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VITROS ECI IMMUNODIAGNOSTIC SYSTEM Adverse Event — Malfunction (MDR 1319681-2008-00053)

VITROS ECI IMMUNODIAGNOSTIC SYSTEM Adverse Event — Malfunction (MDR 1319681-2008-00053) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: VITROS ECI IMMUNODIAGNOSTIC SYSTEM; Generic name: IMMUNODIAGNOSTIC ANALYZER; Manufacturer: ORTHO-CLINICAL DIAGNOSTICS.

DeviceVITROS ECI IMMUNODIAGNOSTIC SYSTEM
Generic nameIMMUNODIAGNOSTIC ANALYZER
ManufacturerORTHO-CLINICAL DIAGNOSTICS
Report number1319681-2008-00053
Event typeMalfunction
Product problemY
Date received2008-02-22
Report sourceHealth Professional, HEALTH PROFESSIONAL
SourceopenFDA MAUDE (device adverse events)

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