BIOSTOP G CEM RESTR 12MM 546312000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-10-08 for BIOSTOP G CEM RESTR 12MM 546312000 manufactured by Depuy Cmw - 9610921.

MAUDE Entry Details

Report Number1818910-2019-108307
MDR Report Key9166364
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2019-10-08
Date of Report2019-09-16
Date of Event2019-09-16
Date Mfgr Received2019-09-16
Device Manufacturer Date2016-12-12
Date Added to Maude2019-10-08
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 Street700 ORTHOPAEDIC DRIVE
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal465810988
Manufacturer Phone6107428552
Manufacturer G1DEPUY CMW - 9610921
Manufacturer StreetCORNFORD RD
Manufacturer CityBLACKPOOL FY4 4QQ
Manufacturer CountryUK
Manufacturer Postal CodeFY4 4QQ
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIOSTOP G CEM RESTR 12MM
Generic NameDEPUY CMW RESORBABLE BIOMATERIALS : CEMENT CENTRALIZER/PLUG
Product CodeJDK
Date Received2019-10-08
Catalog Number546312000
Lot Number16E3103005
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEPUY CMW - 9610921
Manufacturer AddressCORNFORD RD BLACKPOOL FY4 4QQ UK FY4 4QQ


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-10-08

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