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.

A flexible container incorporating flexible front and rear sheets with a perimeter seal in which at least one length or section of the perimeter seal can include a seal weld that has both a permanent seal section and a pressure absorbing seal section. The pressure absorbing seal section is configured to peel, fail, or split when the flexible container, filled with a solution or liquid, is dropped onto a hard surface to thereby absorb the impact of the drop. The flexible container can be provided with one or more dispensing and/or additive ports or without any port. The flexible container may include more than one compartments with a peelable seal separating two adjoining compartments of the flexible container.

A therapeutic pouch is provided. The therapeutic pouch defines a cavity for slidably receiving intravenous therapy equipment, such as an IV bag or other fluid dispenser. A front portion of the therapeutic pouch provides a comforting presentation for the patient, while the rear portion of the therapeutic pouch provides a visibility pouch for securing the IV bag and allowing a healthcare provider visibility of the administration of the fluids retained by the IV bag. The visibility pouch may provide an upper opening and an opposing lower opening, both communicating with the cavity for enabling the IV bag to protrude therefrom and access to IV tubing and ports, respectively. An upper portion of the therapeutic pouch provides a hanging loop for working in unison with the IV bag hole for enabling support from an IV stand or the like.

The present invention relates to a multilayer structure including a base (X), a layer (Y), and a layer (Z), wherein the layer (Y) contains an aluminum-containing compound (A), and the layer (Z) contains an organic phosphorus compound (BO) and a polymer (F) having an ether bond and having no glycosidic bond.

A multi-mix infusion bag is provided. The multi-mix infusion bag includes a lower portion and an upper portion. The lower portion has a lower chamber and the upper portion includes a plurality of chambers. Each chamber is separated and contains a fluid agent. The multi-mix infusion bag is configured to transfer each fluid agent within each chamber of the upper portion into the lower chamber for mixing. The multi-mix infusion bag may include dispensing devices associated with each chamber, wherein the dispensing devices operate to transfer the fluid agents into the lower chamber for mixing.

An aseptic bioprocess package is provided herein. The aseptic bioprocess package includes a 2D flexible container including an interior compartment, a height having an upper half and a lower half, an inlet and an outlet, the inlet and the outlet being disposed on the same half of the 2D flexible container and a channel-forming feature in the interior compartment of the container, the channel-forming feature being configured to maintain a fluid flow path that fluidly connects the interior compartment of the flexible container with the outlet.

A pressure bag (1) has a bag-like shape including an opening (11) at one end thereof and a bottom portion (12) on the opposite side to the opening (11). The pressure bag (1) has a double structure in which an inner sheet (20) and an outer sheet (30) are laid one on top of the other so that the outer sheet (30) is located on the opposite side of the inner sheet (20) from the housing chamber (10). A pressure chamber (15) is provided between the inner sheet (20) and the outer sheet (30). All of the inner sheet (20), the outer sheet (30), and the pressure chamber (15) extend from one side to the other side of the housing chamber (10) via the bottom portion (12).

A system for storing pharmaceuticals or biological media comprising a bag including a flexible sidewall defining an opening; and a vent coupled with the flexible sidewall at the opening and defining a vent passageway between an internal volume of the bag and an external environment, wherein the vent is coupled with the bag at a location spaced apart from and above the opening.

An IV container for precise measurement and dispensing of fluid contained in the IV container. This IV container has an upper fluid-containing portion to contain and measure a first quantity of fluid. The upper fluid-containing portion has a first cross-sectional area, and a first plurality of fluid measurement markings along a side of the upper fluid-containing portion that represent measurement units of a first size. A lower fluid-containing portion is in fluid communication with the upper fluid-containing portion, and can contain and measure a second lesser quantity of fluid. The lower fluid-containing portion has a second cross-sectional area that is less than the first cross-sectional area. The lower fluid-containing portion has a second plurality of measurement markings along a side of the lower fluid-containing portion that represent measurement units of a second size that's smaller than the units of the upper fluid containing portion, and therefore provides enhanced measurement precision.

A multi-mix infusion bag is provided. The multi-mix infusion bag includes a lower portion and an upper portion. The lower portion has a lower chamber and the upper portion includes a plurality of chambers. Each chamber is separated and contains a fluid agent. The multi-mix infusion bag is configured to transfer each fluid agent within each chamber of the upper portion into the lower chamber for mixing. The multi-mix infusion bag may include dispensing devices associated with each chamber, wherein the dispensing devices operate to transfer the fluid agents into the lower chamber for mixing.