CHROMID? CPS ELITE AGAR 416172

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-22 for CHROMID? CPS ELITE AGAR 416172 manufactured by Biomerieux Espa?a.

MAUDE Entry Details

Report Number3009307598-2019-00001
MDR Report Key8812743
Date Received2019-07-22
Date of Report2019-08-26
Date Mfgr Received2019-07-30
Device Manufacturer Date2019-04-03
Date Added to Maude2019-07-22
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 ESPA
Manufacturer StreetISAAC NEWTON, 6 TRES CANTOS
Manufacturer CityMADRID, SPAIN 28760
Manufacturer CountrySP
Manufacturer Postal Code28760
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCHROMID? CPS ELITE AGAR
Generic NameCHROMID? CPS ELITE AGAR
Product CodeJXA
Date Received2019-07-22
Catalog Number416172
Lot Number1007250760
Device Expiration Date2019-07-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMERIEUX ESPA?A
Manufacturer AddressISAAC NEWTON, 6 TRES CANTOS MADRID, SPAIN 28760 SP 28760


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-22

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