This dialysis-fluid supply system, which mixes a diluent and at least two drugs to generate a dialysis fluid, and outputs said dialysis fluid, is provided with: two tanks which mix the drugs and the diluent to generate the dialysis fluid, and store said dialysis fluid; a water supply device and a drug supply device which supply the diluent and the drugs to each of the tanks; mechanisms for outputting, to a dialysis device, the dialysis fluid stored in each of the tanks; and a control unit for controlling the driving of these. During output of the dialysis fluid from at least one of the tanks, the control unit sequentially switches the supply destination tank for the drugs and the diluent, and the dialysis-fluid output source tank, between the two tanks in order to generate the dialysis fluid in the other tank.

This dialysis-fluid supply system, which mixes a diluent and at least two drugs to generate a dialysis fluid, and outputs said dialysis fluid, is provided with: a mixing tank which mixes the drugs and the diluent to generate the dialysis fluid; a storage tank which stores and outputs the dialysis fluid generated by the mixing tank; a transport mechanism for transporting, to the storage tank, the dialysis fluid generated by the mixing tank; an output mechanism for outputting, to a dialysis device, the dialysis fluid stored in the storage tank; and a control unit for controlling the driving of the transport mechanism and the output mechanism.

A processor of a medical device configured to communicate with a remote server can be programmed to protect the medical device from exposure to unauthorized or malicious software. A system or method to implement this form of protection can include, for example, at least one processor on the medical device, a control software module that controls the operation of the medical device and is executable on the processor, a data management module that manages data flow to and from the control software module from sources external to the medical device, and an agent module that has access to a limited number of designated memory locations in the medical device. In addition, a hemodialysis apparatus can be configured to operate in conjunction with an apparatus for providing purified water from a source such as a municipal water supply or a well. A system for controlling delivery of purified water to the hemodialysis apparatus can comprise a therapy controller of the hemodialysis apparatus configured to communicate with a controller of a water purification device, and a user interface controller of the hemodialysis apparatus configured to communicate with the therapy controller, and to send data to and receive data from a user interface.

A system for conducting inhalation studies includes an inhalation exposure chamber and an aerosol delivery line connected to the inhalation exposure chamber. The aerosol delivery line is configured to produce a bi-directional and symmetrical presentation of aerosol to the inhalation exposure chamber. A laminar flow element is configured to create an ante-chamber where complete and turbulent mixing of the aerosol occurs. A radial exhaust and the laminar flow element enable laminar flow of the aerosol through the inhalation exposure chamber.

A suspension device for a drainage container has, on a first side, a first fastening unit for mounting and fastening the drainage container on the suspension device. On a second side, a second fastening unit is present for mounting and fastening the suspension device on a rail. The first fastening unit is arranged in a first fastening part, and the second fastening unit is arranged in a second fastening part. The suspension device further comprises a weighing part with a weighing element, wherein the weighing part is connected or can be connected to the first fastening part and to the second fastening part so as to measure, with the weighing element, a relative displacement, such that a filling quantity of the aspirated body fluid in the drainage container can be determined.

A surgical fluid thermal treatment system can be used during a procedure to heat or cool surgical fluid, e.g., prior to introducing the fluid into the body of a patient. In some examples, the system includes an open basin into which fresh surgical fluid is dispensed and a heater that heats the fluid in the basin. The system may also include a volume measurement device that measures the volume of fluid in the basin. The system may have a user interface that a user interacts with to check fresh fluid into the basin. The user may also interact with the user interface to check medical tools into the basin and check medical tools out of the basin. A controller associated with the system can track the volume of fluid removed from the basin during the course of a procedure.

A filling aid. The filling aid includes a needle housing portion including at least one tab having a starting position and a filling position, and a filling needle cradle including a filling needle, the filling needle cradle slidable connected to the needle housing portion and having a starting position and a filling position, wherein when the at least one tab on the needle housing moves from a starting position to a filling position, the filling needle cradle slides from a starting position to a filling position, and wherein when the at least one tab on the needle housing moves from a filling position to a starting position, the filling needle cradle slides from a filling position to a starting position.

A system for determining components of matter removed from a body includes a container for receiving the matter, a device for weighing the container and the matter therein, an instrument for obtaining information relating to determine the components of the matter based in part on a weight of the matter determined by said device and the information relating to the at least one aspect of the matter obtained by said instrument. A display includes a screen for displaying information relating to the matter provided by said processer. The information may include a height and/or a color of the matter among other aspects. An insert containing an absorbent material may be utilized to separate fat cells from a fluid when liposuction is used to remove the matter. The insert may be porous allowing fluid to enter the absorption.

The specification discloses a portable dialysis machine having a detachable controller unit and base unit. The controller unit includes a door having an interior face, a housing with a panel, where the housing and panel define a recessed region configured to receive the interior face of the door, and a manifold receiver fixedly attached to the panel. The base unit has a planar surface for receiving a container of fluid, a scale integrated with the planar surface, a heater in thermal communication with the planar surface, and a sodium sensor in electromagnetic communication with the planar surface. Embodiments of the disclosed portable dialysis system have improved structural and functional features, including improved modularity, ease of use, and safety features.

Devices, systems, and methods are provided for adherence monitoring, and devices, systems, and methods are provided for monitoring use of consumable dispensers. In general, the devices, systems, and methods can facilitate an individual's adherence to a schedule for consuming consumables and can facilitate monitoring and tracking of the individual's adherence to the schedule. The devices, systems, and methods can allow data regarding the individual's historical adherence to the schedule to be accessible via a computer system. In one embodiment, an accessory is provided that can be configured to attach to consumable dispensers. The accessory can be configured to be removably and replaceably coupled to the dispenser. The accessory can be configured to provide a notification to a user indicating that a certain event occurred and/or that a certain action needs to be taken. The accessory can be configured to sense attachment thereof to and removal thereof from the dispenser.