THERATRON T780 G22

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06,07 report with the FDA on 1997-12-22 for THERATRON T780 G22 manufactured by Theratronics Intl., Ltd..

Event Text Entries

[22182420] It was reported that the cobalt 60 source remained in the "on" position at the end of a pt treatment.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610077-1997-00012
MDR Report Key141656
Report Source01,05,06,07
Date Received1997-12-22
Date of Report1997-12-18
Date of Event1997-12-05
Date Mfgr Received1997-12-05
Device Manufacturer Date1979-08-01
Date Added to Maude1998-01-07
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
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTHERATRON
Generic NameCOBALT TELETHERAPY DEVICE
Product CodeIWD
Date Received1997-12-22
Model NumberT780
Catalog NumberG22
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeNA
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key138207
ManufacturerTHERATRONICS INTL., LTD.
Manufacturer Address413 MARCH RD. P.O. BOX 13140 KANATA, ONTARIO CA K2K 2B7
Baseline Brand NameTHERATRON
Baseline Generic NameCOBALT TELETHERAPY DEVICE
Baseline Model NoT780
Baseline Catalog NoG22
Baseline ID*
Baseline Device FamilyTHERATRON
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1997-12-22

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