Abstract: A method and an accessory device for an ostomy system comprising a monitor device and an ostomy appliance, the ostomy appliance comprising a base plate is disclosed.

Abstract: An ostomy pouch has a body side wall and a distal side wall defining a collection chamber. An opening is provided in the body side wall. A barrier is operably mounted to the body side wall over the opening. The barrier has an inlet opening. An internal collection member is mounted to the barrier. The internal collection member includes a tubular net having a first open end and a second closed end, and a ring-shaped capsule for storing the net inside the capsule in a collected manner. The ring-shaped capsule has an open central region and is mounted to the barrier with the capsule open central region and the barrier inlet opening aligned with one another to define a pouch inlet. The capsule extends into the pouch collection chamber and the first open end of the net is mounted to the capsule overlying the pouch inlet. Excretion is inlet to the pouch and is discharged into the net, paying out the net.

Abstract: An ostomy system configured to detect moisture content in a base plate or a sensor assembly part of the ostomy system, the ostomy system comprising the base plate and/or a sensor assembly part and a monitor device. The base plate or the sensor assembly part includes a first adhesive layer, a plurality of electrodes, and one or more sensing zones each covering one of one or more regions of the first adhesive layer, each of the one or more sensing zones including at least two of the plurality of electrodes. The monitor device is electrically coupled to the plurality of electrodes of the base plate or the sensor assembly part and configured to measure one or more resistances in the one or more sensing zones between the plurality of electrodes, each of the one or more resistances measured by two of the plurality of electrodes at one of the one or more sensing zones, and determine moisture content of the first adhesive layer at each of the one or more sensing zones based on the measured one or more resistances.

Abstract: In one example embodiment, an apparatus for providing negative-pressure therapy may comprise a negative-pressure source, a pressure sensor, and a control valve. The negative-pressure source may be configured to be fluidly coupled to a distribution component. The control valve may be fluidly coupled to the pressure sensor and configured to be selectively coupled to the negative-pressure source, the distribution component, or both. A controller may also be configured to operate the control valve to selectively couple the pressure sensor to at least one of the negative-pressure source and the distribution component through the control valve, and the pressure sensor may provide a feedback signal to the controller indicative of pressure in a feedback path associated with the position of the control valve. The controller may also be configured to operate the negative-pressure source based on the feedback signal.

Abstract: A chest drainage system includes a collection device and a fluid pathway configured to extend from the collection device to a patient. A pressure source is configured to selectively provide sub-atmospheric pressure to the fluid pathway. The system is configured to introduce sub-atmospheric pressure from the pressure source at a substantially constant target pressure and at a dynamic pressure that varies from the target pressure. A method is also disclosed for draining a pleural cavity of a patient. The method involves applying dynamic pressure to the pleural cavity of a patient by changing sub-atmospheric pressure applied to the patient such that the patient's pleura moves without any or limited patient activity, thus facilitating removal of loculated fluid from the pleural cavity. The method may involve the use of the chest drain system.

Abstract: A water leakage detector includes: an electrostatic capacity sensor that is arranged at a bottom portion of a housing; and a leg portion that provides a space between the bottom portion and a floor of the housing including the electrostatic capacity sensor. With this configuration, it may be possible to detect quickly in an earlier stage of water leakage and achieve resistance to deterioration caused by an environment.

Abstract: Systems and methods for controlling a pump system for use in negative pressure wound therapy are described herein. In some embodiments, a method for controlling a pump system includes causing provision of negative pressure, via a flow path, to a wound dressing configured to be positioned over a wound, the flow path configured to fluidically connect the pump system to the wound dressing, measuring a first pressure value in the flow path at a first time, measuring a second pressure value in the flow path at a second time, calculating a first rate of pressure change using the first and second pressure values, and in response to determining that the calculated first rate of pressure change satisfies a threshold rate of change, providing an indication that the wound dressing is full, wherein the method is performed under control of a controller of the pump system.

Abstract: Embodiments of a reduced pressure system and methods for operating the system are disclosed. In some embodiments, the system can include one or more processors responsible for various functions associated with various levels of responsiveness, such as interfacing with a user, controlling a vacuum pump, providing network connectivity, etc. The system can present GUI screens for controlling and monitoring its operation. The system can determine and monitor flow of fluid in the system by utilizing one or more of the following: monitoring the speed of a pump motor, monitoring flow of fluid in a portion of a fluid flow path by using a calibrated fluid flow restrictor, and monitoring one or more characteristics of the pressure pulses. The system can provide external connectivity for accomplishing various activities, such as location tracking of the system, compliance monitoring, tracking of operational data, remote selection and adjustment of therapy settings, etc.

Abstract: Excretion by a diaper wearer in a diaper is predicted by providing in or on the diaper on the wearer an excretion detector capable of detecting excretion by the diaper wearer and a motion sensor capable of detecting movements of the diaper wearer. The sensor continuously detects and at least temporarily records movements of the diaper wearer, and these detected movements are analyzed to determine movement patterns. Then, on detection of excretion by the detector, a movement pattern immediately preceding the detection of excretion is stored or flagged as a critical movement pattern. Thereafter each time movements matching the critical movement pattern are detected, a signal is sent to a user.

Abstract: A tissue closure treatment system and method are provided with an external patient interface. A first fluid transfer component FTC.1 comprises a strip of porous material, such as rayon, with liquid wicking properties. FTC.1 can be placed directly on a suture line for transferring fluid exuded therethrough. An underdrape is placed over FTC.1 and includes a slot exposing a portion of same. FTC.2 comprises a suitable hydrophobic foam material, such as polyurethane ether, and is placed over the underdrape slot in communication with FTC.1. Negative pressure is applied to FTC.2 through a connecting fluid transfer component FTC.3. A negative pressure source can comprises a manual device or a power-operated suction device. The tissue closure method includes a manual operating mode using a manual suction device with an automatic shut off for discontinuing suction when a predetermined volume of fluid has been drained.

Abstract: In one example embodiment, an apparatus for providing negative-pressure therapy may comprise a negative-pressure source, a pressure sensor, and a control valve. The negative-pressure source may be configured to be fluidly coupled to a distribution component. The control valve may be fluidly coupled to the pressure sensor and configured to be selectively coupled to the negative-pressure source, the distribution component, or both. A controller may also be configured to operate the control valve to selectively couple the pressure sensor to at least one of the negative-pressure source and the distribution component through the control valve, and the pressure sensor may provide a feedback signal to the controller indicative of pressure in a feedback path associated with the position of the control valve. The controller may also be configured to operate the negative-pressure source based on the feedback signal.

Abstract: Manifold structures, systems, and methods are disclosed that include using longitudinal members and one or more shaped projections to cause microstrain at a tissue site. In one instance a manifold structure includes a plurality of spaced longitudinal members and at least one shaped projection coupled to at least one of the plurality of longitudinal members for creating a microstrain at a tissue site. The at least one shaped projection includes a columnar member having a distal end and includes an enlarged member positioned at the distal end of the columnar member. The columnar member has a first outer diameter (D1) and the enlarged member has a second outer diameter (D2). The second outer diameter of the enlarged member is greater than the first outer diameter of the columnar member (D2>D1). Other systems, methods, and structures are presented.

Abstract: An electronic device has a home button that is available in a plurality of different contexts to dismiss user interfaces in response a first type of input. The device detects a first input of the first type directed to a displayed first user interface. In response, the device determines whether user interface tactile outputs are enabled. If so, the device performs a first operation and provides a corresponding first tactile output. If not, the device performs the first operation and forgoes providing at least a portion of the corresponding first tactile output. After performing the first operation, the device detects a second input of the first type on the home button. In response, the device performs a second operation that is associated with the home button and provides tactile output that is associated with activation of the home button, regardless of whether user interface tactile outputs are enabled.

Abstract: In one example embodiment, a dressing connector is described that provides a first fluid path between a first connector and a second connector, and a second fluid path between a third connector and a fourth connector. A liquid barrier may be disposed in the first fluid path. The first fluid path and the second fluid path are generally exposed to an exterior surface of the dressing connector. In some embodiments, a tube may also be bonded to the third connector to provide a third fluid path between the dressing connector and another component. In more particular embodiments, the liquid barrier may be a filter, such as a hydrophobic bacterial filter, a sintered polymer filter, and/or a charcoal filter.

Abstract: An electronic device: displays a home button configuration user interface with a plurality of different tactile output settings for the home button. While displaying the home button configuration user interface, the device detects selection of a respective tactile output setting. In response to detecting a first input of a first type on the home button (while the respective tactile output setting is selected), the device determines whether the respective tactile output setting is a first or a second tactile output setting for the home button. If the respective tactile output setting is the first tactile output setting, the device provides a first tactile output without dismissing the home button configuration user interface. If the respective tactile output setting is the second tactile output setting, the device provides a second tactile output without dismissing the home button configuration user interface.

Abstract: A stoma dilation device that includes a tubular support and an inflatable dilation portion located on the tubular support. The inflatable dilation portion includes a stiffening portion and inflation lumen. The device may have a retention portion configured to have a diameter upon full, unrestrained inflation that is greater than the diameter of the dilation portion. The device is designed to be placed in a patient to dilate the stoma for the installation of a catheter feeding tube. The device may be placed and withdrawn with the use of an endoscope which need be inserted into the patient only one time. The single insertion of the endoscope significantly reduces the trauma to the patient in comparison with multiple endoscope insertion methods.

Abstract: A pump for infusing fluid, the pump including a pumping mechanism, a fluid delivery device, a plurality of electric field sensors, and a measurement component. The plurality of electric field sensors is configured to estimate either an electric field that is associated with a patient, or an electric field that is associated with a fluid path of the pump, or both. The measurement component is configured to receive the electric field estimates from each of the electric field sensors and further configured to measure the difference between the electric field estimates.

Abstract: A measuring device 1 for recording a peak level of a liquid flow includes an inlet 2 which opens into an inlet chamber 3 for receiving the liquid flow and a recording chamber 4 in open liquid communication with the inlet chamber 3 for allowing the liquid flow to accumulate up to a level therein. The recording chamber 4 is separated from the inlet 2 for direct liquid communication. At least one outflow opening 9 is provided to allow at least partial escape of the liquid flow, and indicator elements are provided to leave an indication of a level at least approximately at an indication level. A peak level in a liquid flow can thus be recorded very reliably with the measuring device 1.

Abstract: A reduced pressure treatment system includes a porous pad positioned at a tissue site and a canister having a collection chamber, an inlet, and an outlet. The inlet is fluidly connected to the porous pad. A reduced pressure source is fluidly connected to the outlet of the canister to such that fluid from the tissue site may be drawn into the collection chamber. A hydrophobic filter is positioned adjacent the outlet to prevent liquid from exiting the collection chamber through the outlet. A baffle is positioned within the canister to create a tortuous path between the inlet and the outlet to prevent premature blocking of the hydrophobic filter.

Abstract: Meconium stained amniotic fluid can indicate intrauterine fetal distress. The invention provides a system and method for detecting meconium in released amniotic fluid in pregnant women, including a collection body such as a hygienic pad, having a meconium detector. This invention is designed to be employed mainly by a lay person at home; it also may provide possible etiologies for fetal distress.

Abstract: The illustrative embodiments described herein are directed to a system and method for administering reduced pressure at a tissue site. The apparatus includes a reduced pressure source. The reduced pressure source generates a reduced pressure. The apparatus includes a tube having a plurality of lumens. The plurality of lumens includes at least one collection lumen. The reduced pressure source applies the reduced pressure to the tissue site through the plurality of lumens such that the at least one collection lumen receives fluid from the tissue site. The at least one collection lumen stores the fluid received from the tissue site.

Abstract: A wound dressing apparatus includes a wound dressing member dimensioned for positioning relative to a wound bed. The wound dressing member including an internal vacuum reservoir and has a port in communication with the vacuum reservoir for applying subatmospheric pressure to the vacuum reservoir to facilitate removal of fluid from the wound bed. The wound dressing member includes a visual pressure indicator associated therewith for indicating a level of pressure within the vacuum reservoir. The visual pressure indicator includes color indicia having a plurality of colors corresponding to a condition of the pressure within the vacuum reservoir. The wound dressing member includes a lower absorbent member positionable adjacent the wound bed and an upper member which at least partially defines the vacuum reservoir. At least one of the top member and the lower absorbent member has the visual pressure indicator mounted thereto.

Abstract: An apparatus for safety-compliant emptying and filling of a reagent container (24, 40) for a tissue processor (20) comprises a suction line (30, 42) for aspirating a reagent out of the reagent container (24, 40) and a delivery line (32, 44) for filling the reagent container (24, 40) with the reagent, a terminating opening (31, 43) of the suction line (30, 42) being spaced away from a terminating opening (33, 45) of the delivery line (32, 44).

Abstract: A wearable EVD system having a ventricular catheter and transducer supported proximately to a patient's ear by a mount, such as supporting headband or ear clip. An adjustable orifice valve or a spring-loaded needle valve is used to control the amount of CSF that drains into a drip chamber suspended on the patient for periodic measurement and emptying into a similarly located drainage bag, thereby avoiding the need for an IV pole and allowing the patient more mobility without disrupting drainage of CSF.

Abstract: A bagless catheter and incontinence device, which reduces maceration, microbial skin infiltration and infection, urinary tract infection, and offers the user a normal, odor-free, active lifestyle, is provided.

Abstract: An apparatus and method are provided for treating wound with negative pressure. The apparatus includes a wound cover, a first pump for providing said negative pressure at a chosen pressure level to the wound, a canister, a first conduit between the wound cover and the canister, first means for measuring the pressure within the canister, and a second conduit which connects the canister with the first pump. A circulating pump is arranged to intermittently transport a gas volume from the canister to the wound region via a third conduit and back to the canister via the first conduit in order to press out possible exudates from the first conduit to the canister. A second means analyzes the pressure curve over time of said pressure in the canister and a third means indicates by alarm when said pressure curve differs from a normal cyclical form.

Abstract: An artificial Ostomy containment device comprising an implantable intra-abdominal sleeve adapted to interfere with movement of a closure assembly positioned within the sleeve; and a closure assembly comprising a hollow stomal insert sized and shaped to conduct waste content from an intestinal portion in an abdominal cavity through said insert and out of a stoma, and a fixation element coupled to said stomal insert sized and positioned to interfere with said intra-abdominal sleeve.

Abstract: Systems, methods, and apparatuses for providing feedback for reduced-pressure treatment of a tissue site are described. A regulator may include a supply chamber fluidly coupled to the dressing, a control chamber fluidly coupled to the dressing, a charging chamber fluidly coupled to the supply chamber through a port, and a regulator valve operable to control fluid communication through the port based on a pressure differential between the control chamber and a therapy pressure. The feedback system may include one or more mechanical feedback interfaces fluidly coupled to the regulator to provide a signal of at least one of an application of reduced-pressure therapy, a leak condition, a blockage condition, and a canister full condition.

Abstract: Systems, methods, and apparatuses for providing feedback for reduced-pressure therapy are described. A regulator can include a supply chamber fluidly coupled to a dressing, a control chamber fluidly coupled to the dressing, a charging chamber fluidly coupled to the supply chamber through a port, and a regulator valve operable to control fluid communication through the port based on a pressure differential between the control chamber and a target pressure. The feedback system can include a printed circuit board, a pressure sensor and a signal interface communicatively coupled to the printed circuit board. The pressure sensor can be fluidly coupled to the control chamber to determine the pressure in the control chamber. The signal interface can indicate a state of the reduced-pressure therapy. A potential source can be communicatively coupled to the printed circuit board, the pressure sensor, and the indicator.

Abstract: A chest drainage system includes a collection device and a fluid pathway configured to extend from the collection device to a patient. The fluid pathway has a proximal portion configured to extend proximally toward the patient and a distal portion configured to extend distally from the patient. The chest drainage system also includes a pressure source including an accumulator configured to selectively provide sub-atmospheric pressure to the distal portion of the fluid pathway and a valve configured to selectively relieve pressure in the proximal portion of the fluid pathway. The system is configured to open the valve and to introduce the sub-atmospheric pressure from the accumulator of the pressure source when a predetermined pressure differential is detected between the proximal and distal portions of the fluid pathway.

Abstract: A method and apparatus for alerting a user of topical negative pressure therapy apparatus to a full waste canister condition are described, the apparatus comprising a device having vacuum pump means and a waste canister connected to the device and the waste canister operably connected to a wound dressing by aspiration conduit means for aspirating fluid from the wound, the aspiration conduit means, the waste canister and the device providing a fluid flow path therethrough and the vacuum pump means providing fluid flow through the apparatus, the apparatus further comprising fluid flow restriction means in the fluid flow path of said vacuum pump and fluid pressure sensing means upstream and downstream of said fluid flow restriction means.

Abstract: Some embodiments comprise a pump assembly for reduced pressure wound therapy, comprising a housing, a flow pathway through the pump, one or more valves in communication with the flow pathway, a pump supported within or by the housing, and a one-way flow valve in fluid communication with the pump. The pump assembly can have a pressure sensor in communication with the flow pathway through the pump, and at least one switch or button supported by the housing, the at least one switch or button being accessible to a user and being in communication with the controller. The one-way flow valve can be configured to substantially prevent a flow of gas through the one-way flow valve in a direction of flow away from the pump. The pump assembly can have a controller supported within or by the housing, the controller being configured to control an operation of the pump.

Abstract: A surgical sponge and fluid monitoring system and method are provided. The system (100) includes a support ring (104) for securely supporting a container (101) with at least one port opening (206) for placing sponges (204) into the container through the at least one port opening. The support ring includes RFID communication circuitries (305, 307) that interrogate an RFID device (205) in the sponge (204) and an RFID device in the container. The support ring is mechanically linked to a load cell (706, 1329) in the system. The processor (1302) reliably detects when a sponge is placed into the container through the at least one port opening, identifies the type of sponge placed into the container, counts the number of sponges in the container, sorts the types of sponges, and calculates fluid loss for a patient in a surgical procedure. A user interface (1308, 114) keeps the medical professionals informed.

Abstract: NuChain supply chain and disposal chain apparatus are created by NuPurposing containers, conditioning and transforming such containers from fluent material delivery containers into waste collection containers. Novel structural features of the waste collection systems allows bottle docking for the ingress of collection material into fluent material distribution containers as well as operation as a canister waste ingress collection system. The application of counter opposing forces on a canister and a lid operates in sealing and the unsealing and assembly and disassembly. A reduced pressure configured to be drawn away from said container inducing ingress of air into said container by a source of reduced pressure.

Abstract: Negative pressure wound therapy apparatuses and dressings, and systems and methods for operating such apparatuses for use with dressings are disclosed. In some embodiments, controlling the delivery of therapy can be based on monitoring and detecting various operating conditions. An apparatus can have a controller configured to monitor the duty cycle of a source of negative pressure and, based on the monitored duty cycle, determine whether a leak is present. The controller can be configured to provide an indication that a leak is present. For example, the controller can be configured to suspend and/or pause the delivery of therapy, and to restart the delivery of therapy due to a timeout, request from a user, etc. In addition, the controller can be configured to pause and/or restart the delivery of therapy upon a request from the user, such as in response to the user operating a switch.

Abstract: A device for use with a negative pressure bandage for supply negative pressure. The device includes a pump module and a controller module. The pump module contains a power source and a pump. The pump module is removably contained in the controller module. The pump module and controller module can be connected with a connector that provides both a physical and pneumatic connection. The controller module may include one of more visual indicators for allowing the status of the device to be observed at a distance.

Abstract: A valve that is sealable to an associated container having an interior fluid storage region is adapted to permit and stop flow of fluid from the fluid storage region. The valve includes a valve body sealable to the container and a stem mounted to the valve body having a portion in flow communication with the fluid storage region. The stem is movable relative to the valve body between an open position to permit flow from the fluid storage region through the valve, and a closed position to stop flow through the valve. The stem has a grasping region spaced from the valve body. The grasping region is adapted rotate the stem to move the valve between the open and closed positions. The grasping region has first and second sides. One of the sides has a tactile indicator to provide indication of the position of the valve, the other of the side is devoid of the tactile indicator.

Abstract: Embodiments of a reduced pressure system and methods for operating the system are disclosed. In some embodiments, the system can include one or more processors responsible for various functions associated with various levels of responsiveness, such as interfacing with a user, controlling a vacuum pump, providing network connectivity, etc. The system can present GUI screens for controlling and monitoring its operation. The system can be configured to determine and monitor flow of fluid in the system by utilizing one or more of the following: monitoring the speed of a pump motor, monitoring flow of fluid in a portion of a fluid flow path by using a calibrated fluid flow restrictor, and monitoring one or more characteristics of the pressure pulses. The system can be configured to provide external connectivity for accomplishing various activities, such as location tracking of the system, compliance monitoring, tracking of operational data, remote selection and adjustment of therapy settings, etc.

Abstract: A fluid level sensor assembly for monitoring a fluid level in a fluid collection canister of a medical waste fluid collection system. The fluid level sensor assembly includes a fluid level sensor configured for monitoring the fluid level in the fluid collection canister and a fluid level sensor cover configured for preventing direct contact between the fluid level sensor and a fluid in the fluid collection canister. The fluid level sensor cover includes a polymeric cap and polymeric sheath extending from the cap. The elongate tubular sheath surrounds an elongate probe of the sensor with the cap positioned at a base of a sensor body of the sensor to prevent direct fluid contact with the elongate sensor probe and the sensor body.

Abstract: NuChain supply chain and disposal chain apparatus are created by NuPurposing containers, conditioning and transforming such containers from fluent material delivery containers into waste collection containers. Novel structural features of the waste collection systems allows bottle docking for the ingress of collection material into fluent material distribution containers as well as operation as a canister waste ingress collection system. The application of counter opposing forces on a canister and a lid operates in sealing and the unsealing and assembly and disassembly. A reduced pressure configured to be drawn away from said container inducing ingress of air into said container by a source of reduced pressure.

Abstract: A reduced pressure treatment system includes a porous pad positioned at a tissue site and a canister having a collection chamber, an inlet, and an outlet. The inlet is fluidly connected to the porous pad. A reduced pressure source is fluidly connected to the outlet of the canister to such that fluid from the tissue site may be drawn into the collection chamber. A hydrophobic filter is positioned adjacent the outlet to prevent liquid from exiting the collection chamber through the outlet. A baffle is positioned within the canister to create a tortuous path between the inlet and the outlet to prevent premature blocking of the hydrophobic filter.

Abstract: Negative pressure wound therapy apparatuses and dressings, and systems and methods for operating such apparatuses for use with dressings are disclosed. In some embodiments, controlling the delivery of therapy can be based on monitoring and detecting various operating conditions. An apparatus can have a controller configured to monitor the duty cycle of a source of negative pressure and, based on the monitored duty cycle, determine whether a leak is present. The controller can be configured to provide an indication that a leak is present. For example, the controller can be configured to suspend and/or pause the delivery of therapy, and to restart the delivery of therapy due to a timeout, request from a user, etc. In addition, the controller can be configured to pause and/or restart the delivery of therapy upon a request from the user, such as in response to the user operating a switch.

Abstract: A medical waste fluid collection cart may include a controller for controlling one or more functions of the medical waste fluid collection cart and a memory coupled to the controller, the memory configured for storing one or more vacuum levels. The graphical user interface may be communicatively coupled to the controller and/or the memory and may be configured to allow a user to monitor and/or control one or more functions of the medical waste fluid collection cart. The graphical user interface may include a user confirmation screen to allow a user to confirm a vacuum setting. Using the confirmation screen, the user may confirm the vacuum setting using a first selection corresponding to a predetermined low vacuum level or a second selection corresponding to a previously used vacuum level.

Abstract: Systems and methods are provided for sensing fluid in a dressing on a patient and producing an electrical signal. In one instance, a galvanic cell is used as an electronic detection device. The galvanic cell is placed in the dressing and produces voltage when the dressing is substantially saturated. In one instance, the dressing is a reduced-pressure, absorbent dressing. Other systems, methods, and dressings are presented.

Abstract: A bodily fluid drainage assembly can include a fluid bag and one or more covers. The assembly can include one or more volume indicators from which an approximate volume of a bodily fluid that is retained within the bag can be ascertained. In some arrangements, a cover includes a volume indicator that defines an opening through which a transparent or semitransparent portion of the bag can be viewed.

Abstract: A defecation detection apparatus including: a feces/urine receiving member that is placed to face the body of a wearer and that receives discharged feces and urine; a urine suction device that is detachably attached to the feces/urine receiving member and that can sucks urine discharged in the feces/urine receiving member; a temperature sensor that is placed at a defecation position where discharged feces are received in the feces/urine receiving member; and a control section that detects the presence of discharged feces based on a signal remaining after removing a signal that is output from the temperature sensor within a predetermined time after an operation of the urine suction device from a signal that is output from the temperature sensor.

Abstract: A valve assembly is provided which includes a housing having an inlet end and an outlet end and defining a fluid channel and a central chamber. A dissolvable valve member is positioned to obstruct flow through the channel within the chamber. The dissolvable valve member is formed of a material which is dissolvable at a predetermined rate upon contact with a preselected fluid. The preselected fluid is selected from the group consisting of blood, urine, saline and antimicrobial solutions. The dissolvable valve member can be formed from a fluid soluble glass or a starch based material.

Abstract: The present invention relates to a collector for human feces, consisting of: a fixing plate (100) comprising a C-shaped left plate (101) and a C-shaped right plate (101?) of which the ends are connected to each other so as to have a penetrated central portion and be folded over each other; a feces collection bag (200) of which the end is fixed to one lateral side of the fixing plate (100), and which ordinarily is rolled to be inserted between the folded C-shaped left plate (101) and C-shaped right plate (101?) of the fixing plate (100), and is pushed out from a penetrated hole of the fixing plate (100) when feces is injected; and an adhesion means (300). Since the feces collection bag does not come in contact with the anus when being worn, ease of defecation is facilitated due to improved comfort.

Abstract: Methods and device for extracting and collecting tissue, which can be used for example in tissue engineering and grafting applications, are disclosed. In one embodiment, a device can include an outer tube. A rotatable shaft can be disposed within the outer tube can have a tissue harvesting tip formed on its distal end, the tissue harvesting tip being effective to excise tissue upon rotation thereof. A tissue collection device can be included to receive and collected excised tissue, and the tissue collection device can indicate the amount of tissue collected therein. For example, the tissue collection device can include a straining element which collects excised tissue and an indicator by which to assess the amount of collected tissue. In some embodiments, the tissue collection device can translate to indicate the amount of collected tissue.

Abstract: Methods and apparatuses are disclosed for applying negative pressure to a wound site. In some embodiments, the apparatus comprises a source of negative pressure, a processing element, and a memory comprising instructions configured to, when executed on the processing element, cause the apparatus to attempt to generate, via the source of negative pressure, a desired negative pressure at the wound site. If the desired negative pressure has not been generated after a first predetermined period of time, the instructions cause the apparatus to: deactivate the source of negative pressure for a second predetermined period of time, and subsequently attempt to generate the desired negative pressure at the wound site.