FCC ID PQC-MX40WLAN2

PQCMX40WLAN2, PQC MX40WLAN2, PQC-MX40WLAN2, PQC-MX4OWLAN2, POC-MX40WLAN2, P0C-MX40WLAN2

Philips Medical Systems North America Co. INTELLIVUE MX40 WLAN2 PATIENT WORN DEVICE MX40WLAN2

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-MX40WLAN2 is PQC. The remaining characters of the FCC ID, -MX40WLAN2, 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: INTELLIVUE MX40 WLAN2 PATIENT WORN DEVICE

App # Purpose Date Unique ID
1 Original Equipment 2012-04-30 9e6o7XrBF17HdivE5eNNEQ==
2 Original Equipment 2012-04-30 cnyqPXCUyAiTPTasXHRA9A==

Operating Frequencies

Device operates within approved frequencies overlapping with the following cellular bands: LTE 255,Unlicensed NII-3 DOWN | LTE 46,TD Unlicensed DOWN |
Frequency RangePower OutputRule PartsGrant Notes App #
2.405-2.48 GHz0.6 mW15CCC 2.2
2.412-2.462 GHz 2.4 GHz WiFi83 mW15CCC 2.1
5.18-5.32 GHz 5 GHz WiFi22.45 mW15ECC 1.1
5.5-5.58 GHz46.04 mW15ECC 1.2
5.66-5.7 GHz47.66 mW15ECC 1.3
5.745-5.805 GHz66.55 mW15ECC 1.4

Exhibits

Available Exhibits

App #Document Type Submitted
Available
2 USERS MANUALUsers Manual
Adobe Acrobat PDF (2659 kB)
2012-04-30
2012-04-30
2 TEST SETUP PHOTOSTest Setup Photos
Adobe Acrobat PDF (162 kB)
2012-04-30
2012-04-30
2 RF EXPOSURERF Exposure Info
Adobe Acrobat PDF (162 kB)
2012-04-30
2012-04-30
2 LABEL LOCATIONID Label/Location Info
Adobe Acrobat PDF (18 kB)
2012-04-30
2012-04-30
2 LABEL SAMPLEID Label/Location Info
Adobe Acrobat PDF (57 kB)
2012-04-30
2012-04-30
2 LABEL COVER LETTERID Label/Location Info
Adobe Acrobat PDF (37 kB)
2012-04-30
2012-04-30
2 EXTERNAL PHOTOSExternal Photos
Adobe Acrobat PDF (125 kB)
2012-04-30
2012-04-30
2 COVER LETTERCover Letter(s)
Adobe Acrobat PDF (28 kB)
2012-04-30
2012-04-30
2 CONFIDENTIAL REQUEST LETTERCover Letter(s)
Adobe Acrobat PDF (43 kB)
2012-04-30
2012-04-30
2 AUTHORIZATION LETTERCover Letter(s)
Adobe Acrobat PDF (30 kB)
2012-04-30
2012-04-30
2 ADHOC LETTERCover Letter(s)
Adobe Acrobat PDF (34 kB)
2012-04-30
2012-04-30
2 TEST REPORTTest Report
Adobe Acrobat PDF (1311 kB)
2012-04-30
2012-04-30
2 TEST REPORT SRRTest Report
Adobe Acrobat PDF (612 kB)
2012-04-30
2012-04-30
2 INTERNAL PHOTOSInternal Photos
Adobe Acrobat PDF (524 kB)
2012-04-30
2012-06-14
1 USERS MANUALUsers Manual
Adobe Acrobat PDF (2659 kB)
2012-04-30
2012-04-30
1 TEST SETUP PHOTOSTest Setup Photos
Adobe Acrobat PDF (162 kB)
2012-04-30
2012-04-30
1 RF EXPOSURERF Exposure Info
Adobe Acrobat PDF (206 kB)
2012-04-30
2012-04-30
1 LABEL SAMPLEID Label/Location Info
Adobe Acrobat PDF (57 kB)
2012-04-30
2012-04-30
1 LABEL LOCATIONID Label/Location Info
Adobe Acrobat PDF (18 kB)
2012-04-30
2012-04-30
1 LABEL COVER LETTERCover Letter(s)
Adobe Acrobat PDF (37 kB)
2012-04-30
2012-04-30
1 TEST REPORTTest Report
Adobe Acrobat PDF (4699 kB)
2012-04-30
2012-04-30
1 EXTERNAL PHOTOSExternal Photos
Adobe Acrobat PDF (125 kB)
2012-04-30
2012-04-30
1 COVER LETTERCover Letter(s)
Adobe Acrobat PDF (28 kB)
2012-04-30
2012-04-30
1 CONFIDENTIAL REQUEST LETTERCover Letter(s)
Adobe Acrobat PDF (43 kB)
2012-04-30
2012-04-30
1 AGENCY LETTERCover Letter(s)
Adobe Acrobat PDF (30 kB)
2012-04-30
2012-04-30
1 ADHOC LETTERCover Letter(s)
Adobe Acrobat PDF (34 kB)
2012-04-30
2012-04-30
1 INTERNAL PHOTOSInternal Photos
Adobe Acrobat PDF (524 kB)
2012-04-30
2012-06-14

APP # 2 (2012-04-30)

App # Document Type Submitted
Available
2 USERS MANUAL Users Manual
Adobe Acrobat PDF (2659 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
2 TEST SETUP PHOTOS Test Setup Photos
Adobe Acrobat PDF (162 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
2 RF EXPOSURE RF Exposure Info
Adobe Acrobat PDF (162 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
2 LABEL LOCATION ID Label/Location Info
Adobe Acrobat PDF (18 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
2 LABEL SAMPLE ID Label/Location Info
Adobe Acrobat PDF (57 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
2 LABEL COVER LETTER ID Label/Location Info
Adobe Acrobat PDF (37 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
2 EXTERNAL PHOTOS External Photos
Adobe Acrobat PDF (125 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
2 COVER LETTER Cover Letter(s)
Adobe Acrobat PDF (28 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
2 CONFIDENTIAL REQUEST LETTER Cover Letter(s)
Adobe Acrobat PDF (43 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
2 AUTHORIZATION LETTER Cover Letter(s)
Adobe Acrobat PDF (30 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
2 ADHOC LETTER Cover Letter(s)
Adobe Acrobat PDF (34 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
2 TEST REPORT Test Report
Adobe Acrobat PDF (1311 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
2 TEST REPORT SRR Test Report
Adobe Acrobat PDF (612 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
2 INTERNAL PHOTOS Internal Photos
Adobe Acrobat PDF (524 kB)
2012-04-30 00:00:00
2012-06-14 00:00:00

APP # 1 (2012-04-30)

App # Document Type Submitted
Available
1 USERS MANUAL Users Manual
Adobe Acrobat PDF (2659 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
1 TEST SETUP PHOTOS Test Setup Photos
Adobe Acrobat PDF (162 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
1 RF EXPOSURE RF Exposure Info
Adobe Acrobat PDF (206 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
1 LABEL SAMPLE ID Label/Location Info
Adobe Acrobat PDF (57 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
1 LABEL LOCATION ID Label/Location Info
Adobe Acrobat PDF (18 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
1 LABEL COVER LETTER Cover Letter(s)
Adobe Acrobat PDF (37 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
1 TEST REPORT Test Report
Adobe Acrobat PDF (4699 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
1 EXTERNAL PHOTOS External Photos
Adobe Acrobat PDF (125 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
1 COVER LETTER Cover Letter(s)
Adobe Acrobat PDF (28 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
1 CONFIDENTIAL REQUEST LETTER Cover Letter(s)
Adobe Acrobat PDF (43 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
1 AGENCY LETTER Cover Letter(s)
Adobe Acrobat PDF (30 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
1 ADHOC LETTER Cover Letter(s)
Adobe Acrobat PDF (34 kB)
2012-04-30 00:00:00
2012-04-30 00:00:00
1 INTERNAL PHOTOS Internal Photos
Adobe Acrobat PDF (524 kB)
2012-04-30 00:00:00
2012-06-14 00:00:00

APP # 2 (2012-04-30)

App # Document Type Submitted
Available
2 SCHEMATICS Schematics
Adobe Acrobat PDF (170 kB)
2012-04-30 00:00:00
N/A

APP # 1 (2012-04-30)

App # Document Type Submitted
Available
1 TUNE UP PROCEDURE Parts List/Tune Up Info
Adobe Acrobat PDF (45 kB)
2012-04-30 00:00:00
N/A

APP # 2 (2012-04-30)

App # Document Type Submitted
Available
2 OPERATIONAL DESCRIPTION Operational Description
Adobe Acrobat PDF (209 kB)
2012-04-30 00:00:00
N/A

APP # 1 (2012-04-30)

App # Document Type Submitted
Available
1 BLOCK DIAGRAM Block Diagram
Adobe Acrobat PDF (33 kB)
2012-04-30 00:00:00
N/A
1 PARTS LIST Parts List/Tune Up Info
Adobe Acrobat PDF (73 kB)
2012-04-30 00:00:00
N/A
1 SCHEMATICS Schematics
Adobe Acrobat PDF (170 kB)
2012-04-30 00:00:00
N/A

APP # 2 (2012-04-30)

App # Document Type Submitted
Available
2 BLOCK DIAGRAM Block Diagram
Adobe Acrobat PDF (33 kB)
2012-04-30 00:00:00
N/A
2 PARTS LIST Parts List/Tune Up Info
Adobe Acrobat PDF (73 kB)
2012-04-30 00:00:00
N/A

APP # 1 (2012-04-30)

App # Document Type Submitted
Available
1 OPERATIONAL DESCRIPTION Operational Description
Adobe Acrobat PDF (209 kB)
2012-04-30 00:00:00
N/A

Application Forms

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: PQCMX40WLAN2
Unique Application Identifier: 9e6o7XrBF17HdivE5eNNEQ==
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: A4: UNII devices & low power transmitters using spread spectrum techniques

FCC ID
Grantee Code: PQC
Product Code: -MX40WLAN2

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):   06/14/2012
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:   NII - Unlicensed National Information Infrastructure TX
Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant): INTELLIVUE MX40 WLAN2 PATIENT WORN DEVICE

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?   Yes
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. This device is restricted to indoor use only within the 5150-5250MHz band. This device is approved for operation in the Wireless Medical Telemetry Service. This device and its antenna(s) 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:  LARRY STILLINGS
Title of authorized signature:  PRESIDENT

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: PQCMX40WLAN2
Unique Application Identifier: cnyqPXCUyAiTPTasXHRA9A==
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: A4: UNII devices & low power transmitters using spread spectrum techniques

FCC ID
Grantee Code: PQC
Product Code: -MX40WLAN2

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):   06/14/2012
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): Intellivue MX40 WLAN2 Patient Worn Device

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?   Yes
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:   Larry
Last Name:   Stillings
Telephone Number: 603-887-3903 Extension: 201
Fax Number:  603-887-6445
E-mail:  LStillings@cw-inc.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. This device is approved for operation in the Wireless Medical Telemetry Service. This device and its antenna(s) 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:  LARRY STILLINGS
Title of authorized signature:  PRESIDENT

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:

  Timco Engineering, Inc.
849 NW State Road 45 <BR>P.O. Box 370,
Newberry, FL 32669
Date of Grant: 04/30/2012

Application Dated: 04/30/2012
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-MX40WLAN2
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: INTELLIVUE MX40 WLAN2 PATIENT WORN DEVICE
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15E 5180.0  -  5320.0 0.02245  
CC 15E 5500.0  -  5580.0 0.04604  
CC 15E 5660.0  -  5700.0 0.04766  
CC 15E 5745.0  -  5805.0 0.06655  

Power listed is conducted. This device is restricted to indoor use only within the 5150-5250MHz band. This device is approved for operation in the Wireless Medical Telemetry Service. This device and its antenna(s) 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.

CC: This device is certified pursuant to two different Part 15 rules sections.
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: 04/30/2012

Application Dated: 04/30/2012
 
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-MX40WLAN2
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: INTELLIVUE MX40 WLAN2 PATIENT WORN DEVICE
Modular Type: Does not apply
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15E 5180.0  -  5320.0 0.02245  
CC 15E 5500.0  -  5580.0 0.04604  
CC 15E 5660.0  -  5700.0 0.04766  
CC 15E 5745.0  -  5805.0 0.06655  

Power listed is conducted. This device is restricted to indoor use only within the 5150-5250MHz band. This device is approved for operation in the Wireless Medical Telemetry Service. This device and its antenna(s) 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.


CC: This device is certified pursuant to two different Part 15 rules sections.

Mail To:


EA685231
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: 04/30/2012

Application Dated: 04/30/2012
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-MX40WLAN2
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: Intellivue MX40 WLAN2 Patient Worn Device
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.083  
CC 15C 2405.0  -  2480.0 0.0006  

Power listed is conducted. This device is approved for operation in the Wireless Medical Telemetry Service. This device and its antenna(s) 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.

CC: This device is certified pursuant to two different Part 15 rules sections.
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: 04/30/2012

Application Dated: 04/30/2012
 
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-MX40WLAN2
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: Intellivue MX40 WLAN2 Patient Worn Device
Modular Type: Does not apply
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.083  
CC 15C 2405.0  -  2480.0 0.0006  

Power listed is conducted. This device is approved for operation in the Wireless Medical Telemetry Service. This device and its antenna(s) 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.


CC: This device is certified pursuant to two different Part 15 rules sections.

Mail To:


EA577026

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