Abstract: A packaging device for packaging a fluid dispenser (200), said dispenser comprising at least one reservoir (210) containing fluid, and a dispenser unit (220) that is actuated manually so as to dispense said fluid, said packaging device comprising a casing (100) that is provided with a base body (110) and with a cover (120) that is separable from said base body (110), starting from a closed position in which said dispenser (200) is packaged in said casing (100) and going to an open position in which said dispenser (200) may be removed from said casing (100), said casing (100) including at least one projection (130) that is adapted to co-operate with said dispenser (200) at least in the closed position of the cover (120), so as to block said dispenser unit (220) and prevent it from being actuated.

Abstract: A syringe includes a barrel and a rotatable element on the barrel; for example at a proximal location along the length of the barrel. The rotatable element rotates at least partially around the barrel. When a handle is associated with the rotatable element, the barrel may rotate as the handle his held substantially stationary or the handle may be rotated while the barrel and any peripheral device secured thereto remain substantially stationary. When handles are associated with a rotatable element that may be removed from a barrel, a barrel that is disassembled from the rotatable element may be replaced with another barrel of the same or a different configuration. Methods of using a syringe with a rotatable element on a barrel thereof are also disclosed.

Abstract: Methods and systems for an improved feedback milk extraction system are described. According to aspects, the system may communicate with various electronic devices and/or server components to exchange data and perform certain functionalities. The functionalities may include providing visual and audio feedback to a user, supporting unique kit identification as well as associated user profiles and preferred configuration settings, detecting and responding to leaks having various sizes during operation of the breastpump, controlling operation of the breastpump in response to detected leaks and the detected type and/or magnitude of the leak, preemptively contacting customers if a fault condition is detected or imminent, enabling effective labeling of collection containers, and determining volume and flow of expressed breastmilk.

Abstract: An implantable device for releasing one or more substances into a body cavity such as a urinary bladder, is provided. The device includes an inner balloon located within an outer balloon so as to define a lumen between the outer and inner balloons. A first valve is used for filling the lumen; and a second valve is used for filling the inner balloon. The device is delivered to the body using a delivery catheter. The inner portion is filled with the substance or substances to be released into the body cavity. The outer balloon is filled with a substance that is chosen to impart a desired specific gravity to the device. The substances to be released may be contained in particles coated with a soluble coating. The particles may be in suspension or embedded in a matrix.

Abstract: A medical device system is provided herein which has an elongated, flexible hollow member with an expandable infusion segment attached at the most distal end of the device. The device has a plurality of fluid infusion ports on the expandable infusion segment for delivering an intended fluid to a target site in a body lumen. Additionally, a method is provided herein for infusing an intended fluid to a target site within a body lumen.

Abstract: An improved injection port for implantation within a patient having an x-ray discernable marker allowing for the determination of a pressure rating for the injection port when so implanted.

Abstract: A safety insulin pen needle, including a needle hub, a needle tube assembly base arranged on the needle hub, a needle tube, a trigger protector arranged outside the needle hub and a spring arranged between the trigger protector and the needle hub. A guide groove with a special structure is arranged on the side wall of the trigger protector, and a clamping column corresponding to the guide groove is arranged on the outer edge of the side wall of the needle hub, so that the trigger protector is in a to-be-triggered state before use, and is triggered only when in use. Thus, an injection needle can be protected from being exposed to the outside after use, and cross-infection caused by mistakenly touching or reusing is avoided.

Abstract: A needle safety device has an outer tube within which a syringe barrel from which a cannula extends is slideably receivable. A collar in the outer tube is moveable relative thereto and rotatably attachable to the distal end of the barrel. A force member biases the outer tube in a distal direction. A cannula shield able to receive the cannula therein is in the outer tube. The cannula shield is fixedly attached to a cap removably attached to the outer tube. A track is formed in the inner surface of the outer tube. A pin extending radially outwardly from the collar slidingly engages the track. In a pre-injection position, the cannula is entirely within the outer tube. In a full-insertion position, the cannula extends beyond the outer tube. In a locked position, the cannula is irreversibly retained entirely within the outer tube.

Abstract: Various embodiments of an antimicrobial insert for a stopcock medical connector are provided. More specifically, the present invention relates to an antimicrobial insert that is seated within at least a portion of the annular bore of the connector's tap, wherein fluid within the annular bore contacts the antimicrobial insert, thereby preventing microbial proliferation within the stopcock medical connector.

Abstract: A hemodialysis catheter with a plurality of umbrella-like wire members covered with a film which works as a thrombus blocker and can easily and effectively remove the thrombus is disclosed. The hemodialysis catheter has a proximal lumen, the arterial lumen, and a distal lumen, the venous lumen. An elongate member is longitudinally put in either the proximal lumen or the distal lumen, or two elongate members in both lumens. A plurality of umbrella-like wire members are connected to the end of the elongate member. When the hemodialysis catheter is put in the vessel but not in use, the end of the lumen is capped off by the plurality of umbrella-like wire members covered with a film. When it is ready to use, the doctor can pull the elongate member which connects to the plurality of umbrella-like wire members out off the lumen inverting the plurality of umbrella-like wire members and clearing away any thrombus that has formed.

Abstract: An epidural needle assembly is provided, permitting the accurate introduction of a large bore introducer sleeve needle into the epidural space in the spinal column of a patient using the loss of resistance technique. The large bore introducer needle has a beveled side opening at its tip and with a tissue piercing point at the distal extension of the needle. A syringe needle is received within the introducer needle with a distal head of the syringe needle filling the beveled side opening at the distal end of the introducer needle when the syringe hub is fully seated. The lumen of the syringe needle exits the syringe needle head at the side opening of the introducer needle immediately adjacent the tissue piercing point of the introducing needle. The needle assembly may be inserted and advanced, with precise tactile feedback, into a patient, thus accurately detecting the introduction of the introducer needle into epidural space.

Abstract: A liquid medicament dispenser includes a housing and a pump carried by the housing, a reservoir applied to the housing and containing a pre-filled sterile liquid medicament, a sterile tubing set routed through the pump, a sterile administration line carried outside of the housing and coupled aseptically to the sterile tubing set in fluid communication, and an aseptic connector coupled to the reservoir and the sterile tubing set and changeable from a storage state to a use state. In the storage state, the aseptic connector prevents the liquid medicament in the reservoir from moving to the sterile tubing set. In the use state of the aseptic connector, the aseptic connector defines a sterile passageway for the flow of the liquid medicament from the reservoir to the sterile tubing set.

Abstract: A pumping apparatus for use with a pump set to deliver fluid through the pump set to a subject includes a pumping device capable of acting on the pump set to produce a fluid flow within the pump set. A controller is in communication with the pumping device for controlling operation of the pumping device in a feeding configuration and in a flushing configuration. The controller is adapted to store a selected flow rate and a desired fluid volume of a first fluid in the memory and at least one of a flush rate and flush volume of a second fluid. A flush time compensator is capable of being run for determining a compensated feeding configuration of the first fluid based on an amount of time the controller will operate the pump device in the flushing configuration and the desired fluid volume of the first fluid.

Abstract: An autoinjector system for injecting a fluid medicament into a patient includes a re-usable autoinjector, and a disposable cassette loaded with a hypodermic syringe pre-filled with a fluid medicament. The autoinjector includes a first motor for injecting a needle of the hypodermic syringe into the patient and a second motor for expelling the fluid medicament from the syringe.

Abstract: A bioactive material delivery system can include a thermoresponsive polymer membrane and nanowires distributed within the thermoresponsive polymer membrane. Magnetic activation of a thermoresponsive polymer membrane can take place via altering the magnetization or dimensions of nanowires dispersed or ordered within the membrane matrix.

Abstract: Some embodiments an infusion pump system can be used to determine a user's total insulin load (TIL) that provides an accurate indication of the insulin previously delivered to the user's body which has not yet acted. In particular embodiments, the TIL can account for both the bolus deliveries and the basal deliveries that have occurred over a period of time. Such information may be useful, for example, when the infusion pump is operated in conjunction with a continuous glucose monitoring device.

Abstract: The invention faces the technical problem of providing a tight connection between a tube and an dispense interface, while at the same time the biocompatibility of the connection can be improved. The technical problem is solved by an apparatus comprising a tube configured to guide a medium and a dispense interface. The tube comprises a first opening and a second opening, while the dispense interface comprises a recess. The recess has a first opening and a second opening and the tube is at least in part inserted into the recess. The tube is permanently affixed to the dispense interface by a combination of an interference fit and an adhesive, such that the interference fit prevents the adhesive from contaminating the medium.

Abstract: Deflectable catheters, systems, and methods of using deflectable catheters are described herein. An embodiment of a deflectable catheter comprises an elongate member, a handle, and a wire member. The elongate member has a shaft and a flexible member. The shaft defines a first lumen and a second lumen and the flexible member defines a passageway. The flexible member is attached to the shaft such that the passageway defined by the flexible member is in communication with each of the first lumen and second lumen defined by the shaft.

Abstract: A needle safety device (1) has an outer tube (10) within which a syringe barrel (2) is slideably receivable. A collar (14) in the outer tube (10) is moveable relative thereto and rotatably attachable to the distal end of the barrel (2). A force member (16) biases the outer tube (10) in a distal direction. A track (S) is formed in the inner surface of the outer tube (10). A pin (18) extending radially outwardly from the collar (14) slidingly engages the track (S). In a staging position, the barrel is inspectable. In a pre-injection position, the cannula extends a first length beyond the outer tube. In a full-insertion position, the cannula extends a second length greater than the first length beyond the outer tube. In a locked position, the cannula is entirely within the outer tube.

Abstract: In one aspect, a medical injector is provided herein which includes a body; a displaceable plunger disposed in the body; a spring disposed to advance the plunger; a releasable retainer for retaining the plunger in a first state against force of the spring; and, a sleeve disposed on the body, the sleeve being slidable relative to the body. Sliding movement of the sleeve over a predetermined extent relative to the body results in the releasable retainer releasing the plunger thereby allowing the spring to advance the plunger. Advantageously, the subject invention provides a medical injector having an automated plunger drive which is triggered upon sliding movement of the sleeve, thereby minimizing premature or failed activations.