A capping device for disinfection of a medical container is provided. The capping device includes a top portion having an inner surface, a bottom portion having an inner surface and an opening, and a connector. The connector couples the top portion of the capping device to the bottom portion thereof in a manner which permits movement of the top portion between a fully-seated position on the bottom portion of the capping device to form a hollow defined by the inner surface of the top portion of the capping device and the inner surface of the bottom portion thereof, and a position apart from the opening to permit ingress to the vial. The capping device further includes a disinfecting absorbent material disposed inside the hollow and extending through the opening in the inner surface of the bottom portion.

A container closure is provided for use in dispensing fluids from a container, and includes a base constructed and arranged for being attached to a mouth of the container, a first port disposed on the base and in fluid communication with the mouth, a second port disposed on the base in fluid communication with the mouth, and the first and second ports being visually differentiated from each other.

An applicator can have an ampoule body for holding a medical liquid; a tab extending away from the ampoule body and being twistable or deflectable with respect to a longitudinal axis of the ampoule body; and a frangible region in between the tab and the distal portion of the ampoule body, the frangible region being breakable in response to twisting or deflection of the tab. The applicator can have a resilient structure extending between the tab and the ampoule body and configured to allow the twisting or deflection to enable breakage of the frangible region while remaining intact and providing axial rigidity in response to a deflection pressure exerted on the tab during application of the medical liquid. The applicator can have features such as a thumb rest, a bubble portions, a pyramidal body construction, an offset frangible nodule, and various tab and head constructions.

Disclosed is a method and a system for producing an ampoule filled with a medical liquid. A preform is produced by plastic injection moulding that is then inhomogeneously heated and blown to form an ampoule body. Further disclosed is an ampoule produced by means of stretching and blowing, which comprises a connector with a break-off part in which the predetermined breaking point is aligned with the septum of the connector.

A sealing arrangement is for a container (1) and/or container part, such as a closure cap placed onto the container (1). The interior of the container (1) is used to accommodate a medium, particularly a fluid bottled in a sterile manner, which can be removed from the container (1) by a removal device such as a syringe needle. The removal device penetrates sealing material (9) connected to the container. The sealing material (9) is fixedly connected to the outside (7) of the container (1) and/or container parts facing the environment by a fused and/or adhesively bonded connection.

An object is to provide a method for producing a port that can shorten the time for production. Provided is a method for producing a port including: sealingly inserting a sealing plug, through which a hollow needle can be pierced, into a part to be sealed of a port body, wherein the port body includes: a part to be sealed that has a tubular shape with a first end and a second end opposite to the first end; a connection part that has a tubular shape, and is continuous with the first end of the part to be sealed; and the part to be fitted that is formed in any one of an inner peripheral surface of the part to be sealed, an outer peripheral surface of the part to be sealed, and the second end of the part to be sealed; fitting a fitting part of a pulling-out prevention member into the part to be fitted, wherein the pulling-out prevention member includes: a body part that has a first surface and a second surface opposite to the first surface, and the fitting part that is continuous with the body part; and laying the body part on the sealing plug.

A multi-reservoir dispensing, disposable and sterile container has at least two separate and distinct reservoirs positioned adjacent to one another, and which can be readily manufactured using blow-fill-seal technology. The reservoirs contain components of a mixed pharmaceutical formulation, which is prepared at the time of dispensing from the container by blending of the contents of the reservoirs. Liquid flow channels extend from each reservoir and merge together at or near an exit aperture of the container, and a mixing feature can be employed at or downstream of the point of merging. In the container as provided to a user the exit aperture is blocked by a seal, which is removed prior to dispensing.

A needleless access vial includes a vial body for storing a liquid medication. A needleless access port is disposed within an opening along the top of the vial body. A valve having a deformable body is positioned within the access port housing, and is in communication with the access port inlet section and the access port outlet section. The valve is biased toward a closed configuration, and transitions to an open configuration upon engagement of the outlet section by a needleless syringe.

A child-resistant cartridge adapted to be used with an automatic brewing machine. The cartridge has a base and a lidding. The base can contain a pharmaceutical active. The lidding can be a multilayer laminate with an outer layer and an inner layer. The cartridge can be made out of tear resistant materials that are sufficient to prevent 70% of children from accessing the contents of three or more cartridges during a Child-Resistant Screening Test.

A valve includes a valve housing and an elastic valve member accommodated in the valve housing. The valve member is configured to close the valve when the valve is in a closed operating state. The valve member has a valve opening configured to be closed when the valve is in the closed operating state and to provide fluid passage through the valve when the valve is in an open operating state. The valve member is overmolded into the valve housing. The valve is beneficially used as a valve element of a port of a cap for a fluid container, in particular for a container for a medical fluid.