An ejection-type safety intravenous needle includes a sheath, a hub, a cannula fixed on the hub, and a base. An accommodation cavity is formed in the base. The hub is fixed in the accommodation cavity, and the cannula is exposed outside of the accommodation cavity. The sheath encloses the cannula, and a bottom of the sheath is located in the accommodation cavity and provided with a first limiting structure. A second limiting structure cooperating with the first limiting structure is provided at a top of the accommodation cavity. An elastic element is provided in the accommodation cavity, and the elastic element abuts against a bottom end of the sheath. A top and a bottom of the base are provided with a first clamping structure and a second clamping structure, respectively. A third clamping structure cooperating with the first clamping structure and the second clamping structure is provided on the sheath.

A safety cover configured to be coupled to an injection device and to provide a protective enclosure for a needle of the injection device, the safety cover including an outer cover member; an inner cover member coupled to the outer cover member in a concentric arrangement so that the outer cover member encloses at least a portion of the inner cover member, wherein the outer cover member is configured to move relative to the inner cover member from an unlocked position, in which the needle of the injection device is accessible for use, to a locked position, in which the outer cover member and the inner cover member are fixed at one another and the needle of the injection device is inaccessible, wherein the outer cover member includes a body that includes a proximal end, a distal end, and a cavity defined within the body.

A set of at least two drug delivery devices includes a first drug delivery device and a second drug delivery device, The first and second drug delivery devices each include a first set of mutual members that are identical, and the first drug delivery device and the second drug delivery device each include a second set of distinguishing members that differ. The first drug delivery device includes a first connection device for attaching a first dispensing unit to the first drug delivery device and the second drug delivery device includes second connection device for attaching a second dispensing unit to the second drug delivery device, the first and second connection devices differ from each other so that the second dispensing unit is not attachable to the first connection device and the first dispensing unit is not attachable to the second connection device.

Devices having male connectors for preventing connection to non-compatible female connectors are described. An exemplary male connector includes an elongate tip and a collar disposed coaxially around the elongate tip including a plurality of ribs disposed on either an inside surface or an outside surface of the collar for preventing entry of a non-compatible female connector into a channel formed between the elongate tip and the collar. One or more embodiments pertain to a device with a male connector and a compatible female connector including a threaded portion for engaging a corresponding threaded portion of the male connector.

An apparatus includes a housing coupled to a medicament container, which is coupled to a needle. An injection assembly is disposed within the housing and includes an energy storage member and an actuation rod. A distal end portion of the actuation rod is disposed within the medicament container. The energy storage member can produce a force on a proximal end portion of the actuation rod sufficient to move the distal end portion of the actuation rod within the medicament container. This can convey at least a portion of a substance from the medicament container via the needle when a distal tip of the needle is disposed within a first region of a target location. The force is insufficient to move the distal end portion of the actuation rod within the medicament container when the distal tip of the needle is disposed within a second region of the target location.

A needle actuator assembly for a drug delivery system includes a needle actuator body having a guide surface, a needle shuttle having a cam surface, with the needle shuttle moveable along a vertical axis between a first position and a second position. The needle shuttle is configured to move between the first and second position through engagement between the guide surface of the needle actuator body and the cam surface of the needle shuttle. The assembly further including a needle received by the needle shuttle.

A cannula holder capable of securing a cannula to the holder at the time of piercing work, and easily removing the cannula from the holder using tweezers or the like. The cannula holder, to which a piercing needle for piercing an eyeball and a cannula are attached when attaching the cannula used in ophthalmic operations to the eyeball, includes claw portions that are formed on a front end of the cannula holder and which press sides of the cannula either at positions where said claw portions face each other or from multiple directions. A depression may be provided in a side of the front end of the cannula holder, allowing visibility of a part of a back end of the cannula from the depression.

A locking mechanism is provided for use with a reservoir and a reservoir holder so as to prevent unwanted tampering with the reservoir. The mechanism comprises a main body with an aperture that is coupled to the reservoir. A hinged flange is provided on the main body. The flange folds inwards at the pivot point provided by the hinge, toward the aperture of the main body, allowing the mechanism to pass over the ferrule of the reservoir. Once the mechanism is placed over the cartridge, the flange folds toward the reservoir at the pivot point, flexing away from the main body. The flange rests against the underside of the reservoir ferrule, thereby retaining the reservoir within the locking mechanism. The locking mechanism may be for use with either a disposable or a reusable delivery device.

A syringe for use with a medical injector system includes a barrel and a semi-rigid hub, the hub having an outer surface adapted to slidingly move within the barrel, and an inner surface having a continous circumferential wall. The hub further includes an annular engaging portion recessed within at least part of the continous circumferential wall forming a groove, at least one radially extendable and retractable retention member disposed at partially within a proximal cylindrical portion of the hub, and the elastometric seal engaged with a seal engaging portion on the hub and slidingly engaged with the barrel of the syringe. The semi-rigid hub and the elastomeric seal are reciprocally slidable within the barrel, and the at least one radially entendable and retractable retention member is configured to releasably engage the groove upon retraction of the plunger to permit the semi-rigid hub to be selectively withdrawn within the barrel.

A needle actuator assembly for a drug delivery system includes a needle actuator body having a guide surface, a needle shuttle having a cam surface, with the needle shuttle moveable along a vertical axis between a first position and a second position. The needle shuttle is configured to move between the first and second position through engagement between the guide surface of the needle actuator body and the cam surface of the needle shuttle. The assembly further including a needle received by the needle shuttle.