A preassembled medicine mixer comprises a rotary sleeve (4), a guide sleeve I (3), a guide sleeve II (6), a guide part, a dosing barrel (1), and a dosing double needle (2). The guide sleeve I (3) extends into the guide sleeve II (6) and is connected to the rotary sleeve (4). A guide groove (8) is provided on the side wall of the guide sleeve I (3), and two ends of the guide groove (8) are extended by a distance towards opposite directions. A guide spiral groove (7) is provided on an inner wall of the guide sleeve II (6). The guide part is disposed in the guide sleeve I (3) and has a guide block (9) at the outer side thereof. The guide block (9) penetrates through the guide groove (8) and extends into the guide spiral groove (7). In use, the rotary sleeve (4) is rotated to drive the guide part to rapidly move downwards and push a medicine container (17); an upper needle tip of the dosing double needle (2) pierces a sealing plug on the medicine container (17), and a lower needle tip pierces a diaphragm (23) in an interface (22), so that the medicine container (17) is instantly communicated with an infusion container (14), thereby implementing sterile closeness during the entire process of transportation, storage, butt joint, medicine mixing, and infusion.

A flexible multi-chamber bag for storing and reconstituting parenteral nutrition solutions is disclosed. The flexible multi-chamber bag comprises two first peelably sealing walls between the two polymer films extending from the top edge to the bottom edge and separating the first bag into a first chamber, a second chamber and a third chamber, wherein the first chamber is between the second chamber and the third chamber; and at least one of the two first peelably sealing walls split into a second plurality of second peelably sealing walls and the second plurality of the second sealing walls sealed to the bottom edge to form a fourth chamber.

A bodily fluid drainage assembly can include a fluid bag and one or more covers. The assembly can include one or more volume indicators from which an approximate volume of a bodily fluid that is retained within the bag can be ascertained. In some arrangements, a cover includes a volume indicator that defines an opening through which a transparent or semitransparent portion of the bag can be viewed.

Various embodiments of the present technology provide structures for a cover for obscuring medical equipment and methods of making the same. The cover may extend over the medical equipment and comprise a plurality of peripheral flaps that extend over the sides of the medical equipment to conceal at least a portion of the medical equipment. In one embodiment, the cover may comprise a central member configured to extend over the top of the medical equipment. The cover may comprise one or more peripheral flaps extending out from the central member and configured to overlay and conceal a portion of the medical equipment and/or accessories attached to the medical equipment. In some embodiments, the cover may comprise spaces between the peripheral flaps provide access to the medical equipment.

A device and method for enterally hydrating a patient with cooled fluids. The patient may be a paralyzed or limited upper body mobility patient with a functional gastrointestinal system who is nonetheless incapable or not fully capable of drinking unassisted. Here fluids are provided by a suspended container which also has a pouch to admit cooling material such as ice, but to keep the cooling material separate from the fluid. The container may also have optional graduation markings to allow for convenient estimation of fluid use, and an upper open and closeable cap to allow the container to be refilled. The container has a lower fluid conducting tube that terminates in a mouthpiece. The mouthpiece contains a fluid valve formed from at least one slit in an elastic material. Patient mouth force on the valve causes the slit to enlarge, thus enabling cooled fluid to flow into the patient.

Package for supporting a product, in particular a pharmaceutical product, especially in the form of a package for repackaging said product, and preferably usable in entities, such as hospitals, for the therapeutic care of people, comprising a plurality of elements in which one or more elements are formed as respective supporting elements of the product, and are adapted to support, or contain, the product, and especially formed as a respective sachet. The element package has a corresponding portion, in particular outermost, and preferably upper in use, which is adapted to be connected to at least a respective portion of one or more corresponding elements of the package so as to realize the same package, said connecting portion being adapted to be detached from the respective element of the package, to allow detaching the same element from the remaining part of the package.

A portable canister holder is disclosed. The portable canister system comprises a collapsible substantially cylindrical, non-rigid body assembly comprising a plurality of vertical support rods configured to support a plurality of horizontal support restraints. The vertical support rods are able to pivot along with the horizontal supporting restraints, thereby collapsing the body assembly. The lowest horizontal support restraint further comprises a stopper to prevent the canister from being disconnected from the body assembly when in use. The portable canister holder further comprises an articulating joint member having a first end configured to attach to the body assembly and a second end configured to attach to a clamping device. The portable canister holder further comprises an IV holder configured to attach to the body assembly, the IV holder having a plurality of rods configured to support an IV bag.

A gravity infusion IV bag having an elastic suspension arrangement with one or more suspension elements attached at a top end of the bag section and arranged to be hung from a support such that, as fluid flows from the outlet, the weight of the bag section reduces and the elastic suspension arrangement contracts to raise the bag section relative to the support. The one or more suspension elements may be formed from styrene-ethylene-butadiene-styrene (SEBS) and have a 100% Young's modulus in the range 80-120 psi.

A dispensing cap comprising a grasping body, a spout engaging bore and a dispensing coupling. The dispensing coupling has a dispensing cap coupled thereto through a tether. A pouch assembly is likewise disclosed, as is a process of enteral feeding with a pouch and a dispensing cap attachable to the spout. The dispensing cap can be provided and attached to a spout of a pouch (upon removal of a filling cap) wherein the dispensing cap may be provided in a sterilized bag or pouch prior to use. Methods and processes are likewise disclosed.

A drainage bag is provided for a thermal control unit adapted to deliver temperature-controlled liquid to a patient in order to control the patient's temperature. The drainage bag is used to hold and transport the liquid when the liquid inside the thermal control unit is changed. The drainage bag includes a bottom layer, a top layer sealed thereto, and a float secured to the top layer that is positioned adjacent an opening in the top layer. As the liquid from the thermal control unit drains into the opening in the top layer, the liquid lifts the float and the float lifts the top layer of the bag. The bag thereby expands its volume to accommodate the liquid from the thermal control unit. The bag may further be designed to be carried without sealing the opening and without spilling the liquid. A method for using the bag is also disclosed.