Abstract: Enteral feeding pump systems valves assemblies therefor and related fluid flow control methods. The system includes a disposable fluid delivery set with an integral peristaltic tube section and an enteral feeding pump. The system may also include a pinching mechanism for regulating the flow of nutrient formula or water out of the fluid delivery set. Also disclosed is a flow selector valve assembly for an enteral feeding pump system, the valve assembly including a tube adapter having two input flexible tubing channels and one output tubing channel and being configured to position the flexible tubing channels in relation with a receiver. The receiver has an eccentric bearing that is moveable between a first position in which neither of the input flexible tubing channels is compressed, and a second position in which the eccentric bearing compresses one of the input flexible tubing channels therein to prevent flow therethrough.

Abstract: An example of a method of enabling medical fluid transfer between a source container and a destination container can comprise the steps of providing a closed-system fluid transfer module comprising a first closeable, resealable medical connector and a second closeable, resealable medical connector, a multidirectional fluid control valve with a driving interface configured to interface with an electromechanical driver of an electronic medical fluid transfer device, and an intermediate container or an intermediate pumping region; and instructing a user to couple the closed-system fluid transfer module to the electronic medical fluid transfer device.

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: Systems and methods for the intravascular treatment of clot material within a blood vessel of a human patient are disclosed herein. A method in accordance with embodiments of the present technology can include, for example, positioning a distal portion of a catheter proximate to the clot material within the blood vessel. The method can further include coupling a pressure source to the catheter via a tubing subsystem including a valve or other fluid control device and, while the valve is closed, activating the pressure source to charge a vacuum. The valve can then be opened to apply the vacuum to the catheter to thereby aspirate at least a portion of the clot material from the blood vessel and into the catheter.

Abstract: Sensing systems, connectors, and methods include a housing, including a sensor and a locking mechanism, a junction, and a membrane. The junction includes a fluid inlet, a fluid outlet, and a receiving mechanism. The receiving mechanism is removably attachable to the locking mechanism. The membrane is disposed within the junction, and is in fluid communication with the fluid inlet and the fluid outlet. The sensor senses a property of a fluid across the membrane when the locking mechanism is attached to the receiving mechanism.

Abstract: A self-flushing connector includes a housing having a cavity, a first inlet port, a second inlet port, and an outlet port. A collapsible valve is disposed within the cavity. A first flow path extends from the first inlet port to the outlet port. The first inlet port and the second inlet port are fluidly connected through a gap defined between the body of the collapsible valve and an inner wall of the housing defining the cavity. A second flow path extends from the second inlet port to the first flow path. When the collapsible valve is in a closed state, the collapsible valve fluidly disconnects the second flow path from the first flow path while allowing fluid to flow through the first flow path. When the collapsible valve is in an open state, the second flow path is fluidly connected to the first flow path.

Abstract: A device for transferring a toxic substance from a dispensing vessel to at least one receiving vessel comprising: (i) a receiving portion arranged to receive a dispensing vessel containing a toxic substance; and (ii) a transfer apparatus having a first infusion line adapted for fluid communication with the dispensing vessel to transfer a carrier fluid into said vessel and a second infusion line having one end adapted for fluid communication to withdraw and transfer the carrier fluid and the toxic substance from the dispensing vessel and the other end of the second infusion line arranged to connect with the at least one receiving vessel.

Abstract: A catheter includes: a first port; a second port; a first lumen communicating with the first port; a second lumen configured to selectively communicate with the first port and/or the second port; and a switching mechanism part selectively switchable between a first switching state in which the first port and the second lumen communicate with each other and a second switching state in which communication between the first port and the second lumen is blocked.

Abstract: Hand-operated suction and irrigation medical devices are provided. An example medical device comprises a housing having a proximal end and a distal end. The housing defines first and second inlet paths and an outlet path. A first tubular member is partially disposed within the first inlet path and a second tubular member is partially disposed within the second inlet path. Each of the first and second tubular members extends from the proximal end of the housing. A third tubular member is partially disposed within the outlet path and extends from the distal end of the housing. A control member is slidably disposed on the housing and is movable between a first, proximal position and a second, distal position. A passageway provides fluid communication between the first inlet path and an opening to an environment external to the housing such that covering the opening provides control over the flow of fluid through the first inlet path and the first tubular member.

Abstract: A multifunctional dental liner applicator dispenses tooth liner and a stream of air while illuminating the working dental area. The applicator includes a body and a head that is removably attached to a distal end of the body. The head supports a nozzle that is configured to be inserted into a void of a prepared tooth. A liner button on the body controls a valve for dispensing liner out of the nozzle. An air button controls airflow out of openings adjacent the nozzle for drying an area that is receiving liner. Fiber optic fibers extend from a button controlled light source housed in the body to openings adjacent the nozzle for illuminating the working area.

Abstract: A catheter apparatus has a catheter that is inserted into a lumen of the human body, a branch portion which is connected to a base end portion of the catheter and is provided with an insertion hole to pass a guide wire used in inserting the catheter in the lumen of the human body, and a liquid introducing portion for introducing liquid such as a drug solution into the catheter through a tube connected to the branch portion, where at a front end of the catheter is disposed embolus trapping part for trapping an embolus inside the lumen of the human body.

Abstract: The present disclosure relates generally to surgical aspiration and irrigation devices, including methods regarding the same.

Abstract: A core, rotatably fitted within a body of a manifold assembly, includes a flow channel configured so that, when the core is rotated 360 degrees, fluid communication between ports of the body is only established by the channel at a first position, between first and second ports, and at a second position, between third and fourth ports. The channel may define an angle greater than 90 degrees and less than 180 degrees, preferably 120 degrees; and, the rotation, between first and second positions, may be approximately 180 degrees. In a medical injection system, the first and second ports are fill ports of the assembly, the first being coupled to a reservoir, and the second being coupled to a pump; and the third and fourth ports are injection ports of the assembly, the third being coupled to the pump, and the fourth being coupled to an injection line.

Abstract: A syringe is provided having a hub with an orifice, first and second barrels having an interior surface to form respective lumens, a valve, and a test indicator. The first and second barrels slideably receive respective first and second plungers for movement therein. The valve is operable to provide a fluidly communicative path between the orifice of the hub and the first and second barrel lumens. The test indicator is responsive to at least one characteristic of a bodily fluid, the test indicator positioned to be exposed to any bodily fluid drawn into the first barrel lumen and visible from an exterior of the first barrel.

Abstract: A flow control device for medical liquid including a housing having an inlet and an outlet, and a channel formed in an inner surface of the housing, the channel extending at least partly in axial direction; a rotatable member rotatable in relation to the housing without being axially displaced, the rotatable member having at least two apertures; and a core member arranged inside the rotatable member, fixedly connected to the rotatable member. A helical flow path is formed between the lateral surface of the core member and the inner surface of the rotatable member, the at least two apertures of the rotatable member being in communication with said helical flow path, and wherein each of the apertures debouches into the channel in at least one rotational position of the rotatable member.

Abstract: A respiratory access assembly includes a distal plate having one port and cuff and an axially aligned proximal plate including a first port and first cuff and a second port and second cuff. The distal plate is configured to move relative to the proximal plate. The respiratory access assembly includes an actuator, which has a plurality of predetermined positions. The actuator can lock the plates together such that the distal port is aligned with either port of the proximal plate or so that the distal port is not aligned with either port of the proximal plate. A method of using a respiratory access assembly is provided.

Abstract: A method for determining a volume of ablated tissue is provided. The method includes the steps of: supplying energy to tissue to create an ablation volume therein; excising one or more slices of the tissue having a portion of the ablation volume therein; and subjecting at least a portion of the slice to a first contrast agent for a predetermined period of time, wherein the contrast agent is configured to color dead cells within the ablation volume.

Abstract: The invention relates to a device for reducing pressure variations in a fluid flowing in an aspiration branch of a surgical system, which pressure variations are generated by a pump that delivers in a non-continuous manner in the active operating state, with a diffuser arrangement which is arranged, in the aspiration branch, upstream of the pump in the direction of flow of the fluid. The invention also relates to a surgical system, in particular an ophthalmic microsurgical system for lens surgery.

Abstract: The present disclosure relates generally to surgical aspiration and irrigation devices, including methods regarding the same.

Abstract: A variable hemostasis valve is disclosed that may be used during medical procedures to prevent blood loss while permitting the percutaneous introduction, operation, and removal of medical instruments. A flexible tubular seal element is disclosed that is disposed within the variable hemostasis valve to provide a fluid-tight, adjustable seal. After insertion of a medical instrument into the valve through at least a portion of the flexible tubular seal element, a proximal portion of the valve housing may be rotated to cause the tension of the flexible tubular seal element to increase over the inserted medical instrument and engage the valve in a closed position. The proximal portion of the valve housing may then be rotated in an opposite direction to release the seal and return the tubular seal element to a relaxed lumen open position.

Abstract: A fluid control device for directing fluid flow comprising a needleless access device for transferring fluids and methods of directing fluid flow. The fluid control device may have a first port, a second port, a third port and a connecting portion joining the first, second and third ports. A first valve element may be positioned within the first port and a fluid director may be positioned within the connecting portion. The first valve element may move between an opening position, where fluid may flow past the first valve element, and a closed position, where fluid may be prevented from flowing past the first valve element. The fluid director may have at least one passageway for connecting at least two of the first, second and third ports such that fluid may flow therebetween. An actuation mechanism may be used to orient the fluid director and, consequently, the at least one passageway within the connecting portion.

Abstract: The present invention relates to a multi-way valve for use in medicine or medical technology, having at least one basic housing through which a medium can flow in sections, and having an actuator which is held in said basic housing so as to be rotatable about a central axis, wherein the basic housing has at least two connection points for the inflow and outflow of the medium and forms an actuator receptacle which has a peg arranged concentrically with respect to the central axis and which has, on the inner side of the basic housing, a radially encircling cutout, and wherein the actuator has a control element, a substantially hollow cylindrical section which receives the peg of the actuator receptacle at least in sections, at least one throughflow opening for the fluidic connection between two connection points, and at least one radially encircling molding on the outer side of the cylindrical section, and wherein the peg of the actuator receptacle has at least one counterbearing for the actuator to form a seal

Abstract: The invention provides a switching device for an irrigation system. The switching device provides selective communication between a supply port to which a supply of fluid under pressure can be attached and a balloon port to which a fixing balloon of a catheter can be attached, and between the supply port and a port to which a liquid reservoir can be attached. By use of a selection handle, the user can deform conduits in a pre-determined sequence and thus control an irrigation procedure by opening and closing fluid flow in various conduits. The invention further provides an irrigation device incorporating the switching device and a method of controlling a fluid flow e.g. in an irrigation system.

Abstract: The devices and methods shown provide for the minimization of extravasation during arthroscopic surgery. The anti-extravasation surgical portal plug allows a surgeon to drain excess fluids from the soft tissue surrounding the surgical field during arthroscopic surgical procedures.

Abstract: An improved method and equipment for tissue/vessel sealing is disclosed for the sealing, coagulation and transection of tissue during surgical procedures. The improvement is accomplished through better management of heat and moisture present during tissue treatment by having tissue grasping surfaces comprised of an outer non-conducting region and an inner conductive region, and including channels in the jaw assembly to direct steam and moisture away from surrounding tissue. The outer region follows the perimeter each jaw, isolating the treatment zone and preventing steam and excess heat from leaving the tissue treatment zone, reducing thermal margins and unintended patient burns. The outer region also prevents surrounding moisture from affecting the treatment zone and allowing more consistent results.

Abstract: Monopolar electrosurgery devices adapted for resecting tonsil and adenoid tissue. The devices minimize thermal injury by employing a plasma generated by pulsed electrical signals to precisely and effectively cut or coagulate the tissues. Suction may also be applied to the tissues to enhance the cutting, coagulation, and tissue manipulation functions. The devices include an interchangeable tip that may be switched for another tip, depending on which tip may be more suitable for tonsillectomy or adenoidectomy.

Abstract: A system includes (i) a needle for insertion into a port of an implantable infusion device, and (ii) a receiver apparatus having a port location signal receiver module capable of receiving a signal from the implantable infusion device regarding spatial orientation of the port. The system further includes a processor operably coupled to the receiver apparatus and capable of determining the orientation of the needle relative to the port based on the received signal. The system also includes a display operably coupled to the processor. The processor is configured to cause the display to graphically render trajectory of the needle relative to the port. The port is graphically rendered as a target structure having a reference area. The needle is graphically rendered as an object moveable relative to the target structure. Occupation of the reference area by the object indicates trajectory alignment of the port and the needle.

Abstract: A bronchotracheal access valve for a bronchoaspiration apparatus. The valve is characterized in that the rotation of a second member in a given direction with respect to a first member moves the valve from a configuration in which a conduit communicates hydraulically with a sleeve, to a configuration in which the conduit communicates hydraulically with a flush conduit via a duct and a channel to flush an end portion of a catheter.

Abstract: A rotary medical manifold, for delivering various fluids through a patient delivery mechanism is described. The rotary manifold can include a manifold body and a valve stem. The manifold body can include a central cavity, an output port, a first fluid port, and a second fluid port. The valve stem can include an injector port, and a single central fluid passage. The valve stem can be adapted to slidably engage the central cavity of the manifold body and provide selective fluidic connectivity between the injector port and the output port, the first fluid port and the second fluid port.

Abstract: The invention relates to a system for the extraction and infusion of a body fluid, in particular a system for the extraction and infusion of blood, having a fluid distribution device with an outer structural element at which several connection ports are formed and an inner structural element which is arranged, at least partially, in a seat in the outer structural element, is displaceable between positions and has a hollow space configured for the intake and discharge of a fluid. The invention also relates to a method for operating a system for the extraction and infusion of a body fluid.

Abstract: A clamping assembly includes a first clamping member and a second clamping member. The first clamping member defines a first lumen dimensioned to non-rotatably engage a first portion of a tubular member. Rotating the first clamping member effects a rotation of the first portion of the tubular member. The second clamping member defines a second lumen dimensioned to non-rotatably engage a second portion of the tubular member. Rotating the second clamping member in relation to the first clamping member rotates the second portion of the tubular member in relation to the first portion of the tubular member to twist the tubular member to restrict flow through the tubular member.

Abstract: A bronchotracheal access valve for a bronchoaspiration apparatus. The valve is characterized in that the rotation of a second member in a given direction with respect to a first member moves the valve from a configuration in which a conduit communicates hydraulically with a sleeve, to a configuration in which the conduit communicates hydraulically with a flush conduit via a duct and a channel to flush an end portion of a catheter.

Abstract: Visceral fat may be removed from a subject using a cannula that has an interior cavity and an orifice configured to permit material to enter the cavity. This is accomplished by generating a negative pressure in the cavity so that a portion of the tissue is drawn into the orifice. Fluid is then delivered in pulses, via a conduit, so that the fluid exits the conduit within the cavity and impinges against the portion of the tissue that was drawn into the orifice. The fluid is delivered at a pressure and temperature that causes the visceral fat to soften, liquefy, or gellify, without damaging the subject's internal organs that are in the vicinity of the visceral fat. The visceral fat that has been softened, liquefied, or gellified is then suctioned away.

Abstract: A system to minimize fluid turbulence inside a tissue cavity during endoscopic procedures. A body tissue cavity of a subject is distended by continuous flow irrigation using a solenoid operated pump on the inflow side and a positive displacement pump, such as a peristaltic pump, on the outflow side, such that the amplitude of the pressure pulsations created by the outflow positive displacement pump inside the said tissue cavity is substantially dampened to almost negligible levels. The present invention also provides a method for accurately determining the rate of fluid loss into the subject's body system during any endoscopic procedure without utilizing any deficit weight or fluid volume calculation, the same being accomplished by using two fluid flow rate sensors. The present invention also provides a system of creating and maintaining any desired pressure in a body tissue cavity for any desired cavity outflow rate.

Abstract: In one embodiment of the invention, a robotic surgical instrument is provided for the control of flows of one or more fluids into and out of a surgical site. The robotic surgical instrument may include a housing, a flow control system, a hollow tube, and one or more hose fittings. The housing to couple the instrument to a robotic arm. The flow control system mounted in the housing includes one or more controlled valves to control the flow of one or more fluids. The hollow tube has a first end mounted in the housing coupled to the flow control system. A second end of the hollow tube has one or more openings to allow the flow of fluids into and out of the surgical site. The hose fittings have a first end coupled to the flow control system and a second end to couple to hoses.

Abstract: An adaptor for use with a medical catheter comprises a housing having a first tubular channel with a first longitudinal axis, a dial having a second tubular channel with a second longitudinal axis, and an adaptor fitting removably connected to the second tubular channel. The dial is rotatable between an open position and a closed position when the adaptor fitting is connected thereto. In the open position the first tubular channel is fluidly connected to the second tubular channel, and in the closed position the first tubular channel is not fluidly connected to the second tubular channel. The dial may be configured such that it is not rotatable between the open position and the closed position when the adaptor fitting is not connected thereto. The housing may comprise an upper housing member, an intermediate housing member, and a lower housing member.

Abstract: Monopolar electrosurgery devices adapted for resecting tonsil and adenoid tissue. The devices minimize thermal injury by employing a plasma generated by pulsed electrical signals to precisely and effectively cut or coagulate the tissues. Suction may also be applied to the tissues to enhance the cutting, coagulation, and tissue manipulation functions. The devices include an interchangeable tip that may be switched for another tip, depending on which tip may be more suitable for tonsillectomy or adenoidectomy.

Abstract: An eye treatment system includes an eye treatment probe and a console. The console has a cassette receptacle and a fluid drive system including a first peristaltic drive rotor and a second peristaltic drive rotor. The first and second drive rotors are exposed to the receptacle and are substantially coaxial. The cassette includes a cassette body and a fluid pathway network for coupling the fluid drive system of the console with the probe. The cassette body has cassette positioning surface for fittingly engaging the receptacle. The fluid pathway network has a first resilient tubing segment and a second resilient tubing segment, the first and second tubing segments are configured for peristaltic driving engagement by the first and second rotors, respectively, when the cassette is mounted to the console. Various elements of the cassette are configured for interfacing with the components of the console when the cassette is mounted to the console.

Abstract: A combination of a valve assembly and multi-chamber, sequential delivery syringe is disclosed. The combination effectively provides a safety system for transferring hazardous materials from a vial to a site of use. All potentially hazardous materials are flushed from exposed connecting sites prior to disconnections.

Abstract: A connector (100) for a medical device including a body (110) having a proximal end (114), a distal end (112), and a passage (116) extending therethrough between the proximal end and the distal end that fluidly connects the proximal end and the distal end. The proximal end (114) includes a connecting portion (119) for releasably connecting the connector to an external device. The distal end (112) is fluidly connected to a conduit. A cylinder (124) is rotatably disposed in the passage (116) between first position and a second position, wherein the cylinder includes an opening (128) extending generally diametrically therethrough. One or both ends (130,132;230,232) of the cylinder provide manually- or tool-engageable sections (136;236) to enable rotation of the cylinder between open and closed positions, allowing and preventing fluid flow through the connector (100), respectively.

Abstract: An indwelling balloon catheter for an endoscope is provided with a flexible tube including a first lumen and a second lumen, the first lumen and the second lumen being arranged in parallel with each other and extending in an axial direction of the flexible tube over an entire length thereof, and a connector provided with a first connecting pipe and a second connecting pipe which protrude from a body of the connector, protruded portions of the first connecting pipe and the second connecting pipe being configured to be removably inserted into the first lumen and the second lumen, respectively. A cross sectional shape of the first lumen is a non-circular shape, a cross sectional shape of the first connecting pipe corresponding to the cross sectional shape of the first lumen. The first connecting pipe protrudes longer from the connector than the second connecting pipe.

Abstract: An apparatus includes a first valve having an inlet capable of being in fluid communication with a first fluid source, an outlet capable of being in fluid communication with the inlet, and two unidirectional valves. The first valve is capable of being in a first mode in which the inlet is in fluid communication with the outlet through a first flow path, and a second mode in which the inlet is in fluid communication with the outlet through a second flow path isolated from the first flow path. The two unidirectional valves are along the second flow path.

Abstract: A method and apparatus for alerting a colostomate or medical attendant to the presence of fecal matter. The device includes a hollow plug detachably securable to a flexible port positioned about the stoma. The port carries an alarm circuit which is triggered when fecal matter enters the plug lumen which will alert the colostomate to an impending episode. The signal may be vibratory, audible or visible and may be transmitted to a remote location. The device includes an inflatable air cuff which, when inflated, presents a physical barrier to the passage of fecal matter. Gas may pass through filters in the tube. The method involves positioning the device in the stoma, inflating the cuff and generating an alarm when matter is sensed.

Abstract: An administration feeding set for use with a flow control apparatus to deliver fluid from at least one fluid source to a patient. The feeding set includes tubing adapted to extend from the fluid source for flow of fluid through the tubing from the fluid source toward a patient. A locating finger projects outwardly from the tubing and is positioned on the tubing so that when received on the flow control apparatus in an operating position the finger permits a locating member of the flow control apparatus to close. However, when the tubing is received on the flow control apparatus in a non-operating position the finger does not permit the locating member to close thereby to verify whether the tubing is in the operating position on the flow control apparatus.

Abstract: A device is described for fitting and removing a closing means (27, 29) on an end portion (13) of a tubular element (3), comprising: a container (1) defining an internal chamber (18); a rotating platform (19) inside said chamber at the bottom (16) thereof; a receiving housing (26) that is able to receive and hold a first closing means (27) from said end portion of tubular element; and a releasing housing (28) that is able to contain and release a second closing means (29), in said end portion of tubular element; said receiving and releasing housings provided with an opening for passage of the closing means, being fixed on said rotating platform with said opening turned towards said perimeter walls (17) of the container. The device can be used as a connector for peritoneal dialysis and minimizes or eliminates the risks of contamination, also of pathogens, and the risks of peritonitis.

Abstract: A fluid control device for directing fluid flow comprising a needleless access device for transferring fluids and methods of directing fluid flow. The fluid control device may have a first port, a second port, a third port and a connecting portion joining the first, second and third ports. A first valve element may be positioned within the first port and a fluid director may be positioned within the connecting portion. The first valve element may move between an opening position, where fluid may flow past the first valve element, and a closed position, where fluid may be prevented from flowing past the first valve element. The fluid director may have at least one passageway for connecting at least two of the first, second and third ports such that fluid may flow therebetween. An actuation mechanism may be used to orient the fluid director and, consequently, the at least one passageway within the connecting portion.

Abstract: A closed blood sampling system within a pressure monitoring line having a control valve that enables a clearance reservoir to be isolated from the pressure column when no samples are being taken. The valve is a stopcock-like device that includes a rotating valve member and attached control handle with clear visible and tactile indicators for the mode of operation. The rotating valve member has a number of internal and circumferential channels for connecting or disconnecting select ports in the core of the valve. By isolating the clearance reservoir, the quality of the pressure signal is improved such that the sampling line can be lengthened for greater convenience in the intensive care or operating room. The valve may also incorporate a blunt cannula sampling site therewithin.

Abstract: An enterostomy device for providing fluids and nutrients through a stoma formed through the abdominal wall of a patient is described. The enterostomy device, which may be configured as either a gastrostomy device or a jejunostomy device, comprises a low-profile retaining member which is configured to be unobtrusively positioned within the stomach or the intestine, and which is configured to provide sufficient surface area for contacting the stomach or intestine to prevent unintentional removal or release of the enterostomy device from the patient. The enterostomy device is also structured with a low-profile port hub for facilitating the inflation of the retaining member and feeding and venting through the stoma.

Abstract: The invention relates to a medical pump device comprising a rotary valve (13) having preferably only one rectilinear channel (20) which respectively connects the inlet (4) and the outlet (7) of the pump device, or connects the inlet to a pump chamber (15), or said pump chamber to the outlet, upon rotation of the rotary element (19) of the valve. The invention enables a medical pump device to be especially easily produced, said pump device being preferably inserted between an infusion syringe driver or an infusion container and a catheter, and being used to supply small quantities of liquid in an accurately dosed manner.

Abstract: A blood flow reversal valve useful in hemodialysis having rotational detent features enabling audible and tactile feedback to a clinician and alignment features such as visible indicators associated with the blood lines on either side of the valve to confirm normal or reverse flow.