Abstract: A compact, nonelectric fluid dispenser for use in controllably dispensing beneficial agents such as propofol and dexmedetomidine hydrochloride to patients. The dispenser includes a fluid flow control assembly that precisely controls the flow of the medicament solution to the patient and embodies a collapsible, pre-filled drug container that contains the beneficial agents to be delivered to the patient. The unit-dose fluid dispenser of the invention is presented in a sterile and aseptic manner, where the drug has been pre-filled in the system, so that the practitioner cannot mistakenly give the wrong drug to the patient. The dispenser uniquely provides a more efficient medicament delivery system for procedure rooms, such as the endoscopy center, so that a greater number of patients can be treated per day at a higher standard of care with increased profits for the healthcare provider.

Abstract: Embodiments of the present invention relate to a system and method for practicing spectrophotometry using light emitting nanostructures. Specifically, embodiments of the present invention include a physiologic sensor comprising a sensor body configured for placement adjacent pulsatile tissue of a patient, a first light emitting nanostructure device configured to emit light at a first wavelength through the pulsatile tissue, a second light emitting nanostructure device configured to emit light at a second wavelength through the pulsatile tissue, and a light detector configured to detect the light at the first wavelength and the light at the second wavelength after dispersion through the pulsatile tissue.

Abstract: A device for achieving high vacuum stability during phacoemulsification surgery includes a main aspiration line connected to a vacuum source which enables a fluid flow from a phacoemulsification handpiece tip to a drainage reservoir. A first tubing segment is provided in the main aspiration line along with a second tubing segment generally parallel to the first tubing section and a valve disposed in the second tubing segment regulates fluid flow through the second tubing segment in order to limit vacuum surge in the main aspiration line upon clearing of an occlusion in the phacoemulsification handpiece tip.

Abstract: A suction head in fluid communication with a pump head provides a sub-ambient working pressure to a target area, enabling drainage thereof to a waste container. The pump head is coupled non-mechanically to a pump drive. A control system for a suction system is also provided.

Abstract: A system and method are disclosed for automatically limiting the drainage of a bodily fluid such as cerebrospinal fluid (CSF) from a patient into a collection chamber. The collection chamber includes a vent having an hydrophobic filter for the passage of air to facilitate the movement of CSF yet to maintain a closed system. The system includes a buoyant float hingedly connected with the top of the collection chamber in one embodiment. When fluid rises in the collection chamber to a predetermined volume, buoyant force raises the float and causes a seal plug mounted on top of the float to seal one of an inflow port or a vent port. The float is limited to pivoting movement in one plane and to a certain angle within that plane. The system and method avoid overdrainage of CSF from the patient and overfilling of the collection chamber.

Abstract: A barrier of a vacuum pump prevents contamination from entering a vacuum pump air line. The barrier separates parts of the pump and is moveable between an initial state and a distended state. The barrier is assembled within the pump with a pre-load. When the vacuum source is applied to the barrier, the barrier achieves a distended state and when the vacuum source is released, the barrier incrementally self returns to an initial state. The geometry and material construction of the barrier, along with the pre-load, assists in returning the barrier on its own to the initial state from the distended state.

Abstract: A urine collection bag (1) which includes an anti-reflux valve (7) is provided. The bag is made of foil layers (IA, IB) welded together so that the valve is provided by welding four foil layers together. The valve is placed at the inlet (6) and has a width so that it can cooperate with a catheter which is inserted in the inlet. The length is at least 2¼ times the width. Furthermore, a kit of parts which comprises a urine collection bag and a catheter (200) is provided.

Abstract: Drainage belongs to medical equipment, particularly to medical tools and is specified for drainage of cavities. Drainage comprises a first tube, an additional tube, which is fixed upon it, a unit of the clot's splitter and the splitter's fixing element. The additional tube has a smaller diameter with an opening, inside which the conductor is mounted, a unit of clots splitter is installed on the working end of the drainage, it comprises a cylinder, a tube with an opening, placed on it, which is the continuation of the additional tube of the drainage and a spring with a cutter inside the cylinder. A cutter is located diametrically inside the working head, while in the end of the wall of the first tube and the splitter's unit comprises a channel, inside which splitter's fixing element was led, its working end is inside the unit's cylinder and fixes the splitter.

Abstract: A compact, nonelectric fluid dispenser for use in controllably dispensing beneficial agents such as propofol and dexmedetomidine hydrochloride to patients. The dispenser includes a fluid flow control assembly that precisely controls the flow of the medicament solution to the patient and embodies a collapsible, pre-filled drug container that contains the beneficial agents to be delivered to the patient. The unit-dose fluid dispenser of the invention is presented in a sterile and aseptic manner, where the drug has been pre-filled in the system, so that the practitioner cannot mistakenly give the wrong drug to the patient. The dispenser uniquely provides a more efficient medicament delivery system for procedure rooms, such as the endoscopy center, so that a greater number of patients can be treated per day at a higher standard of care with increased profits for the healthcare provider.

Abstract: A low profile surgical access device includes an elongated cannula having an opening defined at a proximal end thereof including an inner peripheral surface dimensioned to facilitate passage of instrumentation therethrough and an outer peripheral surface configured to operatively engage and removably secure to tissue via, e.g., fixation ribs, adhesive, anchors, clips, suction elements, expandable materials and/or combinations thereof. A valve is operatively coupled to the elongated cannula and provides a substantially fluid tight seal when instrumentation is inserted through the cannula. A seal housing is included which is positionable relative to the cannula and which is configured to operatively engage and removably secure to tissue. The instrument seal in the seal housing is positioned in vertical registry with the valve in the elongated cannula.

Abstract: A fluid collection assembly including a container having an interior chamber for collecting fluid, and a quick connect device coupled to the top of the container to couple to a mated connection device on a drainage tube. The quick connect device and the mated connection device may be in an open configuration to permit fluid flow when engaged and in a closed configuration to prevent fluid flow when disengaged. An adjustable hanger may be attached to the container, including an adjustable member that vertically repositions the container.

Abstract: A mucous suction device, comprising in combination, a longitudinally elongated, generally tubular, one-piece plastic body, the body having an axially elongated tapered, first portion extending toward an inlet proximate one end of the body, the body having an axially elongated second portion extending toward an outlet proximate an opposite end of the body, radially outwardly extending annular retention rings in said body second portion, said rings having sharp annular peripheries and said rings being axially resiliently flexible and axially spaced apart, and there being body side porting between said body first and second portions, said side porting being manually controllable to control suction exertion.

Abstract: When a patient is fitted with an external gastrostomy connection to the stomach, ingested food can be removed through the gastrostomy connection using a pump-based or siphon-based system to achieve weight loss. The process of removing ingested food can be improved by alternating the infusion of liquid into the stomach with the removal of material from the stomach. Optionally, stomach acid may be captured and returned to the stomach. Optionally, nutritional supplements or medicines may be added to the infused liquid. Optionally, a flush mount connectorized system with a built in valve may be used to simplify the interface with the gastrostomy hardware that remains installed in the patient. Optionally, the system may be configured to disable itself from further use after a triggering event (e.g., the passage of time or a predetermined number of uses) has occurred.

Abstract: The present invention provides a body fluid suction reservoir including a flexible bag, two plates for supporting the bag, and a spring put between the two plates. The body fluid suction reservoir further includes a lock having a hook and a release part and consisting of a member different from the two plates, by which lock the spring is held in a state compressed between the two plates, and the held state is releasable. The lock has flexibility and is held by one of the plates so as to be deformable from a first state in which the hook is engaged with the other plate to a second state in which the hook is not engaged, and the lock is urged to take the first state.

Abstract: Methods and systems are provided for a sub-atmospheric wound-care (SAWS) system for treating an open wound. The SAWS system includes a regulated vacuum source for developing a negative pressure, a flow rate meter configured to measure a flow rate of liquid removed from the wound, a primary pressure regulating sensor located proximate the wound for directly measuring the negative pressure at the wound, a backup pressure regulating sensor located vacuum tube, a porous dressing suitable to be sealed airtight which is positioned within a wound interface chamber, a collection canister configured to collect said liquid removed from the wound, and an adapter configured to use wall suction a primary regulated vacuum source.

Abstract: A disconnectable connector assembly is provided comprising (a) a first polymeric fitting including a first open end, and a second open end; (b) a stem disposed in the first fitting, the stem including an open end and a closed end, a head comprising the closed end, a side wall including one or more apertures and a plurality of circumferential grooves, and a plurality of resilient members circumferentially engaging circumferential grooves in the side wall, wherein the stem is axially movable, from a first position to a second position, in the direction from the first end of the first fitting toward the second end of the first fitting; and, (c) a second polymeric fitting connected to the first fitting, the second fitting including a first end and a second end, the second fitting being in fluid communication with the stem and the first fitting when the stem is in the first position, and wherein fluid flow between the second fitting and the stem and the first fitting is blocked when the stem is in the second posit

Abstract: Injection shut off valve devices and methods are provided for limiting flow and pressure from a pharmaceutical composition on injection. In some embodiments, the injection shut off valve is coupled to a syringe and can be used to monitor and avoid maximum pressures that can cause damage on injection.

Abstract: A collapsible, hands-free emesis container is provided with improved portability, deployment and emesis reception characteristics. The container includes a receptacle portion for receiving emesis, a chute portion for directing emesis and a retainer to maintain desired positioning of the container about a support structure, which may be the neck of an impaired patient. The container may be provided in a package having size characteristics for easy storage and access by emergency medical service personnel. The container may be formed as a single unitary member.

Abstract: A visceral pleura ring connector that may be utilized to anchor and seal the visceral pleura to a conduit or other device entering the lung from a non-native airway. The visceral pleura ring connector may be positioned around the visceral pleura and an insertion device and seal them together without having to make any holes in the pleura. The visceral pleura ring connector may be utilized with a pulmonary pleural stabilizer to hold the visceral pleura of the lung during surgical procedures involving accessing the lung or lungs of a patient directly through the lung and not the native airways.

Abstract: Multi-functional urine collection devices, embodiments of which can include a self-expanding container having a receptacle for receiving urine from the tubing, a pump for moving urine through the tubing and into a receptacle, extendable tubing that may be shortened and/or lengthened, and/or one or more meters for monitoring, measuring, transmitting or storing a characteristic from the urine.

Abstract: A compact, nonelectric fluid dispenser for use in controllably dispensing beneficial agents such as propofol and dexmedetomidine hydrochloride to patients. The dispenser includes a fluid flow control assembly that precisely controls the flow of the medicament solution to the patient and embodies a collapsible drug container that can be filled in the field with the beneficial agents to be delivered to the patient. The unit-dose fluid dispenser of the invention is presented in a sterile and aseptic manner, where the drug has been pre-filled in the system, so that the practitioner cannot mistakenly give the wrong drug to the patient. The dispenser uniquely provides a more efficient medicament delivery system for procedure rooms, such as the endoscopy center, so that a greater number of patients can be treated per day at a higher standard of care with increased profits for the healthcare provider.

Abstract: A body fluids drainage system includes a urinary catheter, a drainage collection bag, and a connection member connected between the urinary catheter and the drainage collection bag. The connection member houses a valve element formed from a sheet of material and projecting a coherent plane. The valve element defines a longitudinal direction extending between a connecting portion and a flap portion and a recess formed on a periphery of the valve element between the connecting portion and the flap portion.

Abstract: Needleless access port valves are generally discussed herein with particular discussions extended to needleless access port valves having a stretchable or flexible band. In accordance with aspects of the present invention, the band is held in between a flange section of an inlet connector assembly and a shoulder section of the valve body. A plunger integrally formed with the band is movable inside a nozzle to control fluid flow through the inlet of the valve. When the plunger is urged by a medical implement to open the valve inlet, the band flexes to accommodate the moving plunger.

Abstract: A collecting bag for an ostomy appliance, said collecting bag having a front wall and a rear wall, the rear wall having an opening through which waste material may enter the collecting bag, and wherein a manipulation pocket is defined in the front and/or the rear wall of the collecting bag, said manipulation pocket extending into the collecting bag and comprising transfer means adapted to sealed transfer of mechanical movement from the surroundings to the interior of the collecting bag. The sealed transfer of movement can be used to open a passage inside the collecting bag such that flatus gasses may pass through a deodorizing filter, which prior to opening of the passage is protected such that it is not contaminated.

Abstract: A low profile surgical access device includes an elongated cannula having an opening defined at a proximal end thereof including an inner peripheral surface dimensioned to facilitate passage of instrumentation therethrough and an outer peripheral surface configured to operatively engage and removably secure to tissue via, e.g., fixation ribs, adhesive, anchors, clips, suction elements, expandable materials and/or combinations thereof. A valve is operatively coupled to the elongated cannula and provides a substantially fluid tight seal when instrumentation is inserted through the cannula. A seal housing is included which is positionable relative to the cannula and which is configured to operatively engage and removably secure to tissue. The instrument seal in the seal housing is positioned in vertical registry with the valve in the elongated cannula.

Abstract: A universal valve for the Foley type urinary catheter has structure which permits its use as a patient controlled drainage valve, as an interface from which to take sterile samples, and as a connection to a day or night collection bag all without removal of the universal valve from the Foley type urinary catheter. The universal valve may be open or closed by the use of a squeeze mechanism for patient control, or by movement of the threaded connection between the universal valve and a collection bag so that the universal valve is continuously open for drainage into the urine collection bag.

Abstract: A portable urinal that includes a container defining a liquid reservoir and a spout extending therefrom. The spout has an inlet for receiving a liquid. A valve assembly is disposed within the spout. The valve assembly has an interior region and an exterior region. The valve assembly includes a sidewall and one or more sealable openings for permitting flow of a liquid into the reservoir, while resisting undesired flow of the liquid out of the reservoir. The openings defining the line between the interior region and the exterior region. The valve assembly sidewall has a shaped contour structured to direct liquid flow into the openings.

Abstract: An apparatus includes a fluid permeable dressing and a cover membrane configured to extend over the fluid permeable dressing. A tube is coupled to the fluid permeable dressing and is configured to apply suction through the fluid permeable dressing. A fluid reservoir is coupled to the cover membrane, the fluid vessel including an inlet port configured to receive a fluid and an outlet port fluidically coupled to the fluid permeable dressing.

Abstract: The device (1) for providing anti-reflux has a valve element (9) formed from a sheet-shaped material blank. The valve element includes a connecting portion and a flap portion. Retaining means (10a,10b) for retaining the valve element are integral with the device. The connecting portion includes engagement means formed integrally with the valve element for engagement with the retaining means, the valve element projecting a coherent plane.

Abstract: A valve unit for regulating a flow and a disposable urine bag are provided. The valve unit includes an inlet portion and an outlet portion separated from each other by a slide valve. The slide valve includes a female part in direct communication with the inlet portion and the outlet portion and a male part axially displaceable in liquid-proof contact with the female part. The male part includes a closing position wherein a portion of the male part is outside the female part and an open position wherein the male part allows liquid passage between the inlet portion and the outlet portion by means of a communication part. The female part includes a tubular member open at both ends and having a tubular wall extending along the entire length of the male part in the open position for deterring displacement of the male part to the closed position.

Abstract: A disposable liner/lid system useable with a rigid canister and having an adhesive seal to provide improved sealing characteristics and effectively reduce the likelihood of spillage and leakage. The liner includes a flange and the lid includes adhesive that is secured to the interior of the lid and the flange of the liner when installed to provide a seal.

Abstract: An apparatus for cleansing and promoting tissue growth in wounds, in which irrigant fluid optionally containing cell nutrients and/or other physiologically active material from a reservoir connected to a conformable wound dressing and wound exudate from the dressing are recirculated by a device for moving fluid through a flow path which passes through the dressing, a biodegradable scaffold in contact with the wound bed and a means for fluid cleansing and back to the dressing. The apparatus has means for supplying thermal energy to the fluid in the wound. The cleansing means (which may be a single-phase, e.g. micro-filtration, system or a two-phase, e.g. dialytic system) removes materials deleterious to wound healing, and the cleansed fluid, still containing materials that are beneficial in promoting wound healing, is returned to the wound bed. The dressing and a method of treatment using the apparatus.

Abstract: Active and passive wound drainage systems and method are provided. A drainage device includes an input passage for receiving the fluid from a site on or within the patient's body, a container for holding the fluid, and a reversible valve disposed between the input passage and the container. The reversible valve in an original configuration provides unidirectional fluid flow from the input passage toward the container, and in a reversed configuration provides fluid flow from the container toward the input passage.

Abstract: Various embodiments of a fluid collection system having multiple storage chambers are disclosed. In an exemplary embodiment, the system may include a first chamber in fluid communication with a suction source and a second chamber in fluid communication with the first chamber. The second chamber may have a volume less than a volume of the first chamber. The second chamber may also comprise an inlet port for connecting to an external tube. The system may be configured to selectively drain liquid from the second chamber into the first chamber.

Abstract: A wound treatment apparatus is disclosed to provide vacuum therapy to a wound associated with a patient. The wound treatment apparatus comprises a control unit comprising an alarm and a display displaying an alarm log providing information associated with each activation of the alarm. The display also displays information to instruct a user how to operate the wound treatment apparatus. A method of calibrating the control unit is disclosed.

Abstract: An apparatus for cleansing wounds with means for stressing the wound bed and optionally tissue surrounding the wound, in which irrigant fluid from a reservoir connected to a conformable wound dressing and wound exudate from the dressing are recirculated by a device for moving fluid through a flow path which passes through the dressing and a means for fluid cleansing and back to the dressing. The cleansing means (which may be a single-phase, e.g. micro-filtration, system or a two-phase, e.g. dialytic system) removes materials deleterious to wound healing, and the cleansed fluid, still containing materials that are beneficial in promoting wound healing, is returned to the wound bed. The means for stressing the wound bed and optionally tissue surrounding the wound promotes wound healing. The dressing and a method of treatment using the apparatus.

Abstract: The invention relates to an adapter attached to a human or animal body at a stoma, a detachable lid on the adapter, and a connector for connecting an ostomy bag to the adapter. The adapter includes a protruding section extending from the stoma, and a member for mounting a detachable lid onto the end of the protruding section. The adapter and lid are arranged such that the lid can be slid onto and off the adapter in a direction relatively perpendicular to the axis of the protruding section of the adapter. The connector is arranged to connect the ostomy bag to the adapter and to slide the lid off the adapter. In this way, there is no risk of odors or waste leaking from the adapter or the ostomy bag while the bag is being connected to the adapter.

Abstract: Described is, e.g., an apparatus (100), and associated methods of manufacture and use, for draining a fluid, discharged from a urinary catheter (104) installed in a subject's bladder, into a drain container (138) while avoiding undesired pressure states in such bladder. A drain conduit (102) connected to the catheter has a sufficiently small size as to maintain plug-flow between opposite ends of the drain conduit. The discharge end of the drain conduit is connected to a siphon-break apparatus (106) configured to cause a siphon-break disposed at an elevation (132) in approximate agreement with the subject's bladder. The potential energy from fluid downstream of the siphon-break location is decoupled from fluid in the drain conduit.

Abstract: A colostomy bag provided with a stoma ring, a gas outlet and an external deodorizing filter in which a vertical baffle is provided intermediate the stoma ring and the gas outlet and extending from the upper marginal wall of the bag and a level slightly below the lowest point of the stoma ring. The baffle is designed to prevent feces from being squeezed sideways and upwardly into the gas outlet and clogging it.

Abstract: A reduced pressure treatment apparatus includes a drape for positioning over the wound site to create and maintain a substantially air-tight cavity between the wound site and the drape. A multi-lumen suction tube is provided to be attached to a reduced pressure source. The multi-lumen suction tube includes a center lumen and at least one outer lumen and is configured to deliver reduced pressure beneath the drape to the substantially air-tight cavity. The multi-lumen suction tube is adapted to allow fluid to be drawn from the wound site through the center lumen and pressure to be monitored at the wound site through the at least one outer lumen.

Abstract: A suction cup apparatus includes a container body and a valve which covers the container body. The valve has an X-shaped slit therein for resiliently securing a suction catheter. A support member is provided for holding the container body. A flexible arm is also provided, having a first end and a second end, the first end being connected to the support member. A clamp disposed on the second end of the flexible arm for removably securing the flexible arm to a support. In use, the suction cup preferably contains a sterile solution made of water and antibacterial solution with or without a flavoring agent The volume of the suction cup is preferably in the range of 12 oz to 20 oz. But can vary according to use.

Abstract: A method is provided for securing a fluid meter to a fluid collection bag. The method includes the steps of providing a meter ha6 ving a housing defining a fluid receptacle and at least one drain opening, providing a collection bag defining a fluid reservoir and having at least one inlet opening and securing the meter to the bag using an RF welding device to allow fluid communication between the fluid receptacle and the fluid reservoir. In one embodiment, the housing includes a raised surface positioned about the at least one drain opening to which the collection bag is welded.

Abstract: The present invention provides a body fluid suction reservoir including a flexible bag, two plates for supporting the bag, and a spring put between the two plates. The body fluid suction reservoir further includes a lock having a hook and a release part and consisting of a member different from the two plates, by which lock the spring is held in a state compressed between the two plates, and the held state is releasable. The lock has flexibility and is held by one of the plates so as to be deformable from a first state in which the hook is engaged with the other plate to a second state in which the hook is not engaged, and the lock is urged to take the first state.

Abstract: A patient-adjustable device and surgical method for the treatment of urinary incontinence is disclosed herein. More specifically, the device is a mesh surrounded pillow which is implanted near the attachment of the urethra to the bladder, or mid to distal urethra which can be controlled by the patient. The fullness of the pillow can be controlled by the patient using two pressure-sensitive controls under the skin.

Abstract: A lesion or fistula isolating bag, the bag defining a first chamber having a closeable entrance and a second chamber for application to a lesion or fistula and wherein access to the second chamber is made through the first chamber via a valve, the valve being arranged to inhibit passage of fluid from the second chamber to the first, and to allow said access from the first chamber to the second, the bag further comprising a closure for said closeable entrance.

Abstract: A cannula has a tubular body, an inflatable ring affixed within the tubular body adjacent proximal end thereof, and a valve connected to a channel extending to the inflatable ring. The valve is suitable for allowing a liquid to be passed into the inflatable ring from a syringe. The inflatable ring is expandable into the longitudinal channel when the liquid is introduced thereinto. The tubular body has an outer sleeve adjustably receiving an inner sleeve at the distal end of the tubular body. Numerical indicia are formed on the inner sleeve.

Abstract: A system and method are disclosed for automatically limiting the drainage of a bodily fluid such as cerebrospinal fluid (CSF) from a patient into a collection chamber. The collection chamber includes a vent having an hydrophobic filter for the passage of air to facilitate the movement of CSF yet to maintain a closed system. The system includes a buoyant float hingedly connected with the top of the collection chamber in one embodiment. When fluid rises in the collection chamber to a predetermined volume, buoyant force raises the float and causes a seal plug mounted on top of the float to seal one of an inflow port or a vent port. The float is limited to pivoting movement in one plane and to a certain angle within that plane. The system and method avoid overdrainage of CSF from the patient and overfilling of the collection chamber.

Abstract: Disclosed is a device for maintaining an adjustable loop in the drain tube of a urine collection and/or monitoring system. The clip, band or bands act to maintain the adjustable loop such that the adjustment in size of the loop created in the drain tube varies the effective length of the drain tube. Further disclosed is a method for preventing back pressure from developing in the drain tube of urine collection and/or monitoring system.

Abstract: A urine collection apparatus includes an adaptable reservoir that is sized and shaped for conveniently and effectively being transported by a user. The reservoir includes a top portion including an intake valve in fluid communication with the reservoir. The intake valve is provided with an opening such that the male catheter can be selectively biased in fluid communication with an interior of the reservoir. Such an intake valve further has a threaded screw cap directly and adjustably coupled thereto for effectively allowing a selected quantity of air to continuously flow into and out of the reservoir wherein the quantity of air is commensurate with a quantity of fluid discharging and entering the reservoir respectively. The intake valve preferably has a monolithically formed conical tip that terminates proximal to the top portion such that the male catheter can effectively be supported at a fixed relationship with the reservoir during operating conditions.

Abstract: A suction fluid collector includes a transparent reservoir made of a resilient material with an upper opening positioned on one side of a flexible suction bag with at least one transparent side. A plate part made of a resilient material is positioned on another side of the suction bag opposite said reservoir. An urging means arranged between the reservoir and the plate part provides a force tending to expand a gap between the reservoir and the plate part. A suction tube is positioned partially inside the reservoir and extends through the suction bag.