Abstract: Shunt devices and a method for continuously decompressing elevated intraocular pressure in eyes affected by glaucoma by diverting excess aqueous humor from the anterior chamber of the eye into Schlemm's canal where post-operative patency can be maintained with an indwelling shunt device which surgically connects the canal with the anterior chamber. The shunt devices provide uni- or bi-directional flow of aqueous humor into Schlemm's canal.

Abstract: A recovery device assembly comprises an actuator element and a mechanically radially expandable and contractible recovery device operably connected to the actuator element is provided. The recovery device has proximal and distal toroidal balloon blocking elements and a central portion between the blocking elements. The recovery device is at least partially placeable in a first, radially collapsed configuration and in a second, radially expanded configuration by manipulation of the actuator element. When in the second, radially expanded configuration, the proximal and distal blocking elements have radial dimensions greater than the radial dimension of the central portion thereby at least partially defining a collection chamber at the central portion. Also provided are methods of isolating an organ and recovering blood from an organ that use the recovery device assembly provided.

Abstract: The example systems, apparatus and methods use a local perfusion extracorporeal circuit (LPEC) for perfusing a local target region of a body, with a systemic perfusion extracorporeal circuit (SPEC) coupled to the core region of the vasculature using a peripheral placed loop to the body, and a control procedure to cause the local target region of the body to be at a specified pattern of temperature values that are different than the temperature of the core of the body.

Abstract: Provided is an exposure-preventing cap of a novel and simple structure that, by being mounted on a vial, can more reliably inhibit leaking of drug solution to an outside when pulling out and collecting drug solution in a syringe from the vial. An exposure-preventing cap, which is mounted on a mouth of a vial sealed with a rubber stopper, wherein a puncturing hole is formed in a center part of a cap-shaped housing that is attached to a mouth of the vial, and a rubber membrane is arranged at the puncturing hole so as to form an internal space between facing surfaces of the rubber membrane and the rubber stopper. The rubber membrane has a dome shape that is convex facing the rubber stopper.

Abstract: A prosthesis that when implanted in the gastrointestinal tract does not impede the normal function of the pyloric sphincter. In some instances, the prosthesis is implanted as part of, or after, a sleeve gastrectomy procedure. The prosthesis includes a stent with an outer surface and a polymeric cover fully covering the outer surface of the stent. The stent includes a proximal stent flange; a proximal stent segment extending distally from the proximal stent flange; and an enlarged stent segment extending distally from the proximal stent segment.

Abstract: A blood storage container for the anaerobic storage of blood, having enhanced sealing methods and materials for the preservation of stored blood is provided.

Abstract: An extracorporeal circuit has been conceived including: lines (16) which include passages for blood or a medical liquid; a connector (38, 40) at a free end of each of the lines (16); a cassette (18) supporting the lines, and dummy connectors (42, 44) attached to the cassette (18) and each adapted to form a mating connection with a respective one of the connectors (38, 40) at the free ends of the lines (16), wherein the connectors (38, 40) are arranged in accordance with a sequence in which the lines (16) are attached for a blood treatment session or are grouped in accordance with types of liquids to flow through the lines (16) during the blood treatment session. The extracorporeal circuit may be a circuit for dialysis and the circuit includes a hemodialyzer. Further, the connectors (38, 40) and dummy connectors (42, 44) may each be one of a male or female luer lock connector, and the dummy connectors (42, 44) may include both male and female connectors.

Abstract: An assembly for coupling a drug delivery device to a cartridge is disclosed. Optionally the assembly includes a coupling, for example a cannula, having one end extending toward the cartridge. The cartridge is optionally aligned by a guide. Optionally the cartridge has a limited freedom of movement. The coupling is optionally supported by a mount. In some embodiments, the mount is compliant enough that the end of the coupling that extends toward may move to said limited freedom of movement under a force less than a leak threshold of the connection between the coupler and the cartridge.

Abstract: Alzheimer's disease is a neurological disorder marked by progressive memory and cognitive impairments that eventually result in death. Currently, there are no effective therapies or cures that slow or halt the relentless progression of Alzheimer's disease. The invention teaches that the underlying mechanism responsible for the initiation of Alzheimer's disease is due to the insufficient flow of cerebrospinal fluid through apertures in the cribriform plate. The cribriform plate is a flat bony structure at the top of the nasal cavity directly below the olfactory bulbs. Naturally occurring apertures in the cribriform plate provide conduits for cranial nerve 1 fibers passing from the olfactory epithelium below, into the olfactory bulb above. Cerebrospinal fluid in the extracellular compartment above seeps through these apertures and into the nasal submucosa below, where it is removed by lymphatic vessels.

Abstract: Disclosed are devices and methods for treatment of eye disease such as glaucoma. Implants are described herein that create a flow field, such as between the anterior chamber and either the supraciliary space or suprachoroidal space. In addition, the implant can be treated with one or more treatments, including plasma treatments, for creating a variety of surface features and characteristics. Some of the surface features and characteristics can assist in controlling tissue responses to the implanted implant, including promoting or preventing tissue proliferation.

Abstract: Implants and methods for treating ocular disorders are provided. One method involves introducing an implant into an anterior chamber of an eye. The implant is implanted into eye tissue adjacent the anterior chamber such that a proximal end of the implant resides in the anterior chamber following implantation. A therapeutic agent is eluted from the implant into the eye. Desirably, the release of the therapeutic agent from the implant is controlled. The controlled release of the therapeutic agent can be at a chosen rate and/or for a selected duration which can be episodic or periodic. The therapeutic agent can be an antiproliferative agent, an anti-inflammatory drug, or a compound for treating glaucoma or ocular hypertension.

Abstract: A urinary catheter is configured to avoid sliding contact between the outer surface of a catheter tube and the urethra wall. A flexible tubular membrane extends through the catheter tube and has a proximal end secured to an anchor outside the urethra as the catheter tube moves into the urethra, pulling the membrane through the proximal end of the tube so it inverts and covers the outer surface of the tube. Alternatively, a catheter tube of flexible material has a proximal end secured to the anchor, and the catheter tube turns inside out as it is inserted, forming a double wall reflected tube with a proximal reflection point. The sterile interior surface of the membrane or tube becomes the external surface facing the urethral wall as the catheter is deployed, and this external surface maintains static contact with the urethral wall as the catheter is advanced or retracted.

Abstract: Devices, systems and methods are disclosed for the formation of an arteriovenous fistula in the limb of the patient. Embodiments include an apparatus for the creation, modification and maintenance of a fistula, including the modification of an existing dialysis fistula; and a method of supplying oxygenated blood to the venous circulation of a patient. A kit of anastomotic implants is described which supports a broad base of patient anatomies and fistula locations. The devices, systems and methods can be used to treat patients with one or more numerous ailments including chronic obstructive pulmonary disease, congestive heart failure, hypertension, hypotension, respiratory failure, pulmonary arterial hypertension, lung fibrosis and adult respiratory distress syndrome.

Abstract: Flow restrictors for use with a syringe or without a syringe are disclosed for dispensing a liquid medicine for an infant or child. The flow restrictors include a cover having a raised ring, a sleeve for insertion into a bottle, a self-sealing orifice for dispensing the medicine and including an annular cylinder having vertical supports or ribs which extend outward and engage the inside wall of the sleeve. The sleeve includes one or more external protrusions.

Abstract: In certain embodiments, a vial adaptor comprises a housing configured to couple the adaptor with a vial, an access channel, a regulator channel, and a regulator assembly. The access channel is configured to facilitate withdrawal of fluid from the vial when the adaptor is coupled to the vial. The regulator channel is configured to facilitate a flow of a regulating fluid from the regulator assembly to compensate for changes in volume of a medical fluid in the vial. In some embodiments, the regulator assembly includes a flexible member configured to expand and contract in accordance with changes in the volume of the medical fluid in the vial. In some embodiments, the flexible member is substantially free to expand and contract. In some embodiments, the flexible member is not partly or completely located in a rigid enclosure.

Abstract: The present invention is related to a medical aspirator and, in particular, to a medical aspirator comprising: a floor plate; a pressure plate disposed a certain distance away from the floor plate, and defining a discharge hole opened and closed by an opening/closing means; a coil spring installed between the floor plate and the pressure plate; a sealing membrane connecting the edges of the floor plate and the pressure plate, and defining a receiving space capable of receiving bodily fluid between the floor plate and the pressure plate; and a drainage tube connected to the pressure plate, for guiding bodily fluid generated from the body to the receiving space, and including a check valve therein enabling the fluid to flow only in the direction from the body toward the receiving space, wherein the medical aspirator has the effect of preventing contamination from outside air of bodily fluid extracted from the body and stored in the receiving space.

Abstract: An ocular implant comprising a shunt and a fluid absorbing conduit for reducing intraocular pressure, and optionally comprising a biodegradable ring.

Abstract: A sampling device including a body (101) having a sampling chamber (102) adapted to receive a liquid (103) to be sampled. An inlet (104) on the body (101) allows liquid (103) to flow into the sampling chamber (102). A sampling port (105) on the body is adapted to receive a sampling pot or sample receiving container (106) for collecting liquid (103) from the sampling chamber (102) wherein the sampling port includes a safety shield (107) slidaby mounted to the inside (108) of the sampling port, the safety shield slidable between a blocking position in which access to the sampling chamber is restricted and an accessible position in which access to the sampling chamber is allowed.

Abstract: A medical spraying device and method, for irrigating a wound, having a liquid reservoir for a medical irrigation liquid or a connection for such a liquid reservoir and an arrangement for applying pressure to the medical irrigation liquid, such that the irrigation liquid is pushable through a nozzle by the pressure acting on the irrigation liquid in order to produce a spray cone. The nozzle has a plurality of openings, which are arranged at an angle to one another in such a way that the irrigation liquid jets exiting from the openings, at a such flow rate and angle, meet in an atomization space and/or a discharge opening of the nozzle; thus, a spray cone is produced from the atomized irrigation liquid.

Abstract: The invention is about a next-generation blood pump that provides pulsatile blood flow, and has been developed for cardiopulmonary by-pass devices used for maintaining extracorporeal blood circulation during heart surgeries and the supportive devices of circulation system. This device is technically a sort of synchronous power-assisted motor employing direct driver technology. The mentioned blood pump contains a rotor rotating on a magnetic bearing without a shaft and through the helical wings placed into the rotor it provides pulsatile blood supply adequate for the body requirement synchronous with the ECG signals received from the patients. It provides a patient safer and controlled pulsatile blood flow while running at high efficiency.