MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-14 for manufactured by .

MAUDE Entry Details

Report NumberCOR19000100-000
MDR Report Key8343066
Date Received2019-02-14
Date of Report2019-02-14
Date Added to Maude2019-02-14
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 FDA0
Report to FDA3
Event Location3
Manufacturer ContactElisa Gusberti
Manufacturer StreetVia Antonia Pozzi 1
Manufacturer City20149 Milano It
Manufacturer CountryIT
Manufacturer Phone245712171
Manufacturer G1FONA S.r.l
Manufacturer StreetVia Antonia Pozzi 1
Manufacturer City20149 Milano It
Manufacturer CountryIT
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Product CodeMUH
Date Received2019-02-14
Device AvailabilityI
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0


Patients

Patient NumberTreatmentOutcomeDate
10 2019-02-14

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