Pre-loaded syringes for delivering an embolic agent are disclosed herein. Methods related to syringes pre-loaded with an embolic agent are also disclosed.

A priming assembly for a drug delivery device includes a hub, a base connected to the hub and moveable relative to the hub between a first position and a second position, with the base defining a passageway, a cap defining an interior chamber and a passageway in fluid communication with the interior chamber, and a needle connected to the hub and positioned within the interior chamber of the cap, where the passageway of the base is in fluid communication with the passageway of the cap when the base is in the first position, and where the passageway of the base is isolated from the passageway of the cap when the base is in the second position.

A medicant injection device includes a compressible body, a tip, and an outer luer body. The compressible body has a proximal end, a distal end, and a plurality of bellows, and defines an inner cavity for holding a liquid medicant. The tip is positioned at the proximal end of the compressible body. The outer luer body includes internal threads, and is positioned over and engaged with the tip to form a first fitting therewith. The first fitting is configured to be connected with a second fitting. A medicant injection device includes a compressible body having first and second arms, a receptacle interconnected with the compressible body and defining an inner cavity, and a first fitting configured to engage a second fitting. The compressible body is configured to be compressed by forcing the distal end of the first and second arm toward each other.

A sanitizing device used to sanitize a bulb syringe. The device preferably includes a base, a bulb receiver, and a sanitization system. The sanitization system produces a sanitizing gas that is propelled into and possibly around a bulb syringe in order to sanitize the surfaces of the syringe. The sanitization system preferably includes an ionization module, a fan, electrodes, and a power supply. Preferably, the sanitization system is housed in a conical housing which includes a central nozzle and an array of openings centered around the nozzle exit. The sanitization device preferably includes an automatic switch that is activated by the presence of a bulb syringe or upon placing a cover over the device.

The invention provides a syringe for use in an ophthalmic injection. The syringe comprises a body, a stopper and a plunger. The body comprises an outlet at an outlet end and the stopper is arranged within the body such that a front surface of the stopper and the body define a variable volume chamber from which a fluid can be expelled though the outlet. The plunger comprises a plunger contact surface at a first end and a rod extends between the plunger contact surface and a rear portion. The plunger contact surface is arranged to contact the stopper but not couple thereto, such that the plunger can be used to force the stopper towards the outlet end of the body, reducing the volume of the variable volume chamber, but not to move the stopper away from the outlet end.

The invention relates to a shield triggered injection device with a triggering mechanism for injecting doses of a liquid drug. The injection device has a housing structure with a distal end and a proximal end, and a needle shield rotationally mounted relatively to the housing structure such that the needle shield is rotatable between a first position and a second position and which the needle shield when rotated from the first position to the second position is guided helically in a helical track. Further, an axially movable trigger element for releasing a set dose to be automatically ejected upon proximal movement of the trigger element against a bias is provided. The trigger element is provided with an axial locking arm which is biased into the helical track to block the passage through the helical track at least in one rotational direction.

A package (10) for components of a medical apparatus comprising a plurality of panels (12-20) defining a container (11) having an interior space. A first component of the medical apparatus is disposed within the interior space. The first component of the medical apparatus comprises a medicament delivery device. The container (11) comprises a base panel (12) which forms a bottom wall of the container (11). At least one lid panel (16) is connected to the base panel (12) and is foldable into a position in which it extends coplanar with the base panel (12) when the container (11) is manipulated into an open configuration. At least one lid panel (16) includes a sterile surface forming a preparation surface upon which a user may place components of a medical apparatus when the container (11) is in the open configuration. Also disclosed is a medical apparatus comprising such a package with a container of medicament (26) within the interior space of the container (11).

A contrast injector system includes one or more devices for reducing or eliminating risk of cross-patient contamination. In particular, the contrast injector system includes at least one of a sterilization device, vibration device, and illuminator device positioned on a component of the contrast injector system, where the sterilization device, vibration device, and/or illuminator device is in communication with a console of the contrast injector system. The sterilization device has an energy emitter positioned to emit energy to one or more components of the system. The vibration device is positioned on a component of the system so as to induce acoustic vibrations on a surface of such component. The illuminator device includes a light source positioned to illuminate a component of the system.

The present invention includes a device cleaner, and method of use, for cleaning a device port, particularly a medical device port, that may be inserted into the device port cleaner for cleaning and/or disinfecting.

Medical devices such as medical containers can be formed of glass and annealed which produces a clean device having a low bio-burden, or formed by plastic molding which produces a clean device. The clean devices are immediately transferred to a controlled environment such as a clean room or localized area to avoid the need to maintain cleanliness levels in an entire room. Syringe tip closures can be introduced into the housing assembly, where syringe barrels and tip closures are cleaned with filtered ionized air and the tip closures are coupled to the barrels. The syringe barrels can be filled with a substance and a closure member attached. While still in the housing assembly the syringe barrels can be formed into an array and placed in a clean outer container, which is then closed and sealed.