A cleaning management apparatus manages bedside cleaning for an endoscope connected to an examination apparatus. After an examination is completed, a measurement unit measures the operation time of a predetermined operation button of the endoscope. A recording control unit records that a preliminary cleaning has already been performed when the operation time that has been measured satisfies a completion condition. A notification unit gives notice of a message indicating that the preliminary cleaning is completed when the measured operation time satisfies the completion condition.

An endoscope reprocessor includes a bottle connecting instrument and a nozzle. The bottle connecting instrument includes a first advancing and retracting member which shuts off a first flow path at a first position and opens the first flow path at a second position; a first fitting member; and a first retaining member which retains the first advancing and retracting member. The nozzle includes a second advancing and retracting member which shuts off the nozzle at a third position and opens the nozzle at a forth position, a second fitting member to be fitted with the first fitting member, and a second retaining member which retains the second advancing and retracting member.

An endoscope reprocessor includes: a housing unit that houses a medicinal solution bottle such that a sealing portion is located on a top surface; a first guide that guides the housing unit such that the housing unit is capable of advancing and retreating between a first point and a second point; a movable unit that moves in cooperation with advancing of the housing unit; an unsealing member provided in the movable unit and arranged at a position higher than the sealing portion of the medicinal solution bottle housed in the housing unit at the first point, the unsealing member having a shape protruding toward the top surface at a predetermined length to pierce the sealing portion when the medicinal solution bottle reaches the second point by descending as the movable unit advances; and a second guide that guides an advancing direction of the movable unit.

A sterilization system includes a communication hub that is configured to transfer information between devices of the system such as a sterilizing cabinet, biological indicator analyzer, and a server in order to allow a user to track a medical device throughout a sterilization process. The server may provide data to the sterilizing cabinet during a sterilization process that may be used to verify that the medical device is compatible with the sterilizing cabinet, and to automatically select a compatible sterilization cycle to perform on the medical device. Automatic selection of sterilization cycles and confirmation of compatibility reduces the possibility for user error, which could result in contaminated medical devices being placed back into service. Automatic selection of sterilization cycles also allows users to more efficiently configure and perform sterilization cycles while being confident that the medical device will be sterile upon completion.

An apparatus that assists in sterilizing an endoscope inside a sterilizer employing a gaseous sterilant, e.g., hydrogen peroxide, is disclosed. The apparatus may include a dry booster and a flow restrictor that includes two tubes, which may be connected to channels of an endoscope and the dry booster. The flow restrictor may be used to change the flow rates through the channels to assist in delivering sterilant throughout the channels.

A cleaning device for a surgical tool includes a housing having at least one opening for accessing an interior of the housing; a sponge and a heater assembly positioned in the interior of the housing; and a connector. The connector includes a first arm and a second arm extending from an outer surface of the housing. An inner surface of the first arm and an inner surface of the second arm define at least a first recess sized to receive a sidewall of a first tubular body having a first diameter, and a second recess sized to receive a sidewall of a second tubular body having a second diameter, different than the first diameter. The connector is configured to removably attach the housing to the sidewall of the first tubular body or to the sidewall of the second tubular body to supporting the housing relative to the tubular body.

A monitoring system for reprocessing a surgical instrument, where the monitoring system includes: a fluid line provided for supplying a fluid to the surgical instrument, the fluid line being configured to be connected to the surgical instrument; and a fluid line connection for connecting the fluid line to the surgical instrument; wherein the fluid line connection is configured to close an electrical contact in the case of a functional connection of the fluid line to the surgical instrument.

A cleaning device system to clean a surgical scope, which cleaning device system includes an attachment element to attach the cleaning device, being positioned outside the body of a patient, to a trocar. 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.

A method of cleaning a contaminated surface, such as cleaning the elongate interior lumen of an endoscope contaminated with flesh, bone, blood, mucous, faeces or biofilm, said method comprising the steps of: providing a suspension of solid particles in a liquid to said contaminated surface, and flowing said suspension along said surface thereby to remove contaminant from the surface. The suspension is preferably an ice slurry, where the solid material is ice crystals. The slurry preferably has a solid fraction between 50-85% by volume. A freezing point depressant may be present.

A test instrument and a method for producing a test instrument used to evaluate a cleaning, disinfection and/or drying processes of internal flexible channels includes obtaining a medical instrument having a flexible probe section configured for insertion into a body, the flexible probe section including at least one internal flexible channel and at least one external device port, and attaching an access device between the at least one external device port and the at least one internal flexible channel to enable selective access into the internal flexible channel.