BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    KILNER DELUXE SKIN HOOK

    DI: 00192896024922 · Model: 199-375 · SONTEC INSTRUMENTS, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    KILNER DELUXE SKIN HOOK
    Primary DI
    00192896024922
    Version / Model
    199-375
    Catalog Number
    199-375
    Company Name
    SONTEC INSTRUMENTS, INC.
    Labeler DUNS
    040729840
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2018-09-14
    Public Version
    3
    Public Version Date
    2020-09-22
    Public Version Status
    Update
    Public Device Record Key
    f0de65e1-88bd-4d7e-a57f-0b8ef4d71fbf

    Device Description

    KILNER DELUXE SKIN HOOK SMALL TIP

    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
    ["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

    Product Codes

    Code Name
    GDG HOOK, SURGICAL, GENERAL & PLASTIC SURGERY

    GMDN Terms

    Code Name
    42595 Soft-tissue surgical hook, reusable

    Identifiers

    Type ID
    Primary 00192896024922

    Customer Contacts

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

    Device Sizes

    Type Value Unit Text
    Length 4.75 Inch