2ACHL-AIR10CDContinuous Positive Airway Pressure (CPAP) Devices

ResMed Confidential Proprietary Information, not to be reproduced or made available to third parties without prior consent from ResMed and not to be used in any unauthorised way.  ResMed Ltd 2014. DOC NO 378120 PAGE 1 of 92 SPECIFICATION – PRINTED MATERIALS REV 2 Rev Change Note Date document drafted Document prepared by (Name) Document Checked by (Name) 1 C36882 10 Jun 2014 Lisa Oliver Catherine Macalpine Verena Pirnbacher Alison Besley or delegate (refer to change note) 2 C37082 3 Jul 2014 Lisa Oliver Catherine Macalpine Verena Pirnbacher Alison Besley or delegate (refer to change note) AirSense 10 User Guide (device with humidifier) AMER Multi 1. ORACLE DESCRIPTION AirSense10 UG AMER MULTI 2. TRANSLATION DESCRIPTION Refer to the Change History on the English source listed for summary of changes in each version. Rev English source This translation replaces... 1 378013r6 378112 2 378013r6 plus changes as specified below 3. PRINT DETAILS Print according to master spec R370-7240. NOTE: Last page of Portuguese can be printed on the inside back cover. 4. RESMED QC INSPECTION For general sampling and inspection requirements, refer to AWI203-002 Appendix A, Printed or Unprinted Materials and Labels, Criteria 1, 2, 3, 4, 5, 6, 8 and 9 Additional requirement a) None 5. FOR ALL OTHER REQUIREMENTS, REFER TO RESMED SUPPLIER MANUAL AQP119. 6. CHANGE HISTORY This only applies when this document is revised without a change to the related English Reference. Changes must be limited to formatting errors or errors not flowing from the English Reference. REVISION 2 Section Heading Summary of change Technical specifications – Sound Pressure level : 1. For both SlimLine and Standard change results from “27 dBA” to “26.6 dBA”. 2. Remove “SlimLine or Standard and humidification” and its result. Power level : 1. For both SlimLine and Standard change results from “35 dBA” to “34.6 dBA”. 2. Remove “SlimLine or Standard and humidification” and its result. ResMed Confidential Proprietary Information, not to be reproduced or made available to third parties without prior consent from ResMed and not to be used in any unauthorised way.  ResMed Ltd 2014. DOC NO 378120 PAGE 2 of 92 SPECIFICATION – PRINTED MATERIALS REV 2 Changes based on Machines data for tech comms D000-0245r35. REVISION 1 Section Heading Summary of change Covers Update to spine marker - removed the pulse symbol and added with the ResMed logo IFU Added MPMU IFU to the end of all the IFU’s: “The humidifier is intended for single patient use in the home environment and re-use in a hospital/institutional environment.” About the control panel – icon table Updated “Wireless signal strength” to “Wireless signal strength (green)” Added: “Wireless transfer not enabled (gray)” Stopping Therapy Updated “Events per hour” to “Events (AHI) per hour” as per D37-099r9 Technical Specifications Update test results based on D000-0245r33 Technical Specifications - FCC ID Updated from “2ACHL-Air10CD” to “2ACHL-AIR10CD”. TroubleShooting – General Added additional possible cause to “My therapy data has not been sent to my care provider”: Cause: “Data transfer is not enabled for your device” Solution: “ Contact your care provider to enable the data transfer service. ResMed Confidential Proprietary Information, not to be reproduced or made available to third parties without prior consent from ResMed and not to be used in any unauthorised way.  ResMed Ltd 2014. DOC NO 378120 PAGE 3 of 92 SPECIFICATION – PRINTED MATERIALS REV 2 THIS PAGE IS INTENTIONALLY BLANK User guide User guide English | Français | Español | Português User guide 378120r1 Covers.indd 23/07/2014 10:22:13 AM 378120r1 Covers.indd 33/07/2014 10:22:13 AM English 1 ENGLISH Welcome The AirSense ™ 10 AutoSet ™ and AirSense 10 AutoSet for Her are ResMed's premium auto-adjusting pressure devices. The AirSense 10 Elite and AirSense 10 CPAP are ResMed's Continuous Positive Airway Pressure (CPAP) devices. 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 AirSense 10 AutoSet The AirSense 10 AutoSet self-adjusting device is indicated for the treatment of obstructive sleep apnea (OSA) in patients weighing more than 66 lb (30 kg). 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. AirSense 10 AutoSet for Her The AirSense 10 AutoSet for Her self-adjusting device is indicated for the treatment of obstructive sleep apnea (OSA) in patients (female patients with mild to moderate OSA when using AutoSet for Her treatment mode) weighing more than 66 lb (30 kg). 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. AirSense 10 Elite The AirSense 10 Elite device is indicated for the treatment of obstructive sleep apnea (OSA) in patients weighing more than 66 lb (30 kg). 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. AirSense 10 CPAP The AirSense 10 CPAP device is indicated for the treatment of obstructive sleep apnea (OSA) in patients weighing more than 66 lb (30 kg). 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  pathologically low blood pressure  dehydration  cerebrospinal fluid leak, recent cranial surgery, or trauma. 2 Adverse effects You should report unusual chest pain, severe headache, or increased breathlessness to your prescribing physician. An acute upper r…

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ENGLISH FCC information This document provides additional information regarding compliance of the AirSense 10 device with FCC Rules and Industry Canada license-exempt RSS standards. FCC ID: 2ACHL-AIR10CD This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: • This device may not cause harmful interference, • This device must accept any interference received, including interference that may cause undesired operation. This device is designed and manufactured not to exceed the emission limits for exposure to radio frequency (RF) energy set by the Federal Communications Commission of the U.S. Government and Industry Canada. The exposure standard employs a unit of measurement known as the Specific Absorption Rate, or SAR. The SAR limit relevant for the application described in the manual is 1.6W/kg. Tests for SAR are conducted using standard operating positions accepted by the FCC with the device transmitting at its highest certified power level in all tested frequency bands. Although the SAR is determined at the highest certified power level, the actual SAR level of the equipment while operating can be well below the maximum value. This is because the device is designed to operate at multiple power levels so as to use only the power required to reach the network. In general, the closer you are to a wireless base station antenna, the lower the power output. Equipment Authorization has been granted to this model with the reported SAR level(s) evaluated as in compliance with the FCC RF exposure guidelines. SAR information on this equipment is on file with the FCC and can be found under the Display Grant section of www.fcc.gov/oet/ea/fccid after searching on the FCC ID as printed on the equipment. 378111 SAR Addendum.indd 125/06/2014 3:45:18 PM This device has been tested to comply with FCC and IC radiation exposure limits set forth for an uncontrolled environment when used for the documented intended purpose and when mounted and operated as shown in the user guide. The device has been tested for a minimum distance of 20 mm between the device and the human body. This device complies with the FCC radiation exposure limits set forth in an uncontrolled environment.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 for help. Any change or modification to the product is not expressly approved by Resmed and could void the user’s authority to operate the device. Industry Canada, IC: 9103A-AIR10CDMA This device complies with Industry Canada license-exempt RSS standard(s). Operation is subject to the following two conditions: • This device may not cause harmful interference, • This device must accept any interference received, including interference that may cause undesired operation. The device has been designed to comply with safety standards for exposure to radio waves (SAR) in accordance to RSS-102. 378111 SAR Addendum.indd 225/06/2014 3:45:18 PM

Cetecom Inc. Laith Saman 411 Dixon Landing Rd. Milpitas, CA 95035 USA Dear Sir or Madam: Subject: Authority to use FCC exhibits supplied for FCCID: 2ACHL- AIR10CD We, Telit Wireless Solutions, 3131 RDU Center Dr., Suite 135, Morrisville, NC, 27560 hereby authorize Resmed to use our exhibits used for FCC ID: in support of their application reference FCCID: RI7CE910-DUAL for which Cetecom Inc., 411 Dixon Landing Rd. Milpitas, CA 95035, USA is the appointed TCB. Yours sincerely ____________________________________ Brian Tucker Global Vice President of Quality Telit Wireless Solutions, Inc. June 12, 2014 Brian Tucker Tel +1-919-415-1505 Fax +1-919-840-0337 Mobile +1-919-449-8607 E-Mail [email protected] www.telit.com

15 July 2014 To Whom It May Concern: Subject: Validity of Test Results from Testing / Certification of the integrated Module WE, ResMed Ltd, 1 Elizabeth Macarthur Dr, Bella Vista, 2253, Australia confirm that the results from conducted tests acc. to the relevant FCC rule part and as applied to the radio module Telit CE910-DUAL, FCC-ID: RI7CE910-DUAL which is incorporated in our host equipment Wireless Sleep Apnea Device, FCC-ID: 2ACHL-AIR10CD and as reported in the module test report # #NK-12-R-098, 07-27-2012, Nemko Korea Co., Ltd. accurately represent the test results under the new conditions when the identified radio module is integrated in the identified host equipment. By integration of the said radio module into the identified host equipment no changes were made to it or by external adaptation circuitry that impacts the validity of the results of the original module’s test reports. Kind regards, 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

Cetecom Inc. Laith Saman 411 Dixon Landing Rd. Milpitas, CA 95035 USA Dear Sir or Madam: Subject: Confidentiality Request; Certification Application FCC ID: 2ACHL-AIR10CD Telit Wireless Solutions request that the following information from FCC ID: RI7CE910-DUAL, provided to support the FCC application for the 370xx, FCC ID: 2ACHL-AIR10CD, be held permanently confidential on behalf of Resmed: Schematics ks0137b-B_Electric_Diagrams Part List 2000201659_BOM Block Diagram CE910-DUAL_Block Diagram Operational Description CE910-DUAL_Operational Description_ The above material contains trade secrets not customarily released to public that are judged to have the potential to cause detriment to the applicant and provide unjustified benefits to its competitors. This information should not be available for public disclosure for an indefinite period of time. Yours sincerely ____________________________________ Brian Tucker Global Vice President of Quality Telit Wireless Solutions, Inc. June 12, 2014 Brian Tucker Tel +1-919-415-1505 Fax +1-919-840-0337 Mobile +1-919-449-8607 E-Mail [email protected] www.telit.com

18 July 2014 Receiver Federal Communications Commission Equipment Authorization Division, Application Processing Branch 7435 Oakland Mills Road Columbia, MD 21048 Subject: Request for Permanent Confidentiality FCC ID: 2ACHL-AIR10CD To Whom It May Concern: In accordance with §0.457(d) and §0.459 of 47 CFR, ResMed Ltd ACN 003 765 142 requests permanent confidentiality for itself and on behalf of ResMed Inc and its subsidiaries (the ResMed Group) for the following items: 1. Block Diagram 2. Schematic Diagram 3. Part List 4. Operational Description 5. Tune-up Information These items contain detailed system and equipment description and related information about the product which ResMed Ltd considers to be proprietary and confidential to the ResMed Group and a custom design, which otherwise would not be released to the general public. Since this design is a basis from which future technological products will evolve, ResMed Ltd also feels that this information would be of benefit to its competitors, and that the disclosure of the information in these exhibits would harm ResMed Ltd and the members of the ResMed Group by giving our competitors an unfair advantage in the market and diminishing the value of our investment in research even after commercial release of the product. ResMed 1 Elizabeth Macarthur Drive, Bella Vista, NSW, 2153 T +61 (2) 8884-1000 F +61 (2) 8884-2000 E [email protected] ResMed.com.au 25791577 v2 National 18 07 14 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 1 Elizabeth Macarthur Drive, Bella Vista, NSW, 2153 T +61 (2) 8884-1000 F +61 (2) 8884-2000 E [email protected] ResMed.com.au 25791577 v2 National 18 07 14

18 July 2014 Receiver Federal Communications Commission Equipment Authorization Division, Application Processing Branch 7435 Oakland Mills Road Columbia, MD 21048 Subject: Request for Short Term Confidentiality FCC ID: 2ACHL-AIR10CD To Whom It May Concern: In accordance with §0.457(d) and §0.459 of 47 CFR, ResMed Ltd ACN 003 765 142 requests short term confidentiality for itself and on behalf of ResMed Inc and its subsidiaries (the ResMed Group)for the following items: 1. External Photographs 2. Internal Photographs 3. User Manual 4. Test Set-up Photographs until the product will be publicly announced. Number of days: 180 days from Grant date. These items contain detailed system and equipment description and related information about the product which ResMed Ltd considers to be proprietary and confidential to the ResMed Group and a custom design, which otherwise would not be released to the general public. Since this design is a basis from which future technological products will evolve, ResMed Ltd also feels that this information would be of benefit to its competitors, and that the disclosure of the information in these exhibits prior to the commercial release date would harm ResMed Ltd and the members of the ResMed Group by giving our competitors an unfair advantage in the market and diminishing the value of our investment in research and development. ResMed Ltd believes the period of confidentiality requested is necessary to protect the information until the commercial release of the product. ResMed 1 Elizabeth Macarthur Drive, Bella Vista, NSW, 2153 T +61 (2) 8884-1000 F +61 (2) 8884-2000 E [email protected] ResMed.com.au 25791569 v2 National 18 07 14 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 1 Elizabeth Macarthur Drive, Bella Vista, NSW, 2153 T +61 (2) 8884-1000 F +61 (2) 8884-2000 E [email protected] ResMed.com.au 25791569 v2 National 18 07 14

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

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

ResMed Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia Tel: +61 2 8884 1000 Fax: +61 2 8883 3114 ABN 30 003 765 142 Global leaders in sleep and respiratory medicine www.resmed.com Figure 1 Front of CPAP ResMed Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia Tel: +61 2 8884 1000 Fax: +61 2 8883 3114 ABN 30 003 765 142 Global leaders in sleep and respiratory medicine www.resmed.com Figure 3 Underneath of CPAP

ResMed Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia Tel: +61 2 8884 1000 Fax: +61 2 8883 3114 ABN 30 003 765 142 Global leaders in sleep and respiratory medicine www.resmed.com Figure 1 Front of CPAP ResMed Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia Tel: +61 2 8884 1000 Fax: +61 2 8883 3114 ABN 30 003 765 142 Global leaders in sleep and respiratory medicine www.resmed.com Figure 2 Back of CPAP ResMed Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia Tel: +61 2 8884 1000 Fax: +61 2 8883 3114 ABN 30 003 765 142 Global leaders in sleep and respiratory medicine www.resmed.com Figure 3 Underneath of CPAP

ResMed Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia Tel: +61 2 8884 1000 Fax: +61 2 8883 3114 ABN 30 003 765 142 Global leaders in sleep and respiratory medicine www.resmed.com Figure 1 CPU side of FG Main PCBA R370-7326 ResMed Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia Tel: +61 2 8884 1000 Fax: +61 2 8883 3114 ABN 30 003 765 142 Global leaders in sleep and respiratory medicine www.resmed.com Figure 2 Display side of FG Main PCBA R370-7326 ResMed Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia Tel: +61 2 8884 1000 Fax: +61 2 8883 3114 ABN 30 003 765 142 Global leaders in sleep and respiratory medicine www.resmed.com Figure 3 CPU side of CAM PCBA R379-748 ResMed Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia Tel: +61 2 8884 1000 Fax: +61 2 8883 3114 ABN 30 003 765 142 Global leaders in sleep and respiratory medicine www.resmed.com Figure 4 Cellular module and antenna side of CAM PCBA R379-748 ResMed Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia Tel: +61 2 8884 1000 Fax: +61 2 8883 3114 ABN 30 003 765 142 Global leaders in sleep and respiratory medicine www.resmed.com Figure 5 CPAP with covers removed, showing CAM PCBA. Note that CAM PCBA is affixed to end over in assembled unit. ResMed Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia Tel: +61 2 8884 1000 Fax: +61 2 8883 3114 ABN 30 003 765 142 Global leaders in sleep and respiratory medicine www.resmed.com Figure 6 CPAP with covers removed, showing FG main PCBA

FCC ID: 2ACHL AIR10CD IC Cert. No.: 9103A AIR10CDMA SAR Test Report - Appendix A - Plots Page 1 of 11 Plot 1 Date/Time: 5/9/2014 4:51:09 PM Test Laboratory: Cetecom Inc., SAR 3 Lab DUT: ResMed; Type: Medical Device; Serial: 22131321510 Communication System: CDMA2000 (1xRTT, RC3); Frequency: 836 MHz Medium: MSL900_Batch 100818 1 Medium parameters used: f = 836 MHz; σ = 0.992 mho/m; ε r = 53.007; ρ = 1000 kg/m 3 Phantom section: Flat Section Measurement Standard: DASY5 (IEEE/IEC/ANSI C63.19 2007) Procedure Notes: Test Technician: Kathy; Air Temperature: 21.7C; Medium Temperature: 20.7C; Comments: ; DASY Configuration: • Probe: ES3DV3 SN3340; ConvF(6.16, 6.16, 6.16); Calibrated: 4/16/2014; • Sensor Surface: 3mm (Mechanical Surface Detection (Locations From Previous Scan Used)), Sensor Surface: 3mm (Mechanical Surface Detection), z = 2.0, 32.0 • Electronics: DAE4 Sn1233; Calibrated: 3/17/2014 • Phantom: ELI v5.0; Type: QDOVA002AA; Serial: TP:1124 • DASY52 52.8.1(838); Flat-Section 2/Side 1_0mm_836MHz/Area Scan (11x21x1): Measurement grid: dx=15mm, dy=15mm Maximum value of SAR (measured) = 0.0476 mW/g Flat-Section 2/Side 1_0mm_836MHz/Zoom Scan (5x6x7)/Cube 0: Measurement grid: dx=8mm, dy=8mm, dz=5mm Reference Value = 6.137 V/m; Power Drift = 0.20 dB Peak SAR (extrapolated) = 0.055 mW/g SAR(1 g) = 0.045 mW/g; SAR(10 g) = 0.035 mW/g Maximum value of SAR (measured) = 0.0493 mW/g 0 dB = 0.0476 mW/g = 26.44 dB mW/g FCC ID: 2ACHL AIR10CD IC Cert. No.: 9103A AIR10CDMA SAR Test Report - Appendix A - Plots Page 2 of 11 Plot 2 Date/Time: 5/9/2014 4:18:46 PM Test Laboratory: Cetecom Inc., SAR 3 Lab DUT: ResMed; Type: Medical Device; Serial: 22131321510 Communication System: CDMA2000 (1xRTT, RC3); Frequency: 836 MHz Medium: MSL900_Batch 100818 1 Medium parameters used: f = 836 MHz; σ = 0.992 mho/m; ε r = 53.007; ρ = 1000 kg/m 3 Phantom section: Flat Section Measurement Standard: DASY5 (IEEE/IEC/ANSI C63.19 2007) Procedure Notes: Test Technician: Kathy; Air Temperature: 21.8C; Medium Temperature: 20.7C; Comments: ; DASY Configuration: • Probe: ES3DV3 SN3340; ConvF(6.16, 6.16, 6.16); Calibrated: 4/16/2014; • Sensor Surface: 3mm (Mechanical Surface Detection), z = 2.0, 32.0 • Electronics: DAE4 Sn1233; Calibrated: 3/17/2014 • Phantom: ELI v5.0; Type: QDOVA002AA; Serial: TP:1124 • DASY52 52.8.1(838); Flat-Section/Side 2_0mm_836MHz/Area Scan (11x21x1): Measurement grid: dx=15mm, dy=15mm Maximum value of SAR (measured) = 0.375 mW/g Flat-Section/Side 2_0mm_836MHz/Zoom Scan (5x5x7)/Cube 0: Measurement grid: dx=8mm, dy=8mm, dz=5mm Reference Value = 8.652 V/m; Power Drift = 0.18 dB Peak SAR (extrapolated) = 0.526 mW/g SAR(1 g) = 0.382 mW/g; SAR(10 g) = 0.262 mW/g Maximum value of SAR (measured) = 0.440 mW/g 0 dB = 0.375 mW/g = 8.53 dB mW/g FCC ID: 2ACHL AIR10CD IC Cert. No.: 9103A AIR10CDMA SAR Test Report - Appendix A - Plots Page 3 of 11 Plot 3 Date/Time: 5/9/2014 3:53:56 PM Test Laboratory: Cetecom Inc., SAR 3 Lab DUT: ResMed; Type: Medical Device; Serial: 22131321510 Communication System: CDMA2000 (1xRTT, RC3); Frequency: 849 MHz Medium: MSL900_Batch 100818 1 Medium parameters used: f = 849 MHz; σ = 1.01 mho/m; ε r = 52.911; ρ = 1000 kg/m 3 Phantom section: Flat Section Measurement Standard: DASY5 (IEEE/IEC/ANSI C63.19 2007) Procedure Notes: Test Technician: Kathy; Air Temperature: 21.8C; Medium Temperature: 20.7C; Comments: ; DASY Configuration: • Probe: ES3DV3 SN3340; ConvF(6.16, 6.16, 6.16); Calibrated: 4/16/2014; • Sensor Surface: 3mm (Mechanical Surface Detection), z = 2.0, 32.0 • Electronics: DAE4 Sn1233; Calibrated: 3/17/2014 • Phantom: ELI v5.0; Type: QDOVA002AA; Serial: TP:1124 • DASY52 52.8.1(838); Flat-Section/Side 3_20mm_836MHz/Area Scan (11x9x1): Measurement grid: dx=15mm, dy=15mm Maximum value of SAR (measured) = 0.737 mW/g Flat-Section/Side 3_20mm_836MHz/Zoom Scan (5x5x7)/Cube 0: Measurement grid: dx=8mm, dy=8mm, dz=5mm Reference Value = 26.843 V/m; Power Drift = 0.05 dB Peak SAR (extrapolated) = 0.843 mW/g SAR(1 g) = 0.647 mW/g; SAR(10 g) = 0.477 mW/g Maximum value of SAR (measured) = 0.721 mW/g 0 dB = 0.737 mW/g = 2.65 dB mW/g FCC ID: 2ACHL AIR10CD IC Cert. No.: 9103A AIR10CDMA SAR Test Report - Appendix A - Plots Page 4 of 11 Plot 4 Date/Time: 5/9/2014 2:14:56 PM Test Laboratory: Cetecom Inc. SAR 1 Lab DUT: ResMed; Type: Medical Device; Serial: 22131321510 Communication System: CDMA2000 (1xRTT, RC3); Frequency: 1880 MHz Medium: MSL1900_Batch 110615 4 Medium parameters used: f = 1880 MHz; σ = 1.538 mho/m; ε r = 51.322; ρ = 1000 kg/m 3 Phantom section: Flat Section Measurement Standard: DASY5 (IEEE/IEC/ANSI C63.19 2007) Procedure Notes: Test Technician: Mike & Lenny; Air Temperature: 22.3C; Medium Temperature: 21.3C; Comments: ; DASY Configuration: • Probe: ES3DV3 SN3244; ConvF(4.66, 4.66, 4.66); Calibrated: 3/19/2014; • Sensor Surface: 3mm (Mechanical Surface Detection), z = 2.0, 32.0 • Electronics: DAE4 Sn1265; Calibrated: 1/29/2014 • Phantom: ELI 4.0; Type: QDOVA001BB; Serial: 1092 • DASY52 52.8.1(838); Flat-Section/Side 1_0mm/Area Scan (11x21x1): Measurement grid: dx=15mm, dy=15mm Maximum value of SAR (measured) = 0.125 mW/g Flat-Section/Side 1_0mm/Zoom Scan (6x6x7)/Cube 0: Measurement grid: dx=8mm, dy=8mm, dz=5mm Reference Value = 5.765 V/m; Power Drift = 0.02 dB Peak SAR (extrapolated) = 0.152 mW/g SAR(1 g) = 0.105 mW/g; SAR(10 g) = 0.078 mW/g Maximum value of SAR (measured) = 0.116 mW/g 0 dB = 0.125 mW/g = 18.05 dB mW/g FCC ID: 2ACHL AIR10CD IC Cert. No.: 9103A AIR10CDMA SAR Test Report - Appendix A - Plots Page 5 of 11 Plot 5 Date/Time: 5/9/2014 6:51:32 AM Test Laboratory: Cetecom Inc., SAR 1 Lab DUT: ResMed; Type: Medical Device; Serial: 22131321510 Communication System: CDMA2000 (1xRTT, RC3); Frequency: 1880 MHz Medium: MSL1900_Batch 110615 4 Medium parameters used: f = 1880 MHz; σ = 1.538 mho/m; ε r = 51.322; ρ = 1000 kg/m 3 Phantom section: Flat Section Measurement Standard: DASY5 (IEEE/IEC/ANSI C63.19 2007) Procedure Notes: Test Technician: Mike & Lenny; Air Temperature: 21.6C; Medi…

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FCC ID: 2ACHL-AIR10CD IC Cert. No.: 9103A-AIR10CDMA SAR Test Report - Appendix B - Photos Page 1 of 3 Antenna Locations Cellular Antenna FCC ID: 2ACHL-AIR10CD IC Cert. No.: 9103A-AIR10CDMA SAR Test Report - Appendix B - Photos Page 2 of 3 Setup Photos Photo 1: Side 1 at 0 mm Photo 2: Side 2 at 0 mm FCC ID: 2ACHL-AIR10CD IC Cert. No.: 9103A-AIR10CDMA SAR Test Report - Appendix B - Photos Page 3 of 3 Photo 3: Side 3 at 20 mm Photo 4: 15cm Liquid Depth in Elliptical Phantom

FCC ID: 2ACHL-AIR10CD IC Cert. No.: 9103A-AIR10CDMA SAR Test Report - Appendix C - Misc Page 1 of 60 Tissue Parameters Recipe for liquids below 1 GHz: Water 35-58% Sugar 40-60% Salt 0-6% Hydroxyethyl-cellulose <0.3% Preventol-D7 0.1-0.7% Recipe for liquids above 1-3 GHz: Water 52-75% DGBE 25-48% Salt <1.0% SAR measurements were made within 24 hours of the measurement of liquid parameters. Relative permittivity and conductivity are within ±5% of the target. FCC ID: 2ACHL-AIR10CD IC Cert. No.: 9103A-AIR10CDMA SAR Test Report - Appendix C - Misc Page 2 of 60 850 MHz Body Liquid Date Temp (°C) Frequency (MHz) Relative Permativity Conductivity (S/m) 824 53.142 0.975929 825 53.1072 0.97726 835 53.0092 0.990629 836 53.0069 0.992378 837 52.9912 0.993552 848 52.9207 1.00888 849 52.911 1.01014 2014/05/09 20.7 0.9 0.92 0.94 0.96 0.98 1 1.02 1.04 820840 Conductivity (S/m) Frequency (MHz) Conductivity Target Liquid Value 5% Liquid Tolerance -5% Liquid Tolerance 2014/05/09 51 52 53 54 55 56 57 58 59 820840 Relative Permittivity Frequency (MHz) Permittivity Target Liquid Value 5% Liquid Tolerance -5% Liquid Tolerance 2014/05/09 FCC ID: 2ACHL-AIR10CD IC Cert. No.: 9103A-AIR10CDMA SAR Test Report - Appendix C - Misc Page 3 of 60 1900 MHz Body Liquid Date Temp (°C) Frequency (MHz) Relative Permativity Conductivity (S/m) 1851 51.43071.5029 1852 51.42371.5039 1880 51.32181.5381 1900 51.25571.5605 1908 51.24061.5684 1909 51.23581.5702 1851 50.95051.5112 1852 50.9491.5149 1880 51.01371.5723 1900 51.07181.5831 1908 51.0441.5823 1909 51.04151.5817 2014/05/08 21.3 2014/05/12 21 1.42 1.47 1.52 1.57 18451895 Conductivity (S/m) Frequency (MHz) Conductivity Target Liquid Value 5% Liquid Tolerance -5% Liquid Tolerance 2014/05/08 2014/05/12 50 51 52 53 54 55 56 18451895 Relative Permittivity Frequency (MHz) Permittivity Target Liquid Value 5% Liquid Tolerance -5% Liquid Tolerance 2014/05/08 2014/05/12 FCC ID: 2ACHL-AIR10CD IC Cert. No.: 9103A-AIR10CDMA SAR Test Report - Appendix C - Misc Page 4 of 60 Test Equipment SAR1 Lab Equipment Model Serial Instrument description Supplier / Manufacturer Model Serial No. Calibration (date) Calibration Due (date) Robot Staubli TX90 F10/5D3NA 1/A/01 N/A N/A SAM Twin Phantom SPEAG SM 000 T01 DA 1592 N/A N/A Elliptical Phantom SPEAG QD OVA 001 BB 1092 N/A N/A Software SPEAG Dasy52.6.2.482 N/A N/A N/A Device Holder SPEAG SD 000H01 N/A N/A N/A Data Acquisition Electronics SPEAG DAE4 1265 2014/01/29 2015/01/29 SAR Probe SPEAG ES3DV3 3244 2014/03/19 2015/03/19 SAR 3 Lab Instrument description Supplier / Manufacturer Model Serial No. Calibration (date) Calibration Due (date) Robot Staubli TX90 F11/5G2MA 1/C/01 N/A N/A SAM Twin Phantom SPEAG SM 000 T01 DA 1637 N/A N/A SAM Twin Phantom SPEAG SM 000 T01 DA 1638 N/A N/A Elliptical Phantom SPEAG QD OVA 001 BB …

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