FCC ID PQC-ST80IWPIM

Patient Interface Module

by Philips Medical Systems North America Co.

Grantee Code: PQC   Product Code: ST80IWPIM
Latest application date: 2012-06-14

FCC ID Device Details

FCC IDPQC-ST80IWPIM
Mirrorsfcc.id | gov | fccid.ai
Grantee CodePQC
Product CodeST80IWPIM
Applicant BusinessPhilips Medical Systems North America Co. 🇺🇸
Related Domains philips.com audix.com.cn
Equipment ClassPatient Interface Module
Test FirmAudix Technology ( Shanghai ) Co., Ltd.

Operating Frequencies

Frequency RangeApplication PurposeFinal Action Date
2405-2480 MHzOriginal Equipment2012-06-14

Exhibits

DocumentTypeAvailableFile
PQC-ST80IWPIM_User manual_Rev1Users Manual2012-06-14PDF 3 MB
PQC-ST80iWPIM_Internal PhotoInternal Photos2012-06-14PDF 805.5 KB
PQC-ST80IWPIM_External Photo_Rev1External Photos2012-06-14PDF 346.7 KB
PQC-ST80IWPIM_Label & Location_Rev1ID Label/Location Info2012-06-14PDF 294 KB
PQC-ST80iWPIM_Test PhotoTest Setup Photos2012-06-14PDF 560.9 KB
PQC-ST80IWPIM_Test Report_Rev2Test Report2012-06-14PDF 1.9 MB
PQC-ST80IWPIM_ Authorization Letter_Rev1Cover Letter(s)2012-06-14PDF 35.9 KB
PQC-ST80IWPIM_Confidential letter_Rev1Cover Letter(s)2012-06-14PDF 19.7 KB
PQC-ST80IWPIM_MPE Report_Rev1RF Exposure Info2012-06-14PDF 66.2 KB

Application Information

Application ID4NbtgH458F4ai64eCZ1n8A==
Final Action Date2012-06-14
Application PurposeOriginal Equipment
Applicant FRN0004980637
Model-ST80IWPIM
Frequency Range2405-2480 MHz
Equipment ClassDTS - Digital Transmission System
Device DescriptionPatient Interface Module
Responsible PartyDelroy Smith, Principal Scientist / Project Leader, delroy.smith@philips.com , + 1 978 659 3382
AgentByron Byron Byron, Audix Technology (Shanghai) Co., Ltd., byron_kwo@audix.com.cn , +86-21-64955500
Technical ContactByron Kwo, Audix Technology (Shanghai) Co., Ltd., byron_kwo@audix.com.cn , +86-21-64955500
Non-Technical ContactAlan He, Audix Technology (Shanghai) Co., Ltd., alan_he@audix.com.cn , +86-21-64955500
Test FirmByron Kwo, Audix Technology ( Shanghai ) Co., Ltd., byronkwo@audix.com.cn , 021-6495-5500
TCB Emailhotline@acbcert.com
TCB ScopeA4: UNII devices & low power transmitters using spread spectrum techniques
Short-Term ConfidentialityNo
Long-Term ConfidentialityYes
Grant DeferralNo
Modular EquipmentDoes not apply
Composite DeviceNo
Composite PartNo
Cognitive RadioNo
Authorization WaiverNo
Authorization Waiver ApprovedNo
Section 5301 CertificationYes
Related OET Knowledge DataBase InquiryNo
Grant CommentsOutput power listed is conducted. The antenna used for this transmitter must not be co-located with any other transmitters except in accordance with FCC multitransmitter product procedures. End-users and installers must be provided with antenna installation instructions and transmitter operating conditions for satisfying RF exposure compliance.

Applications

Application IDDatePurpose
4NbtgH458F4ai64eCZ1n8A==2012-06-14Original Equipment

Equipment Authorization

FrequencyOutputRules
2405-2480 MHz0.002060015C

Grants

TCB Grant - Application 4NbtgH458F4ai64eCZ1n8A==

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

  ACB, Inc.
6731 Whittier Avenue Suite C110
McLean, VA 22101
Date of Grant: 06/14/2012

Application Dated: 06/14/2012
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-ST80IWPIM
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: Patient Interface Module
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
15C 2405.0  -  2480.0 0.00206  

Output power listed is conducted. The antenna used for this transmitter must not be co-located with any other transmitters except in accordance with FCC multitransmitter product procedures. End-users and installers must be provided with antenna installation instructions and transmitter operating conditions for satisfying RF exposure compliance.

EAS Grant - Application 4NbtgH458F4ai64eCZ1n8A==

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: 06/14/2012

Application Dated: 06/14/2012
 
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-ST80IWPIM
Name of Grantee:  Philips Medical Systems North America Co.
Equipment Class: Digital Transmission System
Notes: Patient Interface Module
Modular Type: Does not apply
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
15C 2405.0  -  2480.0 0.00206  

Output power listed is conducted. The antenna used for this transmitter must not be co-located with any other transmitters except in accordance with FCC multitransmitter product procedures. End-users and installers must be provided with antenna installation instructions and transmitter operating conditions for satisfying RF exposure compliance.



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