BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    PureLife X-Ray Film

    DI: 00812045030740 · Model: 1200502 · Flow X Ray Corporation
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    2
    Pkg Device Count
    130

    Basic Information

    Brand Name
    PureLife X-Ray Film
    Primary DI
    00812045030740
    Version / Model
    1200502
    Company Name
    Flow X Ray Corporation
    Labeler DUNS
    010016319
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    130
    Record Status
    Published
    Publish Date
    2020-07-01
    Public Version
    2
    Public Version Date
    2023-06-28
    Public Version Status
    Update
    Public Device Record Key
    bb983dad-48e6-4a7b-8b14-699d197f7698

    Device Description

    PLD-57 Size 2 Double

    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
    No
    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
    IWZ Film, Radiographic

    GMDN Terms

    Code Name
    40978 Dental x-ray film, non-screen

    Identifiers

    Type ID
    Unit of Use 00312045030745
    Primary 00812045030740