BEUDAMED
    FDA Registration Active 🇺🇸 United States

    VivaSight 2 SLT Kit - 7 mm

    Reg #: 3009171251 · FEI: 3006759904 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    10
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    UPS SUPPLY CHAIN SOLUTIONS, INC.
    Registration Number
    3009171251
    FEI Number
    3006759904
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1860 OUTER LOOP
    City
    Louisville
    State
    KY
    ZIP
    40219
    Country
    US

    Regulatory Submissions

    510(k) Number
    K203749

    Owner / Operator

    Firm Name
    UPS SUPPLY CHAIN SOLUTIONS, INC.
    Operator Number
    9073670
    Address
    1920 Outer Loop, Complex A206
    City
    Louisville
    State
    KY
    Postal Code
    40219
    Country
    US
    Correspondent
    Tim Bishop

    Products

    Device Name Product Code
    Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector) CBI

    Proprietary Names

    VivaSight 2 SLT Kit - 7 mm VivaSight™ 2 DLT Kit 35 Fr - LEFT VivaSight 2 SLT Kit - 8 mm VivaSight 2 SLT + EBB Kit - 8 mm, 9 Fr VivaSight 2 SLT Kit - 7.5 mm VivaSight 2 SLT + EBB Kit - 7 mm, 9 Fr VivaSight™ 2 DLT Kit 37 Fr - LEFT VivaSight™ 2 DLT Kit 41 Fr - LEFT VivaSight™ 2 DLT Kit 39 Fr - LEFT VivaSight 2 SLT + EBB Kit - 7.5 mm, 9 Fr

    Establishment Types

    Repack or Relabel Medical Device