Abstract: A disposable cassette (1) for storing and delivering a medical drug, the cassette (1) comprising a cartridge (7) containing the medical drug, a waste reservoir (8) arranged to receive waste liquid and/or gas, an injection needle (9)arranged to deliver the medical drug, and a valve block (10) being movable between a first position and a second position. The first position establishes a fluid passage between the cartridge (7) and the waste reservoir (8), while preventing fluid flow from the cartridge (7) to the injection needle (9), and the second position establishes a fluid passage between the cartridge (7) and the injection needle (9), while preventing fluid flow from the cartridge (7) to the waste reservoir (8).

Abstract: An auto-injection syringe shaped similar to a credit card and having a biased injection mechanism operable to drive a needle into a user's body by a fixed distance to dispense a dose of fluid at a subcutaneous location. A safety may be provided to avoid undesired actuation of the injection mechanism. After the safety is bypassed, a trigger may be actuated by the user to allow operation of the injection mechanism. A reciprocating needle-cover resists casual view of the needle by the user during and after use of the syringe. A locking mechanism automatically holds the needle-cover at an extended position to isolate the needle from further contact and to resist re-use of the syringe.

Abstract: The priming method includes the steps of: in a state where a contrast agent bag containing a contrast agent is coupled to a second tube moving a second piston in a second syringe backward to introduce the contrast agent to the second syringe, and with a first tube kept open, moving the second piston in the second syringe forward to discharge air in the second syringe to the outside and to fill the first tube with contrast agent.

Abstract: A dosing device having a pumping device delivering at least one medium into a pumping channel running along a pumping axis, as well as an applicator having at least one application opening is known. According to the invention, the applicator has at least one flow channel linking the pumping channel with the application opening and which is oriented transversely to the pumping axis, while the application opening is positioned laterally on the applicator. Use for pharmaceutical applications.

Abstract: Various embodiments of the present invention are directed to limiting a presence of air bubbles in a fluidic medium expelled from a reservoir. In various embodiments, a reservoir is shaped so as to limit a presence of air bubbles in a fluidic medium expelled from the reservoir. Also, in various embodiments, a plunger head within a reservoir is shaped so as to limit a presence of air bubbles in a fluidic medium expelled from the reservoir. In some embodiments, both a reservoir and a plunger head within the reservoir are shaped so as to limit a presence of air bubbles in a fluidic medium expelled from the reservoir.

Abstract: The present disclosure relates to a self-venting cannula assembly. The self-venting cannula assembly including an outer tube that defines a throughbore, an inner tube, a vent aperture, and a filter element. The inner tube is positioned within the outer tube, which defines a vent channel therebetween. The vent aperture is formed in the outer tube to provide fluid communication between the vent channel and an external environment. The filter element is positioned over the vent aperture and prevents particles having a dimension greater than about 0.2 microns from passing therethrough.

Abstract: A method and pump that accurately senses air in a fluid delivery line pulses or activates and deactivates the air sensor(s) multiple times during the pumping phase of the fluid delivery cycle and can generate alarms based upon a single indication or a cumulative indication of air in the line. The pump can include multiple air sensors spaced along the delivery line so that the method can use the multiple signals therefrom to distinguish real moving air bubbles from false positives and/or air bubbles adhered to the inner wall of the line.

Abstract: A pellet loading apparatus has a pellet housing configured to receive and hold a plunger so that a cavity is formed by an interior surface of the pellet housing and the plunger. A pellet is located or formed in the cavity. A dispensing chamber housing is located in a disposable drug delivery device. The dispensing chamber housing is configured to couple with the pellet housing so that the plunger and the pellet can be loaded into the dispensing chamber housing.

Abstract: Apparatus and methods for inhibiting the introduction of air into the body during a percutaneous procedure. The apparatus may include an instrument passage lumen defining a degassing region with a degassing region distal end and a degassing region proximal end, a fluid inlet port at the degassing region distal end, and a fluid outlet port at the degassing region proximal end. So configured, fluid will flow only from the degassing region distal end to the degassing region proximal end.

Abstract: Various embodiments of the present invention are directed to limiting a presence of air bubbles in a fluidic medium expelled from a reservoir. In various embodiments, a plunger head within a reservoir is shaped so as to limit a presence of air bubbles in a fluidic medium expelled from the reservoir. Also, in various embodiments, a reservoir is shaped so as to limit a presence of air bubbles in a fluidic medium expelled from the reservoir. In some embodiments, both a reservoir and a plunger head within the reservoir are shaped so as to limit a presence of air bubbles in a fluidic medium expelled from the reservoir.

Abstract: A method and pump that accurately senses air in a fluid delivery line pulses or activates and deactivates the air sensor(s) multiple times during the pumping phase of the fluid delivery cycle and can generate alarms based upon a single indication or a cumulative indication of air in the line. The pump can include multiple air sensors spaced along the delivery line so that the method can use the multiple signals therefrom to distinguish real moving air bubbles from false positives and/or air bubbles adhered to the inner wall of the line.

Abstract: A syringe device includes a syringe tube having a distal end with a passageway in fluid communication with a cavity thereof. A plunger rod slidingly and sealingly engages within the cavity of the syringe tube. The plunger rod includes at least one aperture in fluid communication with a hollow interior of the plunger rod. A plunger tip is engaged with a distal end of the plunger rod and interacts with an inner surface of the side wall of the syringe tube to separate the cavity into first and second areas. The at least one aperture fluidly connects the hollow interior of the plunger rod and the first area of the syringe tube cavity, such that the generally hollow plunger rod interior allows air to move between an outside of the syringe device and the first area of the cavity during sliding movement of the plunger rod within the syringe tube.

Abstract: A bowel extension device implantable into a body for treatment of short bowel syndrome. The bowel extension device comprises a housing and a displaceable member coupled to the housing. The bowel extension device is configured to apply a tensile force sufficient to promote bowel growth without causing damage to the bowel. In some embodiments, the bowel extension device can be completely contained with the body.

Abstract: A catheter having a drug delivery unit at the distal end thereof. The drug delivery unit includes an actuator capable of assuming an activated and an inactivated configuration. The drug delivery unit also includes a receptacle capable of accepting a therapeutic agent. The actuator and receptacle are in communication with each other such that the actuator transmits force to the receptacle and the receptacle accepts force from the actuator in an activated configuration of the actuator. Also provided is a method of delivering a therapeutic agent to a target site using the catheter of the present invention.

Abstract: Apparatus and methods for inhibiting the introduction of air into the body during a percutaneous procedure.

Abstract: An administering apparatus having a casing including a reservoir for a product to be administered, a piston which can be shifted in the reservoir in an advancing direction towards a reservoir outlet to administer the product, a piston rod, a dosing and drive element for performing a dosing movement for selecting a product dose and a delivery movement for delivering the product dose, and a dose setting member which is moved in the advancing direction during the delivery movement, and which engages the piston rod and the casing such that it can only be moved in the advancing direction jointly with the piston rod and is moved counter to the advancing direction relative to the piston rod during the dosing movement.

Abstract: Medical devices and related methods enable physicians and/or other medical personnel to access percutaneously the interior of a patient. One particular device includes a housing which defines a cavity, a first opening into the cavity, and a second opening into the cavity. The housing is implantable in a patient. The cavity is placed subcutaneously within the patient. The first opening is substantially flush with the surface of the skin of the patient and creates a percutaneous passageway from the exterior of the skin of the patient into the cavity, and the second opening creates a passageway from the cavity into the interior of the patient. A connector is coupled to the second opening and disposed substantially within the cavity to enable a connection between a first device and a second device disposed within the interior of the patient.

Abstract: A syringe includes a body and a plunger disposed therein. The body includes a nozzle formed therein and at least one hub member connected thereto or integrally formed thereon for holding an end of a connector tube. The connector tube includes two ends, each end preferably being connected to a respective hub member to retain the connector tube in contact with the syringe. Preferably, the syringe and the connector tube are packaged in a pre-connected condition for ease of use by the customer. Furthermore, flexible inlet tubing for connection to a syringe for filling the syringe with contrast media, for example, is described. The inlet tubing permits filling of the syringe from either a bag or a bottle and may remain attached to the syringe so that it forms at least a part of the connection to the patient. In addition, an apparatus for facilitating the purge of air from a connector tube that will ultimately be connected between a syringe and a patient is described.

Abstract: A method of dispensing a hazardous pharmaceutical comprising the steps of: connecting a source of flushing fluid to a first port of a fluid delivery set; connecting a pressurizing unit of a powered injector system (including a powered injector and the pressurizing unit) to a second port of the fluid delivery set; purging air from the fluid delivery set; and, after purging air from the fluid delivery set, connecting a third port of the fluid delivery set to a source of the hazardous pharmaceutical. The fluid delivery set can, for example, include a valve system or assembly to control flow of fluid through the fluid delivery set.

Abstract: A mechanism and method for preventing premature activation of an action includes a safety device. The safety device includes a housing that is arranged to enable such an action when the housing is in a desired orientation (e.g., horizontal, vertical). The housing includes a bowl having a concave cavity, a ball located in the cavity and a trigger having an actuator and a sleeve arranged to slide about the ball when the ball is in a predetermined position of the cavity to move the actuator and initiate the action.

Abstract: The present invention is a single use injector device for injecting parenteral medications which operates by hand force. The injector device has a plunger section and a base. As hand force is applied to a moving portion of the plunger section, break tabs or a snap ring resist its motion toward the patient's skin surface. The break tabs or snap ring release abruptly as the hand force reaches a snap point. The motion of the moving portion then drives the medication through the skin surface and into the body of the patient. If the medication is in liquid form, the actual injection may be carried out through a hollow needle attached to the plunger section. Alternatively, the suddenly increased pressure of the medication at the snap point may be used to form a liquid jet for needleless injection. Part or all of the medication may be contained in a glass needle which dissolves in the body after injection. The injector device requires little training to use, reduces perceived pain, and improves injection safety.

Abstract: A closure for a medicament well (1) with a central closing luer-shaped body (2) and, if desired, a round body (2), and a luer-lock skirt extending substantially in parallel with the latter, comprises a void (4), which is provided in the upper end of closure (2) and defined against the outside by a flexible wall (5) on the upper side and on the other side is made to communicate with the outside, via a channel (6) extending through body (2).

Abstract: An improved medication administration system includes a series of one way valves disposed closely adjacent and in direct fluid communication with an auxiliary IV line leading to a patient. A plurality of syringes filled with various selected medications are each secured in a tray against axial and lateral movement by depressing them into correspondingly dimensioned longitudinal grooves. The flanges of the syringes abut a lip of the tray to further restrict axial movement. The nozzles of the syringes are connected to the inlets of the valves so that medication can be adminstered intravenously by simply depressing the appropriate syringe plunger. The tray is surrounded by a supporting outer box which includes retractable clamps for fastening the tray to an operating table. A second similarly shaped box is adapted to be clipped to the first box or clamped to the table. The second box can contain miscellaneous medical equipment.