A blood treatment apparatus is disclosed. The example apparatus includes a blood treatment unit including a fluid inlet and a fluid outlet and a blood line. The apparatus also includes a fluid line including an upstream fluid line configured to receive electrically conductive treatment fluid from a fluid source and pass the electrically conductive treatment fluid to the fluid inlet of the blood treatment unit and a downstream fluid line connected to the fluid outlet of the blood treatment unit for delivering the used electrically conductive treatment fluid to a fluid sink. The apparatus further includes a flow divider arranged in the downstream fluid line and configured to separate the used electrically conductive treatment fluid in the downstream fluid line into to a first fluid section and a second fluid section, thereby electrically isolating the first and second fluid sections.

A medical system, device, and methods are provided having programming to communicate with a mobile device; the medical device further having programming to authenticate the mobile device; the medical device granting access to one or more functions if the mobile device is authenticated.

A method for referencing a pressure or force sensor configured to measure pressure in a tube filled with fluid. The pressure or force sensor is located in an extracorporeal circuit and integrated into or inserted in a clamping device The method includes: (1) referencing a force or pressure reference signal which the pressure or force sensor outputs, with a force or pressure reference signal measured by a force or pressure reference sensor; and (2) using a dialysis fluid side force or pressure reference sensor in a dialysis fluid circuit configured to detect the pressure in the dialysis fluid circuit, for referencing a pressure sensor or force sensor in the extracorporeal circuit. A device uses a dialysis fluid side force or pressure reference sensor in the dialysis fluid circuit that detects pressure in the dialysis fluid circuit, for referencing at least one pressure or force sensor in the extracorporeal circuit.

A medical treatment system is configured to output a predefined test pattern and to receive the signal by way of a microphone in order to test the volume and quality of the audio output in order to ensure the output audio signals effective to wake a sleeping patient. The failure of a processor to confirm the volume and fidelity of the audio output as well as the timeliness of the test pattern causes the processor to deny the resumption of a treatment and to generate an error signal.

Systems and method for monitoring the blood glucose concentration of a patient during a hemodialysis session and automated administration of a medication in response to the glucose concentration falling outside a specified range. The system includes a hemodialysis system and a glucose sensor. The hemodialysis system includes a control system, at least one medication infusion pump, and a dialyzer fluidly connectable to a venous patient line and an arterial patient line. The glucose sensor is in communication with the control system and positioned to continuously measure the blood glucose concentration of the patient during the hemodialysis session. The control system can be programmed to provide automated administration of medication by the at least one medication infusion pump in response to changes in the blood glucose concentration of the patent during the hemodialysis session.

Dialysis systems comprising actuators that cooperate to perform dialysis functions and sensors that cooperate to monitor dialysis functions are disclosed. According to one aspect, such a hemodialysis system comprises a user interface model layer, a therapy layer, below the user interface model layer, and a machine layer below the therapy layer. The user interface model layer is configured to manage the state of a graphical user interface and receive inputs from a graphical user interface. The therapy layer is configured to run state machines that generate therapy commands based at least in part on the inputs from the graphical user interface. The machine layer is configured to provide commands for the actuators based on the therapy commands.

In examples described herein, a system includes an elongate member configured to be introduced into vasculature of a patient. The elongate member includes a pressure sensor configured to generate a pressure signal indicative of pressure in the vasculature adjacent the needle. The system includes processing circuitry configured to receive the pressure signal from the pressure sensor, detect, based on the pressure signal, dislodgment of the elongate member from the vasculature, and generate an output in response to detecting the dislodgment of the elongate member from the vasculature.

The present disclosure relates to a bag holder for receiving a first effluent bag, which serves for receiving effluent resulting from a blood treatment being performed by a blood treatment apparatus and includes at least one closable effluent outlet opening and at least one effluent inlet opening. The bag holder includes one or several rollers for rolling the bag holder and at least one of the following features: a holding device for holding the first effluent bag in the bag holder, a receptacle for receiving the first effluent bag or a section thereof, a pump section for conveying effluent out of first effluent bag being received in the bag holder, at least one effluent outlet line for guiding effluent towards the pump section and/or out of the first effluent bag and/or at least one basin line for guiding effluent into the first effluent bag and/or away from the bag holder.

A blood treatment device includes an extracorporeal blood circuit, dialyzer and dialysis fluid circuit. The blood circuit and dialysis fluid circuit are separated from each other by a membrane in the dialyzer. A weighing device measures and monitors the weight of a bag containing a fluid. A fluid pump pumps fluid out of and into the bag. A control unit interrupts fluid supply by stopping the pump when a weight variation of the bag occurs and temporarily maintains the interruption at least until the malfunction disappears, and automatically restarts the fluid supply if the bag or the weight of the bag stabilizes within a predetermined time and the weight variation does not exceed a predetermined value. The control unit generates an alarm if the bag or weight of the bag does not stabilize within a predetermined time and/or if the weight variation exceeds a predetermined value.

A system for blood treatment can include a dialysis machine and an ultrasonic authentication device connected to the blood treatment machine, the ultrasonic authentication device configured to scan a label and send signals containing label information to the dialysis machine.