A system for cryptographic wireless detection and authentication of fluids includes a computing device configured to receive, from a transmitter attached to a container, a unique identifier associated with a fluid contained in the container, locate, at an immutable sequential listing, at least an identifier-specific record using the unique identifier, and a lot identifier associated with the unique identifier, retrieve, from the immutable sequential listing, at least a lot-specific record using the lot identifier, capture, from the container, at least a secondary datum describing the container, generate an authenticity probability score as a function of the at least an identifier-specific record, the at least a lot-specific record, and the at least a secondary datum, and display to a user an output based on the authenticity probability score.

An illuminated bottle stopper mainly includes a lighting, plug body and light transmission tube, where the lighting is a light transmission decoration of a preset shape with an optoelectronic unit configured on the bottom thereof, the plug body is tapered and assembled on the bottom of the base, a passage is longitudinally configured inside the plug body, one end of the light transmission tube is in connection with the passage of the plug body bottom, and a light source is configured to illuminate the light transmission tube, thereby allowing light to be scattered inside and outside a bottle when the plug body is inserted in the mouth of the bottle.

A stopper for a container has a jacket portion insertable into the container, wherein the jacket portion has a through-opening formed in an axial direction, wherein the stopper has at least two segments, wherein the respective segment has a free end, wherein a first portion of the free end of the respective segment forms a subregion of the jacket portion, and a second portion of the free end of the respective segment protrudes radially inward in relation to the jacket portion, wherein a third portion of the free end of the respective segment protrudes radially outward in relation to the jacket portion, wherein the second portions form a cover portion that can be pierced through in the axial direction and that closes the through-opening, wherein the third portions form a bearing portion of the stopper for bearing against a container edge of the container.

A system for capping a mouth of a container may include: a press-on cap for irreversibly capping the mouth of the container, wherein the press-on cap is made of polymeric material able to withstand high-temperature sterilization and wherein the press-on cap may include: a tubular sleeve extending along an axis of extension and configured to be irreversibly locked to the mouth of the container; a rim that radially projects out of the tubular sleeve at an end of the press-on cap; a capping wall oriented transverse to the tubular sleeve and extending from the rim over a front surface delimited by the rim, wherein the front surface faces outwardly; and a plurality of protrusions, which extend out of the front surface. The front surface may have a height variation relative to the rim across the front surface ranging from −1% to 1% of a characteristic dimension of the capping wall.

Devices and systems for product transfer, such as a dissolvable microcarriers, are described. In one example, the product delivery device may include an inlet port; a conical section that may include a wide end and a narrow end; an outlet port flush with the narrow end of the conical section and extending away from the conical section; and a securement feature configured to connect the wide end of the conical section to a container. In another example, a system for aseptic dry product delivery may include a container at least partially filled with the aseptic dry product; a product delivery device; a pressure source connected to an inlet port; and a receiving vessel where the aseptic dry product is collected.

Devices and systems for product transfer, such as a dissolvable microcarriers, are described. In one example, the product delivery device may include an inlet port; a conical section that may include a wide end and a narrow end; an outlet port flush with the narrow end of the conical section and extending away from the conical section; and a securement feature configured to connect the wide end of the conical section to a container. In another example, a system for aseptic dry product delivery may include a container at least partially filled with the aseptic dry product; a product delivery device; a pressure source connected to an inlet port; and a receiving vessel where the aseptic dry product is collected.

A locking top for blocking a stopper in the neck of a vessel comprises an outer body and a cage that is configured to fit into and lock axially in the outer body. The cage comprises an upper ring, a plurality n of branches connected to the upper ring, n/2 median bridges and n/2 lower bridges arranged in alternation on the periphery of the cage, each connecting together two adjacent branches. When the top is in an intermediate holding position in which the stopper is partially pushed into the neck, the lower bridges surround, at least in part, a collar of the neck; the median bridges located, in an axial direction, between the upper ring and the lower bridges are designed to form an open space between them and the collar.

An improved packaging assembly for storing, distributing, treating, mixing, and dispensing tissue and/or cellular material and/or implantable material. The packaging assembly may include pouches, tubes, and a bag made of a sealable, flexible polymeric material that is open at one end and a needle-free swabable connector attached to the pouch at the other end and acting as a port to allow for the introduction or discharge of biological solutions, rinsing solution, and/or preservation solutions into the packaging assembly. The designed thickness of the wall of the packaging assembly facilitates efficient heat/cold transfer, which is useful for successful controlled rate freezing, quick thawing, and resuscitation of viable cells or tissue. The packaging assembly is also useful for combining additional biological fluids with the cellular material or tissue, and for efficient mixing of the biological fluids with the tissue and/or cellular material in the assembly.

A method for preserving wine or other oxygen sensitive items is disclosed. In some embodiments, the method involves injecting 0.15 gram to 0.5 gram of an inert gas into a container comprising wine and oxygen, without raising a pressure within the container above 10 psig, to form a barrier layer of the inert gas between the wine and the oxygen in the container without displacing all of the oxygen from the container.

A method for preserving wine or other oxygen sensitive items is disclosed. In some embodiments, the method involves injecting 0.15 gram to 0.5 gram of an inert gas into a container comprising wine and oxygen, without raising a pressure within the container above 10 psig, to form a barrier layer of the inert gas between the wine and the oxygen in the container without displacing all of the oxygen from the container.