BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    DIOnavi. Guide (Anchor system)

    DI: 08800049416372 · Model: GUIDE02 11 A04(a,b) · DIO Corporation
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    DIOnavi. Guide (Anchor system)
    Primary DI
    08800049416372
    Version / Model
    GUIDE02 11 A04(a,b)
    Company Name
    DIO Corporation
    Labeler DUNS
    631085206
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2022-12-01
    Public Version
    1
    Public Version Date
    2022-12-09
    Public Version Status
    New
    Public Device Record Key
    79c3cfb4-f55c-49a0-97b3-24f41d483a9d

    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
    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
    Yes
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    Yes
    Sterilization Methods
    Moist Heat or Steam Sterilization

    Product Codes

    Code Name
    NDP Accessories, Implant, Dental, Endosseous

    GMDN Terms

    Code Name
    57949 Dental guided surgery reference plate

    Identifiers

    Type ID
    Primary 08800049416372