FCC ID: 2ACHL-AIR104GU CPAP device with integrated cellular connectivity

5H}20179000049 Go OM Nosrannor REF] 37162 (21)20179000049 5 LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fon] 730"

MADE IN AUSTRALIA IC ID: 9103A-AIR104GU DN 5u]20179000049 Go OM Nojrassor REF] 37163 (21)20179000049 LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fon] 730"

MADE IN AUSTRALIA IC ID: 9103A-AIR104GU DN 5H}20179000049 Go OM Nosrannor REF] 37162 (21)20179000049 5 LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fon] 730"

MADE IN SINGAPORE IC ID: 9103A-AIR104GU DN 5u]20179000049 Go OM Nojrassor REF] 37163 (21)20179000049 LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fon] 730"

MADE IN SINGAPORE IC ID: 9103A-AIR104GU DN 5u]20179000049 Go ojrassor Pee REF] 37164 (21)20179000049 d LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fon] 730"

MADE IN SINGAPORE IC ID: 9103A-AIR104GU DN 5H]20179000049 Go ojrastor fee REF] 37165 (21)20179000049 LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fon] 730"

MADE IN AUSTRALIA IC ID: 9103A-AIR104GU DN 5H]20179000049 Go ojrastor fee REF] 37165 (21)20179000049 LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fon] 730"

MADE IN SINGAPORE IC ID: 9103A-AIR104GU DN 5u]20179000049 Go ojrassor Pee REF] 37164 (21)20179000049 d LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fon] 730"

MADE IN AUSTRALIA IC ID: 9103A-AIR104GU DN 5H}20179000049 Go OM Nojrannsor lak REF] 37159 (21)20179000049 my LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fai 780. MADE IN AUSTRALIA IC ID: 9103A-AIR104GU DN 5u]20179000049 Go ON ojrasssor REA REF] 37158 (21)20179000049 LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fai 780. MADE IN AUSTRALIA IC ID: 9103A-AIR104GU DN 5H}20179000049 Go OM Nojrannsor lak REF] 37159 (21)20179000049 my LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fai 780. MADE IN AUSTRALIA IC ID: 9103A-AIR104GU DN 5H]20179000049 Go osrasuer Pee REF] 37160 (21)20179000049 di LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fai 780. MADE IN AUSTRALIA IC ID: 9103A-AIR104GU DN 5u]20179000049 Go ON ojrasssor REA REF] 37158 (21)20179000049 LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fai 780. MADE IN SINGAPORE IC ID: 9103A-AIR104GU DN 5H}20179000049 Go OM Nojrannsor lak REF] 37159 (21)20179000049 my LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fai 780. MADE IN SINGAPORE IC ID: 9103A-AIR104GU DN 5H]20179000049 Go osrasuer Pee REF] 37160 (21)20179000049 di LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fai 780. MADE IN SINGAPORE IC ID: 9103A-AIR104GU DN Sm] 20179000049 Go nojrasiser PEE REF] 37161 (21)20179000049 df LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fai 780. MADE IN AUSTRALIA IC ID: 9103A-AIR104GU DN Sm] 20179000049 Go nojrasiser PEE REF] 37161 (21)20179000049 df LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fai 780. MADE IN SINGAPORE IC ID: 9103A-AIR104GU DN 5H}20179000049 Go OM Nojrannsor lak REF] 37159 (21)20179000049 my LOT] 1234567 LR76410 R370-4186/1 FCC ID: 2ACHL-AIR104GU ed fai 780. MADE IN AUSTRALIA IC ID: 9103A-AIR104GU DN

AIRCURVE ST-A LABELS for AIR 10 project Title: AIRCURVE ST-A LABELS Project/Product AIR 10 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 2024 Objective id: 77595_Label Design Page 1 of 5 Date last saved: 16-Feb-24 AIRCURVE ST-A LABELS for AIR 10 project 1. Purpose This document contains the labels of the below Air 10 models. Model Name /

Product Code 28541 Marketing Name AirCurve 10 ST-A AirCurve 10 ST-A AirCurve 10 ST-A 28542 28405 2. Lables Given below are the labels present on AirCurve 10 ST-A (28541, 28542 and 28405). View Front View containing, brand name and marketing name. Rear View containing serial number label Photographs Date last saved: 16-Feb-24 Company Confidential Objective id: 77595_Label Design Page 2 of 5 AIRCURVE ST-A LABELS for AIR 10 project View Serial number label Photographs Left Side View no labels Right Side View no labels Date last saved: 16-Feb-24 Company Confidential Objective id: 77595_Label Design Page 3 of 5 AIRCURVE ST-A LABELS for AIR 10 project View Top View no reg labels. App information label only Bottom View Reg labels Reg Label 1 Photographs Date last saved: 16-Feb-24 Company Confidential Objective id: 77595_Label Design Page 4 of 5 AIRCURVE ST-A LABELS for AIR 10 project View Reg Label 2 Photographs Date last saved: 16-Feb-24 Company Confidential Objective id: 77595_Label Design Page 5 of 5

Date: 30-Jun-2022 DEKRA Testing and Certification, S.A.U. Parque Tecnolgico de Andaluca C/ Severo Ochoa 2 & 6 29590 Campanillas Mlaga, Espaa Ref: Confidentiality request for FCC ID: 2ACHL-AIR104GU To whom it may concern:

Pursuant to 0.457(d)(1)(ii) and 0.459 of the Commissions Rules (47 C.F.R.) and 552 (b)(4) of the Freedom of Information Act, ResMed Pty Ltd hereby request requests that a part of the subject FCC application be held confidential to avoid release of sensitive information of the product to the public. For the product stated above, we request that the following information be withheld from public disclose:

Type of Confidentiality Requested Short Term Short Term Short Term Short Term Short Term Short Term Short Term Short Term Short Term Permanent Permanent Permanent Permanent Permanent Exhibit Block Diagrams External Photos Internal Photos Operation Description Parts List & Placement/BOM Tune-Up Procedure Schematics Test Setup Photos Users Manual Permanent Confidentiality:

The above materials contain trade secrets and proprietary information not customarily released to the public. The public disclosure of these matters might be harmful to us and provide unjustified benefits to our competitors. Short-Term Confidentiality:

We hereby request short-term confidentiality for the product stated above to avoid premature release of sensitive information prior to marketing or release of the product to the public. Release date of short term confidentiality is:

45 days from grant date marked 90 days from grant date marked 135 days from grant date marked 180 days from grant date marked Specific date:

We are also aware that we are responsible to notify DEKRA in the event information regarding the product or the product is made available to the public. DEKRA will then release the documents listed above for public disclosure pursuant to FCC Public Notice DA 04-1705. Sincerely, _________________________ By:

Title:

Company:

Telephone:

e-mail:

Christopher Jenkins Associate Manager Systems Engineering ResMed Pty Ltd

+61 2 8884 1000 Christopher.Jenkins@resmed.com.au ResMed Pty Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153, Australia T +61 2 8884 1000 E Christopher.jenkins@ResMed.com.au ResMed.com

Date: June 22, 2022 Re: Declaration about validity of test results from testing/certification of the integrated module We, Related to product:

Type of Equipment:

Brand name:

Model name:

Commercial name:

FCC ID:

IC:

To whom it may concern, ResMed Pty Ltd, 1 Elizabeth Macarthur Dr, Bella Vista NSW 2153, Australia Continuous Positive Airway Pressure (CPAP) Device ResMed 37158, 37159, 37160, 37161, 37162, 37163, 37164, 37165 AirSense 10, AirCurve 10 2ACHL-AIR104GU 9103A-AIR104GU We declare that the u-blox LARA R6001D module has not been modified and has been integrated following modules manufacturer instructions for the installation such as input voltages considering extreme voltages, driver software, environmental conditions, etc... Then, the results from conducted test reports according to FCC and ISED standards supplied by u-blox of module LARA R6001D with FCC ID XPYUBX21BE01 and IC 8595A-UBX21BE01 remain applicable, valid and representative of the module and are representative under the new conditions for the certification of the host device. Sincerely, __________________________ By:

Title:

Company:

Telephone:

e-mail:

Christopher Jenkins Associate Manager Systems Engineering ResMed Pty Ltd

+61 2 8884 1517 Christopher.Jenkins@resmed.com.au ResMed Pty Limited 1 Elizabeth Macarthur Drive Bella Vista NSW 2153 Australia T +61 (2) 8884 1517 christopher.jenkins@resmed.com.au ABN 30 003 765 142 ResMed.com

Date: February 12, 2024 Re: Declaration about validity of test results from testing/certification of the integrated module We, Related to product:

Type of Equipment:

Brand name:

Model name:

Commercial name:

FCC ID:

IC:

ResMed Pty Ltd, 1 Elizabeth Macarthur Dr, Bella Vista NSW 2153, Australia Continuous Positive Airway Pressure (CPAP) Device ResMed 28541, 28542, 28405 AirCurve 10 ST-A 2ACHL-AIR104GU 9103A-AIR104GU To whom it may concern, We declare that the u-blox LARA R6001D module has not been modified and has been integrated following modules manufacturer instructions for the installation such as input voltages considering extreme voltages, driver software, environmental conditions, etc... Then, the results from conducted test reports according to FCC and ISED standards supplied by u-blox of module LARA R6001D with FCC ID XPYUBX21BE01 and IC 8595A-UBX21BE01 remain applicable, valid and representative of the module and are representative under the new conditions for the certification of the host device. Sincerely, __________________________ By:

Title:

Company:

Telephone:

e-mail:

Christopher Jenkins Manager Systems Engineering ResMed Pty Ltd

+61 2 8884 1517 Christopher.Jenkins@resmed.com.au ResMed Pty Limited 1 Elizabeth Macarthur Drive Bella Vista NSW 2153 Australia T +61 (2) 8884 1517 christopher.jenkins@resmed.com.au ABN 30 003 765 142 ResMed.com

Request for Class Permissive Change Date: 19-March-2024 Federal Communications Commission Equipment Authorization Branch 7435 Oakland Mills Rd. Columbia MD 21046 FCC ID: 2ACHL-AIR104GU To whom it may concern:

We, ResMed Pty Ltd, 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia hereby request a Class II Permissive Change for the Product approved under the above-mentioned FCC ID pursuant to Part 2.1043, of Title 47 of the Code of Federal Regulations. The approval update includes adding three equivalent models (28541, 28542, 28405) to the previously approved model (37165), differing by the addition of a new separate PCBA for the following alarm functions:

Generation of visual and auditory alarm signals (medium priority only). Alarm Mute (2-min audio pause). Redundant pressure sensing Power Failure Alarm Alarm System Fault Alarms (e.g., loss of communication with main PCBA) The new models (28541, 28542, 28405) and the approved model (37165) have identical RF module, RF circuitry and Software. Testing is performed to ensure that there is no impact on the RF performance of the device due to addition of the new PCBA for alarms. Sincerely, __________________________ Christopher Jenkins Title: Manager Systems Engineering Company: ResMed Pty Ltd Telephone: 1800 737 633 e-mail: Christopher.jenkins@resmed.com.au ResMed Pty Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153, Australia T +61 2 8884 1000 E Christopher.jenkins@ResMed.com.au ResMed.com

Letter of Declaration Date: 19-March-2024 Federal Communications Commission Equipment Authorization Branch 7435 Oakland Mills Rd. Columbia MD 21046 FCC ID: 2ACHL-AIR104GU To whom it may concern:

We, ResMed Pty Ltd, 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia declares that the similarities and differences between the tested model (28330) and the derived models under test / new models (28541, 28542, 28405) are the following:

Similarities: Hardware (including cellular), Software (including cellular), Colour, Name plaque Difference: Change in REF number on the serial number label. Models 28330, 28541, 28542 and 28405 are identical devices with 28330 used as a test device. We also declare that the similarities and differences between the models 28541, 28542 and 28405 as the following:

Difference: Change in REF number on the serial number label. Similarities: Hardware (including cellular), Software (including cellular), Colour, Name plaque. Models 28541, 28542, and 28405 are identical, with distinct model numbers assigned solely for marketing and geographical identification purposes. Sincerely, __________________________ Christopher Jenkins Title: Manager Systems Engineering Company: ResMed Pty Ltd Telephone:

1800 737 633 e-mail: Christopher.jenkins@resmed.com.au ResMed Pty Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153, Australia T +61 2 8884 1000 E Christopher.jenkins@ResMed.com.au ResMed.com

Date: 15-Feb-2024 DEKRA Testing and Certification, S.A.U. Parque Tecnolgico de Andaluca C/ Severo Ochoa 2 & 6 29590 Campanillas Mlaga, Espaa Ref: Agent letter for FCC ID: 2ACHL-AIR104GU We, hereby authorize ResMed Pty Ltd, 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153, Australia, DEKRA Testing and Certification, S.A.U. Parque Tecnolgico de Andaluca C/ Severo Ochoa n 2 29590 Campanillas - Malaga Spain Agent: Mario Baudet Aranda e-mail: mario.baudet@dekra.com Phone: +34 952 61 93 71 to act as our agent in the preparation of this application for equipment certification, including the signing of all documents relating to these matters. The present authorization considers the development of documents on behalf of the client, written under their own letterhead and related to the necessary information to be provided on their behalf to complete the certification process. We also hereby certify that neither we nor any party to this application are subject to a denial of U.S. Federal benefits, which include FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, U.S.C. 862 because of conviction for possession or distribution of controlled substance. For instances where our authorized agent signs the application for certification on our behalf, I acknowledge that all responsibility for complying with the terms and conditions for Certification, as specified by DEKRA Testing and Certification, S.A.U., still resides with us. This agreement expires one year from the current date. Sincerely, __________________________ Christopher Jenkins Title: Manager Systems Engineering Company: ResMed Pty Ltd Telephone: 1800 737 633 e-mail: christopher.jenkins@resmed.com.au ResMed Pty Limited 1 Elizabeth Macarthur Drive Bella Vista NSW 2153 Australia T +61 (2) 8884 1000 F +61 (2) 8884 2000 E christopher.jenkins@resmed.com.au ABN 30 003 765 142 ResMed.com

Date: 15-Feb-2024 DEKRA Testing and Certification, S.A.U. Parque Tecnolgico de Andaluca C/ Severo Ochoa 2 & 6 29590 Campanillas Mlaga, Espaa FCC ID: 2ACHL-AIR104GU We, certify that:

Sincerely, __________________________ Certifications concerning covered equipment. Section 2.911(d)(5)(i)- (ii) ResMed Pty Ltd, 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153, Australia,

the equipment for which authorization is sought is not covered equipment prohibited from receiving an equipment authorization pursuant to section 2.903 of the FCC rules. as of the date of the filing of the application, the applicant is not identified on the Covered List as an entity producing covered equipment. Christopher Jenkins Title: Manager Systems Engineering Company: ResMed Pty Ltd Telephone: 1800 737 633 e-mail: christopher.jenkins@resmed.com.au ResMed Pty Limited 1 Elizabeth Macarthur Drive Bella Vista NSW 2153 Australia T +61 (2) 8884 1000 F +61 (2) 8884 2000 E christopher.jenkins@resmed.com.au ABN 30 003 765 142 ResMed.com

Date: 15-Feb-2024 DEKRA Testing and Certification, S.A.U. Parque Tecnolgico de Andaluca C/ Severo Ochoa 2 & 6 29590 Campanillas Mlaga, Espaa Certification designating a U.S. agent for service of process. As required by section 2.911(d)(7), FCC ID: 2ACHL-AIR104GU We, Company Name: ResMed Pty Ltd Grantee Code: 2ACHL FRN: 0023645450 Contact Name: Christopher Jenkins Address: 1 Elizabeth Macarthur Dr, Bella Vista, 2153, Australia Tel: 1800 737 633 Email: christopher.Jenkins@resmed.com.au certify that:

Name: TianHeng Consulting, LLC FRN: 0033401258 Contact Person: Hualing Dong Address: 392 Andover Street, Wilmington, MA 01887, United States Tel.: +1 617-997-4010 Email: tianhengconsulting@gmail.com Is our designated U.S. agent for service of process and we acknowledge:

our consent to accept service of process in the United States for matters related to the applicable equipment at the physical U.S. address and email address of the designated U.S. agent the acceptance to maintain an U.S. agent for no less than one year after the grantee has terminated all marketing and importation or the conclusion of any Commission-related proceeding involving the equipment. Applicant Sincerely, ________________ By: Christopher Jenkins Title: Manager, Systems Engineering Company: ResMed Pty Ltd Telephone: 1800 737 633 e-mail: christopher.Jenkins@resmed.com.au Designated U.S. Agent We acknowledge our obligation to accept service of process in the United States for matters related to the applicable equipment at our physical U.S. address and email address stated above. __________________ By: Hualing Dong Title: President Company: TianHeng Consulting, LLC Telephone: +1-617-997-4010 e-mail: tianhengconsulting@gmail.com ResMed Pty Limited 1 Elizabeth Macarthur Drive Bella Vista NSW 2153 Australia T +61 (2) 8884 1000 F +61 (2) 8884 2000 E christopher.jenkins@resmed.com.au ABN 30 003 765 142 ResMed.com

SIMILARITIES AND DIFFERENCES - US/CAN VARIANTS for AIR 10 project Title: SIMILARITIES AND DIFFERENCES -

US/CAN VARIANTS Project/Product AIR 10 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 2022 Date last saved: 30-Jun-22Objective id: Similarities and differences between A10 USCAN Variants 1 of 2 Page SIMILARITIES AND DIFFERENCES - US/CAN VARIANTS for AIR 10 project 1. Purpose This document discusses the similarities and differences between US/CAN variants of the Air10 project applicable to the following device models:

Model Name /

Product Code 37158 37159 37160 37161 37162 37163 37164 37165 Marketing Name AirSense 10 CPAP AirSense 10 Elite AirSense 10 AutoSet AirSense 10 AutoSet FH AirCurve 10 ASV AirCurve 10 S AirCurve 10 VAuto AirCurve 10 ST 2. Equivalence All the device models mentioned in Section 1 have the following same components/parts:

Hardware o Cellular o Flow Generator Software o Cellular o Flow Generator 3. Differences Different models are derived for marketing purposes. The difference between these models are the medical therapy modes and region/customer centric features supported by the device. These settings are configured at manufacturing via a configuration file and is independent of the cellular and flow generator software. In summary, the differences between the device models mentioned in Section 1 are:

Therapy modes Data settings UI language Name plaque Device colour Date last saved: 30-Jun-22Objective id: Similarities and differences between A10 USCAN Variants 2 of 2 Page Company Confidential

Authorization Doc id: UBX-22035000 Rev.: 1.0 Date: 15-Sep-2022 Authorization letter for test reports and technical documents use Addressed to: Federal Communications Commission Equipment Authorization Branch 7435 Oakland Mills Rd. Columbia MD 21046, USA Issued by:

u-blox AG Zrcherstrasse 68, 8800 Thalwil, Switzerland To whom it may concern, We, u-blox AG (Zrcherstrasse 68, 8800 Thalwil, Switzerland), manufacturer and owner of the following radio module approved by FCC United States FCC ID:

Approval Date:

XPYUBX21BE01 12/29/2021 hereby authorize the company ResMed Pty Ltd (1 Elizabeth Macarthur Drive, Bella Vista NSW 2153, Australia) to use the test reports and the technical documents which belong to our module for the FCC certification of the host product integrating our module under FCC ID:

2ACHL-AIR104GU Sincerely, ____________________________________________ Giulio Comar Name :

Certification Manager Position:

+390402529400 Telephone:

giulio.comar@u-blox.com Email:

Author Giulio Comar Department:

cert Page: 1/1 Filename Authorization_for_LARA-R6001D_Test_Reports_use_for_FCC_Certification_ResMed.docx M102 Rev. 1 Copyright u-blox AG. All rights reserved C1-Public

Date: 30-June-2022 DEKRA Testing and Certification, S.A.U. Parque Tecnolgico de Andaluca C/ Severo Ochoa n 2 29590 Campanillas - Malaga Spain Ref: Agent letter for FCC ID: 2ACHL-AIR104GU We,

, hereby authorize ResMed Pty Ltd, 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153, Australia DEKRA Testing and Certification, S.A.U. Parque Tecnolgico de Andaluca C/ Severo Ochoa n 2 29590 Campanillas - Malaga Spain Agent: Mario Baudet Aranda e-mail: mario.baudet@dekra.com Phone: +34 952 61 93 71 to act as our agent in the preparation of this application for equipment certification, including the signing of all documents relating to these matters. The present authorization considers the development of documents on behalf of the client, written under clients own letterhead and related to the necessary information to be provided on clients behalf to complete the certification process. We also hereby certify that neither we nor any party to this application are subject to a denial of U.S. Federal benefits, which include FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, U.S.C. 862 because of conviction for possession or distribution of controlled substance. For instances where our authorized agent signs the application for certification on our behalf, I acknowledge that all responsibility for complying with the terms and conditions for Certification, as specified by DEKRA Testing and Certification, S.A.U., still resides with us. This agreement expires one year from the current date. Sincerely, __________________________ By: Christopher Jenkins Title: Associate Manager Systems Engineering Company: ResMed Pty Ltd Telephone: +61 2 8884 1517 e-mail: christopher.jenkins@resmed.com.au ResMed Pty Limited 1 Elizabeth Macarthur Drive Bella Vista NSW 2153 Australia T +61 (2) 8884 1000 F +61 (2) 8884 2000 E christopher.jenkins@resmed.com.au ABN 30 003 765 142 ResMed.com