HOLLOW GOUGE FOR BROKEN SCREWEXPOSURE 399.680

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-09-03 for HOLLOW GOUGE FOR BROKEN SCREWEXPOSURE 399.680 manufactured by Oberdorf Synthes Produktions Gmbh.

MAUDE Entry Details

Report Number8030965-2019-67911
MDR Report Key8955771
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-09-03
Date of Report2019-08-05
Date Mfgr Received2019-11-11
Device Manufacturer Date2017-08-29
Date Added to Maude2019-09-03
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKARA DITTY-BOVARD
Manufacturer Street1302 WRIGHTS LANE EAST
Manufacturer CityWEST CHESTER PA 19380
Manufacturer CountryUS
Manufacturer Postal19380
Manufacturer Phone6103142063
Manufacturer G1SYNTHES SALZBURG
Manufacturer StreetVORGARTENSTRASSE 206B
Manufacturer CityTUTTLINGEN 1020WIEN
Manufacturer CountrySZ
Manufacturer Postal Code1020 WIEN
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHOLLOW GOUGE FOR BROKEN SCREWEXPOSURE
Generic NameGOUGE,SURGICAL,GEN & PLASTIC SURGERY
Product CodeGDH
Date Received2019-09-03
Returned To Mfg2019-11-11
Catalog Number399.680
Lot Number5943274
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerOBERDORF SYNTHES PRODUKTIONS GMBH
Manufacturer AddressEIMATTSTRASSE 3 OBERDORF 4436 SZ 4436


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-03

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