BEUDAMED
    FDA Registration Active 🇺🇸 United States

    MIDWAY Delivery Catheter (MIDWAY 43 Delivery Catheter; MIDWAY 62 Delivery Catheter)

    Reg #: 3005168196 · FEI: 3005168196 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    PENUMBRA, INC.
    Registration Number
    3005168196
    FEI Number
    3005168196
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    One Penumbra Place
    City
    Alameda
    State
    CA
    ZIP
    94502
    Country
    US

    Regulatory Submissions

    510(k) Number
    K233201

    Owner / Operator

    Firm Name
    PENUMBRA, INC.
    Operator Number
    9072336
    Address
    One Penumbra Place
    City
    Alameda
    State
    CA
    Postal Code
    94502
    Country
    US

    Products

    Device Name Product Code
    Catheter, Percutaneous DQY
    Catheter, Percutaneous, Neurovasculature QJP

    Proprietary Names

    MIDWAY Delivery Catheter (MIDWAY 43 Delivery Catheter; MIDWAY 62 Delivery Catheter)

    Establishment Types

    Manufacture Medical Device