BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Henry Schein

    DI: 10304040115081 · Model: 2020323 · HENRY SCHEIN, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    6

    Basic Information

    Brand Name
    Henry Schein
    Primary DI
    10304040115081
    Version / Model
    2020323
    Catalog Number
    2020323
    Company Name
    HENRY SCHEIN, INC.
    Labeler DUNS
    012430880
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    6
    Record Status
    Published
    Publish Date
    2019-11-01
    Public Version
    1
    Public Version Date
    2019-11-11
    Public Version Status
    New
    Public Device Record Key
    8bfa5450-3de7-4a1f-b671-b1d6a4e5172e

    Device Description

    OBTURATOR - VUL6 - SIZE 25 VC Obt 6pk VCC2

    Device Characteristics

    Single Use
    Yes
    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
    Yes
    PM Exempt
    Yes
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    No
    Has Expiration Date
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    EKM GUTTA-PERCHA

    GMDN Terms

    Code Name
    47751 Warm-bonded endodontic obturation system obturator

    Identifiers

    Type ID
    Primary 10304040115081
    Unit of Use 00304040115084