FDA.reportPublic FDA data

Bard European Distribution Center NV

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30025040683002504068Bard European Distribution Center NV1N2027-01-01Hagelberg 2 Olen Antwerpen BE 2250

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1827561511977884P250050Liverty™ TIPS Stent GraftMIR2026-09-25
1827561759294480P180037Venovo Venous Stent SystemQAN2019-03-13
1827561489855055P170042Covera™ Vascular Covered StentPFV2018-07-30
1827561977743193P130029FLUENCY PLUS ENDOVASCULAR STENT GRAFTPFV2014-06-17
1827561001387635P080007BARD E-LUMINEXX VASCULAR STENTNIO2008-12-04
1827561319940737P070014LIFESTENT FLEXSTAR & FLEXSTAR XL VASCULAR STENT SYSTEMNIP2009-02-13
1827561979670699P060002FLAIR ENDOVASCULAR STENT GRAFTPFV2007-07-23
1827561183885759K130792LIFESTENT BILIARY STENT SYSTEM, LIFESTENT XL BILIARY STENT SYSTEMFGE2013-08-30
1827561912208786K063532BARD E LUMINEXX BILIARY STENTFGE2008-05-30
1827561467465479K060487LIFESTENT FLEXSTAR XL BILIARY STENT SYSTEMFGE2006-03-23
1827561992171367K053404LIFESTENT FLEXSTART BILIARY STENT SYSTEMFGE2005-12-21
1827561257830152K031186LUMINEXX ENDOSCOPIC BILIARY STENTFGE2003-05-06
1827561081840160
1827561363192348

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FGE52013-08-30
PFV32018-07-30
QAN12019-03-13
NIP12009-02-13
NIO12008-12-04