4 X 10MM BARREL, BUR, MEDIUM, 5EA 00509125400

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2020-03-06 for 4 X 10MM BARREL, BUR, MEDIUM, 5EA 00509125400 manufactured by Conmed Corporation.

MAUDE Entry Details

Report Number1017294-2020-00101
MDR Report Key9800693
Report SourceDISTRIBUTOR,FOREIGN
Date Received2020-03-06
Date of Report2020-03-06
Date Mfgr Received2020-02-26
Date Added to Maude2020-03-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
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
Manufacturer ContactMR. JOHN BERGA
Manufacturer Street11311 CONCEPT BLVD.
Manufacturer CityLARGO, FL
Manufacturer CountryUS
Manufacturer Phone3995358
Manufacturer G1CONMED CORPORATION
Manufacturer Street11311 CONCEPT BLVD.
Manufacturer CityLARGO, FL
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name4 X 10MM BARREL, BUR, MEDIUM, 5EA
Generic NameBUR, SURGICAL, GENERAL & PLASTIC SURGERY
Product CodeGFF
Date Received2020-03-06
Catalog Number00509125400
Lot Number930534
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCONMED CORPORATION
Manufacturer Address11311 CONCEPT BLVD. LARGO, FL US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-06

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