A therapeutic bra structure includes a bra body having a bra layered member and a side bra layered member on both sides of the bra layered member separately, a fastener assembly or adhesive assembly combined with a distal edge of the side bra layered member and an elastic adjusting assembly having two elastic adjusting layers. Each elastic adjusting layer has an elastic and permeable layered member, and the two elastic adjusting layers are fixed to an inner side of the bra layered member, and an end adhesive assembly is provided at an outer edge of the elastic adjusting layers for the purpose of combining and positioning. This structure allows users to adjust the elasticity and has the effects of healing the wound stably, facilitating the use and installation of a drainage tube or an artificial blood vessel, and ensuring the safety of wearing bra after breast surgery.

A therapeutic bra structure includes a bra body having a bra layered member and a side bra layered member on both sides of the bra layered member separately, a fastener assembly or adhesive assembly combined with a distal edge of the side bra layered member and an elastic adjusting assembly having two elastic adjusting layers. Each elastic adjusting layer has an elastic and permeable layered member, and the two elastic adjusting layers are fixed to an inner side of the bra layered member, and an end adhesive assembly is provided at an outer edge of the elastic adjusting layers for the purpose of combining and positioning. This structure allows users to adjust the elasticity and has the effects of healing the wound stably, facilitating the use and installation of a drainage tube or an artificial blood vessel, and ensuring the safety of wearing bra after breast surgery.

A blood bag system includes one clamp. The clamp includes a base formed with an insertion hole through which a second tube and a third tube are inserted. A first slit for pressing the outer circumferential surface of the second tube inward such that a second flow channel is closed, and a second slit for pressing the outer circumferential surface of the third tube inward such that a third flow channel is closed, are provided in a wall section forming the insertion hole.

A screen exchange device for reducing the size of a biological tissue according to one embodiment comprises: a disk comprising a plurality of screens each having at least one through-hole configured to reduce the size of a biological tissue, the screens having different through-hole characteristics; a first cover which covers a first side of the disk and includes a first opening through which a biological tissue passes; a second cover which covers a second side of the disk and includes a second opening through which the biological tissue passes; a housing configured to receive the disk; and a manipulator which selects any one screen among the plurality of screens and manipulates the first cover or the second cover such that the selected screen communicates with the first opening and the second opening.

A system to be used to treat Leukemia, comprises a device to power, control and monitor an ultraviolet radiation as well as to monitor a blood contactless conductivity; and a catheter assembly with an inner dialysis catheter, an ultraviolet radiation source and a differential coil sensor. The system is using wavelengths of ultraviolet radiation to destroy infectious microbes that are in the blood and that are inside circulating tumor cells directly and indirectly as well as to destroy infectious microbes at primary tumor location (bone marrow). This is done without withdrawing the blood out of the body. Furthermore, the system measures a blood conductivity to evaluate the treatment process in a real time during the operation.

The present invention is related to the field of tissue regeneration. It concerns more particularly new standardizations and medical devices for the preparation of A-PRP, PRP, BMC, fat tissue, alone or in combination with a biomaterial or cell extract.

A device for dry thawing biological substances and methods for using the same are provided. The dry thawing device can be configured to receive a biological substance within a woven pocket. The woven pocket can include temperature sensors configured to measure a temperature of the interior volume and heating elements configured to heat an interior of the woven pocket 106 based upon the measured temperature to avoid overheating or underheating the biological substance during thawing. The woven pocket can also include mechanical vibrators configured to agitate the biological substance during thawing to achieve an approximately homogeneous temperature profile within the woven pocket.

A method for platelet preservation comprising placing a composition comprising platelets in a gas mixture comprising xenon and oxygen under pressure of about 0-10 Bars at a first temperature of about 18° C.-37° C. for a first period of time, and then subsequently cooling the composition to a second temperature of about 0,1° C.-6° C., and holding the composition under the pressure and in the second temperature for a second period of time.

Methods and container systems for processing biological fluids are disclosed. The container systems include an inner container within an outer container. The inner container wall is made of a porous material of a selected porosity that allows certain components to pass through said porous wall but retains other components. A treating solution is introduced into the chamber of the outer container.

A sample heating/cooling device (2) comprises a plurality of members (6) operable in use to heat and/or cool one or more samples (22). Each member (6) has a sample contact surface and is biased towards a resting position under the operation of a biasing means. The members (6) are movable independently of one another against said bias under the application of a force on the sample contact surface and so are able to conform to the shape of a sample placed on the members to provide a uniform heating/cooling profile. The members (6) may be mounted in a heating/cooling element (4) and adapted to conduct thermal energy between the sample (22) and the element (4). The device (2) is particularly suitable for thawing frozen sample bags having an irregular shape. A corresponding method is also described.