A coupling device configured to form a sample access assembly is provided. The sample access assembly is configured to house a sample. The coupling device includes a heating component and a separating component. Further, the separating component is configured to separate portions of first and second containers that form first and second compartments of the sample access assembly. Moreover, the heating component is configured to heat at least a portion of the sample.

This disclosure relates to scale-down systems for freezing and thawing aqueous liquid mixtures of thermo sensitive substances. In at least one aspect, the system can comprise a first container that has a head-space and a liquid-space, with a substantially constant average transversal cross-section area in the liquid-space that does not change substantially with height. The first container holds a volume of liquid for a height of liquid, has a lateral active heat transfer area having an insulated lateral area ALIM, and has an equivalent radius sized to reproduce the equivalent radius of a second container. The first container further has a lateral heat transfer area in contact with the liquid-space. The first container is smaller than the second container, and the insulated lateral area is equal to or greater than the lateral active heat transfer area.

A label for a tube having a diameter D may have a transparent facestock. A printing area is defined on a first surface of the transparent facestock, the printing area configured to receive data thereon, the printing area covering only a portion of the transparent facestock, whereby a shielding portion of the length of the label is transparent. An adhesive layer is on a second surface of the facestock. A wireless communication inlay is adhered to the adhesive layer in a portion of the label corresponding to the printing area. The printing area and the facestock are sized for the shielding portion to overlap at least partially the printing area when the label is wrapped on a tube.

A label for a tube having a diameter D may have a transparent facestock. A printing area is defined on a first surface of the transparent facestock, the printing area configured to receive data thereon, the printing area covering only a portion of the transparent facestock, whereby a shielding portion of the length of the label is transparent. An adhesive layer is on a second surface of the facestock. A wireless communication inlay is adhered to the adhesive layer in a portion of the label corresponding to the printing area. The printing area and the facestock are sized for the shielding portion to overlap at least partially the printing area when the label is wrapped on a tube.

A method of storing a donor organ prior to implantation into an organ recipient includes bagging a donor organ that has been removed from an organ donor by placing the donor organ into at least one bag and sealing the at least one bag without including any ice in any of the at least one bag within which the donor organ is bagged; placing the bagged donor organ into a portable storage container configured to maintain the donor organ at a temperature of at least 8 degrees Celsius (C) during storage; and storing the donor organ in the portable storage container at the temperature of at least 8 degrees C. prior to transplanting the donor organ into the organ recipient.

The present invention relates to the long-term preservation of biological material. More specifically, it concerns a preservation container comprising: a biological container for containing biological material, a first shield configured for absorbing gamma-rays, a second shield configured for absorbing ambient neutrons, said second shield surrounding the biological container, the preservation container being of low-radioactivity background materials, and a method for preserving a biological material, comprising: a) providing a biological material in a confinement container, b) providing the preservation container of the invention, c) placing the confinement container containing the biological material into said preservation container, d) storing said preservation container containing the biological material in a room located under a material attenuating cosmic rays and induced particles, said material having a thickness equivalent to 1 m to 7000 m of water, for attenuating cosmic rays.

According to an embodiment of the disclosure, a vial cap is configured for sealing attachment to a tube set and to a vial having a hollow interior configured for receiving and storing a liquid sample. The vial cap may comprise an axially extending cylindrical wall and a radially extending cap top disposed within the cylindrical wall, wherein the cap top has an upper surface and a lower surface. The vial cap may include at least two exterior tubes extending upwardly from the upper surface of the cap top, wherein each exterior tube defines a passageway configured to communicate with the tube set. The vial cap may further include at least two interior tubular structures extending downwardly from the lower surface of the cap top, wherein the at least two interior tubular structures each define a passageway configured to communicate with one of the exterior tubes and the hollow interior.

A fluid sample vessel includes inlet and vent tube fittings formed at one end of a container with an opposite open end closed by a needle septum. A support cap is removably engaged to the container to support the container and protect terminal ends of inlet and vent tubular branches coupled to the fittings. The support cap includes a pair of opposite legs with outwardly directed tabs for mounting within a centrifuge while supporting the cryopreservation container.

A method for hyper-fast cooling of samples is described. The samples are secured in a sample container, then the sample container inserted into a cryogenic cooling chamber through an opening of the cooling chamber. The sample container is placed some distance away from a cooling head, but within range of a continuous stream of pressurized liquid coolant emitted by the cooling head, where, the sample is hyper-cooled by spraying the sample container with a continuous stream of the pressurized liquid coolant.

The present invention relates to a product and method for cell preservation, such as cell banking of any type of cells for subsequent scientific or medical use. More closely, the invention relates to a product and a method for cryopreservation of cells using vacuum tubes provided with freeze media/cryopreservation liquid.