MONDIAL 8 (DEVICE 2)

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,05 report with the FDA on 2013-09-26 for MONDIAL 8 (DEVICE 2) manufactured by Heraeus Kulzer Gmbh.

Event Text Entries

[3780534] (b)(4).
Patient Sequence No: 1, Text Type: D, B5


[11247841] (b)(4). Although we have not established that the device caused or contributed to the event, we're reporting it to be compliant with 21 cfr part 803 and out of an abundance of caution. Results: only broken off portion of denture tooth returned. The portion of denture tooth that remained in the all-on-four was not returned as the removal process requires that it be ground out of the acrylic. Therefore nothing remained to return.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3006610834-2013-00016
MDR Report Key3451470
Report Source00,05
Date Received2013-09-26
Date Mfgr Received2013-08-30
Date Added to Maude2013-11-07
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional0
Initial Report to FDA0
Report to FDA0
Event Location0
Manufacturer ContactAUDI BOGUCKI, RDH
Manufacturer Street300 HERAEUS WAY
Manufacturer CitySOUTH BEND IN 46614
Manufacturer CountryUS
Manufacturer Postal46614
Manufacturer Phone5742995409
Manufacturer G1HERAEUS KULZER GMBH
Manufacturer StreetSCHLATTEREST 2
Manufacturer CityWASSERBURG 88142
Manufacturer CountryGM
Manufacturer Postal Code88142
Single Use0
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMONDIAL 8 (DEVICE 2)
Generic NameELM DENTURE, PLASTIC, TEETH
Product CodeELM
Date Received2013-09-26
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerHERAEUS KULZER GMBH
Manufacturer AddressWASSERBURG 88142 GM 88142


Patients

Patient NumberTreatmentOutcomeDate
10 2013-09-26

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