Abstract:
The present invention relates to a blood analysis device including: a membrane configured to separate plasma from blood, a channel into which the plasma separated by the membrane is introduced, an electrode part including electrodes configured to adjoin one surface of the channel and come into contact with the plasma flowing in the channel, and a channel cover configured to adjoin a surface opposite to one surface of the channel which is adjoined by the electrode part, in which when any one of the electrode part and the channel cover adjoins the membrane, a part of the membrane covers an upper portion of the electrode part or the channel cover.
Abstract:
The present invention relates to a brain stimulation device, including: an electrode unit constituted by one or more electrodes and configured to move back and forth to a head of a user to fix the electrodes onto the head of the user; an auxiliary pressing unit configured to move back and forth to the head of the user to fix the electrodes onto the head of the user; and a donut type support unit having a donut type inner side on which the electrode unit and the auxiliary pressing unit are disposed and which surrounds the head, therefore a user can conveniently wear the brain stimulation device without a complicated manipulation for closely attaching the electrodes to his/her head.
Abstract:
The present invention relates to a method of manufacturing a porous carbon electrode, the method including: applying a metal film or metal particles to one surface of a carbon electrode; heat treating the carbon electrode to which the metal film or the metal particles are applied; and forming one surface of the carbon electrode in a porous structure by making the metal film or the metal particles penetrate into one surface of the carbon electrode, and the efficiency of the carbon electrode as an electrode may be improved while increasing a surface area of a carbon structure.
Abstract:
The present disclosure relates to a medical device comprising a multi-functional socket, comprising, a socket capable of being connected with a health information measuring device or a bio sensor module, the type of which are different from each other; and a control portion receiving an identification information from a health information measuring device or a bio sensor module, via the socket, when the socket is connected with the health information measuring device or the bio sensor module, recognizing a type of the health information measuring device or the bio sensor module, and operating an exclusive program for the recognized health information measuring device or the bio sensor module, wherein a type of an exclusive program operated by the control portion differs depending on a type of the health information measuring device or the bio sensor module.
Abstract:
Provided is a non-coding type biosensor. The non-coding type biosensor includes a first electrode including a first sub-electrode and a plurality of second sub-electrodes that are spaced apart from the first sub-electrode, ends of at least some of the plurality of second sub-electrodes being connected to the first sub-electrode, a reaction chamber in which a target material and a mixture solution react with each other, the reaction chamber contacting opposite ends of the plurality of second sub-electrodes, and a second electrode of which one end contacts the reaction chamber.
Abstract:
The present disclosure relates to bodily fluid analyzer with self-diagnosis function comprising, the first sensor part and the first operation part that are used to test or analyze the bodily fluid sample; the second sensor part and the second operation part that are used to self-diagnose of abnormalities of the said first sensor part or the first operation part; and the control part that operates the first operation part or the second operation part based on the predefined conditions and senses the operation status of the first operation part or the second operation part by using the second sensor part or the first sensor part, wherein the first and second sensor parts are used as a means of data entry into the aforementioned bodily fluid analyzer and the said first and second operation parts are used as means of output of the bodily fluid analyzer.
Abstract:
The present specification discloses a microfluidic analysis chip capable of adjusting movement of a specimen or a reagent by a negative pressure generation unit. A microfluidic analysis chip according to the present specification may comprise: a microtube for a main channel, which provides a space in which a specimen input through a specimen inlet formed at one end thereof reacts with a regent while the specimen moves to the other end thereof; a chip housing surrounding the microtube for the main channel; and a negative pressure generation unit which is positioned in the chip housing and connected to the microtube, so as to affect an internal pressure of the microtube for the main channel.
Abstract:
According to one embodiment of the present application, a biosensor, the biosensor comprising: a reaction part including a magnetic nanoparticle complex, a first electrode, and a second electrode; and a sample introduction part forming a passage so that a sample can be introduced into the reaction part from an outside of the biosensor; wherein the magnetic nanoparticle complex includes a first capturing substance for capturing a first target substance, a magnetic nanoparticle, and a reaction substance that performs at least one of an oxidation reaction and a reduction reaction, wherein the magnetic nanoparticle complex is magnetic in the reaction part, and has a property that mobility can be changed according to a change in a condition of the reaction part, wherein the first electrode, a second capturing substance for capturing a second target substance is fixed, wherein the second electrode is an electrode different from the first electrode, and characterized in that at least one of the first target substance and the second target substance is included in the sample, may be provided.
Abstract:
The present disclosure relates to a phase of receipt for receiving the user information and the result of the health diagnosis regarding the user, wherein the results of the health diagnosis regarding the user includes the numeric result value(s) regarding at least one medical checkup item; a phase that decides the risk group in which the user belongs among multiple risk groups by basing on the user information, a phase that decides the risk group in which the user belongs with the multiple risk group categorized according to the degree of the danger predicted regarding the health; and, a phase for deriving medical information related to the user that includes the health risk rating by considering the risk group in which the user belongs and the result of the health diagnosis regarding the user.
Abstract:
A biosensor includes a reaction part including a magnetic nanoparticle complex, a first electrode, and a second electrode; and a sample introduction part forming a passage so that a sample can be introduced into the reaction part from an outside of the biosensor. The magnetic nanoparticle complex includes a first capturing substance for capturing a first target substance, a magnetic nanoparticle, and a reaction substance that performs at least one of an oxidation reaction and a reduction reaction.