FCC ID PQC-MX40WL3

SDIO Wireless Module

by Philips Medical Systems North America Co.

Grantee Code: PQC   Product Code: MX40WL3
Latest application date: 2015-12-24

Device Images

FCC ID Device Details

FCC IDPQC-MX40WL3
Mirrorsfcc.id | gov | fccid.ai
Grantee CodePQC
Product CodeMX40WL3
Applicant BusinessPhilips Medical Systems North America Co. 🇺🇸
Related Domains philips.com
Equipment ClassSDIO Wireless Module
Test FirmBureau Veritas Consumer Products Services, Inc.

Operating Frequencies

Frequency RangeApplication PurposeFinal Action Date
2412-2462 MHzClass II permissive change or modification of presently authorized equipment2015-12-24
5180-5240 MHzClass II permissive change or modification of presently authorized equipment2015-12-24
2412-2462 MHzClass II permissive change or modification of presently authorized equipment2015-06-30
2402-2480 MHzClass II permissive change or modification of presently authorized equipment2015-03-10
5180-5240 MHzClass II permissive change or modification of presently authorized equipment2015-03-10
2402-2480 MHzChange in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 11/14/20142015-03-02
2402-2480 MHzChange in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 08/20/20122015-03-02
5180-5240 MHzChange in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 11/14/20142015-03-02

Exhibits

DocumentTypeAvailableFile
User ManualUsers Manual2015-03-02PDF 219.6 KB
Internal PhotosInternal Photos2015-12-24PDF 228.7 KB
Internal PhotosInternal Photos2015-03-10PDF 551.2 KB
External PhotosExternal Photos2015-12-24PDF 504.2 KB
Host External PhotosExternal Photos2015-12-24PDF 504.2 KB
External PhotosExternal Photos2015-03-10PDF 329.7 KB
EUT PhotosExternal Photos2015-03-02PDF 629.2 KB
Label & LocationID Label/Location Info2015-03-02PDF 169.6 KB
Test Setup PhotosTest Setup Photos2015-12-24PDF 388.8 KB
Test setup photoTest Setup Photos2015-12-24PDF 388.8 KB
Test Setup PhotosTest Setup Photos2015-06-30PDF 216.9 KB
Test Setup PhotosTest Setup Photos2015-03-10PDF 445.9 KB
SAR Test Report part 1RF Exposure Info2015-12-24PDF 4.8 MB
SAR Test Report part 2RF Exposure Info2015-12-24PDF 4.6 MB
Test ReportTest Report2015-06-30PDF 2 MB
DTS Test ReportTest Report2015-03-10PDF 1.5 MB
Test Report Metadata onlyTest Report2015-03-10PDF 1.3 MB
Test Report Metadata onlyTest Report2015-03-10PDF 1.3 MB
UNII Test ReportTest Report2015-03-10PDF 1.5 MB
Permissive Change Request LetterCover Letter(s)2015-12-24PDF 50.1 KB
Product Certification Rep Auth LetterCover Letter(s)2015-12-24PDF 60.1 KB
Authorization LetterCover Letter(s)2015-06-30PDF 66.1 KB
C2PC clarification letterCover Letter(s)2015-06-30PDF 72.5 KB
Permissive Change letterCover Letter(s)2015-06-30PDF 54 KB
Authorization LetterCover Letter(s)2015-03-10PDF 34.4 KB
Permissive Change Request LetterCover Letter(s)2015-03-10PDF 149.7 KB
Supercede Request LetterCover Letter(s)2015-03-10PDF 42.4 KB
Authorization LetterCover Letter(s)2015-03-02PDF 64.2 KB
Authorization Letter from original applicantCover Letter(s)2015-03-02PDF 179 KB
Change of ID LetterCover Letter(s)2015-03-02PDF 67.3 KB
MPE CalculationRF Exposure Info2015-06-30PDF 83.3 KB
MPE CalculationRF Exposure Info2015-03-10PDF 82.3 KB

Application Information

Application IDzUbRcX82M1DaGR3l0OMVlg==
Final Action Date2015-12-24
Application PurposeClass II permissive change or modification of presently authorized equipment
Applicant FRN0017950635
ModelMX40WL3
Frequency Range2412-2462 MHz
Equipment ClassDTS - Digital Transmission System
Device DescriptionSDIO Wireless Module
Responsible PartyDelroy Smith, Principal Scientist / Project Leader, delroy.smith@philips.com , + 1 978 659 3382
Test FirmSarb Shelopal, Bureau Veritas Consumer Products Services, Inc., Sarbjit.Shelopal@bureauveritas.com , +1 925 963 4420
TCB Emailtcb@siemic.com
TCB ScopeA4: UNII devices & low power transmitters using spread spectrum techniques
Short-Term ConfidentialityNo
Long-Term ConfidentialityNo
Grant DeferralNo
Modular EquipmentSingle Modular Approval
Composite DeviceYes
Composite PartNo
Cognitive RadioNo
Authorization WaiverNo
Authorization Waiver ApprovedNo
Section 5301 CertificationYes
Related OET Knowledge DataBase InquiryNo
Grant CommentsCIIPC to add RF category Portable SAR results when module is used in Philips portable host (IntelliVue MX4O) with Philips embedded PCB antenna (r0001). The highest reported SAR values found during evaluation is: Body: 1.17 W/kg. BT function is disabled. Single Modular Approval for mobile platforms. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi- transmitter product procedures. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrator and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrator are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrator must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.

Applications

Application IDDatePurpose
zUbRcX82M1DaGR3l0OMVlg==2015-12-24Class II permissive change or modification of presently authorized equipment
1APn6Fdi6PP9G/LRAVeP/g==2015-12-24Class II permissive change or modification of presently authorized equipment
f8PkvjOIW9QbzbF/a07Tew==2015-06-30Class II permissive change or modification of presently authorized equipment
ptw/fOOS+5S0iOxj/aDe8g==2015-03-10Class II permissive change or modification of presently authorized equipment
j8B3Z5CVuj46CpFumxTqQA==2015-03-10Class II permissive change or modification of presently authorized equipment
S6PH5QvPEgKFm/XlNcVSZQ==2015-03-02Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 11/14/2014
RjOYnXNpTMyRYnbnopJAAg==2015-03-02Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 08/20/2012
QeRxtUkkQy4Dod6dRLbl9w==2015-03-02Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAN Grant Date: 11/14/2014

Equipment Authorization

FrequencyOutputRulesGrant Notes
2402-2480 MHz0.013900015CCC
2402-2480 MHz0.008615CCC
2412-2462 MHz0.173000015CCC
2412-2462 MHz0.17315CCC
5180-5240 MHz0.024715E38, CC
5260-5320 MHz0.024715E38, CC, ND
5500-5580 MHz0.01815E38, CC, ND
5660-5700 MHz0.0215E38, CC, ND
5745-5825 MHz0.024215E38, CC

Grants

TCB Grant - Application zUbRcX82M1DaGR3l0OMVlg==

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

  Bureau Veritas Consumer Products Services, Inc.
775 Montague Expressway
Milpitas, CA 95035
Date of Grant: 12/24/2015

Application Dated: 12/23/2015
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.173  

CIIPC to add RF category Portable SAR results when module is used in Philips portable host (IntelliVue MX4O) with Philips embedded PCB antenna (r0001). The highest reported SAR values found during evaluation is: Body: 1.17 W/kg. BT function is disabled.

Single Modular Approval for mobile platforms. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi- transmitter product procedures. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrator and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrator are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrator must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.


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

EAS Grant - Application zUbRcX82M1DaGR3l0OMVlg==

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: 12/24/2015

Application Dated: 12/23/2015
 
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.173  

CIIPC to add RF category Portable SAR results when module is used in Philips portable host (IntelliVue MX4O) with Philips embedded PCB antenna (r0001). The highest reported SAR values found during evaluation is: Body: 1.17 W/kg. BT function is disabled.

Single Modular Approval for mobile platforms. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi- transmitter product procedures. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrator and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrator are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrator must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.


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

TCB Grant - Application S6PH5QvPEgKFm/XlNcVSZQ==

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

  Siemic Inc.
775 Montague Expressway
Milpitas, CA 95035
Date of Grant: 03/02/2015

Application Dated: 03/02/2015
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.173  
CC 15C 2402.0  -  2480.0 0.0086  

Single Modular Approval for mobile platforms. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.

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

EAS Grant - Application S6PH5QvPEgKFm/XlNcVSZQ==

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: 03/02/2015

Application Dated: 03/02/2015
 
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.173  
CC 15C 2402.0  -  2480.0 0.0086  

Single Modular Approval for mobile platforms. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.


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

TCB Grant - Application RjOYnXNpTMyRYnbnopJAAg==

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

  Siemic Inc.
775 Montague Expressway
Milpitas, CA 95035
Date of Grant: 03/02/2015

Application Dated: 03/02/2015
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Part 15 Spread Spectrum Transmitter
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2402.0  -  2480.0 0.0139  

Single Modular Approval for mobile platforms. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.

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

EAS Grant - Application RjOYnXNpTMyRYnbnopJAAg==

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: 03/02/2015

Application Dated: 03/02/2015
 
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Part 15 Spread Spectrum Transmitter
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2402.0  -  2480.0 0.0139  

Single Modular Approval for mobile platforms. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.


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

TCB Grant - Application QeRxtUkkQy4Dod6dRLbl9w==

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

  Siemic Inc.
775 Montague Expressway
Milpitas, CA 95035
Date of Grant: 03/02/2015

Application Dated: 03/02/2015
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: SDIO Wireless Module
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
38 CC 15E 5180.0  -  5240.0 0.0247  
38 CC ND 15E 5260.0  -  5320.0 0.0247  
38 CC ND 15E 5500.0  -  5580.0 0.018  
38 CC ND 15E 5660.0  -  5700.0 0.02  
38 CC 15E 5745.0  -  5825.0 0.0242  

Single Modular Approval for mobile platforms. Output power listed is Conducted. This device has a 20 MHz and 40 MHz bandwidth mode. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and Order FCC 03-287 as a Client only without Radar Detection.

38: This device has shown compliance, in all grant-listed U-NII sub-bands, with the new rules for U-NII devices adopted under Docket No. 13-49 and may be marketed, manufactured, installed or imported after the June 1, 2016 transition deadline.
CC: This device is certified pursuant to two different Part 15 rules sections.
ND: This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h).

EAS Grant - Application QeRxtUkkQy4Dod6dRLbl9w==

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: 03/02/2015

Application Dated: 03/02/2015
 
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: SDIO Wireless Module
Modular Type: Does not apply
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
38 CC 15E 5180.0  -  5240.0 0.0247  
38 CC ND 15E 5260.0  -  5320.0 0.0247  
38 CC ND 15E 5500.0  -  5580.0 0.018  
38 CC ND 15E 5660.0  -  5700.0 0.02  
38 CC 15E 5745.0  -  5825.0 0.0242  

Single Modular Approval for mobile platforms. Output power listed is Conducted. This device has a 20 MHz and 40 MHz bandwidth mode. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and Order FCC 03-287 as a Client only without Radar Detection.


38: This device has shown compliance, in all grant-listed U-NII sub-bands, with the new rules for U-NII devices adopted under Docket No. 13-49 and may be marketed, manufactured, installed or imported after the June 1, 2016 transition deadline.
CC: This device is certified pursuant to two different Part 15 rules sections.
ND: This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h).

TCB Grant - Application ptw/fOOS+5S0iOxj/aDe8g==

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

  Bureau Veritas Consumer Products Services, Inc.
775 Montague Expressway
Milpitas, CA 95035
Date of Grant: 03/10/2015

Application Dated: 03/09/2015
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.173  
CC 15C 2402.0  -  2480.0 0.0086  

CIIPC to add new antennas (Philips P/N: 453564553001r1444, and 453564252521r1444) and disable BT function.

Single Modular Approval for mobile platforms. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi- transmitter product procedures. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.


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

EAS Grant - Application ptw/fOOS+5S0iOxj/aDe8g==

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: 03/10/2015

Application Dated: 03/09/2015
 
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.173  
CC 15C 2402.0  -  2480.0 0.0086  

CIIPC to add new antennas (Philips P/N: 453564553001r1444, and 453564252521r1444) and disable BT function.

Single Modular Approval for mobile platforms. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi- transmitter product procedures. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.


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

TCB Grant - Application j8B3Z5CVuj46CpFumxTqQA==

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

  Bureau Veritas Consumer Products Services, Inc.
775 Montague Expressway
Milpitas, CA 95035
Date of Grant: 03/10/2015

Application Dated: 03/09/2015
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
38 CC 15E 5180.0  -  5240.0 0.0247  
38 CC ND 15E 5260.0  -  5320.0 0.0247  
38 CC ND 15E 5500.0  -  5580.0 0.018  
38 CC ND 15E 5660.0  -  5700.0 0.02  
38 CC 15E 5745.0  -  5825.0 0.0242  

CIIPC to add new antennas (Philips P/N: 453564553001r1444, and 453564252521r1444) and disable BT function.

Single Modular Approval for mobile platforms. Output power listed is Conducted. This device has a 20 MHz and 40 MHz bandwidth mode. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi- transmitter product procedures. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and Order FCC 03-287 as a Client only without Radar Detection.


38: This device has shown compliance, in all grant-listed U-NII sub-bands, with the new rules for U-NII devices adopted under Docket No. 13-49 and may be marketed, manufactured or imported after the June 1, 2016 transition deadline.
CC: This device is certified pursuant to two different Part 15 rules sections.
ND: This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h).

EAS Grant - Application j8B3Z5CVuj46CpFumxTqQA==

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: 03/10/2015

Application Dated: 03/09/2015
 
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
38 CC 15E 5180.0  -  5240.0 0.0247  
38 CC ND 15E 5260.0  -  5320.0 0.0247  
38 CC ND 15E 5500.0  -  5580.0 0.018  
38 CC ND 15E 5660.0  -  5700.0 0.02  
38 CC 15E 5745.0  -  5825.0 0.0242  

CIIPC to add new antennas (Philips P/N: 453564553001r1444, and 453564252521r1444) and disable BT function.

Single Modular Approval for mobile platforms. Output power listed is Conducted. This device has a 20 MHz and 40 MHz bandwidth mode. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi- transmitter product procedures. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and Order FCC 03-287 as a Client only without Radar Detection.


38: This device has shown compliance, in all grant-listed U-NII sub-bands, with the new rules for U-NII devices adopted under Docket No. 13-49 and may be marketed, manufactured or imported after the June 1, 2016 transition deadline.
CC: This device is certified pursuant to two different Part 15 rules sections.
ND: This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h).

TCB Grant - Application f8PkvjOIW9QbzbF/a07Tew==

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

  Bureau Veritas Consumer Products Services, Inc.
775 Montague Expressway
Milpitas, CA 95035
Date of Grant: 06/30/2015

Application Dated: 06/30/2015
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.173  

CIIPC to add new antennas (Philips P/N: 453564553001, and 453564252521) and disable BT function. Increase transmit power for 802.11 g & 802.11 n-HT20.

Single Modular Approval for mobile platforms. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi- transmitter product procedures. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.


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

EAS Grant - Application f8PkvjOIW9QbzbF/a07Tew==

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: 06/30/2015

Application Dated: 06/30/2015
 
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
CC 15C 2412.0  -  2462.0 0.173  

CIIPC to add new antennas (Philips P/N: 453564553001, and 453564252521) and disable BT function. Increase transmit power for 802.11 g & 802.11 n-HT20.

Single Modular Approval for mobile platforms. Output power listed is Conducted. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi- transmitter product procedures. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter.


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

TCB Grant - Application 1APn6Fdi6PP9G/LRAVeP/g==

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

  Bureau Veritas Consumer Products Services, Inc.
775 Montague Expressway
Milpitas, CA 95035
Date of Grant: 12/24/2015

Application Dated: 12/24/2015
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
38 CC 15E 5180.0  -  5240.0 0.0247  
38 CC ND 15E 5260.0  -  5320.0 0.0247  
38 CC ND 15E 5500.0  -  5580.0 0.018  
38 CC ND 15E 5660.0  -  5700.0 0.02  
38 CC 15E 5745.0  -  5825.0 0.0242  

CIIPC to add RF category Portable SAR results when module is used in Philips portable host (IntelliVue MX4O) with Philips embedded PCB antenna (r0001). The highest reported SAR values found during evaluation is: Body: 1.17 W/kg. BT function is disabled.

Single Modular Approval for mobile platforms. Output power listed is Conducted. This device has a 20 MHz and 40 MHz bandwidth mode. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrator and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrator are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and Order FCC 03-287 as a Client only without Radar Detection.


38: This device has shown compliance, in all grant-listed U-NII sub-bands, with the new rules for U-NII devices adopted under Docket No. 13-49 and may be marketed, manufactured or imported after the June 1, 2016 transition deadline.
CC: This device is certified pursuant to two different Part 15 rules sections.
ND: This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h).

EAS Grant - Application 1APn6Fdi6PP9G/LRAVeP/g==

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: 12/24/2015

Application Dated: 12/24/2015
 
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-MX40WL3
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Unlicensed National Information Infrastructure TX
Notes: SDIO Wireless Module
Modular Type: Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
38 CC 15E 5180.0  -  5240.0 0.0247  
38 CC ND 15E 5260.0  -  5320.0 0.0247  
38 CC ND 15E 5500.0  -  5580.0 0.018  
38 CC ND 15E 5660.0  -  5700.0 0.02  
38 CC 15E 5745.0  -  5825.0 0.0242  

CIIPC to add RF category Portable SAR results when module is used in Philips portable host (IntelliVue MX4O) with Philips embedded PCB antenna (r0001). The highest reported SAR values found during evaluation is: Body: 1.17 W/kg. BT function is disabled.

Single Modular Approval for mobile platforms. Output power listed is Conducted. This device has a 20 MHz and 40 MHz bandwidth mode. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons and must not be co-located or operating in conjunction with any other antenna or transmitter, except in accordance with FCC multi-transmitter product procedures. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrator and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrator are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter. OEM integrators must be provided with antenna installation instructions. Only those antennas tested with the device or similar antennas with equal or lesser gain may be used with this transmitter. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and Order FCC 03-287 as a Client only without Radar Detection.


38: This device has shown compliance, in all grant-listed U-NII sub-bands, with the new rules for U-NII devices adopted under Docket No. 13-49 and may be marketed, manufactured or imported after the June 1, 2016 transition deadline.
CC: This device is certified pursuant to two different Part 15 rules sections.
ND: This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h).

Mail To: