FRAZIER 0033120

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-24 for FRAZIER 0033120 manufactured by Conmed Corporation.

MAUDE Entry Details

Report Number9233031
MDR Report Key9233031
Date Received2019-10-24
Date of Report2019-10-03
Date of Event2019-09-04
Report Date2019-10-03
Date Reported to FDA2019-10-03
Date Reported to Mfgr2019-10-24
Date Added to Maude2019-10-24
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFRAZIER
Generic NameAPPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED
Product CodeGCX
Date Received2019-10-24
Model Number0033120
Catalog Number0033120
Lot Number201905201
Device AvailabilityY
Device Age1 DA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCONMED CORPORATION
Manufacturer Address525 FRENCH ROAD UTICA NY 13502 US 13502


Patients

Patient NumberTreatmentOutcomeDate
10 2019-10-24

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