TACROLIMUS FLEX REAGENT CARTRIDGE 10700795

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 2020-01-14 for TACROLIMUS FLEX REAGENT CARTRIDGE 10700795 manufactured by Siemens Healthcare Diagnostics Inc..

MAUDE Entry Details

Report Number2517506-2020-00012
MDR Report Key9588556
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-01-14
Date of Report2020-02-07
Date of Event2019-12-20
Date Mfgr Received2020-01-15
Device Manufacturer Date2009-12-07
Date Added to Maude2020-01-14
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 ContactCHRISTINA LAM
Manufacturer Street511 BENEDICT AVE
Manufacturer CityTARRYTOWN NY 10591
Manufacturer CountryUS
Manufacturer Postal10591
Manufacturer Phone9145243504
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Street500 GBC DRIVE PO BOX 6101
Manufacturer CityNEWARK DE 197146101
Manufacturer CountryUS
Manufacturer Postal Code197146101
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTACROLIMUS FLEX REAGENT CARTRIDGE
Generic NameTACROLIMUS FLEX REAGENT CARTRIDGE
Product CodeMLM
Date Received2020-01-14
Model NumberTACROLIMUS FLEX REAGENT CARTRIDGE
Catalog Number10700795
Lot NumberGD0288
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Address500 GBC DRIVE PO BOX 6101 NEWARK DE 197146101 US 197146101


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-14

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