PROTAPER NT ROTARY FILE PTRF325

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 2006-04-20 for PROTAPER NT ROTARY FILE PTRF325 manufactured by Dentsply Tulsa.

Event Text Entries

[456176] Eight to ten files separated during a two month period. Further information was requested though none is available as of this report.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8031010-2006-00146
MDR Report Key703740
Report Source05
Date Received2006-04-20
Date of Report2006-03-21
Date Mfgr Received2006-03-21
Date Added to Maude2006-04-27
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. STE. 60 SUSQUEHANNA COMMERCE CENTER W.
Manufacturer CityYORK PA 17404
Manufacturer CountryUS
Manufacturer Postal17404
Manufacturer Phone7178457511
Manufacturer G1DENTSPLY MAILLEFER
Manufacturer Street*
Manufacturer CityBALLAIGUES CH-1338
Manufacturer CountrySZ
Manufacturer Postal CodeCH-1338
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePROTAPER NT ROTARY FILE
Generic NameEKS
Product CodeEKG
Date Received2006-04-20
Model NumberNA
Catalog NumberPTRF325
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key692844
ManufacturerDENTSPLY TULSA
Manufacturer Address* JOHNSON CITY TN * US
Baseline Brand NamePROTAPER NT ROTARY FILE
Baseline Generic NameDENTAL FILEE
Baseline Model NoNA
Baseline Catalog NoPTRF325
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2006-04-20

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