A staple cartridge configured for use with a surgical stapling device is disclosed. The staple cartridge includes an authentication ramp that extends from a proximal end of the cartridge body and defines a ramp axis that is transverse to an axis of the cartridge. The authentication ramp is aligned with a sled cavity in the cartridge and comprises first and second cam surfaces that are configured to move a lockout of the surgical stapling device in a direction away from the cartridge axis upon contact therewith when the staple cartridge is seated into the surgical stapling device.

A staple cartridge configured for use with a surgical stapling device is disclosed. The stapling device includes a lockout for prevent operation of the device. The staple cartridge includes a first cam surface configured to move the lockout from a locked position to an intermediate position when the staple cartridge is initially inserted into the device. The staple cartridge further includes a second cam surface configured to move the lockout from the intermediate position to an unlocked position when the staple cartridge is operably seated in the device. The first cam surface is proximal to the second cam surface and may be vertically displaced therefrom.

A staple cartridge configured for use with a surgical stapling device is disclosed. The stapling device includes a lockout for prevent operation of the device. The staple cartridge includes a first cam surface configured to move the lockout from a locked position to an intermediate position when the staple cartridge is initially inserted into the device. The staple cartridge further includes a second cam surface configured to move the lockout from the intermediate position to an unlocked position when the staple cartridge is operably seated in the device. The first cam surface is proximal to the second cam surface and may be vertically displaced therefrom.

The robotized module for actuating an elongated flexible medical device comprises a pair of actuation members that are either in an actuation configuration or in a free configuration. The pair of actuation members is movable between a first position and a second position. A control member acts in repeated cyclical manner to cause the actuation member, when in the actuation configuration, to move from the first position to the second position, and when in the free configuration, to move from the second position to the first position.

A modular storage system is described for storing and/or shielding a hypodermic needle which includes a modular needle container element for storing and/or shielding a hypodermic needles. The system includes a compartment for storing the needle, defined by first and second walls configured to be end walls, and a front wall and a rear wall extending between the first and second walls; each of the first and second walls has an outer surface directed away from the compartment, and each of the first and second walls include either a male connector on the outer surface of the wall or a female connector extending through the wall. The male connector includes a clip arm and the female connector includes a slot, such that the male connector is configured for engagement in a snap-fit manner to the female connector in the first or second wall of a second container element.

A waste disposal system (30) with a waste receiver (32) for receiving pharmaceutical waste material. A locking assembly (34) is secured to a fixed surface and actuated from a locked configuration to an unlocked configuration. A lock cylinder of the locking assembly may extend forward of a front wall (44) of a receiver body (36) of the waste receiver to engage a locking feature of a cover (82) in the locked configuration. A cover retention feature (124) may prevent axial decoupling of the cover from the receiver body. The receiver body may be formed from two shells (62,64). A reaction agent (150) is positioned within the container volume and spaced apart from a bottom wall of the receiver body. The reaction agent may be positioned within the container volume between the lock passageway (94) and/or a solid receiver volume, and opposing sidewalls of the receiver body. A support may maintain the position of the reaction agent within the container volume.

A touchscreen cover assembly embodiment is configured to create a sterile interface between a touchscreen and a user and includes a sterile frame and a sterile cover member. The sterile frame includes a forward frame surface and a rearward frame surface opposite the forward frame surface. The sterile frame defines an interior opening, and the sterile frame is configured to be secured to the touchscreen such that the rearward frame surface faces the touchscreen and the interior opening is aligned with a user interface of the touchscreen. The sterile cover member includes a forward cover portion and a rearward cover portion. The sterile cover member is configured to be secured to the touchscreen by the sterile frame such that the forward cover portion is positioned between the interior opening and the user interface of the touchscreen and the rearward cover portion is positioned over a housing of the touchscreen.

A touchscreen cover assembly embodiment is configured to create a sterile interface between a touchscreen and a user and includes a sterile frame and a sterile cover member. The sterile frame includes a forward frame surface and a rearward frame surface opposite the forward frame surface. The sterile frame defines an interior opening, and the sterile frame is configured to be secured to the touchscreen such that the rearward frame surface faces the touchscreen and the interior opening is aligned with a user interface of the touchscreen. The sterile cover member includes a forward cover portion and a rearward cover portion. The sterile cover member is configured to be secured to the touchscreen by the sterile frame such that the forward cover portion is positioned between the interior opening and the user interface of the touchscreen and the rearward cover portion is positioned over a housing of the touchscreen.

An improved medical procedure or catheterization tray included in an improved medical procedure or catheterization package. The improved medical procedure or catheterization tray is intuitively arranged. In one example, a catheterization package and catheterization tray has a layout and/or arrangement of components that may help reduce CAUTI rates by facilitating ease of use and aiding in proper aseptic technique during insertion. The medical procedure or catheterization package and/or medical procedure or catheterization tray may include various implements, compartments, and components necessary and/or helpful to the medical procedure or catheterization.

An improved medical procedure or catheterization tray included in an improved medical procedure or catheterization package. The improved medical procedure or catheterization tray is intuitively arranged. In one example, a catheterization package and catheterization tray has a layout and/or arrangement of components that may help reduce CAUTI rates by facilitating ease of use and aiding in proper aseptic technique during insertion. The medical procedure or catheterization package and/or medical procedure or catheterization tray may include various implements, compartments, and components necessary and/or helpful to the medical procedure or catheterization.