Tissue sample cassettes for receiving tissue samples include an upper tray including compartments separated by dividers, a lower tray coupled to the upper tray and having a central recess, and an absorbent material located in the recess of the lower tray. Related systems and methods for automated gross processing of tissue samples are also disclosed.

Embodiments of the disclosure relate to a biosample plate that includes a memory component for storing biosample identification and analysis data, and a wireless communication interface for transferring the data to and from the biosample plate. In one embodiment, the biosample plate comprises a base for receiving a biosample, a memory component coupled to the base for storing identification and analysis information related to the biosample, and a wireless communication interface coupled to the memory component for transferring the information to and from the memory component. The wireless communication interface may include an optical device.

A method for the integrated and automated analysis of DNA or protein, including a single-use cartridge, with an analysis device having a control device, and devices for capturing and processing signals, the control device carrying out a completely automatic process and evaluation of molecular diagnostic analysis via single-use cartridges (Lab-on-a-Chip). Controlling of an analysis process, which occurs in the cartridge, involve the subsequent displacement and thermostatisation of liquids with a first device, and with a second device the signals which are obtained during the analysis are processed. The first and the second devices are synchronized in such a manner that the analysis process of the sample can be carried out in a totally integrated manner thus producing an immediate result.

The biological information detection sensor supply device is provided with a main body case having a supply port to which a biological information measurement device can be attached, a housing unit for housing a biological information detection sensor and a sensor supply film including a cover film and a holding film for sandwiching the biological information detection sensor, and a supply unit for supplying the biological information detection sensor from the housing unit to the supply port. The supply unit supplies the biological information detection sensor to the supply port, and separates the holding film and the cover film from the sensor supply film in a state before the biological information detection sensor is supplied to the supply port. At the supply unit, the biological information detection sensor supplied to the supply port is fitted to the biological information measurement device fitted to the supply port.

Provided herein are systems for determining a stretch condition of a tissue and assessing the stiffness of the tissue. Also provided herein are methods for using the systems for measuring stiffness of a tissue, assessing the effect of an agent on a tissue, and identifying subjects having a disease or disorder associated with increased or decreased stiffness of a tissue.

A system for the integrated and automated analysis of DNA or protein, including a single-use cartridge, with an analysis device having a control device, and devices for capturing and processing signals, the control device carrying out a completely automatic process and evaluation of molecular diagnostic analysis via single-use cartridges (Lab-on-a-Chip). Controlling of an analysis process, which occurs in the cartridge, involves the subsequent displacement and thermostatization of liquids with a first device, and with a second device the signals which are obtained during the analysis are processed. The first and the second devices are synchronized in such a manner that the analysis process of the sample can be carried out in a totally integrated manner thus producing an immediate result.

The present invention relates to the field of biological sample testing technology, and in particular, to a biological sample reaction vessel. A reagent storage portion and a push rod movable relative to the reagent storage portion are packaged in the reaction vessel; the reagent storage portion comprises at least one reagent containing cavity, and the reagent containing cavity is sealed by a sealing element; and the push rod is connected to the sealing element, and the push rod is used for cooperation with an external device to separate the sealing element from the reagent storage portion. In this application, the reagent storage portion and the push rod are both packaged in the biological sample reaction vessel, and in reaction, the biological sample reaction vessel only needs to cooperate with a test cassette. With one operation, that is, inserting the biological sample reaction vessel into the external device, the reagent in the reagent storage portion can be released rapidly.

The biological information detection sensor supply device is provided with a main body case having a supply port to which a biological information measurement device can be attached, a housing unit for housing a biological information detection sensor and a sensor supply film including a cover film and a holding film for sandwiching the biological information detection sensor, and a supply unit for supplying the biological information detection sensor from the housing unit to the supply port. The supply unit supplies the biological information detection sensor to the supply port, and separates the holding film and the cover film from the sensor supply film in a state before the biological information detection sensor is supplied to the supply port. At the supply unit, the biological information detection sensor supplied to the supply port is fitted to the biological information measurement device fitted to the supply port.

A medical test system includes: a test cartridge having a sample collection portion, a test substrate, a result indicator, and a reservoir that stores a test solution; and a measurement station including: a reservoir lock that couples to the reservoir; a tester manipulator that couples to the sample collection portion and is able to insert the test substrate into the reservoir portion in order to apply the test solution to the test substrate; and a sensor able to identify a result. A medical test cartridge includes: a tester portion including: a collection element; substrate; and result indicator; and a base portion including: a reservoir housing a test solution. An automated method of evaluating a medical sample includes: receiving a base portion of a test cartridge; securing the base portion using a retention element; receiving a tester portion of the test cartridge; and inserting the tester portion into the base portion.

A system including a processor and memory coupled to the processor. The memory stores a local testing database having a test configuration profile for a cassette having a lateral flow assay (LFA) strip having a test line and intensity threshold value. An operator input device is coupled to the processor for receiving operator provided results from an operator that is provided to the processor. An LFA test result display for displaying an LFA test result, and an LFA strip reader coupled to the processor for reading the LFA strip is in the system. The processor determines the LFA test result based on comparing a measured intensity value of a portion of the test line in the LFA strip image to the intensity threshold value for the test line, receives the operator provided result from the operator input device, and provides to the LFA test result display the LFA test result.