A chemical-liquid injector includes a piston-driving mechanism (130) that moves a piston member of a syringe containing a contrast medium, which includes an actuator and a ram member which is moved back and forth by the actuator, a control circuit (150) which is electrically connected to the actuator, and an operating knob unit (170) which includes an operating knob that is to be operated by an operator, and a rotation sensor that outputs an electric signal corresponding to a rotation of the operating knob. The control circuit is configured to generate a predetermined control signal accordingly, on the basis of a signal from the rotation sensor, and the piston-driving mechanism is operated according to the control signal.

A fluid infusion system includes an air pump connected to an accumulator tank to produce pressurized air that is stored in the accumulator tank. The system can include one or more fluid bag chambers wherein each fluid bag chamber includes an inflatable bladder positioned inside the fluid bag chamber to apply pressure on the fluid bag supported inside the chamber. The fluid bag can be connected by a tube set to deliver fluid from the fluid bag to a surgical tool at a surgical site. The fluid can, for example, be irrigation fluid or distention fluid. The system can include a controller connected to the pump to control the pump to produce the pressurized air and an adjustable pressure regulator can be connected between the accumulator tank and the inflatable bladder to control the pressure of air delivered to the inflatable bladder and the pressure that the fluid is delivered to the surgical tool. A pressure sensor can be connected between the adjustable pressure regulator and the inflatable bladder to measure the air pressure delivered to the inflatable bladder and send the air pressure measurements to the controller. The controller can configure the system display to show the air pressure measured by the pressure sensor.

A drug delivery pump includes a dosing chamber (16) for delivering a substance (18) therefrom, pushing apparatus, and a thermal energy source (14) arranged to cause a sufficient change in temperature in a portion of the pushing apparatus so that the pushing apparatus imparts a pushing force against the substance to cause the substance to be delivered from the dosing chamber. A controller (90) controls delivery of the substance from the dosing chamber. A thermal insulator (24) thermally insulates the substance in the dosing chamber from the thermal energy source.

There is disclosed a fluid warming system (300) for warming intravenous fluid, comprising: a heater unit (304), including a heating element (314) and at least one temperature sensor; a heat exchanger unit (302), removably attachable to the heater unit (304), which includes an inlet (306) and an outlet (308) through which the fluid can pass, and a controller (316), programmed: to receive at least one temperature measurement (T.sub.CI, T.sub.CO) from said at least one temperature sensor in the heater unit (304); to compute a fluid flow rate (q), corresponding to the rate of flow of fluid from the inlet (306) to the outlet (308) of the heat exchanger unit (302), in dependence on the amount of electrical power (P.sub.H) supplied to the heating element and said at least one temperature measurement (T.sub.CI, T.sub.CO); and to control the electrical power (P.sub.H) supplied to the heating element in dependence on the computed fluid flow rate (q).

A medical drip bag heater includes a flexible sheet of material configured to wrap around a drip bag, heating wires, velcro strips, and a thermostat control. The sheet of material includes a body portion with two side edges and a bottom flap with a bottom edge. The heating wires are embedded into the sheet of material and configured to electrically connect to a power source through a thermostat control. The velcro strips are fixedly attached to the two side edges and the bottom edge. The thermostat control controls the temperature of the heater and displays the temperature.

A dispensing assembly has a dispensing chamber housing, a temperature control device, a thermal sensor, and an interface. The dispensing chamber housing has an inner surface, an outer surface, and a wall thickness. The inner surface partially defines a dispensing chamber for receiving a quantity of a substance. The temperature control device at least partially surrounds the dispensing chamber housing. The temperature control device alters a temperature of a substance in the dispensing chamber. The temperature control device and the thermal sensor are located on a substrate. The substrate is wrapped around an exterior surface of the dispensing chamber housing. The interface is connected to the temperature control device and the thermal sensor. An interface connector is connected to the interface. The distance between the temperature control device and the thermal sensor is approximately equal to the wall thickness of the dispensing chamber housing.

An auxiliary sensor can be used to measure the temperature of individual products in a heating cabinet. By arranging the temperature sensor with respect to the low mass thermal conductors and insulators, the sensor can be focused on the product to obtain the proper temperature irrespective of the immediate environment whether it is at room temperature or even within the heating cabinet.

A blood warmer (10) has a first heating plate (12) and a second heating plate (14) as well as an exchangeable conductor (18, 20, 22, 24) for blood, which is arranged between the first heating plate (12) and the second heating plate (14). The blood warmer (10) has an inlet (66) and an outlet (68) for blood to which the conductor (18, 20, 22, 24) is fluidically connected. Due to the roughness of the surface (46) of the conductor (18, 20, 22, 24), an intermediate space (50) remains between the first heating plate (12) and/or the second heating plate (14) and the conductor (18, 20, 22, 24). A medium (52), which has a higher thermal conductivity than air, is at least partially statically arranged in the intermediate space (50). The blood warmer (10) may also have an electromechanical oscillating circuit and/or a vibration motor.

A surgical fluid thermal treatment system can be used during a procedure to heat or cool surgical fluid, e.g., prior to introducing the fluid into the body of a patient. In some examples, the system includes an open basin into which fresh surgical fluid is dispensed and a heater that heats the fluid in the basin. The system may also include a volume measurement device that measures the volume of fluid in the basin. The system may have a user interface that a user interacts with to check fresh fluid into the basin. The user may also interact with the user interface to check medical tools into the basin and check medical tools out of the basin. A controller associated with the system can track the volume of fluid removed from the basin during the course of a procedure.

The present invention includes: a laminated structure of an insulation substrate; a resistance pattern laminated on one side of the insulation substrate with a pure metal or an alloy which is a mixture of two or more metals at a predetermined ratio and having a resistance value which is set by a pattern having a length and a cross-sectional area; a first insulator layer coated on an upper surface of the resistance pattern by a predetermined method to protect and insulate the resistance pattern; a conductor layer in which a metal material is deposited on the upper surface of the first insulator layer by a predetermined method; and a thin film protective layer deposited on the upper surface of the conductor layer to provide insulation from the conductor layer, waterproofing, corrosion resistance, and chemical resistance.