Abstract: The invention relates to an adapter element for fastening a needle element to a syringe base body, the adapter element having a base body which is configured and provided for receiving the needle element, the base body having at least one through-opening for passing the needle element through and for fixing it, and the base body being configured and provided for being fastened to the syringe base body.

Abstract: Provided is a method performing vascular surgery utilizing a guiding apparatus that includes an adaptor and an introducer, by inserting a longitudinal section of the adaptor into the introducer and operating a valve of the introducer by moving a cursor provided on a side wall of the introducer within a travel region of the cursor. Operating the valve either fixedly attaches or releases the longitudinal section of the adaptor within or from the introducer. The adaptor includes an inner volume that encloses a plurality of ducts and the introducer includes an inner volume that aligns with the inner volume of the adaptor when the valve is fixedly attached the longitudinal section of the adaptor within the introducer, thereby providing ducts that allow an instrument to pass entirely through both the adaptor and the introducer.

Abstract: An apparatus for discharging a dose of a fluid substance to an animal, the apparatus including: a delivery assembly adapted to discharge the dose of the substance to the animal; and a control system operatively associated with the delivery assembly so as to selectively operate the delivery assembly, wherein the control system is adapted to measure the discharge of the fluid substance from the delivery assembly such that the dose is discharged when the delivery assembly is operated.

Abstract: Gas-powered fluid injection systems and methods are disclosed, e.g., for delivering fluids into a patient's body. An injection device comprises a driver housing which forms and/or encloses a gas pressure source, an actuation piston driven by the gas pressure source and a hydraulic fluid pressurized by movement of the actuation piston. The hydraulic fluid flows through an adjustable valve into a plunger lumen which pushes a plunger of a fluid dispensing device, such as a syringe, to dispense an injection fluid, such as a medicament. The injection device has a movable plunger sleeve which receives the plunger of the fluid dispensing device. The plunger sleeve is moved during the activation and de-activation of the injection device such that it relieves residual pressure in the fluid dispensing device thereby preventing the fluid dispensing device from continuing to dispense injection fluid after the injection device has been de-actuated.

Abstract: The application relates to an infusion part comprising a cannula part (7) and a fluid path, whereby a sealing (18) is positioned between the cannula part and an inlet/outlet opening (12) of the fluid path when the cannula part is in position for use in order to keep the fluid path to a cannula tight. The sealing (18) is surrounding the inlet/outlet opening (12) and/ or the distance d1 between a centre line c of the cannula part and a point on an outer surface of the cannula part positioned at or above an upper edge of the sealing (18) is larger than the distance d2 between the centre line c of the cannula part and a point on the outer surface of the cannula part positioned at or below a lower edge of the sealing.

Abstract: A catheter system and method of introducing an intravenous catheter into a patient includes a syringe, an access needle, a pliable catheter, and a guidewire. The syringe has a first chamber and a distal syringe end portion, which defines a conduit distally extending to a distal syringe opening such that the conduit fluidly connects the first chamber to the distal syringe opening. The access needle defines a needle lumen longitudinally extending therethrough and is secured relative to the distal syringe end portion. The pliable catheter is releasably secured relative to the access needle. The guidewire distally extends through the conduit toward the distal syringe opening and is configured to selectively move through the conduit, the distal syringe opening, and along the needle lumen to thereby guide movement of the pliable catheter relative to the access needle for introducing the pliable catheter into the patient.

Abstract: A fluid injector having at least one injector head with a front end configured to releasably receive the at least one syringe is described. The fluid injector further includes at least one pressure jacket releasably associated with the front end of the at least one injector head for securing the at least one syringe during an injection procedure. A connection mechanism releasably connects the at least one pressure jacket to the front end of the at least one injector head. The connection mechanism includes at least one electromagnet.

Abstract: A wearable liquid supplying device for human insulin injection is fixed on a body of human through a ring belt and includes a substrate, a flow-guiding-and-actuating unit, a sensor and a driving chip. The substrate has a liquid storage chamber. The flow-guiding-and-actuating unit has a liquid guiding channel in communication with a liquid storage outlet of the liquid storage chamber and a liquid guiding outlet. The sensor measures a blood glucose level and generates measured data correspondingly. The driving chip receives the measured data from the sensor and controls the actuation of the flow-guiding-and-actuating unit and the open/closed states of the switching valves. The flow-guiding-and-actuating unit is enabled to generate a pressure difference so that the insulin liquid is transported to the liquid guiding outlet through the liquid guiding channel and flows into the microneedle patch for allowing the microneedles to inject the insulin liquid into the subcutaneous tissue.

Abstract: An interventional catheter assembly comprising a catheter for insertion and guidance to a target site in a body lumen or a cavity and an operating head mounted in proximity to a distal end of the catheter and comprising a system for removing obstructive material from the target site is provided. In certain embodiments, the catheter assembly includes at least one aspiration port located proximal to the operating head that communicates with a first sealed lumen for withdrawing fluids and obstructive material from the target site. The catheter assembly may also include at least one liquid infusion port that communicates with a second sealed lumen for supplying fluid to a location in proximity to the target site. Kits including the interventional catheter assembly with an aspiration and/or infusion conduit are also provided.

Abstract: A device and use thereof for supply of gas to an operational space configured to adjoin a temporarily open inner portion of a mammal during surgical operations. The device includes a supply conduit, connectable to the gas source including an outlet end, and a body having at least partly an annular shape extending along a circumferential path around centre axis enclosing the operational space. The body has an inner side, outer side, an open interior channel, and an opening allowing the gas to enter the body from the supply conduit. The body is manufactured in foam rubber-like material having large number of open cells functioning as supply nozzles permitting the supply of a substantially laminar, continuous gas stream into the operational space enabling the formation of a gas cushion in the operational space.

Abstract: The present disclosure relates to administration of fluid medication, in particular medication and dosing regimen for management of pain, more specifically to an anesthetic and dosing regimen for anesthetic for perioperative pain management and/or for palliative care. The present disclosure relates further to a medication pump and a method for delivering medication using the medication pump.

Abstract: A syringe calibrated for use with a predetermined medication and including a barrel, a plunger received through an end of the barrel and movable relative thereto, a tip disposed at one end of barrel and configured to be affixed to a device compatible for use with the syringe, a dosage schedule of the predetermined medication marked on the syringe and expressed as a ratio of a patient characteristic to a dosing unit of measurement, a first set of dosing indicia marked on the syringe and expressed as the predetermined patient characteristic, and a second set of dosing indicia marked on the syringe and expressed as the dosing unit of measurement.

Abstract: The breakaway assembly includes a first breakaway subassembly and a second breakaway subassembly. The subassemblies are configured to connect, which causes bellows sheaths in each subassembly to compress and open pores, allowing fluid to flow through the subassemblies. The subassemblies can be connected to luer tip. The luer tips can be connected to an intravenous (IV) fluid line or other types of lines used in the medical field to move fluids. This allows the movement of fluid from a fluid-holding component to a patient. Unless the subassemblies are locked together, the subassemblies will be disconnected under the correct amount of pressure. This disconnection closes the pores on the subassemblies, which keeps fluid from leaking, and prevents the contamination of the IV line. Luer tips may also be connected to the subassemblies. Some of the luer tips allow for the quick connection of the luer tip to the subassembly through a flange being inserted into a notch or flange acceptor.

Abstract: Certain embodiments provide multi-medicament infusion systems for preventing the cross-channeling of medicaments. The system may include one or more of an infusion pump, medicament reservoirs, a multi-channel fluid conduit, and an infusion set. The medicament reservoirs and/or collars may be sized and shaped differently such that the medicament reservoirs can only be inserted into the system under selected configurations.

Abstract: A fluid dispensing device is provided for dispensing a measured amount of fluid into a living organism. The device includes a rigid fluid reservoir closed by a septum for use in a fluid dispensing device for dispensing a measured amount of fluid into a living organism, wherein the device has a main housing enclosing the operative components of the device, the said fluid reservoir located within the main housing, an injection assembly including a needle, and a trigger mechanism. The needle has a first end adapted to piercing the septum and pushing the septum into the reservoir so that the septum acts as a piston, expelling the fluid through the needle, and a second end adapted to injecting the fluid into the living organism.

Abstract: A flow control apparatus and method for accurate detection of occlusion conditions in a feeding set. A sensor is arranged with respect to a pumping device to produce a signal indicative of pressure in the feeding set. A control circuit that may receive the sensor signal from the sensor indicative of the pressure in the feeding set may also control operation of the pumping device. The control circuit is configured to operate the pumping device in an operational state, and in a reset state subsequent to the operational state in which the pumping device does not produce a pumping action and the pumping device is moved to a position in which the pumping device does not block the feeding set to permit fluid flow in a backflow direction opposite to the patient direction thereby relieving any built up pressure in the feeding set downstream of the pumping device.

Abstract: Embodiments described herein relate generally to medical implant delivery apparatuses and methods. In some embodiments, an apparatus comprises a first cap, a needle hub at least partially disposed within the first cap, a pusher wire and a pusher wire connector disposed within the needle hub, a needle and a second cap. The first cap includes a proximal end, a distal end, and a longitudinal axis. The needle includes a first, beveled end configured to receive an implant, and a second end disposed within a hub pocket of the needle hub. The second cap is connected to the needle hub and disposed at a proximal end of the first cap. The pusher wire, the pusher wire connector, and the needle are substantially aligned with one another along the longitudinal axis of the first cap. In some embodiments, the pusher wire is sized to be received in the bore of the needle.

Abstract: An intelligent bioelectric module for use with a drug delivery system has a case and a set of at least two electrodes in electrical communication with a detection surface of the case. The case is configured so that, in use, the detection surface comes into electrical communication with (i) a second surface of the delivery system when a first surface of the delivery system has been put into contact with a tissue surface of a human or animal subject or (ii) the tissue surface that is adjacent to a portion contacted by the first surface of the delivery system or (iii) both the second surface and the tissue surface.

Abstract: A method, including ejecting irrigation fluid from a distal end of a probe so as to irrigate tissue, and receiving, over a period of time, initial signals indicative of respective temperatures of the distal end, from a temperature sensor in the distal end. The method also includes formulating from the initial signals a temperature range between upper and lower temperature thresholds and, when a further signal from the temperature sensor, received subsequent to the period of time, is indicative of a further temperature above the upper temperature threshold, raising an alarm that a bubble is present in the irrigation fluid.

Abstract: An injection device comprising: a housing arranged to contain a liquid medicament or a medicament cartridge; an electrical coil arranged around an inner surface or an outer surface of the housing; an electricity storage apparatus electrically connected to the electrical coil; and a magnet arranged to be movable axially within a defined space with respect to the electrical coil, such that electrical voltage is induced in the electrical coil and a current is generated to charge the electricity storage apparatus.