Abstract: A tibial trial insert includes an upper plate and lower plate. An adjustment arrangement between the upper and lower plates is actuatable to adjust a gap between the upper and lower plates. The adjustment arrangement includes a first lift with a first lever arm arrangement and a second lift with a second lever arm arrangement. Each lever arm arrangement is indirectly connected to the upper and lower plates and pivotally movable to vary its length and adjust the gap between the upper and lower plates. The first lift includes an actuator coupled to the first lever arm arrangement. Actuation of the actuator varies the length of the first lever arm arrangement. The adjustment arrangement includes a coupling that couples the second lift to the first lift and configured such that the length of the second lever arm arrangement is varied synchronously to the first lever arm arrangement.

Abstract: A tool includes a working end determining device arranged in a shaft region or gripping region thereof for determining and/or detecting a working end of the tool. The working end determining device includes a writable and/or readable data storage device that stores data relating to the working end of the tool. The working end determining device provides data externally with reference to the working end of the tool for detecting the working end of the tool. The working end determining device can be a communication device that includes the data storage device and an antenna device. Alternatively, the working end determining device can be a unit integrated into the tool that is connected to an external control device via an electrical contacting. The integrated unit includes a resistor determining the working end of the tool and/or a storage device storing data with respect to the working end.

Abstract: A method for producing a strainer dish for receiving medical objects to be disinfected or sterilized. A base surface is produced from a sheet metal blank in a first machining step. In a second machining step, the sheet metal blank or base surface is provided with holes to obtain a perforated starting shape. In a third machining step which takes place after the first and second machining steps, a perforated plane is produced, which can be divided into a flat inner section and an edge section. In a fourth machining step which takes place after the third machining step, a strainer dish shape is produced. The raw bottom corresponds to the flat inner section of the perforated plane. A fifth machining step, which takes place after the third machining step, at least partially produces a three-dimensionally structured bottom from the flat inner section.

Abstract: A sieve tray for receiving objects to be disinfected or sterilized includes a base which has a plurality of openings and a base plane delimited by lateral walls. The base is a sheet metal part which has corrugations or indentations which protrude out of the base plane towards the sieve tray interior and/or sieve tray exterior such that the sheet metal part imitates a meshwork structure.

Abstract: An implant, preferably for treating and/or reconstructing, in particular lining and/or sealing and/or relining and/or at least partially filling an acetabular defect, having at least one flat structure which contains a material that is at least partially decomposable or resorbable in vivo. The invention further relates to a surgical kit and the use of an unfinished flat structure for producing an implant.

Abstract: An energy production device for a chargeable energy storage is arranged on a fluid conduit of an existing fluid circuit in a device through which a fluid flows. The fluid flow in the fluid conduit primarily serves a predetermined purpose different from that of the energy production device. The energy production device is arranged to produce energy from the kinetic energy of the fluid flow to charge the chargeable energy storage. A module insertable into the device may include the energy production device. The device may be a washer disinfector for processing medical instruments, systems and/or products that include at least one handpiece having a chargeable energy storage. The energy storage is configured as a rechargeable battery or as a power cell and is adapted to be processed together with the handpiece in the washer disinfector.

Abstract: A medical instrument, medical treatment system and method of assembly. The medical instrument has an instrument body with an RFID tag. An underfloor tag holder receives the RFID tag to fix it in position in such a way that the RFID tag is exposed to the surroundings of the instrument via an opening formed in an instrument body surface, but is set back from the instrument body surface to preferably prevent protrusion beyond the instrument body surface. At least portions of the underfloor tag holder with the RFID tag are enclosed by a separate metal shield having a signal-permeable aperture opening.

Abstract: A keyless coupling for a tool shaft and a handpiece of a surgical instrument having a first coupling section, which is provided on a proximal section of the tool shaft, a second coupling section, which is provided on a distal section of a shaft holder of the handpiece, and a locking/unlocking element. The locking/unlocking element is arranged on the tool shaft and forms a latching section, and the shaft holder has an undercut for receiving the latching section in a locking position of the two coupling sections such that the latching section and the undercut are in latching engagement with one another and secure the two coupling sections against a relative axial movement with respect to one another at least in the pulling direction.

Abstract: A favored angle screw assembly and a rod receiver body for a favored angle pedicle screw assembly. The favored angle screw assembly includes a pedicle screw and the rod receiver body. The rod receiver body includes a tubular wall having a first end with a first opening, a second end with a second opening, and a bore extending from the first opening to the second opening. The bore features a first bore section adjacent to the first opening, a second bore section adjacent the second opening, and a third bore section having a first end adjacent to the first bore section and a second end adjacent to the seat surface. The third bore section defines a transition surface that conforms to a side wall of an oblique three-dimensional shape.

Abstract: A container seal includes a locking bolt, which has on one end portion or central portion thereof a push-in/latch compartment which is open in the transverse direction relative to the lock axis and is formed or provided with an undercut acting in the direction of the latch compartment opening; a clip or tab, wherein the clip or tab is arranged on the other end portion of the locking bolt; and a bolt or bar which is arranged on the free end/end portion of the clip or tab and has on the free end/end portion thereof a latch device which is coupled to the bolt via a predetermined breaking point.

Abstract: A medical product for use during the treatment of a bone defect, having a plurality of individual elements that are connected to one another such that individual elements adjacent to one another engage in one another/are chained to one another. The individual elements of the chain net are subdivided into main elements and connection elements that are designed differently from the main elements. The main elements and the connection elements form, when chained to one another, a grid structure that is flat in the x-y plane.

Abstract: A stackable sieve tray for receiving medical products, preferably for sterilization, has a sieve tray bottom and upward-extending sieve tray sidewalls arranged at the sieve tray bottom. The sieve tray bottom, on its underside, has an indentation in edge regions that holds at least two sieve trays in position with respect to each other in a length and width direction of the sieve trays when the sieve trays are stacked, the indentation of a first sieve tray engaging the sieve tray sidewalls of a second sieve tray.

Abstract: A medical product, preferably for use in the treatment, more particularly in the filling up and/or closure, of a bone cavity, the product having structural elements connected to one another, the structural elements being dividable at least into two groups of structural elements, namely at least into a first group of structural elements and into a second group of structural elements, the structural elements of the first group having a lower hardness than the structural elements of the second group. Furthermore, a method for producing the medical product and a medical kit.

Abstract: A branch-crossed surgical instrument includes a female branch and a male branch, each branch having a terminal portion over the longitudinal extension thereof. The terminal portion of the female branch is passed through by a passage opening, which has a distal and a proximal longitudinal end surface, each having two outer edges and adjusted to receive the terminal portion of the male branch such that the two terminal portions form a plug-through closure in an assembly position of the instrument. The passage opening has a length, wherein the outer edges of the longitudinal end surfaces are exposed in all relative positions of the two branches, in particular in a completely closed position and/or in a completely opened position of the instrument, and not covered by the male branch.

Abstract: A sterile packaging for sterile medicinal products, in particular implants, forms at least one, or in case of a multiple sterile packaging, at least one first sterile barrier and an outer second sterile barrier, separate and independent from the first sterile barrier, and which is accommodated in an outer packaging. The outer packaging is made of a composite material that includes cardboard and at least one coating or film, and is designed and intended to form the second sterile barrier of the sterile packaging.

Abstract: An identification system for automatically identifying a medical tool includes at least one tool holder or packaging having a readable data carrier and designed to hold the medical tool. The system also includes an identification device to identify the medical tool. The tool holder or packaging is designed such that removal of the medical tool automatically closes a circuit provided on the tool holder or packaging and activates an antenna. The identification device is also designed to detect activation of the antenna and to read the data carrier of the tool holder or packaging.

Abstract: A universal drill guide system includes a universal drill guide, interchangeable drill tubes, and interchangeable drill bits. Each interchangeable drill tube corresponds to one of the interchangeable drill bits, and can be detachably coupled to the universal drill guide. A cannulated drill with K-wire retention features a drill bit with a retention mechanism that prevents axial advancement of a K-wire during drilling. A drill removal tool includes a drill remover that can be placed around a drill bit to remove it from bone after a hole is drilled, while leaving a K-wire in place in the bone. A bone screw driver with K-wire retention includes a shaft that can be passed over a K-wire, a distal end for attachment to a cannulated bone screw, and a K-wire retention module for preventing advancement of the K-wire as the screw driver drives the cannulated bone screw into bone.

Abstract: A fixing system for an aligning device of a tibial resection guide for fixating attachment to a limb and an aligning device having the fixing system. The fixing system includes a carrier device having an attachment portion for attaching to an adjustment rod, a fixing magnet arranged on a front side of the carrier device, and a magnetic band adapted to be attracted to the fixing magnet and adapted to be attached to the limb of a patient.

Abstract: A surgical grip for receiving a handpiece shaft for conjoint rotation therewith and/or for receiving a medical tool in such a way as to transmit torque, includes a carrier sleeve on which at least one coupling component provided for coupling the handpiece shaft is attached such that the at least one coupling component can be brought to a coupled position and to an uncoupled position in the operating state, wherein the at least one coupling component can be brought into contact with an activation unit which is arranged between the carrier sleeve and to an outer actuation sleeve, wherein a rotation securing unit present inside the actuation sleeve acts on the activation unit in a spring-biased manner in the operating state such that the activation unit is held secure against rotation relative to the carrier sleeve.