BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    INNESIS PEEK TL CAGE

    DI: 08809763507052 · Model: 52850 · BK MEDITECH CO.,LTD.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

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    Basic Information

    Brand Name
    INNESIS PEEK TL CAGE
    Primary DI
    08809763507052
    Version / Model
    52850
    Company Name
    BK MEDITECH CO.,LTD.
    Labeler DUNS
    687941818
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2023-06-14
    Public Version
    1
    Public Version Date
    2023-06-22
    Public Version Status
    New
    Public Device Record Key
    9dd19f95-70aa-441d-976c-19a87b5a0fa4

    Device Description

    Rasp

    Device Characteristics

    Single Use
    No
    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
    Labeling does not contain MRI Safety Information
    Direct Marking Exempt
    No
    PM Exempt
    Yes
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    Yes
    Sterilization Methods
    Moist Heat or Steam Sterilization

    Product Codes

    Code Name
    HTR Rasp

    GMDN Terms

    Code Name
    35559 Bone file/rasp, manual, reusable

    Identifiers

    Type ID
    Primary 08809763507052