A suction device and system utilizing a moveable and/or portable dry vacuum accumulator for vacuum accumulation. The device has at least one accumulator or reservoir for storing a vacuum charge. The device is initially charged by a vacuum source, such as a vacuum from a wall vacuum source as is conventional in a hospital. The vacuum may be boosted using a vacuum boosting pump that may be pneumatic, hydraulic or even electric. The device can be charged to a second predetermined vacuum level which can be different from both atmospheric pressure as well as a first predetermined vacuum level supplied by the vacuum source. Apparatus is also provided for boosting vacuum or for increasing or decreasing a volume in the at least one accumulator or reservoir.

Apparatuses for collecting breast milk are described herein. The apparatuses include a body having a front side and a rear side opposed to the front side, the body defining a cavity and the rear side defining an opening shaped for receiving a portion of a user's breast. The cavity has an upper region for receiving the portion of the user's breast and a lower region for collecting the breast milk. The opening is positioned adjacent to the upper region of the cavity. The apparatuses may include a suction generating device for modulating the negative pressure in the cavity when the apparatus is pressed against the user's breast.

A nasal fluid-spray device having: a reservoir containing at least one dose (D) of fluid; and a dispenser system that, each time the device is actuated, sprays a dose (D) of fluid through a spray orifice, generating a spray that extends axially from the spray orifice. The device further includes a generator system for generating a secondary flow, which generator system is actuated simultaneously with the dispenser system, the secondary flow generator system having a secondary flow channel provided with an outlet orifice, the outlet orifice arranged downstream from the spray orifice, and the secondary flow extending from the outlet orifice along an axis (B) that forms an angle (α) relative to the axis (A) of the spray and that intersects the axis (A), thereby deforming and/or deflecting the spray.

A manually-actuated, constant reduced-pressure apparatus for use with a reduced-pressure system for treating tissue at a tissue site includes a flexible, collapsible member that is operable to move between a compressed position and an extended position. The collapsible member may be disposed between a carrier member and a slider member that move between a compressed position and an extended position. The carrier member and slider member are urged away from each other by a constant-force biasing member, e.g., a constant force coil spring. As the apparatus moves from the compressed position to the extended position, a constant reduced-pressure is generated and delivered to a reduced-pressure port. Methods of manufacturing a manually-actuated, constant reduced-pressure apparatus and methods of treating a tissue site are also provided.

The methods described herein provide improvements to the measurement of dose content uniformity of inhaler and nasal devices. The methods involve analyzing and measuring a spray pattern of an emitted spray from an inhaler or nasal device. The spray pattern may be used to determine the dose content uniformity of an inhaler or nasal device.

A leak control system (26) for an evacuation system (12) of an insufflation system (1), for controlling leakage of insufflating gas from a vessel (5) of a subject being insufflated. An evacuation conduit (20) connects a Venturi vacuum creating device (14) to the vessel (5) through a pressure relief valve (27) operable from a closed state to an open state in response to a pressure drop across the pressure relief valve (27) in the direction of the arrow A exceeding a predefined pressure drop value. The vacuum creating device (14) is operable in response to a signal from a pressure sensor (10) detecting pressure in the cavity (5) exceeding a predefined pressure value for applying a vacuum to the evacuating conduit (20) to increase the pressure drop across the pressure relief valve (27) to the predefined pressure drop value, for in turn operating the pressure relief valve (27) into the open state. On the pressure in the vessel (5) being reduced below the predefined pressure value, the vacuum creating device (14) is deactivated, and the pressure relief valve (27) transitions into the closed state, thereby preventing further leakage of insufflating gas though the Venturi vacuum creating device (14).

Example embodiments may include an apparatus for providing negative-pressure therapy with a push-to-release actuator. The actuator may be a key insertable through a keyway in the apparatus to engage a movable barrier, such as a piston. The actuator may also be used to lock the barrier in a primed position. Pressing on the actuator can release the barrier and activate the apparatus for negative-pressure therapy. In some examples, the actuator may comprise a shaft, a latch, and a spring biasing the latch toward the shaft. The latch may comprise an opening toward a proximal end of the shaft. The apparatus may comprise a receptacle for receiving the actuator, and a keeper may disposed within the receptacle for coupling to the latch. In some embodiments, the keeper may comprise a base protruding from the wall, and a ledge extending from the base toward the second aperture.

A pressure regulating or pressure relief device comprises an inlet and an outlet chamber with an outlet. The inlet is in fluid communication with the outlet chamber. A valve seat is located between the inlet and the outlet. A valve member is biased to seal against the valve seat, and displaces from the valve seat by an inlet pressure at the inlet increasing above a pressure threshold to allow a flow of gases from the inlet to the outlet via the outlet chamber. The flow of gases through the outlet causes an outlet pressure in the outlet chamber to act on the valve member together with the inlet pressure to displace the valve member from the valve seat.

A nasal delivery device for and a method of delivering a substance to a nasal cavity of a subject, the delivery device comprising: a delivery unit for delivering a flow entraining a substance to one nostril of a subject, the delivery unit including a nosepiece for fitting to a nostril of the subject; and a flow resistor unit for fitting to the other nostril of the subject, the flow resistor unit including a progressive resistor for progressively providing an increasing flow resistance to the delivered flow.

Methods and devices for delivering a dose, such as a medicament, for inhalation. A dose may be stored by a delivery device and dispersed and delivered in a metered fashion to a subject, such as by the subject inhaling via a mouthpiece of the delivery device. One or more chambers of the device may have a toroidal shape and may be arranged to be selectively opened for fluid communication with a flow path of the delivery device, such as by sliding the chamber relative to a portion of the flow path. The flow path may include a restriction that permits air to bypass the chamber, and/or the chamber may be arranged so that fluid entering the chamber interacts with fluid exiting the chamber so as to enhance dispersion of the dose.