FCC ID PQC-SRRFMPBV1

Device for monitoring fetal and maternal heartrate and uterin activity

by Philips Medical Systems North America Co.

Grantee Code: PQC   Product Code: SRRFMPBV1
Latest application date: 2017-09-28

FCC ID Device Details

FCC IDPQC-SRRFMPBV1
Mirrorsfcc.id | gov | fccid.ai
Grantee CodePQC
Product CodeSRRFMPBV1
Applicant BusinessPhilips Medical Systems North America Co. 🇺🇸
Related Domains philips.com
Equipment ClassDevice for monitoring fetal and maternal heartrate and uterin activity
Test FirmCTC advanced GmbH

Operating Frequencies

Frequency RangeApplication PurposeFinal Action Date
2363-2387 MHzOriginal Equipment2017-09-28
2402-2480 MHzOriginal Equipment2017-09-26

Exhibits

DocumentTypeAvailableFile
User manualUsers Manual2017-09-28PDF 4.4 MB
Internal PhotosInternal Photos2017-09-28PDF 1.3 MB
External PhotosExternal Photos2017-09-28PDF 736.2 KB
LabelID Label/Location Info2017-09-28PDF 469.5 KB
Test setup PhotosTest Report2017-09-28PDF 1.1 MB
Test setup PhotosTest Setup Photos2017-09-26PDF 1.1 MB
Test Report MBANTest Report2017-09-28PDF 4.1 MB
Test report mbanTest Report2017-09-28PDF 4.7 MB
Test report BTLETest Report2017-09-26PDF 3.6 MB
Test report SRRTest Report2017-09-26PDF 3 MB
SAR excemptionRF Exposure Info2017-09-28PDF 159.2 KB
Block diagram Metadata onlyBlock DiagramPDF 55.4 KB
Schematics Metadata onlySchematicsPDF 636.3 KB
Technical specification Metadata onlyOperational DescriptionPDF 776.9 KB
mban operational description Metadata onlyOperational DescriptionPDF 334.2 KB
pca material list Metadata onlyParts List/Tune Up InfoPDF 175.4 KB
tune up information Metadata onlyParts List/Tune Up InfoPDF 167.4 KB

Application Information

Application IDWNm47vaHoZlbSmNr5LIbIQ==
Final Action Date2017-09-28
Application PurposeOriginal Equipment
Applicant FRN0017950635
ModelSRRFMPBV1
Frequency Range2363-2387 MHz
Equipment ClassTNT - Licensed Non-Broadcast Transmitter Worn on Body
Device DescriptionDevice for monitoring fetal and maternal heartrate and uterin activity
Responsible PartyDelroy Smith, Principal Scientist / Project Leader, delroy.smith@philips.com , + 1 978 659 3382
Test FirmGerald Schmidt, CTC advanced GmbH, mail@ctcadvanced.com , 49-681-598-0
TCB EmailTCB@ctcadvanced.com
TCB ScopeB2: General Mobile Radio And Broadcast Services equipment in the following 47 CFR Parts 22 (non-cellular) 73, 74, 90, 95, 97, & 101 (all below 3 GHz)
Short-Term ConfidentialityNo
Long-Term ConfidentialityYes
Grant DeferralNo
Modular EquipmentDoes not apply
Composite DeviceYes
Composite PartYes
Cognitive RadioNo
Authorization WaiverNo
Authorization Waiver ApprovedNo
Section 5301 CertificationYes
Related OET Knowledge DataBase InquiryYes
Grant CommentsOutput Power listed is peak conducted.

Applications

Application IDDatePurpose
WNm47vaHoZlbSmNr5LIbIQ==2017-09-28Original Equipment
2rNVRzOQSnzYDKlmJ25V3Q==2017-09-26Original Equipment

Equipment Authorization

FrequencyOutputToleranceEmissionRules
2363-2387 MHz0.001635ppm2M71GXD95I
2392-2397 MHz0.002935ppm2M76GXD95I
2402-2480 MHz0.002915C
2405-2480 MHz0.002915C

Grants

TCB Grant - Application WNm47vaHoZlbSmNr5LIbIQ==

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

  CTC advanced GmbH
Untertuerkheimer Strasse 6-10
66117 Saarbruecken,
Germany
Date of Grant: 09/28/2017

Application Dated: 09/11/2017
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-SRRFMPBV1
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Licensed Non-Broadcast Transmitter Worn on Body
Notes: Device for monitoring fetal and maternal heartrate and uterin activity
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
95I 2363.0  -  2387.0 0.0016 35.0  PM 2M71GXD
95I 2392.0  -  2397.0 0.0029 35.0  PM 2M76GXD

Output Power listed is peak conducted.

EAS Grant - Application WNm47vaHoZlbSmNr5LIbIQ==

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: 09/28/2017

Application Dated: 09/11/2017
 
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-SRRFMPBV1
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Licensed Non-Broadcast Transmitter Worn on Body
Notes: Device for monitoring fetal and maternal heartrate and uterin activity
Modular Type: Does not apply
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
95I 2363.0  -  2387.0 0.0016 35.0  PM 2M71GXD
95I 2392.0  -  2397.0 0.0029 35.0  PM 2M76GXD

Output Power listed is peak conducted.



TCB Grant - Application 2rNVRzOQSnzYDKlmJ25V3Q==

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

  CTC advanced GmbH
Untertuerkheimer Strasse 6-10
66117 Saarbruecken,
Germany
Date of Grant: 09/26/2017

Application Dated: 09/11/2017
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-SRRFMPBV1
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: Device for monitoring fetal and maternal heartrate and uterin activity
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
15C 2405.0  -  2480.0 0.0029  
15C 2402.0  -  2480.0 0.0029  

Output Power listed is peak conducted.

EAS Grant - Application 2rNVRzOQSnzYDKlmJ25V3Q==

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: 09/26/2017

Application Dated: 09/11/2017
 
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-SRRFMPBV1
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: Device for monitoring fetal and maternal heartrate and uterin activity
Modular Type: Does not apply
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
15C 2405.0  -  2480.0 0.0029  
15C 2402.0  -  2480.0 0.0029  

Output Power listed is peak conducted.



Mail To: