DIMENSION? EXL DIMENSION? EXL 200 10636929

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 2020-03-26 for DIMENSION? EXL DIMENSION? EXL 200 10636929 manufactured by Siemens Healthcare Diagnostics Inc..

MAUDE Entry Details

Report Number2517506-2020-00118
MDR Report Key9884334
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-03-26
Date of Report2020-03-26
Date of Event2020-03-03
Date Mfgr Received2020-03-03
Device Manufacturer Date2017-06-09
Date Added to Maude2020-03-26
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 PO BOX 6101
Manufacturer CityNEWARK, DE
Manufacturer CountryUS
Manufacturer Phone6318356
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS INC- BROOKFIELD
Manufacturer StreetREGISTRATION NUMBER 1226181 101 SILVERMINE ROAD
Manufacturer CityBROOKFIELD, CT
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDIMENSION? EXL
Generic NameDIMENSION? EXL? 200 INTEGRATED CHEMISTRY SYSTEM
Product CodeJJE
Date Received2020-03-26
Model NumberDIMENSION? EXL 200
Catalog Number10636929
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Address500 GBC DRIVE PO BOX 6101 NEWARK, DE US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-26

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