AXIOS STENT AND DELIVERY SYSTEM M00553520 5352

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 2020-01-13 for AXIOS STENT AND DELIVERY SYSTEM M00553520 5352 manufactured by Boston Scientific Corporation.

MAUDE Entry Details

Report Number3005099803-2020-00015
MDR Report Key9583740
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-01-13
Date of Report2020-01-13
Date of Event2019-11-13
Date Mfgr Received2019-12-18
Device Manufacturer Date2019-08-06
Date Added to Maude2020-01-13
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 CORPORATION
Manufacturer StreetBALLYBRIT BUSINESS PARK
Manufacturer CityGALWAY
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAXIOS STENT AND DELIVERY SYSTEM
Generic NamePANCREATIC STENT, COVERED, METALLIC, REMOVABLE
Product CodePCU
Date Received2020-01-13
Returned To Mfg2019-11-26
Model NumberM00553520
Catalog Number5352
Lot Number0024222016
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 2020-01-13

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