564results about How to "Reduce contact" patented technology

Devices and methods for altering the spacing and motion at the facet joints of the vertebral column are provided. One embodiment of the invention comprises a prosthesis with surfaces configured to articulate with the facets of the facet joint. A retaining member for anchoring the prosthesis within the facet joint is optionally included. Methods for surgically and less invasively implanting the prosthesis and securing the prosthesis to the articular processes or surrounding soft tissue are also provided.

A circular stapler facilitate performing end to end anastomosis; further an occasional prompt with sound effect warning timely firing the stapler bolts. A circular stapler includes a bolting machine (1) consists of a shaft (11), an actuator (12), and a stapler (13); a hand-held handle (2); an adjusting knob (3); and an anvil (4), a hollow anvil shaft (41);characterized in that: a conic trocar (5) disposed to a most distal end of said bolting machine (1), a cambered surface of said conic trocar (5) formed with, at least, three relieve-pressure grooves (53) equal distant distributed are extended from an apex (51) to a bottom (52); an audio prompt (6) disposed inside said bolting machine (1), said audio prompt (6) includes a printed circuit board (PCB) (61), a buzzer (62) electrically connected to the PCB (61) controlled by a switch, and a battery (64) supplies power to the PCB (61).

A device permits effective engagement of micro-needles with a cutaneous layer thereby to permit for a substance to pass effectively to the cutaneous layer. A flexible or non-flexible material supports an array of micro-needles for receiving the surface of the cutaneous layer so that the proximal ends of the micro-needles pierce to effect a passage of a substance with the micro-needles to the cutaneous layer. A passageway or bladder acts on the substrate to cause the proximal ends of the micro-needles to pass to the cutaneous layer for passage of a substance associated with the micro-needles to the cutaneous layer. The bladder includes apertures located about and spaced from the micro-needles such that suction transmitted though the apertures. The micro-needles are mounted with a movable first substrate. In one form, the first substrate includes a surface with concavities and the micro-needles are mounted in the concavities, and the apertures are located in the concavities. In another form the surface is substantially flat. There can be a third layer spaced relative to the second substrate layer at least partly forming a chamber between the second layer and third layer. There can be a biasing device for urging the first substrate from the cutaneous layer.

A heart rate measuring device is attached around a user's hand, the device having an inner surface, which is in contact with the skin on the hand to which it is attached, and an outer surface, which is other than the inner surface. The inner surface of the measuring device is provided with an electrically conductive inner structure, which functions as an electrode for a contact with the skin of the hand to which the device is attached. An electrically conductive outer structure functions as an electrode for a contact with the user's other hand and it is electrically isolated from the electrically conductive inner structure. The electrically conductive outer structure on the measuring device extends at least to opposite sides of the hand to which the device is attached, and at least part of the electrically conductive outer surface is on the outer surface of the measuring device, on opposite sides of the hand to which the device is attached. The electrically conductive outer structure and inner structure are connected to a measuring unit for heart rate measurement.

A high electron mobility transistor including: a GaN material system based heterostructure; a passivating nitride layer over the heterostructure and defining a plurality of openings; and a plurality of electrical contacts for the heterostructure and formed through the openings.

A device capable of capturing and facilitating the removal of a thrombus in blood vessels (or stones in biliary or urinary ducts, or foreign bodies) uses a soft coil mesh with the aid of a pull wire or string to engage the surface of a thrombus, and remove the captured thrombus. The soft coil mesh is formed by an elongated microcoil element that forms the helical elements of a macrocoil element. The microcoil element provides a relatively elastic effect to the helical elements forming the macrocoil and allows for control of gripping forces on the thrombus while reducing non-rigid contact of the device with arterial walls. The use of multiple coil mesh elements, delivered through a single lumen or multiple lumens, preferably with separate control of at least one end of each coil, provides a firm grasp on a distal side of a thrombus, assisting in non-disruptive or minimally disrupted removal of the thrombus upon withdrawal of the device.

A device permits effective engagement of micro-needles with a cutaneous layer thereby to permit for a substance to pass effectively to the cutaneous layer. A flexible or non-flexible material supports an array of micro-needles for receiving the surface of the cutaneous layer so that the proximal ends of the micro-needles pierce to effect a passage of a substance with the micro-needles to the cutaneous layer. A passageway or bladder acts on the substrate to cause the proximal ends of the micro-needles to pass to the cutaneous layer for passage of a substance associated with the micro-needles to the cutaneous layer. The bladder includes apertures located about and spaced from the micro-needles such that suction transmitted though the apertures. The micro-needles are mounted with a movable first substrate. In one form, the first substrate includes a surface with concavities and the micro-needles are mounted in the concavities, and the apertures are located in the concavities. In another form the surface is substantially flat. There can be a third layer spaced relative to the second substrate layer at least partly forming a chamber between the second layer and third layer. There can be a biasing device for urging the first substrate from the cutaneous layer.

A method for in-line monitoring of via / contact etching process based on a test structure is described. The test structure is comprised of via / contact holes of different sizes and densities in a layout such that, for a certain process, the microloading or RIE lag induced non-uniform etch rate produce under-etch in some regions and over-etch in others. A scanning electron microscope is used to distinguish these etching differences in voltage contrast images. Image processing and simple calibration convert these voltage contrast images into a “fingerprint” image characterizing the etching process in terms of thickness over-etched or under-etched. Tolerance of shifting or deformation of this image can be set for validating the process uniformity. This image can also be used as a measure to monitor long-term process parameter shifting, as well as wafer-to-wafer or lot-to-lot variations. Advanced process control (APC) can be performed in-line with the guidance of this image so that potential electrical defects are avoided and process yield ramp accelerated.

Devices and methods for altering the spacing and motion at the facet joints of the vertebral column are provided. One embodiment of the invention comprises a prosthesis with surfaces configured to articulate with the facets of the facet joint. A retaining member for anchoring the prosthesis within the facet joint is optionally included. Methods for surgically and less invasively implanting the prosthesis and securing the prosthesis to the articular processes or surrounding soft tissue are also provided.

A method of marking a skin for a vehicle interior trim panel comprising providing a skin with a color and an outer surface. A laser is applied to the outer surface such that a portion of the skin surface contacted by the laser changes color relative to a portion of the outer skin not contacted by the laser to create a marking in the outer skin surface indicating the presence of a vehicle component or function. In particular, an image, pattern, or color contrast may be created on the skin. A unique hole pattern and size distribution caused by the laser may provide a skin with a woven fabric texture. In addition, stitches formed on a skin surface may be colored differently from the surrounding skin surface to distinguish their appearance.

A device capable of capturing and facilitating the removal of a thrombus in blood vessels (or stones in biliary or urinary ducts, or foreign bodies) uses a soft coil mesh with the aid of a pull wire or string to engage the surface of a thrombus, and remove the captured thrombus. The soft coil mesh is formed by an elongated microcoil element that forms the helical elements of a macrocoil element. The microcoil element provides a relatively elastic effect to the helical elements forming the macrocoil and allows for control of gripping forces on the thrombus while reducing non-rigid contact of the device with arterial walls. The use of multiple coil mesh elements, delivered through a single lumen or multiple lumens, preferably with separate control of at least one end of each coil, provides a firm grasp on a distal side of a thrombus, assisting in non-disruptive or minimally disrupted removal of the thrombus upon withdrawal of the device.

A method and system for limiting the motion of items, such as camera optics, are disclosed. A motion limiting member can be used to limit the motion of the item using a surface thereof that abuts a structure of the item. Limits on the motion can be defined by a positioning member that is attached to the motion limiting member and that abuts a structure that is fixed with respect to the desired range of motion of the item whose motion is being limited. This abutment facilitates the precise definition of the limit on the motion of the item.

An improved method for measuring and automatically disposing of infectious waste generated during and after surgical and clinical procedures is provided. The infectious waste removal device includes a suction source, a method for pressure verification, separation chamber for isolating fluids, containment reservoir, measurement chamber for determining fluid received, an information source for such fluid volumes, a quantitative method for calculating fluid dynamics, a post use cleaning method, and other attributes for use by the surgical team or healthcare staff in order to while minimize healthcare worker handling of said infectious waste and to limit their possible exposure.