Abstract: One aspect of the invention is a method to vent gas from a body cavity during an endoscopic procedure. A body cavity is in fluid communication with an exhaust gas inlet of a vacuum break device. The vacuum break device has a chamber in fluid communication with both the inlet and an outlet. The chamber may comprise one or more openings in fluid communication with the atmosphere. A conduit in fluid communication with the exhaust gas outlet may be connected directly or indirectly to a suction source. The suction source may be activated.

Abstract: A remote sensing catheter system including an injection catheter and a collection catheter. In one method of use, an external sensor of the system determines the timing of operation of the collection catheter. In another method of use, a sensor determines the volume of medium in the injection.

Abstract: Here is disclosed a urine receiver. The urine receiver which collects urine of a wearer of the urine receiver under suction force has a container member provided with a bottom, a peripheral wall and flange. The container member has a suction tube which extends through the peripheral wall and has a urine suction port opening toward the interior of the container member and a urine evacuation port opening toward the exterior of the container member. The evacuation port is adapted to be connected to a connector of a urine suction means provided externally of the container member.

Abstract: A wound exudate removal and isolation system includes a porous dressing, a canister in fluid communication with the dressing, and a first valve positioned between the dressing and the canister. The first valve is positionable between an open position and a closed position. A disposal line is fluidly connected to the canister and includes a second valve that is positionable between an open position and a closed position. A pump is fluidly connected to the canister and is configured to draw wound exudate from the dressing into the canister when the first valve is open and the second valve is closed. The pump is configured to force wound exudate from the canister into the disposal line when the first valve is closed and the second valve is open.

Abstract: Provided is a device for treatment of wounds using reduced pressure, which includes a pump, a gas barrier cover, a first compressible material which expands after compression, and a second material capable of absorbing wound fluids several times its own weight. The first and second materials are arranged inside the cover and form a reservoir connected to the pump. The device also includes an inlet for connecting the reservoir with a wound, a wound pad to be arranged in the wound cavity, and a sealing covering the wound and the wound pad. A third material with high liquid spreading capability is arranged around at least a major part of the first material, and the second material is in the form of at least one layer arranged outside the third material and separated from the first material by the third material.

Abstract: A sampling device includes a body, a needle, a sealing element and an element for feeding and removing a liquid. The needle has at least one groove located between the sealing element and the sampling end of the needle. The sampling end has a sampling hole opening out on a lateral wall of the end. The sampling device leakage problems encountered in the conventional art to be overcome while at the same time resolving the problems of placing the inside of a tube containing a product to be analyzed at atmospheric pressure.

Abstract: A collector for a negative pressure wound therapy system has a soft collecting bag with a gas-permeable unit and a liquid absorber. The collecting bag is connected to a wound-dressing unit via an inlet connecting set and is connected to a sensor assembly via a detecting connecting set. With the soft collecting bag, the collector occupies less volume. By the gas-permeable unit and the liquid absorber, the liquid and gas entering into the collecting bag quickly isolate. Moreover, multiple collectors connect in series to form a collector combination to reduce the frequency to replace the collector combination so that a longer usage time of the collector combination is available.

Abstract: A removable manifold for a medical/surgical waste collection system. The manifold is dimensioned to be mounted to a receiver integral with the system. The manifold includes a includes at least one fitting through which waste is drawn into the manifold. The fitting opens through an inlet port into a void space internal to the manifold. A backflow prevention valve is disposed in the manifold void space. The backflow prevention valve includes a static hub to which a driver for engaging a complementary valve internal to the receiver. The valve regulates flow between the receiver and the down line components of the waste collection system. The valve is normally closed. When the manifold is fitted to the receiver the driver engages the valve so as move the valve to the open position. This allows fluid flow from the manifold and receiver to the downstream components of the system.

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: In general, this disclosure relates to extracorporeal fluid circuits. In some aspects, an air-release device for allowing air to be released from a liquid in extracorporeal circuitry includes an elongate chamber having a bottom region and a top region and a fluid entry port and fluid exit port at or near the bottom region. The air release device also includes a vent structure at or near the top region of the elongate chamber that includes a porous material capable of swelling when moistened such that the vent structure can inhibit liquid from escaping the air-release device during use.

Abstract: A novel collection device for collection, storage and disposal of biological products, in conjunction with an improved cleansing method. Disclosed is an apparatus which includes a locking closing member handle to allow for safe transport and disposal of medical waste. Closing member allows for secure containment of medical waste and subsequent apparatus cleaning. Closing member design includes a gap between closing member and housing which facilitates device cleaning after waste disposal.

Abstract: A catheter for collecting fluid such as blood from a vessel such as a coronary sinus of a patient has an elongated, flexible tubular portion and an annular sealing member spaced from a distal end of the tubular member. A proximal end of the tubular member is adapted to be connected to a source of suction for applying suction to a collection lumen of the tubular member. The distal end is placed in a blood vessel with the sealing member spaced from opposing surface of the vessel in an absence of a suction applied to the collection lumen. Suction is applied to the collection lumen in an amount sufficient to draw blood from the vessel through the fluid inlet and into the collection lumen and further sufficient to urge the opposing surface of the vessel to migrate into sealing engagement with the sealing member.

Abstract: A collector for a negative pressure wound therapy system has a soft collecting bag with a gas-permeable unit and a liquid absorber. The collecting bag is connected to a wound-dressing unit via an inlet connecting set and is connected to a sensor assembly via a detecting connecting set. With the soft collecting bag, the collector occupies less volume. By the gas-permeable unit and the liquid absorber, the liquid and gas entering into the collecting bag quickly isolate. Moreover, multiple collectors connect in series to form a collector combination to reduce the frequency to replace the collector combination so that a longer usage time of the collector combination is available.

Abstract: An apparatus and method for treating a wound can include a flexible sheet for sealingly engaging a patient's skin around a wound bed, a drain to be located in the wound bed, a vacuum source connected to the drain, and a flow restriction device to control the flow of fluid through an aperture of the flexible sheet.

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 container for use with a hemodialysis apparatus having a vent structure is described. The vent structure is porous, and allows air in the container to vent when the container is being filled with fluid, but expands when the vent structure becomes wet, when filling is complete, thereby closing off the pores and inhibiting (e.g., preventing) fluid from flowing through the vent structure, and reentry of air into the container. The vent structure can also include a micro-porous membrane.

Abstract: The tissue therapy device includes a sealant layer and a suction apparatus. The sealant layer creates a sealed enclosure between it and the surface of a patient by forming an airtight seal around an area of tissue. The suction apparatus is in fluid communication with the sealant layer and together, create a closed, reduced pressure therapy system. The suction apparatus self-creates reduced pressure by decreasing the density of air molecules underneath the sealant layer by expanding the volume of the air molecules.

Abstract: A reduced pressure treatment appliance is provided for enclosing and providing reduced pressure treatment to an object or a portion of an object. In some embodiments, the reduced pressure treatment appliance may be used to treat wounds and other conditions, such as lymphedema, varicose veins, venous insufficiency and stasis, and other infirmities. In other embodiments, the appliance may be used to provide reduced pressure (or vacuum) treatment for non-medical purposes. In some embodiments, the appliance comprises a flexible chamber and a collapsible frame that may be collapsed while the appliance is not in use. In yet other embodiments, the appliance also includes a vacuum system to supply reduced pressure to the volume within the chamber, a pressurized fluid system to inflate the collapsible frame, a drainage system to remove fluids from the appliance, and a treatment port and a forced entry treatment system to introduce fluids and other treatment instrumentalities into the volume within the chamber.

Abstract: The present invention relates to a portable waste containment device that is rapidly deployable. The waste containment device allows containment of liquid or semi-liquid waste until permanently disposed. The present invention also provides a portable waste containment system wherein the waste containment device is enclosed within a package for storage and when pulled from the package the waste containment device is ready for use. Still further, the present invention provides a method of using the portable waste containment device of the present invention.

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 vent assembly is described for use in an extracorporeal fluid unit. A vent structure adjacent to a micro-porous membrane forms the assembly. The vent structure is porous, but expands when the vent structure becomes wet, thereby closing off the pores and inhibiting (e.g., preventing) fluid from flowing through the vent structure. The vent structure also protects the membrane from becoming wet, such as from condensation.

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 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: 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: 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: An aspiration flow control device includes a housing having at least one vacuum port, at least one aspiration port, and an ejection port. The at least one vacuum port is adapted to be connected to a vacuum source, and the aspiration port is adapted to be connected to an aspiration line for receiving fluids from a surgical site. The device further includes a rotating structure having at least three vanes, which structure is configured to rotate within the housing. The at least three vanes divide an enclosed volume within the housing into at least three rotating fluid collection chambers. During rotation of the rotating structure, at least one fluid collection chamber is in communication with at least one vacuum port and the aspiration port through which fluid is received, and at least one other fluid collection chamber is simultaneously in communication with the ejection port through which fluid is expelled.

Abstract: Here is disclosed a urine receiver. The urine receiver which collects urine of a wearer of the urine receiver under suction force has a container member provided with a bottom, a peripheral wall and flange. The container member has a suction tube which extends through the peripheral wall and has a urine suction port opening toward the interior of the container member and a urine evacuation port opening toward the exterior of the container member. The evacuation port is adapted to be connected to a connector of a urine suction means provided externally of the container member.

Abstract: A catheter for collecting fluid such as blood from a vessel such as a coronary sinus of a patient has an elongated, flexible tubular portion and an annular sealing member spaced from a distal end of the tubular member. A proximal end of the tubular member is adapted to be connected to a source of suction for applying suction to a collection lumen of the tubular member. The distal end is placed in a blood vessel with the sealing member spaced from opposing surface of the vessel in an absence of a suction applied to the collection lumen. Suction is applied to the collection lumen in an amount sufficient to draw blood from the vessel through the fluid inlet and into the collection lumen and further sufficient to urge the opposing surface of the vessel to migrate into sealing engagement with the sealing member.

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: 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: Disclosed is a receptacle for use with a medical suction device which is equipped with a cover body and an external case for detachably holding and air-tightly surrounding the receptacle and a patient-side tube for introducing waste liquid into the receptacle, and designed to create a negative pressure in both an interior space of the cover body and the external case and an interior space of the receptacle so as to allow waste liquid to be sucked into the receptacle through the patient-side tube. The receptacle has an air-pervious/liquid-impervious element having air perviousness and liquid imperviousness. The air-pervious/liquid-impervious element at least partly constitutes a portion of the receptacle to be surrounded by the cover body and the external case.

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: Various implementations of a fluid collection system having a flexible liner are disclosed. In one exemplary variation, the fluid collection system may include a container having a top opening, a lid configured to close the top opening, and a flexible liner attached to the lid. The liner may be interposed between the lid and the container when the lid closes the top opening. The liner and the lid may define a substantially sealed interior space therebetween. The lid may include an access port through which the interior space receives fluid. The flexible liner may also be configured to controllably collapse as the fluid is removed from the interior space.

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.

Abstract: An epidural needle has an elongate tube and a hub with a proximal end, a distal end, an open passageway having an inside diameter, and a cavity disposed between the proximal end and distal end. The hub is attached to the elongate tube so that a hollow bore of the elongate tube is in fluid communication and substantial axial alignment with the open passageway. A resilient member defining an opening therethrough is disposed in the cavity and is axially aligned and in fluid communication with the open passageway. The hub has a clamp with a releasable latch disposed about the resilient member. The clamp is selectively movable between an open position wherein the inner diameter of the resilient member is substantially unaffected and a clamp/latch position wherein the clamp causes a strain to the resilient member and thereby reduces the inner diameter of the opening through the resilient member.

Abstract: A catheter for collecting fluid such as blood from a vessel such as a coronary sinus of a patient has an elongated, flexible tubular portion and an annular sealing member spaced from a distal end of the tubular member. A proximal end of the tubular member is adapted to be connected to a source of suction for applying suction to a collection lumen of the tubular member. The distal end is placed in a blood vessel with the sealing member spaced from opposing surface of the vessel in an absence of a suction applied to the collection lumen. Suction is applied to the collection lumen in an amount sufficient to draw blood from the vessel through the fluid inlet and into the collection lumen and further sufficient to urge the opposing surface of the vessel to migrate into sealing engagement with the sealing member.

Abstract: An aspirator, including a bulb that defines first and second ports, a tube adjacent to the first port defined by the bulb, and means for helping to prevent aspirated material inside the bulb from exiting the bulb through the second port defined by the bulb.

Abstract: A drainage chamber for collecting body fluids, in particular liquor, includes a collecting area limited by an outer wall for collecting the body fluid, an inlet connection linked to the collecting area for linking to a drainage catheter (an intraventricular catheter), an outlet connection and a ventilation connection linked to the environment. The drainage chamber has a spring-loaded first closing element, biased in the direction of a first closing position, which in its closing position closes both the inlet connection and the ventilation connection and which is displaceable against the spring tension by means of an actuating mechanism into an open position, in which it releases the inlet connection and the ventilation connection.

Abstract: A container assembly provides for the collection, transporting, and dispensing of a fluid specimen. The container assembly includes a cup-shaped container having an open end for collecting the fluid specimen. A lid is attachable to the container to close the open end thereof. The lid includes an access port for providing communication with the collected fluid specimen through the cover and for permitting extraction of a sample therefrom. A self-sealing closure member is supported by the lid in the access port and seals the access port preventing fluid leakage. The extraction device may be used to extract a sample of the fluid specimen. The extraction device is insertable through the self-sealing closure to permit such extraction. Upon removal of the extraction device, the self-sealing closure recloses the access port.

Abstract: A kit for draining fluids from the body of a patient is provided. The kit eliminates the problem of having to obtain a distinct liquid source and a means for delivering the liquid into a chamber of a chest drain. The kit includes an apparatus configured to receive fluids from the body of the patient. The apparatus defines a chamber to contain a predetermined volume of liquid. The apparatus includes an inlet through which liquid is deliverable to the chamber of the apparatus from an exterior of the apparatus. The kit also includes a container packaged with or attached to the apparatus. The container is prefilled and sealed to contain at least the predetermined volume of liquid. The container includes an outlet configured to deliver at least the predetermined volume of liquid to the chamber of the apparatus through the inlet of the apparatus.

Abstract: A thoracic drainage system for removing liquid from the thoracic cavity of a patient. The system includes a reusable thoracic vacuum regulator and a standard disposable collection container. A disposable water seal chamber is also provided that can be disposed of after each patient and is a separable, independent component. There is also a combination thoracic vacuum regulator having a water seal chamber removable affixed thereto to enable the water seal chamber to be readily removed from the thoracic vacuum chamber in order to carry the water seal chamber along with the patient as that patient is transported.

Abstract: A female urinary incontinence management device having a base member that adhesively attaches to the patient, and a bag member that is sealingly and releasably attached to the base member. The base member is generally triangular having a top portion that, when attached to the patient, extends across and above the symphysis pubis, side portions that extend down along the groin area, and a short bottom portion that extends across the perineal area. The base member includes an upraised ridge portion into which is integrated a “female” part of a means for sealing the bag member with the base member. The bag member includes a similar upraised ridge portion into which is integrated a “male” part of the means for sealing the bag member with the base member. The bag member may be releasably and sealingly coupled to the base member by interlockingly squeezing the “male” and “female” parts together.

Abstract: A fill spout for a drainage device is disclosed which permits the user to supply water directly to a water seal chamber of the drainage device for establishing a water seal therein. The fill spout comprises a funnel having lateral sides for facilitating the entry of the water into the drainage device, a depending lip extending from the fill spout for preventing any run off or spillage, and a tab having an arcuate-shaped rest which permits the user to open and close the fill spout. In use, the user pulls the tab which opens the fill spout and places a water-filled bottle against the rest. The user then pours a predetermined amount of water through the funnel and directly into the water seal chamber.

Abstract: A system for disposing of body fluids collected during surgery comprises a canister and an apparatus for emptying and cleaning the canister. The canister has a lid having an inlet port to receive body fluids during surgery and for insertion of a cleaning fluid sprayer during servicing, an outlet port with a suction tube extending into the canister for removal of fluids therefrom, and a vacuum port for the application of vacuum to the canister. The servicing unit is an appliance having a receiving compartment in which the canister is placed. A connector head in the servicing unit connects the canister to a source of cleaning fluid and to a conduit for evacuating the fluids in the canister through the suction tube and to a decontamination chamber, where they are brought into contact with a disinfecting fluid, and subsequently to a drain.

Abstract: A thoracic drainage system for removing liquid from the thoracic cavity of a patient. The system includes a reusable thoracic vacuum regulator and a standard disposable collection container. A disposable water seal chamber is also provided that can be disposed of after each patient and is a separable, independent component. There is also a combination thoracic vacuum regulator having a water seal chamber removable affixed thereto to enable the water seal chamber to be readily removed from the thoracic vacuum chamber in order to carry the water seal chamber along with the patient as that patient is transported.

Abstract: A method for collecting and disposing of urine and fecal excrement from an individual. The method is the simultaneous and independent use of a disposable urine management device and a disposable fecal management device. The disposable urine management device is independently applied in a releasable manner to the uro-genital area of the individual while the disposable fecal management device is independently applied in a releasable manner to the perineal area of the individual.

Abstract: An improved drainage apparatus for use in pleural aspiration of patients during thoracic surgery. The Apparatus includes three tubes mounted in parallel and connected to one another. A first tube acts as a vacuum input tube; the second tube is a flow monitor tube, while the third tube is filled with water and keeps the vacuum system isolated from the atmosphere.

Abstract: A disposable thoracic drainage device connectable to an aspiration unit, comprising a container body internally forming at least one chamber for collecting the drainage liquid which is connected to an inlet for connection to a patient and to a water-head suction adjustment valve. The water-head suction adjustment valve has a first water head section and a second water head section which are side by side and mutually series-connected by a connecting duct.