Abstract: A breast shield arrangement (300) for a breast pump comprises a first sealing portion (310), a port (320) and an intermediate portion (330) coupled between the first sealing portion (310) and the port (320). The intermediate portion (330) comprises a circumferentially extending wall defining a first volume (V1) which is adapted to receive a part of a breast, a first end (331), a curved portion (332) and a second end (333). The curved portion (332) comprises a second sealing portion (332c) which is adapted to at least partially seal the curved portion (332) against the nipple (310), the areola (320) or the breast (200) when a vacuum is applied at the port (320) creating a second volume (V2) between the first sealing portion (310, 332c) of the breast (200). The curved portion (332) at the second volume is curved outwardly as seen from the first sealing portion (310).

Abstract: The present invention relates to a breast status determination device (10?). The breast status determination device (10?) comprises a breast shield (16?), a nipple elongation measurement unit (17?), and a breast status determination unit (20?). The breast shield (16?) can receive abreast (12) of a user (14) therein. The nipple elongation measurement unit (17?) can measure an elongation of a nipple of the breast (12) received in the breast shield (16?) for a specific pressure in the breast shield (16?) during a milk extraction session. The breast status determination unit (20?) can determine a status of the breast (12) based on the elongation of the nipple (26). The breast status determination device (10?) can allow estimating of milk left in the breast during the milk extraction session, when the breast (12) is empty, and whether a milk ejection reflex is present or absent in the breast (12).

Abstract: A breast pump system has first and second kits, and they have different sets of functional units. However, they have shape features which are designed to provide similar appearance in use, to make the use of the breast pump system more discrete.

Abstract: A breast pump has abreast shield for fitting over at least the nipple of a breast thereby to create a cavity over the breast. A stimulation unit is used to apply a physical stimulus to the nipple and/or to a portion of the breast for stimulating the milk ejection reflex. A negative pressure source is used to apply a static negative pressure to the cavity for holding the breast shield on the breast during milk expression, and promoting expression, while milk is collected in a milk collection container. This provides a low cost and low noise breast pump.

Abstract: A milk storage container for use with a breast pump has a head for attachment to a breast pump and a base part which defines a plurality of individual compartments. The compartments are rigid or semi-rigid so that they can easily be cleaned and sterilized and frozen milk is removable individually from the compartments.

Abstract: A breast pump device is provided, and a controller for operating a pressure source of the breast pump device. A degree of stretching of the nipple is determined during use of the breast pump device. A maximum under-pressure level to be applied during use of the breast pump is determined in dependence on the degree of stretching. This provides automatic pressure level adjustment to provide improved comfort for the user while enabling successful milk expression.

Abstract: A teat has a stimulation portion for stimulating the incisive papilla. The stimulation portion is located at a central region of the teat between a base region and a tip region.

Abstract: A breast pump device is provided and a controller for operating a pressure source of the breast pump device. A milk flow is monitored during a breast pumping session. The pressure source is controlled in dependence on the flow, thereby to switch, the breast pumping, between a first pressure profile of the pressure source for a low energy mode and a second pressure profile of the pressure source for an expression mode. The breast pumping session comprises a plurality of time periods with the low energy mode and a plurality of time periods with the expression mode, in order to reduce electrical power consumption.

Abstract: A breast pump comprises an outer housing for mounting over the breast and an inner breast shield which is transparent at least in the region of the nipple. The outer housing has a window in an upper portion of the outer housing, for enabling, in use, a direct line of sight for the user of the breast pump, through the window to the nipple. The remainder of the outer housing blocks a view of the nipple from at least directly in front.

Abstract: The present application relates to a cold plasma device (1) for treating skin (5). The cold plasma device (1) comprises a cold plasma generator (3) adapted to generate cold plasma that produces reactive species for treating said skin (5), and a manipulator (10) adapted to manipulate said skin (5) to increase exposure of bacteria on said skin to said reactive species during use of the device.

Abstract: The present invention relates to a system, method and corresponding computer program for milk ejection reflex (MER) determination, the system comprising a breast shield arrangement (1) for a breast pump (2) configured to be attached on a first breast of a female, a physiological sensor unit (4) for receiving a physiological reception signal from the second breast, which is opposite to the first breast, wherein the physiological reception signal is indicative of fluid contents in the second breast, and wherein the system is configured to determine a milk ejection reflex based on a change in fluid contents in the second breast. It finds particular application during and in connection with breastfeeding and allows for direct detection of the beginning of the milk flow in the breast, i.e. the occurrence of the MER, without delay and with a high degree of precision.

Abstract: A breast pump (100) is provided comprising a vacuum pump (120) which is configured to be operated at different vacuum profile settings, a controller (140) configured to control an operation of the vacuum pump (120) based on the different vacuum profile settings, and a breast fullness estimator (150) configured to estimate a fullness of a breast based on a duration of a milk expression session. The controller (140) is configured to select a vacuum profile setting based on the breast fullness estimation of the breast fullness estimator (150). Hence, the efficiency of the breast pump is increased as the operation of the vacuum pump is adapted to the estimated breast fullness.

Abstract: The present invention relates to a breast status determination device (10?). The breast status determination device (10?) comprises a breast shield (16?), a nipple elongation measurement unit (17), and a breast status determination unit (20?). The breast shield (16?) can receive abreast (12) of a user (14) therein. The nipple elongation measurement unit (17) can measure an elongation of a nipple of the breast (12) received in the breast shield (16?) for a specific pressure in the breast shield (16?) during a milk extraction session. The breast status determination unit (20?) can determine a status of the breast (12) based on the elongation of the nipple (26). The breast status determination device (10?) can allow estimating the amount of milk left in the breast during the milk extraction session, when the breast (12) is empty, and whether a milk ejection reflex is present or absent in the breast (12).

Abstract: The present invention relates to an oxytocin release stimulation device (10?) that can be arranged at or close to skin of a user (40). The oxytocin release stimulation device (10?) comprises a lighting unit (14?) and a control unit (16?). The control unit (16?) controls the lighting unit (14?) such that the lighting unit (14?) provides light with specific wavelengths and radiant exposures to the skin of the user (40) for a duration that ensures stimulation of a release of oxytocin. Release of oxytocin allows to stimulate a milk ejection reflex and thus to support milk extraction, e.g. when the oxytocin release stimulation device (10) is used with a breast pump (100?). The oxytocin release stimulation device (10?) can furthermore allow to reach an oxytocin level during pregnancy that allows to reduce the risk of postpartum depression or that allows to facilitate induction of labor.

Abstract: A breast shield arrangement (300) for a breast pump comprises a first sealing portion (310), a port (320) and an intermediate portion (330) coupled between the first sealing portion (310) and the port (320). The intermediate portion (330) comprises a circumferentially extending wall defining a first volume (V1) which is adapted to receive a part of a breast, a first end (331), a curved portion (332) and a second end (333). The curved portion (332) comprises a second sealing portion (332c) which is adapted to at least partially seal the curved portion (332) against the nipple (310), the areola (320) or the breast (200) when a vacuum is applied at the port (320) creating a second volume (V2) between the first sealing portion (310, 332c) of the breast (200). The curved portion (332) at the second volume is curved outwardly as seen from the first sealing portion (310).

Abstract: The present application relates to a cold plasma device (13) for treating a surface (6) with cold plasma. The device (13) has a cold plasma generator (14) adapted to generate cold plasma that produces reactive species for treating the surface (6). The device (13) also includes a treatment head (5) that is positionable relative to the surface (6) such that the reactive species are imparted toward the surface (6) during treatment. The device (13) is also provided with an air flow generator (8) to generate an air flow over the surface (6) and a controller (9) configured to control operation of the air flow generator (8) to generate an air flow over the surface (6) after the treatment has been completed such that remaining by-products of the cold plasma are dissipated.

Abstract: The present invention relates to a breast shield arrangement (1) for a breast pump (2) comprising: a breast shield (3) for receiving a user's breast therein, and a sensor (4) for transmitting an input signal into the breast and receiving a corresponding reception signal in response, said reception signal indicating changes in milk flow in the breast.

Abstract: A wearable device may take a set of health inputs from embedded body sensors for the duration of an activity performed by a user of the wearable device. Based on these inputs, the wearable device can calculate a health parameter (e.g., calories burned during the activity). The wearable device can also track its location during the activity, and provide this location to a geolocation data network. The geolocation data network may provide geolocation data (e.g., weather/environmental/terrain data) pertaining to the wearable device's location. The wearable device can then modify its measurements and/or calculated health parameters based on the geolocation data (e.g. Increasing calories burned during a run due to high heat and uphill terrain in the location of the run).

Abstract: The present invention relates to a system, method and corresponding computer program for milk ejection reflex (MER) determination, the system comprising a breast shield arrangement (1) for a breast pump (2) configured to be attached on a first breast of a female, a physiological sensor unit (4) for receiving a physiological reception signal from the second breast, which is opposite to the first breast, wherein the physiological reception signal is indicative of fluid contents in the second breast, and wherein the system is configured to determine a milk ejection reflex based on a change in fluid contents in the second breast. It finds particular application during and in connection with breastfeeding and allows for direct detection of the beginning of the milk flow in the breast, i.e. the occurrence of the MER, without delay and with a high degree of precision.

Abstract: A system (1) and corresponding method for determining an impact of an active substance on an infant comprises: a parameter providing unit (10) for providing age and weight of the infant, an intake estimation unit (20) for estimating the amount of intake of the active substance by a breastfeeding caregiver of the infant, a substance level determination unit (30) for determining a level of the active substance in breast milk at the time of breastfeeding based on a history of the estimated intake of the active substance, and an impact determination unit (40) for determining an impact of the active substance on the infant based on i) the determined level of the active substance in the breast milk at the time of breastfeeding, and ii) the age and weight of the infant. The system (1) allows a determination of the impact of an active substance on the infant.