Abstract: A cap assembly for a medicament delivery device is disclosed. The cap assembly includes a cap configured to be mounted to a proximal end of the medicament delivery device, wherein the cap comprises a cam surface. The cap assembly further includes a squeezer comprising (i) a body defining a first longitudinally extending channel configured to receive a delivery member shield and (ii) a plurality of radial arms flexible in a radial direction. The cap assembly also includes a spinner comprising (i) a proximal end face configured to cooperate with the cam surface of the cap, (ii) a body defining a second longitudinally extending channel configured to receive the squeezer, and (iii) a plurality of holes in the body of the spinner configured to receive the plurality of radial arms of the squeezer.

Abstract: The present disclosure relates to a cap assembly (5) for a medicament delivery device, comprising: a cap (7) having a tubular body (7b) defining an axially extending distal opening (7c) and configured to be mounted to a proximal end of a medicament delivery device, wherein the cap (7) has a bottom structure (7e) defining a proximal end of the distal opening (7c), wherein the bottom structure (7e) has a cam structure (7f) provided inside the tubular body (7b), and wherein the tubular body (7b) has inner walls provided with radial recesses (7d), and an elongated squeeze member (9) configured to be received in the distal opening (7c) of the tubular body (7b), and having a longitudinally extending channel (9d) configured to receive a delivery member shield, and which squeeze member (9) has radial arms (9e) flexible in the radial direction and forming part of a wall of the channel (9d), wherein the squeeze member (9) has a proximal end face (9a) configured to cooperate with the cam structure (7f) of the cap (7), w

Abstract: A cap assembly for a medicament delivery device is disclosed. The cap assembly includes a cap configured to be mounted to a proximal end of the medicament delivery device, wherein the cap comprises a cam surface. The cap assembly further includes a squeezer comprising (i) a body defining a first longitudinally extending channel configured to receive a delivery member shield and (ii) a plurality of radial arms flexible in a radial direction. The cap assembly also includes a spinner comprising (i) a proximal end face configured to cooperate with the cam surface of the cap, (ii) a body defining a second longitudinally extending channel configured to receive the squeezer, and (iii) a plurality of holes in the body of the spinner configured to receive the plurality of radial arms of the squeezer.

Abstract: A cap assembly for a medicament delivery device is disclosed. The cap assembly includes a cap configured to be mounted to a proximal end of the medicament delivery device, wherein the cap comprises a cam surface. The cap assembly further includes a squeezer comprising (i) a body defining a first longitudinally extending channel configured to receive a delivery member shield and (ii) a plurality of radial arms flexible in a radial direction. The cap assembly also includes a spinner comprising (i) a proximal end face configured to cooperate with the cam surface of the cap, (ii) a body defining a second longitudinally extending channel configured to receive the squeezer, and (iii) a plurality of holes in the body of the spinner configured to receive the plurality of radial arms of the squeezer.

Abstract: Disclosed is an apparatus for wireless power transmission between an external power source and an electric mobility vehicle.

Abstract: A sub-assembly of a medicament delivery device is presented, where the sub-assembly includes a plunger rod that is biased, a main body arranged on the plunger rod, and a coupling member movable relative to the main body, where the main body includes a first locking element, the coupling member includes a second locking element, and where the first locking element and the second locking element are configured to be releasably engaged with each other such that the coupling member is prevented from moving relative to the main body.

Abstract: The present invention relates to a drive mechanism for a medicament delivery device, comprising a plunger rod (54) arranged to act on a stopper (28) arranged in a medicament container (16); a compression drive spring (58) operably connected to said plunger rod (54) and capable of applying a force on said plunger rod (54); a spring guide (78) arranged coaxial with, and radially outside, said compression drive spring (58), capable of preventing buckling of said drive spring, wherein said spring guide (78) comprises a resilient force element (86) capable of applying a force on said medicament container (16).

Abstract: A medicament delivery device is presented having an elongated housing extending in a longitudinal direction, which housing is arranged to accommodate a medicament container, an end cap arranged with a first attachment element designed to engage with a second attachment element on the housing for attaching the end cap to the housing, a rotator rotatably arranged inside the housing, an activator axially slidable with respect to the housing from an extended position to a retracted position and operably connected to the rotator such as to rotate the rotator from an initial non-activated rotational position and an activated rotational position when the activator is moved from the extended to the retracted position. The rotator further comprises a blocking element arranged to cooperate with the first attachment element for preventing disengagement of the first attachment element from the second attachment element when the rotator is in the activated rotational position.

Abstract: The present disclosure relates to a cap assembly (5) for a medicament delivery device, comprising: a cap (7) having a tubular body (7b) defining an axially extending distal opening (7c) and configured to be mounted to a proximal end of a medicament delivery device, wherein the cap (7) has a bottom structure (7e) defining a proximal end of the distal opening (7c), wherein the bottom structure (7e) has a cam structure (7f) provided inside the tubular body (7b), and wherein the tubular body (7b) has inner walls provided with radial recesses (7d), and an elongated squeeze member (9) configured to be received in the distal opening (7c) of the tubular body (7b), and having a longitudinally extending channel (9d) configured to receive a delivery member shield, and which squeeze member (9) has radial arms (9e) flexible in the radial direction and forming part of a wall of the channel (9d), wherein the squeeze member (9) has a proximal end face (9a) configured to cooperate with the cam structure (7f) of the cap (7), w

Abstract: The present disclosure relates to a medicament container assembly (11) for a medicament delivery device, comprising: an elongated body (3) configured to receive a medicament container (17) and provided with a radially flexible first gripper arm (3f) extending in the axial direction of the body (3) and an oppositely arranged radially flexible second gripper arm (3g) extending in the axial direction of the body (3), wherein the first gripper arm (3g) and the second gripper arm (3f) are configured to support a neck portion of a medicament container, and a clamp member (13) configured to be arranged radially outside of the first gripper arm (3f) and the second gripper arm (3g), to press the first gripper arm (3f) and the second gripper arm (3g) radially inwards, to prevent proximal displacement of a medicament container.

Abstract: Medicament delivery device comprising: which extends along a longitudinal axis and comprises:a generally tubular elongated housing having a proximal and a distal end, which generally tubular elongated housing is arranged to accommodate a medicament container (28); a drive unit comprising a drive element (116) and plunger rod (68) operably arranged to act on said medicament container (28); a tubular element (72) rotatable arranged in relation to said housing and operably arranged to said plunger rod(68).The invention is characterised in that the plunger rod comprises at least one holding member (80) and in that the tubular element (72) comprises at least one arm (78) extending generally transversal to the longitudinal axis of the device, wherein the at least one arm (78) is arranged to engage the at least one holding member (80) on said plunger rod (68) to releasable hold said drive unit in an energy accumulated state.

Abstract: An application for a disposable support/resuscitation system includes a pressurized gas inlet connected to a pressure relief device. The pressure relief device has a first pressure relief valve that opens at a setable gas pressure and, optionally, has a second pressure relief valve that opens at a pre-determined maximum gas pressure. Changing the first pressure release valve from a low pressure range to a high pressure range requires activation of a pressure range actuation button. A manometer is connected to the pressure relief valve. A manually operated valve is connected to the manometer, and a patient interface port is connected with the manually operated valve. The manually operated valve selectively controls administration of the pressurized gas to the patient. The manometer, pressure relief device, and manually operated valve are made from non-ferromagnetic materials for proper operation in the vicinity of a Magnetic Resonance Imaging System.

Abstract: An application for a disposable support/resuscitation system is disclosed includes a pressurized gas inlet and a pressure relief device interfaced to the pressurized gas inlet. The pressure relief device has a first pressure relief valve that opens at a setable gas pressure and, optionally, has a second pressure relief valve that opens at a pre-determined maximum gas pressure. A manometer is connected to the pressure relief valve. A manually operated valve is connected/interfaced to the manometer, and a patient interface port is connected/interfaced with the manually operated valve. The manually operated valve selectively controls administration of the pressurized gas to the patient and both the manometer and the manually operated valve are in close proximity to the patient. The manometer, pressure relief device, and manually operated valve are made from non-ferromagnetic materials for proper operation in the vicinity of a Magnetic Resonance Imaging System.

Abstract: An application for a PEEP valve includes a filter media in the air flow between a patient interface and exit vent(s). The patient interface is connected to a patient airway system and the exit vents exhaust exhalation gasses into the atmosphere. The filter prevents or reduces the passage of microbes from the patient's exhalation gasses into the atmosphere. The PEEP valve provides positive gas pressure to a patient's lungs, requiring a predetermined exhalation gas pressure to be exceeded before releasing exhalation gasses into the atmosphere.

Abstract: An application for a disposable support/resuscitation system is disclosed includes a pressurized gas inlet and a pressure relief device interfaced to the pressurized gas inlet. The pressure relief device has a first pressure relief valve that opens at a setable gas pressure and, optionally, has a second pressure relief valve that opens at a pre-determined maximum gas pressure. A manometer is interfaced to the pressure relief valve, a manually operated valve is interfaced to the manometer, and a patient interface port is interfaced with the manually operated valve. The manually operated valve selectively controls administration of the pressurized gas to the patient and both the manometer and the manually operated valve are in close proximity to the patient.

Abstract: An application for a PEEP valve includes a filter media in the air flow between a patient interface and exit vent(s). The patient interface is connected to a patient airway system and the exit vents exhaust exhalation gasses into the atmosphere. The filter prevents or reduces the passage of microbes from the patient's exhalation gasses into the atmosphere. The PEEP valve provides positive gas pressure to a patient's lungs, requiring a predetermined exhalation gas pressure to be exceeded before releasing exhalation gasses into the atmosphere.