FCC ID RIASJMRFICMDM3

RIA-SJMRFICMDM3, RIA SJMRFICMDM3, RIASJMRFICMDM3, RIASJMRF1CMDM3, RIA5JMRFICMDM3, R1ASJMRF1CMDM3

St. Jude Medical Implantable Cardiac Monitor SJMRFICMDM3

Data is missing from this FCC ID. This may be due to an application error or missing data from FCC.gov. Be sure to check the "Alternate Sources" links.

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: RIASJMRFICMDM3 is RIA. The remaining characters of the FCC ID, SJMRFICMDM3, 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: Implantable Cardiac Monitor

Application: Implantable Cardiac Monitor
Equipment Class: DTS - Digital Transmission System
Short Link: fcc.id/RIASJMRFICMDM3
Sources: FCC.gov | FCC.report
Registered By: St. Jude Medical - RIA ()

Operating Frequencies

Frequency Range	Power Output	Rule Parts	Line Entry
2.402-2.48 GHz	0.49 mW	15C	1

Application Forms

1 ()

Application for Equipment Authorization FCC Form 731 TCB Version

Applicant Information

Applicant's complete, legal business name:	St. Jude Medical
FCC Registration Number (FRN):	0025428756
Alphanumeric FCC ID:	RIASJMRFICMDM3
Unique Application Identifier:	FWjq4wSEflsBOpzJKymahg==
Line one:	15900 Valley View Court
City:	Sylmar
State:	California
Country:	United States
Zip Code:	91342

TCB Information

TCB Application Email Address:	vkerai@tuvam.com
TCB Scope:	A4: UNII devices & low power transmitters using spread spectrum techniques

FCC ID

Grantee Code:	RIA
Product Code:	SJMRFICMDM3

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

Name:	Jennifer A Wong
Title:	Director, Regulatory Affairs

Telephone Number:

972-526-9622

Extension:

Fax Number:	818-493-3597
Email:	jwong03@sjm.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): 01/01/2017
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):	Implantable Cardiac Monitor

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: TUV SUD America Inc.

First Name: Barry

Last Name: Quinlan

Telephone Number:

978-573-2528

Extension:

Fax Number: 978 977 0182

E-mail: bquinlan@tuvam.com

Grant Comments

Enter any text that you would like to appear at the bottom of the Grant of Equipment Authorization:
Output power 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: Jennifer Wong

Title of authorized signature:

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

Grants

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

TUV SUD BABT
Octagon House, Concorde Way, Segensworth North,
Fareham, PO15 5RL
United Kingdom

Date of Grant: 07/12/2016

Application Dated: 07/12/2016

St. Jude Medical

15900 Valley View Court

Sylmar, CA 91342

Attention: Jennifer Wong , Director, Regulatory Affairs

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:	RIASJMRFICMDM3

Name of Grantee:	St. Jude Medical

Equipment Class:	Digital Transmission System
Notes:	Implantable Cardiac Monitor

Grant Notes	FCC Rule Parts	Frequency Range (MHZ)	Output Watts	Frequency Tolerance	Emission Designator
	15C	2402.0 - 2480.0	0.00049

Output power is conducted.

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

St. Jude Medical
15900 Valley View Court
Sylmar, CA 91342
United States