Abstract: A portable, heated scent, odor, and/or molecule dispense system is provided, as well as devices and methods for doing the same. The portable systems and methods to dispense molecules may contain a liquid, gel, solid, foam, or other material-based formulation so as to attract, repel, kill, mask, or otherwise use the molecules. The portable system and methods may include a housing; a molecule holding pad in the housing; a first chemical reaction heat source in the housing; and a second chemical reaction heat source in the housing, wherein the molecule holding pad is arranged between the first chemical reaction heat source and the second chemical reaction heat source, and wherein the first chemical reaction heat source and the second chemical reaction heat source are each reactive to oxygen.

Abstract: A method and apparatus for sterilizing is provided, wherein an item to be sterilized is loaded into a sterilizing cabinet integrated with a sterilizable wheeled case cart, the sterilizing cabinet comprising an interior, the interior being sterilizable; the sterilizable wheeled cart and the affixed sterilizing cabinet is rolled into the floor loading sterilizer; the sterilizable wheeled case cart and the integrated sterilizing cabinet in the floor loading sterilizer is exposed to a sterilizing cycle; and the integrated sterilizable wheeled case cart and sterilizing cabinet are rolled from the floor loading sterilizer, without requiring vertical translation of the sterilizing cabinet relative to the ground or the case cart.

Abstract: A diffuser includes an adjustable heater having a temperature control knob providing indicia coordinated with like indicia on packets of vaporizable materials of different tendencies to vaporize. By manipulating the temperature control knob to the indicia corresponding to the indicia on the packet, a suitable quantity of energy is delivered to the diffuser resulting in suitable vaporization. One indicia is color coded packets and similarly color coded markings adjacent the temperature control knob.

Abstract: A liquid atomization device includes: an inlet; an outlet; and a liquid atomization chamber. The liquid atomization chamber is provided in an air passage between the inlet and the outlet. The liquid atomization chamber includes a rotary shaft, a pumping pipe, a collision wall, a reservoir, and a drain port. The rotary shaft is rotated by a rotary motor and is disposed in the vertical direction. The pumping pipe includes a lower portion having a pumping port and an upper portion fixed to the rotary shaft, and is rotated in coordination with rotation of the rotary shaft to pump up water through the pumping port and centrifugally discharge the water. The pumping pipe generates, inside the pumping pipe, a whirlpool in the water in the reservoir by the rotation, and forms, at the center of the whirlpool, a void providing communication between the pumping port and the drain port.

Abstract: An aroma diffuser comprises a host and an aromatherapy nebulizer; the host has an air pump received therein; the air pump has an air inlet port and an air outlet port; the aromatherapy nebulizer comprises a nebulizer cap and an essential oil bottle with a dip tube extending from the nebulizer cap into the essential oil bottle for sucking liquid essential oil up. The host sets a mounting ring extending outwards from a sidewall thereof, the aromatherapy nebulizer is installed in the mounting ring in such way that the aromatherapy nebulizer is able to be plugged in or pulled out up and down through the mounting ring, thereby the aromatherapy nebulizer is installed externally to the host.

Abstract: 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.

Abstract: Systems and methods of disinfection of catheter connections are provided. A transfer catheter connector can include a UV-transparent window at its distal end and a seal proximal to the window. A solution set connector can be inserted inside a portion of the transfer catheter connector to connect a solution set and transfer catheter. The solution set connector comprises a lumen covered by a leading membrane surface; and a sealing surface configured to sealingly engage the window surface. The connectors can be connected in a disinfection position configuration in which flow is not permitted between the catheters and the connectors are irradiated with UV light. After disinfection, the connectors are advanced to a flow position in which the piercing member pierces the membrane surface, enabling flow between the catheters. The system comprises clips that prevent advancement to the flow position without interference by the disinfection unit or by a user.

Abstract: An anion essential-oil fragrance machine vibration-wave-conduction cup-bottom-element reinforcement and replaceable water-cup and nozzle structure; especially an anion essential-oil fragrance machine which can prevent the heat-ablation crack of the bottom of the vibration-wave-conduction cup, which is generated by the long-term action of the high-temperature and high-speed-vibration frequency of the oscillation unit. Therefore, it can improve the conduction efficiency, prevent leakage, prolong the life of the machine-body components, improve the stability of the machine-body quality, reduce the non-performing rate and the burden of after-sales maintenance man-hours, and save time and effort.

Abstract: Centrifuges are useful to, among other things, remove red blood cells from whole blood and retain platelets and other factors in a reduced volume of plasma. Platelet rich plasma (PRP) and or platelet poor plasma (PPP) can be obtained rapidly and is ready for immediate injection into the host. Embodiments may include valves, operated manually or automatically, to open ports that discharge the excess red blood cells and the excess plasma into separate receivers while retaining the platelets and other factors in the centrifuge chamber. High speeds used allow simple and small embodiments to be used at the patient's side during surgical procedures. The embodiments can also be used for the separation of liquids or slurries in other fields such as, for example, the separation of pigments or lubricants.

Abstract: Systems and methods disclosed herein provide an improved high voltage plasma-based product treatment by integrating the plasma reactor into the processing container. This unique device can deliver a high throughput rate of raw food, without adverse effects on quality. The system is operationally efficient, and is capable of being scaled up or down to provide lower or higher throughput rates, depending on the product manufacturer or processor's needs. In particular, the system obviates the need for further containerization or packaging of product during pasteurization processing.

Abstract: An autoclave comprises an elongate chamber enclosing an interior atmosphere, a floor configured to support one or more objects, and a plenum extending through a portion of the elongate chamber. The plenum includes an inlet as well as a plurality of outlets. The inlet is configured to receive a plenum flow of the interior atmosphere, while each of the plurality of outlets is configured to release a portion of the plenum flow to a different locus of the elongate chamber.

Abstract: An evaluation device includes: a processing container that has an intake port and an exhaust port; a microorganism supply device that floats microorganisms in the air inside the processing container; a light source that irradiates the microorganisms floating in the air inside the processing container with ultraviolet rays while the intake port and the exhaust port are in a state of being closed; and a microorganism recovery device that is connected to the exhaust port. The microorganism recovery device discharges air that has a volume larger than the capacity of the inside of the processing container through the exhaust port while introducing air that does not contain microorganisms to be evaluated into the inside of the processing container through the intake port after the irradiation with the ultraviolet rays and recovers the microorganisms contained in the air that is discharged.

Abstract: A controlled environment enclosure comprises a robotic arm manipulation system used to protect and unprotect a fluid path within the controlled environment enclosure. The apparatus allows the fluid path to be protected against dangerous decontamination vapors and chemicals before the controlled environment enclosure is decontaminated, the method not requiring the use of gloves or other means that degrade the integrity of the controlled environment enclosure. The apparatus similarly allows the fluid path to be unprotected for use without the use of gloves, the method not requiring the use of gloves or other means that degrade the integrity of the controlled environment enclosure when decontaminated is completed. The apparatus and method allow for the protecting, unprotecting and decontaminating sequences to be automated.

Abstract: An apparatus for decontaminating and storing lab instruments such as pipettes. A carousel feature of the apparatus provides convenient access and allows multiple items to be decontaminated at the same time. The ultraviolet lamp directs UV radiation to surface contaminations of the instruments and effectively eliminates various microorganisms.

Abstract: A handheld portable device for sanitizing a surface or air surrounding a surface. The handheld portable device includes a body that comprises a user input and a far-UVC illumination source disposed at the body. The handheld portable device also includes a power source for providing power to the far-UVC illumination source. Responsive to actuating the user input, such as by a user holding the handheld portable device, the far-UVC illumination source emits far-UVC illumination to sanitize the surface or the air surrounding the surface of pathogens.

Abstract: An air sanitation device is disclosed. The air sanitation device can include a base section, a body section, and an air movement device configured to move air through at least a portion of the air sanitation device. The air sanitation device can move air from an inlet of the air sanitation device, and past an ultraviolet (UV) light source, and out an outlet of the air sanitation device. The air sanitation device can be configured to draw in air from within or below a breathing zone. The air sanitation device can be configured to draw in air from below the breathing zone and output sanitized air. The sanitized air can be outputted at an angle such that the sanitized air flows in a generally downward direction.

Abstract: Disclosed are methods and apparatus that help reduce and prevent infection by controlling and/or reducing the level of contaminants, which include pathogens, allergens and/or odor-causing agents including VOCs. Photocatalytic oxidation is performed in a high humidity environment so that hydrogen peroxide molecules are readily produced.

Abstract: To simplify management of a sterilization process of a filling nozzle, a method for sterilizing a filling nozzle is provided, hot water or a liquid chemical agent is fed to drink supply piping that feeds a drink to a plurality of filling nozzles at the same time, the hot water or liquid chemical agent is discharged from all the filling nozzles, a flow rate of the hot water or liquid chemical agent is detected at all the filling nozzles, a representative temperature of the hot water or liquid chemical agent upstream or downstream of at least one filling nozzle is measured, and the sterilization process is ended when both the flow rate at each filling nozzle and the representative temperature reach respective target values.

Abstract: This disclosure relates to a device and method for disinfecting CPAP components using a chemically reactive substrate. Specifically, the device and method are used to disinfect CPAP components (or, CPAP equipment), including the various parts of a CPAP system, such as hoses, masks, pillows, couplings, humidifiers, etc., that require frequent cleaning and disinfecting. An exemplary device includes, among other things, a chamber, an ultraviolet (UV) light configured to emit UV light within the chamber, and a substrate chemically reactive to the UV light. Exposing the substrate to UV light releases free radicals which are configured to destroy bacteria, mold, and fungus, as well as eliminate odor. The free radicals may be circulated within the chamber and consequently within the CPAP components that are placed within the chamber to provide a thorough disinfection.

Abstract: The present invention involves a fill needle system for aseptically dispensing a pharmaceutical fluid in an aseptic chamber comprises a fill needle tubing in fluid communication with a pharmaceutical fluid source via flexible tubing and extending through a fill needle hub; a fill needle dispensing tip disposed at a dispensing end of the fill needle tubing; a fill needle sheath shaped and arranged to removably mate with and seal aseptically to the fill needle hub to form an aseptically sealed volume enclosing the dispensing tip; and a fluid pressure pulse induction system disposed and configured to compress the flexible tubing in order to dislodge droplets of pharmaceutical fluid retained on the dispensing tip after halting dispensing of the pharmaceutical fluid. An associated method of dispensing pharmaceutical fluid comprises operating the fluid pressure pulse induction system to dislodge the droplets. The system may comprise a controller for automatically controlling the dispensing and droplet dislodging.