A hand-held electromechanical surgical device is configured to selectively connect with a surgical accessory. The surgical device includes a power-pack, an outer shell housing, and a gasket. The power-pack is configured to selectively control a surgical accessory. The outer shell housing includes a distal half-section and a proximal half-section, the distal half-section and the proximal half-section together defining a cavity configured to selectively encase substantially the entire power-pack therein. The gasket is located between the distal half-section and the proximal half-section of the outer shell housing. The gasket is configured to create a seal between the distal half-section and the proximal half-section and to provide a sterile barrier between the power-pack and an outside environment outside the outer shell housing.

A sharps container for safe storage of used pen needles, pen needle assemblies, syringe needles, syringe needle covers, and combinations thereof having a substantially non-porous housing which includes a receiver which receives and actively conveys external pen needles, pen needle assemblies, syringe needles, syringe needle covers, and combinations thereof into the interior of the housing; an internal storage compartment sized to facilitate the safe storage of a plurality of used pen needles or syringe needles and optional needle covers. The internal storage compartment including a material capable of absorbing and storing fluids which may incidentally be associated with the used pen needles or syringe needles. The receiver for pen needles, pen needle assemblies, syringe needles, syringe needle covers, and combinations thereof is visually distinguished from the surrounding portions of the housing by one or both of having a different color or different color patterning relative to the surrounding housing.

A hand-held electromechanical surgical device is configured to selectively connect with a surgical accessory. The surgical device includes a power-pack, an outer shell housing, and a gasket. The power-pack is configured to selectively control a surgical accessory. The outer shell housing includes a distal half-section and a proximal half-section, the distal half-section and the proximal half-section together defining a cavity configured to selectively encase substantially the entire power-pack therein. The gasket is located between the distal half-section and the proximal half-section of the outer shell housing. The gasket is configured to create a seal between the distal half-section and the proximal half-section and to provide a sterile barrier between the power-pack and an outside environment outside the outer shell housing.

A system and method are provided for packaging and sterilizing analyte sensors. The packaging system provides a structure for securing the analyte sensors in a fixed position and fixed orientation within the package.

A packaging system for an elongate tool to be coupled to a surgical device. A segmented packaging body comprises a first distal section, a second distal section, and a proximal section. The first and second distal sections provide a clamshell casing to the distal end of the tool, and the proximal section is pivotally coupled to the first distal section and configured to receive the proximal end of the tool. The packaging body may comprise a living hinge and perforations to facilitate mounting the tool on the surgical device without the user touching the tool, thereby minimizing risk of contamination and/or injury. The proximal section may be detached from the clamshell casing at the perforations after the tool is mounted on the surgical device. Secondary packaging may be provided to receive the packaging body. Methods for mounting the tool disposed within the packaging system are also disclosed.

The present invention concerns a sterile closed loop device for medical-surgical use intended for the collection, the transportation and the processing of prostheses and/or biological samples and the like, having at least one collection compartment provided with an hermetically closable main opening, for the introduction of said prosthesis and/or biological samples and the like to be analyzed, so as to be contained in it, at least one containment chamber, in which a solution is contained for the chemical detachment of bacteria adhering to animate or inanimate surfaces, such as prostheses and the like, and/or bacterial biofilm, said containment chamber being selectively communicating with said collection compartment, so that said solution can be conveyed from said containment chamber to said collection compartment, for the chemical separation of bacteria to said prosthesis and/or biological samples and the like to be analyzed, that can be inserted in said collection compartment, and extraction means of said solution for the chemical detachment of bacteria from said collection compartment. The present invention also concerns a method for collecting, transporting and processing a prosthesis and/or biological samples and the like to be analyzed.

A system and method are provided for packaging and sterilizing analyte sensors. The packaging system provides a structure for securing the analyte sensors in a fixed position and fixed orientation within the package.

Package for elongated sharp-edged objects, in particular for tools useful for surgical applications, which are secured in a fixed position in a package consisting at least partially of plastic, wherein the package comprises an a first enlarged package part which defines an interior into which the object that is to be protected and secured protrudes with its sharp edges in a noncontact manner and a second package part in which the shaft of the object is accommodated and held in a fixed position by holding elements.

A system and method are provided for packaging and sterilizing analyte sensors. The packaging system provides a structure for securing the analyte sensors in a fixed position and fixed orientation within the package.

A method for mounting a tool to a surgical device using a packaging body. A proximal section of the packaging body is articulated about a second boundary relative to a first distal section of the packaging body for removing a proximal end of the tool from a proximal cavity for exposing the proximal end. The proximal end is mounted to the surgical device while a distal end of the tool remains securely retained by first and second distal sections of the packaging body within a distal cavity. After mounting, the distal end is released from the distal cavity by articulating one distal section relative to the other distal section for exposing a first portion of the distal end that was retained by the one distal section. Thereafter, the other distal section is removed for exposing a remaining portion of the distal end that was retained by the other distal section.