UROMAX ULTRA M0062251000 225-100

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 2019-09-18 for UROMAX ULTRA M0062251000 225-100 manufactured by Boston Scientific Corporation.

MAUDE Entry Details

Report Number3005099803-2019-04627
MDR Report Key9081285
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-09-18
Date of Report2019-09-18
Date of Event2019-08-26
Date Mfgr Received2019-08-26
Device Manufacturer Date2018-07-31
Date Added to Maude2019-09-18
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 StreetBALLYBRIT BUSINESS PARK
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 Received2019-09-18
Returned To Mfg2019-09-09
Model NumberM0062251000
Catalog Number225-100
Lot Number0022447572
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
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 2019-09-18

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.