Disc filter holder
    2.
    外观设计

    公开(公告)号:USD1018895S1

    公开(公告)日:2024-03-19

    申请号:US29792704

    申请日:2022-04-19

    Abstract: FIG. 1 is a first perspective view of a disc filter holder of the present invention.
    FIG. 2 is a second perspective view of the disc filter holder of the present invention.
    FIG. 3 is a third perspective view of the disc filter holder of the present invention.
    FIG. 4 is a front view of the disc filter holder of the present invention.
    FIG. 5 is a rear view of the disc filter holder of the present invention.
    FIG. 6 is a left-side view of the disc filter holder of the present invention.
    FIG. 7 is a right-side view of the disc filter holder of the present invention.
    FIG. 8 is a top view of the disc filter holder of the present invention.
    FIG. 9 is a bottom view of the disc filter holder of the present invention.
    FIG. 10 is a first view of the disc filter holder of the present invention in an environmental context holding a disc filter; and,
    FIG. 11 is a second view of the disc filter holder of the present invention illustrating an environmental context holding a disc filter in alignment with two other disc filter holders.
    The broken lines in FIGS. 1-9 depict portions of the disc filter holder that form no part of the claimed design. The remaining broken lines shown in FIGS. 10-11 depict environmental subject matter and form no part of the claimed design.

    FILTRATION DEVICE AND PACKAGING CONFIGURED FOR STERILIZATION

    公开(公告)号:US20240269455A1

    公开(公告)日:2024-08-15

    申请号:US18411879

    申请日:2024-01-12

    CPC classification number: A61M39/18 A61M39/14 A61M2205/75

    Abstract: A system for sterilizing or bioburden-reducing a filter device includes a breathable microbial barrier, a filter device, and a tubing arrangement. The tubing arrangement may be coupled to at least one opening of the filter device. The tubing arrangement may include an aseptic connector, a sealable component, and a port, all of which are in fluid communication with one another. The sealable component may be disposed in the tubing arrangement between the at least one opening of the filter device and the aseptic connector. The sealable component may be reconfigurable between an open configuration, which facilitates the entry of a sterilization vapor into the tubing arrangement and the filter device when subjected to a sterilization or bioburden reduction process, and a closed configuration, where the tubing arrangement is sealed from a surrounding environment. The breathable microbial barrier may at least partially enclose the port of the tubing arrangement.

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