BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Shadow Knotless

    DI: 00811714035888 · Model: 920002-0000-P · RESPONSIVE ORTHOPEDICS LLC
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Shadow Knotless
    Primary DI
    00811714035888
    Version / Model
    920002-0000-P
    Catalog Number
    920002-0000-P
    Company Name
    RESPONSIVE ORTHOPEDICS LLC
    Labeler DUNS
    002745858
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2023-11-06
    Public Version
    1
    Public Version Date
    2023-11-14
    Public Version Status
    New
    Public Device Record Key
    4b5290ef-5577-4475-8224-85af6b778b6a

    Device Description

    Shadow Knotless Instruments

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    Yes
    Over the Counter (OTC)
    No
    Kit
    Yes
    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
    FSM Tray, Surgical, Instrument

    GMDN Terms

    Code Name
    12143 Instrument tray, reusable

    Identifiers

    Type ID
    Primary 00811714035888