OXIFIRST FETAL OXYGEN SATURATION MONITORING SYSTEM N400 NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2002-05-23 for OXIFIRST FETAL OXYGEN SATURATION MONITORING SYSTEM N400 NA manufactured by Nellcor Puritan Bennett.

Event Text Entries

[275657] In 2002, nellcor puritan bennett received info stating that the fetal oxygen saturation module was providing high spo2 readings. Npb received a copy of the pt's strip. Results revealed there was an absence of signal for 1 hr. Current pt condition is unk. Device serial number and sensor lot numbers are unk.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2025525-2002-00014
MDR Report Key396514
Report Source05,06,07
Date Received2002-05-23
Date of Report2002-04-25
Date of Event2002-04-25
Date Mfgr Received2002-04-25
Date Added to Maude2002-05-30
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactJULIE MALLETT
Manufacturer Street2200 FARADAY AVENUE
Manufacturer CityCARLSBAD CA 92008
Manufacturer CountryUS
Manufacturer Postal92008
Manufacturer Phone7606035800
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOXIFIRST FETAL OXYGEN SATURATION MONITORING SYSTEM
Generic NameFETAL PULSE OXIMETER
Product CodeMMA
Date Received2002-05-23
Model NumberN400
Catalog NumberNA
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key385544
ManufacturerNELLCOR PURITAN BENNETT
Manufacturer Address2200 FARADAY AVE. CARLSBAD CA 92008 US
Baseline Brand NameOXIFIRST FETAL OXYGEN SATURATION MONITORING SYSTEM
Baseline Generic NameFETAL PULSE OXIMETER
Baseline Model NoN400
Baseline Device FamilyN400
Baseline Shelf Life [Months]NA
Baseline PMA FlagY
Premarket ApprovalP9900
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 2002-05-23

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