Abstract: Fluid transfer devices for filling a drug pump cartridge with liquid drug contents for administration purposes. Fluid transfer device includes a dual open ended barrel partitioned by a transverse partition into a drug vial port for telescopic mounting on a drug vial and an open ended piston cylinder for slidingly receiving a piston head including a drug pump cartridge port for telescopic mounting on a leading cartridge end of a drug pump cartridge. Sliding insertion of the piston head into the piston cylinder to butt against the transverse partition urges air trapped in the compression chamber into the drug vial which in turn urges its liquid drug contents into the vented drug pump cartridge.

Abstract: In certain embodiments, a vial adaptor comprises a housing configured to couple the adaptor with a vial, an access channel, a regulator channel, and a regulator assembly. The access channel is configured to facilitate withdrawal of fluid from the vial when the adaptor is coupled to the vial. The regulator channel is configured to facilitate a flow of a regulating fluid from the regulator assembly to compensate for changes in volume of a medical fluid in the vial. In some embodiments, the regulator assembly includes a flexible member configured to expand and contract in accordance with changes in the volume of the medical fluid in the vial. In some embodiments, the flexible member is substantially free to expand and contract. In some embodiments, the flexible member is not partly or completely located in a rigid enclosure.

Abstract: A needle-free connection device include a casing, a connection base, a slide element and a resilient valve. The casing includes a first hollow tube having a first liquid transmission channel. The connection base is connected to the casing. The resilient valve includes a second hollow tube and a plug connected thereto, wherein the second hollow tube has a second liquid transmission channel, a third liquid transmission channel is formed between the second hollow tube and the plug, and a fourth liquid transmission channel is formed between the connection base and the plug. The first to the fourth liquid transmission channel are intercommunicated with each other. The connection base includes a third hollow tube, and a fourth liquid transmission channel is formed between the plug and the third hollow tube. The needle-free connection device provides a liquid transmission path sequentially passing through the first to the fourth liquid transmission channel.

Abstract: Systems and methods for protecting biological or other material from contamination through the steps of filling, freeze-drying, packaging, storing and use are disclosed. A system can include a flexible container, at least two membranes configured to transmit air or solvent vapor out of the flexible container, and a port to allow for the introduction or withdrawal of a material or substance into or out of the flexible container. The system can optionally further comprise a membrane frame supporting at least one of the membranes and engaged with at least one column member. The at least one column member can be configured to maintain the membranes and the membrane frame a spaced distance from one or more materials received within the flexible container. Upon application of a downward force, the at least one column member can assume a collapsed configuration.

Abstract: Provided are systems and methods for delivery of fluid to a wound therapy dressing. In exemplary embodiments, a pressure source provides negative pressure to a wound dressing and positive pressure to an actuator that expels fluid from a fluid reservoir.

Abstract: According to an illustrative embodiment a method to promote healing of a wound is provided comprising contacting the wound with a biologically active composition comprising a lipoic acid derivative and gelatin. In another embodiment a topical composition is provided, which can be formulated as a homogenous mixture, such as a spray, mist, aerosol, lotion, cream, solution, oil, gel, ointment, paste, emulsion or suspension or applied on a carrier material, such as a bandage, gauze, foam, sponge, hydrogel, hydrocolloid, hydrofiber, occlusive dressing, adhesive composition or scaffold. Methods for producing such a topical composition and carrier material with the topical composition applied thereto are also disclosed.

Abstract: A BAK removal device is constructed as a plug of microparticles of a hydrophilic polymeric gel that displays a hydraulic permeability greater than 0.01 Da. The polymer hydrophilic polymeric gel comprises poly(2-hydroxyethyl methacrylate) (pHEMA). The particles are 2 to 100 ?m and the plug has a surface area of 30 mm2 to 2 mm2 and a length of 2 mm to 25 mm and wherein the microparticles of a hydrophilic polymeric gel has a pore radius of 3 to 60 ?m.

Abstract: This invention relates to methods of applying to a substrate a hydrophilic coating that becomes lubricious when activated with water or water vapor, and to substrates having such a hydrophilic coating.

Abstract: An adapter insert is for the purpose of reinforcing or stiffening a flexible adapter for said guard system to provide greater support and stabilization in the peristomal region in an effort to help reduce herniation, and to help aid adhesion of a faceplate when worn short term without a guard when output is expected to be minimal, for instance, between meals. The conjoined insert and adapter are positioned between a faceplate and a pouch, their inner apertures surrounding the faceplate flanges or heat weld of an ostomy appliance, and worn under form-fitted clothing negating the need for a security strap.

Abstract: An aqueous humor drainage device for implantation into a tissue passage leading into the anterior chamber of the eye. In one aspect, the device includes a flexible tube and a tissue sealing structure extending radially outward from the tube in at least two different directions. The tissue sealing structure is spaced apart from and intermediate cylindrical outer surfaces of proximal and distal portions of the tube. The tissue sealing structure extends radially outward beyond the cylindrical outer surfaces of the proximal and distal portions of the tube. The tissue sealing structure has a second maximal cross-sectional dimension that is greater than a first maximal cross-sectional dimension of the tube and is configured to interface to the tissue passage and form a seal between the tissue passage and the tissue sealing structure. Other aspects are also described and claimed.

Abstract: An ophthalmic system (100) having an ophthalmic cassette (104) for operative engagement with an ophthalmic apparatus (102) is disclosed. The ophthalmic cassette (104) includes a cassette body (108) having a manifold (124) defining an inlet port (180) in fluid flow communication with first and second fluid pathways (120/122) which are in selective fluid flow communication with respective first and second storage chambers (116/118) such that fluid enters either the first storage chamber (116) or the second storage chamber (118). The ophthalmic apparatus (102) is operable to permit alternate fluid flow communication between the inlet port (108) and either the first storage chamber (116) or the second storage chamber (118) during operation of the ophthalmic system (100).

Abstract: The invention relates to a container for drainage of fluids or wound secretion, comprising an inlet opening to connect with a drainage line and an outlet opening for releasing waste air accumulated inside the container during drainage, which is characterized in that the container is pre-evacuated, and the outlet opening is sealable, so that the container is transferable in a first and in a second operating condition, wherein in the first operating condition the outlet opening is sealed, so that a suction can be achieved at the inlet opening caused by the vacuum inside the container, and in the second operating condition the outlet opening is opened, so that air can enter the container through the outlet opening and neutralize the vacuum present inside the container.

Abstract: A combination therapy pad that includes a first layer and a second layer operatively coupled to the first layer. A fiber-optic array is disposed between the first layer and the second layer. A third layer is operatively coupled to the first layer. The third layer includes a vacuum tube in fluid communication with a vacuum source and a therapeutic fluid tube in fluid communication with a therapeutic fluid source. The third layer provides at least one of vacuum therapy and therapeutic fluid treatment to a wound area.

Abstract: A medical fluid drainage system which may be advantageously used to actively absorb excess fluid from an interstitium in a living host and to transport it from an inlet member 1 in a non edematous body part out of an outlet member 4 via pumps (5, 6, 7) built in series, such as a distal area with functional lymphatic vessels, or directly in a lymphatic vessel, or directly in a blood vessel.

Abstract: A gastrointestinal device for implanting within a patient's gastrointestinal tract, the device having a central axis and a first expandable portion comprising a hollow tubular braided structure of wire and having a first cylinder extending parallel to the central axis, the first cylinder having a length and a first face; a neck portion extending from the first face of the first expandable portion parallel to the central axis, the neck portion having a first end, a second end, a wall extending between the first end and second end, and a diameter sized to fit within a pylorus; and a second expandable portion comprising a hollow tubular braided structure of wire and having a second cylinder extending parallel to the central axis, the second cylinder having a second face located at the proximal end of the second cylinder and oriented transverse to the central axis.

Abstract: An implantable device for treatment of glaucoma of the eye. In one aspect, the device includes an elongate duct for diverting aqueous humor from the anterior chamber of the eye, the elongate duct having a central axis with a proximal end and distal end opposite one another. A least one element is spaced apart from the proximal end and the distal end of said elongate duct and extends radially outward beyond an outer surface of said elongate duct in at least two directions transverse to the central axis of said elongate duct, wherein the at least one element has a distal portion with a tapered profile facing the distal end of said elongate duct. The at least one element is configured to deform in a tissue passage leading into the anterior chamber of the eye as it is inserted into the tissue passage in response to forces applied by surrounding ocular tissue of the tissue passage. Other aspects are also described and claimed.

Abstract: A dialysis catheter includes an entirely subcutaneous first section, with an exterior interface via penetration of the overlying subcutaneous skin layer. In addition the first section of the dialysis catheter includes a detachable portion that enables insertion via a guidewire instead of a peel-away sheath. The dialysis catheter has a layered design that minimizes risk of infection.

Abstract: A transfer device (10) for removing or transferring a medium out of or into a bottle (20) having a bottle neck (34) that can be closed by means of a closure (42), including a first adapter part (12), which can be positioned on the bottle, and a second adapter part (14), which interacts with the first adapter part, which can be displaced in the longitudinal direction of the bottle, and has a conducting element (50) for piercing the closure. After the second adapter part (14) has been displaced along the first adapter part in the direction of the closure (42) and the second adapter part has been locked, the first adapter part (12) is non-releasably fastened to or around the bottle (20).

Abstract: The present invention relates to a mupirocin topical pharmaceutical composition in a pump device, and its use for dispensing predetermined quantities of mupirocin for treating skin lesions.

Abstract: Some embodiments disclosed herein are directed to a pump assembly comprising a voice coil, a magnet and a diaphragm, wherein the voice coil is configured to move the diaphragm to pump a fluid through the pump assembly in response to a drive signal applied to the voice coil. Some embodiments disclosed herein are directed to an apparatus for applying negative pressure to a wound comprising a source of negative pressure configured to be coupled to a dressing, the source of negative comprising a voice coil actuator and a diaphragm, and a controller configured to produce a drive signal for the voice coil actuator.