FDA Device Establishments · JSON-LD · Markdown

ABBOTT VASCULAR

FEI 3005718570 · Export Device to the United States But Perform No Other Operation on Device Manufacture Medical Device · Status: Active

FEI Number3005718570
Owner / OperatorABBOTT LABORATORIES (#1415939)
AddressCASHEL ROAD, CLONMEL Tipperary, ,, IE
Mandatory US AgentAbbott Vascular
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)NIQ
Proprietary namesXIENCE Xpedition Everolimus Eluting Stent System; XIENCE Alpine Everolimus Eluting Stent System; XIENCE Sierra Everolimus Eluting Stent System; XIENCE Skypoint Everolimus Eluting Stent System; XIENCE PRIME Everolimus Eluting Stent System; XIENCE ProS Everolimus Eluting Stent System

External sources

Source: openFDA. Public-domain (CC0).