BONEBRIDGE BCI601 BONE CONDUCTION IMPLANT

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 2020-03-04 for BONEBRIDGE BCI601 BONE CONDUCTION IMPLANT manufactured by Med-el Elektromedizinische Geraete Gmbh.

Event Text Entries

[185658583] The device has not been explanted. If it should be explanted, it is to be returned to the manufacturer for evaluation. When available, a device failure analysis will be submitted as a follow up report.
Patient Sequence No: 1, Text Type: N, H10


[185658584] The user went to the clinic for a follow up on 18. Feb. 2020 and reported intermittent functioning of the device which has been going on for a few months now. The recipient will have a ct-scan and will see the new ent doctor next week.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9710014-2020-00157
MDR Report Key9785154
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-04
Date of Report2020-03-04
Date of Event2020-02-18
Date Mfgr Received2020-02-18
Date Added to Maude2020-03-04
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 ContactLAURA SIMONOTTI
Manufacturer StreetFUERSTENWEG 77A
Manufacturer CityINNSBRUCK 6020
Manufacturer CountryAU
Manufacturer Postal6020
Manufacturer Phone57788
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBONEBRIDGE
Generic NameBCI BONE CONDUCTION IMPLANT
Product CodeMPV
Date Received2020-03-04
Model NumberBCI601 BONE CONDUCTION IMPLANT
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMED-EL ELEKTROMEDIZINISCHE GERAETE GMBH
Manufacturer AddressINNSBRUCK AU


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-04

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