OU9AW8001-LSBluetooth Module

Gua ngdongTranstekMedicalElectronicsCo.,Ltd 1 AW8001Bluetooth4.0module Specification Version1.0 20 13-7-25 Gua ngdongTranstekMedicalElectronicsCo.,Ltd 2 1.1Introduction TheAW8001Moduleisdesignedtobeusedinconjunctionwithanexternal mi crocontrollerrunningtheapplication.TheAW8001integratesacompletePHY,Link ControllerandHostsinglemodeBl uetoothlowenergysubsystemandfeaturesasimple SPIbasedinterfacetotheapplicationmicrocontroller.Qualifiedprofiles,APIsandexample applicationareprovidedaspartoftheμBl ueSDKwhichiseasilyportabletoarangeof di ffer entapplicationmicrocontrollers.ThissystemsegmentationallowstheAW8001tobe us edwi ththebest-fitmicrocontrollerforaspecificapplicationaswellaseaseintegration andendproductqualificationasapplicationandprotocolstackdoesnotsharethesame mic rocontroller. 1.2Features • BluetoothSpecificationv4.0compliantsinglemodelowenergysolution • Comp letePHY,LinkControllerandHostsubsystem • Pr ofilesandexampleapplicationsprovidedin μBlueSDK • Co standpoweroptimizedforslaveoperation • Si mpleSPIbasedApplicationControllerInterface(ACI) • FullL inkControllerandHostsecurity • 1 .9to3.6Voperation • Linearvoltageregulator • Step-downDC/DCvoltageregulatorprovidingupto20%peakcurrentreduction • Su b14m Apeakcurrentwithlinearvoltageregulator • Supportssub10μAaveragecurrentoperation • Batteryvoltagemonitor • Temperaturesensor 1 .3 APPLICATIONS • Sportsandfitnesssensors • Healthcareandmedicalsensors • Continua™VersionTwocertifiedproducts • Re mo tecontrols • Watches • Mob ilephoneperipherals • Automa tionsensors • Proxi mit ytags Gua ngdongTranstekMedicalElectronicsCo.,Ltd 3 2.1ProductInformation AW8001isaBT4.0Module,It’smainphysicalfeaturesaretheBluetoothlowenergy PHYandtheBluetoothlowenergystackthathandlesthelinkcontrollerandhoststack.It alsoincludesadditionalanalogsub-systemsneededfortheBluetoothlowenergyoperation, suchaspowermanagementandseveraloscillatoroptions. AW8001blockdiagram AW 8001hason-chipnon-volatilememoryforstoringserviceconfigurations.This on-chipstorageletsyouselectandcombinethenecessaryservicesforyourapplication, reducing therequirementsonyourapplicationcontrollerforhandlingallreal-time operationsrelatedtotheBluetoothlowenergycommunicationprotocol. AW8001includesapowersupplyvoltagemonitorandatemperaturesensorthat furtherreducestherequirementstotheapplicationcontroller.Thesefeaturesare accessiblethroughtheApplicationControllerInterface(ACI). AW8001alsooffersanoptionaloutputsignalthatisactivatedbeforether adio becomesactive.Thistimingsignalenablesyoutocontrolthepeakcurrentdrainofyour application,avoidingoverloadofyourpowersupply(formostapplicationsthisisusuallya sma llbattery).Youcanal sousethistimi ngsignaltocontroltheapplicationcircuitry, avoidingnoiseinterferencewhentheAW8001radioisoperating. A separateserialinterface(UART)givesyouaccesstotheBluetoothlowenergyDirect TestMode(DTM). ThisinterfaceisusedtocontroltheBluetoothlowenergyradio(RFPHY) andissupportedbycommerciallyavailableBluetoothtestequipmentuse dforBluetooth qualification.Thisserialinterfacealsoenablesyoutotestradioperformanceandto optimizeyourantenna. Gua ngdongTranstekMedicalElectronicsCo.,Ltd 4 2.2Operatingconditions TheoperatingconditionsarethephysicalparametersthatnRF8001canoperatewithin. 2.3DigitalI/Osignallevels ThedigitalI/OsignallevelsaredefinedTable.Theoperatingconditionsare:VDD=3.0V,TA =40oCto+85oC(unlessotherwisenoted). 2.4Radiocharacteristics nRF8001electricalcharacterizationisdefinedinTable.Theoperatingconditionsare: VDD=3.0V,TA=40oCto+85oC(unlessotherwisenoted). Gua ngdongTranstekMedicalElectronicsCo.,Ltd 5 3.1MechanicalInformation 3.2PINInformation VCC MOSI SCK /REQN MISO /RDYN NC RESET GND Gua ngdongTranstekMedicalElectronicsCo.,Ltd 6 3.3ModuleInstallation Step1:ConnecttheModuletotheconnector,thisconnectorcanbeaPCBorPinheaderor another,seefollowingpicture Step2:ConnecttheModulePCBAtotheMainPCBA,seefollowingpicture Step3:InstalltheMainPCBAtotheProduct,seefollowingpicture Caution:Wheninstallthemodule,youmustpayattentiontothe temperatureofthesolderingiron(thesolderingironshouldbeconnect toGround),thetem peratureshouldbesetatabout380°C;youmust payattentiontotheelectrostatictoo,takeactiontoavoidelectrostatic. Andyoumustavoidshortcircuitwhenyouconnectthemodule. ModuleFCCID:OU9AW8001-LS Gua ngdongTranstekMedicalElectronicsCo.,Ltd 7 Step4: The final Product, see following picture M ake sure that the module is fixed in the host and does not allow users to replace or demolition. Guangdong Transtek Medical Electronics Co., Ltd 8 Caution: Any changed or modifications not expressly approved by the party responsible for compliance could void the user`s authority to operate this equipment. 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. 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, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures: —Reorient or relocate the receiving antenna. —Increase the separation between the equipment and receiver. —Connect the equipment into an outlet on a circuit different from that to which the receiver is connected. —Consult the dealer or an experienced radio/TV technician fo…

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version:1.0 GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO., LTD Zone A, 5/F., Investment Building, No. 12, Huizhan East Rd., Torch Development District, Zhongshan, Guangdong, 528437, China TEL:86-760-88282982 www.transtek.cn Contains FCC ID: OU9AW8001-LS User Manual Glass Body Fat Analyzer LS203-B Please do read the user manual carefully and thoroughly so as to ensure the safe usage of this product, and keep the manual well for further reference in case you have problems. Thank you very much for selecting the Transtek Glass Body Fat Analyzer LS203-B. 1 Table of Contents Table of Contents Safety Information Your Scale and Its Environment Efficient Use of Your Scale Overview Device Components LCD Display Initial Start-Up General Instructions Insert the Batteries Install App and Pair-up Start Measuring Select Measurement Unit Daily Measurement Manage Your Health Data Transmission Troubleshooting Error Prompt When Measuring ... When Data Transmitting... Specifications Maintenance Warranty FCC Regulations Appendix Table of Body Fat Level Table of Body Water Level Health Tips – About Body Fat EMC Guidance 3 3 4 5 6 6 7 8 8 9 10 10-11 12 13 14 14 15 16 16 17 17-21 ............................................................................................... ...................................................................................................... ................................................................................................................. ................................................................................................................. .......................................................................................................... ............................................................................................................................. .................................................................................................................... .................................................................................................................. .................................................................................................................. ........................................................................................................ ............................................................................................................................ ............................................................................................................................... ...................................................................................................................................... ............................................................................................................ ...................................................................................................... ................................................................................................. ......................................................................................................................... .......................................................................................................... .............................................................................................................................. ................................................................................................................... ........................................................................................................................ Contraindications 3 . Indications For Use 2 Safety and Usage Information 2 ................................................................................................... ................................................................................................................ ...................................................................................................................... 23 Safety InformationSafety Information The warning signs and symbols are essential to ensure your correct and safe use of this product and protect you and others from injury. Please kindly find the meanings of the warning signs and symbols, which you may encounter in the label and user manual, as follows: Safety and Usage Information Symbol for “THE OPERATION GUIDE MUST BE READ” Transtek’s Body Fat Analyzer offers you a seamless way to manage your health. Please be aware that this device is designed for adults’ self-measuring and self-monitoring body fat level. Any information provided by this device is in no way meant to treat, cure or prevent any disease or illness from happening. This device should not be used by anyone who is acutely or chronically ill, suffering from a disease or taking medications that affect your water levels. The accuracy of readings for these patients has not been verified. Specific medical advice should be obtained from a physician. The device is equipped with automatic data transmission function. It may emit electromagnetic energy so as to perform its intended function. Nearby portable and mobile RF communications equipment can affect the performance of the device. Kindly note that the use of accessories, transducers or cables other than those specified, with the exception of transducers and cables sold by the manufacturer as replacement parts for internal components, may result in increased EMISSIONS or decreased IMMUNITY of the device. Be aware that misuse of electrical equipments can cause electric shock, burns, fire and other hazards. Symbol for “MANUFACTURER” Symbol for “COMPLIES WITH MDD 93/42/ECC REQUIREMENTS” Symbol for “ENVIRONMENT PROTECTION – Waste electrical products should not be disposed of with household waste. Please recycle where facilities exist. Check with your local authority or retailer for recycling advice” Symbol for “TYPE BF APPLIED PARTS” Symbol for “SERIAL NUMBER” Symbol for “DIRECT CURRENT” Symbol for “INDOOR USE ONLY” CAUTION I…

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022311 – 6 Request for Confidentiality Date: 2013-5-20 Subject: Confidentiality Request for: ______OU9AW8001-LS_____ Pursuant to FCC 47 CRF 0.457(d) and 0.459 and IC RSP-100, Section 10, the applicant requests that a part of the subject FCC application be held confidential. Type of Confidentiality Requested Exhibit Short Term Permanent Block Diagrams Short Term External Photos Short Term Permanent* 2 Internal Photos Short Term Permanent Operation Description/Theory of Operation Short Term Permanent Parts List & Placement/BOM Short Term Permanent Tune-Up Procedure Short Term Permanent Schematics Short Term Test Setup Photos Short Term Permanent* User’s Manual *Note: ______(Insert Explanation as Necessary)______ ______Guangdong Transtek Medical Electronics Co., Ltd______ has spent substantial effort in developing this product and it is one of the first of its kind in industry. Having the subject information easily available to "competition" would negate the advantage they have achieved by developing this product. Not protecting the details of the design will result in financial hardship. Permanent Confidentiality: The applicant requests the exhibits listed above as permanently confidential be permanently withheld from public review due to materials that contain trade secrets and proprietary information not customarily released to the public. Short-Term Confidentiality: The applicant requests the exhibits selected above as short term confidential be withheld from public view for a period of ___(specify number of days not to exceed 180 ) 3 ___ days from the date of the Grant of Equipment Authorization and prior to marketing. This is to avoid premature release of sensitive information prior to marketing or release of the product to the public. Applicant is also aware that they are responsible to notify ACB in the event information regarding the product or the product is made available to the public. ACB will then release the documents listed above for public disclosure pursuant to FCC Public Notice DA 04-1705. NOTE for Industry Canada Applications: The applicant understands that until such time that IC distinguishes between Short Term and Permanent Confidentiality, either type of marked exhibit above will simply be marked Confidential when submitted to IC. Sincerely, By: Charles Xie / _Compliance Engineer__ (Signature/Title 4 ) (Print name) 2 - The asterisked items (*) require further justification before permanent confidentiality will be allowed. These also currently require review by the FCC under their Permit-But-Ask policy before the grant is issued and can delay completion of an application. Further justification should be added to the note above. One such example for a potted device would be: “The EUT is FULLY potted using a non-removable epoxy based material. Removal of potting material causes irreparable damage to internal circuitry. See photographs exhibits that outline the device before and after potting.” 3 - Please refer to http://acbcert.com/documents/misc-docs/Memo-Short-Term-Vs-Standard-Confidentiality.pdf for complete details. 4 - Must be signed by applicant contact given for applicant on the FCC site, or by the authorized agent if an appropriate authorized agent letter has been provided. Letters should be placed on appropriate letterhead.

Modular Approval Request Letter FCC ID: OU9AW8001-LS Data: 2013-06-24 Gentlemen: There’s a BT4.0 (single mode) modular that would like to have your authorization as a modular approval. This modular transmitter complies with the modular tran smitters basic requiements (Item 1 to 8) in FCC Part 15 Subpart C Section 15.212 as indicated below: Company Guangdong Transtek Medical Electronics Co., Ltd Model Name AW8001 BT module Model Number AW8001 FCC ID OU9AW8001-LS Requirement of FCC Part 15 Subpart C Section 15.212 YES Reference to AW8001 1. The modular transmitter must have its own RF shi elding. NO The module havn’t its own RF shielding. 2. The modular transmitter must have buffered modul ation/data inputs. YES The modular has buffered data inputs, it is int egrated in chip NRF8001 . Please see schematic.pdf 3. The modular transmitter must have its own power supply regulation. YES All power lines derived from the host device are regulated before energizing other circuits internal to the AW8001 Please see schematic.pdf 4. The modular transmitter must comply with the anten na requirements of Section 15.203 and 15.204(c). YES The AW8001 meets the FCC antenna requirements. It has a unique connector. Please see external photo.pdf 5. The modular transmitter must be tested in a stan d ‐ alone configuration, i.e., the module must not be inside a nother device during testing. NO The AW8001 was tested in the host device configuration via a CO M extender. Please see conducted set ‐ up photo.pdf and spurious set ‐ up 6. The modular transmitter must be labeled with its own FCC ID number, and, if the FCC ID is not visible when the module is installed inside another device, then the outside of the device into which the module is installed must also display a label referr ing to the enclosed module. YES The label position of AW8001 is clearly indicated. Please see the label.pdf 7. The modular transmitter must comply with any specifi c rule or operating requirements applicable to the transmitter and the manufacturer must provide adequate instructions alon g with the module to explain any such requirements. A copy of the se instructions must be included in the application for equipment au thorization. YES The AW8001 is compliant with all applicable FCC rules. Detail i nstructions are given in the Users Manual. Please see Installation guide.pdf 8. The modular transmitter must comply with any applic able RF exposure requirements. For example, FCC Rules in Se ctions 2.1091, 2.1093 and specific Sections of Part 15, including 15. 319(i), 15.407(f), 15.253(f) and 15.255(g), require that Unlicensed PCS , UNII and millimeter wave devices perform routine environmenta l evaluation for RF Exposure to demonstrate compliance. In addition spread spectrum transmitters operating under Section 15.247 are requ ired to address RF Exposure compliance in accordance with Section 15.247( b)(4). YES The AW8001 comply with applicable RF exposure requirements. Plea se see RF safety evaluation. pdf Thank you. Sincerely, Charles Xie / _Compliance Engineer COMPANY: Guangdong Transtek Medical Electronics Co., Ltd Tel: +86-760-88282982 829 Fax: +86-760-85339231 Email: [email protected]

External Photos

2012.08.29 PO# Label ref: 1:1 Size ：9x1mm FCC ID: OU9AW8001-LS FCC ID: OU9AW8001-LS

Internal Photos

SGS-CSTC Standards Technical Services Co., Ltd. Application No..: GZEM1305001786RF Page: 1 of 1 FCC ID: OU9AW8001-LS This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for electronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm. Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Company’s findings at the time of its intervention only and within the limits of Client’s instructions, if any. The Company’s sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or appearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only. RF Exposure Compliance Requirement The product belongs to standalone portable device base the FCC rule part 2.1091&2.1093. The transmission frequencies of the device are between 100 MHz and 6 GHz. The worst case test separation distance is 5mm. The Max Conducted Output Power and SAR Test Exclusion Threshold (mW) are listed below: Transmit frequency (GHz) Max Conducted Output Power (mW) SAR Test Exclusion Threshold (mW) 2.402 0.53 9.7 2.440 0.58 9.6 2.480 0.68 9.5 The SAR Test Exclusion Threshold for 100 MHz to 6 GHz is calculated from: 1) 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  f(GHz) is the RF channel transmit frequency in GHz  Power and distance are rounded to the nearest mW and mm before calculation The result is rounded to one decimal place for comparison 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. According to SAR Exclusion Threshold in KDB 447498 (D01) General RF Exposure Guidance v05, the SAR report is not required.

SGS-CSTC Standards Technical Services Co., Ltd. 198 Kezhu Road, Scientech Park, Guangzhou Economic & Technological Development District, Guangzhou, China 510663 Telephone: +86 (0) 20 82155555 Fax: +86 (0) 20 82075059 Email: [email protected] Report No.: GZEM130500178601 Page: 1 of 47 FCC ID: OU9AW8001-LS Authorized Signature: Richard Li Manager The manufacturer should ensure that all products in series production are in conformity with the product sample detailed in this report. If the product in this report is used in any configuration other than that detailed in the report, the manufacturer must ensure the new system complies with all relevant standards. The report must not be used by the client to claim product certification, approval, or endorsement by NVLAP, NIST, or any agency of the federal government. All test results in this report can be traceable to National or International Standards. This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for electronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm. Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Company’s findings at the time of its intervention only and within the limits of Client’s instructions, if any. The Company’s sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or appearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only 1 Cover Page TEST REPORT Application No.: GZEM1305001786RF Applicant: Guangdong Transtek Medical Electronics Co., Ltd FCC ID: OU9AW8001-LS Product Name: Bluetooth Module Product Description: Wireless control Body Fat Analyzer with 2.4 GHz as carrier. Model No.: AW8001 Standards: 47 CFR PART 15 Subpart C: 2012 section 15.247 Date of Receipt: 2013-05-15 Date of Test: 2013-05-16 to 2012-05-29 Date of Issue: 2013-06-20 Test Result : Pass* * In the configuration tested, the EUT detailed in this report complied with the standards specified above. Please refer to section 3 of this report for further detail. SGS-CSTC Standards Technical Services Co., Ltd. Report No.: GZEM130500178601 Page: 2 of 47 FCC ID: OU9AW8001-LS This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for electronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm. Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Company’s findings at the time of its intervention only and within the limits of Client’s instructions, if any. The Company’s sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or appearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only. 2 Version Revision Record Version Chapter Date Modifier Remark 00 2013-06-20 Original Authorized for issue by: Tested By 2013-05-16 to 2012-05-29 (Storm Shu) /Signature Date Prepared By 2013-06-07 (Storm Shu) /Signature Date Checked By 2013-06-20 (Jeffrey Chen) /Reviewer Date SGS-CSTC Standards Technical Services Co., Ltd. Report No.: GZEM130500178601 Page: 3 of 47 FCC ID: OU9AW8001-LS This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for electronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm. Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Company’s findings at the time of its intervention only and within the limits of Client’s instructions, if any. The Company’s sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or appearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only. 3 Test Summary Test Test Requirement Test method Result Antenna Requirement FCC PART 15 C section 15.247 (c) and Section 15.203 FCC PART 15 C section 15.247 (c) and Section 15.203 PASS 6 dB Bandwidth FCC PART 15 C section 15.247 (a)(2) ANSI C63.10: Clause 6.9.1 PASS Maximum Peak …

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Test Setup Photos Radiated Spurious Emission Test Setup 30MHz to 1G: Above 1G: (full anechoic chamber)