BEUDAMED
    FDA Registration Active 🇺🇸 United States

    50cm Lead Extension Kit

    Reg #: 1928237 · FEI: 1928237 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    32
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    MIDWEST STERILIZATION CORP.
    Registration Number
    1928237
    FEI Number
    1928237
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1204 LENCO AVE.
    City
    JACKSON
    State
    MO
    ZIP
    63755
    Country
    US

    Regulatory Submissions

    PMA Number
    P150004

    Owner / Operator

    Firm Name
    MIDWEST STERILIZATION CORP.
    Operator Number
    1928237
    Address
    1204 LENCO AVE., --
    City
    Jackson
    State
    MO
    Postal Code
    63755
    Country
    US
    Correspondent
    KAREN E ELDRIDGE

    Products

    Device Name Product Code
    Dorsal Root Ganglion Stimulator For Pain Relief PMP

    Proprietary Names

    50cm Lead Extension Kit 50cm DRG Single Lead Trial Kit 50cm SlimTip Trial Lead Kit 90cm DRG Dual Lead Trial Kit Lead Accessories Kit 22cm Big Curve Delivery Sheath Kit 50cm DRG Dual Lead Trial Kit 50cm DRG Single Lead Implant Kit 22cm Small Curve Delivery Sheath Kit 90cm SlimTip Implant Lead Kit 90cm DRG Single Lead Implant Kit Large Needle and Sheath Kit 50cm DRG Dual Lead Implant Kit 90cm SlimTip Trial Lead Kit 50cm SlimTip Implant Lead Kit 90cm DRG Dual Lead Implant Kit 30cm Tunneling Tool Kit Tunneling Tool, DRG Curved Needle Kit 95cm Stylet Kit 55cm Stylet Kit Guidewire Kit Hex Key Kit Torque Wrench Kit Anchor Kit 90cm DRG Single Lead Trial Kit Connector Cable Kit Straight Needle Kit Proclaim™ DRG IPG EPG Trial, DRG, 2 Port Header Port Plug, DRG 22cm Large Curve Delivery Sheath Kit

    Establishment Types

    Sterilize Medical Device for Another Party (Contract Sterilizer)