5266 results about "Stent" patented technology

Apparatus and methods for an implant are provided. The implant may have a constrained configuration and a relaxed configuration. The implant may include an outer stent and an inner valve support. The inner valve support may be positioned within the outer stent. The implant may include a transition section spanning between the outer stent and the inner valve support.

The invention discloses a human body intravascular positioning support, and relates to the field of medical instruments. Comprising a metal wire support which is used for expanding in a blood vessel of a human body to dilate the blood vessel, a plurality of positioning units are arranged on the metal wire support, and each positioning unit comprises a spring and a penetrating type positioning head fixedly connected with the far end of the spring; the near end of the spring is fixedly connected with the metal wire support, and the penetrating type positioning head is used for penetrating into the inner wall of a blood vessel to achieve positioning when the metal wire support is unfolded. Through the design that the spring is combined with the positioning unit of the piercing type positioning head, the unification of stable fixing and safe taking-out of the intravascular positioning stent is achieved.

The invention discloses a whole-process vascular interventional operation training method and system based on a virtual reality technology, and the method comprises the steps: firstly, developing a vascular interventional mechanics and collision simulation module, and achieving the deformation simulation of a blood vessel and a guide wire through the combination of position dynamics, a region shape matching technology and a Cosseerat elastic rod model, the collision between the blood vessel and the guide wire is treated by adopting a wide-to-narrow three-layer progressive collision detection method; secondly, constructing an immersive virtual operation scene through model construction and rendering optimization; visual angle roaming, instrument operation and interface interaction are fused, and multi-mode interaction control driving intervention training is achieved; finally, based on a'module-event 'dual-drive framework, operation tasks such as anesthesia, puncture, radiography, intervention, stent release and hemostasis are sequentially connected in series through a unified state machine, and whole-process training is achieved. The accuracy and stability of blood vessel and guide wire simulation are improved, the training immersion sense is enhanced, interventional operation whole-process training is achieved, and high teaching and practical value is achieved.

A system for preparation of an implant and ab interno insertion of the implant into an eye including a handle having one or more actuators and an elongated shaft having an outer sheath and an elongate member positioned within a lumen of the tubular outer sheath. The system includes a recess sized for holding a patch of material fixed relative to the handle and a cutting member movable relative to the handle and to the recess. The cutting member cuts the patch of material into an implant as the cutting member moves towards a cutting configuration. The implant, once cut, is axially aligned with the lumen of the tubular outer sheath. The inner elongate member is movable relative to the tubular outer sheath to advance the implant into a deployment position in the lumen of the tubular outer sheath for delivery into the eye. Related devices and methods are provided.

The invention relates to the technical field of semiconductor device manufacturing, solves the technical problem that in the prior art, automatic grain digging treatment cannot be carried out on detected LED support defective products, and provides a grain digging control method, device and equipment for LED support defective products. Acquiring a real-time image of the to-be-detected LED bracket under a preset target illumination condition; performing visual detection processing on the real-time image, and judging whether the to-be-detected LED bracket is a defective bracket product or not according to a visual detection processing result; when the to-be-detected LED bracket is judged to be a defective bracket product, defect position detection is carried out on the defective bracket product to obtain defect position information; according to the defect position information, defective stent particles in the defective stent products are removed, and particle digging control over the defective stent products is achieved. According to the automatic grain digging device, automatic grain digging treatment can be accurately carried out on the LED support defective products.

The invention relates to a deep vein thrombectomy support device which has the advantage of being convenient to clean. The inner tube assembly comprises an inner tube, a conical head assembly and a limiting key, the inner tube and the handle assembly are matched in the mode that the inner tube can slide axially but cannot rotate relative to the circumferential direction, the conical head assembly is arranged at the far end of the inner tube, the limiting key is movably installed on the handle assembly, and the limiting key selectively acts on the inner tube; the middle tube assembly comprises a middle tube and a support fixing assembly, the near end of the middle tube is connected to the handle assembly, and the far end of the middle tube is connected with the support fixing assembly; the outer pipe assembly comprises an outer pipe which can be axially and movably arranged on the middle pipe in a sleeving manner; the thrombectomy stent assembly comprises a self-expansion stent and a woven mesh, the near end of the self-expansion stent is connected with the stent fixing assembly, the near end of the woven mesh is connected to the far end of the self-expansion stent, and the far end of the woven mesh is connected to the conical head assembly.

A prosthesis assembly includes a stent frame that is expandable and configured for being positioned in the ascending aorta, and a receiving socket positioned within a proximal end of the prosthesis assembly. The receiving socket defines a recess for allowing flowthrough of blood into the stent frame. The receiving socket is further configured for selectively receiving a heart valve assembly for replacing a native heart of a patient or maintaining a mode of operation where the socket is empty and blood flows through the socket into the stent frame.

The utility model discloses a stitching instrument for stitching an endoscope puncture hole. The stitching instrument comprises a handle part and two operating rods which are assembled on the handle part in a rotatable structure, the lower ends of the two operating rods are respectively provided with a convex needle connecting part, and the lower ends of the two operating rods extend out of the guide cylinder of the handle part; in the rotating action of the two operating rods, the needle connecting parts at the lower ends of the two operating rods are folded or unfolded; when the needle connecting parts of the two operating rods are in a folded state, the guide cylinder located at the handle part is in an axial storage coverage range of a trocar channel through which the guide cylinder needs to penetrate during surgical operation; the lower end of each operating rod is provided with a needle mounting base formed in an outward protruding mode, the needle mounting bases are connected with suture needles through detachable structures, and the suture needles are connected to the needle mounting bases in place to form an inflection assembly structure facing the handle part. According to the stitching instrument, the stitching operation is simplified, the stitching safety, flexibility and efficiency are improved, the forming structure of the stitching instrument is simplified, and the practicability is higher.

The invention provides a degradable combined type tracheal stent and an implantation method, the degradable combined type tracheal stent comprises a plurality of rib plates which are coaxially arranged and are in an annular shape and soft bodies which are connected between every two rib plates and are in a net shape, and axial length adjustability and axial bending deformation of a stent main body are achieved through the soft bodies; the support further comprises a connecting part, the connecting part comprises a first connecting body arranged at the two axial ends of the support body and a second connecting body matched with the first connecting body, and the first connecting body and the second connecting body are matched to achieve axial detachable connection and combination between every two support bodies. The adjustable axial length of the stent main body, bionic axial bending deformation and stable connection and combination between every two stent main bodies are effectively realized. The invention further provides an implantation method of the degradable combined type tracheal stent, the implantation method comprises the steps of obtaining the size of the diseased trachea, determining the diameter and the combination number of the stent body, sleeving the diseased trachea and connecting the combination to complete implantation, and the method is easy to operate and can meet different requirements of clinical complex environments.

The present disclosure relates to a massage apparatus including an arm massage part, the massage apparatus comprising: a frame connection part which connects a buttock frame provided in a main frame and a back frame provided in the main frame, and which rotates about a frame rotation axis on the basis of the movement of the back frame; a driving shaft which passes through the frame connection part and moves along an arc-shaped driving shaft slot on the basis of the movement of the back frame; and an arm massage frame holder which moves along a sliding rail on the basis of the movement of a plurality of links that transmit the movement of the driving shaft.

The invention relates to the field of medical instruments, in particular to an abduction assisting device for shoulder joints, which comprises a support, a support plate for bearing arms is hinged to the top of the support, and a driving mechanism, an adjusting mechanism, a fitting mechanism, a support mechanism and a locking mechanism are arranged on the support; the driving mechanism is used for driving the adjusting mechanism, the laminating mechanism and the supporting mechanism to operate synchronously; the adjusting mechanism is used for driving the supporting plate to rotate around the hinge point so as to adjust the abduction angle. The attaching mechanism comprises an air bag fixedly connected to the supporting plate, and the attaching mechanism is used for synchronously inflating or deflating when the angle is adjusted by the adjusting mechanism so as to be attached to the arm; the supporting mechanism is used for synchronously providing or releasing additional supporting force for the supporting plate when the adjusting mechanism adjusts the angle; the locking mechanism is used for locking the adjusting mechanism after angle adjustment is completed. The use process is simplified, the operation threshold is lowered, the rehabilitation preparation time can be saved, and the clinical use efficiency is improved.

The invention discloses a positioning support convenient to fix and safe to take out in a human blood vessel, and relates to the technical field of surgical operation medical instruments. According to the positioning support, a plurality of positioning thorns with tips are arranged on a metal wire support, and each positioning thorn comprises a metal inner wire and a coating layer; the inner metal wire is connected with a metal wire of the metal wire stent, the diameter of the inner metal wire is smaller than that of the metal wire of the metal wire stent, the coating layer is conical and is made of degradable materials, a preset distance is reserved between the tip end of the inner metal wire and the tip end of the coating layer, and a spiral part is formed in the middle of the inner metal wire; after the coating layer is degraded, the spiral part is changed into a stretching state from a compressed state, the metal inner wire penetrates into the blood vessel wall, and a preset gap is formed between the blood vessel wall surface and the surface of the metal wire stent. The support can be reliably fixed and safely taken out.

The invention provides a portal vein pressure adjusting support and a production method thereof, and belongs to the technical field of medical instruments.The adjusting support comprises a cylindrical support body, the support body is provided with a first section and a second section which are integrally arranged, and the side wall of the first section is provided with a film-shaped component used for sealing and isolating the outer side and an inner cavity of the support body; a pressure adjusting valve is arranged in an inner cavity of the first section, is opened for blood flow to pass through when the pressure in the portal vein is larger than a set threshold value, and is closed to cut off the blood flow when the pressure in the portal vein is smaller than the set threshold value; the stent can automatically adjust the opening and closing state of the shunt channel according to the portal vein real-time pressure, and ineffective shunt is reduced to the maximum extent while it is ensured that the portal vein pressure is reduced to a safe range, so that the occurrence risk of hepatic encephalopathy is reduced.

A stent device includes a stent formed in a tubular shape by weaving wires and a cover covering at least a part of the stent. The cover is partially bonded to parts rather than a whole surface of the stent.

The invention is applicable to the technical field of medical instruments, and provides a subskull epidural micro-invasive flexible brain-computer interface electrode, which comprises a plurality of electrode branches, each electrode branch comprises a linear flexible main body, and the flexible main body comprises a micro power supply circuit and a signal circuit which are solidified. A plurality of electrode units are arranged on the micro power supply circuit and the signal circuit at intervals, and the electrode units are electrically connected with the micro power supply circuit and the signal circuit. The brain-computer interface electrode is in a flexible line type, can be implanted into the middle artery of the meninx, does not need craniotomy, is a micro-invasive brain-computer interface, has data monitoring accuracy close to that of an invasive brain-computer interface, does not need to worry about inflammatory response, immunostimulation, biocompatibility, brain tissue damage and other adverse factors after long-term implantation, and is suitable for popularization and application. And the thrombogenic risk of a vein stent brain-computer interface does not exist.

The present disclosure provides apparatus and methods to both infer stent expansion (vessel expansion or compliance) and probability of procedural success (vessel patency) from pretreatment diagnostic imaging at the point-of-care and also train an inference model to generate such an inference, thus allowing a physician to choose with greater certainty an optimal treatment tool and treatment protocol for treating a vessel of a patient.

The present disclosure relates to a medicament delivery device comprising a housing having a proximal end and contains a container of medicament positioned within the housing in a medicament container holder. The medicament container can be dual chambered, for example a pre-filled medicament container having a needle, a dose of medicament and one or more sliding stoppers. The medicament container holder can be configured with a recess or pocket to accommodate the loading of a dual chambered container and interact with an inside surface of the housing to rotationally fix the container holder relative to the housing and the medicament container. A tubular activation member, e.g., a needle cover, is slidably positioned within a housing of the delivery device to move from a first position to a second position, and then to a final locked position. A plunger rod can only move proximally relative to the needle cover when the needle cover is in the second position.

The invention provides a medical implant, a preparation method thereof and an artificial knee joint. The medical implant comprises a macromolecular porous stent and a hydrogel composite material at least filled in pores of the macromolecular porous stent, and the material of the macromolecular porous stent comprises a degradable macromolecular material and carbon nanotubes distributed in the degradable macromolecular material. The hydrogel composite material comprises a hydrogel material matrix and seed cells distributed in the hydrogel material matrix. According to the invention, the degradable high polymer material and the hydrogel material are combined, the carbon nanotubes are introduced into the degradable high polymer material, and meanwhile, seed cells are arranged in a hydrogel material matrix, so that the implantable stent material which has proper degradation performance and good mechanical properties and is renewable is provided.

The invention relates to a self-expanding stent delivery device and a system comprising the same. The self-expanding stent conveying device comprises a pushing rod; the radial force storage structure extends in the axial direction and is arranged at the far end of the pushing rod, and an inner cavity extending in the axial direction is defined in the radial force storage structure; the positioning line extends in the axial direction and penetrates through an inner cavity of the radial force storage structure; the positioning line is in a natural state; the fixing components are at least arranged at the near end and the far end of the positioning line effective area, and the near end and the far end of the positioning line effective area are fixed to the cavity walls of the inner cavities at the near end and the far end of the radial force storage structure respectively. Through cooperative cooperation of the radial force storage structure, the positioning line and the fixing part, while the auxiliary expansion effect on the self-expanding stent is ensured, displacement of the fixing part possibly caused by release of the radial force storage structure is effectively restrained, and therefore reliable conditions are provided for accurate release of the self-expanding stent.

Provided in the present invention is a vertical assembly and swivel construction method for an arch rib. The vertical assembly and swivel construction method comprises the following steps: constructing a lowering cable fixing foundation and a guy cable fixing foundation; vertically assembling arch rib segments, and mounting and pre-tightening a lowering cable and a guy cable; and performing swivel construction, which comprises coordinatively adjusting the lengths of the lowering cable and the guy cable, such that the lower end of the arch rib segments take a rotatable structure as the axis, and the upper portion of the arch rib segments rotates downwards to reach a design position. By using the construction method of the present invention, swivel construction of an arch rib can be completed without the need to set up a support in water; thus, the impact on channel passage and flood discharge can be avoided, and the construction period is also effectively shortened.

The utility model discloses a breast shield with support brackets, belonging to the technical field of electric breast pumps. The exterior of the breast shield features several brackets of the support members, with the head portion of each support member embedded into the front end of the breast shield and the tail portion embedded into the rear end of the breast shield. The integration of the head portion and tail portion of the support members with the breast shield adopts an overmolding process, embedding the head portion and tail portion into the overmolding regions of the head portion and tail portion of the support member of the breast shield, respectively, forming an inseparable assembly with the breast shield. Compared with prior art, the breast shield offers superior structure and stability, and has lower manufacturing requirements and reduced costs. During use, it is not easy for users to experience separation, detachment, etc.

A delivery system for delivering an implant having both a rigid portion and a flexible portion to a body lumen. The delivery system includes an outer tubular member and an inner tubular member slidably disposed within the lumen of the outer tubular member. The inner tubular member includes at least one opening positioned in a side wall adjacent to a distal end region. An expandable implant, including a rigid portion and a flexible portion, is disposed about the outer surface of the inner tubular member. A distal portion of a thread is wrapped around the flexible portion of the implant and configured to maintain the flexible portion in a radially collapsed configuration during delivery of the implant. A distal end region of the outer tubular member is disposed around the rigid portion of the implant to maintain the rigid portion in a radially collapsed configuration during delivery of the implant.

The invention discloses a biological scaffold viscoelasticity evaluation method and related equipment, and aims to overcome the defects of an existing biological scaffold viscoelasticity test method and biological tissue suitability quantitative evaluation. The method comprises the following steps: determining a target implantation part, and acquiring force relaxation experimental data of a biological scaffold by using an atomic force microscope; judging a contact point of the probe and the bracket based on the data; determining the moment when the force signal is stable after the support is compressed to the preset deformation according to the contact point as a force relaxation starting point; calculating the characteristic time when the force value is attenuated to half by taking the starting point as a timing starting point as a microscopic viscoelasticity index; and finally, realizing quantitative evaluation of viscoelasticity suitability by comparing the characteristic time of the stent and the target tissue.

A stent, such as transluminal stent, is disclosed. The stent includes a tubular member with a proximal end, a distal end, and a central portion therebetween. The elongate tubular member comprises a scaffolding forming a plurality of cells and defining a lumen of the elongate tubular member. A proximal portion of the tubular member forms a retention member, wherein the diameter of the retention member is greater than the diameter of the central portion, and wherein a proximal end of the retention member includes an area of increased scaffolding density.

The application provides an extendable digestive tract cannula and application thereof, and relates to the technical field of medical devices. The application comprises a first cannula, a second cannula and a degradable material. Opposite ends of the first cannula are a proximal end and a distal end, respectively. The first cannula is sleeved with the second cannula, and a double-layer structure is formed at the distal end of the first cannula. The double-layer structure is fixed by the degradable material. When the degradable material degrades, the second cannula moves towards the end face of the distal end of the first cannula. By setting the movable second cannula, the second cannula moves backward after the degradable material degrades, so that the length of the digestive tract cannula is extended. Since the length of the digestive tract cannula is increased, the area of intestinal absorption is also increased, the compensatory absorption function of the intestine at the distal end of the digestive tract cannula is weakened, the isolation effect of chyme and the intestine is improved, and the digestion and absorption effect of the intestine can be reduced for a long time.

The microneedle assembly of the present invention includes: a main body (110) opened at one side thereof and including a solution reservoir (111) formed in the opened side thereof; a dispensing unit (120) disposed at the other side of the main body (110) in such a manner as to fluidically communicate with the solution reservoir (111); a needle supports (130) positioned at a front portion of each of the dispensing units (120), and protrudingly formed at the other end of the main body (110); a microneedles (140) engaged with the front end of the needle support (130); and a first solution release flow channel (150) formed to penetrate through a portion extending outwardly from a front end of the dispensing unit (120) to the front end of the needle support (130).

A delivery device for percutaneously delivering a stented prosthetic heart includes a sheath, a handle, and adjustment device including a fine adjustment mechanism, and an outer stability shaft. The sheath defines a lumen and is configured to compressively constrain the stented prosthetic heart valve. The handle is coupled to the proximal portion of the sheath and includes an actuator mechanism coupled to a proximal portion of the sheath that is configured to selectively move the sheath relative to the housing to release the stented prosthetic heat valve. The adjustment device is coupled to the handle and includes an adjustment lumen through which the sheath and the handle slidably extend. The outer stability shaft is coupled to the adjustment device. The fine adjustment mechanism is configured to selectively move the handle and the sheath relative to the adjustment device and the outer stability shaft.

The present invention relates to apparatus for stabilisation of tremors, both physiological and pathological, of parts of the body, especially the hands. We describe an apparatus for reducing effects of tremors on an area of the human body, the apparatus comprising a gyroscope device and an attachment assembly for attachment of the gyroscope device to a location on the human body in the area, wherein the attachment assembly provides a substantially inelastic attachment to the location and comprises a gyroscope mount. The gyroscope mount comprises a substantially stiff first plate having a shape adapted to substantially correspond with a shape of the human body in the location. In preferred embodiments, the attachment assembly further comprises a second plate mountable to the body such that a clamping force is appliable between the first plate and the second plate.

The invention relates to the technical field of arthroscopic surgery instruments, in particular to a support for a sports medicine arthroscopic surgery, which comprises a support, a lifting platform and a leg fixing mechanism, and the lifting platform locks the height position of the leg fixing mechanism on the support through a limiting bolt; the leg fixing mechanism comprises a fixed frame fixedly connected with the lifting table and a movable frame hinged through a rotating connector. The pull rope is wound around the guide wheel in the sliding rail box to be connected with the shank binding belt, and when the knee joint bends and stretches, the second spring pushes the sliding block to move in a self-adaptive mode; during knee bending, the spring extends to compensate looseness of the pull rope; when the knees stretch, the springs are compressed to absorb redundant tension. The tensile force is always perpendicular to the shank axis through mechanical decomposition, and lateral shearing force is eliminated. A spring dynamic compensation mechanism maintains constant upward effective component force, pulling force direction deviation caused by a traditional fixed fulcrum is avoided, unexpected internal rotation during shank lifting is fundamentally restrained, and knee joint ligaments are protected against abnormal stress damage.