NUCLEUS ABI541 AUDITORY BRAINSTEM IMPLANT N/A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2017-08-04 for NUCLEUS ABI541 AUDITORY BRAINSTEM IMPLANT N/A manufactured by Cochlear Ltd.

Event Text Entries

[81777133] This report is submitted on august 04, 2017, (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[81777134] Per the clinic, the patient experienced no connection with the internal device. Reprogramming attempts were made; however, the issue could not be resolved. Subsequently, the device was explanted on (b)(6) 2017 and the patient was reimplanted with a new device.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number6000034-2017-01512
MDR Report Key6766250
Report SourceHEALTH PROFESSIONAL
Date Received2017-08-04
Date of Report2017-07-24
Date of Event2017-07-12
Date Mfgr Received2017-07-24
Device Manufacturer Date2015-12-09
Date Added to Maude2017-08-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationAUDIOLOGIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. SUJEEWA WIJESINGHE
Manufacturer Street1 UNIVERSITY AVENUE
Manufacturer CityMACQUARIE UNIVERSITY, NSW 2109
Manufacturer CountryAS
Manufacturer Postal2109
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNUCLEUS ABI541 AUDITORY BRAINSTEM IMPLANT
Generic NameNUCLEUS AUDITORY BRAINSTEM IMPLANT SYSTEM
Product CodeMHE
Date Received2017-08-04
Model NumberABI541
Catalog NumberN/A
Lot NumberN/A
Device Expiration Date2017-12-09
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOCHLEAR LTD
Manufacturer Address1 UNIVERSITY AVENUE MACQUARIE UNIVERSITY, NSW 2109 AS 2109


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2017-08-04

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