BRAND

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-05 for BRAND manufactured by .

Event Text Entries

[116004318] Test b5
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5078862
MDR Report Key7749745
Date Received2018-08-05
Date Added to Maude2018-08-05
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
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
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBRAND
Generic NameTD
Product CodeDFD
Date Received2018-08-05
Device Availability*
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0


Patients

Patient NumberTreatmentOutcomeDate
101. Life Threatening 2018-08-05

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