Systems, apparatuses, and methods are discussed herein for an endoscope. The endoscope has a distal tip with an oblique portion and a flat portion, the oblique portion defines a plane that forms an angle between and including 20 and 40 degrees to a central axis of the endoscope. A related sheath may have similar features at the distal tip.

Systems, apparatuses, and methods are discussed herein for an endoscope. The endoscope has a distal tip with an oblique portion and a flat portion, the oblique portion defines a plane that forms an angle between and including 20 and 40 degrees to a central axis of the endoscope. A related sheath may have similar features at the distal tip.

A medical device that includes a first body including a first actuation member including a first connector and a second actuation member. The medical device includes a second body for attachment to, and detachment from, the first body. The second body including an actuation wire, a second connector at a proximal end of the actuation wire, and a valve having one or more channels for receiving a material. Attachment of the first body with the second body results in the first connector engaging the second connector, such that movement of the first actuation member causes a corresponding movement of the actuation wire. Moving the second actuation member into the second body to interact with the valve is configured to selectively direct the material through the one or more channels.

An endoscope processor allows the user to easily confirm the setting state of functions. The endoscope processor includes: a processor executing program code to perform: displaying, by the processor, on a touch panel a plurality of custom buttons each having a function description section describing a function operable by a user and a state section indicating a state of the function; and accepting, by the processor, an operation performed on the custom buttons displayed. The function description section includes an icon section illustrating the function and a name section indicating a name of the function in text form.

A removable and replaceable sheath may be coupled to a medical instrument used during a procedure, and may enable one or more functional features of the medical instrument while maintaining a sterile barrier between the instrument itself and the treatment site. The sheath may be replaced prior to a subsequent use, and sterilization of the medical instrument is not required due to the sterile barrier. Sheaths may include an embedded memory that stores procedure configurations and procedure results, longitudinal channels for delivering power or irrigation, optical elements for providing procedure specific endoscopic views, and other features. One sheath may be fitted to an endoscope for imaging and tissue ablation. Another sheath includes a balloon usable during sinuplasty procedures. Yet another sheath may be fitted to a sonic ablation instrument to provide improved transmission of sonic power to tissue.

A removable and replaceable sheath may be coupled to a medical instrument used during a procedure, and may enable one or more functional features of the medical instrument while maintaining a sterile barrier between the instrument itself and the treatment site. The sheath may be replaced prior to a subsequent use, and sterilization of the medical instrument is not required due to the sterile barrier. Sheaths may include an embedded memory that stores procedure configurations and procedure results, longitudinal channels for delivering power or irrigation, optical elements for providing procedure specific endoscopic views, and other features. One sheath may be fitted to an endoscope for imaging and tissue ablation. Another sheath includes a balloon usable during sinuplasty procedures. Yet another sheath may be fitted to a sonic ablation instrument to provide improved transmission of sonic power to tissue.

A system for visualizing a tissue region of interest comprises a deployment catheter defining a lumen and a hood coupled to and extending distally from the deployment catheter. The hood has a low-profile configuration within a delivery sheath and a deployed configuration when extended distally of the delivery sheath. The hood in the deployed configuration defines an open area in fluid communication with the lumen. A distal portion of the deployment catheter extends into the open area. An imaging element is coupled to an imager support member. When in the deployed configuration, the imaging element is configured to extend distally of the distal portion while the imager support member extends within the deployment catheter. The imaging element comprises a tapered surface and the deployment catheter comprises a complementary tapered surface. Retraction of the imaging element causes the imaging element to shift radially outward from a longitudinal axis.

A system for visualizing a tissue region of interest comprises a deployment catheter defining a lumen and a hood coupled to and extending distally from the deployment catheter. The hood has a low-profile configuration within a delivery sheath and a deployed configuration when extended distally of the delivery sheath. The hood in the deployed configuration defines an open area in fluid communication with the lumen. A distal portion of the deployment catheter extends into the open area. An imaging element is coupled to an imager support member. When in the deployed configuration, the imaging element is configured to extend distally of the distal portion while the imager support member extends within the deployment catheter. The imaging element comprises a tapered surface and the deployment catheter comprises a complementary tapered surface. Retraction of the imaging element causes the imaging element to shift radially outward from a longitudinal axis.

A probe is configured with a flushing port and an evacuation port to establish a flow path to remove blood from a resected tissue. The probe comprises a balloon configured to expand and contact the resected tissue to compress filaments and improve access to the underlying blood vessels for coagulation with an energy source. An endoscope can be used to view the tissue, and the balloon may comprise a transparent material or a viewing port to allow imaging of the bleeding tissue through the balloon. The probe may have a light source to illuminate the tissue with a beam oriented at an oblique angle to the tissue surface, which can decrease interference from blood and may allow more localized coagulation of the blood vessel.

A probe is configured with a flushing port and an evacuation port to establish a flow path to remove blood from a resected tissue. The probe comprises a balloon configured to expand and contact the resected tissue to compress filaments and improve access to the underlying blood vessels for coagulation with an energy source. An endoscope can be used to view the tissue, and the balloon may comprise a transparent material or a viewing port to allow imaging of the bleeding tissue through the balloon. The probe may have a light source to illuminate the tissue with a beam oriented at an oblique angle to the tissue surface, which can decrease interference from blood and may allow more localized coagulation of the blood vessel.