OXIMAX N-560 PULSE OXIMETER

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2014-03-28 for OXIMAX N-560 PULSE OXIMETER manufactured by Mediana.

Event Text Entries

[19925690] Received a report of a n-560 with a missing segment and intermittent segments of the display. No patient harm was reported.
Patient Sequence No: 1, Text Type: D, B5


[20301734] (b)(4). Upon investigation the reported intermittent fault was verified, and isolated to cracked solder joints on both the front board and main pcb board.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2936999-2014-00244
MDR Report Key3817475
Report Source06
Date Received2014-03-28
Date of Report2014-03-10
Date of Event2014-03-01
Date Mfgr Received2014-03-10
Device Manufacturer Date2013-01-01
Date Added to Maude2014-06-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
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 G1MEDIANA
Manufacturer StreetWONJU MEDICAL INDUSTRY PARK DONGHWA-RI, MUNMAK-EUP. WONJU-SI
Manufacturer CityGANWON-DO
Manufacturer CountryKN
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOXIMAX N-560 PULSE OXIMETER
Generic NamePULSE OXIMETER
Product CodeDPZ
Date Received2014-03-28
Returned To Mfg2014-03-13
Model NumberN-560
Catalog NumberN-560
OperatorLAY USER/PATIENT
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMEDIANA
Manufacturer AddressWONJU INDUSTRY PARK DONGHWA-RI, MUNMAK-EUP GANGWON-DO KN


Patients

Patient NumberTreatmentOutcomeDate
10 2014-03-28

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