Abstract: A child-proof discharger for media includes a reservoir, a pump part mounted on the reservoir and an actuable discharge portion mounted on the pump part. The discharge portion guided in an axially displaceable manner on a carrier part disposed on the closure element and can be locked with the aid of manually actuable spring bars. The spring bars are configured on an actuating plate configured on the discharge portion, and respectively have an inner tongue, which can be bent radially inwards relative to an inner wall of the carrier part. Each spring bar is respectively assigned a guide ramp as an entry curve to a contact area that is bounded by radial latches of the blocking setting upon a rotary motion of the discharge portion.

Abstract: A movable protection and/or rewrapping device for a balloon catheter may include a tubular member with a bore extending along a length thereof. The tubular member may have at least one rib disposed on an inner surface of the bore. The tubular member may be flared away from the bore at one end and inwardly tapered at the other end. The rewrapping device may include an actuator configured to open a longitudinal slit in the tubular member.

Abstract: Various embodiments of an antimicrobial stopcock medical connector is provided. More specifically, the present invention relates to a stopcock tap having fluid channels provided on portions of the outer surface of the stopcock tap, whereby fluid bypasses the stopcock through the fluid channels by flowing between the outer surface of the stopcock tap and the inner surface of the stopcock housing. Some embodiments further comprise an antimicrobial coating or insert that is provided in the one or more fluid channel, whereby fluid flowing through the fluid channels contacts the antimicrobial coating or an antimicrobial agent that is eluted from the antimicrobial coating. Further still, some embodiments of the present invention comprise an antimicrobial groove that is positioned opposite the fluid channel, whereby when the stopcock is in an “off” position, the antimicrobial groove contacts fluid within a blocked port thereby preventing microbial growth therein.

Abstract: A method for loading a guidewire into a connector using a guidewire introducer includes inserting a guidewire introducer into a proximal end of a connector, the guidewire introducer having a proximal end, a distal end and a slit along the length of the guidewire introducer between the proximal end and the distal end. The guidewire introducer is advanced past a valve in the proximal end of the connector. A distal end of a guidewire is inserted into the proximal end of the guidewire introducer and advanced through the guidewire introducer and through the y-connector. The guidewire introducer is removed from the connector so that the distal end of the guidewire introducer is outside of the y-connector and proximate to the proximal end of the connector. The guidewire introducer is removed from the guidewire using the slit in the guidewire introducer.

Abstract: An apparatus for performing a medical procedure includes a balloon with a variable profile. The balloon includes at least one inflatable chamber occupied by a fluid, such as air, and solids, such as generally spherical balls. When the chamber is inflated, the solids are spaced apart as a result of their ability to move or flow, but when the chamber is evacuated, the solids become compacted and prevent it from fully collapsing. The balloon may have a plurality of inflatable chambers with solids in different arrangements to achieve different objectives during the medical procedure, such as for example stent deployment. For example, one chamber may be expanded while the other is restrained to alter the balloon geometry, such as for providing focused force or permitting perfusion.

Abstract: Various systems and methods provide iontophoretic delivery of anesthesia at a patient's tympanic membrane. Some implementations provide channel switching enabling a single current sink to pull current through two electrodes in an alternating fashion based on clock pulses. The iontophoretic delivery of anesthesia may be driven by an AC modulated current. Some implementations provide for continuous flow of fresh iontophoresis fluid to the ear canal during iontophoresis. The fluid flows from a source reservoir into the cavity between the tympanic membrane and a plug, and then drains out of the cavity to a reservoir. An iontophoresis system may also detect capacitance between an anode electrode and an auxiliary electrode in a patient's ear canal, watching for reduced capacitance to indicate presence of a bubble in the iontophoresis fluid.

Abstract: The processes for inserting fluid under the skin of a patient using a safety syringe assembly include initially locating an up-alignment marker. The marker is aligned with a bevel in the needle of the safety syringe assembly so the orientation of the needle bevel is always known by the medical professional, even when the needle bevel cannot be seen. The needle is inserted bevel up prior to insertion. Once inserted, the medical professional inverts the safety syringe assembly so that the bevel is down. This is done by merely flicking the wrist of the hand holding the safety syringe assembly. This prevents splash back of any body fluids from the patient to the medical professional. The same safety syringe assembly and the same process are used for withdrawing fluids from the body of the patient.

Abstract: A needle tube having a needle tip for puncturing skin; a needle hub; and a fluid-draining portion for enabling draining of a medicine. The needle hub includes: a retention part (first member) for retaining the needle tube; an insertion part into which the output portion of a syringe is inserted; and a flange-like skin contact portion that is disposed in a manner so as to cover an area surrounding the needle tube and makes contact with and/or faces the skin when a living body is punctured with the needle tube. The fluid-draining portion is disposed in the skin contact portion of the needle hub and enables a user to drain the medicine that has spilled when removing air and is held in the skin contact portion.

Abstract: A medical connector includes: a body member that partitions a flow path between a proximal side opening and a distal side opening; and a male connector connection portion including: a valve body facing the flow path, and a male connector connection port openable and closable by the valve body. The body member comprises a male connector housing portion configured to house a distal end portion of a male connector connected to the male connector connection portion. The male connector housing portion is configured to cause the male connector to communicate with the distal side opening and to prevent inflow of a fluid from the proximal side opening to the male connector housing portion by connection of the male connector to the male connector connection portion.

Abstract: A method and apparatus are provided for use in locating a target region which is situated in the body of a subject, for example for the delivery of drugs. The system includes an assembly for controlling the flow of fluid from a fluid reservoir to a conduit, such as a needle. A sensor detects a characteristic indicative of the fluid pressure in the conduit. The system processes data from the sensor to detect the presence of a pulsatile waveform. A controller may control further operation of the system based on information regarding the presence of the pulsatile waveform and features of the waveform, such as amplitude.

Abstract: In some examples, a fluid delivery device is described. The fluid deliver device includes a housing; a reservoir disposed within the housing, the fluid reservoir defining a fluid outlet at a first end of the fluid reservoir; a plunger assembly disposed within the fluid reservoir, the plunger assembly including a friction clutch; and a seal engaged with an interior surface of the fluid reservoir to prevent movement of a material within the fluid reservoir past the seal; and a motive element in communication with a first end of the plunger assembly and configured to apply a motive force on the first end of the plunger assembly towards the first end of the fluid reservoir, wherein the friction clutch is configured to apply a frictional force to the interior surface of the fluid reservoir to resist the motive force, and wherein operation of the friction clutch enables motive force to overcome the frictional force to allow the plunger assembly to translate towards the first end of the fluid reservoir.

Abstract: A syringe assembly for use as a pre-filled syringe is disclosed. The syringe assembly includes a syringe barrel defining a chamber and having a stopper disposed therein. A plunger rod includes an inner member engaged with a portion of the stopper and an outer member adapted for rotational advancement with respect to the inner member to axially displace the outer member with respect to the inner member. The plunger rod is transitionable from a collapsed position in which a portion of the inner member is nested within the outer member, to an extended position in which the same portion of the inner member extends outside the outer member. The inner member includes a radial extension and the outer member defines a helical track adapted to receive the radial extension therein.

Abstract: A syringe assembly including a syringe barrel defining a chamber having a stopper therein is disclosed. The syringe assembly includes a plunger rod associated with the stopper, the plunger rod includes an outer sleeve having a distal end interconnected to the stopper and a sidewall portion defining an opening therein. The plunder rod also includes an inner sleeve disposed within the outer sleeve including a longitudinally extending track in alignment with the opening in the outer sleeve. The inner sleeve is adapted for telescopic movement with respect to the outer sleeve. The plunger rod also includes a spring mounted in association with the inner sleeve. The syringe assembly further includes a holding mechanism associated with the plunger rod and configured for cooperation with the inner and outer sleeves. Relative movement between the inner and outer sleeves causes the plunger rod to transition from a collapsed position to an extended position.

Abstract: Embodiments of the invention described herein include low cost infusion devices having basal and/or bolus fluid delivery options. Embodiments of the device include a housing, a reservoir to contain the fluid, a source of pressure to exert a force to expel the fluid contained in the reservoir, a bolus port adapted to receive an optional extra dose of fluid, and a cannula in fluid communication with the reservoir and the bolus port. The cannula is adapted for insertion into the user's skin for delivery of the fluid to the user's body. The device can provide a continuous delivery of the fluid along a first fluid flow path from the reservoir to the cannula and the optional extra dose of fluid along a second fluid flow path from the bolus port to the cannula.

Abstract: An infusion device (1) for administering a medical fluid to a patient (P) comprises a pumping mechanism (11) for exerting a force onto a delivery set (2, 3) for delivering a medical fluid from the delivery set towards a patient (P), a sensor device (14) for measuring the force exerted on the delivery set (2, 3) by the pumping mechanism (11), the sensor device (14) being constituted to output a sensor signal indicative of the force exerted onto the delivery set (2, 3), and a processor device (15) for controlling operation of the infusion device (1). Herein, the processor device (15) is constituted to perform a diagnosis routine during which a sensor signal of the sensor device (14) is obtained and compared to an expected sensor signal, to allow for detecting a drift in the sensor signal of the sensor device (14).

Abstract: A balloon catheter includes an elongated catheter shaft, an expandable balloon connected to the elongated catheter shaft, and a sheath that defines a lumen and includes a therapeutic agent disposed within the lumen. The balloon catheter further includes a first configuration and a second configuration. When in the first configuration, the expandable balloon is disposed distally from the sheath such that an outer surface of the expandable balloon does not contact the lumen. Further, when in the second configuration, at least a portion of the outer surface of the expandable balloon is disposed within the lumen of the sheath such that it contacts the therapeutic agent. At least a portion of the therapeutic agent that contacts the outer surface of the expandable balloon is transferred from the lumen of the sheath to the outer surface of the expandable balloon when the balloon catheter is in the second configuration.

Abstract: An injection device is presented having a housing, a container holder, a first and a second energy accumulating member arranged in the interior of the housing adapted to accumulate and store energy, a sleeve, a plunger holder operationally associated with said first energy accumulating member such that the plunger holder and the container holder are axially moveable in relation to the housing a predetermined distance towards the proximal end of the injection device from an initial position to a position following needle penetration, and a plunger rod being operationally associated with said second energy accumulating member such that the plunger rod is axially moveable in relation to the container holder, wherein in the initial position movement of the plunger holder is substantially inhibited by at least one first biasable member that recoils when being overlapped by an opening and/or recess of the sleeve such that the plunger holder is released.

Abstract: A syringe protecting device equipped with an outer cylinder, an inner cylinder and a spring, wherein, when the spring is released from its compressed state, the inner cylinder is moved rearward with respect to the outer cylinder so that a syringe needle is stored inside the outer cylinder, and the syringe protecting device further equipped with a releasable pre-locking mechanism for fixing the inner cylinder to the outer cylinder while maintaining the spring in the compressed state in the front-rear direction, wherein, the pre-locking mechanism fixes the inner cylinder before movement to the outer cylinder by engaging the protruding sections of the ring with the engaging sections of the through groove sections.

Abstract: A valve connector for infusion medical lines includes an outer tubular body, an inner hollow spike and an intermediate sealing member formed by an elastic hollow element including a head with a pre-slit normally closed. The elastic hollow element has a base part substantially generally barrel-shaped and a wall having a differentiated radial thickness.

Abstract: The present application regards examples of a fluid delivery device including a spike including a base end and a pointed end, an inlet opening located along the shaft of the spike between the base end and the pointed end, and an outlet opening located on the pointed end. In an example, the fluid delivery device includes an inner flexible layer, wherein the base end of the spike is attached to the inner flexible layer. The fluid delivery device includes an outer flexible layer, wherein the spike punctures the outer flexible layer in response to the inner flexible layer moving towards the outer flexible layer in response to inflation of a volume of space enclosed by the inner flexible layer.