BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    K2™ Hemi Toe Implant System

    DI: 10381780279501 · Model: 205000 · Ascension Orthopedics, Inc.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    1

    Basic Information

    Brand Name
    K2™ Hemi Toe Implant System
    Primary DI
    10381780279501
    Version / Model
    205000
    Catalog Number
    205000
    Company Name
    Ascension Orthopedics, Inc.
    Labeler DUNS
    942377524
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2018-04-10
    Public Version
    8
    Public Version Date
    2023-05-02
    Public Version Status
    Update
    Public Device Record Key
    72beda70-c301-4cdb-95a4-ef4947db25a9
    Distribution End Date
    2023-03-31

    Device Description

    K2 HEMI TRAY

    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
    Yes
    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
    FSM TRAY, SURGICAL, INSTRUMENT

    GMDN Terms

    Code Name
    12143 Instrument tray, reusable

    Identifiers

    Type ID
    Secondary M2482050001
    Primary 10381780279501

    Customer Contacts

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