Abstract: An insufflation pump includes a pump body having a first end and a second end. The pump body includes a syringe mechanism at the first end and an actuation mechanism at the second end. The syringe mechanism includes a plunger. The plunger of the syringe mechanism and the actuation mechanism are linked by a toggle assembly facilitating transfer of power from the actuation mechanism to the syringe mechanism.

Abstract: A catheter hub assembly. The catheter hub assembly includes a catheter hub body, a septum and a septum retainer, the catheter hub body having a distal end, a proximal and an internal wall defining an internal fluid passageway therebetween, the internal wall defining a transitional step within the internal fluid passageway, the septum positioned within the internal fluid passageway such that a distal end of the septum abuts up against the transitional step, the septum retainer at least partially receivable within the internal fluid passageway and having an outer wall shaped and sized to interlock with the inner wall of the catheter hub body, the outer wall including one or more lateral ribs configured to inhibit rotation of the septum retainer relative to the catheter hub body.

Abstract: A medicament delivery device including at least one contact sensor configured to output a signal representing a state of partial detachment of the device from an injection site, and an alert output module configured to output an alert based on the signal received from the at least one contact sensor.

Abstract: A connector for medical fluid vessels includes a fluid-seal fitting such as a male plug defining a lumen and mating with a cooperating connector, a mechanical fastener such as a screw thread for mating with the cooperating connector, and an outer housing positioned around the plug to form an annular space. Optionally, a cap can be provided with a fluid-seal fitting such as a male plug for mating with the lumen of the connector. The connector includes one or more vent openings for drainage and air-drying of any residual fluid in the annular space when capped, as well as for breaking a vacuum to prevent fluid backflow and thus ensure more accurate dosing. In some embodiments, the vent openings are provided in the outer housing. And in some embodiments, the vent openings are provided in the cap.

Abstract: A connector includes an elastic valve body that includes a top face on which a slit is formed and a bottom face opposite the top face; and a holding section that is in contact with the top face and the bottom face of the elastic valve body and holds the elastic valve body. The holding section surrounds the slit, and the elastic valve body includes a peripheral section that is positioned outward of a portion of the elastic valve body that is held by the holding section. The elastic valve body and the holding section are configured such that a volume of the peripheral section in a state in which the elastic valve body is held by the holding section is larger than a volume of the peripheral section in a state in which the elastic valve body is not held by the holding section.

Abstract: Articulation devices, systems, methods for articulation, and methods for fabricating articulation structures will often include simple balloon arrays, with inflation of the balloons interacting with elongate skeletal support structures so as to locally alter articulation of the skeleton. The skeleton may include a simple helical coil. Liquid inflation fluid may be directed to the balloons from an inflation fluid canister, and may vaporize within the articulation system, with the inflation system preferably including valves controlled by a processor. The articulation structures can be employed in minimally invasive medical catheter systems.

Abstract: The male connector (1) includes a connector body (10) and a lock nut (50). The connector body (10) includes a male luer (11), first female threading (41) that surrounds the male luer (11), a base end portion (20) that is inserted into a tube (8), a fixed protrusion (21) formed on the base end portion (20), and a spiral protrusion (32) between the male luer (11) and the base end portion (20). The lock nut (50) includes second female threading (52) that is screwed together with the spiral protrusion (32). When the spiral protrusion (32) and the second female threading (52) are screwed together, the base end portion (20) and the lock nut (50) clamp the tube (8). First rotation prevention mechanisms (14, 54) that engage with one another are provided on the connector body (10) and the lock nut (50) such that the lock nut (50) does not rotate relative to the connector body (10) when the tube (8) is clamped.

Abstract: An injector for delivering a therapeutic product may include a base having a flexible surface that conforms to various body contours of a patient and defines one or more an injection chambers. The injector may have a height that is substantially less than its width, thereby defining a low profile, which provides a larger more stable base that can pinch or stretch the skin in a controlled manner. The larger base can also accommodate larger volumes via multiple injection chambers and/or large combined primary containers.

Abstract: Embodiments disclosed herein include devices for time release of measured quantities of an active ingredient and storage of animal management information. One embodiment disclosed herein releases an active ingredient, which is useful in the ruminant art, within the rumen and, then, at optionally varied intervals, releases additional doses into the same environment. The active ingredients are compartmentalized and, upon receiving an appropriate signal, use a magnetic field to expel the active ingredient into the rumen of the animal. The doses of active ingredient may be delivered simultaneously, sequentially, or independently. Further, the doses of active ingredient may be the same active ingredient or different active ingredients, in any formulation. Another embodiment described herein stores animal management information, such as identification or dosage information, and wirelessly communicates the stored information to an external device.

Abstract: An apparatus for transdermal injection includes a collet configured to transition between first and second states. In the first state, the collet receives a cartridge with a predetermined elongate shape. In the second state, an inner surface of the collet substantially conforms to the predetermined elongate shape of the cartridge such that expansion of the cartridge, when the cartridge is pressurized, is substantially uniformly opposed.

Abstract: A sealing device for sealing a lead-through for a medical instrument that includes a fastening region for fastening the sealing device on a tube or other medical device, a ring-like supporting region which is connected to the fastening region, and an annular sealing lip with an outer edge which is connected to an inner edge of the support portion, and an inner edge which is provided and designed to fluid-tightly abut at an outer surface of a shaft inserted in the sealing device. The difference of the average diameter of the inner edge of the support portion and the mean diameter of a shaft of a medical instrument, for which the sealing device is provided and designed, is not larger than the difference of the average diameter of the shaft and the mean diameter of the inner edge of the sealing lip.

Abstract: An airtrap for a medical or physiological fluid in one embodiment includes a conical housing having a radius that increases from its top to its bottom when the housing is positioned for operation; a medical or physiological fluid inlet located at an upper portion of the conical housing; a medical or physiological fluid outlet located at a lower portion of the conical housing, the inlet and the outlet positioned and arranged so that medical or physiological fluid spirals in an increasing arc around an inside of the conical housing downwardly from the inlet to the outlet; and a gas collection area located at an upper portion of the conical housing. In another embodiment, the airtrap is shaped like a seahorse having a head section and a tail section. Any of the airtraps herein may be used for example in blood sets, peritoneal dialysis cassette tubing, and drug delivery sets.

Abstract: A driving and dosing device for an injection device for discharging a liquid product includes a housing, a rotatable dose adjustment member for adjusting a product dose to be discharged, a driven member received in the housing, a driving member rotatable relative to the housing and which, during the discharge of product, is coupled to the driven member such that a rotation of the driving member has the effect that the driven member is moved in the distal direction relative to the housing, a pretensioned driving spring which is switched between the dose adjustment member and the driving member during the adjustment of the product dose, wherein the dose adjustment member, during the adjustment of the product dose, is coupled in a rotationally fixed manner to the driving member, such that a rotation of the driving member relative to the dosing member is prevented.

Abstract: A device (1) for dispensing a fluid, in particular to a patient, comprising a container (15), in particular an at least partly collapsible container, with an interior (17) for receiving the fluid. The container (15) comprises a closure piece (20) which is rigidly arranged in the container (15) in particular and on which a dispensing opening (24) is formed, wherein the fluid can be dispensed out of the interior (17) through the dispensing opening. The device (1) comprises a pump device (40) driven by a pump drive (50) in order to pump the fluid out of the interior (17) of the container (15). The pump device (40) is fluidically arranged between the interior (17) and the dispensing opening (24) so that the fluid can be pumped out of the interior (17) to the dispensing opening (24) by the pump device (40).

Abstract: A fluid delivery device includes a housing having a bottom surface configured to be coupled to the skin surface. The fluid delivery device includes a cartridge prefilled with a fluid and configured to be inserted into the housing. The cartridge has a septum configured to be generally perpendicular to the bottom surface when the cartridge is inserted in the housing. The fluid delivery device includes a needle assembly that has a needle that includes a fluid coupling end and a delivery end. The fluid coupling end of the needle is fluidly disengaged from the cartridge in an initial position. The delivery end of the needle extends past the plane of the bottom surface and the fluid coupling end of the needle extends through the septum in a deployed position.

Abstract: A drive and dosing device is described for an injection device for administering a fluid product, in particular a medication, wherein the drive and dosing device can be adjusted to a product dose to be administered. The drive and dosing device has, among other things, a coupling which, upon activation of an activation element, enables rotation of a rotation element relative to a housing, wherein by disengaging the activation element, the rotation of the rotation element relative to the housing is blocked.

Abstract: The mechanism includes a body, a drive member movable in the body, a main spring that is loaded when a dose is set and is released for moving the drive member during a delivery of a dose, and a movable trigger inhibiting a movement of the drive member, a movement of the trigger releasing the main spring and the drive member. The trigger is moved from a start position to an end position relative to the body during a setting of a dose, the end position having a distance from the start position that increases as the dose set increases.

Abstract: A drug delivery device for injecting medicament, the device including a main body having a surface for contacting a patient, an actuation button (110, 420, 436) movably disposed relative to the main body, and a reservoir disposed within the main body for containing a medicament. The device also includes a needle having a distal end for insertion into a patient, and a lumen extending proximally from the distal end, wherein the lumen is fluidly connectable with the reservoir. The device further includes a removable needle cover (114, 400) for selectively covering the distal end of the needle and selectively preventing movement of the actuation button relative to the main body that initiates activation of the device.

Abstract: An epidural needle assembly including an epidural needle assembly and an injection needle assembly. The injection needle assembly is slidably mounted on the needle of the epidural needle assembly between extended and retracted positions. The injection needle assembly includes an injection hub having an injection needle secured thereto which extends forwardly therefrom. When the injection needle assembly is in its retracted position, the forward end of the injection needle is positioned rearwardly of the forward end of the epidural needle. When the injection needle assembly is in its extended position, the forward end of the injection needle is positioned forwardly of the forward end of the epidural needle. When in its extended position, the injection needle is able to create a hole in the skin of a person or animal to permit the epidural needle to be inserted therein.

Abstract: An injection device for the delivery of medicament has an indicator for providing an activation indication. The device includes a housing; a plunger slidably mounted within the housing; an actuation mechanism configured, in use, to move the plunger forward relative to a syringe so as to express medicament from the syringe. The device also includes an indicator element responsive to the forward movement of the plunger and configured to provide an audible and/or tactile and/or visual indication when the plunger reaches or approaches its forward position. The plunger includes an elongate shaft formed of at least two telescopic sections. The actuation mechanism acts on the plunger, in use, to expand the telescopic sections and to sequentially move each of the telescopic sections forwardly within the housing. The indicator element is arranged to be responsive to the forward movement of the trailing telescopic section.