BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Rasp

    DI: 04049197516501 · Model: 259-880-260 · RZ-Medizintechnik GmbH
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Let the assistant research this device

    The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Brand Name
    Rasp
    Primary DI
    04049197516501
    Version / Model
    259-880-260
    Company Name
    RZ-Medizintechnik GmbH
    Labeler DUNS
    312953227
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2023-05-02
    Public Version
    1
    Public Version Date
    2023-05-10
    Public Version Status
    New
    Public Device Record Key
    5f5f3aa0-28e7-4c0e-a474-d7fb92f9569f

    Device Description

    Rasp, 8.8 x 260mm

    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
    Moist Heat or Steam Sterilization

    Product Codes

    Code Name
    HTZ Instrument, Cutting, Orthopedic

    GMDN Terms

    Code Name
    36235 Manual surgical rotary handpiece, reusable

    Identifiers

    Type ID
    Primary 04049197516501