ADVANTA V12 COVERED STENT 85364

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,health pr report with the FDA on 2020-03-05 for ADVANTA V12 COVERED STENT 85364 manufactured by Atrium Medical Corporation.

Event Text Entries

[186840942] On completion of the investigation a follow up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[186840943] It was reported that during the procedure, while the endograft was being stented with a balloon expandable stent, the balloon came off of the end of the apparatus. The balloon was able to be retrieved. No patient harm reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3011175548-2020-00365
MDR Report Key9796142
Report SourceDISTRIBUTOR,FOREIGN,HEALTH PR
Date Received2020-03-05
Date of Report2020-03-05
Date of Event2019-10-28
Date Mfgr Received2020-03-03
Date Added to Maude2020-03-05
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer Street40 CONTINENTAL BLVD
Manufacturer CityMERRIMACK NH 03054
Manufacturer CountryUS
Manufacturer Postal03054
Manufacturer G1ATRIUM MEDICAL CORPORATION
Manufacturer Street40 CONTINENTAL BLVD
Manufacturer CityMERRIMACK NH 03054
Manufacturer CountryUS
Manufacturer Postal Code03054
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameADVANTA V12 COVERED STENT
Generic NameSTENT, ILIAC
Product CodeNIO
Date Received2020-03-05
Model Number85364
Catalog Number85364
Lot Number450599
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerATRIUM MEDICAL CORPORATION
Manufacturer Address40 CONTINENTAL BLVD MERRIMACK NH 03054 US 03054


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-05

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