PROTAPER UNIVERSAL ROTARY FILE F2 25MM PTURF225

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-02 for PROTAPER UNIVERSAL ROTARY FILE F2 25MM PTURF225 manufactured by Tulsa Dental Products Llc.

MAUDE Entry Details

Report Number2320721-2020-00021
MDR Report Key9776039
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-02
Date of Report2020-02-29
Date Mfgr Received2020-01-31
Date Added to Maude2020-03-02
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 Location3
Manufacturer ContactMR. KARL NITTINGER
Manufacturer Street221 W. PHILADELPHIA ST. SUITE 60W
Manufacturer CityYORK, PA
Manufacturer CountryUS
Manufacturer Phone8494229
Manufacturer G1DENTSPLY MAILLEFER
Manufacturer StreetCHEMIN DU VERGER 3
Manufacturer CityBALLAIGUES, 1338
Manufacturer CountrySZ
Manufacturer Postal Code1338
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePROTAPER UNIVERSAL ROTARY FILE F2 25MM
Generic NameFILE, PULP CANAL, ENDODONTIC
Product CodeEKS
Date Received2020-03-02
Model NumberNA
Catalog NumberPTURF225
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTULSA DENTAL PRODUCTS LLC
Manufacturer Address608 ROLLING HILLS DRIVE JOHNSON CITY, TN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-02

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.