MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-30 for NUCLEUS 24 DOUBLE ARRAY CI 11+11+2M NA manufactured by Cochlear Ltd.
[186553807]
This report is submitted on 31 march 2020.
Patient Sequence No: 1, Text Type: N, H10
[186553808]
Per the surgeon, it was reported that the device was explanted on (b)(6) 2019 due to suspected device failure. The patient was re-implanted with another manufacturer's device.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 6000034-2020-00914 |
MDR Report Key | 9901295 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-03-30 |
Date of Report | 2020-03-05 |
Date of Event | 2019-08-23 |
Date Mfgr Received | 2020-03-05 |
Date Added to Maude | 2020-03-30 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. KRISTEL KOHNE |
Manufacturer Street | 1 UNIVERSITY AVENUE |
Manufacturer City | MACQUARIE UNIVERSITY, NSW 2109, |
Manufacturer Country | AS |
Manufacturer Postal | 2109, |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | NUCLEUS 24 DOUBLE ARRAY |
Generic Name | NUCLEUS 24 COCHLEAR IMPLANT SYSTEM |
Product Code | MCM |
Date Received | 2020-03-30 |
Returned To Mfg | 2020-03-05 |
Model Number | CI 11+11+2M |
Catalog Number | NA |
Lot Number | NA |
Operator | LAY USER/PATIENT |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COCHLEAR LTD |
Manufacturer Address | 1 UNIVERSITY AVENUE MACQUARIE UNIVERSITY, NSW 2109 AS 2109 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-30 |