Disclosed herein are a sterilization module and a sterilization system including the same. The sterilization module includes a light source emitting germicidal light to kill pathogens in living cells. The living cells may include living cells and the pathogens. In addition, the germicidal light may be light in a wavelength band capable of ensuring a viability of 70% or more for the normal cells and a viability of less than 70% for the pathogens.

Disclosed herein are a sterilization module and a sterilization system including the same. The sterilization module includes a light source emitting germicidal light to kill pathogens in living cells. The living cells may include living cells and the pathogens. In addition, the germicidal light may be light in a wavelength band capable of ensuring a viability of 70% or more for the normal cells and a viability of less than 70% for the pathogens.

A medical pump, preferably a peristaltic pump or a syringe pump, for conveying a medical fluid. The pump includes a housing with an upper housing shell, a lower housing shell and a front lid, and a seal between the upper housing shell and the lower housing shell. The front lid is pivotably arranged on the lower housing shell.

A medical wetness sensing device includes a base adapted to be disposed on a wearer of the medical wetness sensing device. The base includes a first electrical conductor and a second electrical conductor electrically insulated from the first electrical conductor. The first electrical conductor includes a hinge portion enabling a first portion of the first electrical conductor to deflect, at the hinge portion, relative to a second portion of the first electrical conductor. The medical wetness sensing device includes a controller electrically connected to the first electrical conductor and the second electrical conductor. The controller is configured to detect a presence or an absence of a medical fluid electrically connecting the first and second electrical conductors.

A medical wetness sensing device includes a base adapted to be disposed on a wearer of the medical wetness sensing device. The base includes a first electrical conductor and a second electrical conductor electrically insulated from the first electrical conductor. The first electrical conductor includes a hinge portion enabling a first portion of the first electrical conductor to deflect, at the hinge portion, relative to a second portion of the first electrical conductor. The medical wetness sensing device includes a controller electrically connected to the first electrical conductor and the second electrical conductor. The controller is configured to detect a presence or an absence of a medical fluid electrically connecting the first and second electrical conductors.

The invention relates to device (1) for measuring volumes of a liquid in a container (B) by means of measuring emitted high-frequency radiation, comprising control unit (C), a transmitter (TX), at least one first transmitting antenna (ANT_TX1) and at least one second transmitting antenna (ANT_TX2), at least one receiving antenna (ANT_RX1) and a receiver (RX), wherein the transmitter (TX) is configured to emit high-frequency radiation when in operation, wherein the first transmitting antenna (ANT_TX1) and the second transmitting antenna (ANT_TX2) are configured to emit high-frequency radiation during operation so that radiation can reach the container (B), wherein first receiving antenna (ANT_RX1) is configured to record high-frequency radiation reflected from the container (B), wherein the receiver (RX) is configured to take up the high-frequency radiation received by the receiving antenna (ANT_RX1), wherein the control unit (C) is configured to control the transmitters so that the transmitter (TX) emits high-frequency radiation, and wherein the control unit (C) is also configured to evaluate high-frequency radiation taken up by the receiver (RX) so that a measurement of the volume of the liquid in the container (B) is determined, wherein the measurement of the volume of liquid in the container (B) is determined from channel state information. The invention also relates to device (1) for measuring volumes of a liquid in a container (B) by means of measuring emitted high-frequency radiation, comprising a control unit (C), a transmitter (TX), at least one first transmitting antenna (ANT_TX1) and at least one second transmitting antenna (ANT_TX2), a least one first receiving antenna (ANT_RX1) and a second receiving antenna (ANT_RX2) and a receiver (RX), wherein the transmitter (TX) is configured to emit high-frequency radiation when in operation, wherein the first transmitting antenna (ANT_TX1) and the second transmitting antenna (ANT_TX2) are configured to emit high-frequency radiation during operation so that radiation can reach the container (B), wherein the first receiving antenna (ANT_RX1) is configured to record high-frequency radiation reflected from the container (B), wherein the second receiving antenna (ANT_RX2) is configured to record high-frequency radiation transmitted from the container (B), wherein the control unit (C) is configured to control the transmitters so that the transmitter (TX) emits high-frequency radiation, and wherein the control unit (C) is also configured up to evaluate high-frequency radiation taken up by the r

The invention relates to device (1) for measuring volumes of a liquid in a container (B) by means of measuring emitted high-frequency radiation, comprising control unit (C), a transmitter (TX), at least one first transmitting antenna (ANT_TX1) and at least one second transmitting antenna (ANT_TX2), at least one receiving antenna (ANT_RX1) and a receiver (RX), wherein the transmitter (TX) is configured to emit high-frequency radiation when in operation, wherein the first transmitting antenna (ANT_TX1) and the second transmitting antenna (ANT_TX2) are configured to emit high-frequency radiation during operation so that radiation can reach the container (B), wherein first receiving antenna (ANT_RX1) is configured to record high-frequency radiation reflected from the container (B), wherein the receiver (RX) is configured to take up the high-frequency radiation received by the receiving antenna (ANT_RX1), wherein the control unit (C) is configured to control the transmitters so that the transmitter (TX) emits high-frequency radiation, and wherein the control unit (C) is also configured to evaluate high-frequency radiation taken up by the receiver (RX) so that a measurement of the volume of the liquid in the container (B) is determined, wherein the measurement of the volume of liquid in the container (B) is determined from channel state information. The invention also relates to device (1) for measuring volumes of a liquid in a container (B) by means of measuring emitted high-frequency radiation, comprising a control unit (C), a transmitter (TX), at least one first transmitting antenna (ANT_TX1) and at least one second transmitting antenna (ANT_TX2), a least one first receiving antenna (ANT_RX1) and a second receiving antenna (ANT_RX2) and a receiver (RX), wherein the transmitter (TX) is configured to emit high-frequency radiation when in operation, wherein the first transmitting antenna (ANT_TX1) and the second transmitting antenna (ANT_TX2) are configured to emit high-frequency radiation during operation so that radiation can reach the container (B), wherein the first receiving antenna (ANT_RX1) is configured to record high-frequency radiation reflected from the container (B), wherein the second receiving antenna (ANT_RX2) is configured to record high-frequency radiation transmitted from the container (B), wherein the control unit (C) is configured to control the transmitters so that the transmitter (TX) emits high-frequency radiation, and wherein the control unit (C) is also configured up to evaluate high-frequency radiation taken up by the r

A blood flow stimulator may help encourage blood flow in a limb of a patient. The blood flow stimulator may include a housing configured for sealing about the limb of the patient. The housing may include a sealable volume, and the sealable volume may receive the limb of the patient. The blood flow stimulator may include a seal, and the seal may be coupled with the housing. The seal may engage with at least a portion of the limb, for instance to segregate the sealable volume from a surrounding environment of the blood flow stimulator. The blood flow stimulator may include a conduit extending through the housing. The conduit mat help provide access to the sealable volume, for instance from the surrounding environment. In some examples, an adjustable stent is utilized to enhance blood flow within vasculature of a patient. A stent operator may change a size of the stent.

A computer-implemented method, a medical device, and a system for acquiring user-specific customization data, i.e. user-specific language packages, are provided. The computer-implemented method comprises: determining a first set of user-specific customization data stored on the medical device; comparing the first set of user-specific customization data with a second set of user-specific customization data that is required by a user; and upon determining that the second set of user-specific customization data is different from the first set of user-specific customization data, acquiring, from a data storage external to the medical device, the second set of user-specific customization data or a delta between the first set and the second set of user-specific customization data.

A computer-implemented medical system is provided. The system includes a docking station and a mobile machine. The system is configured to perform operations comprising: receiving, by the mobile machine and from a user, a request to transport the mobile machine to a target location to perform a medical treatment; automatically navigating the mobile machine to the target location; performing, by the mobile machine, the medical treatment on a patient; determining, by the mobile machine, that the medical treatment is completed and the mobile machine is disconnected from the patient; automatically navigating the mobile machine to a stationary docking station of the medical system; and determining that the mobile machine is connected to the docking station through one or more connectors, and in response, receiving, by the mobile machine, at least one of an electrical charge, a refill of one or more supplies, a cleaning, or a drain of waste.