A percutaneous medication device, comprising a syringe to be filled with medical liquid and a needle formation attached to a leading-end of the syringe is provided. The needle formation comprises a needle formation body, from the surface of which a needle projects and a cover portion covers a leading-end of the needle formation body. The needle is inserted into a through-hole formed at the leading-end of the needle formation body and fixed by a fixation member. The needle formation body is mated to the cover portion, a space is formed between an inner surface of the cover portion and the leading-end of the needle formation body, and the needle projects from the leading-end surface of the cover portion through a needle insertion hole formed at the leading-end of the cover portion.

There is provided a cassette unit suitable for use with an auto-injector. The cassette unit comprises a cassette unit housing and a removable cap that in a capping position fits over and thereby, acts to close off, a needle projection aperture of the housing. The cassette unit housing has one or more first engagement features arranged for reversibly engaging one or more second engagement features of the removable cap for reversible lock engagement of the removable cap to the housing; and a shuttle lock control defining one or more blocking elements for selectively blocking movement of said first engagement features relative to said second engagement features. The shuttle lock control is axially movable relative to the cassette unit housing between a first ‘cassette unused’ position; a second ‘cassette unlocked’ position; and after replacement of the removable cap, a third ‘cassette used’ position, locating intermediate the first and second positions.

An injection device comprises a casing, a syringe carrier located within a proximal end of the casing and being movable along a longitudinal axis of the device between a stowed position and a needle insertion position, and a drive assembly located within a distal end of the casing and being movable by an insertion driver in order to move the syringe carrier and a loaded syringe from a stowed position to a needle insertion position. The device further comprises a first formation fixed relative to the casing and a second formation fixed relative to an insertion tube of the drive assembly, the first and second formations defining between them a plurality of stop positions for the insertion tube relative to the casing, spaced along the direction of said longitudinal axis, to prevent significant rearward movement of the insertion tube along said axis when a plunger of a firing cartridge is released from a reaction assembly of the cartridge.

Provided is a cassette unit suitable for use with an auto-injector having an electrically powered drive unit. The cassette unit comprises a cassette unit housing defining a cassette unit housing cavity, a rearward entrance to said cavity and a forward needle projection aperture. The housing cavity may receive a syringe comprising a barrel; a needle at a front end of the barrel; and a plunger that is axially movable within the barrel. The cassette unit also comprises in capping relationship with the rearward entrance of the cassette unit housing, a cassette unit end-cap, said cassette unit end-cap defining a drive rod-receiving opening for receipt of a drive rod for providing forward axial drive to said plunger; and a biasing element defining a biasing relationship between the cassette unit end-cap and an end flange of the syringe barrel, thereby urging the syringe forwards in relation to the cassette unit end cap.

A substance delivery device for delivering a substance from a container includes a body, and a plunger movable with respect to the body so as to expel at least a portion of a substance from the container, a trigger mechanism, a latch member latched in a stationary position at least along the longitudinal axis of the device before use, and a lockout shroud movable along the longitudinal axis relative to the latch mechanism. User manipulation of the trigger mechanism causes the latch mechanism to become unlatched and move along the longitudinal axis and to cause movement of a plunger relative to the body, and in a first position of the lockout shroud along the longitudinal axis relative to the latch member, the lockout shroud prevents the trigger mechanism from unlatching the latch member, whereas in a second position the lockout shroud allows the trigger mechanism to unlatch the latch member.

A drug delivery device (100), including a body (104, 116) having a reservoir (164, 176) disposed therein for containing a medicament and an injection needle (152) for penetrating the skin of a patient, the needle (152) providing a path for the medicament between the reservoir (164, 176) and the patient. The device (100) also includes a needle cover (114) for selectively covering the injection needle (152), an adhesive (264) for selectively adhering the device to the patient, a release liner (500) for selectively covering a patient side of the adhesive (264), and a connecting means (112, 520, 512, 508, 524) for connecting the needle cover (114) and the release liner (500) such that removal of one of the needle cover (114) and the release liner (500) from the device (100) removes the other one of the needle cover (114) and the release liner (500).

A supplementary device is configured to be attached to a drug delivery device. The supplementary device comprises a non-contact sensor configured to output signals indicative of the position of a moveable component within the drug delivery device. The supplementary device further comprises a processor configured to receive the signals output from the non-contact sensor. This processor is additionally configured to determine, based on the signals, whether the drug delivery device is in a pre-activation state or a post-activation state.

A pen needle assembly, comprising an outer cover having an open end, a lid removably connected to the open end of the outer cover, a pen needle disposed in the outer cover, and connecting members disposed on opposite sides of the outer cover. Also disclosed is a pen needle assembly, comprising an outer cover having an open end, a lid removably connected to the open end of the outer cover, a pen needle disposed in the outer cover, and connecting members disposed on opposite sides of the outer cover, wherein a plurality of pen needle assemblies are connected adjacent to each other via the connecting members.

A safety catheter includes a catheter hub, a needle cannula having a tip, and a tip protector. The tip protector includes an outer member and an inner member therein. The outer member has a projection releasably engaging the catheter hub. The inner member has a pair of arms extending to free ends from a base. The inner member is axially shiftable relative to the outer member between a first position wherein the needle tip is distal of the tip protector and the free ends of the arms are spread apart such that the distal tip is not shielded, and a second position wherein the tip is within the inner and outer members and the free ends of the arms are brought into close proximity such that the distal tip is shielded. The inner member is entirely received within the outer member in both the fort and the second positions thereof.

An apparatus including a control unit, a sensor arrangement configured to measure the fill level of a medicament within a container of a drug delivery device, and a cap sensor configured to detect at least partial removal of a cap from the drug delivery device is described. The control unit is configured to be awoken from a dormant state in response to detection by the cap sensor that the cap has been at least partially removed from the drug delivery device. The sensor arrangement is configured to start measurement of the fill level subsequent to the control unit being awoken from the dormant state.