FCC ID QHQ20-10494

Resusci QCPR Manikins

by Laerdal Medical AS

Grantee Code: QHQ   Product Code: 2010494
Latest application date: 2018-09-04

FCC ID Device Details

FCC IDQHQ20-10494
Mirrorsfcc.id | gov | fccid.ai
Grantee CodeQHQ
Product Code2010494
Applicant BusinessLaerdal Medical AS 🇳🇴
Related Domains laerdal.no
Equipment ClassResusci QCPR Manikins
Test FirmIntertek Semko AB

Operating Frequencies

Frequency RangeApplication PurposeFinal Action Date
2402-2480 MHzOriginal Equipment2018-09-04

Exhibits

DocumentTypeAvailableFile
User ManualUsers Manual2018-09-04PDF 639.6 KB
Internal PhotosInternal Photos2018-09-04PDF 349.6 KB
External PhotosExternal Photos2018-09-04PDF 422.1 KB
Label Artwork and LocationID Label/Location Info2018-09-04PDF 265 KB
Test SetupTest Setup Photos2018-09-04PDF 760.1 KB
Test ReportTest Report2018-09-04PDF 2 MB
Confidentiality RequestCover Letter(s)2018-09-04PDF 347.9 KB
Justification LetterCover Letter(s)2018-09-04PDF 765.1 KB
Letter of AgencyCover Letter(s)2018-09-04PDF 322.4 KB
RF ExposureRF Exposure Info2018-09-04PDF 465.7 KB
Block Diagram Metadata onlyBlock DiagramPDF 316.4 KB
Circuit Diagram Metadata onlySchematicsPDF 1.2 MB
Technical Description Metadata onlyOperational DescriptionPDF 202.1 KB
BOM Metadata onlyParts List/Tune Up InfoPDF 43.9 KB

Application Information

Application IDHikQiQe4Vk5cNgYe+942Bg==
Final Action Date2018-09-04
Application PurposeOriginal Equipment
Applicant FRN0007349657
Model20-10494
Frequency Range2402-2480 MHz
Equipment ClassDTS - Digital Transmission System
Device DescriptionResusci QCPR Manikins
Responsible PartyMari Kaada, Corporate Regulatory Affairs Manager, mari.kaada@laerdal.no , +4751511700
Test FirmPar Iggstrom, Intertek Semko AB, par.iggstrom@intertek.com , 46-8-750-00-00
TCB EmailTCB_Admin@intertek.com
TCB ScopeA4: UNII devices & low power transmitters using spread spectrum techniques
Short-Term ConfidentialityNo
Long-Term ConfidentialityYes
Grant DeferralNo
Modular EquipmentLimited Single Modular Approval
Composite DeviceNo
Composite PartNo
Cognitive RadioNo
Authorization WaiverNo
Authorization Waiver ApprovedNo
Section 5301 CertificationYes
Related OET Knowledge DataBase InquiryNo
Grant CommentsLimited Single Modular Approval. This modular is intended to be installed in a specific host as described in the filing. This modular must not be co-located or operating in conjunction with any other antenna or transmitter. Approval is limited to OEM installations only. OEM integrators must be provided with installation instructions and labeling requirements for finished products. OEM integrators and end-users must be provided with transmitter operation conditions for satisfying RF exposure compliance. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the modular.

Applications

Application IDDatePurpose
HikQiQe4Vk5cNgYe+942Bg==2018-09-04Original Equipment

Equipment Authorization

FrequencyOutputRules
2402-2480 MHz0.000490015C

Grants

TCB Grant - Application HikQiQe4Vk5cNgYe+942Bg==

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

  Intertek Testing Services NA, Inc.
70 Codman Hill Road
Boxborough, MA 01719
Date of Grant: 09/04/2018

Application Dated: 09/04/2018
Laerdal Medical AS
Tanke Svilandsgate 30
P.O. Box 377,
Stavanger, 4002
Norway
 
Attention: Mari Kaada , Corporate Regulatory Affairs Manager

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:  QHQ20-10494
Name of Grantee:  Laerdal Medical AS
Equipment Class: Digital Transmission System
Notes: Resusci QCPR Manikins
Modular Type: Limited Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
15C 2402.0  -  2480.0 0.00049  

Limited Single Modular Approval. This modular is intended to be installed in a specific host as described in the filing. This modular must not be co-located or operating in conjunction with any other antenna or transmitter. Approval is limited to OEM installations only. OEM integrators must be provided with installation instructions and labeling requirements for finished products. OEM integrators and end-users must be provided with transmitter operation conditions for satisfying RF exposure compliance. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the modular.

EAS Grant - Application HikQiQe4Vk5cNgYe+942Bg==

COPY FEDERAL COMMUNICATIONS
COMMISSION
WASHINGTON, D.C. 20554

GRANT OF EQUIPMENT
AUTHORIZATION
COPY
Certification

Laerdal Medical AS
Tanke Svilandsgate 30 P.O. Box 377,
Stavanger, 4002
Norway
  Date of Grant: 09/04/2018

Application Dated: 09/04/2018
 
Attention: Mari Kaada , Corporate Regulatory Affairs Manager

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:  QHQ20-10494
Name of Grantee:  Laerdal Medical AS
Equipment Class: Digital Transmission System
Notes: Resusci QCPR Manikins
Modular Type: Limited Single Modular
Grant Notes  FCC Rule Parts Frequency
Range (MHZ)
Output
Watts
Frequency
Tolerance
Emission
Designator
15C 2402.0  -  2480.0 0.00049  

Limited Single Modular Approval. This modular is intended to be installed in a specific host as described in the filing. This modular must not be co-located or operating in conjunction with any other antenna or transmitter. Approval is limited to OEM installations only. OEM integrators must be provided with installation instructions and labeling requirements for finished products. OEM integrators and end-users must be provided with transmitter operation conditions for satisfying RF exposure compliance. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the modular.



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