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.

There is provided a control device for providing a fluidic signal to a medical infusion apparatus, the device comprising a housing and a pressure control sheet, wherein the pressure control sheet is formed from a deformable and resilient material, and the pressure control sheet is secured to and forms a seal with the housing such that the housing and the pressure control sheet together define a first chamber and an independent second chamber, wherein the pressure control sheet is arranged so that the fluid pressure within each chamber can be changed upon input from a user. The control device further comprises a first fluid conduit member in fluid-flow communication with the first chamber and a second fluid conduit member in fluid-flow communication with the second chamber, wherein, in use, inputs from a user change the fluid pressure within the chambers which causes movement of fluid through the fluid conduit members to provide fluidic signals.

A wearable drug delivery device includes an injector having a housing, a reservoir, a needle or cannula, a drive mechanism for urging drug product out of the reservoir, through the needle or cannula, and to a patient, and an activator mechanism disposed on a surface of the housing for activating the drive mechanism. An activation prevention mechanism is coupled to the injector housing and/or activation prevention mechanism to prevent inadvertent actuation of the activator mechanism.

A spring bridge (40), for a spring bridge breathing bag plate system (80) of a closed-circuit respirator (100), includes a spring bridge carrier (42) for the arrangement of at least one spring element (82) of a spring bridge breathing bag plate system (80) and at least one fastening element (44) for holding the spring bridge (40) at the closed-circuit respirator (100). The at least one fastening element (44) is a rotating element and/or a sliding element for the rotatable and/or sliding movement of the spring bridge carrier (42) at and relative to the closed-circuit respirator (100). A spring bridge breathing bag plate system (80) is provided for a closed-circuit respirator (100) as well as for a closed-circuit respirator (100).

A medicine powder delivery device and a medicine bottle thereof and a bottle cap of the medicine bottle are disclosed. The medicine powder delivery device includes a medicine bottle and a gas supply member. The medicine bottle has a bottle body and a bottle cap. The bottle body is filled with a medicine powder. When the bottle body is inverted, the bottle body has an unfilled space that is not filled with the medicine powder. The bottle cap includes a cap body, a medicine delivery tube, and a gas delivery tube. The cap body covers the bottle body. The medicine delivery tube and the gas delivery tube extends into the cap body. The medicine delivery tube communicating with the bottle body the gas delivery tube inserted into the unfilled space of the bottle body. The gas supply member is connected to the gas delivery tube.

A breast pump includes a body including a hood attachment portion, a bottle attachment portion, and an inner passage extending between the hood attachment portion and the bottle attachment portion; a diaphragm configured to generate negative pressure in the inner passage; a handle manually operated to move back and forth; and a link mechanism configured to support the handle in a manner movable back and forth relative to the body. The handle is configured to change pressure of the inner passage from a normal state to a negative state by displacing the diaphragm in a lifting direction. The link mechanism is configured to apply an operation force to the handle that becomes maximal during handle movement when the handle is moved in an operation direction that changes the pressure from the normal state to the negative state.

A nasal ventilation mask supplies breathing gas to an airway of a patient. The mask has a housing defining an internal cavity and having a peripheral end defining an end opening. The end opening is in fluid communication with the internal cavity, and the end opening is configured to be positioned over an airway on a face of a patient. The housing further defines a connector segment having a receiver member. The connector member defines a top wall defining an outer periphery. The receiver member has a portion extending past the outer periphery. The receiving member has an opening in fluid communication with the internal cavity. The mask also has a sealing member operably connected to the housing proximate the end opening. The sealing member is configured to abut the face of the patient, and the receiver member is configured to be operably connected to a supply of breathing gas.

A nebulizer device aerosolizes (or vaporizes) liquid drawn from a liquid reservoir via a fluid flow path into a nebulization chamber. An inlet port is coupled to an external air supply and leads through a check valve and Venturi nozzle (e.g. a duckbill valve) into the chamber to direct an air stream across an opening of the fluid flow path. A discharge port leads from the chamber to a user mask, mouthpiece or canula, where the aerosol or vapor mixture can be inhaled. A filtered outlet port isolates exhaled material from the external environment. Multiple discrete heating elements may be placed around the fluid flow path to preheat the liquid. If the liquid is sufficiently volatile, heating may vaporize the material which can condense back into an aerosol after mixing with the air stream. A set of check valves direct one-way fluid flow and prevent leakage or spillage of material from the device.

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 tattoo ink mixing apparatus has a housing having a cavity, a plunger movable between a first position and a second position, and a dynamic member disposed in the cavity and adapted to engage with the plunger distal end. The dynamic member moves in response to movement of the plunger and alternatively creates a suction force and an expulsion force in the opening of the distal end of the housing as the plunger moves between its first and second positions.