Abstract: Embodiments of a catheter insertion device are discussed comprising: an approximately hollow cylindrical catheter sleeve, at whose distal end a catheter is attached: a needle sleeve with a hollow needle, which is attached thereto and which, when ready for use, extends through the catheter sleeve and the catheter, and; a needle protective element that is arranged inside the catheter sleeve while being able to move on the needle. Said needle protective element has an engaging section that engages with an engaging device, which is formed in the vicinity of the needle tip, when the hollow needle is withdrawn from the catheter sleeve. A check valve is placed inside the catheter sleeve between the catheter and the needle protective element. The hollow needle, when ready for use, extends through said check valve, and the check valve automatically closes once the needle is withdrawn.

Abstract: A retractable catheter for use in an implant delivery system, the catheter including an elongate tubular sheath made of a relatively flexible material, and a pull element for transmitting a pull force to the sheath to retract it longitudinally. The pull element includes an end portion disposed in the relatively flexible material, at least the thickness of the end portion being substantially less than its length.

Abstract: We describe a method and apparatus for monitoring the dripping speed in IV process, as well as detecting the its end. The apparatus includes a camera and a processing unit to analyze the information from the acquired video. Features from the image sequence are extracted and the dripping speed is computed accordingly by discrete Fourier transform. The apparatus is also capable of detecting the end of the dripping process by finding the location of liquid surface in the drip chamber. We also describe the use of barcode to provide information to the monitoring device and program.

Abstract: An auto-injector confines all functional components inside an enclosed housing, to keep its needle out-of-sight, at all times. Within the housing, a needle holder positions a needle at a location. A drive mechanism then simultaneously engages the needle with a fluid source and accelerates it with a predetermined momentum for insertion into a patient. After fluid delivery, the withdrawn needle is moved to storage within the housing for subsequent disposal.

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: The invention provides for an integrated device for forming a cavity in a surface of a tissue of an animal comprising: a) a controller board connected to an energy source for actuating at least one porator; b) a fluid reservoir in fluid communication with the tissue; and c) a tissue interface layer, the tissue interface layer containing the at least one porator, the porator in contact with the tissue for forming the cavity. The invention also provides for methods of making and methods of using the same.

Abstract: An apparatus having a tube section and an expanded end. The tube section is flexible while the end section is rigid. The apparatus has a central bore, large enough to loosely receive an endoscope tube, and the end section has two peripheral bores which communicate with the central bore. There is a collar around the central bore which allows formation an air- and water-tight seal with the head of an endoscope. The tube may be fenestrated at its proximal end and may include medial pleats. This apparatus is mainly used by: sliding an endoscope into the central bore until the endoscope head forms an air- and water-tight seal with the central bore; connecting a lavage tube to one peripheral bore and a vacuum tube to the other peripheral bore; inserting the endoscope and the apparatus into a GI tract; and manually controlling the apparatus to apply lavage and vacuum.

Abstract: A device for injection, comprising a body (1) provided with a first channel (2) for conveyance of a first medical substance and a first connecting component (3) having a first port (4) for introduction of a first medical substance into said first channel (2), the connecting component (3) being connectable to an external unit, and a second channel (5) for conveyance of a second medical substance and a second connecting component (6) having a second port (7) which can be opened by means of an injection component for injecting a second medical substance into said second channel (5), and provided with a third connecting component (8) being common to the first and the second channels (2, 5) and having at least one third port (9) for conveying medical substances out from said first (2) and second (5) channels, the first (3), second (6) and third (8) connecting components and the body (1) being designed as an integrated unit.

Abstract: Disclosed is a therapeutic fluid reservoir to be used with an ambulatory portable infusion device. The reservoir includes a pliable shell defining a varying inner volume that varies based on the volume of therapeutic fluid held inside the reservoir, the varying inner volume having a predetermined maximum volume for containing a corresponding volume of therapeutic fluid and an outlet port for communicating fluid from the reservoir to a patient, the varying inner volume decreasing upon therapeutic fluid being communicated through the outlet port. Upon the reservoir reaching the predetermined maximum volume when being filled with therapeutic fluid, any therapeutic fluid in excess of the predetermined maximum volume driven into the reservoir causes a substantially corresponding amount of therapeutic fluid to exit out of the reservoir via the outlet port and/or at least one other port provided in the pliable shell.

Abstract: A device and method for administering a bioactive agent to internal tissue in a body, by introducing a balloon in a deflated condition into the body, inflating the balloon, introducing the bioactive agent into the balloon at the time of, after, or before the inflation of the balloon, and delivering the bioactive agent from the balloon to the tissue.

Abstract: A percutaneous gastrostomy catheter includes an internal retainer configured to be maintained pressed against the stomach wall and to disengage itself from a tubing by biodegradation; and an external flange, traversed by the tubing, configured to be pressed against an external face of the abdominal wall and exert, in cooperation with the internal retainer, a pressure adapted to press an external face of the stomach wall against an internal face of the abdominal wall. The internal retainer includes an internal flange. A first face of the internal flange is configured to be pressed against an internal face of the stomach wall, the internal flange being detachable from the tubing under the effect of a simple pulling force. The internal retainer also includes an end piece pressed against the second face of the internal flange, such that the internal flange is between the end piece and the external flange, the end piece being made of a completely biodegradable copolymer or polymer having a bond with the tubing.

Abstract: A method for rounding at least a part of an edge of an opening in a tubular body formed of thermo-formable material, wherein a mandrel is brought into contact with the edge and the mandrel has a temperature that allows it to permanently deform the material of the tubular body and a product thereof.

Abstract: The magnetically sealed intravenous access valve is an implantable port and valve for vascular access. The magnetically sealed intravenous access valve includes a housing and a pair of hollow tubes provided for interconnection and communication with the patient's blood vessel. Each tube is partially slidably received within a lower portion of the housing. A hollow key is used to selectively open and close the valve and also to inject medication into the patient's blood vessel. The hollow key is removably received within channels formed through a retainer and a rotatable obturator so that the lower end of the hollow key releasably engages the obturator. Selective rotation thereof allows eccentric spout formed in the obturator to align with an eccentric aperture formed in a valve plate. Fluids flow through the hollow key, the aligned spout and plate opening, the lower portion of the housing, and the opposing tubes for fluid transfer.

Abstract: System and method for tridimensional cartography of a structural surface. Two wires are extended in front and along the structural surface so as to define a reference surface. A measuring unit comprising a laser arrangement and a camera is moved in front of the structural surface so as to progressively scan the surface. Tow distinct light planes directed toward the structural surface are projected by means of the laser arrangement. Images of the structural surface containing lines resulting from an intersection of the light planes with the structural surface and four reference points resulting from an intersection of the light planes with the wires are captured by means of the camera. The images are processed to determine the 3D coordinates of the lines defining the mapping in a reference system bound to the reference surface considering the position and the orientation of the measuring unit based on the reference points.

Abstract: The extensible intravenous (“i.v.”) drip line tubing uses a helical accordion support structure on which the i.v. tubing is attached. The helical accordion backbone has some tendency to spring back, but this is not relied upon to extend and return the i.v. tubing it carries. The carrier structure keeps the i.v. tubing from getting tangle or kinked. A centrally located retractable line, which is located within the center of the helical accordion structure, acts as the retracting mechanism, as it tends to allow the accordion structure to be pulled into an extended position, while upon rewinding the central cord, the helical accordion support structure can be pushed toward a collapsed position without the i.v. drip line tubing becoming tanked, kinked, and thereby blocked. As a safety feature, so the i.v. line does not encounter and strain between it and the point of entry of the i.v. line into the patient, is one or more wrist and or armbands to which the i.v. carrier is attached by a short, strong line.

Abstract: A support apparatus connects with and provides fluid communication between a needle and a syringe. The support apparatus includes at least one arm that is configured to provide cantilever support of the needle and syringe while the needle is inserted in a patient. The arm engages the patient's skin, and may be rigid, malleable, hinged, stretchable, telescoping, and/or have other properties. The support apparatus may form part of an adapter that also includes a pressure sensor. The pressure sensor senses the pressure of fluid in a gastric band system when the needle is inserted in an injection port of the gastric band system. A cable may extend from the pressure sensor to a display device, and may include markings configured to provide measurement from the needle to a patient's xyphoid process. Such a measurement may be factored into a calculation to account for hydrostatic pressure differences in pressure readings.

Abstract: A miniaturized Holographic Fourier transform imaging spectrometer HFTIS, made from simple all-reflective components and with no moving parts, is provided. This HFTIS includes an all-reflective two beam interferometer, which provides two interfering beams; a two-dimensional detector array to detect the interference pattern created by the beams; a computing machine for correcting the distortions in the pattern and calculating the spectrum from the corrected interferogram. The same principle can be used to build spot spectrometers, line-scan imaging spectrometers (also called array spectrometers or line-scan hyperspectral cameras) as well as two-dimensional instantaneous imaging spectrometers (also called staring hyperspectral cameras). In all variants of HFTIS that can be built using this invention, the wave-signal collecting element can also be built of all-reflective components.

Abstract: Provided is to enhance the therapeutic effect of an iontophoretic preparation for treatment of breast cancer or mastitis. An iontophoretic preparation for treatment of breast cancer and/or mastitis containing, as an active ingredient, a nonsteroidal anti-inflammatory analgesic agent and/or an anticancer agent, wherein an electrolyte is topically administered through the nipple part into the mammary gland; subsequently, a donor is applied to the nipple part; and the active ingredient is topically administered through the nipple part into the mammary gland by application of current.

Abstract: A system for efficient drainage of a body cavity includes application of vacuum at very high pressure, preferably in the range of approximately 50-500 torr or higher. The system includes the use of a drainage tube having a plurality of holes formed into the wall of a portion of the tube to be inserted in the body cavity. The area of each of the holes is preferably selected to ensure that the suction force communicated by each of the holes to areas within the body cavity is insufficient to injure the tissues exposed in the body cavity. A one-way valve maintains unidirectional flow of drained fluids and gases away from the body cavity. A vacuum relief valve prevents application of dangerous levels of vacuum pressure by opening to admit atmospheric air when vacuum pressure exceeds a predetermined threshold. A vacuum chamber separates drained fluids from drained gases.

Abstract: A tissue stimulating device that provides a biological stimulation of tissue has a release surface adapted for arrangement adjacent to a tissue to be stimulated. An agent reservoir of the device includes an ionic agent capable of causing a stimulation if present at sufficient high extracellular concentration close to the tissue. An agent releaser is provided in the device for releasing a selected amount of the ionic agent from the agent reservoir to an outside of the release surface at a stimulation occasion for stimulating the tissue. The ionic agent will cause a temporary change in ion permeability of the tissue cell membranes and a depolarization of the tissue cells.