Abstract: A device for aseptic delivery of biological material from a vial includes a tubular barrel, a filter assembly, and a dispersion assembly. The dispersion assembly is at least partially disposed within the tubular barrel. The dispersion assembly includes a dispersion element, a piston, and a one-way valve. The dispersion element is in fluid communication with the vial to disperse the biological material from the vial. The piston is disposed at the distal end of the dispersion assembly and is in sealing contact with the tubular barrel. The one-way valve forms a fluid passageway in fluid communication with the dispersion element and the tubular barrel. The one-way valve is configured to allow a flow of the dispersed biological material from the dispersion element, through the fluid passageway, and into the tubular barrel, and to prevent a flow of the dispersed biological material from the tubular barrel into the dispersion assembly.

Abstract: The present disclosure provides to encapsulate the distal components of a scope to form a distal cap assembly, which removes the need for adhesives and potting often used in conventional distal cap assemblies. In particular, the present disclosure provides a spline structure configured to hold the distal end components in a predefined arrangement. The spline structure, along with the distal end components, is inserted into a mold and the spline structure along with the distal end components is encapsulated (e.g., in a polymer using hot melt, or the like) to form a distal cap. The distal cap locks the distal end components into the spline structure and protects the distal end components from moisture and relative movement. As a benefit, the present encapsulation techniques and distal cap assembly is faster to manufacture and provides less room for error than conventional methods.

Abstract: A medical device includes an operating member, a hub, and an end effector. The operating member includes an actuation portion. The hub includes a channel receiving the actuation portion of the operating member. The actuation portion of the operating member moves within the channel. The end effector is movable between a closed configuration and an open configuration. Distal extension of the operating member transitions the end effector to the open configuration, and proximal retraction of the operating member transitions the end effector to the closed configuration. The medical device is formed through an additive manufacturing process.

Abstract: In an exemplary arrangement, a vapor generator for use in a medical device may include a heating core in fluid communication with a source of fluid and defining at least one fluid pathway along which fluid from the source of fluid travels. The at least one fluid pathway may include one or more surfaces that generate turbulence in the fluid. The vapor generator may also include a coil disposed about the heating core, wherein the coil is configured to receive a current so as to heat the fluid traveling along the at least one fluid pathway, thereby generating a vapor.

Abstract: An example method for manufacturing an object is disclosed. The example method includes determining the material composition of a base material, wherein determining the material composition of the base material includes determining the relative percentage of a first metal and the relative percentage of a second metal forming the base material. The method further includes selecting a common laser processing wavelength to be used in processing the base material. The method further includes processing the base material with a laser to form a processed material, the laser emits a laser beam matching the common laser processing wavelength during the processing of the base material and the material composition of the processed material is substantially similar to the material composition of the base material.

Abstract: A device for aseptic delivery of biological material from a vial includes a tubular barrel, a filter assembly, and a dispersion assembly. The dispersion assembly is at least partially disposed within the tubular barrel. The dispersion assembly includes a dispersion element, a piston, and a one-way valve. The dispersion element is in fluid communication with the vial to disperse the biological material from the vial. The piston is disposed at the distal end of the dispersion assembly and is in sealing contact with the tubular barrel. The one-way valve forms a fluid passageway in fluid communication with the dispersion element and the tubular barrel. The one-way valve is configured to allow a flow of the dispersed biological material from the dispersion element, through the fluid passageway, and into the tubular barrel, and to prevent a flow of the dispersed biological material from the tubular barrel into the dispersion assembly.