MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-11-15 for manufactured by .

MAUDE Entry Details

Report NumberCOR18001750-000
MDR Report Key8074919
Date Received2018-11-15
Date of Report2018-11-15
Date Added to Maude2018-11-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag0
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

Product CodeIZH
Date Received2018-11-15
Device AvailabilityI
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0


Patients

Patient NumberTreatmentOutcomeDate
10 2018-11-15

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.