Abstract: An ostomy appliance comprising an adaptor having a distal end adapted to be coupled to an ostomy wafer and a proximal end adapted to be coupled to a cap, said distal end having an opening in fluid communication with an opening in said proximal end.

Abstract: The invention relates to a safety cartridge (1) for a removable vena cava filter (20), having a proximal end (2) and a distal end (3) and having an inner channel (4) extending between the ends. The cartridge is characterized in that it comprises, on the distal end (3) thereof, a linking device (5) for forming a link with a catheter (30) and, in the inner channel thereof, a projection (6) having a limited size in the axial direction of the cartridge (1) so as to locally reduce the cross-section of the channel (4).

Abstract: An exemplary compounding system and method can include a transfer set that includes a manifold for assisting in transferring a plurality of ingredients from supply container(s) to a final container. The manifold can include a first channel in fluid communication with at least one primary ingredient, and a second channel in fluid communication with a plurality of secondary ingredients. The first channel and second channel can be in fluid isolation from each other such that the at least one primary ingredient does not mix with the plurality of secondary ingredients within the manifold. The transfer set can include a plurality of inlet lines in fluid communication with the manifold and two outlet lines configured for connection to two separate pumps and eventually being in fluid communication with the final container.

Abstract: An exemplary pharmaceutical compounding system and device for mixing materials from at least two distinct material sources can include a transfer set and junction structure that has a junction body, a first inlet port located at a first portion of the junction body, a second inlet port located at a second portion of the junction body, and an outlet port located at a third portion of the junction body. The junction structure can be configured to mix fluid received from both the first inlet port and second inlet port and to deliver the fluid to the outlet port. The junction structure can also include attachment structure located on the junction body and configured to attach the junction structure to the housing of the compounding device at a location downstream of a pump system.

Abstract: A method and apparatus for controlling IV medication delivery and monitoring, the method including providing information tags on IV bags that specify delivery parameters, obtaining delivery parameters for at least one bag, associating a controller with a particular patient, comparing patient information for the particular patient with the delivery parameters, determining the efficacy of delivering the medicant to the patient and affecting pump control as a function of the comparison. The method also includes various timing rules and other verification procedures.

Abstract: A method and apparatus for controlling IV medication delivery and monitoring, the method including providing information tags on IV bags that specify delivery parameters, obtaining delivery parameters for at least one bag, associating a controller with a particular patient, comparing patient information for the particular patient with the delivery parameters, determining the efficacy of delivering the medicant to the patient and affecting pump control as a function of the comparison. The method also includes various timing rules and other verification procedures.

Abstract: The disclosed embodiments provide a valve structure that is hermetically sealed to a lower flange formed on an IV bag to form a one-way outlet accessible with a luer tip syringe that does not have a needle. The valve structure can include a piston in combination with a disc or disc valve. The piston can have a slit septum or opening allowing access to an interior surface of the piston. The disc valve is typically in a closed position that prevents injections or other incursions into the bag, thus preserving the integrity and sterility of the bag contents.

Abstract: Needleless access port valves are generally discussed herein with particular discussions extended to needleless access port valves incorporating a piston comprising slit along an upper piston section for accommodating fluid flow. The slit opens when the piston is compressed by a medical implement, such as a syringe tip, to permit fluid communication between the inlet and the outlet of the vale housing. The slit may be cut using high frequency cutting machine or a multi-axis robot arm and a cutting blade.

Abstract: An exemplary pharmaceutical compounding system and device for mixing materials from at least two distinct material sources can include a valve including a valve housing and a valve structure located within the valve housing. The valve structure can be configured to permit fluid to flow through the valve when in an open position, and can include a gravity wall wherein, when the valve structure is in the open position, fluid moving through the valve structure moves upward against a force of gravity when travelling through the valve and traversing the gravity wall.

Abstract: An ostomy appliance comprising an adaptor having a distal end adapted to be coupled to an ostomy wafer and a proximal end adapted to be coupled to a cap, said distal end having an opening in fluid communication with an opening in said proximal end.

Abstract: The purpose of the invention is to create a urine bag that can be easily folded in order to occupy less space prior to use and that can be easily manipulated by a patient, in particular a paraplegic patient. This is achieved using a urine collection bag (1) formed by two sheets of plastic material that are stacked and welded along the periphery (2) thereof. The collection bag (1) comprises a collection compartment (3), said inlet being in communication with the intake port (4) and delimiting the upper portion of the collection compartment (3). The intake port (4) is provided with a vertical extension (8) closed along their periphery (22) thereof and comprising a urinary c catheter (9). The bag (1) of the invention is characterised in that the in-take port (4) and the inlet (6) are offset vertically, and in that the vertical height (ho) of the bag (1) corresponds to a multiple of the height (hp) of the extension (8).

Abstract: The invention relates to a safety cartridge (1) for a removable vena cava filter (20), having a proximal end (2) and a distal end (3) and having an inner channel (4) extending between the ends. The cartridge is characterized in that it comprises, on the distal end (3) thereof, a linking device (5) for forming a link with a catheter (30) and, in the inner channel thereof, a projection (6) having a limited size in the axial direction of the cartridge (1) so as to locally reduce the cross-section of the channel (4).

Abstract: Ostomy appliance components for cleaning and related maintenance of a surgical stoma. Components take the form of attachments, inserted elements, and/or separate parts in contact with ostomy ports, wafers, and/or other connecting components.

Abstract: Ostomy appliance components providing low profile containment of waste from a surgical stoma. Waste collection pouch configuration, positioning, and positioning structure relate to potential advantages in manufacturing and operation of components.

Abstract: A cap assembly for a self-priming IV set valve includes a body portion that is configured to be removably connected to the IV set valve; a hydrophobic filter that is mounted to the body portion; and an actuator having a free end that is configured to either puncture, move or displace a valve element of the IV set valve. A fluid passageway is disposed either in or along the actuator. When the cap assembly is mounted to the IV set valve, the actuator either punctures, moves or displaces the valve element of the IV set valve such that air and liquid within the IV set valve can flow through the fluid passageway and onto the hydrophobic filter, whereupon the hydrophobic filter of the cap assembly prevents the passage of liquid through the hydrophobic filter while the hydrophobic filter permits the passage of air there-through and into the atmosphere.

Abstract: A connector of a self-priming IV set valve including a connector body having a hollow region, and a valve element that is at least partially positioned in the hollow region that is configured to be moved, displaced or punctured by a cap that is releasably connectable to the connector body. When the cap is mounted to the connector, the cap either punctures or moves the valve element and a passageway is formed in the connector such that air and liquid are permitted to pass through the connector and into the cap. When the cap is not mounted to the connector, the valve element of the connector is configured to open under pressure to permit the passage of liquid through the connector and close when pressure ceases.

Abstract: A self-priming IV set valve includes a connector including a valve element that is positioned inside of the connector, and a cap that is removably connected to the connector. When the cap is mounted to the connector a passageway is formed in the connector such that air and liquid are permitted to pass through the connector and into the cap whereupon a hydrophobic filter of the cap prevents the passage of liquid there through while the hydrophobic filter permits the passage of air out of the cap and into the atmosphere. When the cap is not mounted to the connector, the valve element of the connector is configured to open under pressure and close when pressure ceases. Also disclosed is a method of priming the IV set, a cap assembly for a self-priming IV set valve, and a connector for a self-priming IV set valve.

Abstract: A flexible container for fluid administration is provided having a body defining a cavity, a base, and at least one port comprising a flange in contact with a flange of a terminal port having a punctureable membrane layer. The body has a cross-sectional configuration including a lower body section of a first dimension, a middle body section of a second dimension, and an upper body section of a third dimension, wherein the second dimension is smaller than the first dimension and the third dimension. The flexible container may also include a base having a plurality of creases that are foldable to form two folded ends each including an extension having a base of a first dimension and a tip of a second dimension.