BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    NA

    DI: 00840085220784 · Model: KZC131020 · HYHTE HOLDINGS, INC.
    View on AccessGUDID
    Product Codes
    3
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    NA
    Primary DI
    00840085220784
    Version / Model
    KZC131020
    Catalog Number
    KZC131020
    Company Name
    HYHTE HOLDINGS, INC.
    Labeler DUNS
    073029645
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2021-07-30
    Public Version
    2
    Public Version Date
    2022-12-08
    Public Version Status
    Update
    Public Device Record Key
    25567c92-6900-4ca1-a17e-836b4f10d88b

    Device Description

    VARIABLE ANGLE TAP, GUIDED LONG

    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
    Labeling does not contain MRI Safety Information
    Direct Marking Exempt
    No
    PM Exempt
    No
    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
    KWQ Appliance, Fixation, Spinal Intervertebral Body
    OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
    MAX Intervertebral Fusion Device With Bone Graft, Lumbar

    GMDN Terms

    Code Name
    17507 Bone tap, reusable

    Identifiers

    Type ID
    Primary 00840085220784

    Customer Contacts

    Phone
    7608148047
    Email
    [email protected]