VIDAS? MEASLES IGG 30219

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2019-10-23 for VIDAS? MEASLES IGG 30219 manufactured by Biomerieux Sa.

MAUDE Entry Details

Report Number8020790-2019-00062
MDR Report Key9224266
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2019-10-23
Date of Report2019-10-23
Date Mfgr Received2019-09-23
Device Manufacturer Date2019-05-09
Date Added to Maude2019-10-23
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 ContactMR. JEFF SCANLAN
Manufacturer Street595 ANGLUM ROAD
Manufacturer CityHAZELWOOD MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer Phone3147318694
Manufacturer G1BIOMERIEUX SA
Manufacturer Street376 CHEMIN DE L ORME
Manufacturer CityMARCY L ETOILE, 69280
Manufacturer CountryFR
Manufacturer Postal Code69280
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVIDAS? MEASLES IGG
Generic NameVIDAS? MEASLES IGG
Product CodeLJB
Date Received2019-10-23
Catalog Number30219
Lot Number1007326210
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMERIEUX SA
Manufacturer Address376 CHEMIN DE L ORME MARCY L ETOILE, 69280 FR 69280


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-10-23

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