A test device is configured for diagnostic testing and includes an optical readable medium, in turn including a pattern of spots of material arranged on a surface of the device. Several patterns may be provided. The patterns accordingly formed may be human and/or machine readable. They may notably encode security information, e.g., indicating whether the device has already been used. The spots may notably be inkjet spotted. In addition, a method is provided for decoding information encoded in a pattern of such a test device. In embodiments, liquid is introduced in the device, which comprises additional spots having a substantially different solubility than spots forming the actual pattern. Thus, the additional spots get solubilized in and flushed by the liquid as the latter wets them, and an initially hidden pattern may be read, which is formed of the remaining spots (not solubilized). Encoding methods are also provided.

The invention relates to a container for containing tissue, comprising at least one receiving space for tissue and at least one information surface for arranging data, wherein the information can be arranged by means of a laser. The invention also comprises a device provided with a laser for arranging information on such a container. The invention moreover also comprises a method for arranging information on such a container using a laser.

The invention relates to a fluid sampling assembly comprising a sampling device (1) for analysis of one or more substances in a fluid flow passing through the sampling device (1), a first device (3) comprising a flow meter for measuring the fluid flow, and a control unit (12) with communication means, wherein the control unit (12) is adapted to record information concerning the sampling, and to communicate the information to a memory (4, 7, 13). The invention further relates to a method for assuring quality of measurements using a sampling assembly.

A biological analysis system comprising at least one inlet and one outlet, at least two biological analysis devices connected to one another by a conveyor defining a closed circuit, each biological analysis device comprising a region for the exchange of tube holding racks with the conveyor. The conveyor and the at least one inlet of the biological analysis system comprise a reader of an identifier of a tube holding rack which reader is designed to communicate an identifier it has read to a controller of the biological analysis system, which controller is designed to apply a specific treatment to a tube holding rack identified by the reader of the conveyor and the identifier of which has not previously been read by the reader of the at least one inlet of the biological analysis system.

A first rack of a first color and a second rack of a second color respectively hold blood collecting tubes. After a test is finished, the first and second racks are disposed at a carrying-out section. A result screen showing a test result includes a first region of the first color and a second region of the second color. The first and second regions are displayed in positions corresponding to positions of the first and second racks in the carrying-out section. First symbols are displayed in the first region at positions corresponding to positions of the blood collecting tubes held in the first rack. Second symbols are displayed in the second region at positions corresponding to positions of the blood collecting tubes held in the second rack. A displayed appearance of each of the first and second symbols is changed in accordance with the test result.

A sample changer for a thermoanalytical instrument is provided. The sample charger includes a camera and image processing capabilities which provide improved positional control when depositing a sample object on or picking up a sample object from a sample support. The sample charger includes a moveable member driven for movement between at least a receiving position to pick up the sample object at a releasing sample support and a releasing position to deposit the sample object at a receiving sample support. The camera is mounted to the moveable member for movement therewith. The camera includes a field of view and a depth of focus adapted to capture an at least partial image of the sample object, the releasing or receiving sample support.

Disclosed herein are test substrates, systems and methods for detecting an analyte in a sample. Test substrates of the present disclosure include a predefined pattern, wherein a first region includes a partial pattern of the predefined pattern and a second region that is incomplete and wherein the incomplete portion comprises a reagent that reacts with an analyte in a sample to produce a completed pattern, wherein the completed pattern forms a code.

Tissue sample management systems include a central network, a medical professional system, and a pathology lab system for processing a tissue sample in a matrix having a sectionable code. At least the pathology lab system includes at least one imaging device, and the central network is configured to process images from the at least one imaging device to identify and record at least the sectionable code of the matrix. Methods for tissue sample processing include providing a matrix having a sectionable code and measurement marks, the matrix for receiving a tissue sample, and identifying the sectionable code from an image taken of the tissue sample in the matrix. Tissue sample-receiving matrices include a sectionable alphanumeric code or bar code, a tissue sample receptacle, and measurement marks formed along a sidewall thereof. The matrices include one or more proteins and one or more lipids.

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.

A test device is configured for diagnostic testing and includes an optical readable medium, in turn including a pattern of spots of material arranged on a surface of the device. Several patterns may be provided. The patterns accordingly formed may be human and/or machine readable. They may notably encode security information, e.g., indicating whether the device has already been used. The spots may notably be inkjet spotted. In addition, a method is provided for decoding information encoded in a pattern of such a test device. In embodiments, liquid is introduced in the device, which comprises additional spots having a substantially different solubility than spots forming the actual pattern. Thus, the additional spots get solubilized in and flushed by the liquid as the latter wets them, and an initially hidden pattern may be read, which is formed of the remaining spots (not solubilized). Encoding methods are also provided.