ECHOTIP CELIAC PLEXUS NEUROLYSIS NEEDLE EUSN-20-CPN

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a literature,study report with the FDA on 2019-11-21 for ECHOTIP CELIAC PLEXUS NEUROLYSIS NEEDLE EUSN-20-CPN manufactured by Cook Ireland Ltd.

MAUDE Entry Details

Report Number3001845648-2019-00620
MDR Report Key9353049
Report SourceLITERATURE,STUDY
Date Received2019-11-21
Date of Report2019-10-24
Date of Event2019-11-08
Date Mfgr Received2019-10-24
Date Added to Maude2019-11-21
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 ContactMS. HEATHER RYAN
Manufacturer StreetO HALLORAN ROAD NATIONAL TECHNOLOGY PARK
Manufacturer CityLIMERICK
Manufacturer G1COOK IRELAND LTD
Manufacturer StreetO HALLORAN ROAD NATIONAL TECHNOLOGY PARK
Manufacturer CityLIMERICK
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameECHOTIP CELIAC PLEXUS NEUROLYSIS NEEDLE
Product CodeBSP
Date Received2019-11-21
Catalog NumberEUSN-20-CPN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOOK IRELAND LTD
Manufacturer AddressO HALLORAN ROAD LIMERICK


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-11-21

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