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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: GE OEC MEDICAL SYSTEMS 9900

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GE OEC MEDICAL SYSTEMS 9900 Back to Search Results
Model Number 9900
Device Problem Failure to Power Up (1476)
Patient Problems No Known Impact Or Consequence To Patient (2692); No Information (3190)
Event Date 07/07/2015
Event Type  malfunction  
Event Description
The customer reported that the system could not boot up.There was no patient injury or death reported.
 
Manufacturer Narrative
A ge service representative performed an onsite investigation.The power supply was replaced during the service call.The system was tested and found to be working as intended and put back into service.
 
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Brand Name
9900
Manufacturer (Section D)
GE OEC MEDICAL SYSTEMS
384 wright brothers dr.
salt lake city UT 84116
Manufacturer Contact
384 wright brothers dr.
salt lake city, UT 84116
8015364952
MDR Report Key4949011
MDR Text Key17212936
Report Number1720753-2015-03030
Device Sequence Number1
Product Code JAA
Combination Product (y/n)N
PMA/PMN Number
NA
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Foreign,Health Professional,User Facility,Company Representative
Reporter Occupation Other
Type of Report Initial
Report Date 07/27/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number9900
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received 07/07/2015
Initial Date FDA Received07/27/2015
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured01/01/2000
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
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