Medical packaging is provided for enclosing a single-use medical device with multiple frangible operating lines and corresponding frangible connections to define a removable first end which reveals at the time of use an operative part forming the key part that is to come into contact with the patient. The remaining part of the device including the controlling part is retained in the rest of the packaging but can be used to control the device without hindrance. Each of the multiple frangible operating lines indicating on the packaging the difference between the key part that forms the operating part of the device for one of a plurality of predefined medical procedures wherein the identification of the frangible operating lines immediately educates and instructs the user in the correct usage in a sterile and clean manner.

A device retention assembly includes a delivery system and a device retention mechanism retaining the delivery system. The device retention mechanism includes a tray, a base coupled to the tray, and retaining flanges pivotally coupled to the base. The delivery system is enclosed within an opening defined by the base and retaining flanges. A key locks the device retention mechanism in the closed position retaining the delivery system. The key must be removed to unlock the device retention mechanism to release the delivery system.

A medical kit (100) includes a package (105) having a housing (501) and a lid (103). One or more medical implements (1001,1101,1201,1301) for treating a skin tear wound are arranged in a stacked configuration within the package. An instructional labeling system (106) is coupled to the lid. The instructional labeling system can include an identification (107) of a skin tear type the one or more medical implements are designed to treat, a description (108) of the skin tear type, printed instructions (110) defining one or more steps (111,112,113,114) instructing when to use each medical implement within the package to treat the skin tear wound, and one or more removable adhesive labels (115,116).

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.

A bone material dispensing apparatus for preparing, mixing, and dispensing bone material into a foldable container is provided. In some embodiments, the dispensing apparatus comprises a tray and a foldable container. The tray includes a mixing surface, a dispensing surface and a means to measure the amount of material to be dispensed. A kit including a tray, a foldable container, and a spatula are also provided. A method of using the dispensing apparatus to deliver the bone material to a bone detect is also provided.

The invention relates to a sealed container (1) comprising a flange (5, 6) that delimits a through-passage having an axial axis in the container, a door (7) movably mounted on the flange (5, 6), and a first annular seal (13) located between the flange (5, 6) and the door (7), the flange, the door and the first seal forming a sealed connection device that can be connected to a complementary connection device on a sterile enclosure by bayonet connection means in order to allow sterile communication between the sealed container and the sterile enclosure, characterized in that the container (1) includes a protective cover (20) on the connection device, said protective cover being forcibly clipped onto the container, and in that the container further includes contact pressure means arranged between the protective cover (20) and the connection device so as to apply contact pressure to the connection device in the axial direction proportional to the clipping force.

A package comprises: a sterile barrier packaging film; self-sterilizing components comprising: a plurality of chlorite ions and water, wherein the self-sterilizing components are substantially free of an energy-activated catalyst and of an acid-releasing compound; a package interior formed by hermetically sealing the sterile barrier packaging film; and a headspace within the package interior comprising carbon dioxide present in an amount of greater than or equal to 5% by volume of the headspace. When the package is exposed to ultraviolet (UV) light having a wavelength of 254 nm, the chlorite ions react with the water to generate chlorine dioxide (ClO.sub.2), which is released into the headspace. In the absence of any UV light, there is not chlorine dioxide (ClO.sub.2) generation.

A method of applying a buttress to a surgically cut and stapled site uses an end effector with a buttress applier cartridge assembly to load one or more buttress assemblies to the end effector. The buttress assemblies each include a buttress to support a staple formed therein as well an adhesive for adhering to the end effector. The adhesive of the buttress assemblies can include a pattern to assist in both attachment to the end effector and release from the end effector after cutting and stapling a tissue site. The buttress applier cartridge can include features that accommodate end effectors having various tip configurations, including straight tips and curved or bent tips.

A patient support apparatus comprises a support structure comprising a head end, a foot end, a base, and a patient support deck. The patient support deck comprises a fowler section at the head end and a foot section at the foot end. The fowler section is capable of articulating relative to the base. The patient support apparatus further comprises a pediatric support module comprising a seat section disposed between the fowler section and the foot section. The pediatric support module is integrated into the patient support deck and comprises a lid and a body.

The present disclosure generally pertains to methods and kits for preparing an ACL repair surgical implant, the method including drilling femoral and tibial bone plugs of a tendon graft to create medial to lateral holes, and passing a braided suture around the tendinous portion of the tibial end, through soft tissue, and out the tibial end. Next, an anterior to posterior femoral hole is drilled, and a flat-braided suture is passed through the femoral medial to lateral hole and, using a bent needle, passed through junctions of the femoral bone plug and the tendinous portion and out through junctions of the tibial bone plug and the tendinous portion on both sides of the graft. Ends of the flat-braided suture are crisscrossed through the medial to lateral tibial hole. A bone-to-bone fixation suture assembly is passed through the anterior to posterior femoral hole.