Abstract: A system and method to perform a forensic analysis of a file including: one or more processors; and a memory storing computer-readable instructions that, when executed by the one or more processors, cause the system device to: receive one or more files for analysis; identify a file format for the file; determine whether the file format is a supported multimedia file; parse the file to separate structural elements from the file; generate a profile structural signature for the one or more files; a database including a plurality of profile structural signatures corresponding to known hardware and/or software; determining whether the one or more files matches one of the plurality of profile structural signatures; and providing an indication of an identity of the known hardware and/or software for the one or more files upon a determination that the one or more files matches one of the plurality of profile structural signatures.

Abstract: A swallowing medical device includes: an attachment unit configured to be attached to a target portion of a human body for a medical operation; a control unit configured to control the medical operation; and a storage configured to store use information regarding a use state over time of the attachment unit. The control unit executes a control for restricting use of the attachment unit on the basis of a fact that the use information does not satisfy a set condition for ensuring a characteristic of the attachment unit.

Abstract: A swallowing medical device includes: an attachment unit configured to be attached to a target portion of a human body for a medical operation; a control unit configured to control the medical operation; and a storage configured to store use information regarding a use state over time of the attachment unit. The control unit executes a control for restricting use of the attachment unit on the basis of a fact that the use information does not satisfy a set condition for ensuring a characteristic of the attachment unit.

Abstract: A method for measuring fibroblast growth factor-23 (FGF-23) in a sample, which comprise the following steps: (1) reacting, in an aqueous medium, FGF-23 in a sample with magnetic particles, a first antibody or a fragment thereof which binds to FGF-23, and a second antibody or a fragment thereof which binds to FGF-23, to form on the magnetic particles an immunocomplex comprising the first antibody or a fragment thereof which binds to FGF-23. FGF-23, and the second antibody or a fragment thereof which binds to FGF-23; (2) collecting the magnetic particles in the reaction mixture after step (1) by magnetic force, and separating the magnetic particles collected by magnetic force from the other components: and (3) measuring the immunocomplex on the magnetic particles separated in step (2). The present invention provides a method for measuring FGF-23 in a sample, which have a high sensitivity and have a wide measurement range.

Abstract: A method for measuring fibroblast growth factor-23 (FGF-23) in a sample, which comprise the following steps: (1) reacting, in an aqueous medium, FGF-23 in a sample with magnetic particles, a first antibody or a fragment thereof which binds to FGF-23, and a second antibody or a fragment thereof which binds to FGF-23, to form on the magnetic particles an immunocomplex comprising the first antibody or a fragment thereof which binds to FGF-23, FGF-23, and the second antibody or a fragment thereof which binds to FGF-23; (2) collecting the magnetic particles in the reaction mixture after step (1) by magnetic force, and separating the magnetic particles collected by magnetic force from the other components; and (3) measuring the immunocomplex on the magnetic particles separated in step (2). The present invention provides a method for measuring FGF-23 in a sample, which have a high sensitivity and have a wide measurement range.

Abstract: A feces sampling container having an increased storage stability of a component in a feces sample such as hemoglobin to enable the measurement of a component in a feces sample with a small amount of feces collected. The container includes a container body, and a feces sampling stick having a gripping part on one side and a stick part on the other side, the stick part having a feces sampling part in the vicinity of the tip, wherein the container body comprises an opening part through which the feces sampling part of the feces sampling stick is inserted, and a feces container chamber in which a desiccant is enclosed, wherein the feces sample held by the feces sampling part is dried by a contact of the feces sampling part, which is inserted through the opening part and holding the feces sample, with the desiccant.

Abstract: An assembly used in the injection of a contrast product into a patient is disclosed. This assembly includes a container, an injection flowpath, and a filling flowpath. The injection flowpath extends from the container to the patient, while the filling flowpath extends from a feed source to the container. Part of the injection flowpath is also used by the filling flowpath. One connector is disposed between an upstream filling line tubular section and a pump coupling section within the filling flowpath, while another connector is disposed between a downstream filling line tubular section and this same pump coupling section. This allows the upstream filling line tubular section, the pump coupling section, and the downstream filling line tubular section to differ in one or more respects, for instance with regard to hardness.

Abstract: The present invention provides a method for measuring glycated hemoglobin in a sample, which comprises directly oxidizing glycated hemoglobin in a sample, and then measuring a substance produced or consumed by the oxidation; and a method for measuring glycated hemoglobin in a sample, which comprises directly oxidizing glycated hemoglobin in a sample using an enzyme, and then measuring a substance produced or consumed by the oxidation. A method for measuring glycated hemoglobin of the present invention is useful for diagnosing lifestyle-related disease such as diabetes mellitus.

Abstract: The present invention provides a protein comprising an amino acid sequence in which arginine at position 61 of a protein comprising the amino acid sequence represented by SEQ ID NO: 1 is substituted to an amino acid selected from the group consisting of glycine, alanine, valine, leucine, serine, threonine, proline, cysteine, methionine, asparagine, glutamine, and aspartic acid; and a method for measuring a glycated hemoglobin in a sample, wherein the method comprises reacting a glycated hemoglobin in a sample with a protease to produce a glycated hexapeptide, then reacting the produced glycated hexapeptide with the aforementioned protein, and measuring a substance produced or consumed by the reaction.

Abstract: The object of the invention is to provide a biomedical electrode which enables a user to easily attach by oneself without making any mistake with no specialized knowledge being required.

Abstract: The present invention concerns a device for injecting a liquid product contained in a bag, the device comprising a housing consisting of two half-shells articulated about an axis of rotation in order to allow the relative movement of the half-shells relative to each other between: —an open position in order to put the bag in place and—a closed position for injecting the liquid product contained in the bag, remarkable in that: —one of the half-shells comprises a deformable bladder—called the “active bladder”—having a volume that varies under the action of a hydraulic ram supplying said bladder with hydraulic fluid, and—the other of the half-shells comprises a deformable damping cushion having a constant volume—called the “passive cushion”.

Abstract: The present invention provides a method for stabilizing a cholesterol oxidase, a method for preserving a cholesterol oxidase, and a stabilized composition of cholesterol oxidase. A method for stabilizing a cholesterol oxidase and a method for preserving a cholesterol oxidase which comprises allowing the cholesterol oxidase to coexist with an ?-keto acid in an aqueous medium, and, a stabilized composition of cholesterol oxidase which comprises the cholesterol oxidase being allowed to coexist with an ?-keto acid in an aqueous medium. The method for stabilizing a cholesterol oxidase, the method for preserving a cholesterol oxidase, and a stabilized composition of cholesterol oxidase according to the present invention are useful for clinical diagnosis such as metabolic syndrome.

Abstract: Provided is a method for measuring cholesterol in high-density lipoprotein (HDL) simply and accurately. A method for measuring cholesterol in high-density lipoprotein in a specimen, comprising reacting the specimen with i) a cholesterol ester hydrolase and a cholesterol oxidase, or ii) a cholesterol ester hydrolase, an oxidized coenzyme, and a cholesterol dehydrogenase, in an aqueous medium comprising at least one substance selected from the group consisting of pyridinium salts and quaternary ammonium salts each having a specific structure, and a polyanion to form hydrogen peroxide or reduced coenzyme and measuring the formed hydrogen peroxide or reduced coenzyme.

Abstract: The present invention provides a method for measuring a component to be measured in a sample, comprising converting the component to be measured in the sample into hydrogen peroxide and measuring the formed hydrogen peroxide in the presence of an ?-keto acid using an oxidative-coloring chromogen. The present invention also provides a method for suppressing the influence of a peroxide on a method of converting a component to be measured in a sample into hydrogen peroxide and measuring the formed hydrogen peroxide using an oxidative-coloring chromogen, the suppression method comprising using an ?-keto acid. The measuring method and the suppression method of the present invention using an ?-keto acid suppress the influence of a peroxide to give an accurate measurement of the component to be measured in the sample.

Abstract: The invention concerns an device for injecting a patient with a liquid product contained in a container (4), the system comprising a pressurizing unit for driving the liquid product contained in the container, the system further comprising a calculator for estimating the injection flow rate at the outlet of the container, said injection flow rate at the outlet being estimated on the basis of a law of deformation of the system under the effect of the pressure inside the container.

Abstract: Provided is a measuring method of a component to be measured in a specimen while suppressing an influence of bilirubin. A measuring method of a component to be measured, comprising converting the component to be measured in the specimen to hydrogen peroxide through an enzymatic reaction, reacting the formed hydrogen peroxide with an oxidative-coloring chromogen in the presence of a peroxidase, and measuring an absorbance of the colored reaction solution to thereby determine the component to be measured, wherein a fatty acid or a salt thereof coexists. The measuring method of a component to be measured in a specimen according to the present invention is useful in clinical diagnosis.

Abstract: Provided are: a method for stabilizing an ascorbic acid oxidase; a method for preserving an ascorbic acid oxidase; and a stabilized composition of an ascorbic acid oxidase. A method for stabilizing an ascorbic acid oxidase and a method for preserving an ascorbic acid oxidase, each of the methods comprising allowing an ascorbic acid oxidase to coexist with nitrous acid or a salt thereof, or a nitrous acid ester in an aqueous medium; and a stabilized composition of an ascorbic acid oxidase, which comprises an ascorbic acid oxidase being allowed to coexist with nitrous acid or a salt thereof, or a nitrous acid ester in an aqueous medium. The method for stabilizing an ascorbic acid oxidase, the method for preserving an ascorbic acid oxidase, and the stabilized composition of an ascorbic acid oxidase according to the present invention are useful for clinical diagnosis and the like.

Abstract: Described is a method for preserving an aqueous solution comprising a leuco chromogen, comprising adding at least one compound selected from the group consisting of polyoxyethylene alkylamine and polyoxyethylene alkenylamine to the aqueous solution containing a leuco chromogen, and a method for stabilizing a leuco chromogen, comprising allowing the leuco chromogen to coexist in an aqueous solution comprising at least one compound selected from the group consisting of polyoxyethylene alkylamine and polyoxyethylene alkenylamine.

Abstract: The present invention provides a method for a simple and accurate measurement of triglycerides in low-density lipoprotein in a sample comprising performing the following steps sequentially: (i) a step of generating free glycerol by allowing lipoprotein lipase to act on a sample, in an aqueous medium comprising the sample and a specific surfactant such as polyoxyethylene polyoxyalkylene polycyclic phenyl ether; (ii) a step of removing free glycerol present in the reaction solution of the above step (i); (iii) a step of generating free glycerol by allowing lipoprotein lipase to act on the reaction solution from which free glycerol has been removed in step (ii), in the presence of a specific surfactant such as polyoxyethylene polyoxyalkylene alkyl ether; and (iv) a step of measuring free glycerol generated in step (iii), and a kit used for the method.

Abstract: Methods and kits for measuring a component to be measured by reacting the component in the presence of a fatty acid alkanolamide, with a first antibody which binds to the component, then reacting a labeled second antibody that binds to the component so as to form an immunocomplex comprising the first antibody, the component and the labeled second antibody. The amount of the label in the formed immunocomplex is measured and correlated to the amount and concentration of component.