BEUDAMED
    FDA Registration Active 🇨🇭 Switzerland

    K-wire Kit

    Reg #: 3005827567 · FEI: 3005827567 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    5
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    RUETSCHI TECHNOLOGY AG
    Registration Number
    3005827567
    FEI Number
    3005827567
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Fabrikstrasse 35
    City
    Muntelier Fribourg
    Country
    CH

    Owner / Operator

    Firm Name
    Ruetschi Technology AG
    Operator Number
    10043785
    Address
    Fabrikstrasse 35
    City
    Muntelier
    State
    Fribourg
    Postal Code
    3286
    Country
    CH
    Correspondent
    Adrian Hofer

    US Agent

    Business Name
    ONYX MEDICAL CORPORATION
    Contact Name
    JODIE GILMORE
    Address
    1800 North Shelby Oaks Drive
    City
    Memphis
    State
    TN
    ZIP
    38134
    Country
    US
    Email
    [email protected]
    Phone
    901 3236699

    Products

    Device Name Product Code
    Orthopedic Manual Surgical Instrument LXH

    Proprietary Names

    K-wire Kit Pedicle Screw Instrument Kit T-Handle Kit Removal Kit Compressor Distractor Kit

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)