BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Blood Pressure Cuff - Large Cuff Regular

    Reg #: 3004594267 · FEI: 3004594267 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    15
    Establishment Types
    2
    Classifications
    2

    Registration Details

    Registration Name
    Medtronic Care Management Services
    Registration Number
    3004594267
    FEI Number
    3004594267
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    7980 Century Blvd
    City
    CHANHASSEN
    State
    MN
    ZIP
    55317
    Country
    US

    Regulatory Submissions

    510(k) Number
    K091821

    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
    System, Measurement, Blood-Pressure, Non-Invasive DXN
    Oximeter DQA

    Proprietary Names

    Blood Pressure Cuff - Large Cuff Regular Blood Pressure Cuff - Medium Cuff Contour Blood Pressure Cuff - Medium Cuff Regular Blood Pressure Cuff - Large Cuff Contour Generic cables to connect Commander hub devices to peak flow meter Generic cables to connect Commander hub devices to Pulse Oximeter Generic cables to connect Commander hub devices to the various glucose meters Generic cables to connect Commander hub devices to the various thermometers Commander Flex CD320 Blood Pressure Cuff - Small Cuff Regular Generic cables to connect Commander hub devices to various scales Generic cables to connect Commander hub devices to the various Peak Flow meters Generic cables to connect Commander hub devices to the various stethoscopes Pulse Oximeter PO100 Generic cables to connect Commander hub devices to the various Spirometers

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198