PROFILE GT ROTARY INSTRUMENT GTR0802025

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 2006-03-10 for PROFILE GT ROTARY INSTRUMENT GTR0802025 manufactured by Dentsply Tulsa.

Event Text Entries

[436381] A file separated in the canal during a procedure. The canal was filed with the separated piece in place without sequela.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2320721-2006-00076
MDR Report Key686199
Report Source05
Date Received2006-03-10
Date of Report2006-02-09
Date of Event2006-02-08
Date Mfgr Received2006-02-09
Device Manufacturer Date2005-12-01
Date Added to Maude2006-03-15
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., STE. 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 Received2006-03-10
Returned To Mfg2006-02-24
Model NumberNA
Catalog NumberGTR0802025
Lot Number120805004
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key675424
ManufacturerDENTSPLY TULSA
Manufacturer Address* JOHNSON CITY TN * US
Baseline Brand NamePROFILE GT ROTARY INSTRUMENT
Baseline Generic NameDENTAL FILE
Baseline Model NoNA
Baseline Catalog NoGTR0802025
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2006-03-10

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