LUMAXT50 Implantable Cardioverter... - FCC ID QRILUMAXT50

FCC ID QRILUMAXT50

TestRep 95I

Implantable Cardioverter defibrillator

by BIOTRONIK SE & Co. KG

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Document Details

FCC IDQRILUMAXT50
Document ID1658663
Document TypeTest Report
DescriptionTestRep 95I
Document TitleC-3
ApplicantBIOTRONIK SE & Co. KG
Equipment ClassImplantable Cardioverter defibrillator
Product CodeLUMAXT50
Application IDn4u0jr3ocEotNgWKKSodww==
Application PurposeOriginal Equipment
Application Date2012-06-13
Frequency Range402-405 MHz
FRN0008008591
Test FirmEurofins Product Service GmbH
Certified ByJens Zimmermann Head of Laboratory Department
Short-Term ConfidentialityNo
Long-Term ConfidentialityNo
Grant DeferralNo
Modular EquipmentDoes not apply
Composite DeviceNo
Composite PartYes
Submitted2012-03-19
Available2012-06-13
Created2011-02-22
Modified2012-03-19
Pages54
File TypeAdobe Acrobat PDF
File Size1180018
File SHA-256e0ac13bb8d376ba2ead4574fa810eff33f23f7ba2e98667c22d3d6f0dd8f53dd
PDF Metadata Authorgcw3
PDF Metadata CreatorPScript5.dll Version 5.2.2
PDF Metadata ProducerAcrobat Distiller 8.0.0 (Windows)
FCC.gov SourcesFCC.gov 1658663

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conducted test setupTest Setup Photos2012-06-13PDF 238 KB
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Revised authorisation letterCover Letter(s)2012-06-13PDF 284.4 KB
confidentiality int. photos etcCover Letter(s)2012-06-13PDF 562.5 KB
RF Exp StatementRF Exposure Info2012-06-13PDF 708 KB
RFExpRF Exposure Info2012-06-13PDF 1.4 MB