Abstract: A medical suctioning system includes a device for insertion into an intubated patient's bronchi, the device including a controller end having actuating components that include a control mechanism coupled to a plurality of cables at the controller end, the controller end having a suction control button engaged with a plunger to allow for activation and deactivation of suction through the controller end; a control lever in communication with an articulating lever housed within the controller end, the articulating lever to engage with one or more cables disposed through the controller end and to engage with an articulating tip portion at a distal end opposite the controller end; and a catheter extending away from the controller end to the distal end.

Abstract: A device is provided for pooling a fluid from a container unit having at least one container, and includes an inlet port having at least one inlet channel configured for receiving the fluid or ambient air, and an outlet port having at least one outlet channel configured for delivering the fluid to an attachment. Both inlet and outlet ports are disposed on the device. A cavity is provided for accommodating insertion of the container unit for pooling the fluid from the at least one container. At least one spike is disposed in the cavity and configured for puncturing a stopper of the at least one container when the container unit transitions from an upper position to a lower position.

Abstract: An ostomy appliance (20) including a sealing wafer (22) with a first adhesive (32) having a first opening (34) configured to be attached to a skin surface around an ostomy of a user, and a bag (36) for collecting stomal output that includes a second adhesive (44) configured to engage with the skin surface radially outside of the sealing wafer. The sealing wafer and the bag are configured to be connectible to each other either in direct connection or by a coupling interface. One kind of coupling interface includes one or more pipe sections (50). The ostomy appliance allows for differentiation of adhesive types for different purposes, such as sealing and load carrying.

Abstract: A kit of parts includes a urological device and a catheter. The urological device has a stem defining a lumen, a valve connected to a proximal portion of the stem and located in the lumen, and a head part connected to the stem and extending radially around the valve. The catheter is adapted to insert the urological device into a urethra of a user.

Abstract: An apparatus and method are disclosed for detecting the disconnection of a vascular access device such as a needle, cannula or catheter from a blood vessel or vascular graft segment. A pair of electrodes is placed in direct contact with fluid or blood in fluid communication with the vascular segment. In one embodiment, the electrodes are incorporated into a pair of connectors connecting arterial and venous catheters to arterial and venous tubes leading to and from an extracorporeal blood flow apparatus. Wires leading from the electrodes to a detecting circuit can be incorporated into a pair of double lumen arterial and venous tubes connecting the blood flow apparatus to the blood vessel or vascular graft. The detecting circuit is configured to provide a low-voltage alternating current signal to the electrodes to measure the electrical resistance between the electrodes, minimizing both the duration and amount of current being delivered.

Abstract: A surgical access port and assembly are disclosed for providing access for a medical instrument into an intracorporeal cavity of a patient undergoing surgery. The access port comprises a cannula and a first passage which extends along the cannula and along which a medical instrument is arranged to pass, the passage comprising a first entrance portion disposed at a proximal region the of the cannula and a first exit portion disposed at a distal region of the cannula. The cannula further comprises a second passage which extends along the cannula and along which an electrode is arranged to pass, the second passage comprising a second entrance portion disposed at a proximal region of the cannula and a second exit portion disposed at a distal region of the cannula.

Abstract: Systems, apparatuses, and methods for instilling fluid to a tissue site in a negative-pressure therapy environment are described. Illustrative embodiments may include a pneumatically-actuated instillation pump that can draw a solution from a solution source during a negative-pressure interval, and instill the solution to a dressing during a venting interval. A pneumatic actuator may be mechanically coupled to a disposable distribution system that can provide a fluid path between the solution source and a distribution component. A bacterial filter may be disposed in the fluid path between the actuator and the distribution component to prevent contamination of the actuator during operation. The distribution system may be separated from the actuator and disposed of after operation, and the actuator may be re-used.

Abstract: An apparatus is including a negative pressure wound therapy pump including a pump housing; and a negative pressure wound therapy canister attached to and readily removable from the pump housing; the canister including a flexible conduit; the canister operable to receive suction generated by the pump; the flexible conduit sized, shaped, and located to interface with the pump housing of the pump such that suction produced by the pump is transmitted to the canister via the flexible conduit.

Abstract: A fluid delivery device and method is provided, comprising a handle, a plate, a foam applicator coupled to a bottom surface of the plate and impregnated with an antiseptic solution. A lid member protects the foam applicator from an external environment and defines at least one aperture therein, wherein the lid member is coupled to the plate to form a breakable seal between the plate and the lid member. A tray member, having a bottom surface and at least one sidewall to define a volume therein, contains the foam applicator. The foam applicator is hermetically sealed from the external environment by the lid member, plate and tray member. The lid member is detachable from both the plate and the tray to release the foam applicator from the fluid delivery device and is in a ready-to-use condition without further activation.

Abstract: An absorbent article and method of making the absorbent article are disclosed. The absorbent article having a topsheet, a backsheet, and an absorbent core structure having one or more layers wherein at least one layer is a heterogeneous mass layer, wherein the topsheet and the heterogeneous mass are integrated such that they reside in the same X-Y plane.

Abstract: Disclosed is an absorbent article with biocompostable properties, such as a feminine hygiene pad. Particularly, the present invention is directed to an absorbent sanitary article with a high degree of biocompostability. The sanitary article comprises, in one embodiment, at least a top layer, a back layer, and absorbent core, wherein the absorbent core includes a superabsorbent polymer, and wherein at least the superabsorbent polymer is biocompostable. The absorbent article exhibits improved biocompostable properties and performance comparable to non-biodegradable absorbent articles which include non-biodegradable superabsorbent polymers.

Abstract: A valve with an on-off mechanism for a bag used for conditioning, reconstituting, and/or diluting of injectable products, with the valve integrated to the single access point of a bag; the valve includes an open-close mechanism that enables a syringe or an infusion equipment, both including a luer-lock terminal, to be directly coupled to said valve; the valve comprises five basic components: the tapered base, the mobile tapered part, a smaller diameter sealing O-ring, a larger diameter sealing O-ring, and the cover that protects the terminal with a luer-lock type thread; the valve removes the requirement of using metallic needles or plastic spikes during practical use of the bag.

Abstract: The package comprises a sterile bag filled with liquid diluent, a bottle equipped with a pierceable cap to contain a medicinal substance and a tube extending from the bag and having a coupling and perforation device for the cap. The bag is housed in a first casing, while the bottle and the coupling and perforation device are in a second casing. The tube has a portion, housing a flow diverter adjustable from a first position which impedes any communication between the bottle and the bag, a second position which allows the bag to be put in communication with a sealed side opening for a syringe, or a third position which allows the bottle to be connected with said side opening. Another side opening of the flow diverter a flexible tube with hydrophobic filter is attached, terminating into one of said sterile sealed casings and serving as a pressure compensator.

Abstract: A method of deploying an ocular implant into Schlemm's canal of an eye. The method includes the steps of inserting a distal end of a cannula through a cornea of the eye and into an anterior chamber of the eye, the cannula having a distal opening extending from the distal end and through a side wall; placing the distal opening of the cannula into fluid communication with Schlemm's canal; advancing the ocular implant distally through the cannula with a delivery tool engaged with the ocular implant, a proximal portion of the ocular implant engaging the delivery tool proximal to a distal portion of the delivery tool; and disengaging the ocular implant and the delivery tool when the proximal portion of the ocular implant reaches the cannula distal opening. The invention also includes a system for practicing the method.

Abstract: An integrated system for assessing wound exudates from the wound of a patient is described. The system may contain functionality to detect, process and report various wound parameters. The system also may make treatment determinations based on these findings. The system may detect one or more physiological values of the wound exudates from the wound of the patient. The system may means for comparing the one or more detected physiological values to predetermined physiological values in order to obtain a comparison result in real time. The system may include a processor 15 which provides an electronic signal based on a comparison result in which the electronic signal may correspond to guidelines for treating the wound 13. The system may be integrated with other wound treatment devices, such as negative pressure wound therapy devices (NPWT) 9.

Abstract: The invention relates to glaucoma pump implant (100) developed for use in reducing intra ocular pressure of glaucoma patients. The invention particularly relates to a glaucoma pump implant (100) that allows the glaucoma pump implant (100) to act as an active pump by utilizing diameter changes of pupil (210) and iris (220) caused by light variations.

Abstract: An integrated structure of a preparation syringe includes a stretchable piston, a barrel, a needle, an exposed rubber plug, a sealing sheet, a built-in rubber plug, a sealing rubber plug and an engaging rubber plug. One end of the barrel is provided with the stretchable piston, and another end of the barrel is provided with a clamping column. The exposed rubber plug is provided on a side of the stretchable piston away from the barrel. The built-in rubber plug is provided within the barrel. A Scale mark is provided on a circumferential surface of the barrel. The sealing rubber plug is inlaid and sleeved on the clamping column. The sealing sheet is provided on a side of exposed tuber plug away from the barrel. A blunt end is provided at an end of the needle away form a needle tip. The engaging rubber plug is provided outside the blunt end.

Abstract: A system and apparatus for the collection of serous or serosanguinous fluid from a percutaneous site after surgery. A pump unit with one or more pumps or powered sources provide continuous negative pressure suction to draw fluid from the percutaneous site and pumps the fluid into disposable reservoirs with one-way valves that are easy to handle while maintaining sterility and a seal to prevent the loss of vacuum. Air is continuously removed from the reservoirs. Measurement and analysis of the output is performed automatically.

Abstract: Disclosed is a method for the collection, processing and reuse of amniotic fluid at a C-section site. The method is conducted coincident with and in the operating room wherein the caesarian section is performed. In the method, amniotic fluid is suctioned from the caesarian section collection site using a vacuum line system which includes a canister positioned along the vacuum line. The canister has a port whereby the amniotic fluid can be removed from the canister. The amniotic fluid can be then be mixed with a coagulant or sealant and applied to the wound site of the cesarean section patient. Placental aspirate may also be collected, processed and used in accordance with the method of the present invention.

Abstract: Disclosed is a portable automatic electronic drop administration device and method of operation thereof. The device comprises a microcontroller communicatively coupled to at least an accelerometer and an electromechanical assembly to administer one or more drops of a liquid, semi-liquid or gaseous substance from any flexible container held within. The device detects whether it is in a suitable orientation before automatically self actuating the electromechanical assembly to administer one or more drops. It can be used in a variety of settings including self administration of eye drops, dispensing condiments or precise metering of liquid medications. Additionally, the device may contain sensors and wireless components to track usage and event data that may be communicated to a physician or other healthcare provider remotely.