SAPH AP223-01 MBORE NV W/0.2FLTR BCV&PAV 163830401

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-06-28 for SAPH AP223-01 MBORE NV W/0.2FLTR BCV&PAV 163830401 manufactured by Icu Medical Costa Rica Ltd..

MAUDE Entry Details

Report Number9615050-2019-00210
MDR Report Key8745191
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-06-28
Date of Report2019-06-11
Date of Event2019-06-01
Date Mfgr Received2019-08-13
Date Added to Maude2019-06-28
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 ContactEMILY ARNOULD, BSN, RN
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 NameSAPH AP223-01 MBORE NV W/0.2FLTR BCV&PAV
Generic NameACCESSORIES, PUMP, INFUSION
Product CodeMRZ
Date Received2019-06-28
Returned To Mfg2019-06-17
Catalog Number163830401
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerICU MEDICAL COSTA RICA LTD.
Manufacturer AddressZONA FRANCA GLOBAL LA AURORA HEREDIA CS


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-28

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