BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Integra®Ti6®

    DI: 10381780245889 · Model: KW1102 · Ascension Orthopedics, Inc.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Integra®Ti6®
    Primary DI
    10381780245889
    Version / Model
    KW1102
    Catalog Number
    KW1102
    Company Name
    Ascension Orthopedics, Inc.
    Labeler DUNS
    942377524
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2017-09-05
    Public Version
    6
    Public Version Date
    2023-09-18
    Public Version Status
    Update
    Public Device Record Key
    97f48b35-e2c2-47e0-87b3-8298ca1776d1
    Distribution End Date
    2026-12-31

    Device Description

    Integra® Ti6® The Ti6 TC-Series K-Wire is used for temporary fixation.

    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
    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
    HXI PASSER, WIRE, ORTHOPEDIC

    GMDN Terms

    Code Name
    46165 Orthopaedic guidewire, reusable

    Identifiers

    Type ID
    Secondary M269KW11021
    Primary 10381780245889

    Customer Contacts

    Phone
    +1(800)654-2873
    Email
    [email protected]

    Device Sizes

    Type Value Unit Text
    Device Size Text, specify 3.94in L x .035in diameter