DIMENSION VISTA? K2125 SMN 10445152

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2019-07-31 for DIMENSION VISTA? K2125 SMN 10445152 manufactured by Siemens Healthcare Diagnostics Inc.

MAUDE Entry Details

Report Number2517506-2019-00306
MDR Report Key8845546
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-07-31
Date of Report2019-07-31
Date of Event2019-07-05
Date Mfgr Received2019-07-06
Device Manufacturer Date2019-03-20
Date Added to Maude2019-07-31
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 ContactJAMES MORGERA
Manufacturer Street500 GBC DRIVE P.O. BOX 6101
Manufacturer CityNEWARK DE 197146101
Manufacturer CountryUS
Manufacturer Postal197146101
Manufacturer Phone3026318356
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Street500 GBC DRIVE P.O. BOX 6101
Manufacturer CityNEWARK DE 197146101
Manufacturer CountryUS
Manufacturer Postal Code197146101
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDIMENSION VISTA?
Generic NameDIMENSION VISTA? DIRECT BILIRUBIN FLEX? REAGENT CARTRIDGE
Product CodeCIG
Date Received2019-07-31
Catalog NumberK2125 SMN 10445152
Lot Number19080BA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS INC
Manufacturer Address500 GBC DRIVE P.O. BOX 6101 NEWARK DE 197146101 US 197146101


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-31

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