An object is to provide a blood processing filter favorable in both of the effectiveness (leukocyte removing performance) and the safety (reduction in the amount of elutable substances). The object can be achieved by a blood processing filter comprising a filtration medium including a polyester fiber, wherein a surface area of the filtration medium is 6.0 m.sup.2 or more, and a maximum absorbance of an aqueous extract of the blood processing filter in the range from 240 to 245 nm is 0.03 or less.

A test fixture for testing aerosol provision devices may include a housing, a plurality of testing modules disposed at the housing where each of the testing modules includes a cavity configured to receive a portion of an aerosol provision device, and processing circuitry operably coupled to the testing modules. Each of the testing modules may be configured to interface with an assembly of a respective one of the aerosol provision devices to transition the assembly between an initial state and a transitioned state during a functional test controlled by the processing circuitry. The processing circuitry may be configured to conduct the functional test of at least two of the testing modules simultaneously.

A system and method for reducing gas bubbles, including gaseous microemboli (GME) during cardiopulmonary bypass (CPB) by the use of an oxygenator with venous blood bypass and a filter in the venous blood bypass is provided.

A flow generator includes a housing, a blower structured to generate a flow of pressurized breathable air, and a suspension device to support the blower within the housing and provide a pressure seal between low and high pressure sides of the blower. The suspension device includes a bellows-like portion provided along the perimeter of the blower to absorb shock applied at least radially to the blower and one or more cones provided along upper and/or lower sides of the blower to absorb shock applied at least axially to the blower.

A disposable transfer device has an injection device support surface for receiving an on-body injection device thereon and a flow path arrangement for transfer of fluid into the injection device, the transfer device being configured to define preferential gripping areas for user gripping of an injection device when such device is located on the support surface and interfering areas for interfering with user gripping of the injection device in the interfering areas.

A moisture removal and condensation and humidity management apparatus for a breathing circuit comprises a breathing circuit tubing defining a breathing gas conduit. The breathing gas has a first humidity level and a level of moisture therein. A dry gas conduit is adjacent at least a portion of the breathing gas conduit. The dry gas flow is configured to have a second humidity level lower than the first humidity level. A moisture transmission pathway is provided between the breathing gas conduit and the dry gas conduit, such that humidity in the flow of breathing gas is lowered and moisture is transferred to the dry gas flow. The moisture transmission pathway may be provided by a permeable portion which is permeable to water vapor but impermeable to liquid water, or by one or more perforations which permit drainage of liquid water from the breathing gas conduit to the dry gas conduit.

A steam inhaler includes a steam chamber housing having mounted therein a heater assembly. The steam chamber housing defines a steam chamber adapted to receive water. A fitting mounted to the steam chamber housing has a steam conduit section extended toward an exterior vent opening, a nozzle conduit section extended from the steam conduit, and a fresh air conduit section extended from the steam conduit section at a location downstream of the nozzle conduit section. The fitting is configured such that steam flows freely from the steam chamber, through the steam conduit section toward the exterior vent opening, a suction provided at the nozzle redirects at least a portion of the steam into the nozzle conduit section toward a mask, and the fresh air conduit directs fresh air into the steam conduit section to reduce a temperature of the steam exiting the exterior vent opening.

A pump arrangement for powering a pump in providing a controlled volume of water to a drip nozzle in a drip-feed humidifier. The pump arrangement includes: a pump having a solenoid; a processing unit; and a power supply electrically connected to the solenoid via a switch which is controlled by the processing unit. The power supply is structured to supply power to the solenoid via the switch. The processing unit is programmed to modulate the power provided to the solenoid via the switch such that the power is supplied to the solenoid according to a mirror image power profile for each actuation of the solenoid for retracting the armature. The mirror image power profile includes: an initial portion which decreases at a third overall rate, an intermediate portion which decreases at a second overall rate different than the third overall rate, and a final portion which increases at a first overall rate.

A bridge for facilitating delivery of reduced pressure to a wound site of a patient includes a reduced pressure lumen configured to be fluidly coupled to a reduced pressure source, and a secondary pressure lumen configured to be fluidly coupled to a secondary pressure source at a first end and to the reduced pressure lumen at a second end, thereby facilitating flow of exudate removed from the wound site by the reduced pressure source using the secondary pressure source. The reduced pressure lumen or the secondary pressure lumen includes a skin contacting surface formed of a moisture permeable membrane comprising an air-impermeable film that allows moisture from the patient to transfer into the reduced pressure lumen or secondary pressure lumen through the moisture permeable membrane while maintaining reduced pressure at the wound site.

The present invention relates to a device for a respiration arrangement. The device comprises a conduit having a first opening connectable to an air/gas source such as a resuscitation bag, and a second opening connectable to a face mask, such that a fluid pathway along a longitudinal direction of the conduit is established from the first opening to the second opening. The device further comprises a flow constriction, arranged in the conduit which upon fluid flow through the conduit results in a pressure difference over the flow constriction, the flow constriction at least partly comprising a laminar flow section, wherein the device further comprises at least one pressure connecting port arranged in pressurized communication with fluid between the flow constriction and the first opening, and wherein the pressure connecting port is arranged in the longitudinal direction of the conduit.