Abstract: A rotablator apparatus (10), comprising a rotablator assembly (11), a drive shaft (12), a liquid passing pipe (14), and a liquid pumping part (15). A distal end of the drive shaft (12) is connected to the rotablator assembly (11) and is used for driving the rotablator assembly (11) to rotate. The liquid passing pipe (14) is sleeved on the drive shaft (12), and the liquid passing pipe (14) is provided with a liquid passing cavity (141). The liquid pumping member (15) is in transmission connection with the drive shaft (12), and driven by the drive shaft (12), can convey liquid to the far end of the liquid passing pipe (14) by means of the liquid passing cavity (141).

Abstract: An electrode balloon catheter includes a catheter body (1), an outer balloon (2), an inner balloon (3) and electrode pairs (4). The electrode pairs (4) are arranged on a surface of the inner balloon (3), and both the inner balloon (3) and the outer balloon (2) are provided at an end of the catheter body (1). The inner balloon (3) is located inside the outer balloon (2). The outer balloon (2) is configured to store a conductive medium. The electrodes can be adjusted to desired positions by manipulating the inner balloon (3). This enables adjustability in an energy propagation distance, which eventually results in enhanced lesion treatment efficiency, reduced surgical duration and an extended service life of the electrodes.

Abstract: An electrode balloon catheter and a high-voltage generation processing device are provided. The electrode balloon catheter includes a balloon, an inner catheter and a shock wave generation component. The balloon is disposed over the inner catheter and radially expands or collapses as a result of filling an inflation fluid therein or evacuating the inflation fluid therefrom. The shock wave generation component includes a flexible circuit layer and an electrode arrangement. The flexible circuit layer is disposed on the inner catheter, and the electrode arrangement is provided on the inner catheter to be located within the balloon. The electrode arrangement is connected to the flexible circuit layer and connected to a high-voltage generation processing device via the flexible circuit layer. The flexible circuit layer enables the electrode balloon catheter to have a reduced passage size closer to the size of a pre-dilation balloon.

Abstract: A method of preparing an antibody carrying a universal site-directed coupling interface based on a genetically modified vertebrate is described. The method of constructs a vertebrate model, the vertebrate model is used to produce an antibody carrying a universal site-directed coupling interface. The method includes site-directly knocking in a coding gene of a specific recognition sequence of a certain ligase A or a coding gene of a certain intein A at a certain position A of a certain coding gene A of the immunoglobulin in the genome of the recipient animal, to obtain the vertebrate model. The modified mice can normally stimulate immune responses, produce a polyclonal antibody and a monoclonal antibody with a site-directed linking site. Antibodies with a site-directed linking site can normally carry out site-directed linking, and add various application groups to realize downstream applications of antibodies, such as ELISA, immunofluorescence staining, and immuno-PCR.

Abstract: A rotator cuff balloon (10) includes a limiting structure (100) and a protective structure (200) connected to the limiting structure (100). The limiting structure (100) has a curvature along a coronal plane (102). This rotator cuff balloon (10) conforms to the physiological structure of the shoulder joint in the human body, limits itself in the subacromial space and can reduce a patient's foreign body sensation, dislocation, functional failure and other adverse events. The protective structure (200) is configured to be supported in the space between the humeral head and the acromion of the shoulder joint in the human body to provide support. Moreover, the humeral head of a patient with a rotator cuff injury is raised, avoiding pain arising from inter-tissue collisions, increasing the moment arm of the deltoid muscle and resulting in immediate improvements in the functions of the patient's shoulder joint.

Abstract: Disclosed are a self-switching transmission assembly, a balloon, and a prosthesis for use in a shoulder joint. The self-switching transmission assembly comprises: a communicating tube (11, 11?, 11?) comprising an input end (111, 111?, 111?) and an output end (112, 112?, 112?); an external connection tube (12, 12?, 12?), an end portion thereof being insertable into the communicating tube (11, 11?, 11?) from the input end (111, 111?, 111?) and removable from the communicating tube (11, 11?, 11?) from the input end (111, 111?, 111?); and a sealing tube (13, 13?, 13?), which can be placed in a tube body of the communicating tube (11, 11?, 11?) and moved axially relative to the tube body of the communicating tube (11, 11?, 11?).

Abstract: A rotator cuff balloon (10) is disclosed, the rotator cuff balloon (10) includes a limiting structure (100) and a protective structure (200) connected to the limiting structure (100). The limiting structure (100) defines a curvature along a coronal plane. The rotator cuff balloon (10) conforms to the physiological structure of the human shoulder joint limits itself in the subacromial space and can reduce a patient's foreign body sensation, dislocation, functional failure and other adverse events.

Abstract: A drive shaft (1, 3) for use with a rotation device (10, 20) includes an outer layer (11, 31) and an inner layer (12, 32). The outer layer is a tubular structure, and the inner layer is accommodated in a space defined by the outer layer and defines a central lumen (13, 33) for receiving therein an external mechanism. The outer layer is rotatable about the central lumen, and the inner layer is rollable relative to both the outer layer and the external mechanism and thus allows rolling friction to occur between the drive shaft and the external mechanism. Such a structure of the drive shaft can reduce friction between the drive shaft and a guidewire as well as loss due to such friction, avoiding failure of the guidewire due to excessive friction between the guidewire and the drive shaft. Therefore, it is ensured that the drive shaft is suitable for use with guidewires commonly used in clinical practice, resulting in improved surgical operability and lower surgical cost.

Abstract: The present disclosure relates to a rotational atherectomy device and a medical device including the rotational atherectomy device. The rotational atherectomy device includes a drive shaft and a rotational atherectomy component connected to the drive shaft. The rotational atherectomy component includes a base and a rotational atherectomy block. The rotational atherectomy block is relatively movably assembled on the base. When the rotational atherectomy component rotates, the rotational atherectomy block moves in a direction away from the base.

Abstract: A display substrate includes: a base substrate, as well as a first metal layer, a first insulating layer, a second metal layer, a second insulating layer, and a common electrode metal layer laminated on one side of the base substrate. The common electrode metal layer includes metal line segments and connecting line segments. The metal line segments include first metal line segments and second metal line segments. The connecting line segments connect the adjacent first and second metal line segments. Each connecting line segment is provided with a maintenance line segment. Orthographic projections of the maintenance line segments on the base substrate do not overlap those of gate lines and data lines on the base substrate. The spacing between the orthographic projections of the maintenance line segments and those of the gate lines and data lines is greater than or equal to a preset distance, which is greater than zero.

Abstract: A display substrate includes: a base substrate, as well as a first metal layer, a first insulating layer, a second metal layer, a second insulating layer, and a common electrode metal layer laminated on one side of the base substrate. The common electrode metal layer includes metal line segments and connecting line segments. The metal line segments include first metal line segments and second metal line segments. The connecting line segments connect the adjacent first and second metal line segments. Each connecting line segment is provided with a maintenance line segment. Orthographic projections of the maintenance line segments on the base substrate do not overlap those of gate lines and data lines on the base substrate. The spacing between the orthographic projections of the maintenance line segments and those of the gate lines and data lines is greater than or equal to a preset distance, which is greater than zero.

Abstract: A balloon dilation catheter, a balloon (10) and preparation method therefor. The balloon (10) is prepared by co-mixing at least two of L25, TR55, TR90, and TR70, and has high puncture resistance and low compliance with respect to a balloon (10) made of a single nylon material. The balloon (10) is preferably a hollow multilayer structure, and the puncture resistance of the balloon (10) can be further improved and the compliance can be further reduced with respect to a single-layer structure.