MIDMARK ULTRATRIM DENTAL CHAIR 153758-003

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-31 for MIDMARK ULTRATRIM DENTAL CHAIR 153758-003 manufactured by Midmark Corporation.

MAUDE Entry Details

Report Number1523530-2019-00003
MDR Report Key8845874
Date Received2019-07-31
Date of Report2019-07-30
Date of Event2019-04-14
Device Manufacturer Date2016-03-17
Date Added to Maude2019-07-31
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. ADAM CLUTTER
Manufacturer Street60 VISTA DRIVE
Manufacturer CityVERSAILLES OH 45380
Manufacturer CountryUS
Manufacturer Postal45380
Manufacturer Phone9375268474
Manufacturer G1MIDMARK CORPORATION
Manufacturer Street60 VISTA DRIVE
Manufacturer CityVERSAILLES OH 45380
Manufacturer CountryUS
Manufacturer Postal Code45380
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameMIDMARK ULTRATRIM DENTAL CHAIR
Generic NameDENTAL CHAIR
Product CodeNRU
Date Received2019-07-31
Model Number153758-003
Catalog Number153758-003
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMIDMARK CORPORATION
Manufacturer Address60 VISTA DRIVE VERSAILLES OH 45380 US 45380


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-31

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