OXIFIRST FETAL OXYGEN SATURATION MONITORING SYSTEM N400 N400USA

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 2002-10-23 for OXIFIRST FETAL OXYGEN SATURATION MONITORING SYSTEM N400 N400USA manufactured by Nellcor Puritan Bennett.

Event Text Entries

[20164999] Upon application of fetal sensor, bradycardia was noted. Fspo2 remained at 30% but with the presence of variable decelerations, a cesarean section was performed. Standard resuscitative efforts were applied (no intubation) and the pt was released for routine care 4 days later.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2025525-2002-00035
MDR Report Key423897
Report Source05,06
Date Received2002-10-23
Date of Report2002-10-14
Date of Event2002-09-23
Date Mfgr Received2002-10-15
Date Added to Maude2002-10-28
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 ContactJAMES GARVEY II
Manufacturer Street4280 HACIENDA DRIVE
Manufacturer CityPLEASANTON CA 94588
Manufacturer CountryUS
Manufacturer Postal94588
Manufacturer Phone9254634479
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOXIFIRST FETAL OXYGEN SATURATION MONITORING SYSTEM
Generic NameFETAL PULSE OXIMETER
Product CodeMMA
Date Received2002-10-23
Model NumberN400
Catalog NumberN400USA
Lot NumberNA
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key412948
ManufacturerNELLCOR PURITAN BENNETT
Manufacturer Address2200 FARADAY AVENUE 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
101. Required No Informationntervention 2002-10-23

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.