NOVA STAT PROFILE PHOX ULTRA ANALYZER SYSTEM 42013

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-09 for NOVA STAT PROFILE PHOX ULTRA ANALYZER SYSTEM 42013 manufactured by Nova Biomedical Corp.

MAUDE Entry Details

Report Number1219029-2019-00052
MDR Report Key9171679
Date Received2019-10-09
Date of Report2019-10-08
Date of Event2019-09-09
Date Mfgr Received2019-09-09
Date Added to Maude2019-10-09
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 ContactMS MARIYA CESNULEVICIUS
Manufacturer Street200 PROSPECT ST.
Manufacturer CityWALTHAM MA 024543654
Manufacturer CountryUS
Manufacturer Postal024543654
Manufacturer Phone7816473700
Manufacturer G1NOVA BIOMEDICAL CORP
Manufacturer Street200 PROSPECT ST.
Manufacturer CityWALTHAM MA 024543654
Manufacturer CountryUS
Manufacturer Postal Code024543654
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameNOVA STAT PROFILE PHOX ULTRA ANALYZER SYSTEM
Generic NameBLOOD GAS/ELECTROLYTE/METABOLITE/CO-OXIMETRY ANALYZER
Product CodeCHL
Date Received2019-10-09
Model Number42013
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerNOVA BIOMEDICAL CORP
Manufacturer Address200 PROSPECT ST. WALTHAM MA 024543654 US 024543654


Patients

Patient NumberTreatmentOutcomeDate
10 2019-10-09

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