The invention relates to a medical assembly, preferably a sterilized one, comprising a medical article (5) and a package containing said article, said package comprising a hollow support element (2) inside which said article (5) is free, a first protective element (3), called a stopper, which can be coupled to the support element (2) of said article, such that the support element (2) has a grip part (20) that protrudes from said stopper (3), and a second hollow protective element (4), called a cover. Said cover can be coupled to the stopper (3) in such a way as to delimit, in cooperation with said stopper (3), a chamber (8) inside which there extends said grip part (20) of the support element, and, in the state when the cover is coupled to the stopper, a part of the stopper (3) protrudes from the cover (4).

A medical tool kit is provided for packaging, storing, and transporting medical instruments and tools of various types. The medical tool kit is capable of providing continuing sterilization to the medical instruments and tools kept inside the medical tool kit after the tool case is opened during its normal use in a medical procedure. The medical tool kit is further capable of emitting a GPS tracking signal to identify the location of an opened medical tool kit during an emergency as well as creating hands free communication between the user of the medical tool kit and local emergency institutions.

A body cavity drainage device includes a drainage tube with a distal end configured for insertion into the body cavity of a patient, a fluid outlet at a proximal end of the drainage tube; and an activation apparatus coupled to the drainage tube between the proximal end of the drainage tube and the distal end of the drainage tube. The activation apparatus may be configured to alter a position of the distal end of the drainage tube in response to an input at a control device of the activation apparatus, and a first portion of the drainage tube extending from the activation apparatus toward the distal end may be at least substantially coaxial with a second portion of the drainage tube extending from the activation apparatus toward the proximal end. Methods relate to forming a body cavity drainage devices.

A strainer dish for receiving medical items to be disinfected or sterilized includes a receiving container and at least one handle, which, in a removal position projects out of the receiving container in a grippable manner in order to allow the carrying of the strainer dish, and which, in a locking position, is arranged inside the receiving container to allow the loading of the strainer dish, the handle being shifted from the locking position into the removal position by actuation of a releasable holding element.

A medical device package can include a tray defining a recess configured to receive an elongated medical device therein and a lid configured to cover at least a portion of the recess and retain the elongated medical device therein. A retention member or retention aperture formed in the lid permits a clinician to access to a medical device disposed within the recess to releasably retain the elongated medical device with respect to the tray. While releasably retaining the medical device, the clinician to manipulate the device, for example, to sheath or unsheath the device.

Protecting a blood pressure cuff and its user is in a sanitary and convenient manner. A shield has upper and lower edges, longitudinal side edges, and interior and exterior surfaces. Stitching couples the side edges. The shield forms a funnel-shaped, generally conical configuration. The upper edge is imperforate, devoid of elastic, and has a first circumference. The shield is fabricated of a flexible material. A continuous elastic band is secured to the shield adjacent the lower edge. The elastic band is adapted to constrict the lower edge to a second circumference when in a relaxed, un-stretched orientation.

A buttress is applied to an end effector of a surgical stapler. The buttress is loaded on a platform of a buttress applier cartridge. The end effector is closed upon the platform. An adhesive layer of the buttress secures the buttress to the end effector. The buttress is thus adhered to the end effector when the end effector is opened. The end effector is then actuated on tissue of a patient, thereby stapling the buttress to the tissue.

An apparatus includes a housing, a platform, a buttress assembly and a lockout feature. The housing defines a gap that is configured to receive a portion of an end effector of a surgical stapler. A portion of the platform is exposed in the gap defined by the housing. The buttress assembly is positioned on the platform. The buttress assembly is exposed in the gap defined by the housing. The lockout feature is configured to enable an end effector with an unspent staple cartridge to clamp onto the platform and thereby engage the first buttress assembly. The lockout feature is further configured to prevent an end effector with a spent staple cartridge from clamping onto the platform to thereby engage the first buttress assembly.

A buttress is applied to an end effector of a surgical stapler. The buttress is loaded on a platform of a buttress applier cartridge. The end effector is closed upon the platform. An adhesive layer of the buttress secures the buttress to the end effector. The buttress is thus adhered to the end effector when the end effector is opened. The end effector is then actuated on tissue of a patient, thereby stapling the buttress to the tissue.

A surgical instrument includes a rotatable electrical coupling assembly having a first part and a second part that electrically couple and rotate relative to each other. The second part is carried by and rotates with a tube collar coupled to a transducer. A portion of the transducer is inserted through an aperture of the second part, but does not contact the second part. The first part of the assembly may electrically couple to the second part via pogo pins, brush contacts, or ball bearings. Alternatively, the first part may comprise conductive channels formed in the casing. The second part may comprise a rotatable drum with a conductive trace. In some versions, one or more components may comprise MID components. In another version, the rotatable electrical coupling assembly comprises a rotatable PC board and brush contact. Further still, a circuit board may be provided with the transducer inside a transducer casing.