PROFILE GT ROTARY INSTRUMENT GTR1002021

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2005-06-06 for PROFILE GT ROTARY INSTRUMENT GTR1002021 manufactured by Dentsply Tulsa.

Event Text Entries

[15034678] Doctor reported that a file separated in the canal during a procedure. The separated the piece was retrieved without sequela.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2320721-2005-00221
MDR Report Key617911
Report Source05,07
Date Received2005-06-06
Date of Report2004-09-03
Date of Event2004-09-03
Date Mfgr Received2004-09-03
Date Added to Maude2005-06-30
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 Street221 W. PHILA. ST., SUITE 60 SUSQUEHANNA COMMERCE CENTER W.
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 Received2005-06-06
Returned To Mfg2005-05-26
Model NumberNA
Catalog NumberGTR1002021
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key607597
ManufacturerDENTSPLY TULSA
Manufacturer Address* JOHNSON CITY TN * US
Baseline Brand NamePROFILE GT ROTARY INSTRUMENT
Baseline Generic NameDENTAL FILE
Baseline Model NoNA
Baseline Catalog NoGTR1002021
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2005-06-06

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