BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Reprocess FloPatch

    DI: 00627987360134 · Model: FP120 · 1929803 Ontario Corp
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    4
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Reprocess FloPatch
    Primary DI
    00627987360134
    Version / Model
    FP120
    Company Name
    1929803 Ontario Corp
    Labeler DUNS
    204195374
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2023-05-08
    Public Version
    1
    Public Version Date
    2023-05-16
    Public Version Status
    New
    Public Device Record Key
    8ded378f-4aa2-450d-ab6d-e5941ff32f7f

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    Yes
    Over the Counter (OTC)
    No
    Kit
    No
    Combination Product
    No
    HCT/P
    No
    Contains NRL
    No
    Not Made with NRL
    No
    MRI Safety
    MR Unsafe
    Direct Marking Exempt
    No
    PM Exempt
    No
    Has Serial Number
    Yes
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    Yes
    Has Expiration Date
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    DPW Flowmeter, Blood, Cardiovascular

    GMDN Terms

    Code Name
    62211 Invasive/noninvasive vascular ultrasound probe

    Identifiers

    Type ID
    Package 10627987360131
    Primary 00627987360134
    Package 20627987360138
    Package 30627987360135