URETERAL DILATOR 076000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,other,use report with the FDA on 2020-03-30 for URETERAL DILATOR 076000 manufactured by Cook Inc.

MAUDE Entry Details

Report Number1820334-2020-00709
MDR Report Key9897816
Report SourceDISTRIBUTOR,FOREIGN,OTHER,USE
Date Received2020-03-30
Date of Report2020-03-30
Date of Event2020-03-20
Date Mfgr Received2020-03-20
Device Manufacturer Date2019-10-18
Date Added to Maude2020-03-30
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 ContactMRS. JENNIFER CANADA
Manufacturer Street750 DANIELS WAY
Manufacturer CityBLOOMINGTON IN 47404
Manufacturer CountryUS
Manufacturer Postal47404
Manufacturer Phone8123392235
Manufacturer G1COOK INC
Manufacturer Street750 DANIELS WAY
Manufacturer CityBLOOMINGTON IN 47404
Manufacturer CountryUS
Manufacturer Postal Code47404
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameURETERAL DILATOR
Generic NameEZN DILATOR, CATHETER, URETERAL
Product CodeEZN
Date Received2020-03-30
Catalog Number076000
Lot NumberNS10092052
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOOK INC
Manufacturer Address750 DANIELS WAY BLOOMINGTON IN 47404 US 47404


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-30

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