O3 LARGE SENSOR 3756-9 3756

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2019-10-15 for O3 LARGE SENSOR 3756-9 3756 manufactured by Masimo - 52 Discovery.

MAUDE Entry Details

Report Number3011353843-2019-00086
MDR Report Key9194992
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2019-10-15
Date of Report2019-09-26
Date of Event2019-09-03
Date Mfgr Received2019-09-26
Device Manufacturer Date2019-08-05
Date Added to Maude2019-10-15
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 ContactSTEFAN LISSMANN
Manufacturer Street52 DISCOVERY
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer Phone9492977168
Manufacturer G1MASIMO - MEXICALI
Manufacturer StreetINDUSTRIAL VALLERA DE MEXICALI CALZADA DEL ORO, NO.2001
Manufacturer CityMEXICALI, BAJA CALIFORNIA 21600
Manufacturer CountryMX
Manufacturer Postal Code21600
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameO3 LARGE SENSOR
Generic NameOXIMETER
Product CodeMUD
Date Received2019-10-15
Returned To Mfg2019-09-10
Model Number3756-9
Catalog Number3756
Lot Number19HDP
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMASIMO - 52 DISCOVERY
Manufacturer Address52 DISCOVERY IRVINE CA 92618 US 92618


Patients

Patient NumberTreatmentOutcomeDate
10 2019-10-15

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