The present invention discloses a vessel, comprising: an essentially cylindrical vessel body having an opening, a cylindrical wall and a cylinder base; a first groove formed in the cylindrical wall and extending in axial direction at least a predetermined portion of the vessel body; and a second groove formed in the cylindrical wall and extending in axial direction at least a predetermined portion of the vessel body; wherein the first groove is an orientation groove defining the orientation of the vessel with respect to a guide of a fluid extraction apparatus; and wherein the second groove is a coding groove identifying the type of vessel; and
a vessel extraction apparatus, adapted to extract fluid form a plurality of vessels, comprising: a plurality of receiving openings, wherein each opening is adapted to receive one of the vessels; wherein a first protrusion and a second protrusion are associated to each receiving opening; wherein the first protrusion is adapted to engage with a first groove of a vessel; wherein the second protrusion is adapted to engage with a second groove of a vessel that is of a vessel type corresponding to the respective receiving opening;
wherein the distance from the first protrusion to the second protrusion of a first receiving opening differs from the distance from the first protrusion to the second protrusion of a second receiving opening.

The present invention relates to a universal closure capable of fitting various sized container openings in sealed engagement The present invention also relates a universal dispensing closure capable of fitting various sized container openings in sealed engagement and used to house a secondary supply or dose of product and when the closure is activated dispense the secondary product or dose into a receiving vessel to which it is attached.

A fitting for affixing to a mouth portion of a receiving container and for receiving a drinking straw comprises a tubular body including a side wall having an inner surface and an outer surface, an open bottom end and a closed top end formed by a top wall having a frangible region therein configured to permit passage of the drinking straw therethrough. A seal layer is coupled to the closed top end and is configured to overlap the frangible region. The fitting may also be mounted onto a container body including a container side wall, an integral container bottom wall and an open top end defined by an open mouth portion. A drinking straw may be releasably coupled to the container body.

Embodiments are directed to a removable cap with a conduction seal closure for sealing an opening of a container. The cap has a side wall and a top wall with an open access hole there-through. A flat upper portion surrounds the open access hole, which is sealed by the conduction seal. The conduction seal comprises a first polymer sealing layer, an aluminum foil layer on top of the first layer to heat seal the first layer to the cap, and a second polymer layer arranged on top of the aluminum foil layer for protection. The aluminum foil provides a formable shaping strength such that upon seal piercing, a permanent memory spread of the first and third layers is achieved. Removal of the cap does not damage the seal. Access to the container contents is achieved without probe contact to the as-pierced seal.

The present invention aims to provide a medical rubber stopper that is excellent in chemical resistance and airtightness while having good productivity. The present invention relates to a medical rubber stopper including: a disk-shaped head portion with a flange region; and a cylindrical leg portion protruding from the lower surface of the head portion and having a smaller diameter than the head portion, the lower surface of the flange region and the leg portion being laminated with an inert film, the lower surface of the flange region and/or the outer periphery of the leg portion being provided with an annular groove through which the base rubber is exposed.

In one general aspect, a method for filling multiple containers with a pharmaceutical product is disclosed, which comprises decontaminating sealed nested materials in a transfer chamber, removing from the sealed nested materials one or both of a container nest holding the multiple containers and a closure nest holding multiple closures, transferring from the transfer chamber to a controlled environment enclosure the removed nest, aseptically filling the containers with the pharmaceutical product, and closing the containers with the multiple closures. The nests are configured to allow multiple closures and containers to be simultaneously aligned concentrically, and closed simultaneously. Spring-loaded retaining structures on the closure nest allow it to releasably retain multiple closures above the corresponding multiple containers. In some embodiments the spring-loaded features are monolithically integrated with the closure nest. The product may be lyophilized in partially sealed containers while the sealing closures are releasably retained by the closure nest.

A medicine container closure device for recording and broadcasting information about the contents of a container includes a housing that defines an interior space. The housing is configured to couple to a bottle to selectively close the bottle. A power module and a recording-playback assembly are coupled to the housing and are positioned in the interior space. The recording-playback assembly is operationally coupled to the power module. The recording-playback assembly is configured to record and broadcast information regarding the contents of the bottle, such as a name, a usage, a purpose, and a date to refill the contents.

A device for deterring drug abuse includes a housing configured to contain a drug accessible through an access port. The device includes a physical deterrent configured to move from an unsecured position, wherein the access port of the housing is normally accessible, to a secure position, wherein the access port of the housing is normally inaccessible. The device further includes a locking mechanism that is coupled with the physical deterrent. The locking mechanism has a locked mode, wherein the physical deterrent does not normally move from the secure position to the unsecured position. The locking mechanism is further coupled with a deterrent container having a deterrent substance. The device is configured such that attempts to access the drug when the physical deterrent is in the secure position, and when the locking mechanism is in the locked mode, activate the release of the deterrent substance to the drug.

A closure stopper for pharmaceutical applications has a sealing flange seating in a sealing manner on an end face of the container's closure mouth. The sealing flange has a lower sealing surface and a boundary plane contacting an area protruding farthest downwardly and extending perpendicularly to the closure stopper's center axis. An engagement portion extending below the sealing flange is formed with a smaller radial extent than the sealing flange. Preferably a handling portion extends above the sealing flange. A circumferential sealing projection also is formed on the engagement portion and protrudes by a radial dimension with respect to an axial portion of the engagement portion initially adjoining the sealing flange from underneath and having a portion-radius. The sealing projection, at least with respect to its base portion, vertically overlaps a set-back region formed on the sealing flange and set back with respect to the contact plane.

In some aspects, a keyed cap for a container is provided. Furthermore, in some aspects, a keyed container device including a container and the keyed cap for the container is also provided. Still further, in some aspects, a keyed containing system including a container, keyed cap for the container, and an electronic device having a keying element that is adapted to mate or otherwise fit with a specific keying element on the keyed cap. If a keyed cap has a keying element that does not correctly correspond to a specific keying element on an electronic device, then the keyed cap will not properly mate with the keying element on the electronic device. For example, the two keying elements that do not match may not fit sufficiently far enough within each other to permit the piercing member on the electronic device to reach a septum on the cap.