BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    REMEL

    DI: 00848838065835 · Model: R40132 · REMEL, INC.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

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    Basic Information

    Brand Name
    REMEL
    Primary DI
    00848838065835
    Version / Model
    R40132
    Catalog Number
    R40132
    Company Name
    REMEL, INC.
    Labeler DUNS
    065769564
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2023-01-04
    Public Version
    1
    Public Version Date
    2023-01-12
    Public Version Status
    New
    Public Device Record Key
    73ab1b65-3d38-448d-adc7-13f2bfe4e7fb

    Device Description

    Ethanol (90%) MeOH (4.5%) IPA (5.5%) BTL/250ml

    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
    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
    PPM General Purpose Reagent

    GMDN Terms

    Code Name
    43584 Acid-alcohol solution IVD

    Identifiers

    Type ID
    Primary 00848838065835