A device for administering a fluid can include a cylinder, a piston displaceable in the cylinder and connected to a piston rod, and a tensioning device connected to the piston rod. The tensioning device includes a ramp rotatable via a motor, and a ramp track extending along a helical line. The tensioning device includes a roller which is in contact with the ramp track. To perform a tensioning procedure, the ramp track is rotated such that the roller runs on the region of inclination as far as the second plateau so the piston is moved to its rear end position. To perform a dispensing procedure, the ramp track is rotated until the roller runs over a transfer region and is accelerated toward the first plateau, thereby the piston is moved toward an open dispensing end. A control unit determines whether the tensioning procedure and/or dispensing procedure has taken place correctly.

A device for administering a fluid can include a cylinder, a piston connected to a piston rod, and a tensioning device connected to the piston rod. The tensioning device includes a ramp which is rotatable via a motor, a ramp track, and a roller which is in contact with the ramp track and which is mounted rotatably in a driver. In a tensioning procedure, the ramp track is rotated until the roller runs over a transfer region and, on account of the tensioning, is accelerated toward the first plateau. As a result, the piston is moved toward an open dispensing end. The administering device can be configured with one cylinder, one piston and one piston rod. The tensioning device can include two helical screws which run parallel to each other and which both, when the piston is in its rear end position, contribute to the pretensioning which is present.

A drug self-delivery device comprising a body portion containing a drug vial and a needle assembly, where the body portion is slidably engaged to a trigger portion. When engaged by a user pressing the trigger portion against the user's flesh, the needle assembly relative to the drug vial so as to align a needle port with an integral drug delivery port connected to the drug vial thereby allowing fluid flow of medication through the needle. Seals engaged by a penetration spring prevent loss of medication and prevent the need for direct connection between the needle assembly and the drug vial.

A delivery device for delivering medicament, such as insulin, to a patient includes a housing and a base enclosing an inner cavity. Enclosed within the housing is a reservoir for containing a medicament, a delivery mechanism for delivering the medicament to the patient, and a pump in fluid communication with the reservoir and delivery mechanism. The base has an integrally formed fluid channel in fluid communication with the reservoir and the delivery mechanism and a filter media containing an adsorbent positioned in the fluid channel to contact the medicament and remove at least a portion of a stabilizing compound from the medicament carried through the fluid channel.

Core annular flow is used to enable the subcutaneous delivery of a viscous fluid such as a protein therapeutic formulation. The high-viscosity fluid is surrounded by a low-viscosity fluid, and the low-viscosity fluid lubricates the passage of the high-viscosity fluid. This allows the use of protein formulations that have a higher concentration and a higher viscosity at comparatively reduced injection forces and reduced injection times. Several different embodiments of injection devices that provide core annular flow are described herein.

In one embodiment, a fluid storage device includes a rigid outer housing that defines a septum cavity, a reservoir cavity, and a channel that extends between the two cavities, the outer housing further defining an outlet in fluid communication with the reservoir cavity, a septum provided within the septum cavity, the septum being made of an elastic polymer and facilitating refilling of the fluid storage device, and a thin, collapsible membrane that does not generate significant restoring forces when it is deformed as fluid is drawn from the reservoir cavity and, therefore, does not completely or partially return to its initial non-deformed shape even if the outlet of the device remains open after doses are administered.

A medicament delivery system is described. Embodiments of the medicament delivery system can include a smart user device and a medicament delivery assembly. The medicament delivery assembly can be implemented as a single-use cartridge that can be removably coupled to the smart user device. The smart user device can be configured to determine when to automatically administer a medicament stored in the medicament delivery assembly.

A device for repetitive needleless injection including a handheld unit having at least a cell fillable with a liquid, and a propulsion mechanism to apply a sequence of pressure pulses to the liquid to eject a micro-jet of the liquid from the cell via an orifice with a velocity that is sufficient to enable the micro-jet to penetrate into the surface; a reservoir that is connected to the cell by a conduit to enable the liquid to flow from the reservoir to the cell; a controller that is configured to operate the propulsion mechanism repeatedly; and a unidirectional valve to enable flow of the liquid from the reservoir to the cell and to prevent backflow. The propulsion mechanism includes an impulse generator configured to displace an actuation surface to generate the pulse; a plunger to transmit the pulse to the cell, and a restoration mechanism to retract the plunger.

Disclosed is a medical device component for delivering medication fluid to a patient. The medical device component includes a fluid infusion device to regulate delivery of medication fluid, a body-mountable base unit, and a top cover assembly that is removably couplable to the base unit and to the fluid infusion device. The base unit includes a cannula to deliver medication fluid under the control of the fluid infusion device, and a physiological analyte sensor to measure a physiological characteristic. The base unit also includes an electronics assembly electrically connected to sensor leads to obtain measurements in the analog domain, to convert measurements into digital sensor data, and to communicate conditioned digital sensor data to the fluid infusion device. The top cover assembly is configured to provide both fluid and electrical connections for the base unit, by way of an infusion tube having sensor conductors integrated therein or otherwise associated therewith.

An injection apparatus can include a hand-held unit having a head portion and a body portion. The head portion can include a base member, a needle fluidly coupled to the base member, a movable portion disposed over the needle and being axially movable relative to the base member between an extended position and a retracted position in which a distal point of the needle is exposed, a safety cover removably coupled to the base member, the safety cover comprising one or more extension members, and an adjustment member removably coupled to the movable portion and configured to adjust a penetration depth of the needle by increasing or decreasing a distance between the movable portion and the base member.