A washing device for the ear, nose and throat and the like (10) for domestic use or in medical offices which comprises a body (12) within which the components functional to the operation of the device are housed, a container element (14) defining a tank for a saline solution, a cannula (16) for use by the individual for the washing operations, a cable (18) for connecting to the power supply network.

The invention relates to a device for extracorporeal blood treatment, having a hydraulic system B which comprises multiple lines (7), (9) for providing dialysate for a dialyser (3) and having a control system (15) which comprises multiple electrical components (17A), (17B), (17C). The invention also relates to a method for operating a device for extracorporeal blood treatment which has a hydraulic system which comprises multiple lines for providing dialysate for a dialyser and a control system which comprises multiple electrical components, wherein the dialysate is produced using a liquid supplied to the device for extracorporeal blood treatment. The extracorporeal blood treatment device is a blood treatment device which has a central connection (11) to allow a liquid, in particular permeate (pure water), to be supplied to the machine. The blood treatment device is characterised by a cooling apparatus (19) for cooling at least one of the electrical components (17A), (17B), (17C) of the control system (15), said cooling apparatus using the liquid, in particular permeate (pure water), supplied centrally to the device to dissipate heat from the electrical components. The cooling apparatus (19) has at least one heat sink (21) which can be cooled with a liquid and is in thermal contact with the at least one electrical component (17A), (17B), (17C), wherein the cooling apparatus (19) has at least one inlet (22A) which is fluid-connected to the connection (11) for the inflow of a liquid and at least one outlet (22B) which is fluid-connected to a drain (10), (31).

The present invention provides methods and devices for making a cold slurry at a point of delivery. A point of delivery device delivers cold slurry components to a location at or near a target tissue. The components are combined to form the cold slurry at or near the point of delivery. This approach to generating a cold slurry at the point of delivery allows the characteristics of the cold slurry, such as temperature, particle shape and particle size, to be maintained and controlled.

A system for heating/cooling a target unit. The system including a heater/cooler unit and a heat transfer fluid module. The heater/cooler unit including a heater/cooler that includes a heater/cooler element and a heater/cooler pump, and a heat exchanger that includes a heat exchange element. Where, the heater/cooler pump pumps a first fluid through the heater/cooler element and the heat exchange element and back to the heater/cooler pump. The heat transfer fluid module including a fluid reservoir with a second fluid that is pumped to and through the heat exchanger to transfer heating/cooling between the first fluid and the second fluid and pumped to and through the target unit to transfer heating/cooling between the second fluid and the target unit.

An at least partly implantable system for injecting a substance into a patient's body. The system comprises at least one flexibly bendable infusion needle with a tip end of each of said at least one infusion needle arranged in at least one first housing for penetrating the first housing's outer wall in at least one penetration area and having the respective other end arranged in at least one second housing, the first and second housings being adapted for implantation inside the patient's body, wherein the at least one second housing is provided for implantation inside the patient's body remote from the at least one first housing and wherein the injection needle is sufficiently long to bridge the distance from the at least one second housing for remote implantation to the at least one first housing and further through the first housing up to the outer wall of the first housing. The system further comprises at least one drive unit adapted for being coupled to the at least one infusion needle and arranged at least for advancing the tip end of the at least one infusion needle so that the at least one infusion needle penetrates with the tip end or ends thereof said at least one first housing's outer wall in said at least one penetration area.

Many embodiments of wound filling devices and methods of their use in systems for the application of negative pressure therapy are described herein. In one embodiment, a wound filling device comprises: an inflatable bag member having at least one fluid carrying conduit operably connected thereto to inflate/deflate said bag member; a separate textured covering sock member at least partially covering the inflatable bag member. Another embodiment comprises a three-dimensional wound packing member, and may optionally comprise a plurality of such members linked together. Certain embodiments of wound packing members may comprise a porous bag member adapted to be non-adherent to the wound. Yet other embodiments may comprise a non-porous bag member provided with means to connect a fluid supply to the interior.

This disclosure relates to a method for determining a fluid balance between a first volume flow in a first section of a fluid circuit and a second volume flow of a second section of the fluid circuit. The method may also include adjusting, assuming or detecting a first temperature in the first section of the fluid circuit and a second temperature in the second section of the fluid circuit, or detecting a temperature difference between the first and the second sections. The method may also include detecting a second volume flow in a second section of the fluid circuit and forming a balance from at least the first volume flow and a corrected value of the second volume flow. The corrected value is determined from the detected second volume flow and the second temperature and/or the temperature difference.

A treatment system delivers a breathing gas and frozen stem cells or other biologic particles (FBP) to a bronchus of a lung of a patient in order to treat lung and other conditions. The breathing gas and the FBP are usually delivered through separate lumens. The FBP may be delivered concurrently with other frozen particles, such as frozen saline particles (FSP). The FBP/FSP will remain frozen at all times from preparation to delivery, and will thaw only after they are released into the lung.

An extracorporeal blood treatment device with a function-monitoring system, wherein the extracorporeal blood treatment device for connection to the vascular system of a patient has an input branch and an output branch. The extracorporeal blood treatment device is equipped, in a first circuit, with at least one first pump arranged between the input branch and output branch for moving the patient's blood, and, in a second circuit filled with liquid and thermally connected to the first circuit of the extracorporeal blood treatment device via a heat exchanger, it has temperature-influencing means. The function-monitoring system has, in the second circuit, two temperature sensors which are arranged upstream (TS2.sub.auf) and downstream (TS2.sub.ab), respectively, with respect to the heat exchanger, in addition, temperature sensor TS1.sub.ab is arranged in the output branch of the first circuit, downstream from the heat exchanger. The function-monitoring system moreover comprises a computer system which is operatively connected to the aforementioned temperature sensors and the temperature-influencing means and which, after the temperature has been influenced, establishes, from the detected temperature values, corresponding thermodilution curves (TDK1.sub.ab, TDK2.sub.ab, TDK2.sub.auf) and, in order to determine an indicator of the function of the extracorporeal blood treatment device, relates the TDK2.sub.ab and the TDK.sub.1ab to each other.

An apparatus and method for providing heat exchange in the lungs of the mammal during partial liquid ventilation are provided. The apparatus and method can control delivery and removal of partial liquid ventilation to the lungs of a mammal by responding to pressure change in the lungs to minimize danger of causing barotrauma to the patient.