FCC ID 2ACHL-AIR10CD

2ACHLAIR10CD, 2ACHL AIR10CD, 2ACHL-AIR10CD, 2ACHL-AIR1OCD, 2ACHL-AIRI0CD, 2ACHL-A1R10CD

ResMed Ltd Continuous Positive Airway Pressure (CPAP) Devices AIR10CD

An FCC ID is the product ID assigned by the FCC to identify wireless products in the market. The FCC chooses 3 or 5 character "Grantee" codes to identify the business that created the product. For example, the grantee code for FCC ID: 2ACHL-AIR10CD is 2ACHL. The remaining characters of the FCC ID, -AIR10CD, are often associated with the product model, but they can be random. These letters are chosen by the applicant. In addition to the application, the FCC also publishes internal images, external images, user manuals, and test results for wireless devices. They can be under the "exhibits" tab below.

Purchase on Amazon: Continuous Positive Airway Pressure (CPAP) Devices

Application: Continuous Positive Airway Pressure (CPAP) Devices
Equipment Class: PCB - PCS Licensed Transmitter
Short Link: fcc.id/2ACHL-AIR10CD
Sources: FCC.gov | FCC.report
Registered By: ResMed Ltd - 2ACHL (Australia)

App #	Purpose	Date	Unique ID
1	Original Equipment	2014-07-17	hzHDLfP+FqLnyvPyyl83lg==

Operating Frequencies

Colombia Homologation [?]: 2ACHL-AIR10CD

Frequency Range	Power Output	Tolerance	Emission Designator	Rule Parts	Line Entry
824.7-848.31 MHz	270 mW	0.04ppm	1M28F9W	22H	1
1.85125-1.90875 GHz	530 mW	0.02ppm	1M28F9W	24E	2

Exhibits

Document	Type	Submitted Available
rev SAR spot check report(editorial changes)	RF Exposure Info Adobe Acrobat PDF (1967 kB)	2014-08-08 2014-07-17
rev SAR report(editorial changes)	RF Exposure Info Adobe Acrobat PDF (802 kB)	2014-08-08 2014-07-17
rev p22-24 delta 1 test report(editorial changes)	Test Report Adobe Acrobat PDF (1018 kB)	2014-08-08 2014-07-17
rev p22-24 delta 2 test report(editorial changes)	Test Report Adobe Acrobat PDF (695 kB)	2014-08-08 2014-07-17
label info (new label and location)	ID Label/Location Info Adobe Acrobat PDF (1352 kB)	2014-08-01 2014-07-17
temporary confidentiality request-rev	Cover Letter(s) Adobe Acrobat PDF (92 kB)	2014-07-17 2014-07-17
permanent confidentiality request-rev	Cover Letter(s) Adobe Acrobat PDF (93 kB)	2014-07-17 2014-07-17
SAR - miscellaneous	RF Exposure Info Adobe Acrobat PDF (2070 kB)	2014-07-17 2014-07-17
SAR photos	RF Exposure Info Adobe Acrobat PDF (333 kB)	2014-07-17 2014-07-17
SAR plots	RF Exposure Info Adobe Acrobat PDF (332 kB)	2014-07-17 2014-07-17
test report part 22 24 - cdma module	Test Report Adobe Acrobat PDF (1281 kB)	2014-07-17 2014-07-17
label info	ID Label/Location Info Adobe Acrobat PDF (2268 kB)	2014-07-17 2014-07-17
test set-up	Test Setup Photos Adobe Acrobat PDF (378 kB)	2014-07-17 2015-01-13
user guide regulatory	Users Manual Adobe Acrobat PDF (55 kB)	2014-07-17 2015-01-13
user guide	Users Manual Adobe Acrobat PDF (1948 kB)	2014-07-17 2015-01-13
internal photos	Internal Photos Adobe Acrobat PDF (987 kB)	2014-07-17 2015-01-13
external photos - cdma module	External Photos Adobe Acrobat PDF (382 kB)	2014-07-17 2015-01-13
external photos	External Photos Adobe Acrobat PDF (438 kB)	2014-07-17 2015-01-13
attestation of validity of conducted module test results	Attestation Statements Adobe Acrobat PDF (106 kB)	2014-07-17 2014-07-17
authorization for module data use	Attestation Statements Adobe Acrobat PDF (361 kB)	2014-07-17 2014-07-17
permanent confidentiality request module data	Cover Letter(s) Adobe Acrobat PDF (363 kB)	2014-07-17 2014-07-17
permanent confidentiality request	Cover Letter(s) Adobe Acrobat PDF (93 kB)	2014-07-17 2014-07-17
temporary confidentiality request	Cover Letter(s) Adobe Acrobat PDF (92 kB)	2014-07-17 2014-07-17
internal photos - cdma module	Operational Description Adobe Acrobat PDF (173 kB)	2014-07-17
block diagram	Block Diagram Adobe Acrobat PDF (170 kB)	2014-07-17
test report part 22 24 - delta 2	Test Report Adobe Acrobat PDF (822 kB)	2014-07-17 2014-07-17
cellular antenna info	Operational Description Adobe Acrobat PDF (2342 kB)	2014-07-17
operational description - cdma module	Operational Description Adobe Acrobat PDF (803 kB)	2014-07-17
schematics	Schematics Adobe Acrobat PDF (203 kB)	2014-07-17
parts list	Parts List/Tune Up Info Adobe Acrobat PDF (37 kB)	2014-07-17
spot check sar report after change	RF Exposure Info Adobe Acrobat PDF (2009 kB)	2014-07-17 2014-07-17
revised p22-24 delta 2 test report	Test Report Adobe Acrobat PDF (836 kB)	2014-08-01 2014-07-17
block diagram - cdma module	Block Diagram Adobe Acrobat PDF (144 kB)	2014-07-17
test report part 22 24 - delta 1	Test Report Adobe Acrobat PDF (1117 kB)	2014-07-17 2014-07-17
operational & technical description	Operational Description Adobe Acrobat PDF (359 kB)	2014-07-17
SAR report	RF Exposure Info Adobe Acrobat PDF (427 kB)	2014-07-17 2014-07-17
change information	Operational Description Adobe Acrobat PDF (44 kB)	2014-07-17
output power tune-up info (cdma)	Parts List/Tune Up Info Adobe Acrobat PDF (98 kB)	2014-07-17
schematics - cdma module	Schematics Adobe Acrobat PDF (126 kB)	2014-07-17
revised p22-24 delta 1 test report	Test Report Adobe Acrobat PDF (1079 kB)	2014-08-01 2014-07-17

Application Forms

Application for Equipment Authorization FCC Form 731 TCB Version

Applicant Information

Applicant's complete, legal business name:	ResMed Ltd
FCC Registration Number (FRN):	0023645450
Alphanumeric FCC ID:	2ACHLAIR10CD
Unique Application Identifier:	hzHDLfP+FqLnyvPyyl83lg==
Line one:	1 Elizabeth Macarthur Dr
City:	Bella Vista
State:	N/A
Country:	Australia
Zip Code:	2153

TCB Information

TCB Application Email Address:	nikolaus.wahl@cetecom.com
TCB Scope:	B1: Commercial mobile radio services equipment in the following 47 CFR Parts 20, 22 (cellular), 24,25 & 27

FCC ID

Grantee Code:	2ACHL
Product Code:	-AIR10CD

Person at the applicant's address to receive grant or for contact

Name:	Greg Dockar
Title:	Senior Regulatory Affairs Manager

Telephone Number:

+612 8884 1000

Extension:

Fax Number:	+612 8884 2007
Email:	Greg.Dockar@resmed.com.au

Long-Term Confidentiality

Does this application include a request for confidentiality for any portion(s) of the data contained in this application pursuant to 47 CFR § 0.459 of the Commission Rules?: Yes

Short-Term Confidentiality

Does short-term confidentiality apply to this application?: Yes

If so, specify the short-term confidentiality release date (MM/DD/YYYY format): 01/13/2015
Note: If no date is supplied, the release date will be set to 45 calendar days past the date of grant.

Software Defined/Cognitive Radio

Is this application for software defined/cognitive radio authorization? No

Equipment Class

Equipment Class: PCB - PCS Licensed Transmitter
Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant):	Continuous Positive Airway Pressure (CPAP) Devices

Related OET KnowledgeDataBase Inquiry

Is there a KDB inquiry associated with this application? No

Modular Equipment

Modular Type: Does not apply

Application Purpose

Application is for: Original Equipment

Composite/Related Equipment

Is the equipment in this application a composite device subject to an additional equipment authorization? No

Is the equipment in this application part of a system that operates with, or is marketed with, another device that requires an equipment authorization? No

Test Firm Information

Name of test firm and contact person on file with the FCC:

Firm Name: CETECOM Inc.

First Name: Sabrina

Last Name: Sarne

Telephone Number:

408-586-6249

Extension:

Fax Number: 408 586 6299

E-mail: Sabrina.Sarne@cetecom.com

Grant Comments

Enter any text that you would like to appear at the bottom of the Grant of Equipment Authorization:
Output power is ERP for Part 22 and EIRP for Part 24. SAR compliance for near the body operation has been assessed for a minimum distance of 20 mm between the device including its antenna and the users body, according to the documented intended purpose. Users must be informed of the operating requirements for satisfying RF exposure compliance. The highest reported SAR for near-the-body (min. 20mm) transmission use conditions is 0.90W/kg.

Set the grant of this application to be deferred to a specified date:
No

Equipment Authorization Waiver

Is there an equipment authorization waiver associated with this application? No

If there is an equipment authorization waiver associated with this application, has the associated waiver been approved and all information uploaded?: No

WILLFUL FALSE STATEMENTS MADE ON THIS FORM ARE PUNISHABLE BY FINE AND IMPRISONMENT (U.S. CODE, TITLE 18, SECTION 1001), AND/OR REVOCATION OF ANY STATION LICENSE OR CONSTRUCTION PERMIT (U.S. CODE, TITLE 47, SECTION 312(a)(1)), AND/OR FORFEITURE (U.S. CODE, TITLE 47, SECTION 503).

SECTION 5301 (ANTI-DRUG ABUSE) CERTIFICATION:

The applicant must certify that neither the applicant nor any party to the application is subject to a denial of Federal benefits, that include FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. § 862 because of a conviction for possession or distribution of a controlled substance. See 47 CFR 1.2002(b) for the definition of a "party" for these purposes.

Does the applicant or authorized agent so certify? Yes

Applicant/Agent Certification:

I certify that I am authorized to sign this application. All of the statements herein and the exhibits attached hereto, are true and correct to the best of my knowledge and belief. In accepting a Grant of Equipment Authorization as a result of the representations made in this application, the applicant is responsible for (1) labeling the equipment with the exact FCC ID specified in this application, (2) compliance statement labeling pursuant to the applicable rules, and (3) compliance of the equipment with the applicable technical rules. If the applicant is not the actual manufacturer of the equipment, appropriate arrangements have been made with the manufacturer to ensure that production units of this equipment will continue to comply with the FCC's technical requirements.

Authorizing an agent to sign this application, is done solely at the applicant's discretion; however, the applicant remains responsible for all statements in this application.

If an agent has signed this application on behalf of the applicant, a written letter of authorization which includes information to enable the agent to respond to the above section 5301 (Anti-Drug Abuse) Certification statement has been provided by the applicant. It is understood that the letter of authorization must be submitted to the FCC upon request, and that the FCC reserves the right to contact the applicant directly at any time.

Signature of Authorized Person Filing: Greg Dockar

Title of authorized signature: Senior Regulatory Affairs Manager

Grants

TCB	GRANT OF EQUIPMENT AUTHORIZATION	TCB
Certification
Issued Under the Authority of the
Federal Communications Commission
By:

CETECOM Inc.
411 Dixon Landing Road
Milpitas, CA 95035

Date of Grant: 07/17/2014

Application Dated: 07/17/2014

ResMed Ltd

1 Elizabeth Macarthur Dr

Bella Vista, 2153
Australia

Attention: Greg Dockar , Senior Regulatory Affairs Manager

NOT TRANSFERABLE

EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below.

FCC IDENTIFIER:	2ACHL-AIR10CD

Name of Grantee:	ResMed Ltd

Equipment Class:	PCS Licensed Transmitter
Notes:	Continuous Positive Airway Pressure (CPAP) Devices

Grant Notes	FCC Rule Parts	Frequency Range (MHZ)	Output Watts	Frequency Tolerance	Emission Designator
	22H	824.7 - 848.31	0.27	0.04 PM	1M28F9W
	24E	1851.25 - 1908.75	0.53	0.02 PM	1M28F9W

Output power is ERP for Part 22 and EIRP for Part 24.

SAR compliance for near the body operation has been assessed for a minimum distance of 20 mm between the device including its antenna and the users body, according to the documented intended purpose. Users must be informed of the operating requirements for satisfying RF exposure compliance.

The highest reported SAR for near-the-body (min. 20mm) transmission use conditions is 0.90W/kg.

COPY	FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION	COPY
Certification

ResMed Ltd
1 Elizabeth Macarthur Dr
Bella Vista, 2153
Australia