Embodiments relate to systems, devices, and methods for sanitizing stored contents. System includes main and secondary assemblies. Main assembly includes main opening and main storage section. Secondary assembly includes securing portion, radiation assembly, and control assembly. Securing portion transitions between secured and unsecured states. Secured state is when main and secondary assemblies are secured together. Radiation assembly is configured to emit radiation, and is formed symmetrically relative to a central axis. Control assembly includes first and second safety assemblies and control processor. First safety assembly is configured to determine whether the storage system is in the secured or unsecured state. Second safety assembly is configured to determine whether the secondary assembly is in a safe or unsafe orientation state. Control processor is configured to control the radiation assembly to emit radiation when the storage system is in the secured state and the secondary assembly is in the safe orientation state.

A temperature controlled delivery appliance and a method of operating the same are provided. The temperature-controlled delivery appliance includes a storage container, a climate control system, a sanitization assembly, and a locking mechanism. The sanitization assembly may include an ultraviolet light assembly or an ozone generator that may be selectively activated after a delivery to sanitize the delivered items. The locking mechanism locks the door of the temperature-controlled delivery appliance to prevent user access during a sanitization cycle, as well as to prevent other unauthorized access.

The present disclosure in one aspect provides a sterile packaging container comprising a container body with a cross-sectional shape that is constant along the majority of the longitudinal axis, a cover and a closure assembly that inhibits the passage of microbial contaminants. The container is configured such that the interior of the container can be sterilized. The sterile packaging container described herein allows one to manufacture a sterile packaging tube exercising the smallest possible volume.

A packaging comprising a tray having an opening, a cavity including at least three cavity portions, a plurality of sidewalls, and a base; and a sterile syringe contained within the cavity, wherein the sterile syringe is pre-filled with a medicament or other fluid; wherein a first cavity portion comprises a plunger rod of the sterile syringe, a second cavity portion comprises a barrel of the sterile syringe, and a third cavity portion comprises a needle attachment portion of the sterile syringe, wherein the at least three cavity portions are connected to one another by intermediate narrowed portions, and wherein each of the narrowed portions includes a first sidewall, a second sidewall, a base, and a plurality of geometric features projecting into the narrowed portions to position the sterile syringe away from the plurality of sidewalls.

A surgical instrument system includes a commonly-sized orthopaedic surgical instrument assembly for use in implanting a femoral component, along with a number of orthopaedic surgical instrument assemblies having varying sizes of instruments of use in implanting a tibial tray component and a patella component.

The present disclosure provides a coating apparatus and method for applying a coating of a therapeutic agent, comprising an openable and sealable device compartment, a therapeutic agent positioned in communication with the device compartment, a thermal source for vaporizing the therapeutic agent, and a vacuum source in fluid communication with the device compartment.

The present invention comprises a sterilizing wrap system comprising a base having a support surface and a first sealing surface spaced from the support surface, the support surface supports at least one object requiring sterilization. A wrap is sized to engage the first sealing surface of the base to define a volume encompassing the support surface and the spaced first sealing surface of the base. A first seal maintains a sealed interface between the wrap and the first sealing surface.

A sterilization packaging includes an interior space for receiving medical packaged goods and a sensor unit adapted to measure a first parameter in the interior space. The packaging has a data transmission unit for receiving and transmitting parameter values measured by the sensor unit. The packaging and data transmission unit are matched to one another to allow transmission of parameter values received by the data transmission unit into an outer space around the packaging. A sterilization method includes: introducing packaged goods into packaging and closing the packaging; introducing the closed packaging into a receiving chamber of a sterilizer; starting a sterilization process flow in the sterilizer; detecting parameter values in the packaging and transmitting the parameter values to a control unit of the sterilizer; and controlling the sterilization process flow as a function of the parameter values.

A tray (100) for accommodating a coiled medical device, such as a catheter assembly (700), includes a first compartment (101), a second compartment (102), and a third compartment (103). The catheter assembly (700) and devices associated with a catheterization procedure, such as syringes (701,702) containing sterile water and lubricating jelly and a specimen container (703) can be disposed within the tray. Printed instructions (1001) can be included with the tray (100). One or more layers of wrap material (2200) can be folded about the tray (100) to enclose the tray (100) and other items, such as an additional layer of wrap material (2701), packaged liquid hand sanitizer (2401), and packaged gloves (2402). When a health care services provider (3101) unfolds the wrap material, the same can be used to create a sterile field beneath a patient (3201).

A medical device holder includes a one-piece holder body having end walls, and side walls, extending vertically upward from a base. The end walls are oriented parallel to one another, and the first and the second side walls are oriented so as to converge toward one another in a direction of an opening. A plurality of medical device storage slots are formed by a plurality of internal vertical walls, and a plurality of elongate medical devices wound in opposition to an internal unwinding bias are trapped within the plurality of medical device storage slots.