................................................... 6 5.1 BLANKET 1 MW BLANKET EXEMPTION ..................................................................................................... 6 5.2 MPE-BASED EXEMPTION ........................................................................................................................ 6 5.3 SAR-BASED EXEMPTION ......................................................................................................................... 7 6 MEASUREMENT AND CALCULATION ...................................................................................................... 9 6.1 MAXIMUM TRANSMIT POWER ................................................................................................................... 9 6.2 RF EXPOSURE CALCULATION .................................................................................................................. 9 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-01 Rev. A/0 Aug01,2022 Report No.: SZCR230300053303 Page: 4 of 9 4 General Information 4.1 General Description of E.U.T. Product Type: Portable device Mobile device Fixed device 4.2 General Description of EUT Power supply: DC 3.7V, 400mAh rechargeable battery which charged by charging dock Operation Frequency: 2402MHz to 2480MHz Bluetooth Version: V4.2 Modulation Type: GFSK Number of Channels: 40 Channel Spacing: 2MHz Data rate: 1Mbps Antenna Type: PCB Antenna Antenna Gain: -1.67dBi Remark:The information in this section is provided by the applicant or manufacturer, SGS is not liable to the accuracy, suitability, reliability or/and integrity of the information. 4.3 Separation Distance Minimum test separation distance: 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. SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-01 Rev. A/0 Aug01,2022 Report No.: SZCR230300053303 Page: 5 of 9 4.4 Test Location All tests were performed at: SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch No. 1 Workshop, M-10, Middle section, Science & Technology Park, Shenzhen, Guangdong, China 518057 Telephone: +86 (0) 755 2601 2053 Fax: +86 (0) 755 2671 0594 No tests were sub-contracted. 4.5 Test Facility The test facility is re…

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SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch Report No.: ZEWM2305000714OA01 Rev.00 Page: 1 of 18 ANTENNA PASSIVE TEST REPORT Application No.ZEWM2305000714OA ApplicantShenzhen Hingmed Medical Instrument Co., Ltd. ManufacturerShenzhen Hingmed Medical Instrument Co., Ltd. Product NameAutomatic electronic sphygmomanometer Model No.V03D StandardsANSI/IEEE Std 149-2008 Date Initial Sample(s) Received2023.05.23 Testing Start Date2023.05.23 Testing Finish Date2023.05.23 Report Issue Date2023.05.25 *In the configuration tested, the EUT detailed in this report complied with the standards specified above. Prepared byReviewed ByApproved by SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch Report No.: ZEWM2305000714OA01 Rev.00 Page: 2 of 18 Revision Version Report No.VersionDateMemo ZEWM2305000714OA01002023.05.25Initial creation of report SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch Report No.: ZEWM2305000714OA01 Rev.00 Page: 3 of 18 TABLE OF CONTENTS 1GENERAL INFORMATION....................................................................................................4 1.1Testing Laboratory..............................................................................................................................4 1.2Details of Applicant.............................................................................................................................4 1.3Details of Manufacturer......................................................................................................................4 1.4General Description of EUT..................................................................................................................5 1.5Test Procedure....................................................................................................................................5 1.6Test Specification................................................................................................................................6 1.7Laboratory Environment......................................................................................................................6 2OTA MEASUREMENTS SYSTEM CONFIGURATION......................................................7 2.1Test Configuration...............................................................................................................................7 3TEST EQUIPMENT LIST.......................................................................................................8 4MEASUREMENT UNCERTAINTY.......................................................................................9 5TEST RESULTS.....................................................................................................................10 6PATTERN PLOTS.................................................................................................................12 6.1Return Loss........................................................................................................................................12 6.2VSWR................................................................................................................................................13 6.3Stimulus............................................................................................................................................14 72-D ANTENNA PATTERN(THETA=90°).......................................................................15 83-D ANTENNA PATTERN..................................................................................................16 9THE EUT AND TEST CONFIGURATION.........................................................................17 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch Report No.: ZEWM2305000714OA01 Rev.00 Page: 4 of 18 1General Information 1.1Testing Laboratory Test Lab SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch Address No. 1 Workshop, M-10, Middle section, Science & Technology Park, Nanshan District, Shenzhen, Guangdong, China 518057 ContactErvin Li Tel.+86 18823369694 Fax+86-755-25328600 [email protected] 1.2Details of Applicant Applicant’s NameShenzhen Hingmed Medical Instrument Co.,Ltd. Applicant’s Address 4th Floor, Zhonghangfeixiang Building, NO. 371, Guangshen Road, Baoan District, Shenzhen, Guangdong, China ContactHuangYongBan Tel.13612982871 FaxN/A E-mail [email protected] 1.3Details of Manufacturer Manufacturer’s NameShenzhen Hingmed Medical Instrument Co.,Ltd. Manufacturer’s Address 4th Floor, Zhonghangfeixiang Building, NO. 371, Guangshen Road, Baoan District, Shenzhen, Guangdong, China ContactHuangYongBan Tel.13612982871 FaxN/A E-mail [email protected] SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch Report No.: ZEWM2305000714OA01 Rev.00 Page: 5 of 18 1.4General Description of EUT Device Description: Automatic electronic sphygmomanometer Device Manufacturer: Shenzhen Hingmed Medical Instrument Co.,Ltd. Device Model: V03D Hardware Version: N/A Software Version: N/A 1.5Test Procedure Testing is performed according to the ANSI/IEEE Std 149-2008. SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch Report No.: ZEWM2305000714OA01 Rev.00 Page: 6 of 18 1.6Test Specification IdentityDocument Title ANSI/IEEE Std 149-2008IEEE Standard Test Procedures for Antennas 1.7Laboratory Environment Temperature Min. =19°C，Max. = 25°C Relative humidity Min. =40%，Max. =72% Shield effect0.7-6GHz> 100dB Ground resistance <0.5 SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch Report No.: ZEWM2305000714OA01 Rev.00 Page: 7 of 18 2OTA Measurements System Configuration 2.1Test Configuration Great-Circle-Cut method is used to measure the antenna 3D GAIN of EUT in OTA qualified anechoic chamber. Equipment Under Test (EUT) geometry centre vertical projection at the centre of platform, the distance from EUT to measurement antenna is 5m F-1. OTA Measurement System Configuration SGS-CSTC Standards Technical Services Co…

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SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-01 Rev. A/0 Aug01,2022 Report No.: SZCR230300053302 Page: 1 of 60 Keny Xu EMC Laboratory Manager TEST REPORT Application No.: SZCR2303000533ME Applicant: Shenzhen Hingmed Medical Instrument Co., Ltd. Address of Applicant: 4th Floor, Zhonghangfeixiang Building, NO. 371, Guangshen Road, Baoan District, Shenzhen 518102 China Manufacturer: Shenzhen Hingmed Medical Instrument Co., Ltd. Address of Manufacturer: 4th Floor, Zhonghangfeixiang Building, NO. 371, Guangshen Road, Baoan District, Shenzhen, Guangdong, China Factory: Shenzhen Hingmed Medical Instrument Co., Ltd. Address of Factory: 4th Floor, Zhonghangfeixiang Building, NO. 371, Guangshen Road, Baoan District, Shenzhen, Guangdong, China Equipment Under Test (EUT): EUT Name: Upper Arm blood pressure monitor Model No.: V03D Trade Mark: Hingmed FCC ID: 2A2R4V03D Standard(s) : 47 CFR Part 15, Subpart C 15.247 Date of Receipt: 2023-03-06 Date of Test: 2023-03-10 to 2023-03-20 Date of Issue: 2023-03-20 Test Result: Pass* * In the configuration tested, the EUT complied with the standards specified above. SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-01 Rev. A/0 Aug01,2022 Report No.: SZCR230300053302 Page: 2 of 60 Revision Record Version Chapter Date Modifier Remark 01 2023-03-20 Original Authorized for issue by: Edison Li/Project Engineer Eric Fu/Reviewer SGS-CSTC Standards Technical Services Co., Ltd. Shenzhen Branch SZEMC-TRF-01 Rev. A/0 Aug01,2022 Report No.: SZCR230300053302 Page: 3 of 60 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 Conducted Emissions at AC Power Line (150kHz-30MHz) 47 CFR Part 15, Subpart C 15.247 ANSI C63.10 (2013) Section 6.2 47 CFR Part 15, Subpart C 15.207 Pass Conducted Peak Output Power ANSI C63.10 (2013) Section 11.9.1 47 CFR Part 15, Subpart C 15.247(b)(3) Pass Minimum 6dB Bandwidth ANSI C63.10 (2013) Section 11.8.1 47 CFR Part 15, Subpart C 15.247a(2) Pass Power Spectrum Density ANSI C63.10 (2013) Section 11.10.2 47 CFR Part 15, Subpart C 15.247(e) Pass Conducted Band Edges Measurement ANSI C63.10 (2013) Section 11.13.3.2 47 CFR Part 15, Subpart C 15.247(d) Pass Conducted Spurious Emissions ANSI C63.10 (2013) Section 11.11 47 CFR Part 15, Subpart C 15.247(d) Pass Radiated Emissions which fall in the restricted bands ANSI C63.10 (2013) Sec…

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