# ABBOTT VASCULAR

FEI: 3005718570
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device
Owner/operator: ABBOTT LABORATORIES (#1415939)

Address: CASHEL ROAD, CLONMEL Tipperary, ,, IE

Mandatory US Agent: Abbott Vascular

## Products

Total registered: 1
Top product codes: NIQ
Regulation §: —

Proprietary names: XIENCE 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

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223005718570%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3005718570