The disclosure is directed to methods and systems for cleaning scopes using a camera port (e.g. trocar) which has been modified to include a cleaning system. A trocar is a device designed to allow surgical instruments and tools to be quickly and easily inserted into a body cavity without contacting the surrounding tissue.

A soil-based coupon having an electronically readable verification code printed thereon is used for verification of soil removal by a cleaning process. The coupon includes a soil overlay covering the verification code. The verification code is at least partially revealed by removal of all or part of the soil overlay during the cleaning process. If the data encoded in the verification code can be correctly decoded after completion of the cleaning process, the cleaning process can be verified. The soil overlay can be designed to match the application. The coupons may be used in a cleaning process verification procedure in which one or more computing devices analyze images of the verification codes to determine whether or not cleaning processes can be verified.

A method for controlling an environment within a sterilizer device is disclosed. The method includes equipping an interior space of the sterilizer device with an auxiliary device having a temperature sensor, a humidity sensor, a heating element, monitoring temperature within the sterilizer device, receiving, by the sterilization device, information associated with an initiation of a sterilization cycle of the sterilizer device; monitor duration of the sterilization cycle, receiving, by the sterilization device, information associated with an end of a sterilization cycle of the sterilizer device, determining whether a current humidity measurement is above a predefined threshold, and controlling the heating element to an ON operating state when the current humidity measurement is above the predefined threshold.

Embodiments of a system and method for endoscope cleaning and inspection are disclosed. In an example, an endoscope cleaning and inspection unit includes cleaning and testing capabilities operated via control equipment and a display screen, to operate leak testing equipment, flush control equipment, and optical inspection equipment for leak testing, flushing, rinsing, and inspection of an endoscope interior chamber (lumen) and exterior surfaces. In a further example, the endoscope cleaning and inspection unit may further operate and receive information from a borescope imaging device or a magnification imaging device, using an imaging sensor to capture images of an endoscope lumen or surface respectively, as captured or output on the display screen. Further embodiments provide for control, monitoring, data collection, data input, and data output with such imaging devices via the endoscope cleaning and inspection unit.

A cleaning wizard monitors and provides feedback for cleaning of medical equipment to ensure that cleaning is performed based on best practices. The cleaning wizard receives a video stream comprising an item of medical equipment and inputs a first set of video frames from the video stream into a first machine learning model. The first machine learning model is trained to output whether the first set of video frames corresponds to activity that initiates a cleaning protocol for the item of medical equipment. Responsive to the cleaning protocol being initiated, the cleaning wizard inputs a second set of video frames into a second machine learning model trained to output whether the second set of frames meets criteria of the cleaning protocol. Responsive to all criteria of the cleaning protocol being met, the cleaning wizard transmits a notification to an operator that the cleaning protocol is complete.

A sterile container for sterilizable medical goods includes a receiving space for the medical goods and a data acquisition unit for acquiring parameter data of influencing variables that act on the sterile container. The sterile container includes an NFC module with at least one sensor for acquiring sterility-relevant and/or sterilization-relevant data and a data logger for recording and storing data from the sensor at a recording interval. The sterile container can be monitored by a method that is automatic and sterile-container-specific.

A surgical staple comprising a substrate and one or more coatings which slows the bioabsorption of the substrate. The coating can be selected so as to affect the environment surrounding the staple once the staple is implanted in the patient. The effect on the environment can cause the bioabsorption to occur within a desired time frame.

A modularly structured lid for a sterile container includes a lid component, which has at least one gas exchange portion, on which, on the inner side of a lid, at least one filter device can be arranged, and at least one filter covering by which the at least one gas exchange portion can be completely covered on an outside of the lid. The lid component has at least one standardized clip receiving portion and the filter covering has at least one standardized clip portion, by which the filter covering and the lid component can be interlockingly fixed to each other, and can be mounted and removed without tools. A sterile container can include such a lid and a filter covering for such a lid.

A sterilization tray is disclosed herein. A medical instrument, such as an endoscope, may be placed into the sterilization tray, and the sterilization tray with the medical instrument disposed therein may be placed into a vacuum chamber of a sterilization system. The sterilization tray may also be used to transport the medical instrument to and from a point of care. Sterilization is performed with the instrument in the base component and the lid component disposed atop the base component. Transportation is performed with the instrument in the lid component and the base component disposed atop the lid component.

A sterilization system with integrated instrument recall capabilities and related methods is disclosed. In one aspect, the sterilization system is adapted to determine a failed sterilization cycle of a sterilizer in response to failure of a biological indicator test for the sterilizer, identify sterilization cycles to be recalled based on the failed sterilization cycle, identify one or more patients for whom an item in a recalled sterilization cycle was used, and initiate a patient notification routine comprising at least one of outputting of identifying information of the one or more patients for whom an item in the recalled sterilization cycle was used and notifying the one or more patients for whom an item in the recalled sterilization cycle was used about the recalled sterilization cycle.