Various embodiments disclosed herein relate to needle-based injectors that incorporate a power assembly comprising a stored energy source and a rate control assembly. The power assembly may be further configured to allow the injection to be performed with more force than a user may be capable of delivering, while also allowing the user to maintain control of the injection process after the stored energy source has been released and the injection has begun, such the user may increase or decrease the rate of injection, or stop the injection, during the injection process. In various embodiments, the power assembly may comprise spring- or gas-based stored energy sources, and/or may comprise friction- or tension-based rate control assemblies. Described herein are also methods for injecting an agent using embodiments of the devices described here.

A set of drug delivery devices comprising a first drug delivery device and a second drug delivery device. The first drug delivery device and the second drug delivery device each include a first set of mutual members that are identical in both the first drug delivery device and the second drug delivery device, and the first drug delivery device and the second drug delivery device each comprise a second set of distinguishing members that differ among the first and second drug delivery device. The first drug delivery device includes a first connector for attaching a first dispensing unit to the first drug delivery device and the second drug delivery device includes second connector for attaching a connectors means differ from each other so that a second dispensing unit is not attachable to the first connector and a first dispensing unit is not attachable to the second connector.

An anti-back mechanism for a drug delivery device according to the present application includes a retaining groove, a position retaining protrusion and a clamping groove. The retaining groove is provided on a push rod. The position retaining protrusion is provided in the drug delivery device. The clamping groove has an accommodation cavity into which the position retaining protrusion is inserted. The position retaining protrusion is provided on a ring having a notch and may be clamped with respect to the push rod when the position retaining protrusion is squeezed. When the position retaining protrusion is subjected to a reverse thrust from a cartridge holder of the drug delivery device, the position retaining protrusion may move in a direction opposite to an injection direction, be inserted into the clamping groove to be clamped, and be hooked to the retaining groove to be locked.

A safety syringe comprising a needle redirection device that is desirably configured to bend the needle shaft forwardly of the barrel following an injection to thereby redirect the needle tip from a first position where it projects forwardly in coaxial alignment with the syringe barrel to a second position where the needle tip is covered or protected from incidental or accidental contact and associated needle sticks. Both sliding and pivoting embodiments are disclosed.

A liquid administration device includes an operation unit; a structure that includes an accommodation body configured to accommodate the liquid therein and a needle tube communicatable with the inside of the accommodation body; a cover member that is movable between a protection position and an exposure position; a biasing member that biases the cover member in a distal direction; an exposure restriction unit configured to restrict movement of the cover member to the exposure position when a movement amount of the cover member with respect to the structure reaches a predetermined exposure restriction operation amount; and a movement amount restriction unit.

A method and system are disclosed for driving a plunger in a drug reservoir. In some embodiments, a variable friction element interconnects between a pushing shaft and a wall of the reservoir. For example, rotation of a driving element in a first direction relative to the pushing shaft may advance the pushing shaft in the reservoir. The friction element may have increased friction resistance to rotation of the pushing shaft in the first direction in comparison to frictional resistance to advancing the pushing shaft. For example, the increased friction may result from wedging a radial element between the pushing shaft and the wall of the reservoir.

A drug delivery device with a housing configured to connect to a dispensing unit includes a compartment containing a fluid, a piston rod configured to move in a proximal direction for ejecting the fluid, and a dosing mechanism comprising an actuation member to be actuated by a user. The device includes a conversion mechanism configured to convert a movement of the actuation member to a movement of the piston rod. The conversion mechanism includes a dose selector member, which is rotationally fixed to the housing and axially movable with respect to the housing, and a dosing member, which is rotationally movable with respect to the dose selector member. The drug delivery device includes a friction reduction mechanism provided between the dose selector member and the dosing member to reduce friction between the dose selector member and the dosing member.

A drug delivery device has a housing with a longitudinal axis, a dose setting member actuatable by a user and rotatable around the longitudinal axis to set a dose to be delivered by the drug delivery device, a piston rod that is configured to be axially advanced in a proximal direction to deliver the set dose, and a dosing member for defining the axial advancement of the piston rod upon delivery of the set dose. The dosing member is axially movable along the longitudinal axis and rotationally movable around the longitudinal axis during dose setting, and the dosing member is rotationally fixed to the dose setting member during dose setting. The dosing member comprises a maximum dose stop that is configured to engage with a maximum stop feature provided at the housing to limit movement of the dosing member with respect to the housing upon setting a maximum dose.

The autoinjector has a proximal end and, a longitudinal axis A, and a housing configured to receive a medical container having a barrel defining a reservoir for containing a medical product, and said barrel having a distal end provided with a needle and an opened proximal end configured to receive a plunger rod for pushing a stopper arranged inside the barrel. A needle cover is coupled to and movable with respect to said housing between a first extended position, a retracted position, and a second extended position wherein the needle cover moves back in the distal direction to shield the needle. An injection mechanism is configured to move the plunger rod distally inside the barrel in order to expel the medical product contained inside the barrel. A holder is movable with respect to the housing between a passive position wherein the holder does not trigger the injection mechanism and an active position wherein the holder triggers the injection mechanism. The autoinjector includes blocking means configured to prevent the medical container from moving proximally inside the housing, such that the medical container cannot displace the holder towards the active position if the autoinjector falls down onto a floor, proximal end first.

A container for delivering a medicament to a target location includes a housing having a proximal end and a distal end, the housing including a cap locking tab at the distal end, and a vial containing the medicament. The container includes a plunger slidable within the vial from a proximal end to a distal end of the vial to dispel the medicament, an injection member associated with the distal end of the vial, such that the medicament dispelled from the vial passes through the injection member to the target location, and a slidable interaction member associated with the distal end of the vial configured to slide with the vial. An interaction between the slidable interaction member and the cap locking tab causes the cap locking tab to bias outward, and placement of a safety cap on the container after use locks the safety cap onto the container via an interaction with the cap locking tab. The container may further include a resistance feature to control movement of a plunger rod relative to the vial.