BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Sklar®

    DI: 40649111185299 · Model: 06-3130 · SKLAR CORPORATION
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    500

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    Basic Information

    Brand Name
    Sklar®
    Primary DI
    40649111185299
    Version / Model
    06-3130
    Company Name
    SKLAR CORPORATION
    Labeler DUNS
    006966006
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    500
    Record Status
    Published
    Publish Date
    2018-12-14
    Public Version
    2
    Public Version Date
    2020-02-06
    Public Version Status
    Update
    Public Device Record Key
    9a279fe9-5e4b-4c2d-bac8-bd0e541131d9

    Device Description

    SKLARSAFE SCALPEL #10 BNS 500

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    No
    Over the Counter (OTC)
    No
    Kit
    No
    Combination Product
    No
    HCT/P
    No
    Contains NRL
    No
    Not Made with NRL
    Yes
    MRI Safety
    Labeling does not contain MRI Safety Information
    Direct Marking Exempt
    No
    PM Exempt
    Yes
    Has Serial Number
    Yes
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    No
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    GDX SCALPEL, ONE-PIECE

    GMDN Terms

    Code Name
    47569 Scalpel, single-use

    Identifiers

    Type ID
    Primary 40649111185299
    Unit of Use 00649111185291