SEAL & PROTECT 606.04.705

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 2018-12-26 for SEAL & PROTECT 606.04.705 manufactured by Dentsply Detrey Gmbh.

Event Text Entries

[131421973] While it is unknown if the device used in this case caused or contributed to the patient's symptoms, it is possible as allergic reactions to dental materials are known and reported, with medical consequences being dependent upon the severity of the individual allergic response and subsequent exposure to the same material. Therefore, this event meets the criteria for reportability per 21 cfr part 803. Retain product was evaluated and found to be within specification. A dhr review was conducted with no discrepancies noted.
Patient Sequence No: 1, Text Type: N, H10


[131421976] It was reported that a patient experienced an allergic reaction after treatment with seal & protect. The symptoms reported include swollen lips and lost sensitivity. The patient rinsed with water and after one hour the symptoms abated.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8010638-2018-00015
MDR Report Key8196691
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2018-12-26
Date of Report2018-12-26
Date Mfgr Received2018-11-27
Date Added to Maude2018-12-26
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 DETREY GMBH
Manufacturer StreetDETREY STRASSE 1
Manufacturer CityKONSTANZ, 78467
Manufacturer CountryGM
Manufacturer Postal Code78467
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSEAL & PROTECT
Generic NameVARNISH, CAVITY
Product CodeLBH
Date Received2018-12-26
Model NumberNA
Catalog Number606.04.705
Lot Number17010000103
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDENTSPLY DETREY GMBH
Manufacturer AddressDETREY STRASSE 1 KONSTANZ, 78467 GM 78467


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-12-26

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