Abstract: The subcutaneously implantable vascular access port has two parts including a body and a wing. The body supports a chamber covered by a septum, with a septum held in place over the chamber by a collar. The chamber is coupleable to a vascular structure, such as through tubing extending from the body, for delivery of medical preparations. The body is preferably elongate in form. The wing is configured to be adjustable in width. In one embodiment the wing rotates relative to the body and has an elongate form similar to that of the body. When the wing is rotated it extends laterally from the body and enhances a stability of the body. In another embodiment, the wing is provided as a deformable wing which can expand laterally out of side openings of a cavern in the body into which the deformable wing is inserted.

Abstract: The present invention relates to an injection device (1) comprising:—a body (3) designed to receive a product to be injected, furnished at its distal end with an injection needle (7) and receiving a piston (5) capable of being moved between a storage position and an end-of-injection position under the effect of a distal pressure exerted on a piston rod (8) to the distal end of which it is attached,—means of protecting the injection needle (7) capable of adopting an initial position, during which the injection needle (7) is uncovered, and a final position, in which the said injection needle (7) is covered,—biasing means (26) aiming at moving the said covering element (6) from its initial position to its final position,—immobilization means (16, 31) aiming at keeping the said covering element (6) in its initial position, the said injection device (1) being characterized in that:—the said piston rod (8) comprises at least a first portion (9) and at least one second portion (10) coupled to the said piston (8), th

Abstract: The invention provides a medicine dispenser device for liquids intended to be swallowed, particularly by children and patients who find it difficult to cooperate, the device comprising an elongated cylinder serving as a container for the liquid, the device being provided, in accordance with the requirements of its use and the type of liquid to be dispensed, with at least one dispensing exit outlet at the distal end of the cylinder, the cylinder having a longitudinal axis and the at least one dispensing outlet being positioned to direct at least one stream of dispensed liquid at an angle of between 20° and 170° relative to the distal end of the longitudinal axis of the container, the safety arrangement of the device being such that upon introduction of the distal end of the device into the mouth of a patient, the at least one stream of dispensed liquid is directed to exit towards at least one enveloping surface of the mouth cavity and not in a direction toward the patient's windpipe and the throat opening.

Abstract: An osmotic delivery system is disclosed for delivering an active agent formulation to a fluid environment. The osmotic delivery system typically comprises a reservoir having a lumen that contains the active agent formulation and an osmotic agent formulation and a piston assembly positioned in the lumen to isolate the active agent formulation from the osmotic agent formulation. The piston assembly typically comprises a body constructed and arranged for positioning in the lumen. The body is typically made of a polymeric material that is, for example, resistant to leaching in an organic solvent. In one embodiment, the body is a columnar body having a rim at a distal end thereof for engaging and sealing against a wall of the reservoir and the piston assembly further comprises a spring retained at the distal end of the columnar body for biasing the rim of the columnar body against the wall of the reservoir.

Abstract: A piston for a needleless valve system comprising a head portion configured to be disposed in the needleless valve system and controlling fluid flow through the needleless valve system. The head portion comprising a continuous top surface, and an opening disposed proximate the continuous top surface, wherein the continuous top surface is non-planar when the opening is in an open position.

Abstract: A safety pen needle assembly is provided herein which includes a hub; a needle fixed to the hub having a distal end, formed for insertion into a patient, and a proximal end; a shield; a biasing means disposed to urge the shield from a first position to a second position; and, at least one adjustable tab or locking finger on the hub, the tab or finger being adjustable from a first state to a second state. With the tab or finger being in a first state, the tab or finger interferingly engages the shield so as to restrict movement thereof. The tab or finger in the first state retains the shield in its first position with the proximal end of the needle being exposed. With the tab or finger being in the second state, the tab or finger does not interferingly engage with the shield. As such, the shield is permitted to be urged proximally to the second position by the biasing means. In the second position, the shield covers the proximal end of the needle.

Abstract: A syringe assembly includes a syringe barrel having an inside surface defining a chamber, an open proximal end, a distal end, and an outlet; a plunger assembly disposed at least partially within the syringe barrel, including an elongate plunger rod having a locking flange formed thereon; and a plunger head having a distal sealing surface, the plunger rod being engageable with the plunger head such that the plunger rod is adapted to move the plunger head within the chamber of the syringe barrel through an injection cycle; and a flange lock disposed at the open proximal end of the barrel. The flange lock is integral with the open proximal end of the syringe barrel. During the injection cycle, the flange lock engages the locking flange of the plunger rod so as to prevent removal of the plunger rod from the syringe barrel.

Abstract: A respiratory circuit apparatus and circuit are provided. The circuit includes: an adapter having a plurality of connectors of two or more different internal or outer diameters; and a pressure release valve configured to emanate sound if a pressure of a gas received at the pressure release valve is greater than or equal to an activation pressure of the pressure release valve. The pressure release valve can have a first end of a body portion coupled with one of the plurality of connectors of the adapter. The pressure release valve can be coupled inline in the respiratory circuit via the adapter and in close proximity to a patient location.

Abstract: A balloon catheter device (1700) includes an elongate catheter shaft comprising multifilar cable tubing (1706) having a proximal portion and a distal portion. The proximal portion includes a coating (1708) that allows the shaft to provide a patent fluid passage. The distal cable tube end includes a connection structure (1723) configured to provide desirable strength, pushability, and trackability.

Abstract: A device may include a vibration sensor configured to sense blood flow in a lumen of a person; a cuff coupled to the vibration sensor and configured to contact a limb of the person; a cuff pressurizer coupled to the cuff, the cuff pressurizer configured to adjust a compressive force of the cuff on the lumen; and an energy-generating apparatus coupled to the cuff, the energy-generating apparatus configured to generate energy from a depressurization of the cuff.

Abstract: A warm perfusion system that has the ability to support a tissue or organ at a near normal metabolic rate provides the mechanism not only for restored oxidative metabolism of the organ but for the delivery of cells, cell-based therapeutics, and growth and differentiation factors to a damaged tissue or organ. Subsequent to delivery of therapeutic cells, such as stem cells or progenitor cells, to the damaged organ, the cells can be prompted to grow, multiply and differentiate, thereby restoring damaged tissue.

Abstract: An injection device comprising an outer housing adapted to receive a syringe for holding a volume of a medicament, said syringe comprising a barrel, a needle at one end of the barrel, and a plunger, axially moveable within the barrel, the needle and barrel being such that at least part of the needle is axially moveable in and out of said outer housing but is biased to be normally wholly inside said housing. The injection device further comprises an inner housing intermediate the outer housing and at least part of the barrel and/or plunger, an energy source in communication with the inner housing, and blocking means capable of preventing said inner housing moving axially under the influence of said energy source.

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 percutaneous gastrostomy introduction system may include may include an elongate tube assembly including one or both of a dilator portion and a gastrostomy tube portion, which may be continuously formed or joined by one or more connection joints that may—in certain embodiments—provide for rotation about a common longitudinal axis. The dilator portion includes a helical surface for advancing contact with body tissue and may be disposed near (including up to and defining) a first end of the elongate tube assembly. An engagement structure, including—for example—one or more of a wire loop, a user-graspable handle, or another graspable structure may be included at the first end of the device. Device embodiments may be effective to lessen or prevent tenting of patient tissue during introduction.

Abstract: A catheter includes a flexible tubing having a proximal end and a distal end. The catheter also includes an electrode assembly attached to the distal end of the flexible tubing and having a first magnet therein. The electrode assembly further includes an electrically conductive tip electrode and an electrically nonconductive coupler which is connected between the tip electrode and the distal end of the flexible tubing. The coupler and the tip electrode are coupled by an interlocking connection. The catheter also includes a second magnet spaced from the electrode assembly along a longitudinal axis of the tubing. The first magnet and the second magnet are responsive to an external magnetic field to selectively position and guide the electrode assembly within a body of a patient.

Abstract: Needle assemblies are disclosed. In some embodiments, the needle assembly includes a main housing including an obturator insertion opening and an opposite needle connection opening, a connector housing configured to engage the main housing, the connector housing including obturator, tubing, and plug openings, a self-sealing plug including a channel, the plug positioned within the connector housing so the channel is aligned with the tubing opening, a needle holder base, and a needle. The connector housing is configured to engage the main housing in first and second positions. The obturator opening is axially aligned with the obturator insertion opening and axially aligned with the needle in the first position. The tubing opening is axially aligned with the obturator insertion opening and in fluid connection with the needle in the second position.

Abstract: Devices and methods are provided for inserting a sterile catheter, and for maintaining a sterilely sealed catheter and catheter insertion site over time. In one embodiment, a four-part integrated system is provided that includes (1) a novel vascular catheter with integrated uniform diameter mounting, capping, and needle safety procurement features, (2) a novel vascular catheter dressing designed to specifically mate with and seal to this vascular catheter to achieve a sterile seal both at the catheter-skin insertion site and the catheter-dressing exit site, (3) a hub protection and sterilizing apparatus that serves to stabilize, protect, and sterilize the working end of the catheter hub as it protrudes from the sterile dressing, and that also helps to improve the ergonomics of the catheter-dressing complex in order to avoid snagging on clothing etc., and (4) a whole dressing accessory secondary cover and securement device.

Abstract: A balloon catheter has an elongated flexible shaft made of a metal and at least one inflatable balloon mounted on a distal end area of the flexible shaft. A wall of the shaft providing the mechanical properties for flexibility and pushability is entirely made of metal, the wall has a sheet-like shape, and the wall has an outer diameter up to 0.5 mm and a wall thickness in a range from 0.02 mm to 0.1 mm.

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: A balloon of a balloon catheter including, in its folded state, a central, inflatable body portion having an outer peripheral wall surface and a plurality of hollow lobes being wrapped around the outer peripheral wall surface and being in fluid communication with the inflatable body portion the lobes including free end portions defining gaps therebetween.