A multistage connector assembly for a lumen decontamination system is provided. The assembly includes a main body, a multistage body, a multistage barrier, a connector, and one or more biasing members. The assembly includes a multistage barrier movable in the fluid passageway between a fully closed position in which each stage of the multistage barrier is in a closed position to each independently block flow in the fluid passageway and a fully open position in which each stage is in an open position to allow flow within the fluid passageway. The connector is configured to engage the multistage barrier when coupled to the main body to sequentially open each stage of the multistage barrier to enable flow through the fluid passageway. The biasing member(s) are configured to urge each stage of the multistage barrier towards a closed position that blocks flow in the fluid passageway.

The present application provides a unique way for storing biomaterials, blood, blood products, vaccines, organs in an organ and fluid preservation and transportation system. The organ and fluid preservation and transportation system can comprise a docking system, a container system comprising an upper container, an inner container, an outer container, electronics, and a heating/cooling module. The upper container can attach to the outer container, and/or inner container and create an airtight seal with the environmental conditions staying consistent when sealed wherein the container system can be docked to the docking system wherein the docking system heats or cools down the container system.

An intelligent sterilization method and a sterilization container are disclosed, the intelligent sterilization method comprising: after an intelligent sterilization instruction is issued, the sterilization container sequentially performs the following steps: a sterilizing and drying step, releasing sterilization medium and hot air to an article storage cavity containing a sterilized article, and sterilizing and drying the sterilized article; and a constant temperature aseptic storing step, continuously releasing a small amount of hot air and a small amount of sterilization medium to the article storage cavity to maintain the sterilized article in the article storage cavity at a preset constant temperature and an aseptic condition; wherein the constant temperature is defined as when the sterilized article is in contact with the human body, the human body feels warm and not uncomfortable. The sterilization container includes an article storage cavity, an illumination device, a heating air duct, a microprocessor, and a memory.

A management system that manages a workflow relating to sterilization of a sterilization target is provided. The workflow includes a plurality of stages including a packaging stage in which a set is formed by packaging one or more of the sterilization targets and a first indicator, and the first indicator includes a discoloration area whose color changes according to an achievement degree of a sterilization process. The management system includes: management means for managing management information of the workflow including sterilization related information of the set, wherein the sterilization related information of the set includes a determination result of the achievement degree, and notification means for performing a notification that work related to the workflow is not in a predetermined state, or a notification for preventing work related to the workflow from entering a predetermined state.

A system includes a sensor applicator, a sensor control device arranged within the sensor applicator and including an electronics housing and a sensor extending from a bottom of the electronics housing, and a cap coupled to one of the sensor applicator and the sensor control device, wherein the cap is removable prior to deploying the sensor control device from the sensor applicator.

A safety cabinet can include an enclosure defining an interior compartment accessible through an opening. The safety cabinet includes an interior lighting system. The interior lighting system can include at least one of an illuminating light to enable viewing to cabinet contents and an ultraviolet light configured to disinfect the interior compartment of the safety cabinet. To provide electrical power to the interior lighting system, the safety cabinet includes an electrical connection disposed through the enclosure. The electrical connection can include at least one of a bulkhead connector and an intumescent socket.

A chair sanitizing assembly for disinfecting a chair includes a cylinder that can be attached to a chair and a bottle containing a disinfectant solution that is insertable into the cylinder. A first hose is fluidly coupled to the bottle to receive the disinfectant solution. The first hose extends into a puck and a pump is positioned within the puck to pump the disinfectant solution. A second hose is fluidly coupled to the pump to receive the disinfectant solution when the pump is turned on. A spray nozzle is coupled to the second hose to spray the disinfectant solution onto the chair portion of the chair thereby disinfecting the chair portion prior the user sitting on the chair portion.

The invention relates to a system for testing the sterility of radioactive substances, to the use of the system for testing the sterility of radioactive substances, preferably radioactive pharmaceuticals and/or diagnostic agents, and to a method for testing the sterility of radioactive substances, wherein the system comprises an isolator (8) having a device for membrane filtration (9) and a filter bottle (1) surrounding the shield (5) against ionising radiation.

A hand sanitizing station includes a conduit in fluid communication with a source of sanitizer, the conduit having a fluid outlet. In addition, the hand sanitizing station includes a valve coupled to the conduit and configured to control the volume of sanitizer that exits the fluid outlet, the valve having a control arm. Further, the hand sanitizing station includes a pedal, and a cable connected between the pedal and the control arm of the valve and configured to move the control arm when the pedal is depressed and open the valve a predetermined amount. Movement of the pedal from a first position to a second position causes sanitizer to flow by gravity from the conduit and out of the fluid outlet, and movement of the pedal from the second position back to the first position closes the valve.

A method or system for using an augmented reality device may include displaying information in a surgical field. A method may include receiving an indication of a location of a landmark on a bone of a patient, retrieving a planned location of the landmark on the bone of the patient and receiving information corresponding to the location or the planned location. The location or the planned location may be displayed as a virtual indication using an augmented reality display of the augmented reality device, for example while permitting the surgical field to be viewed through the augmented reality display.