MAC ELECTROCARDIOGRAPH MAC 8 NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2003-02-27 for MAC ELECTROCARDIOGRAPH MAC 8 NA manufactured by Ge Medical Systems Information Technologies.

Event Text Entries

[314990] Customer reported the mac 8 exhibited smoke while charging.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2124823-2003-00011
MDR Report Key445743
Report Source05,07
Date Received2003-02-27
Date of Report2003-02-26
Date Mfgr Received2003-01-24
Device Manufacturer Date1996-06-01
Date Added to Maude2003-03-05
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactANNIE BODE
Manufacturer Street8200 W. TOWER AVE.
Manufacturer CityMILWAUKEE WI 53223
Manufacturer CountryUS
Manufacturer Postal53223
Manufacturer Phone4143622368
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Remedial ActionRP
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameMAC ELECTROCARDIOGRAPH
Generic NameECG ANALYSIS SYSTEM
Product CodeLOS
Date Received2003-02-27
Model NumberMAC 8
Catalog NumberNA
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key434719
ManufacturerGE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
Manufacturer Address8200 WEST TOWER AVE. MILWAUKEE WI 53223 US
Baseline Brand NameMAC ELECTROCARDIOGRAPH
Baseline Generic NameECG ANALYSIS SYSTEM
Baseline Model NoMAC 8
Baseline Catalog NoNA
Baseline IDNA
Baseline Device FamilyMAC ELECTROCARDIOGRAPH
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK991735
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 2003-02-27

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