A sample container handling device is presented. The device comprises a linear transport unit and a release unit comprising a release blade segment. The release blade segment is rotated in a constant rotational direction.

A gripper provides for gripping labware having a variety of diameters and shapes. The gripper includes a support structure having a center axis, a motor, and a gripper stage. The gripper stage includes a plurality of blades, each of the blades having a first end through which a blade rotation axis extends, a second end that is circumferentially and radially moveable to rotate the blade about the blade rotation axis, and c) a center portion. A ring structure is coupled to the motor to rotate the ring structure around the center axis. The ring structure, as it rotates, moves the second end of each blade to rotate the blade about the blade rotation axis of the blade to shift the center portion towards the center axis to contact an outer portion of a vessel extending along the center axis.

The invention relates to a transport device for a laboratory sample distribution system, the transport device comprising a top cover having a transport surface, the transport surface being adapted to carry sample container carriers, an electromagnetic actuation assembly, the electromagnetic actuation assembly being adapted to generate a magnetic field at the transport surface for magnetic drive-interaction with a sample container carrier placed thereon, a support structure for carrying the actuation assembly, a sensor board being arranged in between the support structure and the top cover, the sensor board being adapted to detect a position of a sample container carrier placed on the transport surface with respect to the transport device, and elastic elements which are biased in between the sensor board and the support structure so that the sensor board is held flush against an inside surface of the top cover by a biasing force resulting from the biasing of the elastic elements.

Systems and methods for use in an in vitro diagnostics setting may include an automation track, a plurality of carriers configured to carry a plurality of sample vessels along the automation track, and a characterization station including a plurality of optical devices. A processor, in communication with the characterization station, can be configured to analyze images to automatically characterize physical attributes related to each carrier and/or sample vessel. A method may include receiving a plurality of images from a plurality of optical devices of a characterization station, wherein the plurality of images comprise images from a plurality of perspectives of a sample vessel being transported by a carrier, automatically analyzing the plurality of images, using a processor, to determine certain characteristics of the sample vessel, and automatically associating the characteristics of the sample vessel with the carrier in a database.

A method of configuring a laboratory automation system is presented. The position of a laboratory station is detected automatically. A laboratory sample distribution system and a laboratory automation system adapted to perform such a method are also presented.

In medical analysis devices and automatic specimen examination systems, the specimen conveyance mechanism is constituted by a plurality of belt lines. During installation or maintenance of the specimen conveyance mechanism, it is necessary to confirm the existence of steps at the joints of these belt lines and the parallelism of the conveyance line. According to the present invention, it is possible to lighten the burden of this work with a test tube type or conveyance holder type inspection device provided with a sensor and battery for operation. Also, even when an operator cannot visually confirm the conveyance line from outside, it is possible to confirm the state of the conveyance line.

A control device for wireless tags which are respectively attached to a plurality of articles supported respectively on a plurality of support portions and respectively store identification numbers of the articles, includes positioning portions that are respectively provided corresponding to the plurality of support portions, and input devices that are positioned respectively in the positioning portions. The input devices are individually controllable and each is configured to switch a flag status of one of the wireless tags.

The present disclosure provides a plate comprising an array of wells for chemical or biological reactions, wherein each of the wells comprises a reaction chamber with at least one opening on a surface of the plate. The array of wells consist of a plurality of adjacent blocks of wells, wherein each block of wells consists of a plurality of adjacent rows of wells, and wherein at least one void is provided in each block of wells in between the rows of wells. Here, the void is particularly part of the surface of the plate and lacks a well opening. Furthermore, a method for multiple imaging of such a plate by means of an imaging system is provided with the present disclosure.

The present invention provides a fully automatic fecal occult blood detecting analyzer, which is used to detect a sample box (30). The sample box (30) includes a transparent sleeve and a feces collector and test strips provided in the transparent sleeve. The fully automatic fecal occult blood detecting analyzer includes a feeding chain (10) and a main conveying chain (20); a plurality of clamping devices (40) for clamping the sample box (30) are provided on the feeding chain (10) and the main conveying chain (20), respectively; a transferring device is configured to transfer the sample box (30) from the feeding chain (10) to the main conveying chain (20); a pressing device (90); and an image acquisition device is configured to acquire colored tape information presented on the test strips in the sample box (30) on the main conveying chain (20). The present invention can implement continuous detection and accurate location of a plurality of sample boxes (30) without turning over and tilting the sample boxes (30). Besides, the sample boxes (30) can be pressed accurately so that diluents of fecal samples react with test strips to complete detection.

Vials (samples) as analysis targets to be set in a batch table for serial analyses are allowed to be designated simply and highly flexibly. On a batch table setting screen 100, a sample region designation method selecting button 120, an analysis direction selecting button 121, a plate image display area 125 and other components are arranged. A sample region designation method and an analysis direction are selected simply by clicking the buttons. The start position and the end position of analyses are designated by a drag-and-drop operation using a mouse on a plate image displayed in the plate image display area 125. The vials selected during a process of the drag-and-drop operation are displayed in a color discriminable from other vials. Accordingly, a simple, graphical operation can create a batch table in which the multiple vials mounted on the sample plate are set as analysis targets in a desired order.