The present application refers to a heat transfer liquid for a temperature control device for human body temperature control during extracorporeal circulation, a temperature control device, the use of heat transfer liquid for extracorporeal circulation and a method of human body temperature control using a heat transfer liquid. The heat transfer liquid consists of ethylene glycol or propylene glycol at about 25 volume-percent to about 35 volume-percent, hydrogen peroxide at 0.05 volume-percent or less and sterile, filtered and de-mineralized water as rest.

A diaphragm pump, includes a case, a diaphragm dividing a space in the case into a first space and a second space, a liquid feed flow path including an inflow path to introduce a liquid to be fed into the first space and an outflow path to discharge the liquid to be fed from the first space, a drive unit including a compression/decompression device that repeatedly causes displacement of the diaphragm by repeating compression and decompression of a driving fluid filling the second space, and a valve mechanism to open and close the inflow path and the outflow path. The drive unit includes a pressure release mechanism to release pressure of the driving fluid after the driving fluid is compressed or decompressed by the compression/decompression device.

A hemodialysis enhancement apparatus involves a bladder having elastically deformable surface that forms a variable volume therewithin. The elastically deformable surface has a smooth interior surface such that blood cannot collect to form a blood clot. The hemodialysis enhancement apparatus further includes a rigid housing having a wall surrounding the bladder and defining a housing volume such that a) when the variable volume chamber has a volume equal to the first volume, most of the elastically deformable surface will be spaced apart from the wall, and b) when the variable volume chamber has a volume equal to the second volume, a substantial portion of the elastically deformable surface will abut the wall. A method performed within a hemodialysis system involves, during an initial phase, withdrawing a volume of a patient's blood into a hemodialysis enhancer, and during a subsequent phase, translocating the patient's blood back into the patient's circulation.

A blood loop system for controlling blood oxygen saturation includes a conduit loop, a pump, a flow cell, a matter source, an aeration chamber, a collection chamber and an oxygen probe. The pump is coupled to the conduit loop and positioned to circulate blood through the conduit loop. The flow cell is positioned to measure a characteristic of the blood circulated through the conduit loop. The matter source includes a gas. The aeration chamber is coupled to the conduit loop and is in fluid communication with the matter source to enable the gas to combine with the blood. The collection chamber is in fluid communication with the aeration chamber and is positioned to receive the blood. The oxygen probe is positioned to measure an amount of oxygen in the blood.

A renal failure therapy system having an electrically floating fluid pathway is disclosed. The example system includes a dialyzer, a blood circuit in fluid communication with the dialyzer, and a dialysis fluid circuit in fluid communication with the dialyzer. The system also includes an electrically floating fluid pathway comprising at least a portion of the blood circuit and at least a portion of the dialysis fluid circuit. The only electrical path to ground is via used dialysis fluid traveling through the renal failure therapy system to earth ground. The disclosed system enables at least one electrical component in the at least a portion of the dialysis fluid circuit of the electrically floating fluid pathway to be electrically bypassed.

A fluid warming device for an extracorporeal blood treatment apparatus, comprises: an outlet temperature sensor (31) operatively active at an outlet (22) of a fluid warming path (23) to detect a measured outlet temperature (To) of a fluid leaving the fluid warming device (18); an electronic control unit (29) operatively connected to the outlet temperature sensor (31). The electronic control unit (29) is configured to perform the following procedure: receiving, from the outlet temperature sensor (31) a signal correlated to a measured outlet temperature (To); correcting the measured outlet temperature (To) through a correction model to obtain an actual fluid outlet temperature (Tout); adjusting a heating power (Ph) of heating elements to keep the actual fluid outlet temperature (Tout) at a set reference temperature value (Tset). The correction model is an empirical model of a measurement error (E) derived from a plurality of experimental data sets, the measurement error (E) being a difference between the measured outlet temperature (To) and the actual fluid outlet temperature (Tout).

A sensor system (10) has a medical device provided with a first transmission/reception unit (16) installed inside a medical instrument (12) to output a detection signal of a sensor unit (22), and a second transmission/reception unit (18) detachably installed outside the medical instrument (12) to transmit/receive a signal to and from the first transmission/reception unit (16) in a contactless manner. The first transmission/reception unit (16) and the second transmission/reception unit (18) are arranged so as to be opposed to each other across the medical instrument (12) to transmit/receive the signal by electromagnetic induction.

A system for measurement is provided. The system comprises a core optical module and a scanning interface module. The core optical module is configured to generate a light for generating signals for analyzing an object through the scanning interface module and detect a light including the signals from the object through the scanning interface module. The scanning interface module is changeable for each application and configured to connect with the core optical module by a light transferring unit to scan the object with the transferred light from the core optical module and to receive the light from the object to transfer to the core optical module.

A cartridge insertion system includes a chassis supporting a fluid circuit, the chassis having a forward end with key pins projecting from the forward end and a rear end. The system also includes a medical treatment device with a slot opening closed by doors having a major dimension and having key openings spaced apart a same distance as the key pins on the chassis, such that when the chassis is pushed toward the slot opening, the key pins enter the key openings before the forward end meets the doors. The key pins push against latches that hold the door locked shut, so that the doors will not open if a cartridge without key pins is pressed against the door. When a cartridge with key pins is used, the doors unlock and allow the cartridge to be inserted.

The invention relates to a medical treatment apparatus comprising a tube set 20, a peristaltic pump 6 for conveying fluid, and a monitoring apparatus 15 for monitoring the occlusion of the positive displacement elements 13A, 13B of the peristaltic pump. In addition, the invention relates to a tube set 20 for a medical treatment apparatus, and to a method for monitoring the occlusion of the occlusion elements of a peristaltic pump for conveying a fluid for a medical treatment apparatus. The invention is based on the fact that the occlusion of the positive displacement elements 13A, 13B of the peristaltic pump 6 is monitored in order to monitor the fluid flow in the hose line 5. For this purpose, the electrical resistance or a variable which correlates with the electrical resistance is measured between a first and a second electrode 16A, 16B, the first electrode 16A being arranged on the hose line 5 upstream of the occlusion elements 12 of the peristaltic pump 6 and the second electrode 16b being arranged on the hose line downstream of the occlusion elements such that an electrical contact is produced between the first and second electrode 16A, 16B and the fluid flowing in the hose line 5. The electrodes 16A, 16B are preferably integral component parts of a connecting piece 10, by means of which the hose segment 5A to be inserted into the peristaltic pump 6 is fixed in the form of a loop.