Abstract: A stand for a medical fluid treatment, a system for supporting multi-chamber medical fluid bags and a method for testing whether the multi-chamber bags have been preset properly for therapy are provided. In one embodiment a multi-section stand is provided that is folded in a number of places to produce a structure upon which fluid from a properly preset solution bag flows readily to a patient, but upon which a dual-chamber bag that has not been modified properly for treatment collapses, folds or falls to a position providing visual indication that the chamber seal needs to be released or opened.

Abstract: The present invention relates to glycosyl-etoposide prodrugs, a process for the preparation thereof and the use thereof in combination with functionalized tumor-specific enzyme conjugates for treating cancers.

Abstract: The present invention provides systems, methods and apparatuses for medical fluid delivery systems that employ a pumping cassette. In particular, the present invention provides systems, methods and apparatuses for cassette-based dialysis therapies including hemodialysis, hemofiltration, APD (including tidal modalities) and CFPD. The embodiments described include a combined pump/valve housing, a fail safe pump/valve arrangement, a cassette auto-alignment feature, a pumping membrane material, a multiplexing valve arrangement, an expert fluid pumping management system, an integral port vent and an in-line air separation chamber and combinations of each of these.

Abstract: A flexible bag having expansible and collapsible cells can be used in a liquid dispenser. A rigid manifold, and in one instance a rigid frame is provided in the bag to keep passages open in use and to isolate one of the cells from the remaining cells. The manifold is capable of altering the volume of one of the cells so that the same bag can be used in different applications.

Abstract: Apparatuses and methods for maintaining sterile connections during, for example, dialysis therapy. The present invention provides a container for a medical device and a lid therefore. The lid and the container are configured for an easy snap release using a cam-follower system. The invention also provides a method for using an assembly of the container, lid and a medical device within the container to maintain sterile connections.

Abstract: An element provided with a layer based on fibrin- or fibrinogen-containing material, said element comprising (a) a hydrophobic or substantially hydrophobic support, which has a porous part with a thickness of 0.1 to 5 mm, and whose pores, extending across its thickness have a node spacing of 5 to 100 ?m, one face of said porous part being treated with a compound based on fibrin and/or a fibrinogen-containing material, and (b) a fibrin-based layer covering said treated surface of the support, characterized in that said fibrin-based layer is substantially uniform and homogeneous on said treated surface, and that the fibrin layer and at least the face of the support in contact with the fibrin layer are substantially free of fibrinogen.

Abstract: A flexible container and method for making same are provided. The container comprises a base portion including a bottom, side walls, and an interior, the bottom defining a substantially flat planar surface when the container houses product and the container rests on its bottom, an upper panel portion, that is designed to be received within the interior of the base portion and includes side panels that define a closure member, the upper panel being so constructed and arranged to define a substantially flat surface when the closure member is closed and portions of the upper panel are folded over, the upper panel includes a portion that is sealed to the base portion, and a pair of handles may also be coupled to the base portion.

Abstract: In authentication using a plurality of cipher keys, the authentication time is shortened. In the case that an encipher key to encipher key are required to take an access to each area out of the area to area in a memory of an IC card, a plurality of areas to have an access is informed to the IC card from a reader writer, a plurality of cipher keys corresponding to these areas (for example, cipher key 1, cipher key 2, and cipher key 4) is read out, and reduction processing section generates one reduction key from these cipher keys. A random number which is generated from a random number generation section of the reader writer is transferred to the IC card, and an encipherment section enciphers the random number using the reduction key. The reader writer receives the enciphered random number from the IC card, and deciphers it using the reduction key, and judges the IC card to be proper if the deciphered random number is equal to the generated random number.