FCC ID 2ABOQ-SF1US

2ABOQSF1US, 2ABOQ SF1US, 2ABOQ-SF1US, 2ABOQ-SFIUS, 2ABOQ-5F1U5, 2AB0Q-SF1US, 2ABOO-SF1US, 2ABO0-SF1US

Huntleigh Healthcare Limited, Huntleigh Diagnostic Products Division Wireless Fetal Monitoring Solution SF1US

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: 2ABOQ-SF1US is 2ABOQ. The remaining characters of the FCC ID, -SF1US, 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: Wireless Fetal Monitoring Solution

Application: Wireless Fetal Monitoring Solution
Equipment Class: TNT - Licensed Non-Broadcast Transmitter Worn on Body
Short Link: fcc.id/2ABOQ-SF1US
Sources: FCC.gov | FCC.report
Registered By: Huntleigh Healthcare Limited, Huntleigh Diagnostic Products Division - 2ABOQ (United Kingdom)

App #	Purpose	Date	Unique ID
1	Original Equipment	2014-07-25	GnrzMuDlAPPJsZTJttwvdQ==

Operating Frequencies

Frequency Range	Power Output	Tolerance	Emission Designator	Rule Parts	Line Entry
608.012-612.988 MHz	0.01 mW	1.0000000000ppm	21K6F1D	95H	1

Exhibits

Document	Type	Submitted Available
Test Report	Test Report Adobe Acrobat PDF (1767 kB)	2014-07-25 2014-07-25
Test Set Up Photos	Test Setup Photos Adobe Acrobat PDF (379 kB)	2014-07-25 2014-07-25
Review Q&A	Attestation Statements Adobe Acrobat PDF (148 kB)	2014-07-25 2014-07-25
Tune Up	Parts List/Tune Up Info Adobe Acrobat PDF (360 kB)	2014-07-25 2014-07-25
SAR exemption calculation	RF Exposure Info Adobe Acrobat PDF (156 kB)	2014-07-25 2014-07-25
Label and Location	ID Label/Location Info Adobe Acrobat PDF (77 kB)	2014-07-25 2014-07-25
Internal Photos	Internal Photos Adobe Acrobat PDF (1332 kB)	2014-07-25 2014-07-25
Manual	Users Manual Adobe Acrobat PDF (477 kB)	2014-07-25 2014-07-25
Confidentiaility Request	Cover Letter(s) Adobe Acrobat PDF (52 kB)	2014-07-25 2014-07-25
External Photos	External Photos Adobe Acrobat PDF (429 kB)	2014-07-25 2014-07-25
Agent Authorization	Cover Letter(s) Adobe Acrobat PDF (89 kB)	2014-07-25 2014-07-25
Block Diagram	Block Diagram Adobe Acrobat PDF (196 kB)	2014-07-25
Schematics	Schematics Adobe Acrobat PDF (248 kB)	2014-07-25
Operational Description	Operational Description Adobe Acrobat PDF (928 kB)	2014-07-25

Application Forms

1 (2014-07-25)

Application for Equipment Authorization FCC Form 731 TCB Version

Applicant Information

Applicant's complete, legal business name:	Huntleigh Healthcare Limited, Huntleigh Diagnostic Products Division
FCC Registration Number (FRN):	0023251705
Alphanumeric FCC ID:	2ABOQSF1US
Unique Application Identifier:	GnrzMuDlAPPJsZTJttwvdQ==
Line one:	35 Portmanmoor Road
City:	Cardiff
State:	N/A
Country:	United Kingdom
Zip Code:	CF24 5HN

TCB Information

TCB Application Email Address:	LST.FRE.CertNotice@ul.com
TCB Scope:	B2: General Mobile Radio And Broadcast Services equipment in the following 47 CFR Parts 22 (non-cellular) 73, 74, 90, 95 & 97

FCC ID

Grantee Code:	2ABOQ
Product Code:	-SF1US

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

Name:	Laura J Garcia Deacon
Title:	Regulatory Engineer

Telephone Number:

+44(0)29 20485885

Extension:

7033

Fax Number:	+44(0)29 20492520
Email:	laura.deacon@huntleigh-diagnostics.co.uk

Technical Contact

Firm Name:	UL LLC
First Name:	Bart
Last Name:	Mucha
Line 1:	333 Pfingsten Rd
City:	Northbrook
State:	Illinois
Country:	United States
Zip Code:	60062

Telephone Number:

847-664-1216

Extension:

Fax Number:	847-407-1216
E-Mail:	bartlomiej.mucha@ul.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?: No

If so, specify the short-term confidentiality release date (MM/DD/YYYY format):
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: TNT - Licensed Non-Broadcast Transmitter Worn on Body
Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant):	Wireless Fetal Monitoring Solution

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? Yes

Test Firm Information

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

Firm Name: UL LLC

First Name: Rick

Last Name: Titus

Telephone Number:

847-664-3281

Extension:

Fax Number: 847-313-3281

E-mail: Rick.A.Titus@us.ul.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. This device and its antenna must not be co-located or operating in conjunction with any other antenna or transmitter except in accordance with FCC multi-transmitter product procedures. End-users must be provided with specific operating instructions for satisfying RF exposure compliance.

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: Bart Mucha

Title of authorized signature: Agent

Complete items below if agent signs the application:

Firm Name: UL LLC

Name: Bart Bart Bart

Line 1: Bart

Line 2: Bart

P.O. Box: Bart

City: Bart

State: Bart

Country: Bart

Zip Code: Bart

Telephone Number:

847-664-1216

Fax Number: 847-407-1216

E-mail: bartlomiej.mucha@ul.com

Applications are submitted for FCC ID and Grant requests. Click an above application to view details

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

UL Verification Services Inc. (formerly UL CCS)
47173 Benicia Street
Fremont, CA 94538

Date of Grant: 07/25/2014

Application Dated: 07/25/2014

Huntleigh Healthcare Limited, Huntleigh Diagnostic Products Division

35 Portmanmoor Road

Cardiff, CF24 5HN
United Kingdom

Attention: Laura Garcia Deacon , Regulatory Engineer

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:	2ABOQ-SF1US

Name of Grantee:	Huntleigh Healthcare Limited, Huntleigh Diagnostic Products Division

Equipment Class:	Licensed Non-Broadcast Transmitter Worn on Body
Notes:	Wireless Fetal Monitoring Solution

Grant Notes	FCC Rule Parts	Frequency Range (MHZ)	Output Watts	Frequency Tolerance	Emission Designator
	95H	608.012 - 612.988	0.00001	1.0 PM	21K6F1D

Output power is erp. This device and its antenna must not be co-located or operating in conjunction with any other antenna or transmitter except in accordance with FCC multi-transmitter product procedures. End-users must be provided with specific operating instructions for satisfying RF exposure compliance.

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

Huntleigh Healthcare Limited, Huntleigh Diagnostic Products Division
35 Portmanmoor Road
Cardiff, CF24 5HN
United Kingdom

Date of Grant: 07/25/2014

Application Dated: 07/25/2014

Attention: Laura Garcia Deacon , Regulatory Engineer

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:	2ABOQ-SF1US

Name of Grantee:	Huntleigh Healthcare Limited, Huntleigh Diagnostic Products Division

Equipment Class:	Licensed Non-Broadcast Transmitter Worn on Body
Notes:	Wireless Fetal Monitoring Solution
Modular Type:	Does not apply

Grant Notes	FCC Rule Parts	Frequency Range (MHZ)	Output Watts	Frequency Tolerance	Emission Designator
	95H	608.012 - 612.988	0.00001	1.0 PM	21K6F1D

Mail To:

EA932828

FCC ID 2ABOQ-SF1US

2ABOQSF1US, 2ABOQ SF1US, 2ABOQ-SF1US, 2ABOQ-SFIUS, 2ABOQ-5F1U5, 2AB0Q-SF1US, 2ABOO-SF1US, 2ABO0-SF1US

Huntleigh Healthcare Limited, Huntleigh Diagnostic Products Division Wireless Fetal Monitoring Solution SF1US

Purchase on Amazon: Wireless Fetal Monitoring Solution

Operating Frequencies

Exhibits

Application Forms

Applications are submitted for FCC ID and Grant requests. Click an above application to view details

Grants

Grants authorize equipment for operation at approved frequencies and sale within the USA. Click an above grant to view details