BEUDAMED
    FDA UDI Not in Commercial Distribution 🇺🇸 United States

    Righton

    DI: 04580606430327 · Model: Retinomax 5 · RIGHT MFG. CO., LTD.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Righton
    Primary DI
    04580606430327
    Version / Model
    Retinomax 5
    Catalog Number
    RDA2112BA
    Company Name
    RIGHT MFG. CO., LTD.
    Labeler DUNS
    713383495
    Distribution Status
    Not in Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2022-12-09
    Public Version
    2
    Public Version Date
    2023-06-14
    Public Version Status
    Update
    Public Device Record Key
    3d0ad567-d5c9-4508-956f-7a78aa6fd117
    Distribution End Date
    2022-12-31

    Device Description

    Tulip Chart SET with Carrying case

    Device Characteristics

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

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    HKO Refractometer, Ophthalmic

    GMDN Terms

    Code Name
    36386 Automated ophthalmic refractometer

    Identifiers

    Type ID
    Primary 04580606430327