NOMAD DENTAL 60KV 0.850.0000 FP 0001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,health profession report with the FDA on 2019-06-24 for NOMAD DENTAL 60KV 0.850.0000 FP 0001 manufactured by Aribex.

MAUDE Entry Details

Report Number1017522-2019-00011
MDR Report Key8726362
Report SourceDISTRIBUTOR,HEALTH PROFESSION
Date Received2019-06-24
Date of Report2019-06-21
Date of Event2019-04-09
Date Mfgr Received2019-04-09
Device Manufacturer Date2012-02-09
Date Added to Maude2019-06-24
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. DAVID WATERS
Manufacturer Street11727 FRUEHAUF DRIVE
Manufacturer CityCHARLOTTE NC 28273
Manufacturer CountryUS
Manufacturer Postal28273
Manufacturer Phone7045877297
Manufacturer G1ARIBEX
Manufacturer Street11727 FRUEHAUF DRIVE
Manufacturer CityCHARLOTTE NC 28273
Manufacturer CountryUS
Manufacturer Postal Code28273
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNOMAD DENTAL 60KV
Generic NameEXTRAORAL SOURCE X-RAY SYSTEM
Product CodeEHD
Date Received2019-06-24
Returned To Mfg2019-04-12
Model Number0.850.0000
Catalog NumberFP 0001
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerARIBEX
Manufacturer Address11727 FRUEHAUF DRIVE CHARLOTTE NC 28273 US 28273


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-24

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