The invention relates to an apparatus for clamping a hose line, comprising a clamping body 19, an electromagnetic actuation unit 20 for the clamping body and a monitoring device 23 which monitors the position of the clamping body, the actuation unit 20 comprising a coil 21 for generating a magnetic field. The invention also relates to a medical treatment apparatus, in particular an apparatus for extracorporeal blood treatment, comprising an apparatus 14 for clamping a hose line, and to a method for monitoring an apparatus for clamping a hose line. The monitoring device 23 has a measurement device 24 for measuring an electrical property of the coil 21 that is dependent on the position of the clamping body 19, and an evaluation device 25 for determining the position of the clamping body 19 on the basis of the electrical property of the coil. Given that only one electrical property of the coil 21 is monitored, an additional mechanical component is not required for monitoring. In a preferred embodiment of the invention, the inductance L of the coil 21 is an electrical property that is dependent on the position of the clamping body 19. A measurement device 25 is provided in order to measure the inductance L of the coil.

Methods for checking a connection between a compressed air outlet of a blood treatment apparatus and a pressure measuring line of an extracorporeal blood tubing set. The methods include providing a blood treatment apparatus having a compressed air line. A compressed air device is in fluid communication with the compressed air line for generating pressure within the compressed air line. A compressed air outlet is in fluid communication with both the compressed air line and an exterior of the blood treatment apparatus. The compressed air outlet is connectable with a pressure measuring line and a pressure sensor. The method also includes building up a pressure and an air flow in the compressed air line and/or at the compressed air outlet, measuring a pressure at the compressed air outlet or in the compressed air line, and evaluating an increase of the measured pressure.

The present disclosure relates to a reinfusion tube system that includes a reinfusion fluid tubing with a pre-pump loop section, a post-pump loop section, and a pump loop section; and one of

a check valve positioned at an end or between the ends of the reinfusion fluid tubing such that it is provided to block fluid flow through the check valve in a direction from the post-pump loop section to the pre-pump loop section, and a check valve adapter including a check valve. The check valve adapter can be configured to be connected to an end or to be positioned between the ends of the reinfusion fluid tubing such that the check valve is provided to block fluid flow through the check valve in a direction from the post-pump loop section to the pre-pump loop section.

The invention relates to a circuit arrangement for a protective-conductor connection to at least two fluid-conducting lines 11, 12, in particular to at least two fluid-conducting lines which are guided outwards from the interior of a housing 1 of a medico-technical device, in particular the housing of a blood treatment device. The circuit arrangement comprises a plurality of protection apparatuses 16A, 16B; 17A, 17B for electrical contacting which are designed such that an electrical connection to a fluid in the line can be produced using each protection apparatus for electrical contacting. In the circuit arrangement, at least two protection apparatuses 16A, 16B; 17A, 17B for electrical contacting are assigned to each fluid-conducting line 11, 12. As a result, two protective measures are taken for each fluid-conducting line. In addition, the protection apparatuses 16A, 16B; 17A, 17B of one fluid-conducting line 11; 12 are each electrically connected to another protection apparatus 16A, 16B; 17A, 17B of another fluid-conducting line 11; 12. The protective-conductor concept according to the invention improves safety for the patient and makes it possible to test the protective-conductor connection in a simple manner.

The present disclosure relates to a method for determining syringe parameters. It encompasses, as a first step, the providing of a medical syringe pump with a syringe receptacle having a syringe inserted herein, a drive unit for a slide, a counting device for counting motor steps, at least one sensor, a control device and a storage device. The method as described herein also encompasses, as further steps, moving the slide successively at different positions corresponding to known nominal volumes of the syringe. In a further step, the difference between these two positions is determined and, finally, optionally a number of motor steps of the drive unit of the syringe pump is calculated per nominal volume unit with respect to the inserted syringe.

An object is to provide a blood purifying device and an access flow rate measuring method enabling easy and accurate measurement of an access flow rate of an access vessel. A blood purifying device includes a flow rate calculating unit calculating the access flow rate of an access vessel based on an initial blood indicator for blood distributed through a vein side circuit and flowing through the access vessel of a patient, the flow rate distributed through measuring means when a pump is reversed to cause the priming solution to flow out from an artery side circuit, and a blood indicator for the blood diluted with the priming solution which is obtained when the pump is reversed to dilute, with the priming solution, the blood distributed through the vein side circuit.

Non-invasive heartbeat sensor for determining a heart rate in a conduit of an extracorporeal blood treatment apparatus, comprising one source for directing an optical signal towards the blood flowing in the segment; one detector for receiving an optical informative signal comprising the signal emitted by said source after passing the blood, and emitting respective output signal; a controller receiving the respective output signal and retrieving a heartbeat frequency and a heart rate value, based on the output signal, wherein the informative signal is altered by flow perturbation of the blood partially generated by the flow impulses originated by the heart.

A sensor component for use in a system for measuring concentration of analytes in fluid in a fluid line comprises one or more sensing elements having an optical property that varies with the concentration of the analytes, and engages with the fluid line such that the sensing elements are exposed to the fluid. The sensor component comprises a connector connecting to one or more optical waveguides, and transmits light between the waveguides and the sensing elements. The sensor component comprises one or more of a sampling port configured to provide fluidic access to the fluid line, a data storage medium storing data representing information about the sensor component, and a reflective element. Where it comprises a reflective element, the sensor component transmits light between the waveguides and the reflective element on a separate optical path from an optical path between the waveguides and the sensing elements.

Embodiments of the present invention provide an extra corporeal membrane oxygenation circuit, wherein a pump communicates blood from a patient to an oxygenator and thence back to the patient, comprising: (a) a medium diameter venous line configured to accept blood from the patient and communicate the blood to the pump; (b) a medium diameter arterial line configured to accept blood from the oxygenator and communicate the blood to the patient; (c) one or more shunts connected in a series, where each shunt comprises a medium diameter input connected to a medium diameter output, where the medium diameter output is configured to connect to a medium diameter input of a successive shunt; a small diameter outlet between the medium diameter input and the medium diameter output; and a stopcock connected to the small diameter output such that flow out of the small diameter outlet can be controlled by the stopcock; wherein a first of such shunts is connected to accept blood from the venous line in parallel with the pump and wherein a last of such shunts is connected to communicate blood to the arterial line.

A manual clot aspiration and filtration system enables a method of removing a clot without general anesthesia and the expense of an operating room. An aspiration and filtration system for bodily fluid utilizes a syringe coupled with a filter unit to draw bodily fluid through the filter unit to collect debris on the filter. A flow valve may then be turned and the plunger depressed to force the filtered fluid back into the body. The filter may be configured to capture particles such as blood clots and plaque. The filter unit has a cover that can be removed for inspection and/or removal of the collected debris. When the cover is replaced, trapped air may be removed by turning the flow-valve to a purge direction and pressing the plunger into the syringe to force fluid back toward the filter unit to purge the trapped air through the purge valve.