Abstract: An aspiration needle for use in collecting larger cell samples with a source of vacuum for fine needle aspiration cytology without increasing the size of the needle having a rigid elongate tubular member having distal and proximal extremities. The tubular member has a bore extending therethrough from the distal extremity to the proximal extremity and has an opening at the distal extremity in communication with the bore. A body is secured to the proximal extremity of the tubular member and forms a chamber therein in communication with and in close proximity to the opening into the bore of the tubular member. The chamber is formed by a sloping uninterrupted wall leading distally to the opening to the bore of the tubular member. The body includes a hub proximal of the chamber for receiving the source of vacuum and for establishing communication between the source of vacuum and the chamber.

Abstract: The drug delivery stent assembly includes a hollow tubular wire stent which extends in a path defining a generally cylindrical envelope and which has side walls facing outwardly of the cylindrical envelope with holes therein for delivery of liquid to a site in a vessel where the stent is placed.

Abstract: Heat transfer catheter apparatus and methods of making and using same are disclosed wherein a fluid connection is provided between the distal portions of two adjacent, thin-walled, high strength fluid lumens to define a closed loop fluid circulation system capable of controlled delivery of thermal energy to or withdrawal of thermal energy from remote internal body locations.

Abstract: An aspiration needle apparatus for collecting cell samples from tissue comprising a vacuum container having an enclosed evacuated space evacuated to a subambient pressure and sealed by a penetrable diaphragm. An adapter has a recess to receive the vacuum container. A needle is carried by the adapter and has a distal extremity serving as an aspiration needle to collect the cell sample and has a proximal extremity disposed in the recess and is capable of penetrating the diaphragm of the vacuum container to couple the evacuated space to the flow passage of the needle to supply a subambient pressure to the distal extremity of the needle. An on-off mechanism carried by the adapter includes yieldable means and a member mounted in the recess actuatable by axial movement of the vacuum container into the recess against the force of the yieldable means disposed within the recess.

Abstract: A guiding catheter for use in coronary angioplasty and other cardiovascular interventions which incorporates a transition element in the shaft of the device. The transition element which has a different flexibility than the sections immediately proximal and distal to it, creates a zone in the catheter shaft which is either more or less flexible than the rest of the shaft. The transition element allows a portion of the shaft to be made more rigid or more flexible, without changing the flexibility of the other portions of the shaft. The transition element also allows for a differential flexibility to be added to the catheter shaft.

Abstract: A method for placing an external feeding tube in the gastro intestinal tract of a patient. The device includes a feeding tube and a filling tool for filling a fillable retaining member of a feeding tube. The tool includes a fluid reservoir constructed to contain a fluid therein. The tool further includes a tool body defining a fluid flow path, the tool body constructed to be connected to the fluid reservoir such that the fluid reservoir is in fluid communication with the fluid flow path defined by the tool body. The filling tool further includes a cannula constructed to connect fluidly to a filling lumen of a feeding tube. The cannula is fluidly connected to the fluid flow path.

Abstract: Valve assembly for sealed reception of an elongated object includes a valve body having at least one opening configured and dimensioned to permit entry of an elongated object and defining a central longitudinal axis, an elongated seal member formed of a resilient material and defining an aperture in general alignment with the opening of the valve body whereby the aperture is configured and dimensioned such that insertion of the object into the aperture causes the resilient material defining the aperture to resiliently engage the outer surface of the object in a substantially fluid flight manner, and at least one elongated guard member disposed within the seal member in supporting contact with the inner surface thereof. The guard member is positioned to engage the elongated object upon at least partial insertion of the elongated object into the valve body.

Abstract: A needle assembly having a telescoping shield that extends over the distal end of the needle when released by an actuator that is triggered during a standard sequence of operation of a medical procedure. For example, the telescoping shield extends by a compression spring from a starting retracted position to a venipuncture partially extended position during the standard sequence of operation of drawing a blood sample with an evacuated blood collection tube and needle holder. After the procedure is complete and the needle is removed from the patient the shield continues to extend to a fully extended and locked position over the distal end of the needle rendering the needle safe and preventing needle stick injuries.

Abstract: A self-administration device includes a cylindrical casing opened at one end but closed at the opposite end. The closed opposite end is provided with a drug inflow port and a drug outflow port. An easily deformable and restorable reservoir is housed in the casing and is held by the closed end of the casing. The inflow port and outflow port are opened to the interior of the reservoir while a pushing device is provided at the open end of the casing and is movable along an inner wall of the casing to exert a pressure on the reservoir. A control device is provided for adjusting a moving distance of the pushing device to control a dosage of a liquid drug.

Abstract: A safety needle assembly includes a needle having a longitudinal axis, a length, a pointed distal end, a proximal end and a passageway therethrough. The assembly includes a hub having a longitudinal axis, a proximal end, a distal end and an outside surface with an outside diameter. The hub has an axial opening through it for receiving the needle so that the distal end of the needle projects outwardly. The hub has a circumferential groove in the outside surface and a raised annulus located proximally to the groove. The assembly includes a shield with an open end, a closed end, a sidewall with a longitudinal slot extending from the open end toward the closed end. The shield has a first position exposing the needle and a second position wherein the shield obstructs unintentional access to the needle. The shield has a mounting for holding the shield onto the hub with a first portion having an opening for placement on the hub at the groove.

Abstract: This is a section of a catheter used in making a catheter assembly suitable for accessing a tissue target within the body, typically a target which is accessible through the vascular system. The catheter section uses a braided metallic reinforcing member, typically of superelastic alloy ribbon, situated within the catheter body in such a way to create a catheter having an exceptionally thin wall, controlled stiffness, high resistance to kinking, and complete recovery in vivo from kinking situations. The braid may have a single pitch or may vary in pitch along the axis of the catheter or catheter section. The braided ribbon reinforcing member typically is placed between a flexible outer tubing member and an inner tubing member to produce a catheter section which is very flexible but highly kink. resistant. The catheter sections may be used alone or in conjunction with other catheter sections either made using the concepts shown herein or made in other ways.

Abstract: A needle-syringe assembly, operable in a normal mode and convertible to a retraction mode, comprises an elongated, generally cylindrical barrel, a plunger slidably mounted in the barrel, and a needle holder carrying a hollow needle on the distal end thereof. The barrel forms a hollow nozzle located at the distal end of the barrel. The plunger forms a coaxial cavity extending therethrough, and the plunger includes a helical slot exposing a proximal portion of the coaxial cavity. The needle holder is slidably mounted in the coaxial cavity of the plunger. During the normal mode, a distal portion of the needle holder is engaged within the nozzle by a taper lock. To switch from the normal mode to the retraction mode, the taper lock is disengaged by rotary movement of the plunger relative to the barrel.

Abstract: A catheter for use with a radioactive source within the catheter to irradiate a selected area of a blood vessel in combination with angioplasty procedures, to prevent restenosis of that area of the blood vessel. The catheter has a guidewire channel formed near its distal end to facilitate use of the catheter as a rapid exchange catheter, allowing insertion of the catheter over a guidewire also used in performance of an angioplasty procedure. The catheter can also have a guidewire channel formed near its proximal end to provide an O-ring sealing surface and to facilitate free guidewire movement. The catheter also has a closed end to retain the radioactive source within the catheter. The catheter can also be provided with a centering balloon or a set of centering wire loops to center the radioactive source radially within the blood vessel.

Abstract: A medical device having good surface lubricity in the wet condition, high frictional durability and surface lubricity stability comprises a body and a smoothing or lubricating coating on a surface of the body. The coating is produced by applying a solution of a mixture of maleic anhydride high polymer and polyurethane having allophanate bond on a surface of the body, insolubilizing the resultant coating by heating, and then hydrophilizing the coating with a hydrophilizing agent such as ammonia, amine or alcohol.

Abstract: The drug delivery stent assembly includes a hollow tubular wire stent which extends in a path defining a generally cylindrical envelope and which has side walls facing outwardly of the cylindrical envelope with holes therein for delivery of liquid to a site in a vessel where the stent is placed and the stent being constructed in a manner which permits the stent to be placed in one of two states, one state being where the stent assumes the shape of an enlarged generally cylindrical envelope and the other state being where the stent assumes the shape of a contracted smaller cylindrical envelope.

Abstract: In a needle-less injector combining an actuator and a medicament cartridge, the actuator includes a housing with a forward portion to which the cartridge is connected. An impact member is mounted within the housing inward of the forward portion so as to be movable toward the forward portion, where it may strike components of the cartridge to effect expulsion of a dose of medicament. A chamber is provided within the housing and is pre-filled with a pressurized gas which is in communication with and exerts a constant force on the impact member, tending to urge it towards the forward portion.

Abstract: This invention relates to improved wound dressings that are adapted to being readily sized to fit the shape of the wound so that healing is promoted. In particular, the present invention is directed to a scored spiral wound dressing. More particularly, this invention relates to a spiral wound dressing having superior absorption properties and which is capable of swelling in the presence of wound fluid to closely fit the wound.

Abstract: Disclosed is a syringe with a cap including a syringe main body (30) having a needle attached to the extreme end thereof and the cap (40) for covering the needle (20) of the syringe main body (30), wherein the cap (40) includes a cap securing portion (50) secured to the extreme end of the syringe main body (30) and a cap main body (70) pivotally coupled with the cap securing portion (50) through a hinge portion (60) and the cap main portion (70) includes an accommodating portion for accommodating the needle (20) and a cut-out portion (72) which communicates with the accommodating portion and into which the needle (20) can go in and from which the needle can be taken out, the syringe with cap comprising securing elements (52, 73, 80) capable of securing the cap to the cap securing portion (50) when the syringe is used.

Abstract: A flexible resilient breast pump insert (5) adapted to fit into the rigid funnel portion (1) of a vacuum generating breast pump operable to generate a negative pressure. The insert comprises a mouth portion (6) with an open end shaped to receive and contact the areola of a woman's breast and an inner portion (7) of reduced size to receive the woman's nipple. A lip (9) around the edge of the mouth portion allows it to be connected to the rigid breast pump funnel portion (1) to form a pressure tight seal therewith.

Abstract: The present invention relates to a puncture method and a puncture system. More specifically, the objective of the present invention is to carry out the aspiration of a sample from a human organ or an animal organ and the inner examination thereof, without the outward leak of the fluid and the like in the organ.The puncture method and puncture system of the present invention is in the following structure; making a parasol part arranged on a reservoir adhere through an adhesive to the site to be punctured, inserting a needle body through a sealing part of the reservoir into the site to be punctured to draw out the inner fluid, the leak of the fluid can be prevented by the reverse operation of the sealing part.