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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ELECTROCONVULSIVE THERAPY
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ELECTROCONVULSIVE THERAPY Back to Search Results
Device Problem Insufficient Information (3190)
Patient Problem No Information (3190)
Event Type  Other  
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Brand Name
ELECTROCONVULSIVE THERAPY
Type of Device
ELECTROCONVULSIVE THERAPY
MDR Report Key5419782
Report NumberMW5060068
Device Sequence Number1
Product Code GXC
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Other
Type of Report Initial
Report Date 01/27/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/05/2016
Is this an Adverse Event Report? No
Is this a Product Problem Report? No
Device Operator No Information
Type of Device Usage N
Patient Sequence Number1
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