Abstract: A breathing system for hyperthermic assisted radiation therapy includes at least one heating element that modulates the temperature of air inhaled by a patient, at least one cooling element that modulates the humidity of the air inhaled by a patient, and a controller that maintains the desired humidity and temperature.

Abstract: In an apparatus for collection of waste anesthetic gases, and a method of using such an apparatus, the apparatus has a gas collection chamber with an input port to be connected to an exhaust of an anesthesia delivery system for receiving a first gas flow therefrom that contains a waste anesthetic gas component. An output port from the gas collection chamber is connected to a vacuum system for evacuation of an evacuation gas flow from the gas collection chamber. A bidirectional port leads to and from the gas collection chamber, which has an adsorbing unit connecting the gas collection chamber with an ambient environment surrounding the gas collection chamber. The apparatus provides for safe prevention of discharge of exhaled anesthetic gases into an ambient atmosphere surrounding the apparatus.

Abstract: An application for a PEEP valve includes a filter media in the air flow between a patient interface and exit vent(s). The patient interface is connected to a patient airway system and the exit vents exhaust exhalation gasses into the atmosphere. The filter prevents or reduces the passage of microbes from the patient's exhalation gasses into the atmosphere. The PEEP valve provides positive gas pressure to a patient's lungs, requiring a predetermined exhalation gas pressure to be exceeded before releasing exhalation gasses into the atmosphere.

Abstract: A catheter support comprising a pliant tubular structure of rigidity greater than the penis including a region surrounding the penis shaft, a region surrounding the penis head, and a substantially closed end having an aperture aligned with the penis terminal opening through which the catheter is received. The catheter support limits or eliminates catheter movement substantially radial to the axis of the catheter and thus radially against the inner opening if the penis head, substantially reducing or eliminating abrasion or other insult to the penis surfaces and tissue that interface with the catheter. One embodiment comprises 2 substantially identical elongated halves having longitudinal recesses and hinged together to close around the penis end and catheter providing the catheter support in a structure having improved comfort and wearability.

Abstract: A mouth-to-mouth resuscitation device comprising a straight blow-in tube having a proximal side and a distal side, a filter and one way valve on the proximal side for receiving exhaled breath from a mouth of a rescuer, an opening at the distal side for delivering the exhaled breath into the throat of a victim, an inflatable bladder surrounding the straight blow-in tube which, when inflated, assumes a donut shape which has a diameter of about 1.5? to 2.5?, the bladder located on the straight blow-in tube between about 0.75? and 2.0? from the distal opening, an inflation tube in fluid communication with the inside of the inflatable bladder.

Abstract: Apparatus for use during open system diving to support underwater human respiration. In accordance with various embodiments, an air supply provides a supply of air along a supply conduit. A regulator is adapted for engagement with a diver's mouth to receive air from the supply during an inhale cycle and to direct a mixture of water and exhaust air away from the diver along an exhaust conduit during an exhale cycle. An air/water separator separates the exhaust air from the water in said mixture and directs the separated exhaust air through an exhaust air port. In some embodiments, a one-way stop valve is provided within the air/water separator to prevent back flow. In further embodiments, a bubble diffuser emits the exhaust air as a fine mist of bubbles into the surrounding water.

Abstract: A device for oxygen supply of a user in an aircraft comprising a breathing mask (20), a stowage box (1) for the breathing mask and an oxygen supply hose (22) having one end connected to the stowage box and the other end connected to the breathing mask, wherein the device further comprises means (3) to fix the stowage box in a ceiling of the aircraft, an aperture on the bottom side of the stowage box closed by a door (7) and a leash (28) connected to the stowage box by one end and to the breathing mask by the other end so that, when the door is open, the mask falls and is kept hovered by the oxygen supply hose and the leash.

Abstract: A liquid-collection canister includes a liquid collection chamber defined by at least one wall and a first and second gas-communication pathway formed within the at least one wall. A first aperture is positioned between the first gas-communication pathway and the liquid collection chamber to allow gaseous communication between the liquid collection chamber and the first gas-communication pathway. A second aperture is positioned between the second gas-communication pathway and the liquid collection chamber to allow gaseous communication between the liquid collection chamber and the second gas-communication pathway. A first and a second liquid-air separator are positioned over the first aperture and the second aperture, respectively, to substantially prevent liquid passing through the first and second apertures.

Abstract: A safety shield including a protective device is provided including a piercing member having a proximal end, a distal end and defining a longitudinal axis. A clip defines a first cavity dimensioned for movement of the piercing member therethrough and is oriented in an axis transverse to the longitudinal axis. The first cavity is movable between a movable orientation and a binding orientation. The clip includes a first leg that defines a second cavity dimensioned for movement of the piercing member therethrough and a distal part being configured to engage a medical device. The clip further includes a second leg having a bearing surface that engages the piercing member. The legs are biased for convergent movement such that the first cavity is disposed in the binding orientation and the distal part of the first leg disengages the medical device.

Abstract: A device for delivering a drug includes a body having a proximal end and a distal end and an opening in the distal end thereof. An orifice mechanism at the distal end of the body communicates with the opening. The orifice mechanism includes an inner member having a proximal end and a distal end; a winding helically wound around the inner member; and wherein the winding and the inner member define a first channel for carrying a drug therethrough. An inlet is at the proximal end of the winding and an outlet is at the distal end of the inner member.

Abstract: A medical delivery system for delivering a fluid to a desired location within a body that includes a first member having an aperture, and a second member adapted to be positioned over the first member. The fluid to be delivered is contained within a fluid storage device, formed by at least one of the first member and the second member. The medical delivery system includes means for repositioning the first member relative to the second member between a first state preventing passage of the fluid through the aperture and a second state enabling passage of the fluid outward from the fluid storage device through the aperture.

Abstract: The present invention relates to medical devices that are inserted or implanted into patients and that have antimicrobial coatings that release free radicals into the vicinity of the device. These devices may have coatings that alter their rate of flow release or elution release of an antibacterial agent from a coating on the device upon external stimulation. The coating should therefore be responsive to external control such as by heating, external RF stimulus, sonic control, visible or ultraviolet light exposure and the like. By having control of the release rate, and in some structures without invasion of the patient by mechanical means in addition to the device itself, the release rate can be in response to need at the implant site. The class of compounds to be released are free radical generating or initiating compounds, or compounds that release free radicals upon immersion or stimulation, the free radicals acting as the antimicrobial agent.

Abstract: A number of devices are illustrated for providing a manifold that can simply and selectively couple a number of different therapeutic and diagnostic elements to a catheter or other medical device. Some examples include devices having sliding actuators, rotary actuators, button actuators, or combinations thereof, for easily changing the valve scheme and fluid pathways within a manifold.

Abstract: A flange attaching section has a flange supporting section and a movable section, and the movable section can approach the flange supporting section and separate therefrom due to rotational moving. Even if a flange section of a barrel of a syringe has various thickness, the flange section is easily attached between the flange supporting section and the movable section, and although the attachment is easy, the flange section comes in pressure contact with the flange supporting section in the attached state. Even if, therefore, the flange section of the barrel of the syringe has various thickness, a syringe pump, in which moving of the barrel of the syringe during infusion is prevented securely and the infusion is executed at an accurate speed, is provided.

Abstract: Disclosed are methods and devices for navigating a subarachnoid space in a vertebrate organism including percutaneously introducing a device into the spinal subarachnoid space at an entry location. Navigation of the spinal subarachnoid space is disclosed for the purpose of reaching a desired location in the subarachnoid space or the intracranial space, including areas in and around the spinal cord and brain. Once a desired location is reached, methods and devices for cooling or heating the desired location to cause physiologic changes are suggested.

Abstract: A shieldable needle device including a needle cannula, a hub, a pair of wings extending laterally from opposing sides of the hub, a tip guard axially movable along the needle cannula from a proximal position substantially adjacent the hub to a distal position, and a drive member is disclosed. The drive member includes a first end connected to the hub and a second end connected to the tip guard and is extendable between a folded biased position and an extended position for moving the tip guard from the proximal position to the distal position. The pair of wings, when in a dorsal position, retain the drive member in the folded biased position maintaining the tip guard in a proximal position. Upon release of the wings, the drive member unfolds, extending the tip guard from the proximal position toward the distal position.

Abstract: An aspirating device for an eye includes a tubular member having a predetermined length that enables the tubular member to fit into an open eye and to rest on the surface of the eyeball adjacent one of the eyelids. The tubular member has one or a plurality of spaced openings therein along its length that allow liquid on the surface of the eyeball to be drawn into the tubular member upon the application of suction to the tubular member.

Abstract: Methods of enhancing fluid flow through a vascular site occupied by a vascular occlusion, as well as systems and kits for use in practicing the same, are provided. In practicing the subject methods, the vascular site is flushed simultaneously with a first dissolution fluid (e.g., an organic matter dissolution fluid and/or an inorganic matter dissolution fluid), and a second dissolution fluid attenuating fluid, where flushing is carried out in a manner such that only a surface of the vascular occlusion is contacted with the non-attenuated dissolution fluid. The subject methods, systems and kits for practicing the same find use in the treatment of a variety of different vascular diseases characterized by the presence of vascular occlusions, including both partial and total occlusions.

Abstract: A transdermal drug delivery device for forming a micropore in a tissue membrane of an animal comprising a substrate and a porator that is located on or within the substrate. The porator is constructed of a material that is destroyed upon forming the micropore. The transdermal drug delivery device also comprises at least one reservoir and a controller for controlling the formation of said micropore by the porator and destroying the porator after the formation of the micropore.

Abstract: The invention provides a injection device for administering an injectable product, including a base section adapted to receive a container from which a product dose is dispensed through a needle by displacement of a piston in the container, and a drive unit including a driven member, a drive element and a damping arrangement, the drive unit for applying a force to advance the piston in the container to dispense a dose, wherein the damping arrangement generally counteracts the drive force and counter forces. The invention also encompasses a needle safety sleeve and a blocking structure for use with injection devices.