An anesthetic vaporizer system includes a reservoir containing anesthetic agent, an agent level sensor measuring an agent level of the anesthetic agent in the reservoir, a display, and a controller. The controller is configured to receive agent level measurements from the agent level sensor over a time period, and determine the anesthetic agent is being added to the reservoir from an agent source based on the agent level measurements over the time period. A filling status is determined based on the agent level measurements and a filling status indicator is displayed based on the determined filling status.

Methods and breast pump devices for simultaneous pumping and feeding breastmilk in the nursing position and quantification of breastmilk consumption are provided. A breast pump device includes a nipple shield for receiving a nipple, a housing having a throughput aperture and a fluid path, the fluid path extending from the nipple shield to the throughput aperture, and a negative pressure source. In some embodiments, the housing further includes a gate to control the quantity of breastmilk displaced to a baby. In some embodiments, the gate operates to respond to the amount of breastmilk displaced to the baby, and thereby allows for quantification. In some embodiments, the quantity of breastmilk displaced is also recorded.

The present invention relates to an apparatus for degassing liquids comprising a degassing system, wherein the degassing system has a first degassing chamber, a second degassing chamber, a liquid store, a pump, and a supply line that connects the liquid store to the first degassing chamber; wherein the pump is connected to the first degassing chamber at the intake side and to the second degassing chamber at the pressure side; and wherein the degassing system furthermore has a return line that can be cut off and that connects the two degassing chambers to one another, and wherein the apparatus comprises a controller that is configured to operate the degassing system in a first operating mode and in a second operation mode; wherein the degassing system is connected in the first operation mode such that the pump conducts liquid away from the first degassing chamber and supplies it to a removal unit for degassed liquid; and wherein the degassing system is connected in the second operating mode such that liquid is returned from the second degassing chamber to the first degassing chamber through the return line.

A blood purification device includes a chamber, a liquid feed line, an air introduction unit, a liquid level adjustment unit, and a control unit. The chamber is provided on a blood circuit for extracorporeally circulating patient's blood and introduces purified plasma obtained by purifying plasma separated by a plasma separator provided on the blood circuit, or a replenishing liquid for replenishing the plasma separated by the plasma separator, into the blood circuit. The liquid feed line is capable of sending the purified plasma or the replenishing liquid to the chamber. The air introduction unit is capable of introducing air into the liquid feed line. The liquid level adjustment unit is capable of adjusting a liquid level height in the chamber. At the end of blood purification treatment, the control unit performs a liquid recovery process for sending the purified plasma or the replenishing liquid to the chamber via the liquid feed line while introducing air into the liquid feed line by the air introduction unit and maintains the liquid level height in the chamber at a predetermined liquid level height by the liquid level adjustment unit.

A sensor and method for determining the state of a humidification chamber in a respiratory gas humidifier. The sensor comprises a transmitter for emitting an electromagnetic radiation signal, a receiver for receiving the electromagnetic radiation signal and providing an output signal, and a controller for varying the intensity of the electromagnetic radiation signal emitted by the transmitter and/or the gain setting of the receiver. The controller has two sensor configurations, a first configuration in which the transmitter emits an electromagnetic radiation signal having a first intensity, the receiver has a first gain setting, and the receiver provides a first output signal, and a second configuration in which the transmitter emits an electromagnetic radiation signal having a second intensity, the receiver has a second gain setting, and the receiver provides a second output signal, wherein the first intensity is different to the second intensity, and/or the first gain setting is different to the second gain setting, and the controller determines a state of the humidification chamber by comparing the first and second outputs of the receiver with one or more threshold values.

An intraperitoneal pressure (“IPP”) measurement apparatus is disclosed herein. In an example, the IPP measurement apparatus includes a transfer set or catheter that is fluidly coupled to a patient's peritoneal cavity and a pressure sensor adapted to contact the transfer set or catheter. The pressure sensor is configured to transmit output data indicative of an IPP within the patient's peritoneal cavity. The pressure sensor includes a pressure element configured to measure a pressure imparted by a fluid within the transfer set or catheter. The pressure sensor also includes a pressure amplifier having a first side that contacts a portion of the transfer set or catheter and a second side that contacts the pressure element. The first side has a greater diameter or surface area compared to the second side for amplifying the pressure signal for the IPP measurement.

A tub is configured to contain a supply of water and is configured to be inserted into a chamber of a humidifier. The tub includes a tub base configured to contain the supply of water. The tub also includes a tub lid and a flow plate provided between the tub base and the tub lid. The flow plate includes a water level indicator configured to indicate a level of the supply of water in the tub base. In addition, the water level indicator includes a generally rectangular portion and a generally triangular portion.

A breast shield unit of a breast pump for expressing human breastmilk includes a breast shield (1) to be placed onto a mother's breast, a breastmilk collection container (5) for receiving expressed breastmilk, an adapter (2) for connecting the breast shield (1) to the breastmilk collection container (5) and a valve head (4). A breastmilk channel extends from the breast shield (1) into the breastmilk collection container (5) through the adapter (2) and the valve head (4). The valve head (4) includes a valve (40) which closes and opens the breastmilk channel during the pumping action, wherein a fill level sensor (6) for measuring a fill level of the breastmilk collection container (5) is arranged in the valve head (4). The breast shield unit according to the invention facilitates a fill level measurement without a structural change of the breast shield and breastmilk collection container. Moreover, it facilitates data interchange with external information storage and/or information processing units.

A filter cartridge assembly is disclosed, which includes a housing having a reservoir for collecting fluids entering the housing through a gas return path, a sensor located within the reservoir for detecting a fluid level therein, and a backer plate positioned within the housing adjacent an inlet port to the reservoir and including fluid management structure to shield the sensor from fluid entering the reservoir from the gas return path through the inlet port and causing a false indication of the fluid level in the reservoir.

A system with at least one inflatable member configured for being arranged in a part of the patient's respiratory tract includes a catheter carrying the at least one inflatable member. The catheter includes a fluid line for filling the inflatable member with a fluid; and a pressure monitoring and control member to be arranged outside the patient's body. The pressure monitoring member is in fluid communication with the inflatable member and is configured to receive, during operation, fluid from the inflatable member when the pressure increases above a predetermined threshold pressure and to return the received fluid when the pressure decreases below said predetermined threshold pressure. The pressure monitoring and control member is an elastically expandable balloon made from a material configured to expand elastically when the pressure in the balloon increases above a predetermined threshold pressure and to contract when the pressure decreases below said predetermined threshold pressure.