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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH SYNCHRONY; COCHLEAR IMPLANT

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MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH SYNCHRONY; COCHLEAR IMPLANT Back to Search Results
Model Number MI1200 SYNCHRONY
Device Problem Impedance Problem (2950)
Patient Problem Failure of Implant (1924)
Event Date 03/27/2024
Event Type  malfunction  
Manufacturer Narrative
The device has not been explanted.If it should be explanted, it should be returned to the manufacturer for evaluation.When available, a device failure analysis will be submitted as a follow up report.
 
Event Description
The user's hearing performance with the device is affected.Affected channels were noticed during in situ measurements.The clinic might proceed with revision surgery, although no day has been set yet.
 
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Brand Name
SYNCHRONY
Type of Device
COCHLEAR IMPLANT
Manufacturer (Section D)
MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH
innsbruck
AU 
Manufacturer Contact
laura simonotti
fuerstenweg 77a
innsbruck 6020
AU   6020
57788
MDR Report Key19039148
MDR Text Key339321579
Report Number9710014-2024-00304
Device Sequence Number1
Product Code MCM
UDI-Device Identifier09008737093952
UDI-Public(01)09008737093952
Combination Product (y/n)N
Reporter Country CodeAR
PMA/PMN Number
P000025
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Company Representative
Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date 04/03/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Expiration Date06/25/2021
Device Model NumberMI1200 SYNCHRONY
Was Device Available for Evaluation? No
Was the Report Sent to FDA? No
Initial Date Manufacturer Received 03/27/2024
Initial Date FDA Received04/04/2024
Date Device Manufactured06/25/2018
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Age48 YR
Patient SexMale
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