In some embodiments a system and method are described for safeguarding a hazard, the hazard, for example a needle point, may be moved between a protected retracted position, an active extended position and/or an intermediate position. Optionally in the retracted position, the hazard may be protected inside a housing. Optionally in the extended position, the hazard may be exposed. Optionally, in the intermediate position the hazard may be partially protected and/or concealed, for example by a shield and/or in an indentation. In some embodiments, compromising a shield causes the hazard to be retracted to the retracted position.

One embodiment is directed to a system for injecting, comprising a syringe body defining an interior medicine chamber; a stopper member configured to be inserted into the interior medicine chamber to contain medicine within the medicine chamber; a plunger member configured to be manually manipulated to insert the stopper member relative to the syringe body; and a needle having proximal and distal ends, the proximal end comprising an anchoring geometry configured to be at least partially inserted into the stopper member such that upon retraction of the stopper member, the needle is pulled proximally along with the stopper to be at least partially contained within the interior medicine chamber.

A system for injecting includes a cartridge body defining a proximal opening and a distal needle interface. The system also includes a plunger member defining a plunger interior and configured to be manually manipulated to insert a stopper member relative to the cartridge body. The plunger member includes a needle retention feature disposed in the plunger interior, an energy-storage member disposed in the plunger interior, and an energy-storage member latching member disposed in the plunger interior. The system further includes a needle hub assembly coupled to the distal needle interface of the cartridge body. The needle assembly includes a needle having a needle proximal end feature, a hub, and a needle latching member configured to couple the needle to the hub. The needle is retractable into plunger interior upon manipulation of the plunger member to actuate the energy-storage member latching member.

The invention relates to a syringe with a retractable needle comprising a barrel (2) having a nozzle (19) integrated in a male Luer adapter element (26); a piston (3) slidably arranged in the barrel (2) and coupled to a sealing element (16), said sealing element (16) having a central channel (20); a needle assembly comprising a needle (4), a needle holder (6) and a female Luer adapter element (7); a spring assembly arranged in the piston (3) comprising a spring sleeve (12), a spring (13) mounted on the spring sleeve (12), a spring tensioning element (14) located on the spring sleeve (12) and held in position by the piston wall, and a plunger (15) mounted within the spring sleeve; and a piston cap (10); said piston (3) being coupled to the sealing element (16) by means of the spring tensioning element (14); said spring sleeve (12) being held in position within the piston (3) by a ring element (18) protruding from the inner wall of the piston (3) and supporting the proximal end of the spring sleeve (12), the spring sleeve extending into the channel (20) of the sealing element (16) to the distal end thereof; said spring sleeve (12) comprising at its distal end a circular protrusion (21) on the inside designed to engage a circular recess (22) at the proximal end of the needle holder (6); wherein the piston (3) comprises a holding ring (11) on its inner surface designed to engage with an outer flange (17) of the spring sleeve (12) after actuation of the spring (13).

A device for administering a medicinal liquid by injection is provided. The device comprises a dose assembly comprising collapsible reservoir. The device further includes at least one actuator element onto which the user may apply a force to actuate the device, the force having a component along an axis perpendicular to a longitudinal axis; and a housing comprising a septum. The at least one actuator element is configured and arranged to act on at least a portion of a dose assembly and the at least one actuator element and dose assembly are configured and arranged such that the needle is displaceable along the longitudinal axis and/or in an axis parallel to the longitudinal axis in response to an actuation force so that a portion of the needle moves from an interior to an exterior of the housing and device to allow for dispensation of the medicinal liquid.

A system for measuring injection of a liquid medicine includes a syringe body having proximal and distal ends, a syringe interior, and a syringe flange at the proximal end thereof. The system also includes a stopper member disposed in the syringe interior. The system further includes a plunger member coupled to the stopper member and configured to be manipulated to insert the stopper member distally in the syringe interior relative to the syringe body. Moreover, the system includes a needle coupled to the syringe body at the distal end thereof. In addition, the system includes a sensor flange removably coupled to a syringe body. The sensor flange includes a sensor to measure an injection characteristic and a processor to analyze the injection characteristic to determine an occurrence of an injection event.

The auto-injector consists of a front unit connected to a rear unit, wherein the front unit contains a syringe holder with a syringe coaxially sliding between injecting and secure positions within an activating element preloaded via an ejection spring to secure a trigger button through a stopper located in the rear unit.

The rear unit contains a syringe pusher with a plunger managed via a controller coaxially moved by an injection spring to the front unit upon activating the trigger for injecting medication. After the injection, the activating elements revert to allow the controller to release the syringe which moves into to secure position with the syringe holder and the plunger by the ejection spring.

When the syringe enters a safe position, the controller moves by the injection spring between the activating element and the syringe holder to prevent the syringe from sliding toward the injection side.

Plunger sub-assemblies for automatic injectors include a plunger outer having one or more engagement prongs, a plunger inner having one or more engagement slots which correspond with the engagement prongs of the plunger outer, and a retraction biasing member. The retraction biasing member is retained in a first energized state between the plunger outer and plunger inner when the engagement prongs of the plunger outer are releasably engaged with the engagement slots of the plunger inner. The one or more engagement prongs are capable of flexing substantially radially to release from engagement with the engagement slots of the plunger inner to permit the retraction biasing member to expand from the first energized state to a second expanded state. An automatic injector having a plunger sub-assembly includes a housing, an activation mechanism, and a plunger sub-assembly at least partially mounted within a syringe cartridge having a needle assembly.

A valve actuator that moves in a catheter assembly between a first position where a valve is closed and a second position where the valve is open, the valve actuator including a shaft portion at a distal end of the valve actuator that is configured to pierce the valve, a mating portion at a proximal end of the valve actuator that is configured to engage a Luer device, a diameter reduction region that connects the shaft portion and the mating portion, and a plurality of windows that extend through the valve actuator for flushing fluid, the plurality of windows being disposed in the diameter reduction region, wherein each of the plurality of windows does not extend a full length of the diameter reduction region.

A catheter system may include a catheter assembly and a needle assembly. The catheter assembly may include a catheter hub and a catheter extending distally from the distal end of the catheter hub. The catheter assembly may include a cover coupled to a proximal portion of the catheter hub. The cover may be configured to reduce contact with the catheter assembly during initial insertion of the catheter assembly into vasculature of a patient and/or threading the catheter, which may reduce a risk of bacterial contamination of the catheter. The needle assembly may include an introducer needle, a housing, and a needle hub disposed within the housing. The housing may include a button. A proximal end of the introducer needle may be secured within the needle hub. In response to activation of the button, the needle hub and the introducer needle may move proximally within the housing.