GE COROMETRICS NAUTILUS 2264LAX TOCO TRANSDUCER WITH WING FFCM3260

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-09 for GE COROMETRICS NAUTILUS 2264LAX TOCO TRANSDUCER WITH WING FFCM3260 manufactured by Ge Healthcare.

MAUDE Entry Details

Report Number3007409280-2019-00001
MDR Report Key8773666
Date Received2019-07-09
Date of Report2016-03-07
Date of Event2016-03-07
Date Mfgr Received2016-03-07
Date Added to Maude2019-07-09
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactJENNA VARGAS
Manufacturer Street212 AVENIDA FABRICANTE
Manufacturer CitySAN CLEMENTE CA 92672
Manufacturer CountryUS
Manufacturer Postal92672
Manufacturer G1AVANTE HEALTH SOLUTIONS
Manufacturer Street212 AVENIDA FABRICANTE
Manufacturer CitySAN CLEMENTE CA 92672
Manufacturer CountryUS
Manufacturer Postal Code92672
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameGE COROMETRICS NAUTILUS 2264LAX TOCO TRANSDUCER WITH WING
Generic NameTOCOTRANSDUCER
Product CodeHGM
Date Received2019-07-09
Returned To Mfg2016-03-18
Model Number2264LAX
Catalog NumberFFCM3260
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerGE HEALTHCARE
Manufacturer Address8880 GORMAN RD LAUREL MD 20723 US 20723


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-07-09

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