1. FCC ID
  2. QRI
  3. QRILUMAXT50
  4. LabelLoc

LUMAXT50 Implantable Cardioverter... - FCC ID QRILUMAXT50

FCC ID QRILUMAXT50

LabelLoc

Implantable Cardioverter defibrillator

by BIOTRONIK SE & Co. KG

Document preview loads when visible.

Document Details

FCC IDQRILUMAXT50
Document ID1658655
Document TypeID Label/Location Info
DescriptionLabelLoc
Document TitleNone
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
Created2011-04-19
Modified2011-04-19
Pages1
File TypeAdobe Acrobat PDF
File Size410142
File SHA-256be2c6175047c10a4f380b60cd6cfcb19c7f6ab96464424fbcfa4b919fe180f23
PDF Metadata AuthorNone
PDF Metadata CreatorCanon iR-ADV C5035
PDF Metadata ProducerAdobe PSL 1.1e for Canon
FCC.gov SourcesFCC.gov 1658655

Related FCC Exhibits

DocumentTypeAvailableFile
UserManUsers Manual2012-06-13PDF 1 MB
ExtPhoExternal Photos2012-06-13PDF 337.3 KB
LabelLocID Label/Location Info2012-06-13PDF 400.5 KB
LabelSmplID Label/Location Info2012-06-13PDF 88.3 KB
TestSupTest Setup Photos2012-06-13PDF 301.9 KB
conducted test setupTest Setup Photos2012-06-13PDF 238 KB
TestRep 15.209Test Report2012-06-13PDF 913.1 KB
TestRep 95ITest Report2012-06-13PDF 1.1 MB
Response to FCC ID: QRILUMAXT50 inquiryAttestation Statements2012-06-13PDF 23.8 KB
AutLetCover Letter(s)2012-06-13PDF 277.1 KB
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