Abstract: The present invention relates to a drug aerosol supply apparatus for a respirator, and the objective of the present invention is to prevent secondary respiratory infection due to condensation water. The drug aerosol supply apparatus according to the present invention comprises a T tube, a drug particulate generation unit and a heater. The T tube includes a straight tube having a first end portion to which air provided from a respirator is provided and having a second end portion connected to a mask or a mouthpiece, and a branch tube attached to the straight tube so as to allow communication with the straight tube. The drug particulate generation unit is installed at the branch tube and sprays a drug in a particulate state. The heater for heats the T tube.

Abstract: A vial container includes: a container body in which a solution is accommodated; and a container lid detachably coupled to the top of the container body and having a plurality of lid ventilation holes. The container body includes a solution accommodation portion in which the solution is accommodated, a punching layer closing the bottom of the solution accommodation portion, a residue accommodating groove disposed to surround the periphery of the punching layer, and an entry groove portion provided to face the solution accommodation portion with the punching layer interposed therebetween.

Abstract: A specimen testing device according to an embodiment: a specimen reaction part including a plurality of chambers in which different test reagents are accommodated, respectively, wherein a lysis solution having a specimen mixed therein is supplied to each of the chambers to perform a reaction of the specimen with respect to a test reagent; an optical part which radiates a diagnostic beam to each of the chambers while being sequentially moved along the direction in which the plurality of chambers are arranged, and receives an optical signal from each of the chambers; and a diagnosis part in which a plurality of reaction data for one specimen are obtained on the basis of the optical signal according to the test reagent and the wavelength of the diagnostic beam, and which outputs a test result for the specimen on the basis of the reaction data.

Abstract: A test cartridge includes: a reagent reaction part in which a plurality of chambers accommodating test reagents are arranged; a lysis solution distribution part which is connected to a vial container accommodating a lysis solution, receives the lysis solution, and distributes the lysis solution to the respective chambers; and a container seating part which has a container insertion space into which the vial container is inserted, surrounds the lysis solution distribution part, and is seated on the reagent reaction part.

Abstract: The present invention relates to an immune reaction analysis device. The analysis device of the present invention comprises: an incubation chamber which has a plurality of slits for accommodating cartridges, and in which an incubation for an immunodiagnostic reaction is performed; a cartridge input driving unit for inputting the cartridge into the slit of the incubation chamber; a determination unit for determining the result of the reaction in the cartridge; a cartridge withdrawal driving unit for withdrawing the cartridge accommodated in the slit of the incubation chamber; a cartridge transfer driving unit for transferring the withdrawn cartridge to the determination unit; and a control unit for controlling the cartridge input driving unit, the cartridge withdrawal driving unit, and the cartridge transfer driving unit. The immune reaction analysis device of the present invention provides excellent ease of use and can accurately perform a good number of incubations.

Abstract: Disclosed is an automated liquid-phase immunoassay apparatus used with a cuvette having a plurality of chambers containing a reagent necessary for detection of an analyte in a biological specimen. The apparatus includes a movable cuvette module equipped with the cuvette, an optical reading module for optical assaying of a material resulting from a reaction between the specimen and the reagent, and a dispenser module which is positioned on the cuvette module and which dispenses the specimen and the reagent to the plurality of chambers of the cuvette and washes the specimen and the reagent therefrom.

Abstract: Disclosed is an automated liquid-phase immunoassay apparatus used with a cuvette having a plurality of chambers containing a reagent necessary for detection of an analyte in a biological specimen. The apparatus includes a movable cuvette module equipped with the cuvette, an optical reading module for optical assaying of a material resulting from a reaction between the specimen and the reagent, and a dispenser module which is positioned on the cuvette module and which dispenses the specimen and the reagent to the plurality of chambers of the cuvette and washes the specimen and the reagent therefrom.

Abstract: Provided is a method for detecting and quantifying a nucleic acid in real time and at high speed. The present disclosure provides a real-time high-speed PCR method in which fluorescent signals can be measured from a single-wavelength light source by using a single signal fluorescent material under continuous temperature control. Thus, the PCR method can be performed with a compact lightweight device with a simplified structure.

Abstract: The present invention relates to an automatic in vitro diagnostic apparatus capable of automatically performing a series of examination processes including a pretreatment process for specific components included in a biological sample such as blood and urine. The apparatus of the present invention comprises a base frame 104; a cuvette tray 110 movable back and forth on the base frame 104, for mounting cuvette holders 10 accommodating a plurality of cuvettes arranged thereon alongside each other; a tube tray 120 movable back and forth on the base frame, for mounting tube holders 20 accommodating a plurality of sample tubes containing samples thereon; and a sampling operation unit 500 movable left and right on the base frame 104, for mixing a sample contained in the sample tube with a reagent, and dropping the mixed solution onto an analysis strip provided in the cuvette.

Abstract: The present invention relates to an apparatus for nucleic acid amplification and, more particularly, to an apparatus for nucleic acid amplification capable of rapid nucleic acid amplification by rapidly heating and cooling a reactant in a reaction vessel for a chemical/biochemical reaction requiring a temperature change, and a method for temperature control in nucleic acid amplification.

Abstract: The present invention relates to an ELISA-based, liquid-phase immunoassay apparatus optimized for detecting particular ingredients contained in a biological sample, etc., and a method therefor.

Abstract: Disclosed is an automated liquid-phase immunoassay apparatus used with a cuvette having a plurality of chambers containing a reagent necessary for detection of an analyte in a biological specimen. The apparatus includes a movable cuvette module equipped with the cuvette, an optical reading module for optical assaying of a material resulting from a reaction between the specimen and the reagent, and a dispenser module which is positioned on the cuvette module and which dispenses the specimen and the reagent to the plurality of chambers of the cuvette and washes the specimen and the reagent therefrom.

Abstract: Disclosed is an automated liquid-phase immunoassay apparatus used with a cuvette having a plurality of chambers containing a reagent necessary for detection of an analyte in a biological specimen. The apparatus includes a movable cuvette module equipped with the cuvette, an optical reading module for optical assaying of a material resulting from a reaction between the specimen and the reagent, and a dispenser module which is positioned on the cuvette module and which dispenses the specimen and the reagent to the plurality of chambers of the cuvette and washes the specimen and the reagent therefrom.

Abstract: Disclosed is an automated liquid-phase immunoassay apparatus used with a cuvette having a plurality of chambers containing a reagent necessary for detection of an analyte in a biological specimen. The apparatus includes a movable cuvette module equipped with the cuvette, an optical reading module for optical assaying of a material resulting from a reaction between the specimen and the reagent, and a dispenser module which is positioned on the cuvette module and which dispenses the specimen and the reagent to the plurality of chambers of the cuvette and washes the specimen and the reagent therefrom.

Abstract: The present invention relates to an apparatus for nucleic acid amplification and, more particularly, to an apparatus for nucleic acid amplification capable of rapid nucleic acid amplification by rapidly heating and cooling a reactant in a reaction vessel for a chemical/biochemical reaction requiring a temperature change, and a method for temperature control in nucleic acid amplification.