The present invention is generally related to an apparatus and method for sanitizing a continuous positive airway pressure (CPAP) device, in particular the invention relates to a system, method and device that attach to a CPAP device and sanitizes all of the parts of the CPAP device, including the inner areas of the hose, reservoir and face mask most prone for bacteria buildup. The device has an ozone operating system and one or more ozone distribution lines that distributes ozone to a CPAP device and a non-permeable bag for sanitizing a CPAP mask.

A sterilization system with automated sterilization data processing and related methods. In one aspect, the sterilization system receives mechanical indicator values and chemical indicator values for the sterilization cycle. The system determines whether the mechanical indicator values and chemical indicator values for the sterilization cycle match predetermined criteria. In response to the mechanical indicator and chemical indicator values for the sterilization cycle matching predetermined criteria, the system automatically generates a sterilization record in accordance with the first sterilization cycle data and second sterilization cycle data, stores the sterilization record in a sterilization database, and prints a sterilization label for each sterilized item in the sterilization cycle. Each sterilization label includes a Quick Response (QR) code encoding information for sterilization cycle.

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.

A decontamination system includes a housing having at least one inner surface defining a chamber. An irradiation system supplies ultraviolet germicidal irradiation (UVGI) to the chamber at a level effective to at least one of inactivate SARS-CoV-2 or inactivate at least 90% single-stranded RNA viruses present on an object positioned in the chamber in less than about 2 minutes.

Indicators for indicating the integrity of a seal of a sterilization container are provided. For example, a seal indicator may indicate whether the container is sufficiently sealed to prevent an ingress of contaminants into the container. If the container is sufficiently sealed, the seal indicator is in one state and displays a first indicium, and if the sterilization container is not sufficiently sealed, the seal indicator is in another state and displays a second indicium. Thus, the seal indicator undergoes a visible change in state when the sterilization container transitions from unsealed to sealed, such that the user may be assured that the container is properly sealed to maintain sterility of the articles post-sterilization. Further, the seal indicator undergoes a visible change in state if the seal is subsequently broken, to signal to the user that the seal and the sterility of the container interior has been compromised.

Systems and methods for using solid high-level disinfection chemistries to producing disinfectant solutions. In an embodiment, an apparatus comprises: a first container and a second container. The first container is configured to receive water, sodium percarbonate and tetraacetylethylenediamine. The water, the sodium percarbonate, the tetraacetylethylenediamine react within the first container to produce a mixture comprising peroxyacetic acid. The second container is in fluid communication with the first container, wherein the second container is configured to receive an acid and the mixture. The mixture and the acid mix in the second container to produce a disinfectant solution having a pH between 5.0 and 7.0.

Proposed is a non-contact safety relaying apparatus for transferring an object, the apparatus including: an apparatus body including, a main body formed to have an internal space through which first and second independent spaces communicate, a horizontal partition extending horizontally at a height of a center of the main body, with at least one relaying hole being pierced therethrough, an upper partition extending upward from a first side of the horizontal partition and forming a first relaying space, a lower partition extending downward from a second side thereof and forming a second relaying space, a first door mounted on the main body in such a manner as to open and close the first relaying space, and a second door mounted on the main body in such a manner as to open and close the second relaying space; and an opening and closing unit opening and closing the relaying hole.

There is disclosed a method of monitoring the functionality of individual irradiation emitters within a UVC irradiation disinfecting device comprising: supplying a constant current supply to at least one irradiation emitter; sensing the voltage across the at least one irradiation emitter; sensing the current drawn by the at least one irradiation emitter; analysing the sensed voltage and the sensed current against predetermined values; and determining a failure state of the at least one irradiation emitter based on said analysis.

A method and apparatus for sterilizing medical instruments, including a device for controlling specific humidity, SH, of flow of a gas or gas mixture. The device includes a tank for storing a volume of water. The tank has an inflow port for receiving the gas or gas mixture, and an outflow port for allowing humidified gas or gas mixture at the required SH to exit the tank. The temperature of the water and/or the pressure of the supplied gas or gas mixture are controlled for the required SH.

A reusable apparatus, such as a medical instrument or tool, is decontaminated by applying pressure waves with direct contact of the pressure wave applicator to the reusable apparatus in an open bath in a sufficient dosage to remove contamination but without adversely affecting the ability to reuse the apparatus.