ZEKRYA BUR E015135100000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-01-16 for ZEKRYA BUR E015135100000 manufactured by Dentsply Maillefer.

Event Text Entries

[175246698] Per condition #1 of exemption e2006004, events meeting the definition of a serious injury are required to be reported. Therefore, because medical intervention was necessary to preclude permanent damage in this event, it does meet the criteria for reportability per 21 cfr part 803. The device was not returned for evaluation and the lot number was not provided for retained-product testing and/or dhr review.
Patient Sequence No: 1, Text Type: N, H10


[175246699] In this event it was reported that a carbide bur separated during a dental extraction. The breakage occured on a dog. The broken part has not been retrieved. The dog was given antibiotics but he is fine now.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8031010-2019-00307
MDR Report Key9595978
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2020-01-16
Date of Report2020-01-16
Date Mfgr Received2019-12-17
Date Added to Maude2020-01-16
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 17401
Manufacturer CountryUS
Manufacturer Postal17401
Manufacturer Phone7178494424
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 NameZEKRYA BUR
Generic NameBUR, DENTAL
Product CodeEJL
Date Received2020-01-16
Model NumberNA
Catalog NumberE015135100000
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDENTSPLY MAILLEFER
Manufacturer AddressCHEMIN DU VERGER 3 BALLAIGUES, 1338 SZ 1338


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-16

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