ENDO ANCHOR SYSTEM - HELI-FX TAA HG-18-90-32

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-10-25 for ENDO ANCHOR SYSTEM - HELI-FX TAA HG-18-90-32 manufactured by Medtronic Ireland.

MAUDE Entry Details

Report Number9612164-2019-04502
MDR Report Key9236901
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-10-25
Date of Report2019-11-05
Date of Event2019-04-18
Date Mfgr Received2019-10-30
Date Added to Maude2019-10-25
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 ContactALISON SWEENEY
Manufacturer StreetPARKMORE BUSINESS PARK WEST
Manufacturer CityGALWAY
Manufacturer Phone091708096
Manufacturer G1MEDTRONIC IRELAND
Manufacturer StreetPARKMORE BUSINESS PARK WEST
Manufacturer CityGALWAY
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameENDO ANCHOR SYSTEM - HELI-FX TAA
Product CodeOTD
Date Received2019-10-25
Returned To Mfg2019-10-02
Model NumberHG-18-90-32
Catalog NumberHG-18-90-32
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC IRELAND
Manufacturer AddressPARKMORE BUSINESS PARK WEST GALWAY


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-10-25

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