AUTOMATED IMPELLA CONTROLLER IMPELLA AIC CONTROLLER 0042-0000-EU

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 2019-09-26 for AUTOMATED IMPELLA CONTROLLER IMPELLA AIC CONTROLLER 0042-0000-EU manufactured by Abiomed Inc..

MAUDE Entry Details

Report Number1220648-2019-00201
MDR Report Key9124428
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-09-26
Date of Report2019-09-26
Date of Event2019-09-17
Date Facility Aware2019-09-17
Date Mfgr Received2019-09-17
Device Manufacturer Date2018-12-13
Date Added to Maude2019-09-26
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 ContactMR. RALPH BARISANO
Manufacturer Street22 CHERRY HILL DRIVE
Manufacturer CityDANVERS MA 01923
Manufacturer CountryUS
Manufacturer Postal01923
Manufacturer Phone9786461400
Manufacturer G1ABIOMED INC.
Manufacturer Street22 CHERRY HILL DRIVE
Manufacturer CityDANVERS MA 01923
Manufacturer CountryUS
Manufacturer Postal Code01923
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAUTOMATED IMPELLA CONTROLLER
Generic NameAUTOMATED IMPELLA CONTROLLER
Product CodePYX
Date Received2019-09-26
Model NumberIMPELLA AIC CONTROLLER
Catalog Number0042-0000-EU
Lot Number1380525
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerABIOMED INC.
Manufacturer Address22 CHERRY HILL DRIVE DANVERS MA 01923 US 01923


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2019-09-26

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