Abstract: A storage system for storing used surgical towels, sponges or other medical waste materials includes a rear panel having an upper portion and a lower portion formed from a flexible sheet material. The upper portion of the rear panel has a coupling mechanism for coupling the device to a sterile structure of a surgical room. In certain embodiments, the rear panel may have a weakened partition area for separating the lower portion from the upper portion. A compartment assembly is formed by two or more flexible compartments provided on the lower portion of the rear panel. Each compartment may be liquid impervious and have an upper opening for introducing materials into the compartment. Each compartment has a forward wall that is at least partially transparent so that the contents of the compartment are observable. All components of the storage device may be sterile for use in a sterile environment. In certain embodiments, a storage system may be provided by coupling at least two storage devices together.

Abstract: A package for containing a medical device can have a bottom portion and inner and outer lids releasably sealed to the bottom portion. The bottom portion defines a cavity for receiving a medical device. A flange extends outward sidewalls of the bottom portion and includes an inner flange portion and an outer flange portion. The inner flange portion can be recessed below the outer flange portion. The sealed inner lid permits passage of sterilization. The outer lid provides a moisture-resistant barrier to the package. A corner portion of the outer lid can extend past a corner of the bottom portion. Upon application of a withdrawing force sufficient to break the seals, the inner lid and the outer lid are together capable of being peeled from the bottom portion.

Abstract: A package for household articles is provided with a holistic coding system. The coding system allows consumers to select the articles required for their needs without confusion. The package comprises a plurality of sides forming an interior compartment; a non-opaque colored window and a colored region on at least one side of the package; and a plurality of household articles disposed in the interior compartment. The household articles comprise individual wrappers which have a color; the individual wrappers have the same color as the colored region. The household articles may be hygiene articles.

Abstract: This invention relates generally to improving compliance. More specifically, the invention relates to single-use containers containing liquid formulations for ingestion, strips and packages of such containers, and to compliance improving systems using such containers.

Abstract: The present invention provides a container for storing a blister package and for managing medication with a pharmaceutical composition comprised in the blister package. The container comprises a housing which forms a compartment for the blister package, means for indicating towards a user an appropriate time of accessing the blister package, and means for detecting a users access to a blister package in the compartment. The blister package is moved into and out of the compartment by means of an ejection structure to which the blister package may be fixed. The ejection structure facilitates an enhanced handling of the blister package during insertion and removal of the blister package and facilitates a more accurate indication of a user's access to the blister package.

Abstract: A method for preparing a backup kit for a plurality of patient-specific arthroplasty procedures scheduled at the same medical facility includes providing a database with data from completed arthroplasty procedures using patient-specific arthroplasty kits. The database includes comparisons between preoperatively planned implant size and intraoperatively implanted implant size. The method includes determining a statistically expected implant size deviation from a planned implant size for each implant included in a plurality of patient-specific arthroplasty kits prepared for a shipment to the medical facility using the database. A backup kit of backup implants is assembled for the shipment. The number and size of the backup implants is determined from the statistically expected implant size deviations.

Abstract: A package (1) for an object such as a preferably-sterile medical component, includes: a support element (2) provided with elements (21) for coupling the object (5); a stopper (3) that can be coupled to the support element (2) in such a manner as to define a first chamber (7) for containing the object (5), and such that a grip portion (20) of the support element (2) projects from the stopper (3); and a cover (4) that can be coupled to the stopper (3) in such a manner as to define a second chamber (8) inside which the grip portion (20) of the support element (2) extends, and such that a portion (30) of the stopper (3) coupled to the support element (2) projects from the cover (4).

Abstract: A collapsible single-use sterilization container for use in the sterilization of medical instruments is provided. The sterilization container includes a lid having central portion defined by a frangible region. Upon activation of the frangible region, the central portion may be removed rendering the sterilization container inoperable for future use.

Abstract: The present invention relates to generating a film suitable for medical packaging. The film is generated by blown film co-extrusion to form a multi-layer film which has a heat resistant layer, a barrier layer and a heat seal layer. The barrier layer includes a high barrier resin and a branched co-polymer. The high barrier resin has a density of at least 0.963 g/cm3. The barrier layer includes between 25% and 85% high barrier resin. The heat resistant layer may be comprised of polymers, papers and other materials. The heat seal layer, in some embodiments, comprises any of high density polyethylene and medium density polyethylene, or a combination thereof. In some embodiments, an additional laminate layer may be affixed to the heat resistant layer of the multi-layer film. The final film is between 3.0 and 3.8 mils in thickness, and has a moisture vapor transmission rate of less than 0.08.

Abstract: An identi-meds system comprising: a medication bottle assembly and a supplementary removeably-coupleable tag for accurately identifying contents contained in bottle(s). The medication bottle assembly includes a cap having an outer surface and an inner surface, a bottle having a body, and a prescription label. The supplementary removeably-coupleable tag includes an adhesive backing comprising an adhesive; and a peel-away sheet. The cap, the bottle, and the prescription label comprise the medication bottle assembly to contain and identify at least one medication in Layman's terms. The inner surface of the cap is removably-coupleable to the body of the bottle to contain and access the medication.

Abstract: An elution tool for a radiopharmaceutical elution system includes an elution tool. The tool has a vial chamber sized and shaped for receiving an elution vial. An access opening is aligned with a septum of the elution vial when the elution vial is received in the vial chamber. An elution tool lid is secured to the elution tool body by a hinged connection. The elution tool lid is rotatable at the hinged connection and movable relative to the elution tool body between an occluded position and an exposed position. The tool also includes a latching mechanism for selectively and releasably locking the lid in the occluded position.

Abstract: The medical safety box is a system using RFID (Radio Frequency Identification) technology to ensure that correct delivery of the correct treatment in the form of medication or injection to in-hospital patients is consistently carried out. The system includes a medical box containing whatever medication or injection that needs to be administered to a specific patient. The box has a locking mechanism that can only be opened by an RFID wristband, which is worn by that same specific patient, thus assuring that the medicine in the box is administered to the correct patient.

Abstract: A test appliance (1) with an auditory ossicle prosthesis (2), which is made at least partially of a shape-memory material and which has a first securing element (2a), for mechanical connection to the ear drum or to a member of the auditory ossicle chain, and a second securing element (2b), for connection to another member of the auditory ossicle chain or for connection directly to the inner ear, and a connection element (2c) connecting the two securing elements, wherein the prosthesis is subjected to a shape-modifying thermal treatment upon implantation in the middle ear, is characterized in that it comprises a device for determining an optimized power setting and/or energy application site for the processing of the prosthesis parts that are to be treated thermally during the operation and contains a prosthesis dummy (3) which mimics the prosthesis and which, in those areas where the associated prosthesis is intended to be treated thermally during the operation, is constructed identically to the prosthesis in

Abstract: An apparatus for aseptic insertion includes a container, a first cover, and a second cover. The container includes a first compartment, a second compartment, and a detachable wall disposed between the first compartment and the second compartment. The first cover is sized and configured to attach to the first compartment and the second cover is sized and configured to attach to the container. The detachable wall may defined by a top portion, a portion of a first distal wall of the first compartment, and a portion of a second proximal wall of the second compartment. The detachable wall may be removably attached to the first cover by the top portion of the detachable wall.

Abstract: A storage and support device for storing and supporting components of a Functional Electrical Stimulator Foot Drop Device is disclosed and includes an upstanding hollow tubular member extending upwardly from a base portion. The interior of the tubular member may be used to store certain of the components of the foot drop device, other than the leg cuff portion thereof, during periods of non-use. The leg cuff portion of the foot drop device is wrapped around the tubular member with the tubular member having an exterior curved surface which corresponds to the shape to the disc-shaped electrodes at the inner surface of the leg cuff so that a plastic sheet covering the electrodes will be maintained in intimate contact with the electrodes to extend the life thereof.

Abstract: A carrying case (500) and handle (504) for accommodating a portable topical negative pressure therapy apparatus (200) comprising a device (202) and a waste canister (204) separable therefrom, the waste canister having an aspiration conduit (274) emerging therefrom is described, the carrying bag comprising an apparatus receiving pouch (502), said pouch having opening and closing means (522, 524) at a lower portion thereof and said handle (504) being directly attached to said apparatus.

Abstract: The invention relates to a pharmaceutical composition comprising a pharmaceutically acceptable salt of N-ethyl-N-phenyl-1,2,-dihydro-4-hydroxy-5-chloro-1-methyl-2-oxoquinoline-3-carboxamide, N-methylglucamine, and a pharmaceutically acceptable carrier.

Abstract: A device (1) for the containment of platelet concentrates includes at least a bag (2) defining at least a containment chamber (3) having at least a mouth (4) for the entry of a platelet concentrate and at least a connection element for connection to an infusion line associated with the bag in correspondence to the mouth; the connection element includes a first and a second portion (5a, 5b) integrally associated together and includes at least a constantly open duct (6), passing through the first and the second portion and communicating with the chamber, where the first portion is associable with the infusion line and the second portion is associated with the bag in correspondence to the mouth, the first portion being separable from the second portion in such a way to interrupt the duct and define an opening (8) accessible from outside and including closing element (9) of the opening.

Abstract: The present invention provides an improved package from the administration of active ingredients. The present invention provides a package comprising: a standard portion comprising one or more active ingredients in a plurality of different potencies, and a rescue portion comprising one or more same or different active ingredients. The package may be optionally be used with a patient assessment module. The present invention also provides a kit comprising: a package comprising a standard portion comprising one or more active ingredients in a plurality of different potencies, and a patient assessment module comprising instructions for administration of the standard portion. The package may optionally further comprise a rescue portion.

Abstract: An improved holder and storage system for a tissue-type prosthetic mitral heart valve that constricts the commissure posts of the valve and prevents suture looping. A rod axially movable relative to the holder tensions lengths of attachment sutures that extend between the commissure post tips to create a tent and flex the tips inward, thus helping to prevent looping of any of an array of pre-implanted sutures around the leading tips during delivery of the valve. The holder has a safety mechanism that prevents valve delivery before the rod is deployed. One embodiment automatically deploys the rod upon opening a storage jar. One embodiment permits a delivery handle to directly deploy the rod, while another uses a separate worm screw and coupling. A holder clip that attaches to a packaging sleeve may be formed of flexible members meshed together from which the heart valve and holder are easily pulled free to eliminate a step of decoupling the clip from the sleeve.

Abstract: The invention provides medical devices comprising high-strength alloys which degrade over time in the body of a human or animal, at controlled degradation rates, without generating emboli. In one embodiment the alloy is formed into a bone fixation device such as an anchor, screw, plate, support or rod. In another embodiment the alloy is formed into a tissue fastening device such as staple. In yet another embodiment, the alloy is formed into a dental implant or a stent.

Abstract: A method of producing a particle cassette for a needleless syringe device which alleviates problems of providing a chamber for the confinement of particles which is hermetically sealed from the environment. A predetermined force is applied in the longitudinal direction to push first and second cassette parts together so as to cause plastic deformation of a portion of the first cassette part so as to create said hermetically sealed chamber. The cassette parts are preferably made of PETG and have bonded thereto rupturable membranes preferably made of PET. The sealing is preferably achieved at the end of a protrusion on the first cassette part which is tapered and which interacts with the membrane of the second cassette part.

Abstract: The present is an alternative nutrition and/or intravenous bag concealing sack fabricated from a series of fabric, plastic and/or paper components and an elastic band, positioned in the bottom seam of the sack, providing a means which permit the sack free movement horizontally in and out covering adjacent surfaces.

Abstract: A urinary catheter kit is provided. The catheter kit includes a catheter with a flared end and a package provided with interior protrusions for cooperating with the flared end of the catheter. The largest outer diameter of the flared end of the catheter is slightly larger than the smallest diameter of the package at the protrusions. Thereby, the protrusions will function as a backstop for the catheter. The rigidity of the catheter at the flared end is selected so that—depending on the angle of the flared end—the flared end will be able to flip over if it is subjected to a force over a predetermined level. Thereby the catheter will be able to be entered back into the package.

Abstract: An individually packaged absorbent article including an absorbent article and a package. The package can enclose the absorbent article and can have an outer surface and an inner surface. In certain embodiments, the package can include a package material that is a polymeric film. The package can have two opposing faces, and an opening area. The opening area can be provided substantially on a face of the package, and the package having an overlabel substantially covering the opening area.

Abstract: A housing for accommodating a dental implant is disclosed. The housing comprises a first body portion and a second body portion. The first body has an open end and a pivot end opposite to the open end. The open end is adapted to receive the dental implant. The housing further comprises a pivot element which connects with the first body portion and the second body portion at the pivot ends thereof. The first body portion and the second body portion define an inner space and the second body portion is capable of rotating with respect to the first body portion along the pivot to expose the open end.

Abstract: A sealed foil pouch has a textured opening flange and includes first and second foil sheets having opposing inner surfaces joined together by a seal for defining a sealed area of the pouch located inside the seal and an unsealed area of the pouch located outside the seal. The sealed pouch includes a textured opening flange located adjacent an edge of the pouch for peeling the first and second foil sheets away from one another for breaking the seal and opening the sealed pouch. The textured opening flange is located within the unsealed area of the pouch and includes at least one roughened surface formed on at least one of the first and second sheets. A leg of the seal passes through the textured opening flange. The roughened surface makes it easier to break the leg of the seal for pulling the sheets apart.

Abstract: The present disclosure provides a package for a medical device containing a cavity for receiving the medical device, a first closure having a sealed portal therein and a second closure adjacent the first closure.

Abstract: An individual package of tampon that has a bag body capable of easily accommodating an applicator after use. The individual package of tampon comprises a vertically long, flat bag body (2) consisting of a sheet member and, individually enclosed therein, a tampon with applicator.

Abstract: Endosseous implant to be applied to a human or animal bone, wherein the surface of the implant is made from titanium or a titanium alloy, said implant having a smooth or rough surface texture, which is characterized in that said surface has been treated with at least one selected organic phosphonate compound or a pharmaceutically acceptable salt or ester or an amide thereof; process for producing said implants.

Abstract: An assembly comprising: a protective sheath and a loading device for loading a self-expandable prosthesis into said sheath, the loading device having a conical distal section, which radially compresses the prosthesis and an annular lip that engages with the interior of the distal end of said sheath to guide the prosthesis into the sheath whilst protecting the sheath from damage.

Abstract: A package for household articles provided with a holistic coding system. The coding system allows consumers to select the articles required for their needs without confusion. The coding system includes first coding elements on the dispensing means of package and second coding elements on the articles contained in the package.

Abstract: The present invention relates generally to methods for preparing a dual tendon bundle that is useful as a replacement ligament or tendon graft for, for example, anterior cruciate ligament (ACL) reconstruction. More particularly, the dual tendon bundle prepared according to the present invention has a functional cross section diameter and/or a minimum length that meets or exceeds the standard requirements for replacement ligament or tendon grafts. The present invention further relates to the dual tendon bundle prepared by the disclosed methods and packages comprising the same. Methods of using the dual tendon bundle prepared according to the present invention by providing the dual tendon bundle thus obtained for implanting into a patient in need thereof are also provided.

Abstract: A container for enabling fluid flow therethrough for cleaning or sterilizing of the contents, comprises a tray (10) and lid (20) and having respective bases (11, 21) and side walls (17, 27). The bases (11, 21) have perforations (12, 22) defined by elliptically shaped perforation walls (13, 23) with their major axes vertical to allow easy flow of the cleaning fluid through the container and minimum contact points with the contents or other containers. The internal corners (30) of the perforations (12, 22) in horizontal sections are smoothly curved to minimize debris or deposits collecting and resisting removal. A method of cleaning or sterilizing using the container is also described.

Abstract: Absorbent product including a package, at least one absorbent article and a miniature model.

Abstract: This invention relates to compositions and methods for treating GC-responsive conditions and for reducing and preventing side-effects of GC treatment in patients.

Abstract: A stent scaffolding including a polymer formulation comprising PLLA and polymandelide is disclosed. The polymandelide reduces the molecular weight drop during processing, particularly during sterilization. The stent scaffolding can further include one or more additional stabilizing agents that additionally reduce the molecular weight drop during processing.

Abstract: Package housing for an elongate object (8), including a base element (2) having a housing wall (6) defining a receptacle (4) for the object (8), wherein the receptacle (4) has a longitudinal axis (L) which runs substantially coaxially to the longitudinal axis of the object (8) in the packed state. The base element (2) comprises a head part (10) and a holding part (12) arranged in the direction of the longitudinal axis (L) next to the head part (10), which holding part is connected to the head part (10) by a weakening zone (30) and including at least one holding portion (34), which is intended to hold the object (8) in the holding part (12). According to the invention, the weakening zone (30) is a predetermined breaking point (32).

Abstract: Embodiments disclosed herein relate to thermostable storage of one or more therapeutic agents, including at least one detectable indicator. In an embodiment, the one or more therapeutic agents including at least one detectable indicator are included in at least one glassy substance. Also disclosed are embodiments relating to delivery devices for administration of the thermostable therapeutic agents.

Abstract: Tamper-evident package comprises a container, a primary cap, and a secondary cap. The container comprises a sidewall defining a chamber and a rim defining a mouth to the chamber. The primary cap is removably-attachable to the rim of the container to selectively close the mouth of the container. The secondary cap is positioned over the primary cap to prevent removal of the primary cap when positioned thereover. The secondary cap includes a single-use lock, such as a cable tie, to secure the secondary cap in position over the primary cap. The package thus provides evidence that someone has tampered with or attempted to tamper with the container if the single-use lock is removed or damaged. Method of using the tamper-evident package is also disclosed.

Abstract: A package for a flat medical implant includes a flexible outer component, such as Tyvek®, including a first panel and a second panel foldable over said first panel for closing the package, and an inner component, such as paper, mechanically interlocked with the flexible outer component. A flat medical implant is held by the inner component. While the outer and inner components remains mechanically interconnected to one another, the upper ends of the first and second panels of the outer component are peelable away from one another for opening the package and accessing the flat medical implant at an upper end of the package.

Abstract: A case for modular neck components for hip implants. The case may include indicators based on independent variables associated with physical characteristics of the implant, including leg length, offset, and anteversion. During surgery, the surgeon may be confronted with a need to change a preoperatively-chosen modular neck. For example, the surgeon may desire a change in at least one of the variables, e.g., leg length, offset, and/or anteversion. The case allows the surgeon to quickly and easily select a different modular neck based on an evaluation of one of the variables without requiring reevaluation of the other variables. A method described herein may include preoperative planning in which a template including a grid coordinate system is used, which advantageously provides an intuitive system for the surgeon both preoperatively and during surgery.

Abstract: There is provided an elongated sheet (10) for a medicine packaging bag, which prevents tear of cuts (b, 16) caused by a tension during travel of the sheet, etc. and which allows a medicine packaging bag (A) to easily tear and thus open. The sheet (10) is folded centrally in a width direction and a medicine (a) is introduced between its two-folded halves (11, 11). The sheet (10) is thermal-bonded (12, 13) along an entire width ahead of and behind the medicine (a) and along an entire length of open edge portions of the two-folded halves (11, 11), thus forming the medicine packaging bag. A thermal-bonded portion (13) in the open edge portions is formed inwardly. A large number of fine tearing cuts (16) (4 mm width) are formed inwardly from an end edge (17) of the open edge portions by 1 mm between the thermal-bonded portion (13) and the open edge portions along an entire length in a longitudinal direction of the sheet (10).

Abstract: A package for accommodating, storing, displaying and transporting a medical product. The package has a body formed by a plurality of panels, and at least one of the panels has a first layer and a second layer. A tab is formed integrally with the first layer. The tab is pivotable via at least one hinge formed in the first layer from a first position substantially coplanar with the first layer to a second position where the tab is disposed at an angle to the first layer.

Abstract: A case for an emergency escape breathing apparatus including a substantially rigid hollow shell defining a cylinder housing portion for retaining a cylinder of breathable gas and a delivery device housing portion for removably housing a delivery device for the breathable gas supplied by the cylinder. An access opening is provided which provides access to the interior of the delivery device housing portion through which a delivery device, such as a hood or mask, can be inserted and removed.

Abstract: Embodiments relate to Rifaximin polymorphic, salt, and hydrate forms, methods of producing polymorphic forms and to their use in medicinal preparations and to therapeutic methods using them.

Abstract: The invention is directed toward an osteoimplant for application to a bone defect site to promote new bone growth at the site which comprises a new bone growth inducing composition of demineralized allograft bone material mixed with an aqueous phosphate buffered gelatin which when lyophilized to remove water from the composition crosslinks the gelatin to form a solid structure and when rehydrated is flexible

Abstract: A therapeutic rinse for treating a sore throat including a self heating container having a reservoir. The self heating container is capable of reaching a temperature of at least 130 degrees Fahrenheit when activated. The therapeutic rinse includes a liquid composition having sodium chloride, water, an antibiotic, and a variety of vitamins, minerals and herbs stored in the reservoir of the self heating container. During use, the self heating container is activated and the liquid composition is heated inside the reservoir to about 130 degrees Fahrenheit.

Abstract: The present disclosure relates to medical packaging for the accommodation of medical supplies. The medical packaging discussed herein has a plurality of panels, including a first panel, a second panel, and a third panel, that are releasably secured together to establish a first sterile environment between the first panel and the second panel for the retention of a first medical supply, and a second sterile environment between the second panel and the third panel for the retention of a second medical supply. The panels are configured for relative movement such that movement of the first panel relative to the second panel reveals the first medical supply without compromising the second sterile environment, and movement of the second panel relative to the third panel reveals the second medical supply. The panels are arranged for sequential separation in accordance with the steps of the procedure in which the medical supplies are employed.

Abstract: A container member including a rigid cup portion defining a chamber. The container member has an opening at one end in communication with the chamber and a flexible suspension member extending over the opening. The suspension member has an inner surface facing the chamber, an opposing outer surface and a cavity extending from the outer surface to the inner surface. The cavity is in communication with the chamber and sized to receive at least a portion of the product to be packaged therethrough. The container assembly includes a retainer having a retaining member removably positioned to extend over the cavity. The retaining member holds the at least a portion of the product in position in the chamber such that the at least a portion of the product does not contact the cup portion.