The invention relates to supports (1) for receiving a surgical implant, in particular a bone plate (2), containing an implant receptacle (3), the implant receptacle (3) being of substantially elongate form along a longitudinal axis (4) and having a first part (5) and a second part (6), the first part (5) having a shaft (7) for receiving the surgical implant (2) at a recess (13) of the implant (2), the second part (6) having a first fastening portion (8) for fastening to a holding portion (9) of a container (114). The support (1) furthermore contains at least one elastic element (10), in particular a spring, for securing the implant, which is designed to secure an implant, which is held on the implant receptacle (3), by a force component substantially perpendicular to the longitudinal axis (4). Also disclosed are supports (100) for receiving at least one surgical item, in particular an implant, in particular a screw (101).

Described are medical graft products, systems, and methods for treating fistulae. Certain products of the invention are configured to have portions residing in and around a primary fistula opening, e.g., one occurring in a wall of the alimentary canal. One such product includes a biocompatible graft body which is configured to block at least the primary opening. The graft body includes a capping member, which is configured to contact portions of the alimentary canal wall adjacent to the primary opening, and an elongate plug member extending from the capping member, which is configured to extend into at least a portion of the fistula. In certain embodiments, a graft body component has the capacity to expand or otherwise change form to provide a suitable capping arrangement. Such a component can include a resilient wire frame, e.g., one that is self-expandable or one that requires at least some manipulation in order to expand.

Described are medical graft products, systems, and methods for treating fistulae. Certain products of the invention are configured to have portions residing in and around a primary fistula opening, e.g., one occurring in a wall of the alimentary canal. One such product includes a biocompatible graft body which is configured to block at least the primary opening. The graft body includes a capping member, which is configured to contact portions of the alimentary canal wall adjacent to the primary opening, and an elongate plug member extending from the capping member, which is configured to extend into at least a portion of the fistula. In certain embodiments, a graft body component has the capacity to expand or otherwise change form to provide a suitable capping arrangement. Such a component can include a resilient wire frame, e.g., one that is self-expandable or one that requires at least some manipulation in order to expand.

A system for containing and transporting a medical device may include a container including a bottom face and surrounding side faces as a closed first end and an open second end to form an inner portion for receiving and retaining the medical device. The liner may be extendable over the side faces to line the inner portion of the container to an outer surface of the bottom face of the container. The liner may act as a protective barrier to the container to minimize contamination when receiving and/or retaining a used medical device. First and second covers may be removably attachable to the container, over the liner, to enclose a medical device therebetween. A first cover may have a color or marking indicating the medical device is “clean”, while a second cover may have a color or marking indicating the medical device is “used”.

A packaging system includes a packaging container and a packaging element. The packaging container include a first half having a base surface and an outer wall defining an inset receiving area, a second half sized and configured to couple to the first half in a locking relationship, and a coupling element extending from the base surface of the first half. The packaging element includes a central coupling body defining an opening sized and configured to receive the coupling element of the packaging container therethrough and a plurality of secondary coupling elements each coupled to an outer perimeter of the central coupling body. A plurality of surgical elements are each coupled to one of the plurality of secondary coupling elements.

Devices associated with on-body analyte sensor units are disclosed. These devices include any of packaging and/or loading systems, applicators and elements of the on-body sensor units themselves. Also, various approaches to connecting electrochemical analyte sensors to and/or within associated on-body analyte sensor units are disclosed. The connector approaches variously involve the use of unique sensor and ancillary element arrangements to facilitate assembly of separate electronics assemblies and sensor elements that are kept apart until the end user brings them together.

A receptacle for the safe passing of surgical instruments during surgical procedures, the receptacle comprising: a first pick-up well for receiving one or more surgical instruments and defined by a protective wall and one or more first walls, each of the protective and one or more first walls having a top edge which collectively define an opening to the first pick-up well, and the top edge of the protective wall projecting above the top edges of the one or more first walls; and a handle external to the first pick-up well and comprising an elongate member projecting from the protective wall and adapted to be gripped in a human hand; wherein: the protective wall is located between the elongate member and the first pick-up well; and the elongate member joins the protective wall at a position and orientation such that, in use when a user is gripping the elongate member, the hand of the user does not project above the top edge of the protective wall.

A device for protecting against an airborne contamination of a medical device including an air circulation cooling system is disclosed. The device also includes an enclosure defining a sealed receiving volume for the medical device, the protection device further comprising structure for circulating gas flow, within the enclosure, the gas flow having predetermined composition and/or quality criteria different from the external environment and able to be used by the cooling system of the medical device in operation.

A device for protecting against an airborne contamination of a medical device including an air circulation cooling system is disclosed. The device also includes an enclosure defining a sealed receiving volume for the medical device, the protection device further comprising structure for circulating gas flow, within the enclosure, the gas flow having predetermined composition and/or quality criteria different from the external environment and able to be used by the cooling system of the medical device in operation.

Methods and systems for rotationally aligning a commissure of a prosthetic heart valve with a commissure of a native valve are disclosed. In some examples, a delivery apparatus can include a first shaft configured to rotate around a central longitudinal axis of the delivery apparatus, a second shaft extending through the first shaft and having a distal end portion extending distally beyond a distal end portion of the first shaft, an inflatable balloon coupled to the distal end portion of the first shaft, and a third shaft surrounding the first shaft. The first shaft is configured to rotate within the third shaft and translate axially relative to the third shaft, and the third shaft includes a distal tip portion including a plurality of internal helical expansion grooves and a plurality of external helical expansion grooves that are configured to allow the distal tip portion to flex radially outward.