FCC ID OU52102462001

OU5-2102462001, OU5 2102462001, OU52102462001, OU521O2462OO1, OU52I0246200I, OUS2102462001, 0U52102462001

GE Medical Systems Information Technologies Inc. RFID Module 2102462001

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: OU52102462001 is OU5. The remaining characters of the FCC ID, 2102462001, 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: RFID Module

App # Purpose Date Unique ID
1 Change in Identification 2017-09-13 pRYp0to8QrHnZ3Q154vCNQ==
2 Class II Permissive Change 2018-08-07 WQRpqO9dDUWmDPQnSDC74w==

Operating Frequencies

Exhibits

Available Exhibits

App #Document Type Submitted
Available
2 PC Letter V3Cover Letter(s)
Adobe Acrobat PDF (74 kB)
2018-08-07
2018-08-07
2 FCC Agency LetterCover Letter(s)
Adobe Acrobat PDF (17 kB)
2018-06-04
2018-08-07
2 Co-located TX AttestationsAttestation Statements
Adobe Acrobat PDF (18 kB)
2018-06-04
2018-08-07
2 Host External PhotosExternal Photos
Adobe Acrobat PDF (2315 kB)
2018-06-04
2018-08-07
2 Host Internal PhotosInternal Photos
Adobe Acrobat PDF (2249 kB)
2018-06-04
2018-08-07
2 Host Labeling InfoID Label/Location Info
Adobe Acrobat PDF (171 kB)
2018-06-04
2018-08-07
2 RF Exposure V7RF Exposure Info
Adobe Acrobat PDF (871 kB)
2018-06-04
2018-08-07
2 Test Report V4Test Report
Adobe Acrobat PDF (1922 kB)
2018-06-04
2018-08-07
2 Test Photos RevisedTest Setup Photos
Adobe Acrobat PDF (417 kB)
2018-06-04
2018-08-07
1 Label and LocationID Label/Location Info
Adobe Acrobat PDF (107 kB)
2017-09-12
2017-09-13
1 External PhotosExternal Photos
Adobe Acrobat PDF (443 kB)
2017-09-12
2017-09-13
1 Change In ID Auth LetterCover Letter(s)
Adobe Acrobat PDF (193 kB)
2017-09-12
2017-09-13
1 Change In ID LetterCover Letter(s)
Adobe Acrobat PDF (18 kB)
2017-09-12
2017-09-13
1 Agent AuthCover Letter(s)
Adobe Acrobat PDF (17 kB)
2017-09-12
2017-09-13

APP # 2 (2018-08-07)

App # Document Type Submitted
Available
2 PC Letter V3 Cover Letter(s)
Adobe Acrobat PDF (74 kB)
2018-08-07 00:00:00
2018-08-07 00:00:00
2 FCC Agency Letter Cover Letter(s)
Adobe Acrobat PDF (17 kB)
2018-06-04 00:00:00
2018-08-07 00:00:00
2 Co-located TX Attestations Attestation Statements
Adobe Acrobat PDF (18 kB)
2018-06-04 00:00:00
2018-08-07 00:00:00
2 Host External Photos External Photos
Adobe Acrobat PDF (2315 kB)
2018-06-04 00:00:00
2018-08-07 00:00:00
2 Host Internal Photos Internal Photos
Adobe Acrobat PDF (2249 kB)
2018-06-04 00:00:00
2018-08-07 00:00:00
2 Host Labeling Info ID Label/Location Info
Adobe Acrobat PDF (171 kB)
2018-06-04 00:00:00
2018-08-07 00:00:00
2 RF Exposure V7 RF Exposure Info
Adobe Acrobat PDF (871 kB)
2018-06-04 00:00:00
2018-08-07 00:00:00
2 Test Report V4 Test Report
Adobe Acrobat PDF (1922 kB)
2018-06-04 00:00:00
2018-08-07 00:00:00
2 Test Photos Revised Test Setup Photos
Adobe Acrobat PDF (417 kB)
2018-06-04 00:00:00
2018-08-07 00:00:00

APP # 1 (2017-09-13)

App # Document Type Submitted
Available
1 Label and Location ID Label/Location Info
Adobe Acrobat PDF (107 kB)
2017-09-12 00:00:00
2017-09-13 00:00:00
1 External Photos External Photos
Adobe Acrobat PDF (443 kB)
2017-09-12 00:00:00
2017-09-13 00:00:00
1 Change In ID Auth Letter Cover Letter(s)
Adobe Acrobat PDF (193 kB)
2017-09-12 00:00:00
2017-09-13 00:00:00
1 Change In ID Letter Cover Letter(s)
Adobe Acrobat PDF (18 kB)
2017-09-12 00:00:00
2017-09-13 00:00:00
1 Agent Auth Cover Letter(s)
Adobe Acrobat PDF (17 kB)
2017-09-12 00:00:00
2017-09-13 00:00:00

APP # 2 (2018-08-07)

App # Document Type Submitted
Available
2 PC Letter Cover Letter(s)
Adobe Acrobat PDF (64 kB)
2018-06-04 00:00:00
2018-08-07 00:00:00

Application Forms

Application for Equipment Authorization FCC Form 731 TCB Version


Applicant Information
Applicant's complete, legal business name: GE Medical Systems Information Technologies Inc.
FCC Registration Number (FRN): 0009572553
Alphanumeric FCC ID: OU52102462001
Unique Application Identifier: pRYp0to8QrHnZ3Q154vCNQ==
Line one: 8200 West Tower avenue
City: Milwaukee
State: Wisconsin
Country: United States
Zip Code: 53223

TCB Information
TCB Application Email Address: hotline@acbcert.com
TCB Scope: A1: Low Power Transmitters below 1 GHz (except Spread Spectrum), Unintentional Radiators, EAS (Part 11) & Consumer ISM devices

FCC ID
Grantee Code: OU5
Product Code: 2102462001

Person at the applicant's address to receive grant or for contact
Name: Mike Steinike
Title: Lead System Designer-RF
Telephone Number: 414-362-2417 Extension:
Fax Number: 414-362-2880
Email: michael.steinike@med.ge.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?:   No

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:   DXX - Part 15 Low Power Communication Device Transmitter
Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant): RFID Module

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:   Change in identification of presently authorized equipment. Original FCC ID: M9MOEM805NX Grant Date: 11/02/2012

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:   Laird Technologies, Inc.
First Name:   Adam
Last Name:   Alger
Telephone Number: 2623753091 Extension:
Fax Number:  262 375 4248
E-mail:  adam.alger@lairdtech.com

Grant Comments
Enter any text that you would like to appear at the bottom of the Grant of Equipment Authorization:
This device is allowed only for OEM integration into their enclosure. This grant is valid only when the device is sold to OEM or OEM integrators. OEM integrator is responsible for complying with the instructions and requirements for the housing enclosure. OEM integrators are instructed to ensure that the end use has no manual instructions to remove or install the device.
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:  Thomas Smith
Title of authorized signature:  Director of EMC Compliance

Application for Equipment Authorization FCC Form 731 TCB Version


Applicant Information
Applicant's complete, legal business name: GE Medical Systems Information Technologies Inc.
FCC Registration Number (FRN): 0017065665
Alphanumeric FCC ID: OU52102462001
Unique Application Identifier: WQRpqO9dDUWmDPQnSDC74w==
Line one: 8200 West Tower avenue
City: Milwaukee
State: Wisconsin
Country: United States
Zip Code: 53223

TCB Information
TCB Application Email Address: hotline@acbcert.com
TCB Scope: A1: Low Power Transmitters below 1 GHz (except Spread Spectrum), Unintentional Radiators, EAS (Part 11) & Consumer ISM devices

FCC ID
Grantee Code: OU5
Product Code: 2102462001

Person at the applicant's address to receive grant or for contact
Name: Mike Steinike
Title: Lead System Designer-RF
Telephone Number: 414-362-2417 Extension:
Fax Number: 414-362-2880
Email: michael.steinike@med.ge.com

Technical Contact
Firm Name:
GE Medical Systems Information Technologies
First Name: Michael
Last Name: Steinike
Line 1:
8200 West Tower Avenue
City: Milwaukee
Country:
United States
Zip Code: 53223-3219
Telephone Number:
414.362.2417

Extension:
Fax Number: 414.362.2880
E-Mail:

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?:   No

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:   DXX - Part 15 Low Power Communication Device Transmitter
Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant): RFID Module

Related OET KnowledgeDataBase Inquiry
Is there a KDB inquiry associated with this application?  Yes

Modular Equipment
Modular Type:  Limited Single Modular Approval

Application Purpose
Application is for:   Class II permissive change or modification of presently authorized 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:   Laird Technologies, Inc.
First Name:   Adam
Last Name:   Alger
Telephone Number: 2623753091 Extension:
Fax Number:  262 375 4248
E-mail:  adam.alger@lairdtech.com

Grant Comments
Enter any text that you would like to appear at the bottom of the Grant of Equipment Authorization:
This device is allowed only for OEM integration into their enclosure. This grant is valid only when the device is sold to OEM or OEM intergrators. OEM integrator is responsible for complying with the instructions and requirements for the housing enclosure. OEM integrators are instructed to ensure that the end use has no manual instructions to remove or install the device. This change is to add LMA approval in host as specified within this application.
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:  Thomas T Smith
Title of authorized signature:  Director of EMC Compliance

Complete items below if agent signs the application:

Firm Name:  Laird Technologies Inc
Name:  Thomas Thomas Thomas
Line 1:  Thomas
Line 2:  Thomas
P.O. Box:  Thomas
City:  Thomas
State:  Thomas
Country:  Thomas
Zip Code:  Thomas
Telephone Number:  2624214986
Fax Number:  2623642649
E-mail:  Tom.Smith@lairdtech.com

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:

  ACB, Inc.
6731 Whittier Avenue Suite C110
McLean, VA 22101
Date of Grant: 09/13/2017

Application Dated: 09/12/2017
GE Medical Systems Information Technologies Inc.
8200 West Tower avenue
Milwaukee, WI 53223
 
Attention: Mike Steinike , Lead System Designer-RF

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:  OU52102462001
Name of Grantee:  GE Medical Systems Information Technologies Inc.
Equipment Class: Part 15 Low Power Communication Device Transmitter
Notes: RFID Module
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
15C 0.125  -  0.125  
15C 13.56  -  13.56  

This device is allowed only for OEM integration into their enclosure. This grant is valid only when the device is sold to OEM or OEM integrators. OEM integrator is responsible for complying with the instructions and requirements for the housing enclosure. OEM integrators are instructed to ensure that the end use has no manual instructions to remove or install the device.

COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

GE Medical Systems Information Technologies Inc.
8200 West Tower avenue
Milwaukee, WI 53223
United States
  Date of Grant: 09/13/2017

Application Dated: 09/12/2017
 
Attention: Mike Steinike , Lead System Designer-RF

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:  OU52102462001
Name of Grantee:  GE Medical Systems Information Technologies Inc.
Equipment Class: Part 15 Low Power Communication Device Transmitter
Notes: RFID Module
Modular Type: Does not apply
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
15C 0.125  -  0.125  
15C 13.56  -  13.56  

This device is allowed only for OEM integration into their enclosure. This grant is valid only when the device is sold to OEM or OEM integrators. OEM integrator is responsible for complying with the instructions and requirements for the housing enclosure. OEM integrators are instructed to ensure that the end use has no manual instructions to remove or install the device.



Mail To:


EA468977
TCB GRANT OF EQUIPMENT
AUTHORIZATION
TCB
Certification
Issued Under the Authority of the
Federal Communications Commission
By:

  ACB, Inc.
6731 Whittier Avenue Suite C110
McLean, VA 22101
Date of Grant: 08/07/2018

Application Dated: 05/29/2018
GE Medical Systems Information Technologies Inc.
8200 West Tower avenue
Milwaukee, WI 53223
 
Attention: Mike Steinike , Lead System Designer-RF

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:  OU52102462001
Name of Grantee:  GE Medical Systems Information Technologies Inc.
Equipment Class: Part 15 Low Power Communication Device Transmitter
Notes: RFID Module
Modular Type: Limited Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
15C 0.125  -  0.125  
15C 13.56  -  13.56  

This device is allowed only for OEM integration into their enclosure. This grant is valid only when the device is sold to OEM or OEM intergrators. OEM integrator is responsible for complying with the instructions and requirements for the housing enclosure. OEM integrators are instructed to ensure that the end use has no manual instructions to remove or install the device.

This change is to add LMA approval in host as specified within this application.


COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

GE Medical Systems Information Technologies Inc.
8200 West Tower avenue
Milwaukee, WI 53223
United States
  Date of Grant: 08/07/2018

Application Dated: 05/29/2018
 
Attention: Mike Steinike , Lead System Designer-RF

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:  OU52102462001
Name of Grantee:  GE Medical Systems Information Technologies Inc.
Equipment Class: Part 15 Low Power Communication Device Transmitter
Notes: RFID Module
Modular Type: Limited Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
15C 0.125  -  0.125  
15C 13.56  -  13.56  

This device is allowed only for OEM integration into their enclosure. This grant is valid only when the device is sold to OEM or OEM intergrators. OEM integrator is responsible for complying with the instructions and requirements for the housing enclosure. OEM integrators are instructed to ensure that the end use has no manual instructions to remove or install the device.

This change is to add LMA approval in host as specified within this application.



Mail To:


EA279283

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