OXIMAX N-595 PULSE OXIMETER N595

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2015-02-06 for OXIMAX N-595 PULSE OXIMETER N595 manufactured by Covidien.

Event Text Entries

[18258912] Covidien received a report of a n595 monitor that does not have any audio. The monitor does not sound the audio post tone when it is turned on. No patient harm was reported.
Patient Sequence No: 1, Text Type: D, B5


[18429258] (b)(4)
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2936999-2015-00116
MDR Report Key4492374
Report Source05,06
Date Received2015-02-06
Date of Report2015-01-08
Date of Event2015-01-08
Date Mfgr Received2015-01-08
Device Manufacturer Date2005-08-30
Date Added to Maude2015-03-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactDENISE BRAXTON
Manufacturer Street6135 GUNBARREL AVE.
Manufacturer CityBOULDER CO 80301
Manufacturer CountryUS
Manufacturer Postal80301
Manufacturer Phone3038768909
Manufacturer G1COVIDIEN
Manufacturer StreetNEW MERVUE INDUSTRIAL PARK MICHAEL COLLINS ROAD
Manufacturer CityGALWAY
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOXIMAX N-595 PULSE OXIMETER
Generic NamePULSE OXIMETER
Product CodeDPZ
Date Received2015-02-06
Model NumberN-595
Catalog NumberN595
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer AddressNEW MERVUE INDUSTRIAL PARK MICHAEL COLLINS ROAD GALWAY EI


Patients

Patient NumberTreatmentOutcomeDate
10 2015-02-06

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