BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    BAYONET CURETTE

    DI: 00192896079199 · Model: 413-051 · SONTEC INSTRUMENTS, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    BAYONET CURETTE
    Primary DI
    00192896079199
    Version / Model
    413-051
    Catalog Number
    413-051
    Company Name
    SONTEC INSTRUMENTS, INC.
    Labeler DUNS
    040729840
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2018-09-20
    Public Version
    2
    Public Version Date
    2019-09-10
    Public Version Status
    Update
    Public Device Record Key
    d009d71f-3835-4ecd-85ee-fcabd2257233

    Device Description

    BAYONET CURETTE DOWN ANGLE RING TIP TITANIUM

    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
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

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

    Product Codes

    Code Name
    HXB PROBE

    GMDN Terms

    Code Name
    62558 General-purpose curette

    Identifiers

    Type ID
    Primary 00192896079199

    Customer Contacts

    Phone
    +1(800) 821-7496
    Email
    [email protected]

    Device Sizes

    Type Value Unit Text
    Device Size Text, specify 90 Degree Tip
    Length 10.25 Inch
    Device Size Text, specify 3 Millimeter Tip