BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Medtronic Care Management Services

    Reg #: 3004594267 · FEI: 3004594267 · Expires 2026
    View on FDA
    Products
    3
    Proprietary Names
    19
    Establishment Types
    2
    Classifications
    3

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    Registration Details

    Registration Name
    Medtronic Care Management Services
    Registration Number
    3004594267
    FEI Number
    3004594267
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    200 Medtronic Dr
    City
    Lafayette
    State
    CO
    ZIP
    80026
    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
    Scale, Stand-On, Patient FRI
    System, Measurement, Blood-Pressure, Non-Invasive DXN
    Oximeter DQA

    Proprietary Names

    Stand-on Patient Scale SC250 Stand-on Patient Scale SC100 ForaCare Blue Tooth Weight Scale Test n Go 550 IHEALTH Scale HS4 Generic cables to connect Commander hub devices to various scales Commander Flex CD320 Generic cables to connect Commander hub devices to the various glucose meters Pulse Oximeter PO100 Generic cables to connect Commander hub devices to peak flow meter Generic cables to connect Commander hub devices to Pulse Oximeter Blood Pressure Cuff - Large Cuff Regular Blood Pressure Cuff - Medium Cuff Regular Blood Pressure Cuff - Large Cuff Contour Blood Pressure Cuff - Medium Cuff Contour Generic cables to connect Commander hub devices to the various Spirometers Blood Pressure Cuff - Small Cuff Regular Generic cables to connect Commander hub devices to the various thermometers Generic cables to connect Commander hub devices to the various Peak Flow meters Generic cables to connect Commander hub devices to the various stethoscopes

    Establishment Types

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