The systems, methods, and apparatus disclosed herein are directed to an exchangeable working channel for a surgical instrument comprising a proximal portion, a distal portion, and an instrument channel configured to receive the exchangeable working channel. The exchangeable working channel may comprise a shaft comprising a proximal region and a distal region; an inner surface defining a lumen extending through the shaft; and an outer surface configured to interface with the instrument channel of the surgical instrument. The exchangeable working channel may further comprise one or more locking members configured to releasably couple to the proximal portion or the distal portion of the surgical instrument. The exchangeable working channel may increase a service life of the surgical instrument as a worn working channel can be exchanged with a new one.

A video display apparatus includes an apparatus main body, a lid body, a hinge shaft configured to axially support the lid body with respect to the apparatus main body, main body-side shaft holding sections, the hinge shaft being inserted through the main body-side shaft holding sections, lid-side shaft holding sections formed in the lid body, the hinge shaft being inserted through the lid-side shaft holding sections, a first seal member configured to prevent infiltration of liquid from a gap between the lid-side shaft holding sections and the main body-side shaft holding sections into the hinge shaft, a hinge lid disposed in a stepped hole, into which the hinge shaft is inserted, provided in one of the lid-side shaft holding sections, and a second seal member provided in the stepped hole and configured to prevent infiltration of the liquid into the hinge shaft.

A warming device (30) for warming the lens portion (2) of an optical instrument (I), such as a laparoscope, to a temperature above ambient to prevent lens fogging comprising: a double walled cylindrical tube (3) having an intemal wall (3b), and an external wall (3a), an upper surface and an open distal portion (7) with a central cavity (4) therebetween; a protrusion (9) extending from said upper surface, sized and shaped to receive the lens portion; a circular cap (5) sized to attach to said distal portion of said double walled cylindrical tube; and, a heating element (15) enclosed within said central cavity and thermally coupled to said insulation layer.

Embodiments of a system and method for processing and recognizing non-contact types of human input to prevent contamination are generally described herein. In example embodiments, human input is captured, recognized, and used to provide active input for control or data entry into a user interface. The human input may be provided in variety of forms detectable by recognition techniques such as speech recognition, gesture recognition, identification recognition, and facial recognition. In one example, the human input recognition techniques are used in connection with a device cleaning workflow used to obtain data and human input during cleaning procedures while minimizing cross-contamination between the contaminated device or person and other objects or persons. In another example, the human input recognition techniques are used in connection with a device tracking workflow used to obtain data and human input while tracking interactions with and locations of the contaminated or uncontaminated device.

A modular endoscope system comprises a first modular section comprising imaging and illumination units, and a patient-insertable second modular section that can be detached to the first modular section via an attachment mechanism, wherein the first modular section is positionable at a distal end section of the second modular section and is configured to illuminate and image a portion of a patient anatomy. A method of using a modular endoscopy system comprises attaching a first modular section of the modular endoscopy system to a second modular section of the modular endoscopy system, positioning at least a portion of the modular endoscopy system within a patient, illuminating and imaging a portion of a patient anatomy via the first modular section, removing the modular endoscopy system from the patient, and detaching the second modular section from the first modular section after removal of the modular endoscopy system from the patient.

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.

A device and method for cleaning or defogging a surgical scope during minimally invasive surgery, including a casing which houses a sponge and a heating element configured to be accessible to the surgical scope and the casing is configured to removably attach to a trocar during a surgical procedure.

A device may be configured for white balancing a medical videoscopic camera system prior to videoscopic medical procedures, as well as optionally simultaneously or non-simultaneously applying a fog-prohibiting agent to the distal lens of a medical videoscope such as an endoscope or laparoscope. The device combines a white balancing mechanism, protective mechanism, and defogging mechanism in one simple easy to use device.

In an embodiment, the present specification is an alarm/warning system for notifying a user cleaning an endoscope that the main connector/electrical connector of endoscope has not been covered by a connector cover. The warning system indicates an absence of a connector cover cup when the connector of the endoscope is not connected to a main control unit.

A single use container (10, 40, 70) for holding a plurality of endoscope valves during a cleaning and disinfection procedure defines a plurality of chambers (34, 64, 84) which are isolated from each other and configured to receive a single valve such that a valve in one chamber cannot contact a valve in another chamber. A plurality of apertures (36, 58, 86) in each chamber allow fluid flow therethrough. A closure device (14, 44, 92) is operable to close each chamber (34, 64, 84). An attachment device (38, 68, 77) is configured for attaching the container (10, 40, 70) to an endoscope and to prevent detachment without breaking of the attachment device (38, 68, 77).