GORE VIATORR? TIPS ENDOPROSTHESIS PTB086275W

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-08-02 for GORE VIATORR? TIPS ENDOPROSTHESIS PTB086275W manufactured by W.l. Gore & Associates.

MAUDE Entry Details

Report Number3007284313-2019-00234
MDR Report Key8854194
Report SourceCOMPANY REPRESENTATIVE
Date Received2019-08-02
Date of Report2019-09-05
Date of Event2019-07-05
Device Manufacturer Date2017-09-25
Date Added to Maude2019-08-02
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactVICKIE LANG
Manufacturer CityAZ
Manufacturer Phone9285263030
Manufacturer G1MEDICAL PHOENIX 1 B/P
Manufacturer Street32360 N. NORTH VALLEY PARKWAY
Manufacturer CityPHOENIX AZ 85085
Manufacturer CountryUS
Manufacturer Postal Code85085
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameGORE VIATORR? TIPS ENDOPROSTHESIS
Generic NameSHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS
Product CodeMIR
Date Received2019-08-02
Returned To Mfg2019-07-22
Catalog NumberPTB086275W
Lot Number17268196
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerW.L. GORE & ASSOCIATES
Manufacturer AddressFLAGSTAFF AZ


Patients

Patient NumberTreatmentOutcomeDate
10 2019-08-02

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