Abstract: An embodiment provides a system having a non-invasive ventilation patient interface. In one example, the system includes a headgear element and a non-invasive ventilation patient interface detachably coupled to the headgear element. The non-invasive ventilation patient interface includes a conduit having an entrainment opening and a nasal opening disposed along a conduit axis. A pressure sensing element is provided proximate to the nasal opening. One or more orifices proximate to the entrainment opening are configured to expel a jet of gas. One or more surfaces have a first end and a second end, with the first end being proximate to the one or more orifices and directing a flow of the jet of gas expelled from the one or more orifices, the second end being closer to the nasal opening than the first end.

Abstract: Provided is an apparatus (100) for transporting sweat droplets (112) to a sensor. The apparatus comprises a chamber (102) for filling with sweat. The chamber has an inlet (104) lying adjacent the surface of the skin (106), which inlet permits sweat to enter and fill the chamber. The chamber has an outlet (114) from which a sweat droplet protrudes once the chamber has been filled. The apparatus further comprises a fluid transport assembly which is designed to enable the sweat droplet protruding from the outlet to become detached from the outlet of the chamber. The sweat droplet is subsequently transported by the fluid transport assembly to the sensor. Once the protruding droplet has been released from the outlet, the outlet is made available for a subsequent sweat droplet to protrude therefrom upon further filling of the chamber.

Abstract: Provided is a system (300) for determining a sweat rate per gland and measuring biomarker concentration. The system comprises an apparatus and a sensor (166). The apparatus receives sweat from the skin and transports the sweat as discrete sweat droplets to the sensor. The sensor senses each of the counted sweat droplets. The system further comprises a processor which counts the number of sensed sweat droplets during a time period. The processor also determines time intervals between consecutive sensed sweat droplets, and receives a measure of the volume of each of the counted sweat droplets. The time intervals and the measure of the volume are then used by the processor to identify sweat burst and rest periods of the sweat gland or glands producing the sweat. This identification process necessarily involves assigning the sweat burst and rest periods to the sweat gland or glands, such that the processor is permitted to determine the number of sweat glands involved in producing the sweat.

Abstract: An implantable blood flow control system has an open passageway defined inside a radially inner wall, behind which is a closed passageway. The radially inner wall includes electroactive polymer actuator members for providing a variable flow restriction. The flow restriction has an undulating shape so that the volume of the closed passageway may remain constant during actuation of the electroactive polymer actuator members. In this way, the chamber behind the actuator members does not impede free movement of the actuator members. The undulating pattern presents no sharp edges, where blood coagulation could otherwise occur.

Abstract: A sleep monitoring system (10) for monitoring the sleep of a pair of subject comprises a pair of CO2 sensors (21,21?) for mounting in different sleeping regions within a space (1) and a processor (31) communicatively coupled to the pair of CO2 sensors. The processor is adapted to, for each CO2 sensor in a particular sleeping region, monitor (203) a CO2 concentration from sensor data produced by the CO2 sensor in said particular sleeping region to detect a presence of a subject in said sleeping region; to register (207) the monitored CO2 concentration upon detecting (205) said presence; to determine (303) a degree of crosstalk between said CO2 sensors upon detecting said presence; and to derive (305, 313) sleep pattern information for said subject from the registered CO2 concentration during said presence as a function of the determined degree of crosstalk, wherein the sleep pattern information comprises at least an indication that the subject is awake and an indication that the subject is asleep.

Abstract: Disclosed is an air purification system (10) including an air purification apparatus (100) comprising an air inlet (112); an air outlet (114) for expelling air in a target direction (116) into a region and including an adjustment mechanism (121) arranged to adjust said target direction in response to a target direction adjustment signal from a control system for aiming the air outlet at the face of a person in said region; at least one pollutant removal structure (101) in between the air inlet and the air outlet; and an air displacement apparatus (113) for displacing air from the air inlet to the air outlet through the at least one pollutant removal structure, and a sensor (151, 160, 135) adapted to determine a breathing parameter of the person, wherein the air purification apparatus is configured to expel said air as a function of said breathing parameter. A computer program product for configuring such a control system is also disclosed.

Abstract: A sleep monitoring system (10) for monitoring the sleep of a pair of subject comprises a pair of C02 sensors (21,21?) for mounting in different sleeping regions within a space (1) and a processor (31) communicatively coupled to the pair of CO2 sensors. The processor is adapted to, for each CO2 sensor in a particular sleeping region, monitor (203) a CO2 concentration from sensor data produced by the CO2 sensor in said particular sleeping region to detect a presence of a subject in said sleeping region; to register (207) the monitored CO2 concentration upon detecting (205) said presence; to determine (303) a degree of crosstalk between said CO2 sensors upon detecting said presence; and to derive (305, 313) sleep pattern information for said subject from the registered CO2 concentration during said presence as a function of the determined degree of crosstalk, wherein the sleep pattern information comprises at least an indication that the subject is awake and an indication that the subject is asleep.

Abstract: Disclosed is an air purification system (10) including an air purification apparatus (100) comprising an air inlet (112); an air outlet (114) for expelling air in a target direction (116) into a region and including an adjustment mechanism (121) arranged to adjust said target direction in response to a target direction adjustment signal from a control system for aiming the air outlet at the face of a person in said region; at least one pollutant removal structure (101) in between the air inlet and the air outlet; and an air displacement apparatus (113) for displacing air from the air inlet to the air outlet through the at least one pollutant removal structure, and a sensor (151, 160, 135) adapted to determine a breathing parameter of the person, wherein the air purification apparatus is configured to expel said air as a function of said breathing parameter. A computer program product for configuring such a control system is also disclosed.

Abstract: An air purification apparatus (100) for purifying air in a target space external to the apparatus is disclosed that comprises at least one pollutant removal structure (130; 131, 132) for removing a pollutant from the air in fluid connection with a major vent (110) and a directional vent arrangement comprising a directional inlet (112) for drawing air into the air purification apparatus from a region of the target space in an aiming direction of the directional inlet; and a directional outlet (114) for expelling air in a further aiming direction towards the region.

Abstract: A micro fluidics system includes a closed, expandable volume for mixing a fluid, and a flexible membrane for allowing mixing in the closed, expandable volume. The system further includes a surface having at least one channel for fluidically coupling a first side of the surface to the closed, expandable volume on a second side of the surface. The channel includes a first channel opening fluidically coupling the first side of the surface to the channel and a second channel opening fluidically coupling the channel to the closed, expandable volume. The expandable volume is defined by the flexible membrane closing the second channel opening when there is no fluid in the expandable volume.

Abstract: The invention relates to a micro fluidics system (1) comprising: a closed, expandable volume (35) for mixing a fluid; a flexible membrane (40) for allowing mixing in the closed, expandable volume (35), characterized in that the micro fluidics system (1) further comprises: a surface (5) comprising at least one channel (20, 20a, 20b, 20c, 20d) for fluidically coupling a first side (10) of the surface (5) to the closed, expandable volume (35) on a second side (15) of the surface (5), the channel (20, 20a, 20b, 20c, 20d) comprising a first channel opening (25) fluidically coupling the first side (10) of the surface (5) to the channel (20, 20a, 20b, 20c, 20d) and a second channel opening (30) fluidically coupling the channel (20, 20a, 20b, 20c, 20d) to the closed, expandable volume (35), the expandable volume (35) being defined by the flexible membrane (40) closing the second channel opening (30) when there is no fluid in the expandable volume (35).

Abstract: A Gas-free Fluid chamber for PCR. The present invention relates to a device with a fluid chamber suitable for performing a polymerized chain reaction for gas-free filling. Such devices may be used in the field of e.g. molecular diagnostics.

Abstract: The present invention relates to a lamp unit, especially to a UHP lamp unit, comprising a housing, a lamp positioned within said housing, a reflector assigned to said lamp for reflecting light emitted by said lamp through a transmission window, and at least one thermal bridge and/or heat sink unit being assigned to the reflector and/or to the lamp and/or to the housing. The or each thermal bridge and/or heat sink unit is preferably made from a material having a good thermal conductivity, e.g. the or each thermal bridge and/or heat sink is made from metal or ceramics.

Abstract: The invention provides a system, a processing apparatus, a sample unit, a reagent unit and a method for processing a biological sample in the inside of the sample unit. The system comprises at least a processing apparatus and a sample unit, the sample unit comprises a plurality of microfluidic elements, the processing apparatus comprises actuation means capable of actuating at the microfluidic elements such that a quick, cheap and accurate analysis of the biological sample is possible.