BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    Aquarius XH

    DI: D7075798000 · Model: 579800 · IVOCLAR VIVADENT, INC.
    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
    Aquarius XH
    Primary DI
    D7075798000
    Version / Model
    579800
    Catalog Number
    579800
    Company Name
    IVOCLAR VIVADENT, INC.
    Labeler DUNS
    176935203
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2018-10-29
    Public Version
    2
    Public Version Date
    2021-06-23
    Public Version Status
    Update
    Public Device Record Key
    eed63863-dc42-42ca-8baf-6d7c4cee7871
    Distribution End Date
    2021-06-22

    Device Description

    Aquarius XH 50 g

    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
    No

    Product Codes

    Code Name
    EJT Alloy, gold-based noble metal

    GMDN Terms

    Code Name
    35858 Dental casting noble alloy

    Identifiers

    Type ID
    Primary D7075798000