A robotic assembly associated with gripping an object may determine, using an angle sensor, a relative position of a first gripping arm in relation to a second gripping arm of a robotic assembly. The robotic assembly may separate, using an actuator, the first gripping arm and the second gripping arm of the robotic assembly. The robotic assembly may position the gripping arms around an object, so the first gripping arm and second gripping arm accommodate the object. The robotic assembly may then join the first gripping arm and the second gripping arm until the first roller, second roller, and third roller are in contact with the object. The robotic assembly may apply pressure to the object using a plurality of compression springs between the first gripping arm and second gripping arm allowing the robotic assembly to grip the object.

The present invention provides devices and systems for use at the point of care. The methods devices of the invention are directed toward automatic detection of analytes in a bodily fluid. The components of the device are modular to allow for flexibility and robustness of use with the disclosed methods for a variety of medical applications.

An analysis system 1 includes analysis apparatuses 2A to 2E which are dispersively installed in a plurality of installation places and are connected through a network 3 so as to be communicable with each other. At least one analysis apparatus in each installation place includes: an information collection unit 20 that collects analysis progress information of the host analysis apparatus and the other analysis apparatuses and required movement time information of each of the other analysis apparatuses indicating the required movement time which is the time required for an operator to move from the installation place of the host analysis apparatus to the installation places of the other analysis apparatuses; a search unit 21 that searches for an analysis apparatus that is available first among the host analysis apparatus and the other analysis apparatuses on the basis of the collected analysis progress information and the collected required movement time information; and a display control unit 22 that displays information indicating the searched analysis apparatus that is available first on a display unit 12 of the analysis apparatus.

The present invention provides devices and systems for use at the point of care. The methods devices of the invention are directed toward automatic detection of analytes in a bodily fluid. The components of the device are modular to allow for flexibility and robustness of use with the disclosed methods for a variety of medical applications.

Provided are a method and device for recognizing hook effect in immune turbidimetry, and a computer readable medium. This method generates a reaction curve using light signals measured in a predetermined time period by immune reaction of analyte in a sample, and uses distribution information of the reaction curve in the predetermined time period to determine whether the sample has hook effect. This method only uses measurement information of a small predetermined time period in entire reaction time to determine whether a sample has hook effect, and terminates the test in time, thus accelerating the speed of immune turbidimetry detection of samples with hook effect.

The accuracy of deviation determination is based on a regression line of measurement data in an automatic analysis system that includes a plurality of first computers that display measurement data obtained by allowing a sample to react with a reagent, and a second computer that analyzes the measurement data acquired from each of the first computers and transmits results of the analysis to the first computers. The second computer acquires reference data including information on the automatic analyzers, the reagent, and the measurement data; generates, based on the reference data, integrated regression line information commonly applicable to the plurality of automatic analyzers associated with the information on the automatic analyzers and the information on the reagent; and transmits the integrated regression line information to the first computers. The first computers acquire the integrated regression line information transmitted from the second computer and display the integrated regression line information.

The present invention is related to the field of microfluidics and compound distribution within microfluidic devices and their associated systems. In one embodiment, present invention aims to solve the problem of molecule and compound absorbency into the materials making up laboratory equipment, microfluidic devices and their related infrastructure, without unduly restricting gas transport within microfluidic devices.

A sample measurement method of performing first measurement for a blood coagulation test and second measurement for a test different from the blood coagulation test includes: dispensing a sample for use in the first measurement into a first container from a sample container; dispensing the sample for use in the second measurement into a second container different from the first container from the sample container from which the sample for use in the first measurement has been dispensed; performing the first measurement based on the sample dispensed into the first container; and performing the second measurement based on the sample dispensed into the second container.

A blood coagulation analyzing method according to one or more aspects may include: calculating a coagulation time based on data representing a coagulation curve of a change in an optical detection value of a blood specimen added with a reagent for starting a coagulation reaction; calculating an index value related to derivatives calculated concerning the coagulation curve represented by the data used in the calculating the coagulation time; and determining whether an early reaction error has occurred based on a comparison result obtained by comparing the index value to a predetermined threshold.

The present invention is related to the field of microfluidics and compound distribution within microfluidic devices and their associated systems. In one embodiment, present invention aims to solve the problem of molecule and compound absorbency into the materials making up laboratory equipment, microfluidic devices and their related infrastructure, without unduly restricting gas transport within microfluidic devices.