A system for warming intravenous fluids is provided including a positioning holder configured to receive and support a tube for providing at least one intravenous fluid to a patient and a plurality of elongate heating fingers, wherein each elongate heating finger is configured to be independently manipulated such that said elongate heating finger contacts the tube to transfer heat to the at least one intravenous fluid provided via the tube.

A tube received, at least in part, by a breastmilk warmer includes a first segment having a first thermal conductivity, a second segment having a second thermal conductivity different from the first thermal conductivity, and a third segment having a third thermal conductivity different from at least one of the first and second thermal conductivities. The first segment is configured to be coupled to a source of fluid. The second segment is fluidly coupled to the first segment and disposed in a labyrinthine manner within a breastmilk warmer. The third segment is fluidly coupled to the second segment and is configured to be coupled to a feeding apparatus. The tube also includes a fluid lumen extending from the first segment through the second segment and to the third segment. The fluid lumen has a uniform diameter from the first segment to the third segment.

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.

The present invention relates in one aspect to an infusion fluid warmer which comprises a casing shell having an upper wall structure and a lower, opposing, wall structure. The casing shell encloses a fluid channel or passage extending through the casing shell in-between the upper and lower wall structures and fluid inlet and outlet ports coupled to opposite ends of the fluid channel or passage to allow a flow of infusion fluid through the casing shell. A housing shell is formed in a thermally conducting and electrically insulating material and a heating element is bonded to the housing shell and thermally coupled thereto. The fluid channel or passage extends through the housing shell or extends around the housing shell such that heat energy is transferred to the infusion fluid by direct physical contact with housing shell material.

The present invention relates in one aspect to an infusion fluid warmer which comprises a casing shell having an upper wall structure and a lower, opposing, wall structure. The casing shell encloses a fluid channel or passage extending through the casing shell in-between the upper and lower wall structures and fluid inlet and outlet ports coupled to opposite ends of the fluid channel or passage to allow a flow of infusion fluid through the casing shell. A housing shell is formed in a thermally conducting and electrically insulating material and a heating element is bonded to the housing shell and thermally coupled thereto. The fluid channel or passage extends through the housing shell or extends around the housing shell such that heat energy is transferred to the infusion fluid by direct physical contact with housing shell material.

A heating system for medical fluid that comprises a receptacle for medical fluid to be heated, a heating element powered by a power supply inducing a leakage current (to ground) ranging between 100 and 10 μA. The heating system further comprises an interface device (for example, an electrical insulation and thermal interface device) disposed between the heating element and the medical fluid contained in the receptacle, allowing the heating system to induce a leakage current in the medical fluid that is less than 10 μA at the applied part.

A heating system for medical fluid that comprises a receptacle for medical fluid to be heated, a heating element powered by a power supply inducing a leakage current (to ground) ranging between 100 and 10 μA. The heating system further comprises an interface device (for example, an electrical insulation and thermal interface device) disposed between the heating element and the medical fluid contained in the receptacle, allowing the heating system to induce a leakage current in the medical fluid that is less than 10 μA at the applied part.

A treatment system includes a delivery device which delivers a combination of a breathing gas and frozen ice or other particles to a patient in order to induce hypothermia. The treatment system also includes a temperature system for measuring the temperature of exhaled gases and a controller which can adjust the duration or rate at which the ice particles are delivered in order to control the patient's core temperature based on the measured exhalation gas temperature.

Embodiments include cryogenic systems and methods for treating pain or spasm associated with a nerve of a patient. A target nerve may be located and a distal end of a cryogenic system needle may be inserted into a tissue at a desired location in proximity to the target nerve. The needle includes an outer lumen and an inner lumen extending distally within the outer lumen, the inner lumen including a distal opening that is open to the outer lumen. A cooling fluid may be delivered from a cooling fluid source to the needle via a fluidic pathway, the fluidic pathway including the cooling fluid source, the inner lumen, and the outer lumen, wherein a flow of the cooling fluid cools the needle so that the needle cools the target nerve at the desired location sufficiently such that the pain or spasm is inhibited.

The invention relates to a device for treating an individual suffering from cardiac or circulatory arrest or from a stroke, comprising a blood withdrawal device (BE) that is applied to the individual (P), an analysis unit (BA) which is directly or indirectly connected to the blood withdrawal device for detecting a blood analysis result (BAE) providing at least one characteristic of the blood, directly or indirectly connected to a blood return device (BR) that is applied to the individual (P) and is designed to deliver a substance to the individual via the return device (BR).