GORE ACUSEAL VASCULAR GRAFT ECH060040

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 2020-01-20 for GORE ACUSEAL VASCULAR GRAFT ECH060040 manufactured by W.l. Gore & Associates.

MAUDE Entry Details

Report Number2017233-2020-00047
MDR Report Key9605774
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-01-20
Date of Report2020-03-23
Date of Event2019-12-23
Device Manufacturer Date2019-01-04
Date Added to Maude2020-01-20
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 ContactSIBYLLE STAERK
Manufacturer Street1500 N. 4TH STREET
Manufacturer CityAZ
Manufacturer Phone9285263030
Manufacturer G1MEDICAL WEST B/P
Manufacturer Street1505 N. FOURTH STREET
Manufacturer CityFLAGSTAFF AZ 86004
Manufacturer CountryUS
Manufacturer Postal Code86004
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameGORE ACUSEAL VASCULAR GRAFT
Generic NamePROSTHESIS, VASCULAR GRAFT
Product CodeDSY
Date Received2020-01-20
Catalog NumberECH060040
Lot Number6204461PP010
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerW.L. GORE & ASSOCIATES
Manufacturer AddressFLAGSTAFF AZ


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-20

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