One embodiment is directed to a safety syringe system, comprising: an off-the-shelf syringe assembly comprising a syringe body and a plunger tip; a needle assembly removably coupleable to the distal end of the syringe body such that medicinal fluid may be transferred through a retractable needle coupled to a needle housing comprising the needle assembly upon insertion of the plunger tip relative to the syringe body; and a plunger control assembly coupled to the plunger tip and configured to facilitate manual insertion of the plunger tip relative to the syringe body; wherein upon insertion of the plunger tip to a final insertion state and release of an associated manual insertion load, the plunger tip may be proximally withdrawn, pulling the retractable needle proximally relative to the needle housing to a safe locked and retracted state wherein it is no longer exposed for injection.

The present disclosure relates to drug-delivery apparatuses, and in particular, to a drug-delivery apparatus with a fluidic subsystem that can be used to deliver multiple injections to a patient from a drug container storing a drug fluid. The fluidic subsystem may include multiple injection-needle compartments and re-sealable septa to allow multiple accesses to the drug container, while also preserving the sterility of the drug fluid and of the fluid pathway through which the fluid is delivered to a patient. In some embodiments, the fluidic subsystem may be used to deliver drug fluids that do not contain any preservatives (e.g., non-preserved drugs).

Device for preventing needle reuse and injury has a needle cap or enclosure, a body, and a needle. The needle cap and/or body is movable relative to the other from (i) a first position wherein the needle is received within and enclosed by the needle cap to prevent needle injury; (ii) to a second position wherein the needle is passed through the needle cap to penetrate tissue; and (iii) to a third position wherein the needle is within and enclosed by the needle cap, and the needle cap and body are locked to prevent needle reuse and injury. The needle cap conceals the needle from view before, during and after the patient injection. An intra-needle one-way valve allows liquid flow therethrough in a direction from an inlet toward an outlet of the needle, and prevents liquid flow in an opposite direction to prevent cross-contamination between the needle and a syringe.

A device for transferring fluids in a closed system transfer device using flash for last drop extraction and to reduce coring. The device including a piercing member having a distal end and a proximal end and defining a longitudinal fluid channel. A first opening positioned at the distal end of the piercing member wherein the first opening is in fluid communication with the longitudinal fluid channel. A cover or flash positioned over the first opening. The cover including a pre-cut pattern wherein the cover opens along the pre-cut pattern upon application of a distally directed force from the longitudinal fluid channel. The distal end including the first opening having a steep taper to facilitate last drop extraction.

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.

A syringe assembly includes a main part with a bottom part and a top part. A compressible portion is connected to the top part, and a press unit is formed to the top the compressible portion. A needle is fixed to the top part and located within the compressible portion. The tip of the needle is located corresponding to a film of the press unit. The bottom part has a first lip and a second lip formed to the inner periphery thereof. The top part has a first groove and a second groove in the outer periphery thereof. Multiple collars are telescopically connected to each other, and are connected between the top part and the bottom part. The main part is located in the multiple collars. Each collar has two engaging portions which form two engaging grooves to be engaged with each other when collapsing the collars.

Embodiments of the invention include a medicament device configured to provide stepwise instructions for using the device to a user in a particular sequence is provided. The device includes a device housing configured to receive a container, the housing including a control interface, the control interface including at least one responsive member reactive to a user input, an actuation mechanism configured to interact with the container, a signal output component associated with the device housing, and circuitry associated with the device housing configured to control a provision of the stepwise instructions to the user in the particular sequence. The container includes a first housing for containing a medicament, a second housing, and an injection member, wherein the first and second housings are movable relative to one another. The container further includes an injection member which is retractable within the second housing to prevent an unintentional contact with the injection member.

It is known to deliver drugs through the skin, i.e. transdermally, by using a needle that is used in conjunction with a device.

A device (10) comprises a device body (12) which has an opening (14) for receiving a needle assembly (100) in use. The device also comprises a loading mechanism (16) which is moveable in use to receive the needle assembly (100) via the opening (14) and secure the needle assembly (100) relative to the device body (12). The loading mechanism (16) is configured to receive and secure the needle assembly (100) upon force exerted on the loading mechanism (16) in a single direction (F.sub.D1).

A system for injecting includes a syringe 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 syringe 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 syringe 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.

A system for injecting includes a syringe 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 syringe body, the plunger member. 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 syringe 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 at least partially retractable into plunger interior. The needle proximal end feature includes an annular distally facing surface.