DIMA PRINT ORTHO 66069096

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-08-08 for DIMA PRINT ORTHO 66069096 manufactured by Kulzer Gmbh - Hq.

MAUDE Entry Details

Report Number3005665377-2019-00001
MDR Report Key8873302
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-08-08
Date of Report2019-08-08
Date of Event2019-07-12
Date Mfgr Received2019-07-12
Date Added to Maude2019-08-08
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 ContactDR. ALBERT ERDRICH
Manufacturer StreetLEIPZIGER STRASSE 2
Manufacturer CityHANAU, 63450
Manufacturer CountryGM
Manufacturer Postal63450
Manufacturer G1KULZER GMBH - HQ
Manufacturer StreetLEIPZIGER STRASSE 2
Manufacturer CityHANAU, 63450
Manufacturer CountryGM
Manufacturer Postal Code63450
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDIMA PRINT ORTHO
Generic NameMAINTAINER
Product CodeDYT
Date Received2019-08-08
Catalog Number66069096
Lot NumberXG032N01
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerKULZER GMBH - HQ
Manufacturer AddressLEIPZIGER STRASSE 2 HANAU, 63450 GM 63450


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-08-08

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