18 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA OPTI22

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 2019-11-26 for 18 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA OPTI22 manufactured by Edwards Lifesciences.

MAUDE Entry Details

Report Number3008500478-2019-00172
MDR Report Key9377193
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-11-26
Date of Report2019-11-07
Date of Event2019-11-07
Date Mfgr Received2019-11-07
Device Manufacturer Date2018-04-26
Date Added to Maude2019-11-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. AMRITHA SRINIVASAN
Manufacturer Street12050 LONE PEAK PARKWAY MLE-2
Manufacturer CityDRAPER UT 84020
Manufacturer CountryUS
Manufacturer Postal84020
Manufacturer Phone9492504062
Manufacturer G1EDWARDS LIFESCIENCES LLC
Manufacturer Street1 EDWARDS WAY
Manufacturer CityIRVINE CA 92614
Manufacturer CountryUS
Manufacturer Postal Code92614
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name18 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA
Generic NameCANNULA, CATHETER
Product CodeDQR
Date Received2019-11-26
Model NumberOPTI22
Catalog NumberOPTI22
Lot Number61338640
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerEDWARDS LIFESCIENCES
Manufacturer Address1 EDWARDS WAY IRVINE CA 92614 US 92614


Patients

Patient NumberTreatmentOutcomeDate
101. Life Threatening 2019-11-26

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