An auto-injector for administering a dose of a liquid medicament (M) is presented having an elongate case, a carrier subassembly comprising a tubular carrier slidably arranged inside the case, where the carrier adapted to contain a syringe with a hollow injection needle. The injector also has, a drive spring and a plunger for forwarding load of the drive spring to a stopper of the syringe, wherein the syringe is lockable for joint axial translation with the carrier. A control spring is arranged around the carrier for translating the carrier in a proximal direction (P) for advancing the needle beyond a proximal end of the auto-injector, and a trigger button is used for releasing the control spring on actuation.

A needle guard for a manual tattooing device includes a device body and a spring-loaded plunger having a tattoo needle at one end. The plunger is mounted for translational movement within the device body by manual activation of the plunger. The device includes a locking mechanism such that, in a first position, the plunger can be translated to extend the tattoo needle outside of the device body. However, in a second position of the locking device, translational movement of the plunger is prevented, which in turn prevents the exposure of the tattoo needle outside the confines of the device body.

Systems and methods are disclosed for processing sensor data collected by a drug delivery device with an external computing device. The drug delivery device may include a reservoir and a delivery cannula having a proximal end in fluid communication with the reservoir and a distal end to be received within a patient. The drug delivery device may further include one or more sensors configured to generate sensor data representative of a condition and/or operational state of the drug delivery device, and a communication module configured to transmit information to the external computing device. The external computing device may process the information received from the drug delivery device according to information stored in a memory of the external computing device to determine the condition or the operational state of the drug delivery device and/or generate instructional or informational prompts to be displayed to a user or patient.

The present utility model provides an electrically powered needle-free injector (100), comprising: a needle-free injector body (120); and a needle-free injection end (130) extending distally from the needle-free injector body (120) for medicine administration, the needle-free injector body (120) comprises: a housing (3), an inside of which is divided into a pressurized injection chamber (123) and a motor chamber (124); a pressurized injection assembly (170) disposed within the pressurized injection chamber (123); a needle-free injector locking mechanism (180) at least partially disposed within the pressurized injection chamber; and a motor assembly (190) disposed within the motor chamber (124). The present utility model has a beneficial effect that it may provide a power source for the needle-free injector to electrically take medicine and inject by a built-in motor; it works reliably, is used conveniently, and has a small size.

A substance delivery device (autoinjector) for use with a container (such as a syringe) containing the substance includes: a body arranged to house or hold the container; a plunger which is movable with respect to at least a portion of the body, the plunger being arranged to act upon the container so as to move the container with respect to the portion of the body; wherein the plunger is also arranged to expel at least a portion of the substance from the container; and wherein the device includes elements for adjusting the amount of substance to be expelled from the container. The device can also have elements for priming the container, and can accommodate containers of different size or shape.

A drug delivery device, in the form of an injector, may include one of a number of systems for limiting the delivery of a medical fluid or drug product in case of movement of (e.g., removal of) the injector relative to the patient as determined by a proximity sensor. The drug delivery system may in the alternative or in addition include systems for indicating the amount of medical fluid or drug product delivered (or not delivered) in case of movement of (e.g., removal of) the injector relative to the patient as determined by the proximity sensor. The injector may be, for example, an on-body injector or an hand-held autoinjector.

A reporting injection device, including a barrel in fluid communication with a needle connected with a first end of the barrel, a piston including a plunger, the piston positioned within a second end of the barrel and the plunger having a fluid-tight interaction with an interior of the barrel, and a microprocessor in electronic communication with a switch and a wireless module, the microprocessor configured to send an administration data from the wireless module after triggering the switch.

A safe auto-needle device for injection, comprising: a main housing; a syringe-support for receiving a disposable prefilled syringe; said syringe comprises: a piston; a proximal end; and a distal end terminating in a needle covered by a needle sheath (NS); a drive mechanism for advancing said syringe-support distally towards an injection site; a tubular needle shield; moveable from: a needle covering position, to partially exposed, to needle irreversibly concealed; said generally tubular needle shield comprising a distal end for contacting an injection site, and a proximal end; a spring urging distal movement of said needle shield; and said needle shield comprising a spring seat; an NS remover, designed to mate with and irreversibly grip said NS, for removal of said NS prior to injection; a locking mechanism preventing premature advancement of said needle; a plunger rod for engaging said piston, wherein depressing of said plunger is manually controllable; wherein in use of said device, said NS remover is removed; said distal end of said needle shield is pressed upon an injection site, releasing said locking mechanism, and driving said syringe-support and said syringe, distally until needle penetration; and upon depressing of said plunger, a medicament may be injected. The invention additionally provides a novel two-component NS remover.

Disclosed are systems that include a syringe having a barrel configured to hold a fluid and a plunger configured to draw the fluid into the barrel when the plunger is pulled backward through the barrel. The syringe is configured to inhibit forward movement of the plunger. For example, the systems can include mating pockets configured to engage barbs to inhibit forward movement of the plunger.

A method of sterilizing a prefilled syringe comprises assembling a syringe assembly and performing at least one ethylene oxide (EtO) sterilization procedure cycle. The assembling step includes inserting a tip cap at a first end of a plunger, filling a non-glass barrel with sterilization sensitive material at a second end of the barrel, and inserting the plunger into the barrel at a second end to seal the sterilization sensitive material within the barrel. The EtO sterilization procedure cycle comprises undergoing a preprocessing stage, a wash and conditioning stage, an EtO sterilization stage and a wash and post exposure stage. Upon completing the EtO sterilization procedure cycle, a resultant pH of the sterilization-sensitive material does not exceed an acceptable pH range as defined by the United States Pharmacopeia. The disclosure also discusses inserting an assembled prefilled syringe into a procedure tray prior to performing the EtO sterilization procedure cycle.