COCHLEAR? VISTAFIX? VXI300 IMPLANT 4MM 93101

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 2019-07-01 for COCHLEAR? VISTAFIX? VXI300 IMPLANT 4MM 93101 manufactured by Cochlear Bone Anchored Solutions Ab.

MAUDE Entry Details

Report Number6000034-2019-01064
MDR Report Key8751522
Report SourceCOMPANY REPRESENTATIVE
Date Received2019-07-01
Date of Report2019-06-10
Date Facility Aware2019-06-10
Report Date2019-07-02
Date Reported to FDA2019-07-02
Date Reported to Mfgr2019-06-10
Date Mfgr Received2019-06-10
Date Added to Maude2019-07-01
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 ContactMR. YI FENG
Manufacturer Street1 UNIVERSITY AVENUE
Manufacturer CityMACQUARIE UNIVERSITY, NSW 2109
Manufacturer CountryAS
Manufacturer Postal2109
Manufacturer G1COCHLEAR BONE ANCHORED SOLUTIONS AB
Manufacturer StreetKONSTRUKTIONSV PO BOX 82
Manufacturer City43533
Manufacturer CountrySW
Manufacturer Postal Code43533
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCOCHLEAR? VISTAFIX? VXI300 IMPLANT 4MM
Generic NameCOCHLEAR BAHA CONNECT SYSTEM
Product CodeFZE
Date Received2019-07-01
Model Number93101
Catalog Number93101
Lot NumberCOH1237890
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Age3 MO
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCOCHLEAR BONE ANCHORED SOLUTIONS AB
Manufacturer AddressKONSTRUKTIONSV?GEN 14 PO BOX 82 M?LNLYCKE, 435 22 SW 435 22


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-07-01

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