IQ 200 URINE ANALYZER IQ200 SELECT INSTRUMENT NON ROHS COMPLIANT C10684

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 2020-02-04 for IQ 200 URINE ANALYZER IQ200 SELECT INSTRUMENT NON ROHS COMPLIANT C10684 manufactured by Beckman Coulter Ireland Inc..

MAUDE Entry Details

Report Number2122870-2020-00016
MDR Report Key9668618
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-02-04
Date of Report2020-02-04
Date of Event2020-01-22
Date Mfgr Received2020-01-22
Date Added to Maude2020-02-04
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 ContactMR. HARRY LONG
Manufacturer Street1000 LAKE HAZELTINE DRIVE M/S R590C
Manufacturer CityCHASKA MN 55318
Manufacturer CountryUS
Manufacturer Postal55318
Manufacturer Phone9523681224
Manufacturer G1BECKMAN COULTER
Manufacturer Street1000 LAKE HAZELTINE DRIVE M/S R590C
Manufacturer CityCHASKA MN 55318
Manufacturer CountryUS
Manufacturer Postal Code55318
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameIQ 200 URINE ANALYZER
Generic NameCOUNTER, CELL, AUTOMATED (PARTICLE COUNTER)
Product CodeGKL
Date Received2020-02-04
Model NumberIQ200 SELECT INSTRUMENT NON ROHS COMPLIANT
Catalog NumberC10684
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBECKMAN COULTER IRELAND INC.
Manufacturer AddressLISMEEHAN O?CALLAGHAN?S MILLS ,CO. CLARE EI


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-02-04

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