HYGENIC H09105

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-06-25 for HYGENIC H09105 manufactured by Coltene Whaledent Inc..

MAUDE Entry Details

Report Number2416455-2019-00002
MDR Report Key8731711
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-06-25
Date of Report2019-07-01
Date Mfgr Received2019-06-17
Date Added to Maude2019-06-25
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 ContactTRICIA CREGGER
Manufacturer Street235 ASCOT PARKWAY
Manufacturer CityCUYAHOGA FALLS OH 44223
Manufacturer CountryUS
Manufacturer Postal44223
Manufacturer G1COLTENE WHALEDENT INC.
Manufacturer Street235 ASCOT PARKWAY
Manufacturer CityCUYAHOGA FALLS OH 44223
Manufacturer CountryUS
Manufacturer Postal Code44223
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHYGENIC
Generic NameDENTAL DAM
Product CodeEIE
Date Received2019-06-25
Catalog NumberH09105
OperatorHEALTH PROFESSIONAL
Device Availability*
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCOLTENE WHALEDENT INC.
Manufacturer Address235 ASCOT PARKWAY CUYAHOGA FALLS OH 44223 US 44223


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-06-25

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