2AS8A-BE23TBlood Pressure Monitor

Shenzhen Jamr Technology Co., Ltd. A101-301, D101-201, Jamr Science & Technology Park, No. 2 Guiyuan Road, Guixiang Community, Guanlan Street, Longhua District, 518100 Shenzhen, PEOPLE'S REPUBLIC OF CHINA. Shanghai International Holding Corp. GmbH (Europe) Eiffestrasse 80, 20537 Hamburg, Germany Version Number: 1.0 Revison date: 2024.07.15 Blood Pressure Monitor Model Number: BE23T ---------------------------------------------------------------- USER’S MANUAL 1 CONTENTS 1 Introduction and Intended Use............................................................2 2 Important Information on Blood Pressure and its Measurement........4 3 Components of Your Blood Pressure Monitor.....................................5 4 Using Your Monitor for the First Time.................................................6 5 Measurement Procedure....................................................................7 6 Care and Maintenance.......................................................................14 7 Warranty/service...............................................................................14 8Certifications.....................................................................................15 9 Technical Specifications....................................................................15 10 EMC Declaration..............................................................................16 2 1 Introduction and Intended Use The device is a fully automatic digital blood pressure measuring device using oscillometric technique to measure systolic and diastolic blood pressure as well as the pulse by wrapping around the upper arm withcuff circumference ranging from 15cm to 28cm, 22cm to 42cm and 32cm to 52 cm. Cuff range from 15cm to 28cm is used for children age more than 3 years old, and Cuff range from 22cm to 42cm and 32cm to 52 cm is used for adults. The device can be used in medical facilities or at home, and only for indoor use. Contraindication:The device is not used for patients under dialysis therapy or on anticoagulant, antiplatelets, or steroids. The device is provide accurate blood pressure measurement values that are effective and suitable for clinical and home use. Before using, please read this instruction manual carefully and then keep it in a safe place. 1.1 Remember... • Only a health-care professional is qualified to interpret blood pressure measurements. • This device is NOT intended to replace regular medical checkups. • The device is intended for use by adults only and not intended for use on children and pregnant patient.The effectiveness has not been established in pregnant (including pre-eclamptic) patients. •In cases of irregular heartbeat, measurements made with this instrument should only be evaluated after consultation with a physician. • The products, including accessories, shall be processed in accordance with local regulations after reaching the life cycle. • Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the competent authority of the Member State in which the user and/or patient is established. 1.2 Warnings and Precautions Warning: Do not use the AC adapter if the unit or the power cord is damaged. Turn off the power and unplug the power cord immediately. Warning: The device is not suitable for use in the presence of flammable anesthetic mixtures with air or with oxygen or nitrous oxide. Warning: If the patient is an intended operator, the functions of monitoring blood pressure and pulse rate can be safely used by patient. The routine clean and changing batteries can be performed by the patient. Warning: The device provides a DC input port connected to external ac adapter. 3 It is recommended that use the adapter specified by the manufacturer. The adapter should meet the following conditions: class II equipment, output voltage: DC 5V, current:≥1A, and comply with IEC 60950, IEC 60601-1 or IEC 62368-1, provide at least two MOOP insulation between ac input and dc output. External adapter connected to medical electrical equipment through the DC input port must comply with the respective IEC or ISO standards (e.g. IEC 60950 or IEC 62368-1 for data processing equipment). Further more all configurations shall comply with the requirements for medical electrical systems (see IEC 60601-1-1 or clause 16 of the 3Ed. of IEC 60601-1, 60601-1-2, respectively). Anybody connecting external adapterto medical electrical equipment configurations a medical system and is therefore responsible that the system complies with the requirements for medical electrical systems. Attention is drawn to the fact that local laws take priority over the above mentioned requirements. If in doubt, consult your local representative or the technical service department. Warning: Too frequent measurementscan cause injury to the PATIENT due to blood flow interference. Warning: Don’t place the cuff over wound part. Warning: Pressurization of the CUFF can temporarily cause loss of function of simultaneously used monitoring ME EQUIPMENT on the same limb. Warning: Regularly checking the operationof the blood pressure monitor to ensure that it does not cause long-term damage to the patient's blood circulation. Warning: Apply CUFF and its pressurization on the side of the patient's mastectomy or lymph node removal can cause injury. Warning: To avoid any possibility of accidental strangulation, keep this device away from children and do not drape tubing around your neck. Caution: The user must check that the equipment functions safely and see that it is in proper working condition before being used. Caution: To avoid damaging the device, keep this unit away from children and pets. Caution: The standard material used for the bladder and tubing is latex-free. Caution: The device is intended to monitor, not to diagnose. Unusual values have to be always discussed with a physician. Underany circumstance, you should not alter the dosages of any drugs prescribed by a p…

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ShenzhenJamrTechnologyCo.,Ltd 09-27-2024 EurofinsElectricalandElectronicTestingNA,Inc. 914WestPatapscoAvenue Baltimore,MD21230 RE:AttestationStatementsPart2.911(d)(5)(i)requestfor(FCCID:2AS8A-BE23T) [ShenzhenJamrTechnologyCo.,Ltd](“theapplicant”)certifiesthattheequipmentfor whichauthorizationissoughtisnot“covered”equipmentprohibitedfromreceivingan equipmentauthorizationpursuanttosection2.903oftheFCCrules. Sincerely, FushengLuo ShenzhenJamrTechnologyCo.,Ltd 09-27-2024 EurofinsElectricalandElectronicTestingNA,Inc. 914WestPatapscoAvenue Baltimore,MD21230 RE:AttestationStatementsPart2.911(d)(5)(ii)requestfor(FCCID:2AS8A-BE23T) [ShenzhenJamrTechnologyCo.,Ltd](“theapplicant”)certifiesthat,asofthedateof thefilingoftheapplication,theapplicantisnotidentifiedontheCoveredListasan entityproducing“covered”equipment. Sincerely, FushengLuo

ShenzhenJamrTechnologyCo.,Ltd AgentAuthorizationLetter 2024-09.27 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:FushengLuo Position:RAManager CompanyName:ShenzhenJamrTechnologyCo.,Ltd Address:A101-301,D101-201,JamrScience&TechnologPark,No.2Guiyuan Road,GuanlanStreet,LonghuaDistrict,China Tel/Fax86-755-85292057/86-755-27980758 E-Mail:[email protected]

ShenzhenJamrTechnologyCo.,Ltd LongTermConfidentialityRequestLetter 2024.09.27 EurofinsElectricalandElectronicTestingNA,Inc. 914WestPatapscoAvenue Baltimore,MD21230 USA RE:CONFIDENTIALITYREQUESTFOR(FCCID:2AS8A-BE23T) ToWhomItMayConcern: Thisletterservesasanofficialrequestforconfidentialityundersections0.457and0.459of CFR47.Wehaverequestedthatthe -e.g.Blockdiagram -e.g.SCH -e.g.OperationalDescription requiredtobesubmittedwiththisapplicationbepermanentlywithheldfrompublicreview. Theabovedocumentsarecompanyproprietaryinformationthatcouldnevergetinto thepossessionofyourcompetition. Pleasecontactmeifthereisanyinformationyoumayneed. Sincerely, Name:FushengLuo Position:RAManager CompanyName:ShenzhenJamrTechnologyCo.,Ltd Address:A101-301,D101-201,JamrScience&TechnologPark,No.2Guiyuan Road,GuanlanStreet,LonghuaDistrict,China Tel/Fax86-755-85292057/86-755-27980758 E-Mail:[email protected]

Model No.: BE23T FRONT VIEW OF SAMPLE BACK VIEW OF SAMPLE Model No.: BE23T LEFT VIEW OF SAMPLE RIGHT VIEW OF SAMPLE Model No.: BE23T TOP VIEW OF SAMPLE BOTTOM VIEW OF SAMPLE Model No.: BE23T

ModelNo.:BE23T Page1of4 INTERNALPHOTOOFSAMPLE INTERNALPHOTOOFSAMPLE ModelNo.:BE23T Page2of4 INTERNALPHOTOOFSAMPLEPCB ModelNo.:BE23T Page3of4 ModelNo.:BE23T Page4of4 INTERNALPHOTOOFSAMPLEPCB BTantenna

Shenzhen Most Technology Service Co., Ltd. No.5, 2nd Langshan Road, North District, Hi-tech Industrial Park, Nanshan, Shenzhen, Guangdong, China. RF Exposure Evaluation Report Report Reference No. ..................... : FCC ID.. ........................................... : MTEB24080015-H 2AS8A-BE23T Compiled by ( position+printed name+signature) .. : File administrators Alisa Luo Supervised by ( position+printed name+signature) .. : Test Engineer Sunny Deng Approved by ( position+printed name+signature) .. : Manager Yvette Zhou Date of issue ..................................... : Aug. 02,2024 Representative Laboratory Name .: Shenzhen Most Technology Service Co., Ltd. Address ............................................ : No.5, 2nd Langshan Road, North District, Hi-tech Industrial Park, Nanshan, Shenzhen, Guangdong, China. Applicant’s name ............................ : Shenzhen Jamr Technology Co., Ltd. Address ............................................ : A101-301, D101-201, Jamr Science & Technology Park, No. 2 Guiyuan Road, Guixiang Community,Guanlan Street, Longhua District, 518100 Shenzhen, PEOPLE'S REPUBLIC OF CHINA Test specification/ Standard ..........: 47 CFR Part 1.1307 47 CFR Part 2.1093 TRF Originator .................................. : Shenzhen Most Technology Service Co., Ltd. Shenzhen Most Technology Service Co., Ltd. All rights reserved. This publication may be reproduced in whole or in part for non-commercial purposes as long as the Shenzhen Most Technology Service Co., Ltd. is acknowledged as copyright owner and source of the material. Shenzhen Most Technology Service Co., Ltd. takes no responsibility for and will not assume liability for damages resulting from the reader's interpretation of the reproduced material due to its placement and context. Test item description .....................: Blood Pressure Monitor Trade Mark ....................................... : N/A Model/Type reference....................... : BE23T Listed Models .................................. : N/A Modulation Type ............................... : GFSK Operation Frequency ........................ : From 2402MHz to 2480MHz Hardware Version .............................. JMR_PCB-BE22-AC621B-A-V1.0 Software Version ............................... V1 Rating ............................................... : DC 5V by Adapter DC 4.5V by Batteries Result................................................ : PASS Report No.: MTEB24080015-H Page 2 of 5 T E S T R E P O R T Equipment under Test : Blood Pressure Monitor Model /Type : BE23T Listed Models : N/A Remark N/A Applicant : Shenzhen Jamr Technology Co., Ltd. Address : A101-301, D101-201, Jamr Science & Technology Park, No. 2 Guiyuan Road, Guixiang Community,Guanlan Street, Longhua District, 518100 Shenzhen, PEOPLE'S REPUBLIC OF CHINA Manufacturer : Shenzhen Jamr Technology Co., Ltd Address : A101-301, D101-201, Jamr Science & Technology Park, No. 2 Guiyuan Road, Guixiang Community,Guanlan Street, Longhua District, 518100 Shenzhen, PEOPLE'S REPUBLIC OF CHINA Test Result: PASS The test report merely corresponds to the test sample. It is not permitted to copy extracts of these test result without the written permission of the test laboratory. Report No.: MTEB24080015-H Page 3 of 5 1. R e v i s i o n H i s t o r y Revision Issue Date Revisions Revised By 00 2024.08.02 Initial Issue Alisa Luo Report No.: MTEB24080015-H Page 4 of 5 2. S A R E v a l u a t i o n 2.1 RF Exposure Compliance Requirement 2.1.1 Standard Requirement According to KDB447498D01 General RF Exposure Guidance v06 4.3.1. Standalone SAR test exclusion considerations Unless specifically required by the published RF exposure KDB procedures, standalone 1-g head or body and 10-g extremity SAR evaluation for general population exposure conditions, by measurement or numerical simulation, is not required when the corresponding SAR Exclusion Threshold condition, listed below, is satisfied. 2.1.2 Limits The 1-g and 10-g SAR test exclusion thresholds for 100 MHz to 6 GHz at test separation distances ≤ 50 mm are determined by: [(max. power of channel, including tune-up tolerance, mW)/(min. test separation distance, mm)] · [√f(GHz)] ≤ 3.0 for 1-g SAR and ≤ 7.5 for 10-g extremity SAR, where The test exclusions are applicable only when the minimum test separation distance is ≤ 50 mm and for transmission frequencies between 100 MHz and 6 GHz. When the minimum test separation distance is < 5 mm, a distance of 5 mm is applied to determine SAR test exclusion Report No.: MTEB24080015-H Page 5 of 5 2.1.3 EUT RF Exposure Measurement Data BLE GFSK Test channel Peak Output Power (dBm) Tune up tolerance (dBm) Maximum tune-up Power (dBm) Lowest(2402MHz) -7.391 -7.391±1 -6.391 Middle(2440MHz) -7.069 -7.069±1 -6.069 Highest(2480MHz) -6.784 -6.784±1 -5.784 Worst case: GFSK Channel Maximum Peak Conducted Output Power (dBm) Maximum tune-up Power Calculated value Exclusion threshold SAR Test Exclusion (dBm) (mW) Highest(2480MHz) -6.784 -5.784 0.26 0.08 3.0 Yes .......................THE END OF REPORT.........................

ShenzhenMostTechnologyServiceCo.,Ltd. No.5,2ndLangshanRoad,NorthDistrict,Hi-techIndustrialPark,Nanshan, Shenzhen,Guangdong,China. TESTREPORT FCCRulesPart15.247 ReportReferenceNo........................: FCCID................................................: MTEB24080015-R 2AS8A-BE23T Compiledby (position+printedname+signature)..:FileadministratorsAlisaLuo Supervisedby (position+printedname+signature)..:TestEngineerSunnyDeng Approvedby (position+printedname+signature)..: ManagerYvetteZhou Dateofissue.........................................:Aug.02,2024 RepresentativeLaboratoryName.:ShenzhenMostTechnologyServiceCo.,Ltd. Address ................................................. : No.5,2ndLangshanRoad,NorthDistrict,Hi-techIndustrialPark, Nanshan,Shenzhen,Guangdong,China. Applicant’sname...............................: ShenzhenJamrTechnologyCo.,Ltd. Address ................................................. : A101-301,D101-201,JamrScience&TechnologyPark,No.2 GuiyuanRoad,GuixiangCommunity,GuanlanStreet,Longhua District,518100Shenzhen,PEOPLE'SREPUBLICOFCHINA Testspecification/Standard ............ : FCCRulesPart15.247 TRFOriginator......................................:ShenzhenMostTechnologyServiceCo.,Ltd. ShenzhenMostTechnologyServiceCo.,Ltd.Allrightsreserved. Thispublicationmaybereproducedinwholeorinpartfornon-commercialpurposesaslongasthe ShenzhenMostTechnologyServiceCo.,Ltd.isacknowledgedascopyrightownerandsourceofthe material.ShenzhenMostTechnologyServiceCo.,Ltd.takesnoresponsibilityforandwillnotassume liabilityfordamagesresultingfromthereader'sinterpretationofthereproducedmaterialduetoits placementandcontext. Testitemdescription ........................ : BloodPressureMonitor TradeMark...........................: N/A Model/Typereference ......................... : BE23T ListedModels.....................................:N/A ModulationType..................................:GFSK OperationFrequency..........................:From2402MHzto2480MHz HardwareVersion.................................JMR_PCB-BE22-AC621B-A-V1.0 SoftwareVersion ................................... V1 Rating ..................................................... : DC5VbyAdapter DC4.5VbyBatteries Result ..................................................... :PASS ReportNo.:MTEB24080015-RPage 2 of 38 TESTREPORT EquipmentunderTest:BloodPressureMonitor Model/Type:BE23T ListedModels:N/A RemarkN/A Applicant: ShenzhenJamrTechnologyCo.,Ltd. Address: A101-301,D101-201,JamrScience&TechnologyPark,No.2 GuiyuanRoad,GuixiangCommunity,GuanlanStreet,Longhua District,518100Shenzhen,PEOPLE'SREPUBLICOFCHINA Manufacturer:ShenzhenJamrTechnologyCo.,Ltd Address : A101-301,D101-201,JamrScience&TechnologyPark,No.2 GuiyuanRoad,GuixiangCommunity,GuanlanStreet,Longhua District,518100Shenzhen,PEOPLE'SREPUBLICOFCHINA TestResult : PASS Thetestreportmerelycorrespondstothetestsample. Itisnotpermittedtocopyextractsofthesetestresultwithoutthewrittenpermissionofthetest laboratory. ReportNo.:MTEB24080015-RPage 3 of 38 Contents 1.REVISIONHISTORY................................................................................................................4 2.TESTSTANDARDS...................................................................................................................5 3.SUMMARY......................................................................................................................................6 3.1.GeneralRemarks6 3.2.ProductDescription6 3.3.EquipmentUnderTest6 3.4.ShortdescriptionoftheEquipmentunderTest(EUT)6 3.5.EUToperationmode7 3.6.BlockDiagramofTestSetup7 3.7.TestItem(EquipmentUnderTest)Description*7 3.8.AuxiliaryEquipment(AE)Description7 3.9.AntennaInformation*8 3.10.EUTconfiguration8 3.11.Modifications8 4.TESTENVIRONMENT.............................................................................................................9 4.1.Addressofthetestlaboratory9 4.2.Environmentalconditions9 4.3.TestDescription10 4.4.Statementofthemeasurementuncertainty10 4.5.EquipmentsUsedduringtheTest11 5.TESTCONDITIONSANDRESULTS............................................................................12 5.1.ACPowerConductedEmission12 5.2.RadiatedEmission15 5.3.MaximumPeakOutputPower22 5.4.PowerSpectralDensity23 5.5.6dBBandwidthand99%Bandwidth24 5.6.BandEdgeComplianceofRFEmission25 5.7.SpuriousRFConductedEmission27 5.8.AntennaRequirement28 6.TESTSETUPPHOTOSOFTHEEUT..........................................................................29 7.EXTERNALANDINTERNALPHOTOSOFTHEEUT........................................30 APPENDIXI.DutyCycle31 APPENDIXII.PowerSpectralDensity33 APPENDIXIII.ConductedPeakOutputPower34 APPENDIXIV.99%Bandwidth35 APPENDIXV.6dBBandwidth36 APPENDIXVI.ConductedOutOfBandEmission37 ReportNo.:MTEB24080015-RPage 4 of 38 1.RevisionHistory RevisionIssueDateRevisionsRevisedBy 002024.08.02InitialIssueAlisaLuo ReportNo.:MTEB24080015-RPage 5 of 38 2.TESTSTANDARDS Thetestswereperformedaccordingtofollowingstandards: Thetestswereperformedaccordingtofollowingstandards: FCCRulesPart15.247:FrequencyHopping,DirectSpreadSpectrumandHybridSystemsthatarein operationwithinthebandsof902-928MHz,2400-2483.5MHz,and5725-5850MHz. ANSIC63.10:2013:AmericanNationalStandardforTestingUnlicensedWirelessDevices ReportNo.:MTEB24080015-RPage 6 of 38 3.SUMMARY 3.1.GeneralRemarks Dateofreceiptoftestsample:2024.07.29 Testingcommencedon:2024.07.30 Testingconcludedon: 2024.08.02 3.2.ProductDescription ProductName:BloodPressureMonitor Model/Typereference:BE23T PowerSupply： DC5VbyAdapter DC4.5VbyBatteries TestingsampleID： MTYP06253 Bluetooth: SupportedType:BLE Modulation:GFSK Operationfrequency:2402MHz~2480MHz Channelnumber:40 Channelseparation:2MHz Antennatype: PCBAntenna Antennagain:-12.02dBi 3.3.EquipmentUnderTest Powersupplysystemutilised Powersupplyvoltage: ○ 230V/50Hz ○ 120V/60Hz ○ 12VDC ○ 24VDC ● Other(specifiedinblankbelow) DC5VbyAdapter DC4.5VbyBatteries 3.4.ShortdescriptionoftheEquipmentunderTest(EUT) ThisisaBloodPressureMonitorFormoredetails,refertoth…

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Report No.: E202212139826-1 Page 2 of 20 Statement 1. The report is invalid without "special seal for inspection and testing"; some copies are invalid; The report is invalid if it is altered or missing; The report is invalid without the signature of the person who prepared, reviewed and approved it. 2. The sample information is provided by the client and responsible for its authenticity; The content of the report is only valid for the samples sent this time. 3. When there are reports in both Chinese and English, the Chinese version will prevail when the language problems are inconsistent. 4. If there is any objection concerning the report, please inform us within 15 days from the date of receiving the report. 5. Without the agreement of the laboratory, the client is not authorized to use the test results for unapproved propaganda. ------------ The following blanks ------------ Report No.: E202212139826-1 Page 3 of 20 TABLE OF CONTENTS 1. TEST RESULT SUMMARY ...................................................................................................................... 5 2. GENERAL DESCRIPTION OF EUT ......................................................................................................... 6 2.1 APPLICANT INFORMATION ...................................................................................................................... 6 2.2 MANUFACTURER ........................................................................................................................................ 6 2.3 FACTORY ...................................................................................................................................................... 6 2.4 BASIC DESCRIPTION OF EUT ................................................................................................................... 6 2.5 TEST SCENE .................................................................................................................................................. 6 2.6 SAMPLE WORK DESCRIPTION ................................................................................................................. 6 2.7 ASSISTIVE DEVICE INFORMATION......................................................................................................... 7 2.8 SAMPLE CONNECTION DIAGRAM .......................................................................................................... 7 3. LABORATORY .......................................................................................................................................... 8 4. MEASUREMENT UNCERTAINTY .......................................................................................................... 9 5. EQUIPMENT AND TOOLS USED DURING TEST .............................................................................. 10 6. ANTENNA RADIATION PERFORMANCE MEASUREMENT ........................................................... 11 6.1 LI MITS ......................................................................................................................................................... 11 6.2 TEST PROCEDURE ..................................................................................................................................... 11 6.3 CONFIGURATION OF SYSTEM UNDER TEST ...................................................................................... 12 6.4 TEST PHOTOS ............................................................................................................................................. 12 6.5 TEST RESULTS ........................................................................................................................................... 13 7. PHOTOGRAPH OF THE EUT ................................................................................................................. 19 ------------ The following blanks ------------ Report No.: E202212139826-1 Page 4 of 20 REPORT ISSUED HISTORY Report Version Report No. Description Compile Date 1.0 E202212139826-1 Original Issue 2023-03-15 ------------ The following blanks ------------ Report No.: E202212139826-1 Page 5 of 20 1. TEST RESULT SUMMARY Test Item Test Frequency Test Method Test Scene Test Result Gain 2400 MHz ~2500MHz ANSI IEEE 149-2021 Part 8 scene 1 / 1) Radiation efficiency 2400 MHz ~2500MHz ANSI IEEE 149-2021 Part 10 scene 1 / 1) Radiation pattern 2400 MHz ~2500MHz ANSI IEEE 149-2021 Part 7 scene 1 / 1) Note 1)：Customer-defined test, test results do not make judgment. ------------ The following blanks ------------ . Report No.: E202212139826-1 Page 6 of 20 2. GENERAL DESCRIPTION OF EUT 2.1 APPLICANT INFORMATION Name: Shenzhen Jamr Technology Co., Ltd. Address: A101-301, D101-201, Jamr Science & Technology Park, No. 2 Guiyuan Road, Guixiang Community, Guanlan Street, Longhua District, Shenzhen 518100, PEOPLE'S REPUBLIC OF CHINA 2.2 MANUFACTURER Name: Shenzhen Jamr Technology Co., Ltd. Address: A101-301, D101-201, Jamr Science & Technology Park, No. 2 Guiyuan Road, Guixiang Community, Guanlan Street, Longhua District, Shenzhen 518100, PEOPLE'S REPUBLIC OF CHINA 2.3 FACTORY Name: Shenzhen Jamr Technology Co., Ltd. Address: A101-301, D101-201, Jamr Science & Technology Park, No. 2 Guiyuan Road, Guixiang Community, Guanlan Street, Longhua District, Shenzhen 518100, PEOPLE'S REPUBLIC OF CHINA 2.4 BASIC DESCRIPTION OF EUT Product Name: Upper Arm Type Blood Pressure Monitor Product Model: Bluetooth module antenna gain Trade Name: / Product Size: / Software Version / Hardware Version / Antenna Type： PCB Antenna Frequency Band: 2400MHz – 2500MHz Sample submitting way: ■Provided by customer □Sampling Sample No: E202212139826-0001 Note: 2.5 TEST SCENE Scene Scene description Test scene 1 Free space 2.6 SAMPLE WORK DESCRIPTION Serial No. Work description a) The sample is erected according to the standard, so that the sample can be tested under normal operation Report No.: E202212139826-1 Page 7 of 20 2.7 ASSISTIVE DEVICE …

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Model No.: BE23T CE TEST SETUP RE TEST SETUP Model No.: BE23T RE TEST SETUP