Abstract: Disclosed herein are glass pharmaceutical vials having sidewalls of reduced thickness. In embodiments, the glass pharmaceutical vial may include a glass body comprising a sidewall enclosing an interior volume. An outer diameter D of the glass body is equal to a diameter d1 of a glass vial of size X as defined by ISO 8362-1, wherein X is one of 2R, 3R, 4R, 6R, 8R, 10R, 15R, 20R, 25R, 30R, 50R, and 100R as defined by ISO 8362-1. However, the sidewall of the glass pharmaceutical vial comprises an average wall thickness Ti that is less than or equal to 0.85*s1, wherein s1 is a wall thickness of the glass vial of size X as defined by ISO 8362-1 and X is one of 2R, 3R, 4R, 6R, 8R, 10R, 15R, 20R, 25R, 30R, 50R, and 100R as defined by ISO 8362-1.

Abstract: Disclosed herein are glass pharmaceutical vials having sidewalls of reduced thickness. In embodiments, the glass pharmaceutical vial may include a glass body comprising a sidewall enclosing an interior volume. An outer diameter D of the glass body is equal to a diameter d1 of a glass vial of size X as defined by ISO 8362-1, wherein X is one of 2R, 3R, 4R, 6R, 8R, 10R, 15R, 20R, 25R, 30R, 50R, and 100R as defined by ISO 8362-1. However, the sidewall of the glass pharmaceutical vial comprises an average wall thickness Ti that is less than or equal to 0.85*s1, wherein s1 is a wall thickness of the glass vial of size X as defined by ISO 8362-1 and X is one of 2R, 3R, 4R, 6R, 8R, 10R, 15R, 20R, 25R, 30R, 50R, and 100R as defined by ISO 8362-1.

Abstract: An airfoil assembly for a turbine engine comprising an outer band, an inner band radially spaced inwardly from the outer band to define an annular region, and multiple airfoils circumferentially spaced within the annular region. Each corresponding airfoil of the multiple airfoils can project from a surface at a root and can further include an outer wall defining a pressure side and a suction side. A projection can extend upwardly from the surface on the pressure side and a valley can extend into the surface on the suction side to define a contour in the surface.

Abstract: A vehicle has a plurality of control apparatuses, a user input, a geographic position component, an object detection apparatus, memory, and a display. A processor is also included and is programmed to receive the destination information, identify a route, and determine the current geographic location of the vehicle. The processor is also programmed to identify an object and object type based on object information received from the object detection apparatus and to determine at least one warning characteristic of the identified object based on at least one of: the object type, a detected proximity of the detected object to the vehicle, the location of the detected object relative to predetermined peripheral areas of the vehicle, the current geographic location of the vehicle, and the route. The processor is also configured to select and display on the display an object warning image based on the at least one warning characteristic.

Abstract: A negative pressure respiratory treatment hood for human medical patients. A rigid hood, preferably of unitary fabrication from a clear material, is positioned over the patient's head. The patient's body extends out of an opening in a front wall of the hood. A hinged door may be attached to the front wall of the hood, and is closed and partially closes the opening, and a shroud is sealing connected to the hood and is draped over the patient so as to form a pressure seal. A negative pressure source is connected to the hood and forms a negative pressure environment around the patient's head. Access openings have a resilient material across them, with small openings in the resilient material, to permit access to the patient by medical personnel and/or medical equipment.

Abstract: Multilayer polyimide-fluoropolymer insulation structures exhibiting excellent copper heat seal strength and superior internal adhesion strength comprise a layer of polyimide having first and second major surfaces and at least a first fluoropolymer layer wherein the first fluoropolymer layer comprises fluoropolymer, metal oxide and ammonium salt. Protected wire or cable using the multilayer insulation structures, are also described.

Abstract: Multilayer polyimide-fluoropolymer insulation structures exhibiting excellent heat seal strength and superior internal adhesion strength comprise a base layer of polyimide having first and second major surfaces and a first fluoropolymer layer. The first fluoropolymer layer may be on the first major surface of the polyimide layer. Alternatively, it may be separated from the first major surface of the polyimide layer by an intervening layer. The first fluoropolymer layer comprises from about 70 to about 98% by weight of fluoroethylene propylene polymer (‘FEP’) and from about 30 to about 2% by weight of polytetrafluoroethylene polymer (‘PTFE’) or poly(tetrafluoroethylene-co-perfluoro[alkyl vinyl ether]) (‘PFA’) based on the total weight of the first fluoropolymer layer. Structures having fluoropolymer layers on both surfaces of the polyimide layer are also provided. Protected wire or cable using the composite, and methods are also described.

Abstract: Multilayer polyimide-fluoropolymer insulation structures exhibiting excellent heat seal strength and superior internal adhesion strength comprise a base layer of polyimide having first and second major surfaces and a first fluoropolymer layer. The first fluoropolymer layer may be on the first major surface of the polyimide layer. Alternatively, it may be separated from the first major surface of the polyimide layer by an intervening layer. The first fluoropolymer layer comprises from about 70 to about 98% by weight of fluoroethylene propylene polymer (‘FEP’) and from about 30 to about 2% by weight of polytetrafluoroethylene polymer (‘PTFE’) or poly(tetrafluoroethylene-co-perfluoro[alkyl vinyl ether]) (‘PFA’) based on the total weight of the first fluoropolymer layer. Structures having fluoropolymer layers on both surfaces of the polyimide layer are also provided. Protected wire or cable using the composite, and methods are also described.

Abstract: A surgical/medical tube such as an endotracheal tube 10 is provided having a tubular body 12 equipped with an inflatable cuff 22 and respective, separate cuff inflation and fluid removal lumens 24, 30. A fluid removal opening 32 communicates with lumen 30 and is located proximal to cuff 22. A projection 38, 38a, 40, 42 is located in close proximity to the opening 32 and is configured to prevent contact between the opening 32 and the adjacent tracheal wall.

Abstract: A dielectric composite is provided that is useful for wrapping wire or cable or for supporting electronic circuitry. The composite comprises a polyimide layer having first and second major surfaces; a first fluoropolymer layer on the first major surface on the polyimide layer, said first fluoropolymer layer comprising at least about 55% PFA; and a second fluoropolymer layer on the second major surface on the polyimide layer, said second fluoropolymer layer comprising at least about 55% PFA. Protected wire or cable using the composite, and methods are also described.

Abstract: A surgical/medical tube such as an endotracheal tube (10) is provided having a tubular body (12) equipped with an inflatable cuff (22) and respective, separate cuff inflation and fluid removal lumens (24, 30). A fluid removal opening (32) communicates with lumen (30) and is located proximal to cuff (22). A projection (38, 38a, 40, or 42) is located in close proximity to the opening (32) and is configured to prevent contact between the opening (32) and the adjacent tracheal wall.

Abstract: A medical device tube comprising a cannula having a formed end and a connector that tightly holds the formed end of the cannula between first and second portions of the connector.

Abstract: A laryngeal airway device, having an airway tube which has an internal passage in the airway tube wall for receiving a cuff inflation line, and a dome having an inlet and an outlet, where the dome is connected at its inlet with the distal end of the airway tube. The device also includes an annular spoon-shaped inflatable cuff connected with the periphery of the outlet of the dome; a cuff inflation line configured to be in fluid communication with the internal space of the cuff; and a multi-lobed aperture formed in the dome. The aperture is configured to be in fluid communication with the proximal end of the airway tube. The dome has protrusions forming the multi-lobed aperture, such that a flap is configured to prevent the obstruction of the aperture by a patient's epiglottis when the device is inserted into the patient.

Abstract: A method is provided for exercising an engine-driven, electrical generator. The generator has a first operation mode wherein the generator generates a predetermined output voltage at a predetermined frequency with the engine running a predetermined operating speed and a second exercise mode. The method includes the step of running the engine at a predetermined exercise speed with the generator in the exercise mode. The predetermined exercise speed is in the range of 40% to 70% of the predetermined operating speed of the engine. In addition, in the exercise mode, the generator generates an exercise voltage that is less than the predetermined output voltage.

Abstract: A laryngeal airway device, having an airway tube which has an internal passage in the airway tube wall for receiving a cuff inflation line, and a dome having an inlet and an outlet, where the dome is connected at its inlet with the distal end of the airway tube. The device also includes an annular spoon-shaped inflatable cuff connected with the periphery of the outlet of the dome; a cuff inflation line configured to be in fluid communication with the internal space of the cuff; and a multi-lobed aperture formed in the dome. The aperture is configured to be in fluid communication with the proximal end of the airway tube. The dome has protrusions forming the multi-lobed aperture, such that a flap is configured to prevent the obstruction of the aperture by a patient's epiglottis when the device is inserted into the patient.