Abstract: A tampon including a pledget, a wicking member disposed in direct contact with the pledget, and a withdrawal cord is disclosed. The wicking member is non-coaxially arranged with respect to the withdrawal cord.

Abstract: Systems and methods for treating cellulite including an apparatus that applies or a method involving disrupting, stretching, re-orienting or tearing septa to eliminate or reduce the appearance of cellulite. In one approach, an expandable member is placed between tissue layers to stretch or tear septa connecting tissue layers between which fat deposits are contained.

Abstract: A nasal mucus suction device includes an air pump and a head structure. The air pump has an intake tube and an outlet tube. The head structure is coupled to the intake tube and the outlet tube of the air pump, and defines a channel between a nasal mucus suction inlet and a gas outlet. The channel includes a first channel section in communication with the nasal mucus suction inlet, and a second channel section in communication with the gas outlet. The first channel section includes at least one mucus storage cavity, the second channel section is in communication with the intake tube and the outlet tube of the air pump. The first channel section has a maximized path length, and includes an anti-backflow channel structure. The second channel section includes a noise reduction space.

Abstract: A biomaterial collection system has a receptacle, pouch or bag for collection and a status detection device for indicating pouch volume based on a distance between opposed sides or panels of the receptacle. The receptacle is a collection vessel having a sealed volume defined by at least two opposed panels, and an interior volume defined by a distance between the opposed panels. A detection circuit including a Hall effect sensor and rare-earth magnet provides a signal indicative of the distance. The collection vessel may be employed in conjunction with procedures such as ileostomy, urostomy and colostomy for indication of a nearly full collection vessel that requires emptying.

Abstract: In one embodiment, an irrigated medical system includes a medical tool, an irrigation line configured to fluidically connect an irrigation reservoir storing irrigation fluid to the medical tool, and provide at least some of the irrigation fluid to the medical tool, a force sensor configured to be coupled with the irrigation reservoir, and provide a signal responsively to a force exerted by the irrigation reservoir on the force sensor over time as irrigation fluid in the irrigation reservoir is depleted, and a controller configured to find an irrigation rate of the irrigation fluid flowing in the irrigation line responsively to the signal.

Abstract: The present patent specification provides a medical device including an outer tube, an operation portion and a control portion. The operation portion is at least partially located in the outer tube. The control portion has a channel communicating with the outer tube along a first direction; a second end of the control portion is coupled with a first end of the outer tube so that the channel and the outer tube communicate with each other along the first direction. The control portion includes a control module including a suction control unit, a suction, a suction valve actuator and a switching unit. The suction control unit has a stopping unit and is configured to move along a second direction which is different from the first direction. The suction valve actuator is located at a side opposite the suction control unit with the channel therebetween and the suction valve actuator is configured to be activated by the suction control unit.

Abstract: A catheter having opposed tissue contacting surfaces for creating an anastomosis between two blood vessels is utilized to facilitate a method for percutaneously placing a biologic graft at a procedural site. The method may comprise steps of inserting a guidewire into a blood vessel, placing a sheath over the guidewire, advancing a biologic graft over the guidewire into the blood vessel at a biologic graft attachment site, advancing a catheter over the guidewire, pushing a distal tip of the catheter through the biologic graft, a vessel wall of the blood vessel, and into a lumen of the blood vessel, and creating an anastomosis between the biologic graft and the blood vessel by activating the catheter to apply energy to the vessel wall and to a wall of the biologic graft.

Abstract: A vacuum aspiration control system for use with a vacuum source and an aspiration catheter includes a connecting tube configured to connect the vacuum source with a lumen of an aspiration catheter. An on-off valve is operatively coupled to the connecting tube, and a sensing unit is configured to detect flow within the connecting tube and provide a signal representative of flow. A controller receives the signal to decide whether to open or close the valve. The controller may automatically close the valve to stop flow when flow through the connecting tube is unrestricted, or according to a predetermined timing sequence. The controller can further periodically open a closed valve to determine whether flow has entered an acceptable range. The controller can still further engage pulsed aspiration with a pressure manipulation assembly when flow is restricted or occluded.

Abstract: A shunt is described that expands to an hourglass shape. As the shunt expands, both of its ends radially flare outwards relative to its middle section and the length of the shunt foreshortens, which causes the flared ends to engage the tissue surrounding a puncture or aperture within a patient's tissue.

Abstract: Pressure control unit for an ophthalmic irrigation/aspiration system having a chamber with an upper part for storing air and a lower part for storing a surgical fluid to be irrigated or aspirated, the pressure control unit including a negative pressure source, a positive pressure source and an adjustable valve arrangement. The adjustable valve arrangement includes a vacuum port connected to the negative pressure source and a pressure port connected to the positive pressure source. The adjustable valve arrangement also includes a main port in controllable fluid communication with the vacuum port and the pressure port and the main port is connected to an upper part of the chamber.

Abstract: Embodiments disclosed herein relate to a base plate and/or a sensor assembly part of an ostomy appliance. In embodiments, the base plate and/or the sensor assembly part comprises a first adhesive layer, a masking element, and a plurality of electrodes. The first adhesive layer includes a stomal opening with a center point and a proximal surface configured to be attached to a skin surface of a user. The masking element is arranged on a distal surface of the first adhesive layer, and is more insulative than the first adhesive layer. Further, the plurality of electrodes are arranged on a distal side of the first adhesive layer. Each electrode includes a sensing part and a conductor part and the masking element is arranged between the conductor parts and the first adhesive layer.

Abstract: A syringe for withdrawing an aspirate from a body for micro fat grafting is provided. The syringe includes a barrel having an inner wall extending therein. The inner wall has one or more apertures formed therein allowing the aspirate to contact an absorbent positioned between the inner wall and an outer wall of the barrel. A plunger moves longitudinally within the barrel along the inner wall and has a gasket attached to a proximal end forming a seal against the inner wall. The absorbent may take many forms to absorb a non-fat cell portion of the aspirate. A related method includes retracting the plunger from a first position to draw the aspirate from a harvest site of a body into the barrel, exposing the aspirate to the absorbent, and moving the plunger toward the first position so a remaining portion of the aspirate is no longer exposed to the absorbent.

Abstract: Polymeric compositions, methods, and delivery devices for inhibiting bleeding are disclosed. The method includes applying a dried material topically to a wound site, where the material may include a cross-linked biologically compatible polymer which forms a hydrogel when exposed to blood and where the material may not include an active agent such as thrombin. A spring-loaded delivery device as described herein may be used to apply the dried material.

Abstract: A lid for an ostomy implant is provided. A base includes an attachment means for attachment to the implant and a sliding part. The sliding part is arranged such that when the sliding part is slid along a first sliding route, the sliding part causes the lid to be attachable to or detachable from the implant, and when the sliding part is slid along a second sliding route, the sliding part causes the lid to open, for evacuating a stoma to which the ostomy implant is connected, and closed, for preventing leaks from the stoma, while the lid remains attached to the implant.

Abstract: A visualized surgical assembly is provided, characterized in that the visualized surgical assembly includes a disposable drainage tube and a functional tube for providing visualization function, the disposable drainage tube and the functional tube are connected detachable along the axial of the tube body, and the functional tube is provided with a self-destructive part for cutting the disposable drainage tube. A corresponding endoscope is also provided. The visualized surgical assembly is a combination structure of the disposable drainage tube and the functional tube which can provide visualization function. The disposable drainage tube can removable connect with the functional tube, and the functional tube can be repeated disinfection, which can reduce the cost and avoid the risk of cross infection.

Abstract: Systems and methods for delivering a device for regulating blood pressure between a patient's left atrium and right atrium are provided. The delivery apparatus may include a first catheter, a hub having one or more engagers disposed thereon configured to releasably engage with a first expandable end of the shunt in a contracted delivery state within a lumen of a sheath, and a second catheter extending through a center lumen of the first catheter and the hub, wherein the first catheter, the hub, and the second catheter are independently moveable relative to the sheath. The inventive devices may reduce left atrial pressure and left ventricular end diastolic pressure, and may increase cardiac output, increase ejection fraction, relieve pulmonary congestion, and lower pulmonary artery pressure, among other benefits. The inventive devices may be used, for example, to treat subjects having heart failure, pulmonary congestion, or myocardial infarction, among other pathologies.

Abstract: A disposable urine trap in the form of a foldable pad that envelops the male genitalia and closes around the organ to form a barrier that prevents urine from escaping the trap. The pad includes an asymmetric pair of wings that are separated by a gap and attached to the main body of the pad. The first wing is preferably rectangular in that the distal angles are substantially right angles with parallel side edges and a perpendicular distal edge, and has a length that exceeds a length of a second wing, which terminates so that the distal edge of the second wing is angled to form an obtuse and an acute angle with respect to its generally parallel sides.

Abstract: According to certain embodiments, an apparatus for applying negative pressure to a wound can include a negative pressure source, a sensor, and a controller. The negative pressure source can be configured to couple via a fluid flow path to a wound dressing and provide negative pressure to the wound dressing. The sensor can be configured to monitor a magnitude or frequency of pressure in the fluid flow path generated by the negative pressure source. The controller can be configured to determine an activity classification, such as breathing, changing positions while lying, sitting, walking, standing, jumping, traversing stairs, leg extending, leg bending, and performing chair squats, based on a change in the magnitude of pressure over time while the negative pressure source maintains the magnitude of pressure in the fluid flow path below a negative pressure threshold. The controller can output an indication of the activity classification.

Abstract: A fistula bandage comprising a bandage and an adjustment device for adjusting a tension of the bandage, where the adjustment device comprises: a first engagement portion connected to a first end of the bandage; and a second engagement portion connected to a second end of the bandage; wherein the second engagement portion comprises: a base having a first sliding slot and connected to the second end of the bandage; a moving member slidingly engaged with the base and connected to the first engagement portion; a driving mechanism supported on the base and driving the moving member to slide in a first direction relative to the base; and a stopping mechanism connected to the driving mechanism. The driving mechanism drives the first engagement portion to move relative to the second engagement portion, thereby achieving the purpose of adjusting the tension of the bandage.

Abstract: The present disclosure provides a gastroretentive drug delivery device having an expandable structure. The drug delivery device includes: a capsule body; an arm moving part movable within the capsule body; an elastic body positioned between one end of the capsule body and the arm moving part and acting to move the arm moving part toward the other end of the capsule body; an arm support part movable within the capsule body; a capsule cap configured to engage the other end of the capsule body; a rail formed within the capsule body; and an arm configured to be unfolded by longitudinal movement of the arm moving part and move along the rail. A disintegrable immediate-release formulation is positioned between the arm moving part and the arm support part. A disintegrable sustained-release formulation is positioned between the arm support part and the capsule cap.