FCC ID PQC-WMTS-ITS2

PQCWMTS-ITS2, PQC WMTSITS2, PQC-WMTS-ITS2, PQC-WMTS-1TS2, PQC-WMT5-IT52, POC-WMTS-ITS2, P0C-WMTS-ITS2

Philips Medical Systems North America Co. ITS MODULE WMTS-ITS2

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: PQC-WMTS-ITS2 is PQC. The remaining characters of the FCC ID, -WMTS-ITS2, 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: ITS MODULE

Application: ITS MODULE
Equipment Class: TNB - Licensed Non-Broadcast Station Transmitter
Short Link: fcc.id/PQC-WMTS-ITS2
Sources: FCC.gov | FCC.report
Registered By: Philips Medical Systems North America Co. - PQC (United States)

App #	Purpose	Date	Unique ID
1	Original Equipment	2010-07-07	JeP9WXrvibCLpwyGJgWafw==

Operating Frequencies

Device operates within approved frequencies overlapping with the following cellular bands: LTE 11,1500 Lower UP |

Frequency Range	Power Output	Tolerance	Emission Designator	Rule Parts	Line Entry
1.3959-1.3991 GHz	17 mW	1.1Hz	1M1F1D	95H	1
1.4279-1.4311 GHz	17 mW	1.1Hz	1M1F1D	95H	2

Exhibits

Document	Type	Submitted Available
Users Manual	Users Manual Adobe Acrobat PDF (43 kB)	2010-07-07 2010-07-07
Label Location	ID Label/Location Info Adobe Acrobat PDF (80 kB)	2010-07-07 2010-07-07
Cover Letter	Cover Letter(s) Adobe Acrobat PDF (31 kB)	2010-07-07 2010-07-07
Test Setup Photos	Test Setup Photos Adobe Acrobat PDF (239 kB)	2010-07-07 2010-07-07
Test Report	Test Report Adobe Acrobat PDF (544 kB)	2010-07-07 2010-07-07
Label Sample	ID Label/Location Info Adobe Acrobat PDF (96 kB)	2010-07-07 2010-07-07
Confidential Letter	Cover Letter(s) Adobe Acrobat PDF (315 kB)	2010-07-07 2010-07-07
Agency Letter	Cover Letter(s) Adobe Acrobat PDF (23 kB)	2010-07-07 2010-07-07
Internal Photos	Internal Photos Adobe Acrobat PDF (639 kB)	2010-07-07 2010-08-21
External Photos	External Photos Adobe Acrobat PDF (196 kB)	2010-07-07 2010-08-21
Operational Description	Operational Description Adobe Acrobat PDF (110 kB)	2010-07-07
Block Diagram	Block Diagram Adobe Acrobat PDF (12 kB)	2010-07-07
Schematics	Schematics Adobe Acrobat PDF (124 kB)	2010-07-07
Parts List	Parts List/Tune Up Info Adobe Acrobat PDF (74 kB)	2010-07-07

Correspondence

App #	Document	Date
1	[Re-Sent]Short-Term Confidential Expiration Email generated [Aug 13 2010]	2010-08-13 10:21:29
1	[Re-Sent]Short-Term Confidential Expiration Email generated [Aug 13 2010]	2010-08-13 10:22:32

Application Forms

1 (2010-07-07)

Application for Equipment Authorization FCC Form 731 TCB Version

Applicant Information

Applicant's complete, legal business name:	Philips Medical Systems North America Co.
FCC Registration Number (FRN):	0004980637
Alphanumeric FCC ID:	PQCWMTSITS2
Unique Application Identifier:	JeP9WXrvibCLpwyGJgWafw==
Line one:	3000 Minuteman Road
City:	Andover
State:	Massachusetts
Country:	United States
Zip Code:	01810-1099

TCB Information

TCB Application Email Address:	TEI@TIMCOENGR.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:	PQC
Product Code:	-WMTS-ITS2

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

Name:	Delroy Smith
Title:	Principal Scientist / Project Leader

Telephone Number:

+ 1 978 659 3382

Extension:

Fax Number:	1-978-685-5624
Email:	delroy.smith@philips.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): 08/21/2010
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: TNB - Licensed Non-Broadcast Station Transmitter
Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant):	ITS MODULE

Related OET KnowledgeDataBase Inquiry

Is there a KDB inquiry associated with this application? No

Modular Equipment

Modular Type: Limited Single Modular Approval

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: Compliance Worldwide, Inc.

First Name: Mark

Last Name: McSweeney

Telephone Number:

603-887-3903

Extension:

Fax Number: 603 887 6445

E-mail: mark@complianceworldwide.com

Grant Comments

Enter any text that you would like to appear at the bottom of the Grant of Equipment Authorization:
Power listed is conducted. Limited modular approval. This Grant is valid only when this module is installed by the Grantee in their host models with their specific antennas as detailed in this filing. Use of this module in other hosts or use of different antennas not listed in this filing requires additional certification filing. Compliance of this device in all final host configurations is the responsibility of the grantee. Any accessories to be used with the host devices are limited to those listed in this filing. This device is approved for operation in the Wireless Medical Telemetry Service. Installers must be provided with antenna installation instructions and end-users must be provided with transmitter operating conditions 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: Larry Stillings

Title of authorized signature: President

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:

Timco Engineering, Inc.
849 NW State Road 45 <BR>P.O. Box 370,
Newberry, FL 32669

Date of Grant: 07/07/2010

Application Dated: 07/07/2010

Philips Medical Systems North America Co.

3000 Minuteman Road

Andover, MA 01810-1099

Attention: Delroy Smith , Principal Scientist / Project Leader

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:	PQC-WMTS-ITS2

Name of Grantee:	Philips Medical Systems North America Co.

Equipment Class:	Licensed Non-Broadcast Station Transmitter
Notes:	ITS MODULE
Modular Type:	Limited Single Modular

Grant Notes	FCC Rule Parts	Frequency Range (MHZ)	Output Watts	Frequency Tolerance	Emission Designator
	95H	1395.9 - 1399.1	0.017	1.1 Hz	1M1F1D
	95H	1427.9 - 1431.1	0.017	1.1 Hz	1M1F1D

Power listed is conducted. Limited modular approval. This Grant is valid only when this module is installed by the Grantee in their host models with their specific antennas as detailed in this filing. Use of this module in other hosts or use of different antennas not listed in this filing requires additional certification filing. Compliance of this device in all final host configurations is the responsibility of the grantee. Any accessories to be used with the host devices are limited to those listed in this filing. This device is approved for operation in the Wireless Medical Telemetry Service. Installers must be provided with antenna installation instructions and end-users must be provided with transmitter operating conditions for satisfying RF exposure compliance.

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

Philips Medical Systems North America Co.
3000 Minuteman Road
Andover, MA 01810-1099
United States