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.

The present invention relates to an endoscopic treatment instrument, and more particularly, to an endoscopic treatment instrument including a detachable end-effector and a contamination prevention cover. The endoscopic treatment instrument includes an end-effector for performing treatment in the endoscopic surgery or an endoscope treatment, a connection section being detachably coupled to an end of the end-effector, and a contamination prevention cover being coupled to the connection section or the end-effector and surrounding a portion of an outer peripheral surface of the connection section so as to prevent contamination of the connection section. According to an embodiment of the present invention, since only the end-effector is separable for replacement and the cover is formed to protect a control unit, it is possible to prevent cross infection between patients caused by the contamination of the end-effector and the control unit.

A receptacle for receiving a medical device and a method of making and using the receptacle. The receptacle includes an elongate base, a cover, the cover and elongate base hingedly secured to one another, the cover and the elongate base cooperating to define an envelope having mouth extending into an interior area of the envelope, and a biasing member communicating with the cover and configured to bias the mouth in an open position for receiving the medical device through the mouth into the interior area.

A multifunctional enclosure is described having an elongated sleeve configured with an enlarged opening for the insertion of an elongated member of a medical probe. The multifunctional enclosure is configured to prevent the elongated member of the medical probe from swinging and becoming damaged during transport. The multifunctional enclosure may further comprise an attachment component for securing the medical probe to the multifunctional enclosure. Furthermore, at least one vent may be configured onto the multifunctional enclosure, such as on a first end closure portion. The vent may allow for adequate flow for sterilization and/or drying.

An endoscope tray is provided. The tray comprises an interior for storage of an endoscope. The tray has a lid configured to cover the tray. The lid has an exterior surface having a recess and/or projection, and the tray has a bottom exterior surface having a recess and/or projection such that the recess and/or projection of the lid is configured to mate with the recess and/or projection of the bottom exterior surface of the tray. Systems and methods are also provided.

A system and methods for providing and reclaiming a single use imaging device for sterile environments is disclosed and described. The system may include a single use high definition camera used for general purpose surgical procedures including, but not limited to: arthroscopic, laparoscopic, gynecologic, and urologic procedures, may comprise an imaging device that is a sterile and designed to ensure single use. The imaging device may have a single imaging sensor, either CCD or CMOS, encased in a housing.

An endoscope is provided that includes a first component, a second component, a light source, an image capturing element, and a light guide. The second component has a proximal end and a distal end with proximal end coupled to the first component. The light source is integrated in the first component and includes a laser and a converter. The laser emits primary light and the converter converts the primary light at least partially into secondary light that has a different wavelength. The image capturing element is arranged at the distal end. The light guide has an optical fiber that extends through the second component. The converter is coupled to the proximal end such that the primary and secondary light is injected into the optical fiber, is conducted from the proximal end to the distal end, and emitted at the distal end.

An arthroscope's insertion shaft has near its distal end a solid state camera. The shaft has an outer diameter of no more than 6 mm, and has rigidity and strength for insertion of the camera into joints for arthroscopic surgery. Light conductor(s) have a flattened region shaped to lie between an endoscope camera and an inner surface of an outer wall of an endoscope shaft. The flattened region is shaped to conduct illumination light though the space between the camera and inner surface of the other wall to a distal end of the endoscope shaft for illumination of a surgical cavity to be viewed by the camera. The flattened region is formed by heating a region of a plastic optical fiber, and squeezing the heated region in a polished mold.

A sterilized endoscope kit, comprising a sterilized endoscope, a sterilized treatment instrument, a sterilized guide wire, and a packaging material. The sterilized endoscope includes a first lumen. The sterilized treatment instrument is inserted into the first lumen, the sterilized treatment instrument includes a second lumen. The sterilized guide wire is inserted into the second lumen. The sterilized endoscope, the sterilized treatment instrument, and the sterilized guide wire are arranged in the packaging material, and the packaging material provides a sterile environment for the sterilized endoscope, the sterilized treatment instrument, and the sterilized guide wire. A method for manufacturing a sterilized endoscope kit, comprising inserting a sterilized guide wire into a first lumen of a sterilized treatment instrument, inserting the sterilized treatment instrument into a second lumen of a sterilized endoscope, and placing the sterilized guide wire, the sterilized treatment instrument, and the sterilized endoscope into a packaging material.

Systems and methods that can improve the safety and efficacy of chest tube thoracostomy are described. For example, this document provides systems and methods that facilitate direct visual confirmation of the proper placement of a chest tube within the thoracic space.