BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Xience Prime

    Reg #: 2939561 · FEI: 3004635528 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    8
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    ABBOTT VASCULAR
    Registration Number
    2939561
    FEI Number
    3004635528
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    3200 Lakeside Dr
    City
    SANTA CLARA
    State
    CA
    ZIP
    95054
    Country
    US

    Regulatory Submissions

    PMA Number
    P110019

    Owner / Operator

    Firm Name
    ABBOTT LABORATORIES
    Operator Number
    1415939
    Address
    100 ABBOTT PARK RD., D-03Q3, AP52-1
    City
    Abbott Park
    State
    IL
    Postal Code
    60064
    Country
    US

    Products

    Device Name Product Code
    Coronary Drug-Eluting Stent NIQ

    Proprietary Names

    Xience Prime Xience Xpedition Coronary Drug-Eluting Stent System XIENCE XPEDITION Drug Eluting Stent System XIENCE ALPINE Drug Eluting Stent System XIENCE SIERRA Drug Eluting Stent System XIENCE Skypoint Drug Eluting Stent System Xience ProS XIENCE PRIME Drug Eluting Stent System

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility