BEUDAMED
    FDA Registration Active 🇺🇸 United States

    RapidVac Tubing with Sponge Guard, SEA3715

    Reg #: 3009380063 · FEI: 3009380063 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    12
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Medtronic Distribution Center
    Registration Number
    3009380063
    FEI Number
    3009380063
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    5300 Airways Blvd
    City
    Memphis
    State
    TN
    ZIP
    38116
    Country
    US

    Regulatory Submissions

    510(k) Number
    K980915

    Owner / Operator

    Firm Name
    Medtronic, Inc.
    Operator Number
    2112641
    Address
    710 Medtronic Parkway
    City
    Minneapolis
    State
    MN
    Postal Code
    55432
    Country
    US

    Products

    Device Name Product Code
    Apparatus, Exhaust, Surgical FYD

    Proprietary Names

    RapidVac Tubing with Sponge Guard, SEA3715 OptiMumm Smoke Sponge Guard Tubing, E3635 OptiMumm Smoke Prefilter, E3630 OptiMumm Smoke Reducer Fitting, E3655 OptiMumm ULPA Filter, E3625 RapidVac Tubing, SEA3710 OptiMumm Smoke Prefilter Reducer Adapter, E3660 OptiMumm Smoke Prefilter Reducer Adapter, E3665 RapidVac Laparoscopic Tubing, SEA3720 RapidVac Tubing, SEA3705 OptiMumm Smoke Tubing, E3645 RapidVac Wand, Laser Resistant, SEA3725

    Establishment Types

    Repack or Relabel Medical Device