BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    AeroDR T50

    DI: 04560141935372 · Model: A4UW · KONICA MINOLTA, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    AeroDR T50
    Primary DI
    04560141935372
    Version / Model
    A4UW
    Company Name
    KONICA MINOLTA, INC.
    Labeler DUNS
    692076161
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2016-12-15
    Public Version
    4
    Public Version Date
    2023-02-03
    Public Version Status
    Update
    Public Device Record Key
    fa3ae596-9074-47d4-9667-90a4ed669982

    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
    MR Unsafe
    Direct Marking Exempt
    No
    PM Exempt
    No
    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
    KPR System, X-Ray, Stationary

    GMDN Terms

    Code Name
    40655 Basic diagnostic x-ray system table, powered

    Identifiers

    Type ID
    Primary 04560141935372

    Premarket Submissions

    Submission Number Supplement Number
    K121109 000