ELECSYS TOXO IGM 04618858190

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2019-11-27 for ELECSYS TOXO IGM 04618858190 manufactured by Roche Diagnostics.

MAUDE Entry Details

Report Number1823260-2019-90271
MDR Report Key9384221
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2019-11-27
Date of Report2019-11-27
Date of Event2019-10-25
Date Mfgr Received2019-11-01
Date Added to Maude2019-11-27
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 ContactMICHAEL LESLIE
Manufacturer Street9115 HAGUE ROAD
Manufacturer CityINDIANAPOLIS IN 46250
Manufacturer CountryUS
Manufacturer Postal46250
Manufacturer G1ROCHE DIAGNOSTICS GMBH
Manufacturer StreetSANDHOFERSTRASSE 116
Manufacturer CityMANNHEIM (BADEN-WURTTEMBERG), 68305
Manufacturer CountryGM
Manufacturer Postal Code68305
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameELECSYS TOXO IGM
Generic NameENZYME LINKED IMMUNOABSORBENT ASSAY, TOXOPLASMA GONDII
Product CodeLGD
Date Received2019-11-27
Model NumberTOXO IGM
Catalog Number04618858190
Lot Number409463
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerROCHE DIAGNOSTICS
Manufacturer Address9115 HAGUE ROAD INDIANAPOLIS IN 46250 US 46250


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-27

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.