UP-51MD

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 99 report with the FDA on 2006-11-09 for UP-51MD manufactured by Sony Emcs Corp. Kohda Tech. Ctr.

Event Text Entries

[1122953] On october 24, 2006, sony electronics inc. Received maude report from fda stating that in 2005, (more than 1 year ago) one of our medical devices, up51md video printer, was observed smoking and was cracked. Promptly, sony contacted the user facility that initiated the reported event, but they had no other records or reports to document the reported event. The printer in question was no longer available for examination to determine if the reported event was a result of a problem with the printer or a result of mis-handling at the user facility. The event was not otherwise reported to sony nor was the printer in question sent to any sony facility for repair. An internal review was made for all reported complaints and repairs on the up51md printer, and no similar events have been reported. In light of the fact that there was no patient involvement and in light of the lack of information about the printer in question, sony concludes that, as far as its investigation was able to determine, no mdr incident has occurred in this case.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2246606-2006-00001
MDR Report Key1370094
Report Source99
Date Received2006-11-09
Date of Report2006-11-03
Date of Event2005-06-02
Date Facility Aware2006-10-24
Report Date2006-11-09
Date Added to Maude2009-10-14
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameUP-51MD
Generic NameCAMERA, MULTI FORMAT, RADIOLOGICAL
Product CodeLMC
Date Received2006-11-09
Model NumberUP-51MD
Catalog NumberUP-51MD
Lot Number19223
ID Number42458800 (PROD CODE)
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age1 YR
Device Sequence No1
Device Event Key0
ManufacturerSONY EMCS CORP. KOHDA TECH. CTR
Manufacturer Address1 AZA-SUZUMERGAIRI OHAZA-SAKAZAKI, KOHDA-CHO AICHI-KEN JA


Patients

Patient NumberTreatmentOutcomeDate
10 2006-11-09

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