Abstract: The invention includes a device having a chamber within a syringe. A fluid passageway extends through a syringe piston. A valve is associated with the passageway controlling fluid passage through the piston. The invention includes a piercing structure having a head segment and a body portion, with a channel through the body portion and through at least one surface of the head without passing through the tip. In another aspect the invention encompasses a method of preparing an agent for administration to an individual. A first component is provided within a syringe and a second component is provided within a vial. A closed valve is associated with a fluid passageway between the vial and the syringe barrel through a piston. Valve repositioning allows fluid passage and sliding of the piston joins the first and second components. Repeated sliding of the piston mixes the components to produce the medication agent.

Abstract: A blood collection assembly includes a needle cannula, a hub mounted on the needle cannula, and a spring biased pivoting shield pivotably mounted to the hub and moveable about a pivot axis between a retracted position and a shielded position encompassing a distal end of the needle cannula. A needle holder is mated at a first end with the hub, and is adapted for receiving a blood collection container such as an evacuated tube through the opposing end. A retaining member is attached to the pivoting shield and is releasably engageable with the hub to maintain the pivoting shield in the retracted position against the spring bias. Insertion of a blood collection tube into the needle holder causes the retaining member to release from engagement with the hub, thereby causing the pivoting shield to move toward the shielded position due to the spring bias.

Abstract: A guided filter system for temporary placement of a filter in an artery or vein is disclosed. The system includes a guidewire slideable through a wire guide included in a distal region of a support wire. The support wire has an expandable filter, which is operable between a collapsed or enlarged condition. A variety of endovascular devices, including angioplasty, atherectomy, and stent-deployment catheters, are insertable over the guidewire and/or the support wire. Methods of using the guided filter system to direct and exchange endovascular devices to a region of interest, and to entrap and remove embolic material from the vessel are also disclosed.

Abstract: Embodiments of an implantable electrolytic pump include a first expandable diaphragm and a second flexible diaphragm, and first and second chambers each for containing a fluid, wherein the first expandable diaphragm separates the first and second chambers and provides a fluid barrier therebetween, and the second chamber is formed between the first expandable diaphragm and the second flexible diaphragms. The pump may further include electrolysis electrodes within the first chamber for causing generation of a gas therein and to thereby expand the expandable diaphragm so that fluid is forced from the second chamber into a cannula.

Abstract: A stylet is provided which makes it possible to improve the handling of a catheter while also facilitating insertion of the catheter. A catheter set having such a stylet is also provided. A stylet with a hole and a stylet without a hole include, respectively: a stylet main body; an engaging part; a film-like linking part for linking the stylet main body and the engaging part; and a soft tip end part which is provided at a tip end of the engaging part. The engaging part has a tapered tubular shape which can expand and contract thanks to an alternating arrangement of soft parts and rigid parts in the peripheral direction. The stylet main body is then pulled rearwards from a state in which the stylet with a hole and the stylet without a hole are assembled with a catheter, thereby enabling the engaging part, which can engage with the edge of the opening of the catheter, to contract in the radial direction and be withdrawn.

Abstract: A drainage pump unit for aspirating body fluids comprises a suction pump housing and a suction pump arranged in the suction pump housing. A fluid collection container can be secured releasably on the suction pump housing. A flat band-shaped capacitive filling level sensor is arranged on the suction pump housing for the purpose of detecting a filling level in the fluid collection container. The drainage pump unit also comprises an elastically configured coupling element with a first surface and a second surface lying opposite the first surface, and the coupling element, in the secured state of the fluid collection container, bears with the first surface on the filling level sensor and with the second surface on an outer wall of the fluid collection container. By virtue of the elastically configured coupling element, this drainage pump unit permits a filling level measurement even in the case of low filling amounts.

Abstract: An IV line temperature controlled warming device includes a housing and a fluid cassette or cartridge that receives fluid from an IV line and includes intravenous line tubing arranged in a preformed configuration. The configuration includes tubing sections arranged in generally circular and concentric portions and a central serpentine tubing section that basically reverses fluid flow and facilitates flow in opposing directions within adjacent tubing sections. The fluid cassette is retained within the device on a base plate partially disposed within a device housing interior, while a housing cover is selectively opened and closed to permit access to the base plate. The base plate includes a heater plate disposed thereon, while the cover and heater plate each include heating elements to apply heat to opposing surfaces of the tubing cassette. The heating elements are controlled by a controller in response to measured temperatures of the heater plate and fluid.

Abstract: The invention relates to a microdialysis catheter comprising a multilumen tube (10) and a membrane (11), said tube exhibiting at least two longitudinally arranged inner channels (13,14), said channels extending from a proximal (20) end of the tube to the distal end (21) of the tube, whereat through-holes (12,15) are provided, one from each of said at least two channels to the outside of said tube, said channels (13,14) blocked for passage of liquid distally of the respective through-holes, a tubular membrane (11) arranged circumferentially around the tube (10) such as to cover the at least two through -holes (12,15), said membrane is sealingly fastened (22) to the tube thereby forming a dialysis chamber (18) between the tube and the membrane.

Abstract: One embodiment is a medical device comprising an elongate catheter having a proximal end, a distal end, and a lumen extending therethrough and a tip disposed at the distal end of the elongate catheter, the tip extending distally of the distal end of the catheter, the tip comprising a soft body portion and a rigid ring distal the soft body portion.

Abstract: A surgical drain tube assembly and its associated method of manufacture. The drain tube assembly has an extruded intake tube that defines multiple internal conduits. The intake tube has a first end and an opposite second end. The internal conduits run between the first end and the second end. The extruded intake tube contains multiple slices that run from the first end to a termination point. Each of the slices communicates with a different one of the internal conduits inside the intake tube. The internal conduits are therefore transformed into open grooves that are capable of draining fluids at any point along their lengths. The extruded intake tube can also be cut into separate arms that converge at the termination point. The intake tube is coupled to a single conduit collection tube that draws fluid from all the conduits of the intake tube.

Abstract: A removable clamp, for supporting a membrane filter in a medical infusion system, includes connected and opposing walls. A locking feature, which may be connected to an end of one of the walls, engages and disengages a terminal end of the other wall. The filter may be inserted between the opposing walls of the clamp, and an inner surface of each of the opposing walls may be secured against corresponding major surfaces of the inserted filter, by only pressing at least one of the opposing walls of the clamp toward the other of the opposing walls.

Abstract: A removable clamp, for supporting a membrane filter, includes connected and opposing walls. A locking feature, which may be connected to an end of one of the walls, engages and disengages a terminal end of the other wall. When the filter is inserted between the opposing walls of the clamp, and the locking feature engages the terminal end of the other wall, an inner surface of each of the opposing walls is secured against corresponding major surfaces of the inserted filter, in order to support the filter without extending over vent holes of the filter.

Abstract: A surgical instrument including a fixed or removable handle and a tubular member having a lumen extending therethrough with apertures at its proximal and distal ends permitting visualization of and access to body tissues. An access window in a distal portion of the instrument is formed through the wall of the tubular member and in communication with the lumen.

Abstract: A skin treatment apparatus that includes, a disposable electrode carrier with a plurality of voltage-applying dome-shaped elements protruding from the surface of the electrode carrier. Further, the protruding elements are spaced apart in a pattern. The apparatus operates to apply a voltage to at least some of the protruding elements. The apparatus applies a voltage to the protruding elements with a magnitude that is sufficient to result in an electrical break down of the skin and thereby cause electric current enabling the desired treatment.

Abstract: A kit for charging an infusion pump having a reservoir for holding a local anesthetic. The kit includes a first stopcock having an input port, a first input/output port and a second output port and a manual control for selectively coupling either the first input/output port or the second output port to the input port. The kit further includes a second stopcock having an input port, first and second output ports and a manual control for selectively coupling either the first output port or the second output port to the input port. The second output port of the first stopcock is adapted for coupling to the input port of the second stopcock. The kit further includes a syringe adapted to be coupled to the first input/output port of the first stopcock and tubing for coupling the input port of the first stopcock to a source of the liquid and for coupling the output port of the second stopcock to an input port of the pump.

Abstract: An iontophoresis apparatus and method is disclosed that is suited to deliver a plurality of treatment methods such as, but not limited to, body site conductivity enhancement followed by low voltage iontophoresis.

Abstract: Devices, systems, and methods for accessing the internal and external tissues of the heart are disclosed. At least some of the embodiments disclosed herein provide access to the external surface of the heart through the pericardial space for localized delivery of leads to the heart tissue. In addition, various disclosed embodiments provide devices, systems, and methods for closing a hole in cardiac tissue.

Abstract: A transdermal device such as a patch can include a drug source, a porator, and an energy storage device on-board the patch. The porator operates free of any concurrent connection to any external source of power. A switch can be used to make the selective electrical connection between the porator and the energy storage device. The switch can be arranged to respond to a manual user action after the patch has been adhered to skin, including separation of the porator from a remainder of the patch. Optionally, a series of switches can make electrical connections between the porator and respective individual energy storage devices.

Abstract: An injection port comprises a body, a fluid reservoir, a septum, and a plurality of fasteners. The fluid reservoir is defined in part by the body and the septum. A needle may be inserted through the septum to reach the reservoir. The fasteners are integral with the body. The fasteners are simultaneously rotatable from a non-deployed position to a deployed position. The fasteners are retracted relative to the body when the fasteners are in the non-deployed position. The fasteners are extended relative to the body when the fasteners are in the deployed position. The fasteners are also simultaneously rotatable from the deployed position to the non-deployed position. The injection port may be coupled with a gastric band via a conduit. The conduit may provide fluid communication between an inflatable member of the gastric band and the reservoir of the injection port as part of a closed fluid circuit.

Abstract: A number of parameters related to the operation of a fluid delivery device are determined based on pressures within the device sensed using multiple pressure sensors. In one example, the volume of therapeutic fluid within a reservoir of a fluid delivery device is estimated based on a measured pressure differential. In another example, the rate at which a therapeutic fluid is added to or removed from the reservoir is estimated based on the measured pressure differential.