30257 results about "General surgery" patented technology

The invention discloses a thrombus excision system. An embolus is extracted through a mechanical embolus extraction device, a blood vessel is dredged, and revascularization of the blood vessel is achieved. A saccule guide catheter is put at the near end of the embolus part when the embolus is extracted, blood flow is temporarily blocked, and thus a fine crushed embolus generated in the embolus extraction process is prevented from being flushed to the far end of the blood vessel; meanwhile, for a relatively large embolus, a part of thrombus can also be sucked by virtue of the saccule guide catheter, and then the residual thrombus can be extracted by virtue of a thrombus exsector. The thrombus exsector, the saccule guide catheter and a delivery microcatheter are arranged on the thrombus excision system disclosed by the invention, wherein the thrombus exsector is used as a main component, an excision spring is arranged, and the release state of the excision spring is a conical spiral state. Compared with the prior art, the thrombus excision system has the advantages that the thrombus exsector is very soft, the minimal through size is 0.014' (0.36mm), the thrombus exsector can easily enter a cerebral vessel, a near-end protection technology is adopted in the operation process, and thrombus suction is combined with mechanical embolus extraction, so that the success rate of the operation is improved, and the complications are reduced.

In some implementations, a low dead space airway adapter for sampling fluid flowing through a ventilation assembly includes an outer wall configured to couple to an endotracheal (ET) tube adapter and an internal projection positioned at least partially within an internal cavity defined by the outer wall and configured to extend within an internal cavity of the ET tube adapter when the airway adapter is in use. The internal projection can include a fluid passageway configured for fluid communication with at least a portion of the internal cavity of the ET tube adapter and a free end comprising an opening in fluid communication with the fluid passageway. At least a portion of the free end can be chamfered around the opening and configured to contact an inner surface of the ET tube adapter when the outer wall is coupled to the ET tube adapter.

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.

In an embodiment, a cryoablation probe includes a shaft, where the shaft has a supply tube, a return tube surrounding the supply tube, an insulated portion, wherein a vacuum circuit runs through the insulated portion between the return tube and an insulating shaft, and an expansion chamber extending distally to the insulated portion. The probe further includes a distal tip configured to seal a distal end of the return tube. The distal tip has a tip portion extending distally from the distal end of the return tube and a plug portion configured to be inserted inside of the return tube. The probe includes a compressive element surrounding the return tube and the plug portion of the distal tip, configured to seal the distal tip to the return tube.

A patient specific instrument is disclosed for correcting a condition present in a patient. The patient specific instrument includes a body that includes an inferior side having a bone engagement surface shaped to match a first surface of a first bone and a second surface of a second bone of a joint. The instrument also includes a superior side having a first guide feature and a second guide feature that together, with the bone engagement surface overlying the first surface and the second surface, are positioned to guide resection of the first bone and the second bone during a surgical osteotomy for correcting the condition. The body is configured to seat transverse to the joint with the bone engagement surface engaging the first surface of the first bone and the second surface of the second bone.

The present application discloses a shapewear garment comprising an upper portion, comprising a front panel and a back panel, the front panel at least partially cover an abdominal region of a wearer when worn, and the back panel at least partially cover a lower back region of the wearer; a pants portion connected to the upper portion and located below the upper portion, the pants portion extend at least around a crotch and buttocks region of the wearer; and an abdominal compression panel disposed in a stacked arrangement with the front panel and joined thereto, the abdominal compression panel at least partially cover the abdominal region of the wearer.

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.

A pill container has a body, at least one lid, and at least one elastic assembly. The body comprises a first wall, a second wall, and at least one compartment. The first wall and second wall are two opposite sides of the body. The compartment is located between the first wall and the second wall. The lid is pivotably mounted on the second wall of the body. The elastic assembly is located on the second wall, and has a flexural segment and a first protruding section. The first protruding section is located on the flexural segment and contacts the second wall. The first protruding section supports a space between the flexural segment of the elastic assembly and the body.

An introducer can include an introducer needle and an introducer sheath having a transition therebetween that eases tissue over a distal end of the introducer sheath without catching tissue thereon tissue despite an excised portion of the introducer needle. The introducer needle can include a needle shaft having a longitudinal needle slot extending from a proximal portion of the needle shaft through a distal needle tip, which results in an excised portion of a heel of a bevel of the needle tip. The introducer sheath can include a sheath body and a tapered sheath tip. The sheath body can be over the needle shaft sealing the needle slot thereunder but for a sheath-body opening in a proximal portion of the sheath body for an access guidewire. The introducer can include the transition from the bevel of the needle tip to at least the taper of the sheath tip.

A fluidics system includes a cassette having a saline subsystem, a contrast subsystem, and a vacuum subsystem. The fluidics system further includes a splitter and a first tubing set coupled to the cassette and splitter, the first tubing set having a single saline channel, a single contrast channel, and a single vacuum channel. The fluidics system further includes two or more hub assemblies, at least one of the two or more hub assemblies configured to have a third saline flow-path, a third contrast flow-path, and a third vacuum flow-path to provide saline, contrast and vacuum to the lumen of a catheter coupled to the at least one of the two or more hub assemblies. The fluidics system further includes a second tubing set having a plurality of tube groups, each tube group coupled to the splitter and to one of the two or more hub assemblies.

A quick-fill pill organizer has a box, multiple retrieving covers, and a packaging cover. The box has multiple compartments. Each compartment has a retrieving opening and a packaging opening. The retrieving cover is mounted on the retrieving opening and corresponds to the compartment one-to-one such that the corresponding compartment connects to or is blocked from the outside. The packaging cover is mounted on the packaging openings such that all the compartments connect to or are blocked from the outside at the same time. When the retrieving openings are upward, the retrieving cover of the specific compartment can be opened. When the packaging openings are upward, the packaging cover can be opened or closed such that all of the compartments connect to or are blocked from outside at once.

A urinary drainage system includes an air pressure apparatus. The air pressure apparatus includes a connector and an adapter. The connector includes a reduced diameter portion, a connector lumen extending from an upstream opening to a downstream opening in the reduced diameter portion, and a lateral port configured for drawing a fluid sample from the connector lumen. The adapter is sealing coupled to the connector and includes an adapter lumen receiving the reduced diameter portion, the downstream opening in fluid communication with the adapter lumen. A luminal space is defined in the adapter lumen around the reduced diameter portion of the connector. The adapter further includes an air intake port including a port lumen orthogonal to the adapter lumen, which is configured to provide a positive air flow to the luminal space to draw a fluid through the downstream opening in the reduced diameter portion of the connector.

A device may include a flexible tube comprising: a distal end, a proximal tip, the proximal tip comprising a suction line extension being configured for placement in a uterine cavity of a uterus after childbirth, a tube center of the flexible tube; and at least one lumen around the tube center, the at least one lumen comprising a suction line, the suction line being in communication with a source of negative pressure and the suction line extension, the suction line extension being configured for applying the negative pressure to the uterine cavity using the source of the negative pressure thereby causing mechanical hemostasis of bleeding blood vessels of a uterine wall of the uterine cavity. Embodiments include an anchoring mechanism being proximate to the suction line extension along the flexible tube, the anchoring mechanism being configured for maintaining the suction line extension in a desired position within the uterine cavity.

Rapidly insertable central catheters (“RICCs”), introducers, and insertion devices including combinations and methods thereof are disclosed. For example, a RICC system can include an introducer and a RICC insertion assembly including a RICC assembly disposed in a RICC insertion device. The RICC assembly can include a RICC, an access guidewire, and a splittable casing over a catheter tube of the RICC and the access guidewire forming a longitudinal composite. The RICC insertion device can include a frame and a nose cover forming a split channel that splits away from a through channel of a nose of the frame. The RICC insertion device can be configured for advancing the RICC assembly by rolling the longitudinal composite across roller wheels disposed in the frame. The through channel can be configured for advancing the catheter tube therethrough while the split channel can be configured for both splitting and passing the splittable casing therethrough.

A wand for a blind assembly comprising (a) an elongated member, (b) a rotatable member located at or adjacent one end thereof, (c) guide member located at or adjacent another end thereof; and (d) a cord having a loop, wherein the loop passes from a position remote from the rotating member, engages the rotating member, passes about the guide member and returns to the remote position after reengagement of the rotating member, wherein the loop adjacent to or within the elongated member is retained between the rotating member and the guide to restrict movement of the loop perpendicularly of the elongated member, and wherein the loop remote from the rotating member is adapted to engage and rotate a drive member of a blind assembly.

An introducer can include an introducer needle (134) and an introducer sheath (136) having a transition therebetween that eases tissue over a distal end of the introducer sheath without catching tissue thereon tissue despite an excised portion of the introducer needle. The introducer needle can include a needle shaft (140) having a longitudinal needle slot (146) extending from a proximal portion of the needle shaft through a distal needle tip (144), which results in an excised portion of a heel of a bevel (150) of the needle tip. The introducer sheath can include a sheath body (162) and a tapered sheath tip (170). The sheath body can be over the needle shaft sealing the needle slot thereunder but for a sheath-body opening (166) in a proximal portion of the sheath body for an access guidewire.

A method of preparing and / or delivering an osteochondral plug may include, positioning a tissue graft on a cutting guide, wherein the tissue graft may have been removed from a larger body of tissue to define a shaped surface. The tissue graft may include a top surface having a cartilage surface. The method may further include advancing a first cutter along a cutting direction toward the tissue graft to cut the tissue graft to form the osteochondral plug having an external wall parallel to the cutting direction and transverse to the top surface. Positioning the tissue graft on the cutting guide may include placing the shaped surface on a registration surface of the cutting guide. The registration surface may have a reference shape that corresponds to a shape of at least part of the shaped surface.

The present invention relates generally to improved systems and methods for removing undesirable material residing in vessels. More specifically, the present invention relates to systems and methods for using at least one cannula to remove substantially en bloc, from a site of obstruction or interest, undesirable material without fragmentation and without excessive fluid loss.

Various implementations include a sheath system and corresponding expandable introducer. The system includes an elongated introducer body and an elongated core member received within the central lumen of the introducer body. A portion of the introducer body expands in response to the outwardly directed radial force exerted on the central lumen of introducer body by the core member as it moves between the unexpanded and expanded positions.

A pill dispenser includes a dispenser body, a pill dispensing cover, and a pill outlet cover. The dispenser body is hollow. A fixed cylinder is disposed at a center of the dispenser body. Partition plates are connected between the fixed cylinder and the dispenser body to define pill cavities. The partition plates are disposed in a circumferential array. At least one end of each of the partition plates extends out of the dispenser body. Clamping grooves are defined in the pill dispensing cover. A periphery of each of the partition plates is clamped in a corresponding one of the clamping grooves, so the pill dispensing cover is fixed to the dispenser body. The pill dispensing cover includes pill dispensing openings one-to-one corresponding to the pill cavities. When the pill dispensing cover is fixed to the dispenser body, each of the partition plates abuts against the pill dispensing cover.

The present invention provides a dry powder inhaler comprising: one or more doses of powdered medication; an outlet through which a user may inhale a dose of medication; an airway comprising a vortex chamber having a wall, an exit, a powder inlet channel, and optionally one or more bypass inlet channels, wherein the powder inlet channel and or the bypass inlet channels are tangential to the wall. A mesh is located at the exit of the vortex chamber. The mesh is formed from circumferential elements and radial elements which together define a plurality of openings. When a user inhales on the outlet, medication is entrained in an air flow and flows through the vortex chamber and the mesh in the airway and out through the outlet.

The present application relates to a kind of snare cutting knives for endoscope, including proximal handle, tube body assembly, cutting assembly and limiting component;Proximal handle is equipped with limiting sliding slot;The proximal end of tube body assembly is connected with proximal handle, and the distal end of tube body assembly is equipped with insulating protection tube;Cutting assembly includes cutting ring and cutting head, and cutting head is set to the distal end of cutting ring;Limiting component includes sliding part and limiting control wire, sliding part is slidably arranged in limiting sliding slot, and the proximal end of limiting control wire is fixedly connected with sliding part, and sliding part is used to drive limiting control wire axial movement;When limiting control wire moves to the distal end of insulating protection tube, cutting head and insulating protection tube abut each other and are fixed;When limiting control wire exits insulating protection tube, cutting head can continue to move relative to insulating protection tube.

An intracardiac echocardiography (“ICE”) catheter handle, including a housing having a longitudinal axis, the housing having a proximal end and a distal end. A first actuator can be positioned on a first portion of the housing in a plane aligned with the longitudinal axis, the first actuator coupled to a first controller, the first actuator and first controller configured to control a catheter coupled to the first controller in a first direction and a second direction in the first plane. A second actuator can be positioned on a second portion of the housing in a second plane aligned with the longitudinal axis, the second actuator coupled to a second controller, the second actuator and second controller configured to control a catheter coupled to the second controller in a third direction and a fourth direction in the second plane, wherein first plane is aligned orthogonally to the second plane.

The invention discloses a bending-adjustable catheter, and relates to the technical field of interventional medical instruments, the bending-adjustable catheter comprises an inner tube, an outer tube, a bending-adjustable supporting tube and a handle, the inner tube comprises an inner tube bending section located at the far end, the inner tube bending section can be bidirectionally bent, and the inner tube bending section at the far end of the inner tube extends outwards from the outer tube; position anchoring of the outer pipe can be achieved through the anchoring structure; the far end of the bending adjusting supporting pipe is connected with the bending adjusting section of the inner pipe, the far end of the outer pipe is fixed to the bending adjusting supporting pipe, and the elasticity modulus of the bending adjusting supporting pipe is smaller than that of the inner pipe. The handle is provided with an inner pipe pushing piece. When the outer tube is anchored to the inner wall of a blood vessel, axial acting force is applied to the inner tube through the inner tube pushing piece, the inner tube control bending section is bent under the action of the axial acting force and supporting force applied by the bending adjusting supporting tube, large-angle bending adjusting can be achieved at the far end of the inner tube, overall rotation of the inner tube and the outer tube is matched, and the far end of the inner tube can rotate in a three-dimensional space. The bending of the adjustable-bending catheter in any direction is realized, and the adjustable-bending catheter can better pass through a roundabout blood vessel.

A system that includes a workpiece and a robotic gripper apparatus. The workpiece includes a pair of opposed first retention features. Each first retention feature includes a first proximal end, a first distal end, and an outer periphery. The pair of opposed grippers are moveable between a first position in which the pair of opposed grippers engage the pair of opposed first retention features. Each gripper includes a mounting feature having a second proximal end, a second distal end, and an inner periphery. When the pair of opposed grippers are in the first position, a first portion of the inner periphery near the first proximal end engages a first portion of the outer periphery near the second proximal end and a second portion of the inner periphery near the first distal end is separated from a second portion of the outer periphery near the second distal end.

A hair care appliance is provided. The hair care appliance includes a handle and a body coupled to the handle via a rotational hinge joint. The body can be movable via the rotational hinge joint between a straight configuration in which the body is aligned with a longitudinal axis of the handle and a bent configuration in which the body extends along an axis transverse to the longitudinal axis of the handle. A fluid flow path extends between an inlet in the handle and an outlet in the body. The hair care appliance can be operated with minimal loss of fluid flow in either the straight configuration and the bent configuration. The hair care appliance includes a fan assembly in the handle and a heater assembly in the body that are positioned to create a balanced center of mass of the hair care appliance when operated by a user.

A method of extracting a thrombus from a thrombus site in a cerebral artery of a patient by advancing a first catheter into an internal carotid artery of the patient; advancing a funnel catheter within the first catheter; moving the funnel catheter and the first catheter with respect to each other to place the funnel outside of the first catheter; expanding the funnel into contact with an inner wall of the internal carotid artery at or proximal to a distal end of a carotid siphon, thereby reducing blood flow past the funnel; advancing a clot-mobilizer distally through the first catheter toward the thrombus and beyond the carotid siphon; engaging thrombus material from the thrombus with the clot-mobilizer; moving the clot-mobilizer and thrombus material proximally at least partially into the funnel; applying suction to aspirate thrombus material; and moving the funnel, the clot-mobilizer and the thrombus material proximally within the vasculature.

Systems for producing a cosmetic effect in skin tissue of a patient are provided. The systems include a treatment module and an actuation assembly. The treatment module includes at least one coring element configured to remove a portion of skin tissue when the coring element is inserted into and withdrawn from the skin tissue. The actuation assembly is operably attached to the treatment module and can translate and / or actuate the treatment module in one or more directions relative to a surface of the skin tissue. The system can perform a microcoring procedure that provides a cosmetic effect to the patient. Methods of performing a microcoring procedure are also provided.

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.

Disclosed herein is a catheter, which in some embodiments includes a distal section configured to enter a skin insertion site. The distal section can include a tapered junction having one or more dilation structures configured to dilate the skin insertion site. The distal section can further include a distal portion extending from a distal end of the tapered junction, the distal portion having a diameter smaller than a proximal portion of the catheter. In combination, the tapered junction, the one or more dilation structures, and the specific actions of the user urging the catheter into the insertion site can result in an improved fit of the catheter in the insertion site.