80 results about "Intravenous tubes" patented technology

The invention concerns an arrangement to couple an intravenous hose having a roller clamp with an infusion pump. A hose clamp has clamping surfaces in the form of legs which can move relative one another about a hinge, the legs being enveloped on their outside by a biased clamping spring, and the device is formed by an expander rib that is fastened on the inside of the door and can be brought into engagement with the legs of the hose clamp so to produce the open position after closing the door to expand the legs. The housing has a receiver, into which the hose clamp can be snapped, and that a locking device is present in the housing that prevents the closing of the door if the hose clamp is not inserted into the receiver and permits the closing of the door when the hose clamp is fully inserted.

An IV line temperature controlled warming device includes a housing and a fluid cassette or cartridge that receives fluid from an IV line and includes intravenous line tubing arranged in a preformed configuration. The configuration includes tubing sections arranged in generally circular and concentric portions and a central serpentine tubing section that basically reverses fluid flow and facilitates flow in opposing directions within adjacent tubing sections. The fluid cassette is retained within the device on a base plate partially disposed within a device housing interior, while a housing cover is selectively opened and closed to permit access to the base plate. The base plate includes a heater plate disposed thereon, while the cover and heater plate each include heating elements to apply heat to opposing surfaces of the tubing cassette. The heating elements are controlled by a controller in response to measured temperatures of the heater plate and fluid.

Venous reservoirs are interposed between the patient and the arterial pump and serve to remove air bubbles and provide compliance that accommodates variations in the volume of blood circulating in the extracorporeal circuit during cardiopulmonary bypass (CPB). The invention is a reservoir that incorporates automated means to remove air bubbles from the venous line prior to the blood entering the arterial blood pump. In another form, the reservoir includes means that handles foam prior to the blood entering the blood pump. In yet another form, the invention is means that improve air removal in a soft shell venous reservoir. These features are applicable to CPB circuits using gravity drainage or vacuum assisted venous drainage.

An intravenous connector is provided having a valve body having first end configured to receive a syringe for administering medicine to a patient; a spike element having a tapered hollow spike terminating in a tip at a first end and having a second end configured for attaching to an intravenous tube, the spike element secured in the valve body such that the tip is disposed proximate the first end of the valve body and the second end of the spike element is located at a second end of the valve body; and a pliable seal member disposed in the valve body around the tapered hollow spike and exposed at the first end of the valve body. An antimicrobial material comprising a silane quaternary ammonium salt is incorporated on or within the seal member and is coated on the valve body and the spike element.

A priming indicator for a fluid infusion system includes a luer cap or other component of the infusion system having an indicator surface covered by a membrane. The membrane exhibits a first visual characteristic, such as being opaque, when dry and exhibits a second characteristic, such as becoming less opaque, when wet. Once the membrane becomes wet, indicia on the surface, which may be provided on a rod at least partially covered by the membrane, becomes visible, thereby indicating an intravenous tube to which the luer cap is secured has been primed or is nearly primed. The indicator may alternately be employed at an upstream end of an infusion set, such as at the port of a medical bag providing a supply of fluid, to indicate a low level of fluid in the medical bag.

The invention relates to a blood treatment device by extracorporeal circulation comprising a filter having a primary chamber and a secondary chamber separated by a semi-permeable membrane; a blood circuit comprising an arterial line intended to come from the patient, the filter's primary chamber and the venous line intended to return to the patient; a dialysate circuit comprising the filter's secondary chamber and at least a drain line for circulating the waste intended to come from the filter and intended to go to a drain; a first bag in fluid communication with the drain line; at least a first gravimetric weighing means linked to the first bag, fluid flow rate adjustment means acting on the drain line; a control unit linked to the first gravimetric weighing means and with the fluid flow rate adjustment means; a second bag in fluid communication with the drain line, the control unit being capable of receiving weight signals from the first gravimetric weighing means and of controlling the fluid flow rate adjustment means to load one of the bags with liquid while the other bag unloads liquid, and vice-versa.The invention also relates to a single-use drain line for use in a treatment device according to the invention.

A clip is provided that is especially well adapted for holding IV lines. The clip includes a first member and a second member. The first member defines a groove, and the second member defines a second groove substantially corresponding to the first groove of the first member. An axial member is also included. The first member and the second member are configured to rotate about the axial member.

The current techniques provide a system for monitoring a physiological parameter of a patient using microneedles that are coupled to an optical system, allowing spectroscopic measurements to be made immediately below the outer layer of the epidermis. In embodiments of the present invention, the results of the spectroscopic measurements are used to control the administration of a drug through an intravenous tube. In other embodiments, the microneedles may be coated with a drug for administration to the patient. In other embodiments, the microneedles may be mounted in a probe, wherein an actuator is used to move the needles into contact with the skin, and a drug delivery system is used to infuse the drug into the patient. A method for making needles is also provided.

The present invention relates to an intravenous tube fixer capable of drawing and testing returned blood. It mainly includes a drawing-testing unit capable of producing suction action and a needle group. Said needle group has a needle body communicated with said drawing-testing unit, a tube seat which can be removably connected with said drawing-testing unit, and a flexible tube through which the needle body can be passed. Said invention also provides the concrete working principle and its operation method.

The measurement of blood flow in a dialysis shunt is obtained by injection of an indicator material into a venous line leading from dialysis equipment to the shunt. The blood flow in an arterial line leading from the shunt at a location downstream of the venous line to the dialysis equipment is monitored by an arterial line sensor for the presence of the indicator material. A detector connected to the sensor provides a dilution curve in response to the presence of the indicator material and the blood flow in the shunt is calculated from the area under the dilution curve. The locations of the arterial and venous lines in the shunt can be reversed to obtain a measurement of blood recirculation from the venous line into the arterial line.