Abstract: A drug delivery device may include an Inertial Measurement Unit (IMU) is provided. The IMU may include an accelerometer, a magnetometer, or a gyroscope. Motion parameters may be detected when the drug delivery device is shipped, being prepared for activation for use, or during use. The IMU may provide data indicative of a rapid deceleration, such as when a package containing the drug delivery device is dropped, or some other physical event experienced by the drug delivery device. The drug delivery device may also include internal or external pressure sensors or a blood glucose sensor that may coordinate with the IMU to provide additional feedback regarding the status of the device or user. A controller of the drug delivery device may generate a response depending on the particular parameters being monitored or may change device operational parameters as a result of detected system events.

Abstract: A safety needle (10) and a safety needle device (1). The safety needle device (1) comprises the safety needle (10), an outer protective cover (60), and a sealing membrane (70). The outer protective cover (60) cooperates with the sealing membrane (70) to seal and package the safety needle (10). The safety needle (10) comprises a needle sleeve housing (20), a syringe assembly holder (40), a needle (30), and an elastic safety cover (50). The syringe assembly holder (40) is provided at a rear end of the needle sleeve housing (20). The needle (30) is movably provided inside the needle sleeve housing (20) and the syringe assembly holder (40). The elastic safety cover (50) is provided in the needle sleeve housing (20) so as to be capable of rotating and extending and retracting.

Abstract: A guide wire of the present disclosure includes a core shaft having a distal end portion decreasing in diameter, a coil body wound to cover the distal end portion, and a distal end fixing portion fixing the core shaft and the coil body to each other. The distal end portion includes a small diameter portion, a large diameter portion, and a tapered portion between the small diameter portion and the large diameter portion. The core shaft and the coil body are fixed at a portion excluding the tapered portion. A first bending rigidity FR1 of the large diameter portion, a second bending rigidity FR2 of the small diameter portion, and a length L of the tapered portion satisfy the following expressions (1) and (2). In the following expressions (1) and (2), the unit of L is mm (millimeter).

Abstract: The present disclosure relates to an assisted injection device for injecting a composition contained in a medical container. The injection device includes a body configured to receive the medical container in a fixed position relative to the body. The injection device includes a spring-loaded piston rod translationally movable inside the body along a spring axis. The injection device includes a lever pivotably mounted on the body about a first pivot axis orthogonal to the spring axis at a first distance form the spring axis. The injection device includes a selective blocking system coupled to the lever by a second pivot axis orthogonal to the spring axis. The lever is pivotable between a rest position. The selective blocking system engages the piston rod to prevent any translation movement of the piston rod and a second position wherein the selective blocking system releases the piston rod.

Abstract: A medical device (100) for securing a catheter (700) to a support (600) is described, comprising a base element (200) having a first side (201) fixable to the support (600), and a second side (202) opposite the first side (201), and comprising a top element (500) having a first side (501) connectable with the second side (202) of the base element (200). When the first side (501) of the top element (500) is connected with the second side (202) of the base element (200), the top element (500) and the base element (200) are arranged for forming a feedthrough for the catheter (700) between the second side (202) of the base element (200) and the first side (501) of the top element (500). At least one of the base element (200) and the top element (500) comprises a deformable fluidum filled chamber (430), the deformable fluidum filled chamber (430) arranged such that the catheter (700) is locally tightly held between the base element (200) and the top element (500) when positioned there between.

Abstract: Injection monitoring circuitry is provided for coupling to part of an injection device having a syringe and a plunger rod. The injection monitoring circuitry has an input to receive force measurement data from a force sensor, the force measurement data includes a plurality of timestamped force measurements of force applied by a user to the injection device when an injection is administered to an injection site. Processing circuitry is provided to determine from the force measurement data when an end of injection has been reached, the end of injection corresponding to the plunger rod having reached an end position in a distal portion of the barrel of the syringe during administration of the injection by the user. Machine readable instructions and an injection monitoring method are also provided.

Abstract: A puncture needle includes: a rod-shaped main body; and a blade surface located at a distal end portion of the main body, which includes: first, second, and third blade surface portions. The first blade surface portion and the second blade surface portion form a blade edge at a ridge line where the first blade surface portion and the second blade surface portion meet, wherein a needle tip is located at a distal end of the blade edge. The third blade surface portion is contiguous with a proximal side of at least the first blade surface portion, and the third blade surface portion is a single flat surface that is inclined with respect to a central axis of the main body. In a side view of the main body, a line extending along the third blade surface portion intersects with the first blade surface portion.

Abstract: Systems and methods are provided for measuring depth, position, and/or angle of a cannula in a medical drug delivery device. In particular, a drug delivery device having a cannula is positioned adjacent to tissue, a voltage pulse is provided to the cannula, a charge is measured at an electrode in the drug delivery device, and the depth of penetration of the cannula is determined based in part on the charge at the first electrode. Systems and methods described herein can be used to determine subcutaneous insertion depth in a wearable bolus injector. In some implementations, insertion depth determination is achieved through capacitive sensors which measure needle depth in a drug delivery device.

Abstract: Automatic injection devices (i.e., auto-injectors) and methods are disclosed that use gas-generating chemical reactions for parenteral delivery of therapeutic fluids. The generated gas may place the auto-injector in a punctured configuration to puncture a patient's skin with a needle, an injected configuration to deliver the therapeutic fluid through the needle and into the puncture site, and/or a retracted configuration to withdraw the needle from the puncture site.

Abstract: A multiple carrier injection system includes an adapter, having at least one arm, and a pen needle assembly. The pen needle assembly includes a hub retaining a needle and a bullet having a cover to seal the bullet, where the bullet encloses the hub in a first position. The arm engages the adapter to the hub, and the arm causes the hub to rotate within the bullet to move the hub into a second position.

Abstract: A liquid medicine administration device includes a prefilled syringe and a gasket biasing member assembly. The biasing member assembly includes: a gasket pressing member configured to press a gasket; a flange attachment member attached to the prefilled syringe; a biasing member housed between the pressing member and the flange attachment member; and an operating member including an engagement holding portion. The pressing member includes an engagement portion to be engaged with the flange attachment member. When the engagement holding portion is located at an abutment position, deformation of a deformable portion is inhibited by abutment between the engagement holding portion and an abutment portion of a deformable portion, and engagement between the engagement portion and the attachment member body portion is held.

Abstract: Drug delivery system, injection device, transfer apparatus, vial holder and method of administering and transferring are disclosed which provide for passive warming of chilled injectable transferred through the transfer apparatus and into the injection device. The injection device may include a skin-facing surface including a skin boundary displacement extension or structure around a needle injection site to create a high pressure zone in the tissue. Radio frequency tracking and monitoring features for tracking patient compliance also may be provided.

Abstract: A gastric jejunal (GJ) feeding tube device for GJ feeding of an infant or child is provided. The device comprises a GJ button comprising a GJ button body, a gastric port, a jejunal port, a gastric channel, and a jejunal channel. The device also comprises a multi-lumen tube comprising a multi-lumen tube body, a multi-lumen tube proximal end, and a multi-lumen tube distal end. The device also comprises a jejunal tube comprising a jejunal tube body, a jejunal tube proximal end, a jejunal tube distal end, a spring, and a ring. The spring provides a kink-resistant feature. The ring is positioned at the jejunal tube proximal end. The jejunal tube and the GJ button are operatively connected at the ring and the mating surface by radial compression. The ring has a higher durometer than the jejunal tube body and an outer diameter that does not substantially decrease distally.

Abstract: A balloon catheter has an outer shaft which surrounds a shaft lumen. The outer shaft has a proximal outer shaft portion connected to a distal outer shaft portion. An inner shaft is in a distal portion of the shaft lumen. A guide wire lumen is in the inner shaft. An opening at a proximal end portion of the inner shaft permits the guide wire to be guided out from the outer shaft. A metallic tube is in the shaft lumen. The proximal end portion of the inner shaft is engaged with the metallic tube. A separate, elongate and metallic stiffening element is in the shaft lumen, and is connected to the metallic tube and protrudes from the metallic tube into the distal portion of the shaft lumen and into the proximal portion of the shaft lumen to stiffen portions of the outer shaft.

Abstract: A peripheral intravenous catheter assembly may include a low-drag septum. The septum may include a body having a distal end and a proximal end, which may be sealed. The septum may include a slot disposed within an outer surface of the body and oriented along a longitudinal axis of the body. The slot may include a distal end spaced apart from the distal end of the body, and a proximal end spaced apart from the proximal end of the body. An introducer needle may extend through the slot.

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 pump module for an infusion pump includes a plunger-cylinder unit that can be coupled to the infusion pump in order to deliver fluid from a fluid feed line into a fluid drain line to a patient. The plunger-cylinder unit has a delivery chamber that is fluidically connected to the fluid feed line and the fluid drain line. The delivery chamber is delimited by the cylinder (14). The plunger can be moved linearly/back and forth in the axial direction. A plunger seal seals the plunger in relation to the cylinder. The section of the wall of the cylinder, over which the plunger seal passes during the back-and-forth motion of the plunger, is sealed in a sterile manner in relation to the surroundings.

Abstract: The present invention provides a drug delivery system (1) comprising a drug delivery device (2, 3) carrying at least one reservoir (40a, 40b), and a needle unit (4) being attachable to the drug delivery device (2, 3) in axial extension thereof and adapted to establish a flow way between the at least one reservoir (40a, 40b) and a drug delivery site. The needle unit (4) comprises a needle structure (11) comprising a front needle portion (12) for entering the drug delivery site, and at least one back needle portion (13a, 13b) for insertion into the at least one reservoir (40a, 40b), and a needle shield (20).

Abstract: A nasogastric tube structure is disclosed which comprises a first tube, a clamping member and a positioning member. The first tube has a front necking opening, a rear opening, a stopper ring on a wall thereof adjacent to the rear opening and an engaging groove on the wall thereof adjacent to the stopper ring. The clamping member comprises two corresponding positioning segments and a C-shaped clip portion for connecting the two positioning segments and engaging with the engaging groove. The positioning member is sleeved on the two positioning segments.

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.