2ACHL-A10STACDWireless Continuous Positive Airway Pressure Device

User guide User guide English 288010 cover.indd 230/09/2015 1:55:25 PM 288010 cover.indd 330/09/2015 1:55:25 PM English 1 ENGLISH Welcome The AirCurve ™ 10 ST-A is a bilevel positive airway pressure device. WARNING Read this entire guide before using the device. CAUTION In the US, Federal law restricts this device to sale by or on the order of a physician. Indications for use AirCurve 10 ST-A The AirCurve 10 ST-A device is indicated to provide non-invasive ventilation for patients weighing more than 30 lb (13 kg) or more than 66 lb (30 kg) in iVAPS mode with respiratory insufficiency or obstructive sleep apnea (OSA). It is intended for home and hospital use. The humidifier is intended for single patient use in the home environment and re-use in a hospital/institutional environment. Contraindications Positive airway pressure therapy may be contraindicated in some patients with the following pre-existing conditions:  severe bullous lung disease  pneumothorax or pneumomediastinum  pathologically low blood pressure, particularly if associated with intravascular volume depletion  dehydration  cerebrospinal fluid leak, recent cranial surgery, or trauma. Adverse effects You should report unusual chest pain, severe headache, or increased breathlessness to your prescribing physician. An acute upper respiratory tract infection may require temporary discontinuation of treatment. The following side effects may arise during the course of therapy with the device:  drying of the nose, mouth, or throat  nosebleed  bloating  ear or sinus discomfort  eye irritation  skin rashes. 2 At a glance The AirCurve 10 ST-A includes the following:  Device  HumidAir ™ humidifier (if supplied)  Air tubing  Power supply unit  Travel bag  SD card (already inserted). Contact your care provider for a range of accessories available for use with the device including:  Air tubing (heated and non-heated): ClimateLineAir ™ , ClimateLineAir Oxy, SlimLine ™ , Standard  HumidAir humidifier  Side cover for use without the humidifier  Filter: Hypoallergenic filter, standard filter  Air10 ™ DC/DC converter (12V/24V)  SD card reader  Air10 oximeter adapter  Air10 USB adapter  Power Station II  Air10 tubing elbow English 3 About your device 1 Air outlet 6 HumidAir humidifier 2 Air filter cover 7 Screen 3 Retention clip 8 Adapter cover 4 Power inlet 9 SD card cover 5 Serial number and device number 10 LED alarm indicator About the control panel Start/Stop button Press to start/stop therapy. Press and hold for three seconds to enter power save mode. Dial Turn to navigate the menu and press to select an option. Turn to adjust a selected option and press to save your change. Home button Press to return to the Home screen. Different icons may be displayed on the screen at different times including: Ramp Time Wireless signal strength (green) Humidity Wireless transfer not enabled (grey) Humidifier warming No wireless connection Humidifier cooling Airplane Mode Alarm muted 4 Setup CAUTION Do not overfill the humidifier as water may enter the device and air tubing. 1. With the device on a stable level surface, grip the retention clip on the back of the device and pull up to open. Note: The retention clip is shown in the open position. 2. (a) Plug the power connector into the device power inlet then (b) push down the retention clip to secure in place. Connect one end of the power cord into the power supply unit and the other end into the power outlet. 3. Connect the air tubing firmly to the air outlet located on the rear of the device. 4. Open the humidifier and fill it with water up to the maximum water level mark. Do not fill the humidifier with hot water. 5. Close the humidifier and insert it into the side of the device. 6. Connect the free end of the air tubing firmly onto the assembled mask. See the mask user guide for detailed information. Recommended masks are available on www.resmed.com. Note: Ensure the device is placed so that the LED alarm indicator is clearly visible. English 5 Starting therapy 1. Fit your mask. 2. Press Start/Stop or breathe normally if SmartStart ™ is enabled. You will know that therapy is on when the Monitoring screen is displayed. The pressure bar shows the inspiratory and expiratory pressures in green. The green bar will expand and contract as you breathe in and out. The screen will go black automatically after a short period of time. You can press Home or the dial to turn it back on. If power is interrupted during therapy, the device will automatically restart therapy when power is restored. The AirCurve 10 ST-A device has a light sensor that adjusts the screen brightness based on the light in the room. Stopping therapy 1. Remove your mask. 2. Press Start/Stop or if SmartStart is enabled, therapy will stop automatically after a few seconds. Note: If Confirm Stop is enabled, a message is displayed asking if you want to stop therapy. Turn the dial to select Yes and then press the dial to stop therapy. Once therapy has stopped, the Sleep Report gives you a summary of your therapy session. Usage hours –Indicates the number of hours of therapy you received last session. Mask Seal–Indicates how well your mask sealed: Good mask seal. Needs adjusting, see Mask Fit. Humidifier–Indicates if your humidifier is working properly: Humidifier working. Humidifier might be faulty, contact your care provider. If set by your care provider, you will also see: Events per hour–Indicates the number of apneas and hypopnoeas experienced per hour. More Info–Turn the dial to scroll down to view more detailed usage data. 6 Power save mode Your AirCurve 10 ST-A device records your therapy data. In order to allow it to transmit the data to your care provider, you should not unplug the device. However, you can put it into power save mode to save electricity. To enter power save mode:  Press and hold Start/Stop for three seconds. The screen goes black. To exit power save mode:  Press Start/Stop once. The Home sc…

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20 April 2015 To whom it may concern Subject: Signature Delegation Regarding documents issued by ResMed Ltd to CETECOM for the purposes of obtaining Federal Communications Commission (FCC) and Industry Canada (IC) Registrations for AirSense, and AirCurve Series with 3G, Mr David Mulcahy – VP Product Development, is authorised to sign on my behalf. Sincerely, Greg Dockar | Senior Regulatory Affairs Manager | ResMed Ltd. 1 Elizabeth Macarthur Drive | Bella Vista NSW 2153, Australia  Office: +61 2 8884 2175 |Cell: +61 (0) 418 226 401  E-mail and : [email protected] |  www.resmed.com ResMed Ltd 1 Elizabeth Macarthur Drive Bella Vista NSW 2153 Australia T +61 (2) 8884 1000 F +61 (2) 8884 2000 E [email protected] ABN 30 003 765 142 ResMed.com

External Front Side View External Back Side View External Left Side of Device External Right Side of Device Therapy Hose AC/DC Power Supply

Display Side of Flow Generator Mother Board Back of Flow Generator Mother Board Cellular Module & Antenna Side of CAM_Board CPU side of CAM Board Alarm PCB Top Side Alarm PCB Bottom Bottom Side Front of device with Cover removed

Test Report No.: NK-12-R-098 FCC and IC Certification Telit Communications S.p.A. FCC ID: RI7CE910-DUAL / IC: 5131A-CE910DUAL Page 47 of 52 Appendix C – EUT Photographs ● Front Side View of EUT Test Report No.: NK-12-R-098 FCC and IC Certification Telit Communications S.p.A. FCC ID: RI7CE910-DUAL / IC: 5131A-CE910DUAL Page 48 of 52 ● Rear Side View of EUT Test Report No.: NK-12-R-098 FCC and IC Certification Telit Communications S.p.A. FCC ID: RI7CE910-DUAL / IC: 5131A-CE910DUAL Page 49 of 52 ● Side View of EUT Test Report No.: NK-12-R-098 FCC and IC Certification Telit Communications S.p.A. FCC ID: RI7CE910-DUAL / IC: 5131A-CE910DUAL Page 50 of 52 ● Side View of EUT Test Report No.: NK-12-R-098 FCC and IC Certification Telit Communications S.p.A. FCC ID: RI7CE910-DUAL / IC: 5131A-CE910DUAL Page 52 of 52 ● View of Antenna

© 2015 RF Exposure Lab, LLC This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. 802 N. Twin Oaks Valley Road, Suite 105 • San Marcos, CA 92069 • U.S.A. TEL (760) 471-2100 • FAX (760) 471-2121 http://www.rfexposurelab.com CERTIFICATE OF COMPLIANCE SAR EVALUATION ResMed Ltd. Dates of Test: September 18, 2015 1 Elizabeth Macarthur Drive Test Report Number: SAR.20150907 Bella Vista, NSW 2153 Revision A Australia This wireless mobile and/or portable device has been shown to be compliant for localized specific absorption rate (SAR) for uncontrolled environment/general exposure limits specified in ANSI/IEEE Std. C95.1-1992 and had been tested in accordance with the measurement procedures specified in IEEE 1528-2013 and IEC 62209-2:2010 (See test report). I attest to the accuracy of the data. All measurements were performed by myself or were made under my supervision and are correct to the best of my knowledge and belief. I assume full responsibility for the completeness of these measurements and vouch for the qualifications of all persons taking them. RF Exposure Lab, LLC certifies that no party to this application is subject to a denial of Federal benefits that includes FCC benefits pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. 853(a). Jay M. Moulton Vice President Testing Cert. # 2387.01 FCC ID: 2ACHL-A10STACD Model(s): 28326 Marketing Names: AirCurve 10 ST-A Hardware Version: BOM 28326 Software Version: SX558 Test Sample: Engineering Unit Same as Production Serial Number: 22151827473 Equipment Type: Wireless CPAP Device Classification: Portable Transmitter Next to Body TX Frequency Range: 824 – 848 MHz, 1850 – 1910 MHz Frequency Tolerance: ± 2.5 ppm Maximum RF Output: 850 MHz (CDMA) – 25.0 dBm; 1900 MHz (CDMA) – 25.0 dBm Conducted Signal Modulation: CDMA Antenna Type: Internal Application Type: Certification FCC Rule Parts: Part 2, 22H, 24E KDB Test Methodology: KDB 447498 D01 v05r02, KDB 941225 D01 v02 Industry Canada: RSS-102 Issue 5, Safety Code 6 Max. Stand Alone SAR Value: 0.56 W/kg Reported Separation Distance: 20 mm – End; 0 mm All Other Sides Report Number: SAR.20150907 © 2015 RF Exposure Lab, LLC Page 2 of 75 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. Table of Contents 1. Introduction ................................................................................................................................... 3 SAR Definition [5] .............................................................................................................................. 4 2. SAR Measurement Setup .............................................................................................................. 5 Robotic System ................................................................................................................................. 5 System Hardware .............................................................................................................................. 5 System Electronics ............................................................................................................................ 6 Probe Measurement System ............................................................................................................. 6 3. Probe and Dipole Calibration ....................................................................................................... 14 4. Phantom & Simulating Tissue Specifications ............................................................................... 15 Head & Body Simulating Mixture Characterization .......................................................................... 15 5. ANSI/IEEE C95.1 – 1992 RF Exposure Limits [2] ........................................................................ 16 Uncontrolled Environment ............................................................................................................... 16 Controlled Environment ................................................................................................................... 16 6. Measurement Uncertainty............................................................................................................ 17 7. System Verification ...................................................................................................................... 18 Tissue Verification ........................................................................................................................... 18 Test System Verification .................................................................................................................. 18 8. SAR Test Data Summary ............................................................................................................ 19 Procedures Used To Establish Test Signal ..................................................................................... 19 Device Test Condition ..................................................................................................................... 19 9. FCC 3G Measurement Procedures ............................................................................................. 20 9.1 Procedures Used to Establish RF Signal for SAR ................................................................ 20 9.2 SAR Measurement Conditions for CDMA2000 .................................................................... 20 SAR Data Summary – 835 MHz Body - CDMA ............................................................................... 24 SAR Data Summary – 1900 MHz Body - CDMA ............................................................................. 25 10. Test Equipment List ................................................................................................................. 26 11. Conclusion ........................................................................................…

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Test Report No.: NK-12-R-098 FCC and IC Certification Telit Communications S.p.A. FCC ID: RI7CE910-DUAL / IC: 5131A-CE910DUAL Page 2 of 52 TABLE OF CONTENTS 1. Scope 4 2. Introduction (Site Description) 5 2.1 Test facility 5 2.2 Accreditation and listing 6 3. Test Conditions & EUT Information 7 3.1 Operating During Test 7 3.2 Environmental Conditions 7 3.3 Description of EUT 7 4. Measuring Instrument Calibration 8 5. Summary of Test Results 9 6. Recommendation / Conclusion 9 7. Description of Test 10 7.1 Effective Radiated Power / Equivalent Isotropic Radiated Power 10 7.2 Radiated Spurious & Harmonic Emission 11 7.3 Conducted Output Power 12 7.4 Conducted Spurious Emission 13 7.5 Frequency Stability / Temperature Variation 15 7.6 Conducted Output Power 16 8. Test Data 17 8.1 Conducted Output Power 17 8.2 Effective Radiated Power (ERP) 18 8.3 Equivalent Isotropic Radiated Power (EIRP) 19 8.4 Occupied Bandwidth / 26 dB Emission Bandwidth 20 8.5 Radiated Spurious & Harmonic Emission (Cellular) 21 8.6 Radiated Spurious & Harmonic Emission (PCS) 23 8.7 Frequency Stability / Temperature Variation (Cellular) 25 8.8 Frequency Stability / Temperature Variation (PCS) 26 8.9 Receiver Spurious Emissions 27 Test Report No.: NK-12-R-098 FCC and IC Certification Telit Communications S.p.A. FCC ID: RI7CE910-DUAL / IC: 5131A-CE910DUAL Page 3 of 52 9. Accuracy of Measurement 28 10. Test Plots (Cellular) 30 11. Test Plots (PCS) 37 12. Test Equipment List 44 Appendix A: Labelling Requirement 45 Appendix B: Photographs of Test Set-up 46 Appendix C: EUT Photographs 47 Test Report No.: NK-12-R-098 FCC and IC Certification Telit Communications S.p.A. FCC ID: RI7CE910-DUAL / IC: 5131A-CE910DUAL Page 4 of 52 1. Scope Measurement and determination of electromagnetic emissions (EME) of radio frequency devices including intentional and/or unintentional radiators for compliance with the technical rules and regulations of the Federal Communications Commission under FCC Part 2 & Part 22 & 24 and Industrie Canada under RSS-Gen & 132 & 133. Responsible Party : Contact Person : Manufacturer : Telit Communications S.p.A. Brian Tucker Tel No. : +919 439 7977 Telit Communications S.p.A. Viale Stazione di Prosecco 5/B, 34010 Sgonico, Trieste, Italy  FCC ID: RI7CE910-DUAL  IC 5131A-CE910DUAL  Model: CE910-DUAL  Brand Name: Telit  EUT Type: DUAL BAND CDMA Module  Classification: Licensed Potable Transmitter(PCB)  Applied Standard: FCC 47 CFR Part & 2, 22, 24 RSS-Gen, 132,133  Test Procedure(s): ANSI C63.4 (2003)  Dates of Test: June 18, 2012 ~ July 25, 2012  Place of Tests: Nemko Korea Co., Ltd. Test Report No.: NK-12-R-098 FCC and IC Certification Telit Communications S.p.A. FCC ID: RI7CE910-DUAL / IC: 5131A-CE910DUAL Page 5 of 52 2. Introduction (Site Description) 2.1 Test facility The measurement procedure described in American National Standard for Methods of Measurement of Radio-Noise Emissions from Low-Voltage Electrical and Electronic Equipment in the Range of 9 kHz to 40 GHz (ANSI C63.4-2003) was used in determining radiated and conducted emissions emanating from Telit Communications S.p.A. FCC ID : RI7CE910-DUAL and IC: 5131A-CE910DUAL These measurement tests were conducted at Nemko Korea Co., Ltd. The site address is 300-2, Osan-Ri, Mohyeon-Myeon, Cheoin-Gu, Yongin-Si, Gyeonggi-Do, KOREA The area of Nemko Korea Corporation Ltd. Test site is located in a mountain area at 80 kilometers (48 miles) southeast and Incheon International Airport (Incheon Airport), 30 kilometers (18miles) south-southeast from central Seoul. It is located in the valley surrounded by mountains in all directions where ambient radio signal conditions are quiet and a favorable area to measure the radio frequency interference on open field test site for the computing and ISM devices manufactures. The detailed description of the measurement facility was found to be in compliance with the requirements of §2.948 according to ANSI C63.4 2003. Fig. 1. The map above shows the Seoul in Korea vicinity area. The map also shows Nemko Korea Corporation Ltd. and Incheon Airport. Nemko Korea Co., Ltd. 67-1 & 300-2,Osan-Ri,Mohyeon- Myeon, Cheoin-Gu, Yongin-Si, Gyunggi-Do, KOREA 449-852 Tel) +82-31-322-1700 Fax) +82-31-322-2332 Test Report No.: NK-12-R-098 FCC and IC Certification Telit Communications S.p.A. FCC ID: RI7CE910-DUAL / IC: 5131A-CE910DUAL Page 6 of 52 2.2 Accreditation and listing Accreditation type Accreditation number FCC part 15/18 Filing site Registration No. 97992 CAB Accreditation for DOC Designation No. KR0026 KOLAS Accredited Lab. (Korea Laboratory Accreditation Scheme) Registration No. 155 Canada IC Registered site Site No. 2040E VCCI registration site(RE/CE/Telecom CE) Member No. 2118 EMC CBTL - KCC(RRL)Designated Lab. Registration No. KR0026 SASO registered Lab and Certification Body Registration No. 2008-15 Test Report No.: NK-12-R-098 FCC and IC Certification Telit Communications S.p.A. FCC ID: RI7CE910-DUAL / IC: 5131A-CE910DUAL Page 7 of 52 3. Test Conditions & EUT Information 3.1 Operating During Test The EUT was tested at the lowest channel, middle channel and the highest channel with maximum RF power and all data were recorded in the report. 3.2 Environmental Conditions Temperature 24°C ~ 28°C Relative Humidity 30% ~ 55% 3.3 Description of EUT Frequency Band Tx 824.70 MHz ~ 848.31 MHz 1851.25 MHz ~ 1908.75 MHz Rx 869.70 MHz ~ 893.31 MHz 1931.25 MHz ~ 1988.75 MHz Output Power (Conducted power) Cellular CDMA : 0.292 W(24.65 dBm) PCS CDMA : 0.278 W(24.44 dBm) Emission Designator 1M28F9W Antenna Type Magnet Mount Antennas Antenna Gain 5.12 dBi for Cellular, 6.12 dBi for PCS Dimensions 28.2 mm(W) x 28.2 mm(D) x 2.4 mm(H) Weight Approx. 4.7 g Operating Temperature -30°C ~ +85 °C Test Report No.: NK-12-R-098 FCC and IC Certification Telit Communications S.p.A. FCC ID: RI7CE910-DUAL / IC: 5131A-CE910DUAL Page 8 of 52 4. Measuring Instrument Calibration All measurements were made with instruments calibrated according to the recomme…

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FCC Recognized A2LA Accredited IC recognized # 3462E-1 CETECOM Inc. 6370 Nancy Ridge Drive Suite 101  San Diego, CA 92121  U.S.A. Phone: + 1 (858) 362 2400  Fax: + 1 (858) 587 4809  E-mail: [email protected]  http://www.cetecom.com CETECOM Inc. is a Delaware Corporation with Corporation number: 2905571 V5.0 2015-10-27 © Copyright by CETECOM FCC Test Report ResMed Ltd. Model Number: 28326 Product Description: Continuous Positive Airway Pressure (CPAP) Device FCC ID: 2ACHL-A10STACD 47 CFR Part 22, 24 TEST REPORT #: EMC_CONN-046-15001_FCC 22_24_WWAN_v1.2 DATE: 11/14/2015 Test Report #: EMC_CONN-046-15001_FCC 22_24_WWAN_v1.2 FCC ID: 2ACHL-A10STACD Date of Report: 11/14/2015 Page 2 of 45 Table of Contents 1 Assessment ............................................................................................................................... 3 2 Administrative Data ................................................................................................................. 4 2.1 Identification of the Testing Laboratory Issuing the Test Report .................................................. 4 2.2 Identification of the Client ............................................................................................................. 4 2.3 Identification of the Manufacturer ................................................................................................. 4 3 Equipment under Test (EUT) ................................................................................................... 5 3.1 Specification of the Equipment under Test .................................................................................... 5 3.2 Identification of the Equipment under Test (EUT) ........................................................................ 6 3.3 Identification of Accessory equipment........................................................................................... 6 3.4 Environmental conditions during Test: .......................................................................................... 6 3.5 Dates of Testing: ............................................................................................................................ 6 4 Subject of Investigation ............................................................................................................ 7 5 Summary of Measurement Results .......................................................................................... 8 6 Measurements......................................................................................................................... 10 6.1 RF Power Output .......................................................................................................................... 10 References ............................................................................................................................ 10 6.1.1 Measurement requirements: ................................................................................................. 10 6.1.2 Limits: .................................................................................................................................. 10 6.1.3 Conducted Output Power Measurement .............................................................................. 11 6.1.4 6.2 Spurious Emissions Radiated ....................................................................................................... 13 References ............................................................................................................................ 13 6.2.1 Measurement requirements: ................................................................................................. 13 6.2.2 Limits: .................................................................................................................................. 13 6.2.3 Radiated out of band measurement procedure: ................................................................... 15 6.2.4 Sample Calculations for Radiated Measurements ............................................................... 16 6.2.5 Measurement Survey: ........................................................................................................... 16 6.2.6 Test Conditions: ................................................................................................................... 16 6.2.7 Test Results for Radiated Spurious Emissions: .................................................................... 17 6.2.8 7 Test Equipment and Ancillaries used for tests ....................................................................... 44 8 Revision History ..................................................................................................................... 45 Test Report #: EMC_CONN-046-15001_FCC 22_24_WWAN_v1.2 FCC ID: 2ACHL-A10STACD Date of Report: 11/14/2015 Page 3 of 45 1 Assessment The following device was tested against the applicable criteria specified in FCC rules parts 2, 22 and 24 of Title 47 of the Code of Federal Regulations. No deviations were ascertained during the course of the tests performed. Company Description Model # ResMed Ltd. Continuous Positive Airway Pressure (CPAP) Device 28326 Responsible for Testing Laboratory: 11/14/2015 Compliance Milton Ponce de Leon (Test Lab Manager) Date Section Name Signature Responsible for the Report: 11/14/2015 Compliance Anthony Planinac (EMC Engineer) Date Section Name Signature The test results of this test report relate exclusively to the test item specified in Section3. CETECOM Inc. USA does not assume responsibility for any conclusions and generalizations drawn from the test results with regard to other specimens or samples of the type of the equipment represented by the test item. The test report may only be reproduced or published in full. Reproduction or publication of extracts from the report requires the prior written approval of CETECOM Inc. USA. Test Report #: EMC_CONN-046-15001_FCC 22…

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FCC: Recognized A2LA Accredited IC recognized # 3462E-1 CETECOM Inc. 6370 Nancy Ridge Drive Suite 101  San Diego, CA 92121  U.S.A. Phone: + 1 (858) 362 2400  Fax: + 1 (858) 587 4809  E-mail: [email protected]  http://www.cetecom.com CETECOM Inc. is a Delaware Corporation with Corporation number: 2113686 V4.0 2012-07-20 The BLUETOOTH trademarks are owned by Bluetooth SIG, Inc., U.S.A. and licensed to CETECOM Inc. © Copyright by CETECOM EMC_CONN-046-15001_TEST_PHOTOS FOR ResMed Ltd. Model Number: 28326 Product Description: Continuous Positive Airway Pressure (CPAP) Device FCC ID: 2ACHL-A10STACD Test Report #: EMC_CONN-046-15001 FCC ID: 2ACHL-A10STACD Date of Report 10-13-2015 1 Conducted Unit Test Report #: EMC_CONN-046-15001 FCC ID: 2ACHL-A10STACD Date of Report 10-13-2015 Test Report #: EMC_CONN-046-15001 FCC ID: 2ACHL-A10STACD Date of Report 10-13-2015 Test Report #: EMC_CONN-046-15001 FCC ID: 2ACHL-A10STACD Date of Report 10-13-2015 2 Radiated unit Test Report #: EMC_CONN-046-15001 FCC ID: 2ACHL-A10STACD Date of Report 10-13-2015 Test Report #: EMC_CONN-046-15001 FCC ID: 2ACHL-A10STACD Date of Report 10-13-2015 3 AC conducted setup Test Report #: EMC_CONN-046-15001 FCC ID: 2ACHL-A10STACD Date of Report 10-13-2015 Radiated Setup 9 kHz – 30 MHz: Test Report #: EMC_CONN-046-15001 FCC ID: 2ACHL-A10STACD Date of Report 10-13-2015 4 Radiated Setup 30 MHz – 1 GHz: Test Report #: EMC_CONN-046-15001 FCC ID: 2ACHL-A10STACD Date of Report 10-13-2015 5 Radiated Setup 1 GHz – 3 GHz: Test Report #: EMC_CONN-046-15001 FCC ID: 2ACHL-A10STACD Date of Report 10-13-2015 6 Radiated Setup 3 GHz – 18 GHz:

Report Number: SAR.20150304 © 2015 RF Exposure Lab, LLC Page 37 of 75 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. Appendix C – SAR Test Setup Photos Test Position End 20 mm Gap Report Number: SAR.20150304 © 2015 RF Exposure Lab, LLC Page 38 of 75 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. Test Position Top 0 mm Gap Report Number: SAR.20150304 © 2015 RF Exposure Lab, LLC Page 39 of 75 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. Test Position Front 0 mm Gap Report Number: SAR.20150304 © 2015 RF Exposure Lab, LLC Page 40 of 75 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. Front of Device Report Number: SAR.20150304 © 2015 RF Exposure Lab, LLC Page 41 of 75 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. Antenna Distances in Device to Back Top and Bottom Antenna Size 35mm x 5mm x 6mm Report Number: SAR.20150304 © 2015 RF Exposure Lab, LLC Page 42 of 75 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. Antenna Location on Back & Distance to End Report Number: SAR.20150304 © 2015 RF Exposure Lab, LLC Page 43 of 75 This report shall not be reproduced except in full without the written approval of RF Exposure Lab, LLC. Antenna Location on End