METAFIX 579.0004 NOT APPLICABLE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-27 for METAFIX 579.0004 NOT APPLICABLE manufactured by Corin Medical.

MAUDE Entry Details

Report Number9614209-2020-00031
MDR Report Key9887618
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-27
Date of Report2020-03-27
Date of Event2020-03-03
Date Mfgr Received2020-03-03
Device Manufacturer Date2018-01-03
Date Added to Maude2020-03-27
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 FRANCK DIDIER
Manufacturer StreetTHE CORINIUM CENTRE CIRENCESTER
Manufacturer CityGLOUCESTERSHIRE, GL7 1YJ
Manufacturer CountryUK
Manufacturer PostalGL7 1YJ
Manufacturer G1CORIN MEDICAL
Manufacturer StreetTHE CORINIUM CENTRE CIRENCESTER
Manufacturer CityGLOUCESTERSHIRE, GL7 1YJ
Manufacturer CountryUK
Manufacturer Postal CodeGL7 1YJ
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMETAFIX
Generic NameHIP STEM
Product CodeLZO
Date Received2020-03-27
Model Number579.0004
Catalog NumberNOT APPLICABLE
Lot Number372203
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCORIN MEDICAL
Manufacturer AddressTHE CORINIUM CENTRE CIRENCESTER GLOUCESTERSHIRE, GL7 1YJ UK GL7 1YJ


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2020-03-27

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