Abstract: An article of safety outerwear has a body including: a trunks outerwear part, adapted to receive the lower region of the torso of a wearer in use and having apertures through which the legs of the wearer protrude; and a pair of tubular leg parts, each adapted to receive therethrough a leg of the wearer and extending between an upper end, connected to the trunks outerwear part, and a lower end disposed adjacent to the ankle of said leg. Each leg part includes a tubular vent portion, extending from about the knee to about the ankle of the leg received in the leg part in use. The vent portion is constructed substantially from mesh. The mesh has an open texture for high breathability, presents a smooth surface to the legs in use, and is adapted to provide the wearer with protection against abrasion in normal working and athletic activities.

Abstract: Apparatus and a method for treating an irregularity in a wall of a vessel of a patient defined by an irregular or afflicted wall portion with adjacent normal wall portions comprises a catheter having a distal end portion for being guided through the vessel to the site of the irregularity. A balloon associated with said distal end portion of the catheter for selective inflating to contact the walls of the vessel urges a stent carried by the distal end portion of the catheter in a constricted condition for passage through the vessel into an expanded form with the stent spanning the afflicted wall portion and contacting the adjacent wall portions. The catheter is formed with lumens for inflating the balloon, for receiving a guidewire for guiding the catheter through the vessel, and for connecting a port in the catheter proximate the afflicted wall portion to enable delivery of a therapeutic agent into the vessel to contact the stent and the irregular wall portion.

Abstract: A liner for a ladle is formed of a body of refractory material defining a hollow interior which is bounded by a continuous sidewall. Within the interior is a barrier of refractory material which faces the interior surface of part of the sidewall and is spaced inwardly therefrom in the hollow interior of the body to define with said facing part of said sidewall a spout for discharging molten metal, in use, from the ladle. The barrier has two longitudinal edge surfaces received at two facing inner portions of the sidewall respectively which are extended inwardly. By providing these inward extensions the barrier can be positioned within the interior of the liner thereby obviating the need for an outward extension from the liner body to define a spout. This enables the liner to be used with ladle shells without the shell requiring modification to accommodate such an outward extension.

Abstract: A muzzle stabilizer for a repeating firearm is described. The muzzle stabilizer includes a tubular body having two or more gas vents for venting gas in an average direction that exerts a corrective force for counterbalancing muzzle climb during periods of repeating discharges. An attachment flange, which has a coupler adapted to mate with a corresponding coupler on the end of the muzzle of the firearm, is disposed at a first end of the tubular body. A gas regulator is engaged with a second end of the tubular body for adjusting the venting of gas through at least one of the gas vents. The gas vents can include a plurality of ninety-degree vents of graduated sizes radially arranged about the tubular body. The muzzle stabilizer can include a multistage expansion chamber through which high pressure and temperature gas expands before it is vented through the gas vents.

Abstract: A medical device system that is insertable in a body lumen for treating and/or preventing injury to a body lumen wall is disclosed. The system comprises a stent comprising a sidewall having a first edge and a second edge, and a balloon capable of being disposed within the sidewall. The balloon has a first end portion that is capable of contacting the first edge of the sidewall and a second end portion that is capable of contacting the second edge of the sidewall when the balloon is expanded. At least the first end portion of the balloon comprises a first biologically active material. When the balloon is expanded, the first end portion of the balloon extends axially beyond the first edge of the sidewall in order to deliver the first biologically active material to a portion of the body lumen wall that is adjacent to the first edge of the sidewall. Methods for deploying the system are also disclosed.

Abstract: An endotracheal device for use with a supra-laryngeal mask including a video display for providing images of the area ahead of the endotracheal device to facilitate insertion without damaging the surrounding tissue; the endotracheal device having a flexible portion and a rigid portion maintaining a light and an image guide for transmitting illuminating light ahead of the endotracheal device and for transmitting reflected light from the area ahead of the endotracheal device.

Abstract: A passenger kiosk, comprising a computing arrangement receiving data from a plurality of data feed arrangements, the data including airport operational parameters for an airport facility, a set of advertisements and inventory management rules and a kiosk display displaying one of the advertisements based on one of the airport operational parameters and one of the inventory management rules.

Abstract: A medical device, polymer composition, and method for delivering substantially water-insoluble drugs to tissue at desired locations within the body. At least a portion of the exterior surface of the medical device is provided with a polymer coating. Incorporated in the polymer coating is a solution of at least one substantially water-insoluble drug in a volatile organic solvent. The medical device is positioned to a desired target location within the body, whereupon the drug diffuses out of the polymer coating.

Abstract: A catheter for placement of an in situ implant is provided. This catheter may include a first elongate shaft having a proximal end and a distal end, a second elongate shaft having a proximal end and a distal end, a first sharpened distal tip disposed at the distal end of the first shaft and a second sharpened distal tip disposed at the distal end of the second shaft. The first shaft and the second shaft may also be secured to one another at the distal end of the first shaft according to the invention. Still further, according to other teachings, the first sharpened distal tip may extend beyond the second sharpened distal tip in a catheter that practices the invention.

Abstract: Apparatus and a method for treating an irregularity in a wall of a vessel of a patient defined by an irregular or afflicted wall portion with adjacent normal wall portions comprises a catheter having a distal end portion for being guided through the vessel to the site of the irregularity. A balloon associated with said distal end portion of the catheter for selective inflating to contact the walls of the vessel urges a stent carried by the distal end portion of the catheter in a constricted condition for passage through the vessel into an expanded form with the stent spanning the afflicted wall portion and contacting the adjacent wall portions. The catheter is formed with lumens for inflating the balloon, for receiving a guidewire for guiding the catheter through the vessel, and for connecting a port in the catheter proximate the afflicted wall portion to enable delivery of a therapeutic agent into the vessel to contact the stent and the irregular wall portion.

Abstract: The present invention provides an interactive multimedia apparatus (1, 11, 21) comprising a digital musical instrument (3, 14, 24, 41) and having a plurality of control members (42, 44, 45, 46) including at least one limited state (on/off) control member (44) and one or more dynamic range state control members (42, 45, 46). A central control unit (2, 12, 22) is also provided having a store of digital media stored thereon and a suite of software for interpreting the state of the control members (42, 44, 45, 46) in order to select, open and render the digital media. A control unit is associated with the digital musical instrument (3, 14, 24, 41) and has a CPU and a sensing means for identifying the state of the control members (42, 44, 45, 46).

Abstract: The invention provides a system which comprises a medical device that delivers a combination of therapies. These therapies include the administration of radiation, biologically active materials, cryotherapy, and thermotherapy. The present invention is also directed to a method of treating body lumen surfaces using the system of the invention. A system is provided for delivering a biologically active material to a surface of a body lumen being exposed to a radioactive source. In one aspect, the system comprises an implantable medical device which has two opposing ends, each having a surface, and a middle portion. The two opposing ends comprise a biologically active material and the middle portion of the medical device is substantially free of any biologically active material. In another aspect, the system delivers a genetic material to a surface of a body lumen which is exposed to a radioactive source.

Abstract: A method of supporting at least two different investor groups with different maximum leverage ratios in one investment fund is disclosed. Each different investor group may have an associated tracking account. According to various embodiments, the method includes establishing contractual arrangements between investors of the investor groups, the investment fund and an external lender. The contractual arrangements limit the recourse of the external lender to assets allocable to the investors of an investor group if the tracking account associated with such investor group triggers a margin call on a loan from the external lender. Alternatively, the contractual arrangements may limit the recourse of the external lender to assets allocable to the investors of an investor group if the trading account triggers a margin call to the extent that such call is allocable to such investor group.

Abstract: The inventors have found that both the drug dose and drug release profiles are significant factors for the safety and efficacy of drug coated stents. The inventors have identified optimum dosing and release kinetics for drug coated stents. In particular, the inventors have determined dosing and release kinetics that permit the delivery of the lowest effective drug dosage, thus enhancing patient safety and minimizing any side effects from the drug.

Abstract: A laryngoscope with a detachable camera, the system providing illuminating light to and images of the area ahead of the laryngoscope to facilitate insertion of the laryngoscope without damage to the surrounding tissue, the system including a keyed attaching device for facilitating attachment of camera and laryngoscope in a correct orientation.

Abstract: The invention provides a system which comprises a medical device that delivers a combination of therapies. These therapies include the administration of radiation, biologically active materials, cryotherapy, and thermotherapy. The present invention is also directed to a method of treating body lumen surfaces using the system of the invention. A system is provided for delivering a biologically active material to a surface of a body lumen being exposed to a radioactive source. In one aspect, the system comprises an implantable medical device which has two opposing ends, each having a surface, and a middle portion. The two opposing ends comprise a biologically active material and the middle portion of the medical device is substantially free of any biologically active material. In another aspect, the system delivers a genetic material to a surface of a body lumen which is exposed to a radioactive source.

Abstract: A combination laryngoscope and video display for providing images of the area ahead of the laryngoscope to facilitate insertion without damaging the surrounding tissue; the laryngoscope having a detachable blade and a rigid, detachable light and image guide attachment device for providing illuminating light ahead of the blade and for detecting the reflected light.

Abstract: An analyzer, preferably a desktop analyzer, includes: a component transport system; a liquid dispense or aspirating station; a member removably located on the transport system. The removable holder includes: a probe tip dispenser; a fluid supply section for holding a sample; a test element recess for holding one or more test elements or test element holders, wherein the removable holder is configured to contain the test element recess such that a test element can be acted upon by the liquid dispense or aspirating station, while the test element is in the recess; and a measurement device to analyze a sample. Another aspect provides a removable centrifuge model on the transport system, which separates samples, such as whole blood before analysis.

Abstract: This invention relates generally to medical devices, such as stents, for delivering a biologically active material to a desired location within the body of a patient. In particular, the invention relates generally to a medical device for delivering a biologically active material to a surface of a body lumen. More particularly, the invention is directed to a medical device comprising two opposing end sections, each having a surface, and a middle portion. The middle portion comprises a plurality of struts and the two opposing end sections comprises non-structural elements.

Abstract: The invention features a catheter assembly and methods for delivering a hydrogel-lined stent to a body lumen, and methods for lining a stent with a hydrogel. The assembly includes a catheter which has a balloon at least a portion of which is coated with a hydrogel and an expansible stent mounted on the balloon in a contracted condition for passage with the catheter to a site of a body. Expansion of the balloon lodges the stent in the body with hydrogel coated on the inner surfaces of the stent as a lining.