Drug delivery safety devices having trigger activation systems activated by pressure against the skin of a patient and which automatically shield the needle after withdrawing the needle from the skin of the patient.

A needle module for a drive-controlled handheld unit for repeatedly piercing human or animal skin, comprising a housing; a needle holder, which can be moved back and forth in the housing in a longitudinal direction of the housing; a piercing device on the needle holder, which can be moved, on account of the movement of the needle holder, between a proximal and a distal position, in which a piercing tip of the piercing device is arranged outside the housing; a coupling component, which is coupled to the needle holder in such a way that a driving movement provided with a repetition frequency by a drive device that can be coupled to the coupling component can be introduced onto the needle holder; and a damping component, which is arranged between the needle holder and the coupling component and is configured to damp a transfer of force therebetween.

A system for mixing drug products and injecting includes a syringe body, proximal and distal stopper members disposed in the syringe body, a plunger member, and a needle hub assembly coupled to the distal needle interface of the syringe body. The proximal and distal stopper members form a proximal drug chamber between there between and a distal drug chamber between the distal stopper member and a distal end of the syringe body. The plunger member includes a needle retention feature, an energy-storage member, and an energy-storage member latching member all disposed in disposed in a plunger interior. First and second sizes of the respective proximal and distal drug chambers can be modified by movement of the proximal and distal stopper members relative to the syringe body. The needle is at least partially retractable into plunger interior upon manipulation of the plunger member relative to the syringe body.

Drug delivery safety devices having trigger activation systems activated by pressure against the skin of a patient and which automatically shield the needle after withdrawing the needle from the skin of the patient.

Embodiments provided herein include a resettable injection training device having a body, a plunger slidable relative thereto, an injection simulation member and retractable and extendable shield, wherein the shield releasably locks in a retracted position prior to use. After use of the training device, the shield extends over the injection simulation member to prevent contact with the injection simulation member. Resetting of the slidable shield occurs by applying a force onto a distal end of the shield to retract the shield until a shield locking surface interacts with a locking surface on the body to maintain the shield in a retracted position. Release of the shield from a retracted position to an extended position may occur by moving the plunger toward a distal end of the body until a contact region at a proximal end of the plunger releases the shield locking surface from the body locking surface to release the shield.

An apparatus for use with a syringe for providing a safety syringe, the safety syringe including a plunger configured during an inward stroke to expel a substance from a hypodermic needle attached at an open end of a barrel of the syringe, the apparatus including: a biasing member configured to bias a sheath towards a closed position at least partially covering the hypodermic needle, wherein the biasing member is configured to be released at a point on the inward stroke of the plunger to urge the sheath towards the closed position.

A pneumatically activated retractable-needle syringe comprising a syringe barrel, a plunger, a needle, a needle hub, a locking tip, a propellant gas release cell and a rupture mechanism is provided. The plunger has a retraction lumen defined therein for receiving the needle when the retractable-needle syringe is actuated.

A syringe is provided, including a syringe barrel, a needle set and a push rod. A front end part is provided in the syringe barrel. An end of the needle set has an open area, the open area is transversely provided with a first snap part. The push rod is slidably disposed within the syringe barrel, and an end of the push rod facing the front end part has a second snap part. When the push rod is slidingly moved to the front end part, the second snap part is engaged with the first snap part.

Vented syringes are described herein. A vented syringe includes a syringe body and a plunger body. The syringe body defines a syringe cavity. The plunger body is at least partially disposed within the syringe cavity. The plunger body includes an air intake channel defined within the plunger body. The vented syringe further includes a plunger seal that is sealingly engaged with the syringe cavity to cooperatively define a syringe volume. The vented syringe further includes a one-way valve in fluid communication with the air intake channel and the syringe volume, wherein the one-way valve is configured to prevent fluid flow from the syringe volume to the air intake channel and permit fluid flow from the air intake channel to the syringe volume.

A syringe for medical use, the syringe having a selectively retractable needle and a multifunctional needle holder and retainer ring assembly including a needle holder with a head section having an inwardly tapering frustoconical section of the fluid pathway and a rearwardly facing annular surface surrounding the rear opening, and an elastomeric retainer ring with a substantially unexpanded collar extending rearwardly beyond the rearwardly facing annular surface to increase needle pushout force, reduce activation force and improve fluid flow through the syringe. Annular projections inside the retainer ring and on the outer surface of the head section of the needle holder are also disclosed.