THERATRON T780C G85

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,07 report with the FDA on 1998-07-14 for THERATRON T780C G85 manufactured by Theratronics International Ltd.

Event Text Entries

[120603] A report was received that the treatment table collapsed while a pt was supported on it. According to the service rep investigating the event, the pt was not injured.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610077-1998-00013
MDR Report Key179555
Report Source01,05,07
Date Received1998-07-14
Date of Report1998-07-13
Date of Event1998-06-26
Date Mfgr Received1998-06-29
Device Manufacturer Date1991-01-01
Date Added to Maude1998-07-31
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 Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTHERATRON
Generic NameCOBALT THERAPY DEVICE
Product CodeIWD
Date Received1998-07-14
Model NumberT780C
Catalog NumberG85
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeNA
Device Eval'ed by Mfgr*
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key174592
ManufacturerTHERATRONICS INTERNATIONAL LTD
Manufacturer Address413 MARCH RD P.O. BOX 13140 KANATA, ONTARIO CA
Baseline Brand NameTHERATRON
Baseline Generic NameCOBALT TELETHERAPY DEVICE
Baseline Model NoT780C
Baseline Catalog NoG85
Baseline ID*
Baseline Device FamilyTHERATRON
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK850543
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1998-07-14

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