Systems and methods for cleaning and disinfecting contaminated tube lumens are described herein. One system includes an ultraviolet light source and a sterile fluid reservoir fluidly coupled to a liquid light guide. The system is configured to allow simultaneous access and propagation of ultraviolet light and fluid in a tube having a lumen to be cleaned and disinfected. The light guide can be moved inside the tube and simultaneously emit ultraviolet light through its walls and at its distal end into the interior of the contaminated tube. A flush of sterile fluid from an open end of the liquid light guide removes debris and micro-organism detached from the inner surface during light exposure. The sterile fluid can be a high refractive index ionic solution promoting light propagation.

A method of protecting an ear canal of a patient during a surgical procedure using a protective sheath includes forming the protective sheath using additive manufacturing based on a digital model of anatomy of the patient, where the protective sheath includes a passageway extending therethrough. The method may further include inserting the protective sheath into the patient so that the passageway extends at least partially within the ear canal of the patient. The method may further include inserting at least one instrument during the surgical procedure through the passageway of the protective sheath and into the middle ear of the patient.

A memory stores identification information on a subject related to preliminary cleaning acquired by an ID acquirer a non-contact manner. A registration processing unit determines whether or not to register preliminary cleaning execution information in a server apparatus based on the identification information stored in the memory. The registration processing unit determines, when identification information on an endoscope and identification information on a cleaning operator are stored in the memory, to register preliminary cleaning execution information including the identification information on the endoscope and the identification information on the cleaning operator.

An endoscope can comprise a proximal section, an insertion section extending longitudinally from the proximal section and comprising an elongate tubular body disposed along an insertion section longitudinal axis and a lumen extending through the elongate tubular body, and a distal section extending from the insertion section and comprising an elevator portion comprising an elevator configured to position and orient one or more endotherapy tools extending from the lumen, and a camera module comprising an illumination unit and an imaging unit. The camera module can be positioned longitudinally spaced apart from the elevator portion in an in-line configuration, such that the insertion tube longitudinal axis passes through the elevator portion and the camera module. The camera module can be user-detachable from the elevator portion. The camera module can be cleaned and sanitized for reuse and the insertion section can be disposable.

An elevator for an endoscope comprises a first end secured to the endoscope, a second end movable by an actuator, a flexible portion positioned between the first and second ends that is rotatable when the second end is moved by the actuator, and a guide portion extending between the flexible portion and the second end to receive an endotherapy instrument extending from the endoscope, the guide portion comprising a chute to guide the endotherapy instrument leaving the endoscope. A method of forming an elevator comprises forming from a planar sheet of material an elongate body comprising a length between first and second ends, a width, and a thickness, forming a guide body in the elongate body, bending the elongate body such that first and second lengths of the elongate body oppose each other to form an interior space, and bending the guide body to extend into the interior space.

A container for endoscopes, usable for the containment of endoscopes during washing, sterilization, drying and for the subsequent storage of endoscopes subjected to such operations, characterized in that it is provided with signaling means (7) applied to said container (2) and adapted to emit a signal if the pressure inside the same container (2) is below a pre-established value.

A method of using a vacuum chamber to assist in detecting and removing moisture from an instrument having a lumen, e.g., an endoscope is disclosed. Second derivatives of pressure with respect to time are calculated and differences therebetween summed. These summations may be compared to a threshold value to determine whether residual moisture remains on the instrument in the chamber. The vacuum chamber may include a rack for hanging instruments having lumens, such as endoscopes.

An endoscope can comprise a proximal section, an insertion section extending longitudinally from the proximal section and comprising an elongate tubular body disposed along an insertion section longitudinal axis and a lumen extending through the elongate tubular body, and a distal section extending from the insertion section and comprising an elevator portion comprising an elevator configured to position and orient one or more endotherapy tools extending from the lumen, and a camera module comprising an illumination unit and an imaging unit. The camera module can be positioned longitudinally spaced apart from the elevator portion in an in-line configuration, such that the insertion tube longitudinal axis passes through the elevator portion and the camera module. The camera module can be user-detachable from the elevator portion. The camera module can be cleaned and sanitized for reuse and the insertion section can be disposable.

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 medical valve may comprise a valve stem and an operation portion. The operation portion may include a stationary portion, a movable portion which is movable relative to the stationary portion and fixed relative to the valve stem, a seal disposed between the stationary portion and the movable portion, and a biasing member. Movement of the movable portion in a first direction may cause deformation of the biasing member, such that a restorative force of the biasing member urges movement of the movable portion in a second direction opposite the first direction. A frictional force between the seal and one of the stationary portion and the movable portion resists the movement of the movable portion in the second direction.