CP910 PROCESSING UNIT (SMOKE) 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 2017-12-11 for CP910 PROCESSING UNIT (SMOKE) N/A manufactured by Cochlear Ltd.

Event Text Entries

[94466565] This report is submitted on december 12, 2017, by cochlear limited on behalf of cochlear americas. (b)(4)..
Patient Sequence No: 1, Text Type: N, H10


[94466566] Per the clinic, the patient experienced skin reaction and infection at implant site, subsequently the patient was administered oral antibiotics (date and duration not reported).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number6000034-2017-02271
MDR Report Key7107276
Report SourceHEALTH PROFESSIONAL
Date Received2017-12-11
Date of Report2017-12-01
Date Mfgr Received2017-12-01
Date Added to Maude2017-12-11
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. KRISTEL KOHNE
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 NameCP910 PROCESSING UNIT (SMOKE)
Generic NameNUCLEUS HYBRID COCHLEAR IMPLANT SYSTEM
Product CodePGQ
Date Received2017-12-11
Model NumberCP910
Catalog NumberN/A
Lot NumberN/A
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 2017-12-11

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