NICOLET EEG GROUP 842-693200

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2019-11-08 for NICOLET EEG GROUP 842-693200 manufactured by Natus Neuro Incorporated.

MAUDE Entry Details

Report Number3010611950-2019-00065
MDR Report Key9296660
Report SourceUSER FACILITY
Date Received2019-11-08
Date of Report2019-10-10
Date of Event2019-10-10
Date Mfgr Received2019-10-10
Date Added to Maude2019-11-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. JANESSA BOONE
Manufacturer Street3150 PLEASANT VIEW ROAD
Manufacturer CityMIDDLETON WI 53562
Manufacturer CountryUS
Manufacturer Postal53562
Manufacturer Phone6088298603
Manufacturer G1NATUS NEUROLOGY INCORPORATED
Manufacturer Street3150 PLEASANT VIEW ROAD
Manufacturer CityMIDDLETON WI 53562
Manufacturer CountryUS
Manufacturer Postal Code53562
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNICOLET EEG GROUP
Generic NameVIDEO CART MONOPOD DOME CAMERA
Product CodeGWQ
Date Received2019-11-08
Returned To Mfg2019-10-22
Model Number842-693200
Catalog Number842-693200
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerNATUS NEURO INCORPORATED
Manufacturer Address3150 PLEASANT VIEW ROAD MIDDLETON WI 53562 US 53562


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-11-08

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