BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Revision Cannula

    DI: 08031497002224 · Model: ASA0050 · TECRES SPA
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

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    Basic Information

    Brand Name
    Revision Cannula
    Primary DI
    08031497002224
    Version / Model
    ASA0050
    Company Name
    TECRES SPA
    Labeler DUNS
    435428396
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2022-09-23
    Public Version
    1
    Public Version Date
    2022-10-03
    Public Version Status
    New
    Public Device Record Key
    68d44bb7-748d-4c5a-83b6-af7502984430

    Device Description

    Revision Cannula is intended to be used to distal femoral bone cement delivery through Tecres' Cemex System.

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    No
    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
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    KDD Kit, Surgical Instrument, Disposable

    GMDN Terms

    Code Name
    47737 Orthopaedic cement injection cannula

    Identifiers

    Type ID
    Primary 08031497002224