BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    PDT, Inc.

    DI: 00813677023223 · Model: T731 Micro-Friedman Bone Rongeur · PDT, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    PDT, Inc.
    Primary DI
    00813677023223
    Version / Model
    T731 Micro-Friedman Bone Rongeur
    Catalog Number
    T731
    Company Name
    PDT, INC.
    Labeler DUNS
    125850144
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2024-07-01
    Public Version
    1
    Public Version Date
    2024-07-09
    Public Version Status
    New
    Public Device Record Key
    404270d7-7543-4fdb-a34a-4fd54263a242

    Device Description

    T731 Micro-Friedman Bone Rongeur

    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
    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, Dry Heat Sterilization

    Product Codes

    Code Name
    EMH Forceps, Rongeur, Surgical

    GMDN Terms

    Code Name
    15713 Dental rongeur

    Identifiers

    Type ID
    Primary 00813677023223