Abstract: A guiding device is provided. An implantable apparatus includes a member to be anchored. A position-limiting wire is detachably connected to the implantable apparatus. A proximal end of the position-limiting wire is connected to the control handle. A distal end of the guiding catheter is provided with a guiding member. A distal end portion of the guiding catheter is bendable. A proximal end of the delivery catheter and a proximal end of the guiding catheter are respectively connected to the control handle. When the control handle is manipulated to make the guiding member on the guiding catheter move along the position-limiting wire toward the distal end, the distal end portion of the guiding catheter is bent and deformed, such that the distal end of the guiding catheter abuts against the member to be anchored of the implantable apparatus.

Abstract: A heart valve prosthesis anchored to an interventricular septum. The heart valve prosthesis includes a valve supporting frame and a fixing device. The valve supporting frame includes a valve stitching section and an artificial valve. The artificial valve is fixedly connected to the valve stitching section. The fixing device includes a fixing and supporting section and a fixing member. One end of the fixing and supporting section is connected to a proximal end of the valve stitching section, and another end of the fixing and supporting section is connected to the interventricular septum of a patient by the fixing member, to support the heart valve prosthesis and prevent the heart valve prosthesis from axially moving.

Abstract: A heart valve prosthesis anchored to an interventricular septum. The heart valve prosthesis includes a valve supporting frame and a fixing device. The valve supporting frame includes a valve stitching section and an artificial valve, and the artificial valve is fixedly connected to the valve stitching section; the fixing device includes a fixing and supporting section and a fixing member, one end of the fixing and supporting section is connected to a proximal end of the valve stitching section, and another end of the fixing and supporting section is connected to the interventricular septum of a patient by the fixing member, to support the heart valve prosthesis and prevent the heart valve prosthesis from axially moving.

Abstract: The present application relates to a transcatheter prosthetic valve replacement system including a delivery catheter, a frame, a prosthetic valve, and one or more clamping devices. The prosthetic valve is fixed in the frame. The clamping device is connected to a periphery of the frame. The frame and the clamping device can be preloaded in the delivery catheter. The clamping device includes a clamping member, a collar, and a control member. One end of the clamping member is a fixation end which is fixedly connected to the frame, and the other end of the clamping member is a deployable resilient segment which can be compressed and released. The collar is slidably sleeved on the clamping member. One end of the control member is connected to the collar, and the other end of the control member is manipulated outside the body. From being compressed to being fully released, the clamping member in sequence has two configurations.

Abstract: The present application relates to a stepwise-clamping type valve prosthesis including a frame body and a clamping member. The frame body has a channel allowing blood to flow therethrough. The clamping member includes a first clamping member and a second clamping member. One end of the first clamping member is connected to the frame body, and the other end of the first clamping member is a free end. The second clamping member is connected to the first clamping member. The clamping member has three states in sequence from being restricted to being fully released. In the first state, the first clamping member and the second clamping member are both restricted and restricted. In the second state, the second clamping member is restricted, and the first clamping member extends in a radial direction of the frame body and is capable of reaching a position between a valve leaflet and a heart wall.

Abstract: The present application relates to a separately releasable aortic valve stent, which includes a valve sewing segment, a positioning member, and a prosthetic valve. The prosthetic valve is connected to the valve sewing segment. The valve sewing segment and the positioning member are two independent components and connected to each other via a guiding device. The positioning member is able to be released prior to the valve sewing segment. A slide connection structure is disposed on the valve sewing segment. One end of the guiding device is connected to the positioning member, and another end of the guiding device passed through the slide connection structure is connected to the positioning member. The valve sewing segment is slidable along the guiding device.

Abstract: A heart valve prosthesis anchored to an interventricular septum. The heart valve prosthesis includes a valve supporting frame and a fixing device. The valve supporting frame includes a valve stitching section and an artificial valve. The artificial valve is fixedly connected to the valve stitching section. The fixing device includes a fixing and supporting section and a fixing member. One end of the fixing and supporting section is connected to a proximal end of the valve stitching section, and another end of the fixing and supporting section is connected to the interventricular septum of a patient by the fixing member, to support the heart valve prosthesis and prevent the heart valve prosthesis from axially moving.

Abstract: A method and an apparatus for pattern recognition is provided in the present invention, applied to the field of artificial intelligence. The method includes: acquiring a two-dimensional image of a target object and a two-dimensional feature of the target object according to the two-dimensional image of the target object; and acquiring a three-dimensional image of the target object and a three-dimensional feature of the target object according to the three-dimensional image of the target object; identifying the target object according to the two-dimensional feature and the three-dimensional feature of the target object. The method can reduce restrictions on acquiring the image of the target object, for example, reduce the restrictions on the image of the target object in terms of postures, lighting, expressions, make-up and occlusion, thereby improving an accuracy of recognizing the target object and improving a recognition rate and reducing recognition time at the same time.

Abstract: Provided is a detachable endoscopic clamp, related to medical apparatuses, which aims to solve the problem that the existing endoscopic clips are hard to remove and can only provide a weak clipping force. The detachable endoscopic clip includes at least two engagement members and at least two resilient members. Ends of the engagement members and ends of the resilient members from conjugates, and at least one of the conjugates is detachable. The endoscopic clip can be easily detached and removed after a surgery.

Abstract: Provided is a detachable endoscopic clamp, related to medical apparatuses, which aims to solve the problem that the existing endoscopic clips are hard to remove and can only provide a weak clipping force. The detachable endoscopic clip includes at least two engagement members and at least two resilient members. Ends of the engagement members and ends of the resilient members from conjugates, and at least one of the conjugates is detachable. The endoscopic clip can be easily detached and removed after a surgery.

Abstract: A magnesium phosphate bone cement includes a powder agent and a liquid agent. A liquid-to-solid ratio of the liquid agent to the powder agent is 0.1-0.5 ml/g. The powder agent comprises following components: phosphate accounting for 32-70 wt %, magnesium oxide accounting for 28-65 wt %, and silicon-containing compound accounting for 1-15 wt %. Preferably, the powder agent further comprises ammonium dihydrogen phosphate, and degradable and adhesion-promoting material, wherein the ammonium dihydrogen phosphate accounts for 5-30 wt % of a total weight of the phosphate.

Abstract: A method and an apparatus for pattern recognition is provided in the present invention, applied to the field of artificial intelligence. The method includes: acquiring a two-dimensional image of a target object and a two-dimensional feature of the target object according to the two-dimensional image of the target object; and acquiring a three-dimensional image of the target object and a three-dimensional feature of the target object according to the three-dimensional image of the target object; identifying the target object according to the two-dimensional feature and the three-dimensional feature of the target object. The method can reduce restrictions on acquiring the image of the target object, for example, reduce the restrictions on the image of the target object in terms of postures, lighting, expressions, make-up and occlusion, thereby improving an accuracy of recognizing the target object and improving a recognition rate and reducing recognition time at the same time.

Abstract: An interspinous process bracing system comprises an interspinous process brace and a delivery device. The interspinous process brace includes a flexible and foldable bag, and a filler. An injection opening is provided at a proximal end of the bag. The delivery device comprises a delivery tube. A distal end of the delivery tube is detachably connected to the injection opening. The filler can be injected, through the delivery tube and the injection opening, into the bag to expand the bag, forming the interspinous process brace. The system achieves interspinous process bracing through a minimally invasive surgery and thereby reduces injuries.

Abstract: A prosthesis (100) for preventing a valve regurgitation, comprising a fixation unit (110), a connection piece (120) and a closure assisting piece (130); the fixation unit (110) comprises a fixation piece (111) and an anchor (112); the connection piece (120) is flexible, and a distal section thereof is connected to a proximal section of the fixation piece (111), and a proximal section thereof is connected to a distal section of the closure assisting piece (130); the fixation piece (111) is fixed on the atrial wall or a valve ring of a patient via the anchor (112); the deployed width of the fixation piece (111) is less than two-thirds of the circumference of a valve tissue annulus; the closure assisting piece (130) is located between autologous valve leaflets of the patient when in a free state; the maximum width of the closure assisting piece (130) is less than the maximum deployed width of a single autologous valve leaflet; and the proximal end of the anchor (112) is provided with an anti-disengagement end (1

Abstract: An implant with anchoring device for heart valve disease comprises a cardiac valve prosthesis (1), at least two sets of anchoring needles (2) and at least two sets of anchoring needle releasing devices (3). Proximal end of the anchoring needles (2) are provided with anti-disengagement ends (23). The anchoring needle releasing devices (3) are detachably connected to the cardiac valve prosthesis (1). The anchoring needle releasing devices (3) comprise delivery tubes (31) and shafts (32). Distal sections of the anchoring needle releasing devices (3) are in preset shapes. The shafts (32) can be pushed to force the anchoring needles (2) to move toward the distal ends of the delivery tubes (31), so that the cardiac valve prosthesis (1) is fixed between autogenous tissue (6) and the anti-disengagement ends (23) to achieve accurate positioning and firm anchoring of the cardiac valve prosthesis (1).

Abstract: An interspinous process bracing system, comprising an interspinous process brace and a delivery device. The interspinous process brace includes a flexible and foldable bag (100), and a filler (200). An injection opening (110) is provided at a proximal end of the bag. The delivery device comprises a delivery tube (310). A distal end of the delivery tube (310) is detachably connected to the injection opening (110). The filler (200) can be injected, through the delivery tube (310) and the injection opening (110), into the bag to expand the bag, forming the interspinous process brace. The system achieves interspinous process bracing through a minimally invasive surgery and thereby reduces injuries.

Abstract: A prosthesis (100) for preventing a valve regurgitation, comprising a fixation unit (110), a connection piece (120) and a closure assisting piece (130); the fixation unit (110) comprises a fixation piece (111) and an anchor (112); the connection piece (120) is flexible, and a distal section thereof is connected to a proximal section of the fixation piece (111), and a proximal section thereof is connected to a distal section of the closure assisting piece (130); the fixation piece (111) is fixed on the atrial wall or a valve ring of a patient via the anchor (112); the deployed width of the fixation piece (111) is less than two-thirds of the circumference of a valve tissue annulus; the closure assisting piece (130) is located between autologous valve leaflets of the patient when in a free state; the maximum width of the closure assisting piece (130) is less than the maximum deployed width of a single autologous valve leaflet; and the proximal end of the anchor (112) is provided with an anti-disengagement end (1

Abstract: An implant with anchoring device for heart valve disease comprises a cardiac valve prosthesis (1), at least two sets of anchoring needles (2) and at least two sets of anchoring needle releasing devices (3). Proximal end of the anchoring needles (2) are provided with anti-disengagement ends (23). The anchoring needle releasing devices (3) are detachably connected to the cardiac valve prosthesis (1). The anchoring needle releasing devices (3) comprise delivery tubes (31) and shafts (32). Distal sections of the anchoring needle releasing devices (3) are in preset shapes. The shafts (32) can be pushed to force the anchoring needles (2) to move toward the distal ends of the delivery tubes (31), so that the cardiac valve prosthesis (1) is fixed between autogenous tissue (6) and the anti-disengagement ends (23) to achieve accurate positioning and firm anchoring of the cardiac valve prosthesis (1).

Abstract: The present disclosure relates to a vertebral balloon dilation system, comprising a rigid pushing tube (2), a balloon (1) made of membrane material and fixedly connected with a sealing head (11), a sleeve tube (3) sleeved on the pushing tube (2) and the balloon (1), and a liner core (4) slidably inserted into the pushing tube (2). When the vertebral balloon dilation system is operated, the sleeve tube (3) slides axially towards the proximal end of the pushing tube (2), and the balloon (1) is exposed. According to the present disclosure, the balloon (1) can be fed to the center or to the opposite side of the vertebral body simply by puncturing at only one side without drilling out a cavity in advance, thus simplifying surgical procedures, shortening duration of surgery, reducing the incidence of complications, alleviating the pain of patients and reducing the economic burden of patients.

Abstract: A bone idler implanting system comprises a bag (1) and a delivery device (2). A distal end of the bag (1) is fixedly connected to a sealing head (11); the sealing head is closed at its distal end and has a blind hole (111) at its proximal end, and the blind hole (11) has an opening towards the interior of the bag (1). The bag (1) has micro-pores (12). The delivery device (2) comprises a liner core (23), a delivery tube (21), and a sleeve tube (22). The delivery tube (21) is a rigid tube, and a distal end of the delivery tube (21) is detachably connected to a. proximal end of the bag (1). When the delivery device (2) is operated, the sleeve tube (22) slides axially towards the proximal end of the conveying tube (21), and the bag (1) is exposed.