A medical instrument processor includes an enclosure, a liquid distribution system, and a disinfectant concentration measuring subsystem. The enclosure is configured to hold a medical instrument. The liquid distribution system is configured to deliver a disinfection solution to a medical instrument within the enclosure. The liquid distribution system has a liquid outlet. The disinfectant concentration measuring subsystem includes a first mixing chamber in fluid communication with the liquid outlet, a pump that is configured to simultaneously pump the disinfection solution and the reagent solution into the first mixing chamber, and a concentration analysis assembly that is operable to determine a concentration of disinfectant in a sample solution that is output from the first mixing chamber. The reservoir is in fluid communication with the first mixing chamber.

A bottle closing device for placing press-fit closures, such as crown corks, crown caps, and similar closures, on bottles or similar containers. The abstract of the disclosure is submitted herewith as required by 37 C.F.R. §1.72(b). As stated in 37 C.F.R. §1.72(b): A brief abstract of the technical disclosure in the specification must commence on a separate sheet, preferably following the claims, under the heading “Abstract of the Disclosure.” The purpose of the abstract is to enable the Patent and Trademark Office and the public generally to determine quickly from a cursory inspection the nature and gist of the technical disclosure. The abstract shall not be used for interpreting the scope of the claims. Therefore, any statements made relating to the abstract are not intended to limit the claims in any manner and should not be interpreted as limiting the claims in any manner.

An electrolyzed water generating device of the present invention includes an electrolytic solution supplying unit and an electrolysis unit including an electrolysis electrode pair. The electrolytic solution supplying unit is provided so as to supply an aqueous solution of an electrolyte for generating electrolyzed water to the electrolysis unit. The electrolysis unit is provided so that the aqueous solution of the electrolyte for generating electrolyzed water is electrolyzed using the electrolysis electrode pair to generate an electrolyzed water. The electrolyte for generating electrolyzed water contains an alkali metal chloride and a substance that makes an aqueous solution acidic. The electrolyzed water generating device generates an electrolyzed water having a pH of more than 6.5 and less than 8.0.

Techniques for automatically eradicating microorganisms (e.g., germs, bacteria, and/or viruses) from appliance handles using ultraviolet (UV) light are provided. In one aspect, a system for eradicating biological contaminants from a handle on an appliance door is provided. The system includes a UV light emitter for producing UV disinfecting light during a cleaning cycle; and a waveguide coating on the handle, coupled to the UV light emitter, for propagating the UV disinfecting light over a surface of the handle. The system can also include a control module for controlling the UV light emitter; and at least one sensor for providing data to the control module as to when to initiate or halt a cleaning cycle. A method for eradicating biological contaminants from a handle on an appliance door using the present system is also provided.

A cleaning apparatus is actuated to move At least one object from a vehicle floor to a container. A vehicle seat is sprayed with a cleaning fluid from a nozzle.

Peroxyformic acid compositions for removal of biofilm growth and other contaminants and impurities from industrial processing hard surfaces are disclosed. In particular, peroxyformic acid compositions may be dosed on site and/or generated in situ for the reduction and prevention of biofilms on the hard surfaces. Methods of employing the peroxyformic acid compositions for removal of biofilm growth and other impurities such as aldehydes and alcohols from industrial CO.sub.2 effluent are also disclosed which beneficially provide ambient biofilm control and break down more rapidly than other peracids, allowing for extended runs between CIP cleaning, including a reduction and/or elimination of cleaning of the scrubbers and other industrial surfaces.

An aseptic filling machine capable of performing molding and filling at the same time that has a compact facility size, requires a reduced initial investment, requires a reduced running cost because of its simplified process, and ensures an aseptic condition with reliability, and an aseptic filling method therefor. An aseptic filling machine includes a pre-heating sterilizing portion that sterilizes a preform, a heating portion that heats the sterilized preform, a molding and filling portion that fills the heated preform with a sterilized content under high pressure, thereby molding the preform into a bottle and at the same time filling the preform with the content, and a sealing portion that seals the bottle filled with the content. Before the aseptic filling machine starts operating, each portion is sterilized. During operation of the aseptic filling machine, aseptic air is supplied to each portion to maintain the aseptic condition.

An endoscope reprocessor includes: an endoscope housing portion; a medicinal solution tank in which a medicinal solution is stored; a medicinal solution transfer portion that transfers the medicinal solution from the medicinal solution tank to the endoscope housing portion; a comparison portion that compares the concentration of the medicinal solution and a first reference concentration; a first adjustment portion that increases a reaction rate of the medicinal solution in a state in which the concentration of the medicinal solution is lower than the first reference concentration; and a control portion to which the comparison portion and the first adjustment portion are connected, and which drives the first adjustment portion in a case where the comparison portion determines that the concentration of the medicinal solution is lower than the first reference concentration.

To simplify management of a process of sterilization of a filling nozzle.

In a method for sterilizing a filling nozzle, hot water or a liquid chemical agent is fed to drink supply piping (7) that feeds a drink to a plurality of filling nozzles (2a) at the same time, the hot water or liquid chemical agent is discharged from all the filling nozzles (2a), a flow rate of the hot water or liquid chemical agent is detected at all the filling nozzles (2a), a representative temperature of the hot water or liquid chemical agent upstream or downstream of at least one filling nozzle is measured, and a sterilization process is ended when both the flow rate at each filling nozzle and the representative temperature reach respective target values.

A hazardous drug deactivation wipe kit includes a first pouch having a one-way valve coupled to an end thereof, a second pouch, and a third pouch. The first pouch contains a wipe saturated in a hypochlorite solution, the second pouch contains a wipe saturated in thiosulfate solution, and the third pouch contains a wipe saturated in isopropyl alcohol solution. The deactivation wipe kit may be used in a clean room to deactivate most hazardous drugs on a work surface.