FCC ID PQC-WMTS-ITS2

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

Philips Medical Systems North America Co. ITS MODULE

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 . 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.

Philips Medical Systems North America Co.

Full Company Details: Philips Medical Systems North America Co. - PQC
Company Code: PQC
Address:
   Philips Medical Systems North America Co.
   3000 Minuteman Road
   Andover, MA 01810-1099
   United States
App # Purpose Date Unique ID
1 Original Equipment 2010-07-07 JeP9WXrvibCLpwyGJgWafw==

Approved Operating Frequencies

Line EntryFrequency RangePower OutputToleranceEmission DesignatorRule Parts
11395.9-1399.10.0171.1Hz1M1F1D95H
21427.9-1431.10.0171.1Hz1M1F1D95H

Exhibits

All Available Documents

Document Type Submitted / Available
SchematicsSchematics / Adobe Acrobat PDF (124 kB) 2010-07-07 /
Internal PhotosInternal Photos / Adobe Acrobat PDF (639 kB) 2010-07-07 / 2010-08-21
Cover LetterCover Letter(s) / Adobe Acrobat PDF (31 kB) 2010-07-07 / 2010-07-07
Agency LetterCover Letter(s) / Adobe Acrobat PDF (23 kB) 2010-07-07 / 2010-07-07
Agency LetterCover Letter(s) / Adobe Acrobat PDF (23 kB) 2010-07-07 / 2010-07-07
Test ReportTest Report / Adobe Acrobat PDF (544 kB) 2010-07-07 / 2010-07-07
Label LocationID Label/Location Info / Adobe Acrobat PDF (80 kB) 2010-07-07 / 2010-07-07
Label LocationID Label/Location Info / Adobe Acrobat PDF (80 kB) 2010-07-07 / 2010-07-07
Block DiagramBlock Diagram / Adobe Acrobat PDF (12 kB) 2010-07-07 /
Confidential LetterCover Letter(s) / Adobe Acrobat PDF (315 kB) 2010-07-07 / 2010-07-07
Test Setup PhotosTest Setup Photos / Adobe Acrobat PDF (239 kB) 2010-07-07 / 2010-07-07
Label SampleID Label/Location Info / Adobe Acrobat PDF (96 kB) 2010-07-07 / 2010-07-07
Users ManualUsers Manual / Adobe Acrobat PDF (43 kB) 2010-07-07 / 2010-07-07
Label SampleID Label/Location Info / Adobe Acrobat PDF (96 kB) 2010-07-07 / 2010-07-07
Confidential LetterCover Letter(s) / Adobe Acrobat PDF (315 kB) 2010-07-07 / 2010-07-07
Users ManualUsers Manual / Adobe Acrobat PDF (43 kB) 2010-07-07 / 2010-07-07
Operational DescriptionOperational Description / Adobe Acrobat PDF (110 kB) 2010-07-07 /
Test ReportTest Report / Adobe Acrobat PDF (544 kB) 2010-07-07 / 2010-07-07
Cover LetterCover Letter(s) / Adobe Acrobat PDF (31 kB) 2010-07-07 / 2010-07-07
External PhotosExternal Photos / Adobe Acrobat PDF (196 kB) 2010-07-07 / 2010-08-21
Parts ListParts List/Tune Up Info / Adobe Acrobat PDF (74 kB) 2010-07-07 /
External PhotosExternal Photos / Adobe Acrobat PDF (196 kB) 2010-07-07 / 2010-08-21
Test Setup PhotosTest Setup Photos / Adobe Acrobat PDF (239 kB) 2010-07-07 / 2010-07-07
Internal PhotosInternal Photos / Adobe Acrobat PDF (639 kB) 2010-07-07 / 2010-08-21

APP # 1 (2010-07-07) Documents

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

Grants

TCB Grant from App #1 (2010-07-07)

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.

EAS Grant from App #1 (2010-07-07)

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
  Date of Grant: 07/07/2010

Application Dated: 07/07/2010
 
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.



Mail To:


EA964603

Applications for this FCC ID

Form App # 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

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