NDEHP SAPPHIRE SET NV +1.2FLTR 1632402 163240455

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-10-23 for NDEHP SAPPHIRE SET NV +1.2FLTR 1632402 163240455 manufactured by Icu Medical Costa Rica Ltd..

MAUDE Entry Details

Report Number9615050-2019-00440
MDR Report Key9227215
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-10-23
Date of Report2019-09-30
Date of Event2019-09-27
Date Mfgr Received2019-09-30
Device Manufacturer Date2014-02-01
Date Added to Maude2019-10-23
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 ContactCHRISTOPHER ZANONI
Manufacturer Street600 N. FIELD DR.
Manufacturer CityLAKE FOREST IL 60045
Manufacturer CountryUS
Manufacturer Postal60045
Manufacturer Phone2247062300
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNDEHP SAPPHIRE SET NV +1.2FLTR
Generic NameACCESSORIES, PUMP, INFUSION
Product CodeMRZ
Date Received2019-10-23
Returned To Mfg2019-10-14
Model Number1632402
Catalog Number163240455
Lot Number3895371
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerICU MEDICAL COSTA RICA LTD.
Manufacturer AddressZONA FRANCA GLOBAL LA AURORA HEREDIA CS


Patients

Patient NumberTreatmentOutcomeDate
10 2019-10-23

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