INVOS 5100C-US

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2019-08-28 for INVOS 5100C-US manufactured by New Mervue Industrial Park.

MAUDE Entry Details

Report Number8020893-2019-00166
MDR Report Key8942875
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-08-28
Date of Report2019-08-28
Date Mfgr Received2019-08-07
Device Manufacturer Date2014-11-21
Date Added to Maude2019-08-28
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 ContactAVI KLUGER
Manufacturer Street5920 LONGBOW DRIVE
Manufacturer CityBOULDER CO 80301
Manufacturer CountryUS
Manufacturer Postal80301
Manufacturer Phone3035306582
Manufacturer G1NEW MERVUE INDUSTRIAL PARK
Manufacturer StreetMICHAEL COLLINS ROAD
Manufacturer CityGALWAY
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINVOS
Generic NameOXIMETER, TISSUE SATURATION
Product CodeMUD
Date Received2019-08-28
Model Number5100C-US
Catalog Number5100C-US
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerNEW MERVUE INDUSTRIAL PARK
Manufacturer AddressMICHAEL COLLINS ROAD GALWAY


Patients

Patient NumberTreatmentOutcomeDate
10 2019-08-28

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