BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Rumex

    DI: 00840159905463 · Model: 16-010 · RUMEX INTERNATIONAL CORP.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Rumex
    Primary DI
    00840159905463
    Version / Model
    16-010
    Catalog Number
    16-010
    Company Name
    RUMEX INTERNATIONAL CORP.
    Labeler DUNS
    041546137
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2020-06-04
    Public Version
    1
    Public Version Date
    2020-06-12
    Public Version Status
    New
    Public Device Record Key
    bc01a952-b157-4992-8a79-4f5a62ffd3a0

    Device Description

    Rumex Corneoscleral Punch (0.50, 0.75, 1.00, 1.50 mm Tips), Length 110 mm, Titanium Handle

    Device Characteristics

    Single Use
    No
    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
    No
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    Yes
    Sterilization Methods
    ["Dry Heat Sterilization", "Ethylene Oxide", "Moist Heat or Steam Sterilization"]

    Product Codes

    Code Name
    HNJ Punch, Corneo-Scleral

    GMDN Terms

    Code Name
    13232 Corneoscleral punch

    Identifiers

    Type ID
    Primary 00840159905463