Provide is a blood collection container capable of suppressing the occurrence of blood clots involving bubbles when blood containing heparin is coagulated, and capable of suppressing the production of fibrin in serum after separation when blood containing heparin is separated into serum and blood clots. A blood collection container according to the present invention includes: a blood collection container main body having an opening at one end thereof and a closed bottom at the other end thereof; a serine protease disposed in the blood collection container main body; and a heparin neutralizing agent disposed in the blood collection container main body, wherein when a region in which the serine protease is disposed is defined as a first region, and a region in which the heparin neutralizing agent is disposed is defined as a second region, the second region includes a region present on an other end side with respect to an end on the other end side of the first region.

Provide is a blood collection container capable of suppressing the occurrence of blood clots involving bubbles when blood containing heparin is coagulated, and capable of suppressing the production of fibrin in serum after separation when blood containing heparin is separated into serum and blood clots. A blood collection container according to the present invention includes: a blood collection container main body having an opening at one end thereof and a closed bottom at the other end thereof; a serine protease disposed in the blood collection container main body; and a heparin neutralizing agent disposed in the blood collection container main body, wherein when a region in which the serine protease is disposed is defined as a first region, and a region in which the heparin neutralizing agent is disposed is defined as a second region, the second region includes a region present on an other end side with respect to an end on the other end side of the first region.

A kit preparation that enables drug dose adjustment. The kit preparation includes a bag which contains an infusion solution or pure water and at least one drug enclosing part in which a drug is enclosed and which is provided with a sealing part. The drug enclosing part is connected to the bag via the sealing part; and, when the sealing part is released, the bag is communicated with the drug enclosing part and thus the drug is poured into the bag so that a dispensing work can be carried out.

A kit preparation that enables drug dose adjustment. The kit preparation includes a bag which contains an infusion solution or pure water and at least one drug enclosing part in which a drug is enclosed and which is provided with a sealing part. The drug enclosing part is connected to the bag via the sealing part; and, when the sealing part is released, the bag is communicated with the drug enclosing part and thus the drug is poured into the bag so that a dispensing work can be carried out.

Device for blocking a fluid product reservoir with a neck, having a cap, a fixing ring to hold the cap on the neck, the fixing ring having a cylindrical structure with wall parts separated by lateral windows, each wall part having at least one inner radial projection to hold the cap in the fixing ring, each lateral window having a lower edge provided with at least one rigid lug extending radially inwards from the lower edge. The rigid lugs, in the blocking position of the fixing ring, are arranged under a neck of the reservoir, to thus fix the fixing ring on the reservoir. A blocking cover is provided having a cylindrical wall and an upper wall and arranged around the fixing ring to lock said fixing ring in its blocking position. The upper surface of the cap has a deformation profile that engages, after assembly, with the fixing ring.

To provide a method for manufacturing a medical glass container prevented from breakage and deformation and a fire blasting device. A method for manufacturing a medical glass container includes a processing process of placing a glass container 10 on the outer peripheral surface of each of a first roller 61 and a second roller 62, which are disposed side by side in such a manner that the axis lines are parallel to each other, so that the axis line of the glass container 10 is parallel to the axis lines of the first roller 61 and the second roller 62 and the entire outer peripheral surface in an inner surface 15 of the glass container 10 corresponding to a region deteriorated by processing is made to abut on the outer peripheral surface of each of the first roller 61 and the second roller 62, and then applying a flame ejected from a point burner 30 to the region deteriorated by processing in the inner surface 15 of the glass container 10 while rotating the glass container 10 by rotating the first roller 61 and the second roller 62 around the axis lines.

To provide a method for manufacturing a medical glass container prevented from breakage and deformation and a fire blasting device. A method for manufacturing a medical glass container includes a processing process of placing a glass container 10 on the outer peripheral surface of each of a first roller 61 and a second roller 62, which are disposed side by side in such a manner that the axis lines are parallel to each other, so that the axis line of the glass container 10 is parallel to the axis lines of the first roller 61 and the second roller 62 and the entire outer peripheral surface in an inner surface 15 of the glass container 10 corresponding to a region deteriorated by processing is made to abut on the outer peripheral surface of each of the first roller 61 and the second roller 62, and then applying a flame ejected from a point burner 30 to the region deteriorated by processing in the inner surface 15 of the glass container 10 while rotating the glass container 10 by rotating the first roller 61 and the second roller 62 around the axis lines.

A medical bag comprising: a bag main body comprising a flexible sheet material having an interior portion partitioned via a partition part into a first space and a second space that is smaller than the first space, a first liquid housed in the first space, and a second liquid housed in the second space. When the volume of the first liquid is set as L1 and the volume of the second liquid is set as L2, L1/L2 is 2.0 to 6.0. The partition part has a breaking strength of 5 to 25 kPa.

A medical device configured as a tube holder for use in collecting bodily fluids, especially for use as a blood collection tube holder, the device embodying two coaxially alignable needles, the first needle being a forwardly facing fluid collection needle and the second needle being a rearwardly facing fluid discharge needle. The first and second needles are satisfactorily supported by a frontal attachment and body, respectively, that are disposed in relative sliding engagement along an interface that is transverse to the first and second needle and that extends at least from the second needle to an opening into a needle retraction chamber that projects rearwardly from the body.

System and associated method for capturing, preserving, and transporting a bodily fluid, including a collection jar having a base body, a lid body, and a cartridge having a plunger therein and disposed in the lid body, the cartridge housing a preservative when the plunger is in a first plunger position and permitting a release of the preservative into an internal cavity of the collection jar when the plunger is in a second plunger position, and a transportation packaging having an outer container, at least one insulation foam support, at least one phase change material bottle, and at least one collection jar holding tray, where the phase change material bottle has an indented portion corresponding to an indented portion of the collection jar holding tray, and where the collection jar is configured for placement in the at least one collection jar holding tray during transportation.