Abstract: Methods and devices for use and handling of intravenous and/or subcutaneous needles, and, more particularly, to safety devices for shielding needles or other sharp articles or devices that present a safety hazard are disclosed. In an embodiment, a needle protective sheath can include a top wall, a bottom wall, and a pair of side walls joining the top and bottom walls. A finger shield extends from the top wall at a front opening of the sheath and is attached to the top wall by a hinge portion. The finger shield can be rotated about the hinge portion to block the front opening so as to secure a needle within the sheath.

Abstract: A transport assembly for shipping components of a medicament delivery device to final assembly is presented, where the transport assembly has a plunger rod, a first resilient member configured to bias the plunger rod, an elongated plunger rod holder configured to receive the plunger rod, a transport securing sleeve configured to receive a portion of the plunger rod holder, and configured to move axially from a first position relative to the plunger rod holder in which the transport securing sleeve prevents the plunger rod holder to disengage from the plunger rod to a second position located distally relative to the first position, enabling disengagement of the plunger rod holder from the plunger rod, a rear end cap, and a second resilient member configured to bear against the rear end cap and configured to bias the transport securing sleeve in the proximal direction away from the second position.

Abstract: A removal member for removing a needle protective cap includes a housing having a longitudinal axis and receiving the cap along an insertion direction, the housing having a first support area and a second support area the first area being carried by a blocking element, movable relative to the housing between a cap insertion configuration, in which the orthogonal projections of the first and second areas in a transverse plane substantially perpendicular to the longitudinal axis are separated by an insertion distance, and a cap blocking configuration, in which the first and second areas are located in separate transverse planes, and in which the orthogonal projections of the first and second areas in said transverse plane are separated by a blocking distance less than the insertion distance and adapted to block the translation of the cap relative to the removal member in a removal direction opposite to the insertion direction.

Abstract: Access assemblies include an instrument valve housing and a valve assembly disposed within a cavity of the instrument valve housing. The valve assembly includes a guard assembly, and a seal assembly disposed adjacent to the guard assembly. The seal assembly includes first, second, third, and fourth seal sections. The first seal section is nested within the second seal section, the first and second seal sections are nested within the third seal section, and the first, second, and third seal sections are nested within the fourth seal section.

Abstract: An injector device comprising an elongate housing having a proximal end and a distal end, and configured to receive a container of medicament, a needle sleeve mounted within the housing and moveable between an extended position in which the needle sleeve at least partially extends from the distal end of the housing, and a retracted position in which the needle sleeve is received further within the housing than in the extended position, a piston rod moveable longitudinally within the housing, a piston spring configured to bias the piston rod towards a distal end of the housing to engage a container of medicament when received within the housing, and a release mechanism configured to control actuation of the piston rod.

Abstract: A treatment system includes a guide sheath, and a catheter provided with a pressure-controlled element. The pressure-control element preferably includes an expanded configuration adapted to extend across a small feeder vessel branching from the splenic vein. The pressure-control element is positioned with the feeder vessel, and a therapeutic agent is delivered under pressure directly into the feeder vessel, where it is forced to penetrate deep into tissue. Pressure responsive elements for monitoring intravascular pressure are also provided to time delivery of the therapeutic agent for maximum uptake by the target organ. Methods for treating tissues and organs via vascular pathways are provided.

Abstract: A plunger for a medical syringe includes a plunger body having a longitudinal axis, a lateral surface, a front side and a rear side, wherein a first sealing bead is associated with the front side of the plunger, the rear side is used for connecting to a plunger rod and, in addition, a front part of the plunger including the front side is covered with a film-like cover layer for otherwise separating the plunger from the medical substance in the use position. In addition, the cover layer be configured with different thicknesses, wherein the thickness is greatest in the region of the longitudinal axis and decreases radially outwards from the longitudinal axis.

Abstract: A method and system of and for securing a lumen or catheter, after placement in a patient, to prevent unwanted removal or dislodgement of the lumen or catheter caused by patient movement and/or further medical interventions such as cardiopulmonary chest compressions, electrical defibrillation, surgical procedures, and the like. The method and system comprising simple and sterile materials that preclude the use of excessive suturing and ineffective ad-hoc methods with tape and gauze. The catheter is secured by a rubber on plastic frictional force and will resist external forces while preventing the tube structure from bending and subsequent occlusion. The device can be comfortably attached to the patient in all of the anatomical locations typically targeted for large catheter installment. The method of securement is rapid and requires only a single personnel to handle the device and the catheter tube simultaneously.

Abstract: An injector includes a housing, a needle hub movably mounted within the housing and an injection needle supported by the hub. The hub and the needle are axially translatable between retracted and injection positions. A needle shield, having an aperture, is movably connected to the housing between first and second positions. The needle extends through the needle shield aperture in the injection position of the needle and the first position of the needle shield, and the needle is blocked from extending through the needle shield aperture in the second position of the needle shield. When the needle shield is in the second position and the hub and the needle are in the injection position, the needle shield covers the tip of the needle and subsequent movement of the needle shield toward the first position axially translates the hub and the needle back toward the retracted position.

Abstract: A wearable drug delivery device that can deliver a liquid drug stored in a container to a patient is provided. The container can be a prefilled cartridge that can be loaded into the drug delivery device by the patient or that can be preloaded within the drug delivery device when provided to the patient. A sealed end of the container is pierced to couple the stored liquid drug to a needle conduit that is coupled to a needle insertion component that provides access to the patient. A drive system of the drug delivery device can expel the liquid drug from the cartridge to the patient through the needle conduit. The drive system can be controlled to provide the liquid drug to the patient in a single dose or over multiple doses.

Abstract: A surgical instrument for suction and irrigation, includes: an insertion tube inserted into the body of a patient; an instrument body coupled to the insertion tube and disposed outside the body of the patient; an irrigation fluid control valve coupled to the instrument body; and a drainage fluid control valve coupled to the instrument body and separated a predetermined distance from the irrigation fluid control valve in a longitudinal direction of the instrument body.

Abstract: A medical injection device for supporting a medical container, the medical container comprising a barrel adapted to contain a composition and a needle extending from a distal end of the barrel, wherein the medical injection device comprises: a body configured to receive at least a part of the medical container, a plunger axially movable relative to the body along an axis of the body, needle cover movable relative to the body along the axis, the needle cover being configured to move successively between storage position wherein the needle cover covers the needle, an injection position wherein the needle cover exposes at least partially the needle, a safety position wherein the needle cover covers the needle and is prevented from moving back to the injection position.

Abstract: A novel seal is provided along with a valve for implementing the seal in the form of a hemostatic catheterization valve. A pressure-sensing form of the hemostatic valve is also provided. The novel seal includes a pair of cooperating conical gaskets divided through their apexes into a plurality of edge-abutting semi-conical flaps. The seals are angularly fixed in orientation relative to each other using registering structures such as complementary tabs and sockets. More specifically, the seams where the semi-conical flaps abut are angularly off-set between the two conical gaskets by a predetermined amount.

Abstract: A catheter assembly 10 comprises a catheter 12 including a longitudinally extending wall 16 with inner and outer surfaces. The inner surface of the wall defines a bore 22 extending longitudinally through the catheter defining a first lumen 52 and a second lumen 54. At least one of the first and second lumens communicates with an opening in the outer surface of the wall at a distal end of the catheter. An elongated separator 14 includes a longitudinally extending surface that at least partially defines the second lumen. The longitudinally extending surface of the separator is disposed asymmetrically relative to the bore when viewed in cross-section taken transverse to the longitudinal extent of the separator adjacent to a distal end of the separator. At least a portion of the separator is movable relative to the bore and the inner surface of the catheter wall.

Abstract: Some embodiments relate to a catheter system having a changeable or adjustable working length. The catheter system can comprise a proximal end, a distal end, and a first axial lumen configured to receive a guidewire formed through at least a portion of the catheter body. A first opening can be formed through a portion of the catheter body and be in communication with the first lumen. The sheath can be rotatable, axially movable, or otherwise changeable from at least a first position to a second position, wherein the sheath can substantially cover the first opening in the catheter body in the first position, and can substantially expose the first opening in the catheter body in the second position.

Abstract: An injection device for delivering a dose of medicament from a syringe (5), the injection device comprising a housing (10), a plunger (210) moveably mounted within the housing (10), an actuation mechanism (200), a trigger mechanism (40), and a plunger velocity regulator. The actuation (mechanism (100) is arranged to provide a forward biasing force to urge the plunger (210) forward in use to express a dose of medicament, and the trigger mechanism (40) is arranged to releasably hold the plunger (210) against the force of the actuation mechanism (200). The plunger velocity regulator comprises a cam surface (262) associated with the housing, and a cam member (252) associated with the plunger (210) and arranged to engage the cam surface (262) during actuation movement of the plunger (210) such that axial movement of the plunger (210) relative to the housing (10) causes relative rotational movement of the cam member (252) which limits the forward velocity of the plunger movement.

Abstract: A plunger assembly is configured for slidable advancement through a reservoir of a vessel containing a material to be administered. The plunger assembly includes a plunger rod having a distal end configured to be inserted into the reservoir. An elastomeric plunger extending from the distal end of the plunger rod is configured to sealingly engage a sidewall of the reservoir. At least one printed circuit board is embedded within the plunger, and at least one electronic component is electrically connected with the at least one printed circuit board.

Abstract: An autoinjector including a plunger for engaging with the bung, a collar located around the plunger, an insertion spring biasing the collar relative to the rear of the device, and a delivery spring biasing the plunger relative to the collar. The device further includes a stop feature defining the limit of axial movement of the syringe body through the housing, and a collar release mechanism for releasing the collar from the rear of the device to commence insertion and a plunger release mechanism for releasing the plunger from the collar while substantially preventing rearward axial movement of the collar, following insertion, to commence delivery of the medicament. Following release of the plunger from the collar, the plunger is configured to move axially and rotationally relative to the collar, the direction of rotation being changed one or more times with axial movement of the plunger.

Abstract: An integrated guidewire includes a wire and a flexible tube. The wire is sized and shaped to move in an anatomical material transportation system of a patient. The flexible tube is sized and shaped to move in the anatomical material transportation system, having proximal and distal ends, the proximal-end is coupled to a device external to the patient, the flexible tube is configured to transfer fluids between the distal-end and the device, and the wire and the flexible tube are intertwined with respect to one another.

Abstract: An administration assembly for a medicament delivery device is presented having a plunger rod, a plunger rod holder and an activation sleeve configured to receive a portion of the plunger rod holder. The triggering member is configured to move the activation sleeve from a first position to a second position relative to the plunger rod holder. The plunger rod is configured to be axially locked relative to the plunger rod holder when the activation sleeve is in the first position. The plunger rod is released from being axially locked when the activation sleeve is moved towards the second position.