586results about "Filtering accessories" patented technology

Various embodiments of the present invention are directed to patches for medical devices. In various embodiments, an adhesive patch of a medical device may have selective areas with adhesive material of varying adhesion strengths. In other embodiments, an adhesive patch of a medical device may include adhesive material that may be activated by a catalyst to increase or decrease the adhesion strength of the adhesive material. In further embodiments, a medical device may include a pierceable membrane containing an agent, the pierceable membrane positioned to be pierced by a needle and to cause some of the agent to be carried to the user-patient.

Various embodiments of the present invention are directed to patches for medical devices. In various embodiments, an adhesive patch of a medical device may have selective areas with adhesive material of varying adhesion strengths. In other embodiments, an adhesive patch of a medical device may include adhesive material that may be activated by a catalyst to increase or decrease the adhesion strength of the adhesive material. In further embodiments, a medical device may include a pierceable membrane containing an agent, the pierceable membrane positioned to be pierced by a needle and to cause some of the agent to be carried to the user-patient.

A system is disclosed for delivering gas during a laparoscopic surgical procedure performed within a patient's abdominal cavity requiring smoke evacuation which includes a gas delivery device having a housing with a port for receiving pressurized insufflating gas from a gas source, a pump assembly for circulating gas throughout the system, and a disposable gas conditioning unit or filter cartridge configured for operative association with the gas delivery device.

Various embodiments of the present invention are directed to patches for medical devices. In various embodiments, an adhesive patch of a medical device may have selective areas with adhesive material of varying adhesion strengths. In other embodiments, an adhesive patch of a medical device may include adhesive material that may be activated by a catalyst to increase or decrease the adhesion strength of the adhesive material. In further embodiments, a medical device may include a pierceable membrane containing an agent, the pierceable membrane positioned to be pierced by a needle and to cause some of the agent to be carried to the user-patient.

An apparatus, system or method enables microbubbles to be created on demand for use as the contrast agent within a contrast medium administrable to a patient for purposes of a medical procedure. The system comprises a reservoir, a pressurizing device, a microbubble generator, and a controller. The reservoir stores a liquid. The pressurizing device conveys the liquid, along with the medium formed therewith, through the system. The microbubble generator is used to create the microbubbles within the liquid to form the medium. The microbubble generator has an inlet for receiving the liquid and an outlet for communication of the medium to the patient. The controller controls the operation of the system so that the microbubbles created by the microbubble generator are generated according to the demands of the medical procedure and are administrable within the medium to the patient.

Implantable drug delivery systems target delivery of small volumes of drugs to specific tissues. In some cases, a drug delivery system includes an implantable osmotic pump connected to a drug-containing housing, with that housing connected to a needle, cochlear implant or other type of component for ultimate delivery to the target tissue. In some implementations, a subcutaneous port receives a fluid from an external pump. The port is connected to a needle or other component for delivery of one or more drugs to the target tissue. Both solid and liquid drug formulations can be used. In embodiments using solid drugs, a separate drug vehicle (such as saline) can be used to dissolve a portion of the solid drug, with the drug-loaded vehicle then delivered to the target tissue.

A device for priming and venting a hazardous drug within an intravenous administration set. The device includes various access ports and fluid channels to permit direct injection of a hazardous drug into the fluid reservoir, while eliminating the possibility of undesirable exposure to the hazardous drug. The device further includes priming and flushing ports to enable flushing of a hazardous drug from the system following an infusion procedure.

Flat filter for venting gas in intravenous medical lines, comprising a case formed by a frontal plate and by a dorsal plate between which a hydrophilic filtering membrane is interposed. The dorsal plate has a single through hole for gas venting in communication with an elongated collecting channel formed on the inner surface of the dorsal plate and along which a hydrophobic membrane of complementary shape is applied.

An implantable system includes cells that produce and release a therapeutic agent, or agents, to a host in need. The system can include cells capable of eluting therapeutic agents in response to changing physiological conditions within a host. The system may comprise naked cells, encapsulated cells, or a mixture of non-encapsulating and encapsulated cells. The system may also comprise cells, and / or cell groups, of different origins. The implantable device may be placed intra-vascular, within bone marrow, within soft tissue, in the peritoneal cavity, or intra-hepatic, etc. The system can be comprised of a stent, or like devices. Such stents and like devices may optionally include port(s), catheter(s), and containment envelope systems for holding the above cells.

A device for priming and venting a hazardous drug within an intravenous administration set. The device includes various access ports and fluid channels to permit direct injection of a hazardous drug into the fluid reservoir, while eliminating the possibility of undesirable exposure to the hazardous drug. The device further includes priming and flushing ports to enable flushing of a hazardous drug from the system following an infusion procedure.

To ensure that there is no misconnection between a needle, such as for example a spinal or epidural needle, and the appropriate medication, the needle hub the needle is formed, by molding or extrusion, to have a given configuration. An adapter is placed between the needle and a conventional fluid store, or medical line. The end of the adapter that connects to the needle assembly is formed to have a configuration that is complementary to that of the hub of the needle assembly, so that the adapter and the needle hub may be readily mated to each other. The other end of the adapter is formed to have another configuration, for example a conventional luer, that is readily connectable to a conventional fluid store, such as a syringe that has a conventional luer. The adapter is formed by inter-fitting two elements to effect an integral locking mechanism to prevent the uncoupling of the fluid store and the adapter, once they are securely coupled. By thus configuring the hub of the needle to have a given configuration that is matable only to the end of an adapter that has a complementary configuration, and further providing an adapter that prevents the removal of the fluid store connected thereto, the potential for mis-connecting the needle to a fluid store that contains a different medicament is greatly reduced, if not totally eliminated.

There is disclosed a filter package comprising a housing and a cover that is adapted to enclose a sterile disposable filter wherein the package cover is penetrable at a point axially aligned with the filter and has at least one pre-formed break line along which the package cover, when subjected to appropriate force, ruptures so as to permit withdrawal of the filter by a syringe coupled thereto.

Various embodiments of the present invention are directed to patches for medical devices. In various embodiments, an adhesive patch of a medical device may have selective areas with adhesive material of varying adhesion strengths. In other embodiments, an adhesive patch of a medical device may include adhesive material that may be activated by a catalyst to increase or decrease the adhesion strength of the adhesive material. In further embodiments, a medical device may include a pierceable membrane containing an agent, the pierceable membrane positioned to be pierced by a needle and to cause some of the agent to be carried to the user-patient.

A method and system for developing a conceptual model to facilitate generating a business-aligned information technology (IT) solution. Requirements of the IT solution are defined. A conceptual model is developed by business and IT stakeholders. The conceptual model represents an IT solution design and includes systems, conceptual components and operational concepts. The conceptual components represent hardware components and software components of the IT solution. The operational concepts indicate interactions among the conceptual components that are needed to perform business functions. A computing system generates documentation of the conceptual model. The documentation is available and accessible to the business and IT stakeholders and includes documentation of the operational concepts. The architecture and design of the IT solution is developed along with related documentation.

The present invention provides a closable male luer connector (101) in which an inner portion (121) within the spigot (111) of the connector is movable from a sealing position to an open position on connection of the connector to a female luer connector (10). The movement of the inner portion may be caused by, for example, action of the female connector on a projecting arm (122b) or a screw thread arrangement.

An injection device for injecting an injection solution prepared from a powdered medication in sterile water immediately before use which is administered by a syringe. A winged cannula has a hollow needle and a needle holder with wings. A female Luer Lock connector is joined to the winged cannula by a flexible connecting tube and has an insertion region for the connecting tube and a connection region for placing the syringe, filled with the injection solution, against a skin surface, and also has a continuous bore that is continuous from the insertion region to the connection region of the Luer Lock connector. A porous filter element permeable to the injection solution is provided in the continuous bore of the Luer Lock connector.

A syringe filter for containing a filter membrane is disclosed and includes first and second fluid distribution surfaces configured to be positioned on opposing sides of a membrane. An inlet port is in fluid communication with the first fluid distribution surface and a first plurality of distribution pathways formed on the first fluid distribution surface. An outlet port is in fluid communication with the second fluid distribution surface and a second plurality of distribution pathways formed on the second fluid distribution surface. The first plurality of distribution pathways is configured to distribute fluid flow from the inlet port to one side of the membrane while the second plurality of distribution pathways is configured to direct fluid flow from another side of the membrane to the outlet port.

An assembly is provided which includes an infusion device coupled to a standard medication syringe. The medication syringe may be coupled to a stopcock valve having multiple ports and to which syringes, vial adapters, infusion tubing, and multiple other items may be coupled. The infusion device includes a source of power based on a resistance force such as vacuum, spring or gas power. The infusion device converts the resistance based force to usable work in the form of a force applicator. The force applicator includes a driver section on one section of a reciprocating arm and an attachment to the power source on another section of the arm. The driver is pulled outward (excursion) to increase the size of the chamber, creating a force that tends to return the driver back inward, causing incursion. The driver can be attached removably to the syringe plunger to induce the infusion process.

The invention provides a process of assembling a medical filter to solve the technical problems that in the prior art, an existing medical filter is low in assembling efficiency, low in cleanliness and the like, and belongs to the technical field of medical device assembling. The process includes the following steps of firstly, feeding an upper cover; secondly, assembling a ventilating membrane; thirdly, feeding a lower cover; fourthly, assembling a filter membrane; fifthly, assembling the whole; sixthly, discharging the finished product, namely, taking out the assembled filter. By means of the process, the medical filter is automatically assembled, and therefore production efficiency and cleanliness are improved.

An extracorporeal blood circuit, comprising an expansion chamber for air-blood separation, wherein a filter (38) retains the solid particles in the blood. The filter has a trunco-conical filtering wall with a vertical axis surmounted by a top head (43) provided with upper openings (44) conformed and arranged such as to define a fluid passage which is asymmetrical with respect to the vertical axis. The top head does not retain air bubbles internally thereof, thus preventing a situation in which the air bubbles are directed towards an outlet of the expansion chamber and thus towards the patient. The extracorporeal circuit is used in a dialysis apparatus.

A combined filter for removing an aqueous fluid and entities, such as bacteria, existing in such aqueous fluid, from a nonaqueous fluid is described. The combined filter consists of a hydrophilic filter and a hydrophobic filter that are arranged in fluid communication and serially to be placed along the flow path of a fluid. The hydrophilic filter and the hydrophobic filter may touch one another or be located some distance from one another. Also, a structure may be inserted into the space between the hydrophilic filter and the hydrophobic filter that will maintain the space between the hydrophilic filter and the hydrophobic filter without significantly restricting the flow of fluid. And, in one embodiment, the combined filter may be composed simply of material having both hydrophilic and hydrophobic characteristics on the molecular level. Preferably, however, the filters and spacing structure are contained within an encasement having an inlet and an outlet. As any filter or spacer is located farther downstream with respect to the intended flow of fluid, the dimensions of that filter or spacer in the direction perpendicular to the intended flow of fluid increase to a sufficient extent that, as the stream of fluid expands perpendicularly to its intended direction of flow, the possibility of the fluid contacting any solid element other than a filter is decreased.