BEUDAMED
    FDA Registration Active 🇨🇱 Chile

    MODULAR HYBRID GLENOID

    Reg #: 3014302784 · FEI: 3014302784 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    BIOMET CHILE S.A.
    Registration Number
    3014302784
    FEI Number
    3014302784
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Av. Santa Clara No. 085 Floor 7, HUECHURABA
    City
    Santiago de Chile Region Metropolitana
    Country
    CL

    Regulatory Submissions

    510(k) Number
    K060694

    Owner / Operator

    Firm Name
    ZimmerBiomet Americas DFE
    Operator Number
    10056779
    Address
    1800 W Center St.
    City
    Warsaw
    State
    IN
    Postal Code
    46580
    Country
    US

    US Agent

    Business Name
    Zimmer Biomet
    Contact Name
    Holly Seppanen
    Address
    1800 West Center Street
    City
    Warsaw
    State
    IN
    ZIP
    46580
    Country
    US
    Email
    [email protected]
    Phone
    952 8470494

    Products

    Device Name Product Code
    Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented KWT
    Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented KWS

    Proprietary Names

    MODULAR HYBRID GLENOID

    Establishment Types

    Export Device to the United States But Perform No Other Operation on Device