Abstract: A dry-powder inhaler may include a first casing portion, a second casing portion, and a hinge arrangement connecting the first casing portion and the second casing portion. The dry-powder inhaler may be assembled by folding the first casing portion and the second casing portion together. The first casing portion may include a cavity for receiving a dose blister foil, said cavity being adapted to contain a dry-powder medicament. The first casing portion and the second casing portion when folded together may be adapted to form an inlet for allowing a lidding foil extending out there from and an outlet for providing the medicament.

Abstract: A dry powder inhaler is disclosed. The dry powder inhaler includes a first housing member and a second housing member being rotatable in relation to one another to prepare administering a medicament dose from at least one medicament reservoir. An air inlet, a first air outlet, and a second air outlet are provided. The air inlet and the first air outlet are connected by a first air channel via a dosage mechanism configured to arrange a dose from the reservoir into the first air channel. The air inlet and the second air outlet are connected by a second air channel. An inhalation chimney is provided internally forming the proximal portion of the first air channel and comprising the first air outlet at a first end thereof.

Abstract: A dry powder inhaler may include a housing having a lower housing part defining at least one air inlet and at least one air outlet. At least one container may be disposed in the lower housing part. The at least one container may include a cavity for a dry powder drug. A chamber may be disposed above the at least one container for deaggregation of the dry powder drug after emptying of the dry powder drug from the cavity. Upon inhalation by a user at the at least one air outlet, air may flow from the at least one air inlet into and through the chamber to empty the dry powder drug from the cavity and convey the dry powder drug to the at least one outlet.

Abstract: A dry-powder inhaler may include a first casing portion, a second casing portion, and a hinge arrangement connecting the first casing portion and the second casing portion. The dry-powder inhaler may be assembled by folding the first casing portion and the second casing portion together. The first casing portion may include a cavity for receiving a dose blister foil, said cavity being adapted to contain a dry-powder medicament. The first casing portion and the second casing portion when folded together may be adapted to form an inlet for allowing a lidding foil extending out there from and an outlet for providing the medicament.

Abstract: A dry powder inhaler may include a housing having a lower housing part defining at least one air inlet and at least one air outlet. At least one container may be disposed in the lower housing part. The at least one container may include a cavity for a dry powder drug. A chamber may be disposed above the at least one container for deaggregation of the dry powder drug after emptying of the dry powder drug from the cavity. Upon inhalation by a user at the at least one air outlet, air may flow from the at least one air inlet into and through the chamber to empty the dry powder drug from the cavity and convey the dry powder drug to the at least one outlet.

Abstract: A method and arrangement for facilitating through-line mismatch RF testing using an air-isolated coaxial line having an inner conductor surrounded by a coaxial shielding. At least one circular opening is provided through the shielding. A radially adjustable piston is provided in each opening such that it is electrically connected to the shielding and such that its protrusion from an inside of the shielding towards the inner conductor is adjustable. The position of the radially adjustable piston is calibrated with a known level of RF mismatch so that a desired level of mismatch can be created through adjustment of the piston. By adjusting the piston so that it does not protrude beyond the inside of the shielding, the arrangement is effectively set to zero and does not have to be disconnected after use.

Abstract: The present invention relates to a container for solids or liquid and a method of opening a container. The container comprises a hollow body which holds the contents and a closure which cooperates with the body to close the container. The closure comprises an opening member which is movable from a retracted position to an opening position in which the closure can be opened. The container further comprises a locking member for securing the opening member, the locking member being movable between a locking position in which the opening member is kept secured in the retracted position and an unlocked position in which the opening member is movable into the opening position.

Abstract: The present invention relates to a method and an arrangement of facilitating through-line mismatch RF testing using an air-isolated coaxial line (1) having an inner conductor (2) surrounded by a coaxial shielding (3). At least one opening (4) is provided through the shielding (3). A radially adjustable piston (5) is provided in each opening (4) such that it is electrically connected to the shielding (3) and such that its protrusion from an inside of the shielding (3) towards the inner conductor (2) may be varied. Hereby is provided for an adjustable and easy characterized mismatch, which does not have to be disconnected after use, but simply set to zero.

Abstract: The administration of at least one drug in the form of dry powder by inhalation through an air flow path may be accomplished by an inhalation system including a delivery device having a mouthpiece through which the powder is inhaled. The inhalation system includes a dose cassette defining at least one drug cavity containing dry powder of a dose to be delivered and being sealed by a lid. Further, the inhalation system includes a resilient member configured to be introduced into the air flow path to guide/direct the air flow into the drug cavity upon removal of the lid.

Abstract: A method for filling a cavity with a quantity of particulate material, comprising the steps of filling a chamber with its open side facing upwards with the quantity of particulate material, positioning the opening of the cavity opposite the opening of the filled chamber, and thereafter rotating the chamber and the cavity so that the cavity is positioned with its open side facing upwards and the chamber with its open side facing downwards, whereby the quantity of particulate material is emptied into the cavity. A corresponding device comprising a chamber, filling means for filling the chamber with the quantity of particulate material, operating means for positioning the opening of the cavity opposite the opening of the chamber, and conveyor belt for rotating the chamber and the cavity so that the cavity is positioned with its open side facing upwards and the chamber is positioned with its open side facing downwards.

Abstract: The present invention relates to a container for solids or liquids, comprising a hollow body which holds the content, a closure which cooperates with the body to close the container and a compliance aid device arranged on the container for indicating the time at which the last dose was taken or when the next dose is due. The compliance aid comprises a movable first part and a fixed second part provided on the hollow body, wherein the first part is automatically moved to a new indicating position in relation to the second part upon moving the closure in relation the hollow body.

Abstract: The present invention relates to a container for solids or liquid and a method of opening a container. The container comprises a hollow body which holds the contents and a closure which cooperates with the body to close the container. The closure comprises an opening member which is movable from a retracted position to an opening position in which the closure can be opened. The container further comprises a locking member for securing the opening member, the locking member being movable between a locking position in which the opening member is kept secured in the retracted position and an unlocked position in which the opening member is movable into the opening position.

Abstract: The present invention relates to a manually actuated delivery device for the delivery of a dose of liquid comprising a housing (1) which includes an outlet through which liquid, in use, is delivered. An actuating member (2) is moveably disposed relative to the housing (1) between a first position and a second position, the user moving the actuating member (2) into the second position to actuate the delivery device. A liquid delivery assembly (3) is located at least partly within the housing (1) the liquid delivery assembly (3) comprising a liquid delivery unit (4) a carrier unit (5) for the liquid delivery unit (4) and a coupling member (6) which couples the movement of the actuating member (2) and the carrier unit (5). The movement of the carrier unit (5) activates a counting mechanism (7a, 7b) which indicates how many doses have been delivered.

Abstract: An inhalation device for administering a powdered medicament by inhalation including a suction tube through which the medicament is drawn on inhalation by a user, a blister pack, a housing which carries the blister pack and has housing surfaces, the suction tube being removably connected to the housing and having a distal end which can interact with the blister pack and a proximal end through which the user inhales, and a resilient member that resiliently biases the suction tube into a position where it is spaced from the housing surfaces to facilitate grasping of the suction tube by the user when the inhalation device is ready for use.

Abstract: The present invention relates to an inhalation device for administering a powdered medicament by inhalation. The inhalation device (1) comprises a suction tube (4) through which the medicament is drawn on inhalation by a user and a blister pack assembly (5). The suction tube (4) has a distal end (7) which interacts with the blister pack assembly (5) and a proximal end (8) through which the user inhales. The inhalation device (1) is also provided with biasing means (6) which raise the suction tube (4) away from the blister pack assembly (5).

Abstract: Valves are disclosed including a housing having at least one fluid inlet and at least one fluid outlet, a valve seat for at least one of the fluid inlets and fluid outlets, a diaphragm movable between a first position engaged with the valve seat and a second position disengaged from the valve seat, the diaphragm having a surface area which is greater than the size of the valve seat so that the surface area of the diaphragm is greater than the surface area necessary for abutment against the valve seat, an actuator for actuating the diaphragm between the first and second positions, and an activator for displacing the diaphragm whereby at least partially portions of the surface area of the diaphragm are exposed to the valve seat upon displacement of the diaphragm.