UROMAX ULTRA M0062251170 225-117

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 2020-01-14 for UROMAX ULTRA M0062251170 225-117 manufactured by Boston Scientific Corporation.

MAUDE Entry Details

Report Number3005099803-2019-06528
MDR Report Key9586010
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-01-14
Date of Report2020-03-23
Date of Event2019-12-01
Date Mfgr Received2020-02-24
Device Manufacturer Date2017-02-01
Date Added to Maude2020-01-14
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 ContactCAROLE MORLEY
Manufacturer Street300 BOSTON SCIENTIFIC WAY
Manufacturer CityMARLBOROUGH MA 01752
Manufacturer CountryUS
Manufacturer Postal01752
Manufacturer Phone5086834015
Manufacturer G1BOSTON SCIENTIFIC IRELAND LIMITED
Manufacturer Street780 BROOKSIDE DRIVE
Manufacturer CityGALWAY
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUROMAX ULTRA
Generic NameDILATOR, CATHETER, URETERAL
Product CodeEZN
Date Received2020-01-14
Returned To Mfg2020-01-21
Model NumberM0062251170
Catalog Number225-117
Lot Number0020209917
Device Expiration Date2020-01-26
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer Address300 BOSTON SCIENTIFIC WAY MARLBOROUGH MA 01752 US 01752


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-14

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