41results about How to "Easily act" patented technology

A portable intra-oral capture and display system, designed for use by a dental practitioner in connection with a patient seated in a dental chair, includes: a handpiece elongated for insertion into an oral cavity of the patient, where the handpiece includes a light emitter on a distal end thereof for illuminating an object in the cavity and an image sensor for capturing an image of the object and generating an image signal therefrom; a monitor interconnected with the handpiece, where the monitor contains electronics for processing the image for display and a display element for displaying the image, where the interconnection between the monitor and the handpiece includes an electrical connection for communicating the image signal from the image sensor in the camera to the electronics in the monitor; and a receptacle on the dental chair for receiving the monitor, wherein the receptacle conforms to the monitor such that the monitor may be withdrawn from the receptacle in order to allow the display element to be seen by the dental practitioner or the patient.

Systems and methods for determining the configuration of a connection between two devices by measuring an electrical characteristic are provided. Using the measured electrical characteristic, a device is able to select an appropriate communication interface, such as serial, Universal Serial Bus (USB), FireWire, parallel, PS/2, etc., and configure itself appropriately. Systems and methods which determine the physical orientation of a connector with respect to another connector may also be provided alone or in combination with such systems and methods for selecting communication interfaces. The physical orientation of a connector can be determined by measuring an electrical characteristic and a device can then configure itself appropriately. In accordance with the principles of the present invention, device designs can decrease in size and cost as well as simplify operation for the end-user.

A method of determining glycated hemoglobin is provided, by which a ratio of the glycated hemoglobin in a sample can be determined accurately and easily. The ratio of glycated hemoglobin can be determined by degrading a glycated hemoglobin in a whole blood sample selectively with a protease to give a glycated hemoglobin degradation product`; causing a redox reaction between a glycation site of the glycated hemoglobin degradation product and a fructosyl amino acid oxidoreductase; and determining this redox reaction. Further, as shown in FIG. 1, in a whole blood sample, there is a correlation between the ratio of the glycated hemoglobin determined by this method and an HbA1c concentration. Thus, without determining the glycated alpha-amino group as a characteristic structure of HbA1c, an amount of HbA1c can be determined accurately and easily from the determined ratio of the glycated hemoglobin.

A die cushion apparatus of a press machine in which a discharge opening of a fluid hydraulic pump/motor is directly connected to a pressure chamber on a cushion pressure production side of a fluid hydraulic cylinder and the torque of a rotating shaft of the fluid hydraulic pump/motor is controlled by an electric motor to control a pressure (die cushion pressure) of the pressure chamber on the cushion pressure production side. It is therefore possible to control the die cushion pressure with excellent responsiveness with respect to a die cushion pressure command and prevent occurrence of a surge pressure. The die cushion apparatus also has excellent energy efficiency since energy required for a die cushioning action that a cushion pad receives when effecting die cushioning of a press machine is regenerated as electrical energy through the fluid hydraulic cylinder, fluid hydraulic pump/motor, and electric motor.

On a lower case serving as a supporting base, a movable unit is supported to be able to vibrate in an X direction, with a first elastic member interposed therebetween. In the movable unit, a panel assembly is supported on a movable base to be able to vibrate in a Z direction, with a second elastic member interposed therebetween. A vibration generator is mounted on the panel assembly and supported by a third elastic member on the movable base. When the vibration generator generates vibration in the X direction, the entire movable unit vibrates in the X direction. When the vibration generator generates vibration in the Z direction, the panel assembly vibrates in the Z direction. When the panel assembly is pressed with a finger, the force of the pressing operation can be detected by a second detector which is a force sensor.

A threaded container closure assembly in which the container comprises one or more radially extending members proximate the distal end thereof that initially engage with one or more radially extending members or partial radially extending members on a mating closure or top proximate the distal end thereof so that the container and top become at least partially interconnected and are thereby not too easily and inadvertently separated while the user attempts to cause engagement of the threads for screwing down the top onto the container.

An inlet port (17A) of a first exhaust gas purifying device (16) is provided on a side opposite to an engine (8) by sandwiching an axis (O1-O1) of a cylindrical body (17) of the first exhaust gas purifying device (16). An exhaust pipe (26) connecting the engine (8) and the first exhaust gas purifying device (16) is constituted by a lateral pipe line (27) extending in a left and right direction of an upper revolving structure (3) on a front side of the first exhaust gas purifying device (16) and having a bellows pipe (28) in the middle for absorbing relative displacement between the engine (8) and the first exhaust gas purifying device (16) and a bent pipe line (29) bent having a U-shape rearward from a tip end side of the lateral pipe line (27) and connected to the inlet port (17A) of the first exhaust gas purifying device (16).

Ossicular replacement prostheses are manufactured from a non-biodegradable shape memory polymer. Such prostheses can include TORPs, PORPs, and incudo-stapedial joints (ISJs). The prostheses are reshaped upon application of a stimulus to capture a portion of one or more ossicles. The force of capture of a reshaped polymeric prosthesis is less than a comparable reshaped shape memory alloy prosthesis and thereby prevents recipient discomfort and/or pressure induced necrosis of the bone. In addition, biocompatible shape memory polymers can be designed with recoverable strain that is orders of magnitude higher than shape memory alloys. Furthermore, prostheses can be manufactured in a single size and easily trimmed or otherwise modified by the surgeon during the implantation procedure to tailor the prosthesis in size and/or shape for the particular anatomy. Such modification does not negatively effect the ability of the prostheses to engage the ossicle.

An injector in which it is possible to switch a pressure booster on or off so that it is possible to control not only the injection duration, but also the progression of the injection pressure within a broad range during the injection.

A radiotherapy apparatus includes a source of radiation, a patient support for locating a patient in the field of the source of radiation, a position detector for determining a position of a patient relative to the radiotherapy apparatus, a comparator for comparing the output of the position detector with a predetermined position, and a feedback system for informing the patient of the output of the comparator.

A method of measuring an analyte in a sample with excellent sensitivity using a redox reaction is provided. In this method, a reducing substance or an oxidizing substance derived from the analyte is measured in the presence of a tetrazolium compound and sodium azide using the redox reaction, and an amount of the analyte is determined from the amount of the reducing substance or oxidizing substance thus measured. The tetrazolium compound and the sodium azide are present at a ratio in a range from 20:3 to 20:12. Preferably, a solution containing the tetrazolium compound and the sodium azide is aged and then added to the sample.

A movement member which reciprocates includes a thick portion and a thin portion, a bearing portion formed in the thick portion is slidingly supported by the guide shaft, and a sliding portion formed in the thin portion is slidingly guided by the sliding guide portion. Power of the motor is transmitted to a pinion gear via a speed reduction gear and a speed reduction mechanism inside a gear box, and a movement reaction force is applied from the pinion gear to the rack portion. Since the rack portion is positioned on an axis Os, a force is effectively applied to the movement member by the power from the motor.

To provide a roll, a rolling mill and rolling method capable of not only effectively correcting the plate crown of a material to be rolled but also reducing the edge drop and preventing a roll from damage caused by the increase of the local line pressure between the rolls.

A roll crown is formed by a continuous curve having a local maximum point and a local minimum value point where the central region held between the local maximum point and the local minimum point represents one function and the end region from the local maximum point to the nearer roll end represents another function having an inclination of steeper gradient (or having a radius decreasing more sharply toward the roll end) than that of the extension of the function in the central region.

The current invention concerns a kit suitable for the non-surgical treatment of skin lesions including warts, verrucae, corns, and skin tags said kit comprising a cryogenic body comprising a housing hosting a coolant container and further comprising a cryogenic applicator head, whereby the housing and the cryogenic applicator head extend axially; said cryogenic applicator head is provided with a cryogenic tip for performing a cryogenic treatment to a skin lesion, whereby said coolant container contains a coolant suitable for cooling said tip; the kit further comprises an acid body comprising an acid container containing an acidic composition and having an acid outlet, and an acid dispenser head that axially extends from said acid container, is in fluid communication with said acid outlet, and is suitable for applying a dose of said acidic composition to a skin lesion. The invention also concerns a dosage regimen.