PROFILE GT ROTARY INSTRUMENT GTR1002017

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2003-11-26 for PROFILE GT ROTARY INSTRUMENT GTR1002017 manufactured by Dentsply Tulsa.

Event Text Entries

[296831] The doctor reported breaking files. At the time of this report there was no further info available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2320721-2003-00226
MDR Report Key499779
Report Source05
Date Received2003-11-26
Date of Report2003-10-30
Date Mfgr Received2003-10-30
Date Added to Maude2003-12-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationDENTIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactDR. PATRICIA KIHN
Manufacturer Street570 WEST COLLEGE AVE.
Manufacturer CityYORK PA 17404
Manufacturer CountryUS
Manufacturer Postal17404
Manufacturer Phone7178457511
Manufacturer G1DENTSPLY TULSA
Manufacturer Street608 ROLLING HILLS DRIVE
Manufacturer CityJOHNSON CITY TN 37604
Manufacturer CountryUS
Manufacturer Postal Code37604
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePROFILE GT ROTARY INSTRUMENT
Generic NameDENTAL FILE
Product CodeEMR
Date Received2003-11-26
Returned To Mfg2003-10-30
Model NumberNA
Catalog NumberGTR1002017
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key488556
ManufacturerDENTSPLY TULSA
Manufacturer Address608 ROLLING HILLS DR. JOHNSON CITY TN 37604 US
Baseline Brand NamePROFILE GT
Baseline Generic NameDENTAL FILE
Baseline Model NoNA
Baseline Catalog NoGTR1002017
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2003-11-26

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