ZRYPO3iHealth Pulse Oximeter

1 iHealth PO3 Fingertip Pulse Oximeter OPERATION GUIDE INDEX INTRODUCTION AND INTENDED USE........................................................................................ 2 CONTENTS AND DISPLAY INDICATORS...................................................................................... 2 PRODUCT DESCRIPTION ............................................................................................................ 3 SPECIFICATIONS......................................................................................................................... 3 CAUTIONS.................................................................................................................................. 3 Cautions .......................................................................................................................... 3 USING YOUR PULSE OXIMETER ................................................................................................. 5 CARE AND MAINTENANCE......................................................................................................... 6 TROUBLESHOOTING .................................................................................................................. 6 IMPORTANT INFORMATION REQUIRED BY THE FCC................................................................. 7 EXPLANATION OF SYMBOLS ON DEVICE ................................................................................... 7 SERVICE CENTER........................................................................................................................ 8 2 INTRODUCTION AND INTENDED USE Thank you for selecting iHealth Pulse Oximeter product. PO3 is intended to measure blood oxygen saturation (SpO 2 %)(the amount of oxygen in your blood) and pulse rate(bpm). It is designed for adult and can be used in family, homecare, commdevicey care. The PO3 is a medical device and is not intended to diagnose or treat any medical condition or disease. This Bluetooth pulse oximeter can be used with an iPod, iPhone or iPad. iPhone and iPod touch are trademarks of Apple Inc., registered in the U.S. and other countries. iPad is a trademark of Apple Inc. The iHealth Bluetooth pulse oximeter is designed for the following models: iPod touch 5th generation iPhone 4S iPhone 5 New iPad iPad 4 The iOS version of these device should be V5.0 or higher. iHealth is a trademark of iHealth Lab Inc. CONTENTS AND DISPLAY INDICATORS 3 PRODUCT DESCRIPTION Pulse oximeter measures the amount of oxygen in your blood and the pulse rate. The oximeter works by shining two light beams into the small blood vessels or capillaries of the finger, reflecting the amount of oxygen in the blood and displaying the measurement on the screen. The oxygen saturation(SpO2) is measured as a percentage of full capacity. Typically, a SpO2 reading between 96%-99% is considered normal. High altitudes and other factors may affect what is considered normal for a given individual. SPECIFICATIONS 1. Model: PO3 2. Display System: LED 3. Power Source: Battery 3.7V Li-ion 330mAh 4. peak wavelength: 660nm/880nm; 5. SpO2 Measuring Range: 70-99% 6. Average Root Mean Square(A RMS ) of SpO2 Accuracy: 70-99%, <2 digits; <70%, no definition. 7. Pulse Rate Measuring Range: 30-250bpm 8. Pulse Rate Accuracy: ±2bpm or ±2% larger one 9. Automatic Shut-off: After 8 seconds of no indication on the sensors 10. Operation Environment: 5°C-40°C; Humidity <80% 11. Storage Environment: -20°C-55°C; Humidity <95% CAUTIONS Cautions 1. Do not use the pulse oximeter in a magnetic resonance(MR) environment. 2. The pulse oximeter might misinterpret excessive movement as good pulse strength. Limit finger movement as much as possible when using the device. 3. Do not use the pulse oximeter on the same hand/arm when using a blood pressure cuff or monitor. 4. The pulse oximeter has no alarms and it will not sound if the amount of oxygen in your blood is low or if your pulse is too high or too low. 4 5. The pulse oximeter must be clean for a proper reading. 6. Your finger must be clean for proper reading. 7. Any of the following conditions may cause inaccurate measurements of the pulse oximeter, BUT NOT LIMITED TO: - Flickering or very bright light; - Poor blood circulation; - Low hemoglobin; - hypotension, severe vasoconstriction, severe anemia or hypothermia - Nail polish, and/or artificial nails; and - Any tests recently performed on you that required an injection of intravascular dyes 8. The pulse oximeter may not work if you have poor circulation. Rub your finger to increase circulation, or place the device on another finger. 9. The pulse oximeter measures oxygen saturation of functional hemoglobin. High levels of dysfunctional hemoglobin(caused by sickle cell anemia, carbon monoxide, etc.) could affect the accuracy of the measurements. 10. Do not use the pulse oximeter in a combustible environment(oxygen enriched environment). 11. Do not use the pulse oximeter outside the specified operating and storage temperature ranges. 12. Field strengths from fixed transmitters, such as base stations for radio(cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast towers and TV broadcast towers may affect accuracy. 13. The materials used in the pulse oximeter are conformed to the biocompatibility and nontoxic and no hazard to the body. 14. Use in emergency vehicles with communication systems may affect accuacy. 15. The packing material of the pulse oximeter is recyclable, and they must be collected and disposed according to the related regulation in the country or region where the package of the device or its accessories in opened. 16. Any material of the pulse oximeter that may cause pollution in the environment, must be collected disposed strictly compiled with the local rules and requirements. CHARGE THE BATTERY Plug the iHealth Pulse Oximeter PO3 into a USB port for three hours or until the battery indicator turns off. 5 USING YOUR PUL…

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Subject: Confidentiality Request for: _____FCC ID:ZRYPO3 THIS MUST BE SIGNED BY THE APPLICANT/AGENT AND SHOULD BE PLACED ON APPROPRIATE LETTERHEAD Request for Confidentiality Date: 2013-3-7 ____ 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* 1 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)______ _____Andon Health 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 ) 2 ___ 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: Project Manager_ ____ (Signature/Title 3 ) (Print name) 1 - 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.” 2 - Please refer to http://acbcert.com/documents/misc-docs/Memo-Short-Term-Vs-Standard-Confidentiality.pdf for complete details. 3 - 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.

SGS-CSTC Standards Technical Services (Shanghai)Co., Ltd. Report No.: SHEM1302000240ME －Appendix A Page: 1 of 4 Page 1 of 4 PO3 External Photos Application No.: SHEM1302000240ME Applicant: Andon Health Co., Ltd Address of Applicant: No. 3 JinPing Street, YaAn Road, Nankai District, Tianjin 300190, China Equipment Under Test (EUT): Product Name: Activity Monitor Brand Name: iHealth Model No.: PO3 SGS-CSTC Standards Technical Services (Shanghai)Co., Ltd. Report No.: SHEM1302000240ME －Appendix A Page: 2 of 4 Page 2 of 4 1 Contents Page 1 CONTENTS..........................................................................................................2 2 EXTERNAL PHOTOS........................................................................................3 SGS-CSTC Standards Technical Services (Shanghai)Co., Ltd. Report No.: SHEM1302000240ME －Appendix A Page: 3 of 4 Page 3 of 4 2 External Photos SGS-CSTC Standards Technical Services (Shanghai)Co., Ltd. Report No.: SHEM1302000240ME －Appendix A Page: 4 of 4 Page 4 of 4 End

SGS-CSTC Standards Technical Services (Shanghai)Co., Ltd. Report No.: SHEM1302000239ME －Appendix B Page: 1 of 5 Page 1 of 5 PO3 Internal Photos Application No.: SHEM1302000239ME Applicant: Andon Health Co., Ltd Address of Applicant: No. 3 JinPing Street, YaAn Road, Nankai District, Tianjin 300190, China Equipment Under Test (EUT): Product Name: Activity Monitor Brand Name: iHealth Model No.: PO3 SGS-CSTC Standards Technical Services (Shanghai)Co., Ltd. Report No.: SHEM1302000239ME －Appendix B Page: 2 of 5 Page 2 of 5 1 Contents Page 1 CONTENTS..........................................................................................................2 2 INTERNAL PHOTOS.........................................................................................3 SGS-CSTC Standards Technical Services (Shanghai)Co., Ltd. Report No.: SHEM1302000239ME －Appendix B Page: 3 of 5 Page 3 of 5 2 Internal Photos SGS-CSTC Standards Technical Services (Shanghai)Co., Ltd. Report No.: SHEM1302000239ME －Appendix B Page: 4 of 5 Page 4 of 5 SGS-CSTC Standards Technical Services (Shanghai)Co., Ltd. Report No.: SHEM1302000239ME －Appendix B Page: 5 of 5 Page 5 of 5 End

SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. 588 W est Jindu Road,Songjiang District,Shanghai,China Telephone: +86 (0) 21 6191 5666 Fax: +86 (0) 21 6191 5678 [email protected] Report No.: SHEM130200024001 Page 1 of 40 Tony Wu E&E Section Manager SGS-CSTC (Shanghai) Co., Ltd. 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 FCC Part 15C TEST REPORT Application No. : SHEM1302000240ME Applicant: Andon Health Co., Ltd FCC ID: ZRYPO3 Equipment Under Test (EUT): NOTE: The following sample(s) submitted was/were identified on behalf of the client as Product Name: iHealth Pulse Oximeter Brand Name: iHealth Model: PO3 Added Model: N/A Standards: FCC PART 15 Subpart C: 2011 Date of Receipt: Feb.22, 2013 Date of Test: Feb.27, 2013 to Mar.07, 2013 Date of Issue: Mar.15, 2013 Test Result : PASS * *In the configuration tested, the EUT detailed in this report complied with the standards specified above. SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. Report No.: SHEM130200024001 Page: 2 of 40 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 thesample(s) tested and such sample(s) are retained for 90 days only Version Revision Record Version Chapter Date Modifier Remark 00 / Mar.15, 2013 / Original Authorized for issue by: Engineer Zenger Zhang Print Name Clerk Amy Wang Print Name Reviewer Keny Xu Print Name SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. Report No.: SHEM130200024001 Page: 3 of 40 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 thesample(s) tested and such sample(s) are retained for 90 days only 2 Test Summary Test Item Test Requirement Test method Result Antenna Requirement FCC Part 15, Subpart C Section 15.203/15.247 (c) --- PASS AC Power Line Conducted Emission FCC Part 15, Subpart C Section 15.207 ANSI C63.10 (2009) Section 6.2 PASS Minimum 6dB Bandwidth FCC Part 15, Subpart C Section 15.247 (a)(2) ANSI C63.10 (2009) Section 6.9 PASS Conducted Peak Output Power FCC Part 15, Subpart C Section 15.247 (b)(3) ANSI C63.10 (2009) Section 6.10 PASS Power Sp…

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SGS-CSTC Standards Technical Services（ （（ （Shanghai） ）） ） Co., Ltd. No. 588 West Jindu Road, Songjiang District, Shanghai, China Telephone: +86 (0) 21 61915666 Fax: +86 (0) 21 61915678 [email protected] Report No.: SHEM130200024005 Page 1 of 9 Tony Wu E&E Section Manager SGS-CSTC (Shanghai) Co., Ltd. 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 FCC MPE REPORT Application No.: SHEM1302000240ME Applicant: Andon Health Co., Ltd Equipment Under Test (EUT): NOTE: The following sample(s) submitted was/were identified on behalf of the client as Product Name: iHealth Pulse Oximeter Brand Name: iHealth Model: PO3 Added Model: N/A FCC ID: ZRYPO3 Standards: 47 CFR Part 1.1307(2011) 47 CFR Part 2.1093 (2011) KDB447498 D01 Date of Receipt: Feb.22, 2013 Date of Test: Feb.27, 2013 Date of Issue: Mar.15, 2013 Test Result : PASS* * In the configuration tested, the EUT complied with the standards specified above. SGS-CSTC Standards Technical Services（ （（ （Shanghai） ）） ） Co., Ltd. Report No.: SHEM130200024005 Page: 2 of 9 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 thesample(s) tested and such sample(s) are retained for 90 days only Version Revision Record Version Chapter Date Modifier Remark 00 / Mar.15, 2013 / Original Authorized for issue by: Zenger Zhang Engineer Print Name Amy Wang Clerk Print Name Keny Xu Reviewer Print Name SGS-CSTC Standards Technical Services（ （（ （Shanghai） ）） ） Co., Ltd. Report No.: SHEM130200024005 Page: 3 of 9 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 thesample(s) tested and such sample(s) are retained for 90 days only 2 Contents Page 1 COVER PAGE .............................................................................................................. 1 VERSION.............................................................................................................................................1 VERSION.............................................................................................................................................2 2 CONTENTS.…

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SGS-CSTC Standards Technical Services (Shanghai)Co., Ltd. Report No.: SHEM1302000240ME －Appendix C Page: 1 of 4 Page 1 of 4 PO3 Test Setup Photos Application No.: SHEM1302000240ME Applicant: Andon Health Co., Ltd Address of Applicant: No. 3 JinPing Street, YaAn Road, Nankai District, Tianjin 300190, China Equipment Under Test (EUT): Product Name: Activity Monitor Brand Name: iHealth Model No.: PO3 SGS-CSTC Standards Technical Services (Shanghai)Co., Ltd. Report No.: SHEM1302000240ME －Appendix C Page: 2 of 4 Page 2 of 4 1 Contents Page 1 CONTENTS..........................................................................................................2 2 TEST PHOTOS...................................................................................................3 2.1 RADIATED EMISSION TEST SETUP....................................................................3 2.2 CONDUCTED EMISSIONS ON MAINS TERMINALS TEST SETUP...........................4 SGS-CSTC Standards Technical Services (Shanghai)Co., Ltd. Report No.: SHEM1302000240ME －Appendix C Page: 3 of 4 Page 3 of 4 2 Test Photos 2.1 Radiated Emission Test Setup 30MHz to 1GHz Above 1GHz SGS-CSTC Standards Technical Services (Shanghai)Co., Ltd. Report No.: SHEM1302000240ME －Appendix C Page: 4 of 4 Page 4 of 4 Zoom View 2.2 Conducted Emissions on Mains Terminals Test Setup End