VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM 1922814

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-05 for VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM 1922814 manufactured by Ortho-clinical Diagnostics.

MAUDE Entry Details

Report Number1319681-2020-00008
MDR Report Key9792228
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-05
Date of Report2020-03-05
Date of Event2020-02-16
Date Mfgr Received2020-02-17
Device Manufacturer Date2017-10-24
Date Added to Maude2020-03-05
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. JAMES A STEVENS
Manufacturer Street100 INDIGO CREEK DRIVE
Manufacturer CityROCHESTER NY 14626
Manufacturer CountryUS
Manufacturer Postal14626
Manufacturer Phone5854533000
Manufacturer G1ORTHO-CLINICAL DIAGNOSTICS
Manufacturer Street100 INDIGO CREEK DRIVE
Manufacturer CityROCHESTER NY 14626
Manufacturer CountryUS
Manufacturer Postal Code14626
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVITROS ECIQ IMMUNODIAGNOSTIC SYSTEM
Generic NameCHEMISTRY ANALYZER
Product CodeKHO
Date Received2020-03-05
Catalog Number1922814
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerORTHO-CLINICAL DIAGNOSTICS
Manufacturer Address100 INDIGO CREEK DRIVE ROCHESTER NY 14626 US 14626


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-05

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