2ACHL-AIR114GContinuous Positive Airway Pressure (CPAP) Device

ResMed Pty Ltd

Click to zoom

Application Details

Equipment Class: PCB - PCS Licensed Transmitter
Date of Grant: Feb 16, 2021
Application Purpose: Original Equipment
Date of Application: Feb 16, 2021
Equipment Note: Continuous Positive Airway Pressure (CPAP) Device
Frequency Range: 1850.70000000 - 1909.30000000
Company: ResMed Pty Ltd
Country: Australia

Documents & Files

Select a file to view

Document Text

Text extracted from the exhibit documents filed with the FCC. Open a document above to read the original.

Users Manual

User guide English User guide Setting Up Device Tu b Tubing Mask Power Supply Power Cord i ENGLISH Contents Welcome ............................................................................................................................................... 1 Indications for use .................................................................................................................. 1 Contraindications .................................................................................................................... 1 Adverse effects ...................................................................................................................... 1 ResMed Product Software License Terms............................................................................. 2 At a glance ............................................................................................................................................ 3 About your device ................................................................................................................... 4 Setting up your device ......................................................................................................................... 5 Navigating the touch screen ................................................................................................................ 7 Additional features .................................................................................................................. 8 Connecting your AirSense 11 device and smart device ......................................................... 9 Starting/Stopping therapy ................................................................................................................... 9 About the heated tubing .................................................................................................................... 10 Therapy data ....................................................................................................................................... 11 Cleaning and caring for the device .................................................................................................... 12 Disassembling ...................................................................................................................... 13 Cleaning ................................................................................................................................ 13 Checking ............................................................................................................................... 14 Replacing the air filter ........................................................................................................... 15 Reassembling ....................................................................................................................... 15 Traveling ............................................................................................................................................. 15 Traveling by plane ................................................................................................................. 15 Troubleshooting ................................................................................................................................. 16 General warnings ............................................................................................................................... 17 Technical specifications ..................................................................................................................... 18 Guidance and manufacturer’s declaration electromagnetic emissions and immunity ................. 23 Symbols .............................................................................................................................................. 24 Servicing ............................................................................................................................................. 25 Limited warranty ................................................................................................................................. 25 Further information ............................................................................................................................ 26 English 1 Welcome The AirSense™ 11 AutoSet™ (including AutoSet for Her) device is ResMed's premium auto-adjusting pressure device. The AirSense 11 Elite and the AirSense 11 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 11 AutoSet (including AutoSet for Her) The AirSense 11 self-adjusting system is indicated for the treatment of obstructive sleep apnea (OSA) in patients weighing more than 66 lb (30 kg), including female patients with mild to moderate OSA in AutoSet for Her mode. The AirSense 11 self-adjusting system is intended for home and hospital use. AirSense 11 CPAP (including Elite) The AirSense 11 CPAP system is indicated for the treatment of obstructive sleep apnea (OSA) in patients weighing more than 66 lb (30 kg). The AirSense 11 CPAP system is intended for home and hospital use. 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 thera…

Text truncated - open the document above for the full version.

External Photos

AIRSENSE 11 PHOTOGRAPHS for PACIFIC project Title: AIRSENSE 11 PHOTOGRAPHS Project/Product PACIFIC 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 2020 Date last saved: 20-Nov-20Objective id: AirSense 11 Photographs.docx Page 1 of 5 AIRSENSE 11 PHOTOGRAPHS for PACIFIC project Company Confidential Date last saved: 20-Nov-20Objective id: AirSense 11 Photographs.docx Page 2 of 5 This document contains the photographs for the Air 11 Pacific Project, and is applicable to the following device models:  39420 AirSense 11 AutoSet  39421 AirSense 11 CPAP  39422 AirSense 10 Elite  39423 AirSense 11 AutoSet  39424 AirSense 11 CPAP  39425 AirSense 10 Elite Front View Rear View AIRSENSE 11 PHOTOGRAPHS for PACIFIC project Company Confidential Date last saved: 20-Nov-20Objective id: AirSense 11 Photographs.docx Page 3 of 5 Left Side View Right Side View AIRSENSE 11 PHOTOGRAPHS for PACIFIC project Company Confidential Date last saved: 20-Nov-20Objective id: AirSense 11 Photographs.docx Page 4 of 5 Top View Bottom View AIRSENSE 11 PHOTOGRAPHS for PACIFIC project Company Confidential Date last saved: 20-Nov-20Objective id: AirSense 11 Photographs.docx Page 5 of 5 PCBA Top View PCBA Bottom View Unilab(Shanghai) Co.,Ltd. Report No. : UL05420151102FCC/IC042-7 Page 1 of 3 EUT EXTERNAl PHOTOS View of EUT-1 View of EUT-2 Unilab(Shanghai) Co.,Ltd. Report No. : UL05420151102FCC/IC042-7 Page 2 of 3 View of EUT-3 View of EUT-4 1 2 2 1 Unilab(Shanghai) Co.,Ltd. Report No. : UL05420151102FCC/IC042-7 Page 3 of 3 View of EUT-5 Unilab(Shanghai) Co.,Ltd. Report No. : UL05420151102FCC/IC042-8 Page 1 of 1 EUT INTERNAL PHOTOS View of EUT-1 View of EUT-2

ID Label/Location Info

OF 4 4.0 eLB1392-074 Melanie Webster 22 February 2021 PAGE REV SPEC NO. 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. © 2021 ResMed. SPECIFICATION FCC & ISED Labelling Submission Air 11 OF 4 4.0 eLB1392-074 Melanie Webster 22 February 2021 PAGE REV SPEC NO. 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. © 2021 ResMed. SPECIFICATION FCC & ISED Labelling Submission Air 11 OF 4 4.0 eLB1392-074 Melanie Webster 22 February 2021 PAGE REV SPEC NO. 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. © 2021 ResMed. SPECIFICATION FCC & ISED Labelling Submission Air 11 OF 4 4.0 eLB1392-074 Melanie Webster 22 February 2021 PAGE REV SPEC NO. 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. © 2021 ResMed. SPECIFICATION FCC & ISED Labelling Submission Air 11

Internal Photos

Test Report

DEKRA Testing and Certification, S.A.U. Parque Tecnológico de Andalucía, c/ Severo Ochoa nº 2 · 29590 Campanillas · Málaga · España C.I.F. A29 507 456 Report No: (NIE) 63467RRF.001 2021-02-03 Test report No: NIE: 63467RRF.001 Partial Test report USA FCC 15.31(h), 22, 24, 27,15.209,15.247 CANADA RSS-130, RSS-132, RSS-133, RSS-139, RSS-247, RSS-Gen (*) Identification of item tested Continuous Positive Airway Pressure (CPAP) Device (*) Trademark ResMed (*) Model and /or type reference 39000 AirSense 11 (*) Derived model not tested 39420 AirSense 11 AutoSet, 39421 AirSense 11 CPAP, 39422 AirSense 11 Elite, 39423 AirSense 11 AutoSet, 39424 AirSense 11 CPAP, 39425 AirSense 11 Elite. Other identification of the product HW Version: 1.0 SW Version: SW04600 FCC ID: 2ACHL-AIR114G IC: 9103A-AIR114G (*) Features 4G LTE Cat 1, 3G, BLE Applicant RESMED Pty Ltd 1 Elizabeth Macarthur Drive, BELLA VISTA, NSW, 2153, AUSTRALIA Test method requested, standard USA FCC Part 15.31(h) (10-1-19 Edition). Measurement standard. USA FCC Part 22 (10-1-19 Edition). Public Mobile Services. USA FCC Part 24 (10-1-19 Edition). Personal Communications Services. USA FCC Part 27 (10-1-19 Edition). Miscellaneous Wireless Communications Services. USA FCC Part 15.209 (10-1-19 Edition). Radiated emission limits; general requirements. USA FCC Part 15.247 (10-1-19 Edition). Operation within the bands 902 - 928 MHz, 2400 -2483.5 MHz, and 5725 - 5850 MHz. CANADA RSS-130 Issue 2, Feb. 2019. CANADA RSS-132 Issue 3, Jan. 2013. CANADA RSS-133 Issue 6 Amendment 1, Jan. 2018. CANADA RSS-139 Issue 3, Jul. 2015. CANADA RSS-Gen Issue 5 (March 2019). CANADA RSS-247 Issue 2 (February 2017). -Transmitter out of band radiated emissions with simultaneous transmissions. Guidance for Performing Compliance Measurements on Digital Transmission System, Frequency Hopping Spread Spectrum System, and Hybrid Systems Devices Operating Under Section 15.247 of the FCC Rules. 558074 D01 Meas Guidance v05r02 dated April 2, 2019. KDB 971168 D01 Power Meas License Digital Systems v03r01, April. 2018. ANSI C63.10-2013: American National Standard for Testing Unlicensed Wireless Devices. ANSI C63.26-2015. Approved by (name / position & signature) Rafael López Martín EMC Consumer & RF Lab. Manager Date of issue 2021-02-03 Report template No FDT08_23 (*) “Data provided by the client” DEKRA Testing and Certification, S.A.U. Parque Tecnológico de Andalucía, c/ Severo Ochoa nº 2 · 29590 Campanillas · Málaga · España C.I.F. A29 507 456 Report No: (NIE) 63467RRF.001 Page 2 of 44 2021-02-03 Index Competences and guarantees ...................................................................................................................... 3 General conditions ......................................................................................................................................... 3 Uncertainty ..................................................................................................................................................... 3 Data provided by the client ............................................................................................................................ 3 Usage of samples .......................................................................................................................................... 5 Test sample description ................................................................................................................................. 5 Identification of the client ............................................................................................................................... 6 Testing period and place ............................................................................................................................... 6 Document history ........................................................................................................................................... 6 Environmental conditions .............................................................................................................................. 6 Remarks and comments ................................................................................................................................ 7 Testing verdicts .............................................................................................................................................. 8 Summary ....................................................................................................................................................... 8 Appendix A: Test results FCC 22, 15.247, 15.209 / RSS-132, RSS-247 ...................................................... 9 Appendix B: Test results FCC 24, 15.247, 15.209 / RSS-133, RSS-247 ....................................................20 Appendix C: Test results FCC 27, 15.247, 15.209 / RSS-139, RSS-130, RSS-247 ...................................31 DEKRA Testing and Certification, S.A.U. Parque Tecnológico de Andalucía, c/ Severo Ochoa nº 2 · 29590 Campanillas · Málaga · España C.I.F. A29 507 456 Report No: (NIE) 63467RRF.001 Page 3 of 44 2021-02-03 Competences and guarantees DEKRA Testing and Certification is a testing laboratory accredited by the National Accreditation Body (ENAC - Entidad Nacional de Acreditación), to perform the tests indicated in the Certificate No. 51/LE 147. DEKRA Testing and Certification is a FCC-recognized accredited testing laboratory with appropriate scope of accreditation that include testing performed in this test report. DEKRA Testing and Certification is an ISED-recognized accredited testing laboratory with appropriate scope of accreditation that include testing performed in this test report. In order to assure the traceability to other national and international laboratories, DEKRA Testing and Certification has a calibration and maintenance program for its measurement equipment. DEKRA Testing and Certification guarantees the reliabilit…

Text truncated - open the document above for the full version.

Test Report

DEKRA Testing and Certification, S.A.U. Parque Tecnológico de Andalucía, c/ Severo Ochoa nº 2 · 29590 Campanillas · Málaga · España C.I.F. A29 507 456 Report No: (NIE) 63467RRF.002 2021-02-03 Test report No: NIE: 63467RRF.002 Partial Test report USA FCC 15.31(h), 22, 24, 27, 15.209, 15.247 CANADA RSS-132, RSS-133, RSS-139, RSS-247, RSS-Gen (*) Identification of item tested Continuous Positive Airway Pressure (CPAP) Device (*) Trademark ResMed (*) Model and /or type reference 39000 AirSense 11 (*) Derived model not tested 39420 AirSense 11 AutoSet, 39421 AirSense 11 CPAP, 39422 AirSense 11 Elite, 39423 AirSense 11 AutoSet, 39424 AirSense 11 CPAP, 39425 AirSense 11 Elite. Other identification of the product HW Version: 1.0 SW Version: SW04600 FCC ID: 2ACHL-AIR114G IC: 9103A-AIR114G (*) Features 4G LTE Cat 1, 3G, BLE Applicant RESMED Pty Ltd 1 Elizabeth Macarthur Drive, BELLA VISTA, NSW, 2153, AUSTRALIA Test method requested, standard USA FCC Part 15.31(h) (10-1-19 Edition). Measurement standard. USA FCC Part 22 (10-1-19 Edition). Public Mobile Services. USA FCC Part 24 (10-1-19 Edition). Personal Communications Services. USA FCC Part 27 (10-1-19 Edition). Miscellaneous Wireless Communications Services. USA FCC Part 15.209 (10-1-19 Edition). Radiated emission limits; general requirements. USA FCC Part 15.247 (10-1-19 Edition). Operation within the bands 902 - 928 MHz, 2400 -2483.5 MHz, and 5725 - 5850 MHz. CANADA RSS-132 Issue 3, Jan. 2013. CANADA RSS-133 Issue 6 Amendment 1, Jan. 2018. CANADA RSS-139 Issue 3, Jul. 2015. CANADA RSS-Gen Issue 5 (March 2019). CANADA RSS-247 Issue 2 (February 2017). -Transmitter out of band radiated emissions with simultaneous transmissions. Guidance for Performing Compliance Measurements on Digital Transmission System, Frequency Hopping Spread Spectrum System, and Hybrid Systems Devices Operating Under Section 15.247 of the FCC Rules. 558074 D01 Meas Guidance v05r02 dated April 2, 2019. KDB 971168 D01 Power Meas License Digital Systems v03r01, April. 2018. ANSI C63.10-2013: American National Standard for Testing Unlicensed Wireless Devices. ANSI C63.26-2015. Approved by (name / position & signature) Rafael López Martín EMC Consumer & RF Lab. Manager Date of issue 2021-02-03 Report template No FDT08_23 (*) “Data provided by the client” DEKRA Testing and Certification, S.A.U. Parque Tecnológico de Andalucía, c/ Severo Ochoa nº 2 · 29590 Campanillas · Málaga · España C.I.F. A29 507 456 Report No: (NIE) 63467RRF.002 Page 2 of 41 2021-02-03 Index Competences and guarantees ...................................................................................................................... 3 General conditions ......................................................................................................................................... 3 Uncertainty ..................................................................................................................................................... 3 Data provided by the client ............................................................................................................................ 3 Usage of samples .......................................................................................................................................... 5 Test sample description ................................................................................................................................. 5 Identification of the client ............................................................................................................................... 6 Testing period and place ............................................................................................................................... 6 Document history ........................................................................................................................................... 6 Environmental conditions .............................................................................................................................. 6 Remarks and comments ................................................................................................................................ 7 Testing verdicts .............................................................................................................................................. 8 Summary ....................................................................................................................................................... 8 Appendix A: Test results FCC 22, 15.247 / RSS-132, RSS-247 ................................................................... 9 Appendix B: Test results FCC 24, 15.247 / RSS-133, RSS-247 .................................................................20 Appendix C: Test results FCC 27, 15.247 / RSS-139, RSS-247 ................................................................31 DEKRA Testing and Certification, S.A.U. Parque Tecnológico de Andalucía, c/ Severo Ochoa nº 2 · 29590 Campanillas · Málaga · España C.I.F. A29 507 456 Report No: (NIE) 63467RRF.002 Page 3 of 41 2021-02-03 Competences and guarantees DEKRA Testing and Certification is a testing laboratory accredited by the National Accreditation Body (ENAC - Entidad Nacional de Acreditación), to perform the tests indicated in the Certificate No. 51/LE 147. DEKRA Testing and Certification is a FCC-recognized accredited testing laboratory with appropriate scope of accreditation that include testing performed in this test report. DEKRA Testing and Certification is an ISED-recognized accredited testing laboratory with appropriate scope of accreditation that include testing performed in this test report. In order to assure the traceability to other national and international laboratories, DEKRA Testing and Certification has a calibration and maintenance program for its measurement equipment. DEKRA Testing and Certification guarantees the reliability of the data presen…

Text truncated - open the document above for the full version.

Test Report

DEKRA Testing and Certification, S.A.U. Parque Tecnológico de Andalucía, c/ Severo Ochoa nº 2 · 29590 Campanillas · Málaga · España C.I.F. A29 507 456 Report Nº: (NIE) 63467RRF.003 2020-11-30 Test report No: NIE: 63467RRF.003 Partial Test report REFERENCE STANDARD: USA FCC Part 22, Part 24 & Part 27 CANADA RSS-130, RSS-132, RSS-133 & RSS-139 (*) Identification of item tested Continuous Positive Airway Pressure (CPAP) Device (*) Trademark ResMed (*) Model and /or type reference 39000 AirSense 11 (*) Derived model not tested 39420 AirSense 11 AutoSet, 39421 AirSense 11 CPAP, 39422 AirSense 11 Elite, 39423 AirSense 11 AutoSet, 39424 AirSense 11 CPAP, 39425 AirSense 11 Elite. Other identification of the product HW Version: 1.0 SW Version: SW04600 FCC ID: 2ACHL-AIR114G IC: 9103A-AIR114G (*) Features 4G LTE Cat 1, 3G, BLE Applicant RESMED Pty Ltd 1 Elizabeth Macarthur Drive, BELLA VISTA, NSW, 2153, AUSTRALIA Test method requested, standard USA FCC Part 22 (10-1-19 Edition). Public Mobile Services. USA FCC Part 24 (10-1-19 Edition). Personal Communications Services. USA FCC Part 27 (10-1-19 Edition). Miscellaneous Wireless Communications Services. CANADA RSS-130 Issue 2, Feb. 2019. CANADA RSS-132 Issue 3, Jan. 2013. CANADA RSS-133 Issue 6 Amendment 1, Jan. 2018. CANADA RSS-139 Issue 3, Jul. 2015. ANSI C63.26-2015. KDB 971168 D01 Power Meas License Digital Systems v03r01, April. 2018. Approved by (name / position & signature) Rafael López Martín EMC Consumer & RF Lab. Manager Date of issue 2021-02-03 Report template No FDT08_23 (*) “Data provided by the client” DEKRA Testing and Certification, S.A.U. Parque Tecnológico de Andalucía, c/ Severo Ochoa nº 2 · 29590 Campanillas · Málaga · España C.I.F. A29 507 456 Report No: (NIE) 63467RRF.003 Page 2 of 77 2021-02-03 Index Competences and guarantees ...................................................................................................................... 3 General conditions ......................................................................................................................................... 3 Uncertainty ..................................................................................................................................................... 3 Data provided by the client ............................................................................................................................ 3 Usage of samples .......................................................................................................................................... 5 Test sample description ................................................................................................................................. 5 Identification of the client ............................................................................................................................... 5 Testing period and place ............................................................................................................................... 6 Document history ........................................................................................................................................... 6 Environmental conditions .............................................................................................................................. 6 Remarks and comments ................................................................................................................................ 7 Testing verdicts .............................................................................................................................................. 8 Summary ....................................................................................................................................................... 8 Appendix A: Test results FCC Part 22 / RSS-132 .......................................................................................10 Appendix B: Test results FCC Part 24 / RSS-133 .......................................................................................29 Appendix C: Test results FCC Part 27 / RSS-130, RSS-139 ......................................................................52 DEKRA Testing and Certification, S.A.U. Parque Tecnológico de Andalucía, c/ Severo Ochoa nº 2 · 29590 Campanillas · Málaga · España C.I.F. A29 507 456 Report No: (NIE) 63467RRF.003 Page 3 of 77 2021-02-03 Competences and guarantees DEKRA Testing and Certification S.A.U. is a testing laboratory accredited by the National Accreditation Body (ENAC -Entidad Nacional de Acreditación), to perform the tests indicated in the Certificate No. 51/LE 147. DEKRA Testing and Certification is a FCC-recognized accredited testing laboratory with appropriate scope of accreditation that include testing performed in this test report. DEKRA Testing and Certification is an ISED-recognized accredited testing laboratory with appropriate scope of accreditation that include testing performed in this test report. In order to assure the traceability to other national and international laboratories, DEKRA Testing and Certification S.A.U. has a calibration and maintenance program for its measurement equipment. DEKRA Testing and Certification S.A.U. guarantees the reliability of the data presented in this report, which is the result of the measurements and the tests performed to the item under test on the date and under the conditions stated on the report and, it is based on the knowledge and technical facilities available at DEKRA Testing and Certification S.A.U. at the time of performance of the test. DEKRA Testing and Certification S.A.U. is liable to the client for the maintenance of the confidentiality of all information related to the item under test and the results of the test. The results presented in this Test Report apply only to the particular item under test established in this document. IMPORTANT: No parts of this report may be reproduced or quoted ou…

Text truncated - open the document above for the full version.

Test Report

Unilab(Shanghai) Co.,Ltd. Report No. : UL05420151102FCC/IC042-2 Page 1 of 375 RF Test Report Test in accordance with Federal Communications Commission(FCC) CFR TITLE 47, Parts 2, 22, 24,27 & Industry Canada (IC), RSS-GEN, 130,132,133,139 Product Name : ELS61-US Model No. : ELS61-US FCC ID: QIPELS61-US IC ID: 7830A-ELS61US Applicant : Gemalto M2M GmbH Address : Siemensdamm 50, 13629 Berlin, Germany Date of Receipt : 11-02-2015 Test Date : 11-17-2015~11-28-2015 Issued Date : 01-21-2016 Report No. : UL05420151102FCC/IC042-2 Report Version : V1.0 Notes： The test results only relate to these samples which have been tested. Partly using this report will not be admitted unless been allowed by Unilab. Unilab is only responsible for the complete report with the reported stamp of Unilab. Unilab(Shanghai) Co.,Ltd. Report No. : UL05420151102FCC/IC042-2 Page 2 of 375 Test Report Certification Issued Date : 01-21-2016 Report No. : UL05420151102FCC/IC042-2 Product Name : ELS61-US Applicant : Gemalto M2M GmbH Address : Siemensdamm 50, 13629 Berlin, Germany Manufacturer : Gemalto M2M GmbH Address : Siemensdamm 50, 13629 Berlin, Germany Mo…

Text truncated - open the document above for the full version.

Contact Information

Applicant

Christopher Jenkins(Associate Manager - Systems Engineering)

[email protected]+61288841517Fax: +61288842007

Test Firm

DEKRA Testing and Certification, S.A.U.Rafael Lopez Martin

[email protected]34-9562-61 91 00Fax: 34-9562-61 91 13

Technical Specifications

#	Rule Parts	Frequency Range	Power Output	Emission	Tolerance
11	24E	1.85 GHz - 1.91 GHz	130.00 mW	18M0W7D	14.59 Hz

Confidentiality

Long Term

Grant Notes

Output power is conducted. This devices is authorized for portable operation and the highest reported SAR corresponding to Simultaneous transmission LTE Band 2 (Body Exposure) and BLE measured is 1,426 W/Kg. Multi-transmitter, supporting simultaneous transmission, configurations have been evaluated as described in this filling. Other multi-transmitter configurations have not been evaluated and shall be evaluated according to KDB Publication 447498 and §2.947(f), §15.31(h) and §15.31(k) composite system and §2.1 terms and concepts.

Other Applications from ResMed Pty Ltd

2ACHL-AIR11M1TA

NIV Device with Integrated Cellular and Bluetooth Connectivity

Apr 13, 2026

Equipment Class

JAB - Part 15 Class B Digital Device

2ACHL-AIR11M1U

Continuous Positive Airway Pressure (CPAP) Device

Apr 10, 2023

Equipment Class

JAB - Part 15 Class B Digital Device

2ACHL-AIR11M1G22

Continuous Positive Airway Pressure (CPAP) Device

Dec 29, 2022

Equipment Class

CXX - Communications Rcvr for use w/ licensed Tx and CBs

2ACHL-AIR11M1B

Bilevel device with integrated cellular and Bluetooth connectivity

May 31, 2022

Equipment Class

CXX - Communications Rcvr for use w/ licensed Tx and CBs

2ACHL-A10STACD

Wireless Continuous Positive Airway Pressure Device

Nov 12, 2015

Equipment Class

PCB - PCS Licensed Transmitter

Documents & Files

Select a file to view

Users Manual

↗

Cover Letter(s)

↗

External Photos

↗

ID Label/Location Info

↗

Internal Photos

↗

Test Report

↗

Test Setup Photos

↗

Document Text

Text extracted from the exhibit documents filed with the FCC. Open a document above to read the original.

Users Manual

Text truncated - open the document above for the full version.

External Photos

ID Label/Location Info

Internal Photos

Test Report

Text truncated - open the document above for the full version.

Test Report

DEKRA Testing and Certification, S.A.U. Parque Tecnológico de Andalucía, c/ Severo Ochoa nº 2 · 29590 Campanillas · Málaga · España C.I.F. A29 507 456 Report No: (NIE) 63467RRF.002 2021-02-03 Test report No: NIE: 63467RRF.002 Partial Test report USA FCC 15.31(h), 22, 24, 27, 15.209, 15.247 CANADA RSS-132, RSS-133, RSS-139, RSS-247, RSS-Gen (*) Identification of item tested Continuous Positive Airway Pressure (CPAP) Device (*) Trademark ResMed (*) Model and /or type reference 39000 AirSense 11 (*) Derived model not tested 39420 AirSense 11 AutoSet, 39421 AirSense 11 CPAP, 39422 AirSense 11 Elite, 39423 AirSense 11 AutoSet, 39424 AirSense 11 CPAP, 39425 AirSense 11 Elite. Other identification of the product HW Version: 1.0 SW Version: SW04600 FCC ID: 2ACHL-AIR114G IC: 9103A-AIR114G (*) Features 4G LTE Cat 1, 3G, BLE Applicant RESMED Pty Ltd 1 Elizabeth Macarthur Drive, BELLA VISTA, NSW, 2153, AUSTRALIA Test method requested, standard USA FCC Part 15.31(h) (10-1-19 Edition). Measurement standard. USA FCC Part 22 (10-1-19 Edition). Public Mobile Services. USA FCC Part 24 (10-1-19 Edition). Personal Communications Services. USA FCC Part 27 (10-1-19 Edition). Miscellaneous Wireless Communications Services. USA FCC Part 15.209 (10-1-19 Edition). Radiated emission limits; general requirements. USA FCC Part 15.247 (10-1-19 Edition). Operation within the bands 902 - 928 MHz, 2400 -2483.5 MHz, and 5725 - 5850 MHz. CANADA RSS-132 Issue 3, Jan. 2013. CANADA RSS-133 Issue 6 Amendment 1, Jan. 2018. CANADA RSS-139 Issue 3, Jul. 2015. CANADA RSS-Gen Issue 5 (March 2019). CANADA RSS-247 Issue 2 (February 2017). -Transmitter out of band radiated emissions with simultaneous transmissions. Guidance for Performing Compliance Measurements on Digital Transmission System, Frequency Hopping Spread Spectrum System, and Hybrid Systems Devices Operating Under Section 15.247 of the FCC Rules. 558074 D01 Meas Guidance v05r02 dated April 2, 2019. KDB 971168 D01 Power Meas License Digital Systems v03r01, April. 2018. ANSI C63.10-2013: American National Standard for Testing Unlicensed Wireless Devices. ANSI C63.26-2015. Approved by (name / position & signature) Rafael López Martín EMC Consumer & RF Lab. Manager Date of issue 2021-02-03 Report template No FDT08_23 (*) “Data provided by the client” DEKRA Testing and Certification, S.A.U. Parque Tecnológico de Andalucía, c/ Severo Ochoa nº 2 · 29590 Campanillas · Málaga · España C.I.F. A29 507 456 Report No: (NIE) 63467RRF.002 Page 2 of 41 2021-02-03 Index Competences and guarantees ...................................................................................................................... 3 General conditions ......................................................................................................................................... 3 Uncertainty ..................................................................................................................................................... 3 Data provided by the client ............................................................................................................................ 3 Usage of samples .......................................................................................................................................... 5 Test sample description ................................................................................................................................. 5 Identification of the client ............................................................................................................................... 6 Testing period and place ............................................................................................................................... 6 Document history ........................................................................................................................................... 6 Environmental conditions .............................................................................................................................. 6 Remarks and comments ................................................................................................................................ 7 Testing verdicts .............................................................................................................................................. 8 Summary ....................................................................................................................................................... 8 Appendix A: Test results FCC 22, 15.247 / RSS-132, RSS-247 ................................................................... 9 Appendix B: Test results FCC 24, 15.247 / RSS-133, RSS-247 .................................................................20 Appendix C: Test results FCC 27, 15.247 / RSS-139, RSS-247 ................................................................31 DEKRA Testing and Certification, S.A.U. Parque Tecnológico de Andalucía, c/ Severo Ochoa nº 2 · 29590 Campanillas · Málaga · España C.I.F. A29 507 456 Report No: (NIE) 63467RRF.002 Page 3 of 41 2021-02-03 Competences and guarantees DEKRA Testing and Certification is a testing laboratory accredited by the National Accreditation Body (ENAC - Entidad Nacional de Acreditación), to perform the tests indicated in the Certificate No. 51/LE 147. DEKRA Testing and Certification is a FCC-recognized accredited testing laboratory with appropriate scope of accreditation that include testing performed in this test report. DEKRA Testing and Certification is an ISED-recognized accredited testing laboratory with appropriate scope of accreditation that include testing performed in this test report. In order to assure the traceability to other national and international laboratories, DEKRA Testing and Certification has a calibration and maintenance program for its measurement equipment. DEKRA Testing and Certification guarantees the reliability of the data presen…

Text truncated - open the document above for the full version.

Test Report

Text truncated - open the document above for the full version.

Test Report

Text truncated - open the document above for the full version.

Technical Specifications

#	Rule Parts	Frequency Range	Power Output	Emission	Tolerance
11	24E	1.85 GHz - 1.91 GHz	130.00 mW	18M0W7D	14.59 Hz

Confidentiality

Long Term

Grant Notes