COROMETRICS 118 NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,05 report with the FDA on 2003-12-31 for COROMETRICS 118 NA manufactured by Ge Medical Systems Information Technologies.

Event Text Entries

[359092] The customer reports the device would not register a blood pressure reading. No pt injury reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2124823-2003-00083
MDR Report Key507977
Report Source00,05
Date Received2003-12-31
Date of Report2003-12-30
Date of Event2003-07-30
Date Mfgr Received2003-11-24
Date Added to Maude2004-01-28
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 Location0
Manufacturer ContactPAUL HANNEMAN
Manufacturer Street8200 W TOWER AVE
Manufacturer CityMILWAUKEE WI 53223
Manufacturer CountryUS
Manufacturer Postal53223
Manufacturer Phone4143622404
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameCOROMETRICS
Generic NameFETAL MONITOR
Product CodeKNG
Date Received2003-12-31
Model Number118
Catalog NumberNA
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key496927
ManufacturerGE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
Manufacturer Address8200 WEST TOWER AVE. MILWAUKEE WI 53223 US
Baseline Brand NameCOROMETRICS
Baseline Generic NameFETAL MONITOR
Baseline Model No118
Baseline Catalog NoNA
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2003-12-31

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