NDEHP SAPPHIRE YLW STRIPED+PAV 1637402 163740455

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 2019-08-27 for NDEHP SAPPHIRE YLW STRIPED+PAV 1637402 163740455 manufactured by Icu Medical Costa Rica Ltd..

MAUDE Entry Details

Report Number9615050-2019-00364
MDR Report Key8935301
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-08-27
Date of Report2019-08-08
Date of Event2019-07-28
Date Mfgr Received2019-09-20
Device Manufacturer Date2018-10-01
Date Added to Maude2019-08-27
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 YLW STRIPED+PAV
Generic NameELECTRIC INFUSION PUMP ADMINISTRATION SET, SINGLE-USE
Product CodeMRZ
Date Received2019-08-27
Model Number1637402
Catalog Number163740455
Lot Number946365H
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
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 2019-08-27

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