A method and apparatus for decontaminating substantially enclosed environments by using ultrasonic cavitation of a cleaning fluid to produce a low pressure, low air flow mist that can be activated by a nonthermal plasma actuator to create a cloud of activated hydroxyl species with the capacity to decontaminate articles, open surfaces or substantially enclosed spaces of pathogens, including bacteria, and other pathogenic microorganisms. An automated system and related non-transitory computer medium are also disclosed.

A method and apparatus for decontaminating substantially enclosed environments by using ultrasonic cavitation of a cleaning fluid to produce a low pressure, low air flow mist that can be activated by a nonthermal plasma actuator to create a cloud of activated hydroxyl species with the capacity to decontaminate articles, open surfaces or substantially enclosed spaces of pathogens, including bacteria, and other pathogenic microorganisms. An automated system and related non-transitory computer medium are also disclosed.

A method and apparatus for decontaminating substantially enclosed environments by using ultrasonic cavitation of a cleaning fluid to produce a low pressure, low air flow mist that can be activated by a nonthermal plasma actuator to create a cloud of activated hydroxyl species with the capacity to decontaminate articles, open surfaces or substantially enclosed spaces of pathogens, including bacteria, and other pathogenic microorganisms. An automated system and related non-transitory computer medium are also disclosed.

A method and apparatus for decontaminating substantially enclosed environments by using ultrasonic cavitation of a cleaning fluid to produce a low pressure, low air flow mist that can be activated by a nonthermal plasma actuator to create a cloud of activated hydroxyl species with the capacity to decontaminate articles, open surfaces or substantially enclosed spaces of pathogens, including bacteria, and other pathogenic microorganisms. An automated system and related non-transitory computer medium are also disclosed.

A system and method for neutralizing a biological organism is provided. The system includes a first element is made from paraformaldehyde. A second element is configured to generate heat and decompose the paraformaldehyde into formaldehyde gas. In one embodiment, the second element is configured to have an exothermic and self-sustaining alloying reaction in response to being thermally energized by an initiator.

A decontamination system, method, and sterilant kit for a device, such as a lumen device, is depicted. The decontamination system, in some embodiments, includes a device container, a wicking pad, and a sterilant fluid delivery device. The device container, such as a terminal package or a decontamination chamber, defines a device receiving area. The wicking pad is in fluid communication with the device receiving area. The sterilant fluid delivery device is in fluid communication with the wicking pad. The sterilant fluid delivery device is configured to wet the wicking pad with sterilant fluid. The wicking pad is configured to evaporate sterilant fluid into the device receiving area.

The present invention is an improved method for decontamination of a space and an integrated device that completes the decontamination cycle extremely fast while still being compact, lightweight, simple to operate and easy to move as a single unit. The method of the present invention delivers less biocide than is used in prior art methods at a very high rate of flux, allows the biocide to reside in the space being decontaminated to achieve a predetermined kill level, and then aerates the space. Because a nominal amount of biocide is used, there is less biocide to remove from the space than in prior art methods thereby reducing the time required for aeration and shortening the downtime for safe entry of the facility.

A cleansing and packaging system for pipeline preparation of specialty medical instruments and method for cleansing and packaging instruments are provided herein. The cleansing and packaging system includes a first sealable cleansing compartment and a second sealable packaging compartment. A conveyor device transports medical instruments to be cleansed through a sealing entry door to the cleansing compartment, then to the packaging compartment through a sealing joining door, and then out of the packaging compartment through a sealing exit door. The cleansing compartment includes a sanitation system and a sterilization system, each which includes its own inspection devices that operate continuously to confirm the success of sanitation and sterilization operations. The packaging compartment includes a packaging system, which may include its own inspection devices that operate continuously to confirm the quality of the packaging of medical instruments. The pipeline approach provides greater availability of limited specialty medical instruments to hospital physicians.

The present invention relates to a method for sterilizing an article inside a sealed container by placing a polyoxymethylene melt formable co-polymer fiber that has been irradiated between about 1 and 200 kGy and then heated at from about 20 C. to about 90 C. for a selected period of time.

The present invention relates to a dry composition, which upon addition of an aqueous medium forms a substantially homogenous paste suitable for use in haemostasis procedures. The paste forms spontaneously upon addition of the liquid, hence no mechanical mixing is required for said paste to form. The invention further relates to methods of preparing said dry composition, a paste made from said dry composition and use of said paste for medical and surgical purposes.