Abstract: Methods and systems for managing configurable devices are disclosed. A configurable device may be a type of hardware device that may be configured for various purposes. The operation of the configurable device may depend on its configuration. To manage the configurable devices, a system may configure the configurable devices to provide desired functionalities. Once configured, the configured configurable devices may be deployed to a deployment site where they may provide their respective functionalities. As part of the process of configuring and deploying the configurable devices, the configurable devices may be moved between various locations. To protect and otherwise physically manage the configurable devices, the configurable device may be packaged with compliant packaging. The compliant package may facilitate configuration of the configurable devices.

Abstract: A disclosed system for transporting items to destination locations, for example when receiving inventory at large retail locations, includes a conveyor assembly comprising a plurality of docking locations; an item identifier operable to read identification data; an orchestrator operable to, based at least on the identification data, pair items with transporter solutions; and a sorting controller operable to, based at least on the identification data and the pairings, route items to specific docking locations where transporter solutions are docked. Transporter solutions may include autonomous ground vehicles (AGVs) that bid on delivery tasks and can adjust shelf height in order to facilitate loading and unloading. The AGVs can thus provide an effectively seamless conveyor solution—either rollers on the conveyor surface move items or rollers on the underside of the AGV move the AGV with the items.

Abstract: A system and method for determining an optimal combination drug product for a particular patient includes a processor that receives patient information and determines an optimal combination drug product based on the received information. A system which can provide information regarding predicted events or pathologies based on received patient information and guidance on subsequent steps to ameliorate, treat or intervent. A drug production device includes a plurality of drug containers, each of which are coupled to a drug dispensing channel. A controller controls the dispensing of drug through each channel, and a combination drug product is produced from the dispensed drugs. A combination drug product includes a plurality of discrete units of a first drug, and a plurality of discrete units of a second drug. A transdermal patch includes a plurality of drug compartments, each containing a quantity of drug product, and a controller for controlling the release of drugs from each compartment.

Abstract: A package for a point of sale card that includes a first panel, a second panel coupled to the first panel by an activatable adhesive applied to one of the first panel or the second panel, and a card enclosure region defined between the first panel and the second panel, the card enclosure region configured to receive a point of sale card therein. The activatable adhesive is selectively activated along a perimeter surrounding the card enclosure region to secure the first panel and the second panel together at the perimeter and prevent access to the card enclosure region without irreparable damage to the first panel or the second panel.

Abstract: A method for providing a dried solid product containing an active pharmaceutical ingredient is disclosed and includes providing a primary packaging container, providing a drying cartridge different from the primary packaging container, the drying cartridge made of a material adapted to hold a liquid product to be dried, wherein the liquid product contains an active pharmaceutical ingredient and the drying cartridge is made of a material having a thermal conductivity higher than the thermal conductivity of glass. The method also includes filling the liquid product into the drying cartridge, drying the liquid product in the drying cartridge to form a dried solid product containing the active pharmaceutical ingredient, transferring the dried solid product into the primary packaging container.

Abstract: A method of manufacturing a light scattering film, the method includes providing a light transmissive base having a film shape. A plurality of holes is defined in the light transmissive base, using a perforating device. Each of the plurality of holes has a diameter ranging from about 100 nm to about 5 ?m. A spacing between each of the plurality of holes is about twice to about five times as large as an average diameter of each of the plurality of holes.

Abstract: A package for a frozen food includes a plurality of spherically-shaped portions of hard ice cream. A first sealing member at least partially conforms to the shape of each spherical portion of the plurality of spherically-shaped portions. A second sealing member is adhered to the first sealing member. The first and second sealing members cooperatively form a plurality of storage cavities. Each storage cavity selectively encloses a corresponding spherical portion of the plurality of spherically-shaped portions, wherein each corresponding spherical portion includes a concave depression.

Abstract: Methods and apparatuses can be configured to facilitate sorting of paper from garbage and/or single stream recycling and subsequently process that separated paper to remove the contaminants from the paper so that the paper is in an acceptable condition for recycling. In some embodiments, the apparatus and method may utilize at least one dryer device that is configured to heat the paper without combusting the paper to remove water from the paper. The dryer device can also be configured to mix the paper as it is dried while also removing particulate contaminants off of the paper to clean the thrown away paper sufficiently so that the paper is in a condition that is acceptable for recycling into a paper product (e.g. a cardboard box, paper plate, sheets of paper, etc.).

Abstract: A method of degasification of a carbonated beverage-filled container in an apparatus for blowing and filling containers, the apparatus including a mold enclosing a blown and carbonated beverage-filled container. The container includes a dispensing opening, an injection head that is movable along a longitudinal axis, passing by the dispensing opening of the container, between a sealing position in which the injection head is in a sealing engagement with the dispensing opening and a non-sealing position in which the injection head spaced from the dispensing opening. The method includes the steps of moving the injection head away from the sealing position to a first non-sealing position, moving the injection head from the first non-sealing position back to the sealing position, and after moving the injection head back, moving the injection head away from the sealing position to a second non-sealing position that is different from the first non-sealing position.

Abstract: The present invention relates to improved methods of making compositions and compositions made by these methods having improved stability and/or extended release of an active agent or drug upon administration. These compositions may generally comprise an active agent or drug non-covalently immobilized or bound to an excipient substrate. The active agent or drug may include a wide variety of drugs. Binding of the active agent or drug to the substrate may be achieved by evaporating a solvent containing the active agent dissolved therein or by triggering co-precipitation by addition of a precipitating solvent. Additional steps of vacuum removal of surrounding atmosphere and replacement with inert gas may provide additional stability. Present methods and compositions also facilitate manufacturing of drug products and may make these processes safer in some cases.

Abstract: The present invention relates to a pressure sensitive, hot melt processable adhesive composition comprising a polar plasticizing oil, a polar polyethylene copolymer and polyisobutylene and a layered adhesive construction and a medical device comprising the adhesive composition according to the invention.

Abstract: A layered adhesive construct includes a backing layer and a layer of a pressure sensitive, hot melt processable adhesive composition. The adhesive composition includes a polar plasticizing oil or a combination of polar plasticizing oils in a content above 10% (w/w), and 10-50% (w/w) of a polar polyethylene copolymer. The polyethylene copolymer has a melt flow index below 2 g/10 min (190° C./21.1N), and the polar plasticizing oil is a liquid rosin derivative, animal oils and derivatives, esters, ethers, glycols, poly propylene oxide, or alpha-butoxy-polyoxypropylene.

Abstract: The instant invention relates to low acidic species (AR) compositions comprising a protein, e.g., an antibody, or antigen-binding portion thereof, and methods, e.g., cell culture and/or protein purification methods, for producing such low AR compositions. Methods for using such compositions to treat a disorder, e.g., a disorder in which TNF? is detrimental, are also provided.

Abstract: Methods and systems for continuously bagging pellets formed from a tacky and/or polymer containing formulation include improved drying systems and techniques. The methods and systems may include directing a flow of air to help contain moisture within a dryer, transport pellets out of the dryer, and/or dry pellets as they move away from the dryer. The methods and systems may include conditioning (e.g., drying, coating, classifying) the pellets using a conditioning unit prior to bagging the pellets.

Abstract: A system for preparing food product minimizes bacterial contamination and outgrowth within the packaged food product, includes a powered slicer to sequentially separate slices of food product to create a stack of food product slices. The system also includes a first spray nozzle for depositing a first predetermined amount of the antimicrobial preparation onto the first face of the log or other food product piece each time a slice is removed as well as a a second spray nozzle for depositing a second predetermined amount of the antimicrobial preparation into a vacuum pouch prior to reception of a stack within the pouch. In an embodiment, the spray system is implemented with respect to a mixer/blender to pretreat a mix prior to further processing.

Abstract: Prefilled reservoir apparatuses for use in ambulatory infusion devices include a rigid top and a flexible bag that forms at least a portion of a reservoir containing a liquid medicament composition. The reservoir apparatuses include a septum assembly that includes a fluid flow path in communication with the reservoir and a self-sealing septum disposed in or over the fluid flow path. The septum is positioned and configured to be pierced by a cannula of a base of an infusion device when the reservoir apparatus is received by the base.

Abstract: The main objective of this invention is a Mobile plant for dosing, mixing and packaging of powdery products, characterized because it is comprised of a carrying structure and several areas for: reception and weighing, loading, mixing, sack filling, sewing and labelling, metal detection, palletizing and cleaning. This invention is included within the industrial plants technical sector of manufacturing and mixing of powdery products.

Abstract: A package for golf balls, commonly known as a “sleeve”, includes a body having a plurality of side walls and end walls that define a hollow interior for receiving and containing the golf balls. The end walls close off ends of the body. At least one of the side walls contains a plurality of openings spaced apart from one another along a length of the side wall, Each opening is formed at a location that corresponds to and is in registration with a portion of one golf ball that is in closest proximity to the inner surface of the side wall, so as to allow each golf ball to be marked individually (by stencil or otherwise), from the outside of the body, or sleeve, by the user (golfer) by accessing the surface of the ball through the corresponding opening in the side wall.

Abstract: The invention provides a method of packaging a sterilized product. The method includes the steps of providing a product and sterilizing the product. The sterilized product is enclosed in a first layer, which is substantially hermetically sealed to form a first sealed enclosure. The first sealed enclosure is enclosed in a second layer, which is substantially hermetically sealed to form a second sealed enclosure. The second sealed enclosure is enclosed in a third layer, which is substantially hermetically sealed to form a third sealed enclosure. The third sealed enclosure is enclosed in a fourth layer, which is substantially hermetically sealed to form a packaged product.

Abstract: A method of using and a steel reinforced concrete protector in an anode cavity which comprises a cored hole, a drilled hole or a cut chase formed in concrete. The protector comprises a sacrificial anode assembly and a separate backfill. The sacrificial anode assembly comprises a sacrificial metal element that is a metal less noble than steel and an activator to maintain an activity of the sacrificial metal element. The at least one spacer prevents the sacrificial metal element and the activator from contacting the surface of the anode cavity. The spacer and the sacrificial metal element have a coupling mechanism which facilitates connection of the sacrificial metal element to the spacer. The backfill is a pliable and viscous material which contains an electrolyte, and the backfill facilitates embedding the anode assembly in the anode cavity. The invention also relates to a prepackaged sacrificial anode assembly and a method of increasing a shelf life of the sacrificial anode.

Abstract: In one aspect, an absorbent product includes a package and at least n absorbent articles contained in the package (n is greater than 10). Each of the absorbent articles has a body contacting surface and a garment contacting surface. Each of the absorbent articles includes a component material disposed between the body contacting surface and the garment contacting surface. The component material has a printed graphic which is seen through either the body contacting or garment contacting surfaces. The n graphics of the n absorbent articles are different from each other, and preferably have a predetermined association. In another aspect, a method is directed to printing a graphic on a sheet material which will become a component material for the absorbent articles. In another aspect, a method is directed to producing the absorbent product including the package and the n absorbent articles contained in the package.

Abstract: Provided is a method for manufacturing a container containing a content fluid, including: a molding step of stretching a bottomed tubular preform that is heated to a temperature at which the preform is stretchable so as to form the container by means of pressure of the content fluid injected into the preform through a mouth portion; a sealing step of sealing the content fluid by fitting a cap body to the mouth portion; and a pressurizing step of increasing an inner pressure of the container, wherein the container includes an invertible deforming portion that is freely invertible and deformable toward an inside of the container, and in the pressurizing step, the inner pressure of the container is increased by reducing a volume of the container by inverting and deforming the invertible deforming portion toward the inside of the container.

Abstract: A surgical instrument having opposed jaws that can be selectively moved between open and closed positions. Various embodiments include components for measuring the thickness of tissue clamped between the opposed jaws. Some embodiments are configured to ascertain the amount of compressive force that is being applied to the tissue while the thickness of the tissue is being determined. The tissue thickness data is displayed on the instrument itself and/or on a display that is remote from the instrument. The various embodiments may comprise different types of surgical instruments such as surgical staplers and graspers. A jaw arrangement with jaws shaped to define a cradle that corresponds to a cross-sectional shape of an object is also disclosed. The components that generate the thickness data may be electrically or mechanically actuated.

Abstract: A protective cover for a nasal cannula completely encloses the two prongs of the nasal cannula when properly installed. This protective cover will keep the nasal cannula from contacting potentially unclean surfaces when the nasal cannula is not in use. An optional UV light may be present in the protective cover to provide UV cleaning of the nasal cannula prongs when the cover is closed.

Abstract: A method is disclosed for making a pharmaceutical composition for pulmonary administration, the method comprising a step in which an inhalable pharmaceutically active material is acoustically blended in a resonant acoustic blender. The invention also relates to compositions for inhalation prepared by the method.

Abstract: An ultrasonic surgical blade comprising a body having a proximal end and a distal end. The distal end of the body is movable relative to a longitudinal axis by vibrations produced by a transducer. The body comprises a longitudinally extending bore formed within the ultrasonic surgical blade. The ultrasonic surgical blade is configured to emit a spray from the bore at the distal end thereof to substantially prevent fluid from contacting the distal end of the ultrasonic surgical blade.

Abstract: A sterile individual set for use in a process of manufacturing a biopharmaceutical product. To make it quicker and easier to grasp and use fluidic type functional members, the sterile individual set includes a sterile flexible bag having a peripheral wall defining a sterile internal space and a fluidic type functional member arranged at least partially inside the sterile internal space. The functional member includes one or more communication duct(s) arranged in the sterile internal space. The sterile individual set also includes structural association elements capable of holding together several portions of the communication duct or ducts that are to be bundled together into a bundle. The structural association elements have an external surface with lower static and dynamic friction coefficients so as to make the functional member easier to handle by slippage of the bundle of communication ducts with respect to the peripheral wall of the flexible bag.

Abstract: Disclosed herein are processes for continuously bagging pellets. The pellets can be formed from a tacky and/or polymer-containing formulation. Other embodiments relate to systems for continuously bagging pellets. Still other embodiments related the individual components of the processes and systems for continuously bagging pellets.

Abstract: A process for purifying fibrinogen from a fibrinogen containing source by precipitation of fibrinogen by a precipitating agent from a fibrinogen containing solution in the presence of one or more chelating agent(s) and removal of the supernatant from the fibrinogen paste, characterised in that fibrinogen is extracted from the paste forming a liquid fraction containing fibrinogen, and an undissolved residue, which is separated from the liquid.

Abstract: A mixing pouch forms a packaging product that includes a first compartment containing a supply of a liquid ingredient and a second compartment that contains a supply of a powdered ingredient with a breakable seal between the two compartments to separate the two ingredients. Rupturing the breakable seal creates a common interior cavity and allows the mixing of the two ingredients to create a mixed product. One end of the mixing pouch is formed with a dispenser through which the mixed product is dispensed for use. An apparatus, such as a positionable clamp or an adhesive strip on the exterior of the mixing pouch, can reduce the size of the common interior cavity to facilitate the dispensing of the mixed product. Preferably, the mixing pouch is a flexible plastic member having a dispensing end formed with a channel closed by a tear-away portion.

Abstract: A nightwear vending machine to be placed in and around the grounds of all hospitals, clinics and health care centres in the UK. The vending machine will sell women's, men's and children's pyjamas, night dresses, night gowns and slippers to all members of the public and be available 24 hours a day.

Abstract: A protective certificate cover system and method of manufacture thereof is provided having a certificate or diploma, a protective cover having two panels, a cover aperture formed in one panel configured to be aligned with a printed name area on the certificate when the certificate is closed within the cover. An envelope has a viewing window so the printed name area is visible when the closed cover containing the certificate is inserted into the envelope. A transparent sleeve is provided permitting the envelope containing the cover to be shrink wrapped and sealed.

Abstract: A pharmaceutical container comprising a pair of containers interconnected with a coupling is described. The containers are intended to contain two components of a pharmaceutical such that when mixed a finished, ready to use, pharmaceutical mixture results. The coupling includes cutting devices that can cut through a frangible membrane when the containers, joined by the coupling are twisted with respect to one another.

Abstract: An improved method for the manufacture of an oil-in-water emulsion comprises using a microfluidisation device whose interaction chamber comprises a plurality of Z-type channels upstream of a back pressure chamber.

Abstract: The present invention presents methods for making oxidation-resistant and wear-resistant polyethylenes and medical implants made therefrom. Preferably, the implants are components of prosthetic joints, e.g., a bearing component of an artificial hip or knee joint. The resulting oxidation-resistant and wear-resistant polyethylenes and implants are also disclosed.

Abstract: A mask storage device and a method of preventing defect formation on a mask are provided. The method includes providing a mask storage device comprising a first and second shell configured to form a sealed space in a closed state and a desiccant positioned within the mask storage device. The method further includes placing a mask inside the mask storage device and sealing the mask storage device with the mask and desiccant inside the sealed space.

Abstract: Provided is a novel oxygen-absorbing resin composition having excellent oxygen-absorbing performance and suppressing odor generation after absorption of oxygen even if a material responsive to a metal detector is not used. Further provided is an oxygen-absorbing resin composition having excellent oxygen-absorbing performance in a wide range of humidity conditions from low humidity to high humidity. Such an oxygen-absorbing resin composition contains a copolymerized polyolefin compound and a transition metal catalyst, in which the copolymerized polyolefin compound contains at least one constituent unit having a tetralin ring.

Abstract: This invention relates to the filling or dispensing of radiopharmaceuticals in sample vials. Radiopharmaceuticals must be dispensed in a cleanroom environment according to cGMP regulations. Single-use filling cassette-type dispensing systems can be used for filling or dispensing of radiopharmaceuticals in sample vials. A single-use filling cassette is the core of such a dispenser system. A flexible bag container comprising a flexible bag and a filling cassette was found. The filling cassette is assembled within the flexible bag under aseptic conditions. The assembled filling cassette defined a closed system since each opening is connected to a sample vials or sterile filter avoiding contamination from outside.

Abstract: Oxygen is a major quality-deteriorating factor with respect to many food products in that it may cause the growth of molds and the development of rancid off-flavors, which reduce the quality or shelf life of many food products. The present invention provides an improved food packaging and a method for prolonging the shelf life and quality of packaged foods by packaging the food in a packaging material together with a microbial oxygen absorber, such as Lactococcus spp., Streptococcus spp., Lactobacillus spp., Leuconostoc spp., Brevibacterium spp., Propionibacterium spp., and Bifidobacterium spp.

Abstract: An implant storage and insertion system for a shape memory orthopedic implant allows the implant to be constrained in a deformed state, protected, insulated, held for insertion, and properly positioned in bone. The implant storage and insertion system includes a restraining block having an impact surface. The restraining block engages an implant at a first end, and further a medical instrument engages the restraining block and positions the restraining block at a bone such that the impact surface may be impacted to insert a second end of the implant into the bone.

Abstract: An oats processing equipment comprises at least two groups of awners and at least two groups of oat grinders, with awners within the same group being connected in parallel or in series, and oat grinders within the same group being connected in parallel or in series, preferably 3 to 4 groups of awners and oat grinders are included. An oat processing method comprises steps of: (S00) classifying oats subjected to surface processing according to grain sizes; (S10) feeding oats of a certain class into a plurality of groups of awners for more than two stages of awn removing; and (S20) feeding the oats subjected to the awn removing into a plurality of groups of oat grinders for more than three stages of grinding. The inputted load of a single awner and an oat grinder is limited, thus achieving the technical effect of grinding oats gently and separating the oats finely.

Abstract: Embodiments relate to a reinforced nestable container and a method of forming a reinforced nestable container able to withstand a high pressure processing. The container has an open end, a closed end, and a sidewall extending between the open end and the closed end and defines an interior. The closed end has a cone bottom including a first step that steps towards the closed end and forms a flexible point such that the base can flex and return to its original position and shape; a generally flat portion that extends towards the center of the closed end; a second step that steps towards the open end and in to an inner-profile having a first radius in one direction and a second radius in an opposite direction, forming an s-curve; at least one strengthening fillet; and a base plateau, whereby at least the s-curve formed by the first step, the flat portion and the second step spread tension such that the container can withstand pressure therein.

Abstract: A trocar seal comprising an elastomeric membrane having an opening adapted to receive a surgical instrument. The membrane is configured with a plurality of pleats circumscribing the opening and extending laterally from opening. The pleats comprise a plurality of pleat walls increasing in height as the pleats extend laterally from the opening. In one embodiment, the pleats are conically arranged.

Abstract: A device and a method for manufacturing an item of packaging for a group (27) of smokable articles (11), in particular cigarettes, having a wrapping, preferably an inner wrapping, of, in particular, a thin packaging material, such as paper, tinfoil or the like, in which a material web (31) of the packaging material is severed into individual blanks (10) and in which the article groups (27) to be wrapped are in each case wrapped with the individual blanks (10). Flavoring and/or aromatic portions (42) for the smokable articles are applied to the packaging-material web (31), which flavoring and/or aromatic portions (42), after application, are at least in regions reduced in their height by a processing means, preferably in that they are spread flat and/or pressed flat by the processing means (47).

Abstract: An oxygen scavenging composition capable of providing good oxygen absorption capabilities wherein the oxygen scavenging agent is a sulfite salt with a Group I cation, combined with an acidifying agent and optionally a hygroscopic salt. The compositions can be formed into films, coatings, 3-dimensional solids, fibers, webs, and shaped products or structures which are incorporated into, applied to, or otherwise become a part of a container structure, including container closures, seals, gaskets, liners, and the like.

Abstract: A beverage dispensing kiosk that contains empty beverage containers and fills them with water and other beverages. The beverage containers comply with applicable regulations and standards to be designated “compostable.” The kiosk uses municipal water as the base, purifies the water, and adds constituents to meet the taste of the ultimate consumer. The delivered beverage may be commonly known as bottled water or as a soft drink, such as a cola beverage.

Abstract: A storage method of storing a package with its contents under irradiation of light. At least part of the package is made of polyamide (A) which is obtained by polycondensation of a diamine component comprising 70 mol % or more of m-xylylenediamine and a dicarboxylic acid component comprising 70 mol % or more of ?,?-linear aliphatic dicarboxylic acid having 4 to 20 carbon atoms. The oxygen transmission of the package including polyamide (A) is reduced by irradiation of light, to prevent the spoilage of the contents.

Abstract: The present disclosure is directed to embodiments of automated crimping systems, methods of crimping prosthetic valves, and methods of using automated crimping systems to crimp prosthetic valves. In some embodiments, an automated crimping system includes a crimper controller, a rotary actuator, an outer crimper housing, and a crimper mechanism mounted within the outer crimper housing. In some embodiments, an automated method of crimping a prosthetic valve includes inserting a prosthetic valve into an automated crimping system, activating the automated crimping system, and removing the crimped prosthetic valve from the automated crimping system. In some embodiments, a method of crimping a prosthetic valve comprises partially crimping the prosthetic valve at a first speed to a partially crimped configuration and further crimping the prosthetic valve at a second speed.

Abstract: The present invention relates to a contact lens including at least one clay and at last one silicone component, wherein the at least one clay is applied to the surface of the contact lens and the contact lens does not include any diffusible material whose release from the contact lens is inhibited by the at least one clay.

Abstract: A method for detecting and removing foreign particles in polymeric resin powder comprising drying the resin powder; removing static energy from the resin powder; producing a layer of resin powder 0.2 to 0.8 mm in height in a feeding tray which feeds a conveyor; conveying the layer of resin powder with a transparent conveyor belt at a speed of between 12.2 and 36.64 meters/minute into a foreign particle detection zone; illuminating the polymeric resin powder in the detection zone from above and below with a light; continuously imaging the resin powder from above with a high speed digital CCD camera; continuously analyzing the images with a control device to detect particles having nonwhite colors; and actuating a suction system with the controller to suction off any detected particles to produce a polymeric resin powder having a reduced number of foreign particles.