BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Vivoo Sediva Sedimentation Test Tube

    Reg #: 3018126397 · FEI: 3018126397 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    VIVOSENS INC
    Registration Number
    3018126397
    FEI Number
    3018126397
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    44 Tehama Street, Suite 409
    City
    San Francisco
    State
    CA
    ZIP
    94105
    Country
    US

    Owner / Operator

    Firm Name
    Vivosens Inc
    Operator Number
    10085777
    Address
    44 Tehama Street, Suite 409
    City
    San Francisco
    State
    CA
    Postal Code
    94105
    Country
    US
    Correspondent
    Gozde Buyukacaroglu

    Products

    Device Name Product Code
    Tube, Sedimentation Rate GHC

    Proprietary Names

    Vivoo Sediva Sedimentation Test Tube

    Establishment Types

    Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility