FCC ID 2ANMMTHFT1

2ANMM-THFT1, 2ANMM THFT1, 2ANMMTHFT1, 2ANMMTHFTI

GSK Consumer Healthcare The product consists of a single use Analyzer module that connects to a smartphone application via Bluetooth Low Energy. The product also includes a sterile swab and collection container and an extraction fluid-filled dispenser. THFT1

Theraflu Theraflu Flue Test I-FLU-C02

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: 2ANMMTHFT1 is 2ANMM. The remaining characters of the FCC ID, THFT1, 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: The product consists of a single use Analyzer module that connects to a smartphone application via Bluetooth Low Energy. The product also includes a sterile swab and collection container and an extraction fluid-filled dispenser.

Application: The product consists of a single use Analyzer module that connects to a smartphone application via Bluetooth Low Energy. The product also includes a sterile swab and collection container and an extraction fluid-filled dispenser.
Equipment Class: DTS - Digital Transmission System
Short Link: fcc.id/2ANMMTHFT1
Sources: FCC.gov | FCC.report
Registered By: GSK Consumer Healthcare - 2ANMM (Switzerland)

App #	Purpose	Date	Unique ID
1	Original Equipment	2020-08-24	6OykRkNU7/9V1/kv1lVlYQ==

Operating Frequencies

Frequency Range	Power Output	Rule Parts	Line Entry
2.402-2.48 GHz	0.1 mW	15C	1

Exhibits

Document	Type	Submitted Available
Test Rpt	Test Report Adobe Acrobat PDF (966 kB)	2020-08-24 2020-08-24
Label info	ID Label/Location Info Adobe Acrobat PDF (216 kB)	2020-08-24 2020-08-24
Confidentiality Letter	Cover Letter(s) Adobe Acrobat PDF (834 kB)	2020-08-24 2020-08-24
POA Letter	Cover Letter(s) Adobe Acrobat PDF (685 kB)	2020-08-24 2020-08-24
User Manual BT brochure FDA	Users Manual Adobe Acrobat PDF (2518 kB)	2020-08-24 2021-02-20
User Manual BT carton FDA	Users Manual Adobe Acrobat PDF (606 kB)	2020-08-24 2021-02-20
External Photos	External Photos Adobe Acrobat PDF (1507 kB)	2020-08-24 2021-02-20
Tsup App A	Test Setup Photos Adobe Acrobat PDF (715 kB)	2020-08-24 2021-02-20
User Manual Package Insert	Users Manual Adobe Acrobat PDF (191 kB)	2020-08-24 2021-02-20
Internal Photos	Internal Photos Adobe Acrobat PDF (4361 kB)	2020-08-24 2021-02-20
Parts List	Parts List/Tune Up Info Adobe Acrobat PDF (87 kB)	2020-08-24
Schematics	Schematics Adobe Acrobat PDF (377 kB)	2020-08-24
Operational Description	Operational Description Adobe Acrobat PDF (2426 kB)	2020-08-24
Block Diagram	Block Diagram Adobe Acrobat PDF (1014 kB)	2020-08-24

Application Forms

Application for Equipment Authorization FCC Form 731 TCB Version

Applicant Information

Applicant's complete, legal business name:	GSK Consumer Healthcare
FCC Registration Number (FRN):	0026272195
Alphanumeric FCC ID:	2ANMMTHFT1
Unique Application Identifier:	6OykRkNU7/9V1/kv1lVlYQ==
Line one:	GSK Consumer Healthcare
Line two:	route de l'Etraz 2
P.O. Box:	1279
City:	Nyon
State:	N/A
Country:	Switzerland
Zip Code:	1260

TCB Information

TCB Application Email Address:	TEI@TIMCOENGR.COM
TCB Scope:	A4: UNII devices & low power transmitters using spread spectrum techniques

FCC ID

Grantee Code:	2ANMM
Product Code:	THFT1

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

Name:	Didier Falconnet
Title:	Development Director

Telephone Number:

0041798428307

Extension:

Fax Number:	0041225674842
Email:	didier.m.falconnet@gsk.com

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): 02/20/2021
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: DTS - Digital Transmission System
Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant):	The product consists of a single use Analyzer module that connects to a smartphone application via Bluetooth Low Energy. The product also includes a sterile swab and collection container and an extraction fluid-filled dispenser.

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: EMC Services Pty Ltd

First Name: Geoffrey

Last Name: Garrett

Telephone Number:

+61299754555

Extension:

E-mail: geoff@emc.net.au

Grant Comments

Enter any text that you would like to appear at the bottom of the Grant of Equipment Authorization:
Power listed is conducted.

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: Robert Middleton

Title of authorized signature: Branch Manager

Grants

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

Timco Engineering, Inc.
849 NW State Road 45
Newberry, FL 32669

Date of Grant: 08/24/2020

Application Dated: 08/24/2020

GSK Consumer Healthcare

route de l'Etraz 2P.O. Box 1279,

Nyon, 1260
Switzerland

Attention: Didier Falconnet , Development Director

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:	2ANMMTHFT1

Name of Grantee:	GSK Consumer Healthcare

Equipment Class:	Digital Transmission System
Notes:	The product consists of a single use Analyzer module that connects to a smartphone application via Bluetooth Low Energy. The product also includes a sterile swab and collection container and an extraction fluid-filled dispenser.

Grant Notes	FCC Rule Parts	Frequency Range (MHZ)	Output Watts	Frequency Tolerance	Emission Designator
	15C	2402.0 - 2480.0	0.0001

Power listed is conducted.

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

GSK Consumer Healthcare
GSK Consumer Healthcare route de l'Etraz 2P.O. Box 1279,
Nyon, 1260
Switzerland