There is provided an automatic analyzer and a method of storing reagents in an automatic analyzer, in which restrictions on installation of reagent packs are smaller than those of the device in the related art. The automatic analyzer includes a reagent storage 105 that stores reagent packs 201, 301 containing reagents. The reagent storage 105 includes: a first holding unit 403 capable of holding only an immune reagent pack 201 containing a first reagent among the reagents; a second holding unit 404 capable of holding only a biochemical reagent pack 301 containing a second reagent that is different from the first reagent; and a third holding unit 405 capable of holding both the immune reagent pack 201 and the biochemical reagent pack 301.

A management system including a processor, the processor is configured to acquire an image obtained by imaging an outer surface of each of plural sample containers and a boundary container, the sample container containing a sample and in which subject information of a subject from whom the sample is collected is given to the outer surface, the boundary container in which group boundary information indicating a boundary between plural groups of subjects is given to the outer surface, recognize the subject information and the group boundary information based on the image, and associate a test result related to the sample contained in each of the sample containers with a test order which includes the subject information and in which the group is divided corresponding to the group boundary information, based on a result of the recognition and the test order.

Automated systems for processing a biopsy sample are disclosed herein, as well as methods for automating the processing of a biopsy sample. A benefit to the automated systems and methods herein can be the efficient and cost-effective processing of large numbers of biopsy samples. Another benefit to the automated systems and methods herein can be increased personnel safety for processing biopsy samples. Additional benefits to the automated systems and methods herein can be greater patient safety by increasing accuracy in biopsy sample processing, and preventing errors in biopsy sample processing that may lead to misdiagnosis and improper treatments.

The invention relates to a configuration control device for a laboratory instrument, a laboratory instrument with a configuration control device for instrument-controlled treatment of at least one laboratory sample and a method for configuring the laboratory instrument by means of the configuration control device. By using user-dependent configuration data, the requirement for the user of having to perform a completely manual configuration of the laboratory instrument, which is effected by the user-dependent configuration data, is dispensed with.

A processing system includes a processing unit configured to process a cartridge, in particular a microfluidic cartridge, and is further configured to process a biological sample received in the cartridge. The processing unit includes a computing unit configured to compare input or read in sample data with input or read in first cartridge data in order to determine a compatibility of the sample with the cartridge. The computing unit is further configured to output a first error message in response to a determination of incompatibility between the sample and the cartridge. A method includes using the processing system to determine a compatibility between a sample and a cartridge.

Disclosed herein are a detection device and a detection method. The detection device comprises: a consumable cassette (1) configured to have a detection side (A) provided with a consumable, the consumable cassette (1) being provided with a circuit board (3) carrying a test information; and a detection instrument configured to read the test information from the circuit board (3) and perform a detection to the consumable based on the test information to obtain a detection result. Also provided is a detection method comprising: providing the detection device (S1); placing the consumable cassette (1) into the detection instrument (S2); obtaining a test information by the detection instrument (S3); determining, according to the test information, whether the consumable is in compliance with a detection requirement (S4); and performing a detection to the consumable by the detection instrument to obtain a detection result when the consumable is in compliance with the detection requirement (S5). The test information is obtained with lower cost. An accuracy and an efficiency of the detection are improved.

A signal reference value (SLocal) is set at which a blood coagulation reaction time (T) of a blood coagulation time reference sample measured on the basis of the result of comparing a signal value (amount of transmitted light, amount of scattered light, amount of fluorescence, or turbidity) pertaining to blood coagulation time that varies temporally according to the mixing and reaction of the blood coagulation time reference sample and a reagent and a signal reference value (S) corresponds to an expected value (Te) for the blood coagulation reaction time that has been set beforehand so as to correspond to the blood coagulation time reference sample. As a result, it is possible to use the blood coagulation time reference sample to determine the state of the reagent and enhance the reliability of measurement results by setting a unique signal reference value for each reagent container.

Systems, devices and methods are disclosed for collecting laboratory specimens from laboratory specimen boxes once a specimen has been placed inside a box.

Provided is an automatic analysis device that can suppress concentration of a reagent made to react with a specimen. This automatic analysis device is provided with: a reagent container which accommodates a reagent and which has attached thereto a perforable lid; a perforation unit for perforating the lid; and a reagent suction nozzle that is inserted into a hole formed by perforation and that sucks up the reagent. The automatic analysis device is characterized by being further provided with a state storage unit that stores the state as to whether the reagent container is in an unused state or in a used state, and a state update unit that, when the lid is perforated by the perforation unit while the reagent container is in an unused state, updates the state stored in the state storage unit to the used state.

A treatment device (1) for treating histological or cytological samples has a plurality of containers (6) for different treatment agents and a detection apparatus (2) for detecting a code which unequivocally identifies a type of a treatment agent or a type of a group of treatment agents from a package or replacement container of a treatment agent or group of treatment agents. The device furthermore has an evaluation apparatus (18) that, based on a detected code, ascertains which of the containers is or are to be replenished or replaced, and an indicating apparatus (4) which communicates to a user the ascertained container (6) or containers (6) that is or are to be replenished or replaced. The indicating apparatus may include a display (5) presenting a schematic image of the plurality of containers (6) with image(s) of each ascertained container being marked, and/or a light source (15) that illuminates each ascertained container.