Abstract: A catheter assembly for use in accessing a vasculature of a patient during renal replacement or other therapies is disclosed. In one embodiment, the catheter assembly includes a catheter body that defines first and second lumens. The catheter body defines a distal tip region that includes a venous lateral opening that is in fluid communication with the first lumen and includes a distal-facing portion. The distal tip region further includes an arterial lateral opening that is in fluid communication with the second lumen, includes a distal-facing portion, and is substantially un-staggered with respect to the venous lateral opening. A distal end opening is defined on the distal tip region and is sized to pass a fluid therethrough. In one embodiment, the distal end opening is in fluid communication with a third lumen of the catheter body that can withstand high fluid flow rates associated with power injection of contrast media.

Abstract: An access port for providing subcutaneous access to a patient is disclosed. In one embodiment, the port includes an internal body defining a fluid cavity that is accessible via a septum. A compliant outer cover including silicone is disposed about at least a portion of the body. A flange is included with the port body and is covered by the outer cover. The flange radially extends about a perimeter of the port body proximate the septum so as to impede penetration of a needle substantially into the outer cover in instances where the needle misses the septum. The flange can further include both an anchoring feature for securing the outer cover to the port body and an identification feature observable via x-ray imaging technology for conveying information indicative of at least one attribute of the access port. The outer cover provides a suitable surface for application of an antimicrobial/antithrombotic coating.

Abstract: A catheter connection system and a method of connecting the catheter connection system to a catheter. The catheter connection system includes a hub assembly and a collar. The hub assembly includes a cannula extending from a distal end thereof, and a collet defining an inner surface spaced apart from the cannula to permit passage of a catheter wall between the body and the cannula. The collet includes a proximal barb on an outer surface and the collar includes an attachment barb on an inner surface, engagement of the respective barbs acting to provide a permanent connection between the collar on the collet, while permitting free rotation of the collar about the collet.

Abstract: A power injection catheter for high flow rate delivery of fluids. The power injection catheter may include a pressure relief mechanism for preventing overpressurizing within the lumen of the catheter. The pressure relief mechanism may be configured to prevent sudden pressure build-up inside the catheter lumen by absorbing, buffering or releasing pressure inside the lumen during pressure spikes. The power injection catheter may also take the form of a multi-lumen catheter capable of simultaneous infusions of a single fluid through two or more of the lumens in the catheter.

Abstract: A catheter connection system is described herein, including a hub assembly and a connector assembly, the hub assembly including a cannula configured for insertion into a catheter lumen and the connector assembly including a collet and collar. The collet is connected to the hub assembly and positioned about a distal portion of the cannula such that an inner surface of the collet is spaced from an outer surface of the cannula. The collar and collet include features that interact with one another to provide a locking engagement. Also described is a multifunction adaptor to establish a connection between a catheter and another instrument, such as a tunneler or syringe.

Abstract: A catheter connection system is disclosed. In one embodiment, a catheter connection system may include at least two components and a deformable sealing element positioned between the at least two components configured to allow, upon deformation, fluid flow through the at least two components. In another embodiment, the catheter connection system may include a sealing element positioned between at least two components, wherein the components are coupled to one another by a locking member.

Abstract: A valved catheter that allows placement and withdrawal of an accessing device or attachable unit without the risk of air embolism or blood loss. In one variation, the valved catheter includes a catheter tube having a necked portion in its proximal end that forms an integral valve, the necked portion being surrounded by a compression sleeve that biases the valve in a closed position. In another variation, the valved catheter is a dual lumen catheter with a corresponding bifurcating extension for engaging the valves in the catheter in order to establish fluid communication through the catheter.

Abstract: A catheter connector for a subcutaneously placed catheter. The catheter connector can be configured for a single lumen catheter or a multiple lumen catheter. The connector facilitates precise positioning of both distal and proximal ends of a catheter, providing enhanced functionability and patient comfort.

Abstract: A catheter connector for a subcutaneously placed catheter. The catheter connector can be configured for a single lumen catheter or a multiple lumen catheter. The connector facilitates precise positioning of both distal and proximal ends of a catheter, providing enhanced functionability and patient comfort.

Abstract: A multifunction adaptor for an open-ended catheter that allows placement of the catheter while minimizing the risk of air embolism or blood loss through the open (proximal) end of the catheter body. In one variation, the design allows passage of a standard guidewire for “over-the-guidewire” placement techniques and a connection for catheter flushing using a standard syringe. In another variation, the multifunction adaptor is configured for coupling a tunneler to the proximal end of a catheter.

Abstract: A catheter assembly for use in accessing a vasculature of a patient during renal replacement or other therapies is disclosed. In one embodiment, the catheter assembly includes a catheter body that defines first and second lumens. The catheter body defines a distal tip region that includes a venous lateral opening that is in fluid communication with the first lumen and includes a distal-facing portion. The distal tip region further includes an arterial lateral opening that is in fluid communication with the second lumen, includes a distal-facing portion, and is substantially un-staggered with respect to the venous lateral opening. A distal end opening is defined on the distal tip region and is sized to pass a fluid therethrough. In one embodiment, the distal end opening is in fluid communication with a third lumen of the catheter body that can withstand high fluid flow rates associated with power injection of contrast media.

Abstract: A multi-lumen catheter configured for insertion into the vasculature of a patient for fluid infusion into or fluid aspiration from the patient is disclosed. The multi-lumen catheter includes one or more cross sectionally variable lumens, wherein the cross sectional area of the lumen(s) may be selectively increased, particularly during fluid infusion, in order to enable relatively greater fluid flow rate therethrough. In one embodiment, the multi-lumen catheter includes a deformable first septum for providing an increased cross sectional area for a lumen under high flow rate pressurization, such as power injection. A deformable second septum also deforms to allow for first septum deformation and additionally provides an urging force to restore the first septum to an un-deformed state once lumen pressurization has ceased. In another embodiment, a bi-positional septum is used to selectively increase the cross sectional area of a lumen of the catheter during power injection.

Abstract: A catheter connector system that allows trimming of the proximal end of a catheter (single or multiple lumen) prior to the placement of a connector hub. In one variation, the catheter connector system comprises a catheter, a connector sheath including a soft collet, and a connector hub including a cannula for engaging the catheter and a connector hub interface for receiving the connector sheath.

Abstract: A catheter connector system that allows trimming of the proximal end of a catheter (single or multiple lumen) prior to the placement of a connector hub. In one variation, the catheter connector system comprises a catheter, a connector sheath including a soft collet, and a connector hub including a cannula for engaging the catheter and a connector hub interface for receiving the connector sheath.

Abstract: A valved catheter that allows placement and withdrawal of an accessing device or attachable unit without the risk of air embolism or blood loss. The valved catheter includes a catheter tube having a necked portion in its proximal end that forms an integral valve, the necked portion being surrounded by a compression sleeve that biases the valve in a closed position.

Abstract: Disclosed is a temperature sensing device and system including a processor, a memory, and optics for collecting incident infrared energy to produce a temperature signal. The device and system function in accordance with a disclosed method to derive one or more signal parameters from the infrared energy, such as signal strength and signal dilution, and compare the parameter(s) with acceptable, pre-defined limits. A filtered or unfiltered temperature indication is provided if all parameters lies within pre-defined limits, and a different temperature indication is displayed if one or more parameters exceeds pre-defined limits.

Abstract: Disclosed is a temperature sensing device and system including a processor, a memory, and optics for collecting incident infrared energy to produce a temperature signal. The device and system function in accordance with a disclosed method to derive one or more signal parameters from the infrared energy, such as signal strength and signal dilution, and compare the parameter(s) with acceptable, pre-defined limits. A filtered or unfiltered temperature indication is provided if all parameters lies within pre-defined limits, and a different temperature indication is displayed if one or more parameters exceeds pre-defined limits.

Abstract: A particularly useful method is disclosed for sterilizing micro-isolators in which a sipper bottle is contained. In the present invention, sterilization is effected by using a microprocessor control to regulate the pressure within a sterilization chamber in response to temperature conditions. Pressure within the chamber is regulated so that as temperature is raised and lowered, the boiling point of water in the sipper bottle is never exceeded. Prior to sterilization, the chamber is evacuated of air to permit effective distribution of steam. Subsequent to sterilization, the chamber is again evacuated in order to evaporate condensed steam that covers the micro-isolator and its contents. During each of these evacuations, the microprocessor control regulates the rate of vacuum draw down so that the boiling point of water in the sipper bottle is again not exceeded. This method permits micro-isolators to be sterilized with sipper bottles full of water, without losing a significant volume of water.

Abstract: Means are provided for the monitoring of a sterilization procedure employing alkylene oxide, particularly ethylene oxide, to sterilize medical equipment, especially heat-sensitive equipment, and especially for monitoring the aeration of the so-sterilized goods and articles to desorb the retained alkylene oxide, which means employ interaction of the alkylene oxide with a cation-exchange resin and subsequent aeration of the cation exchange resin coupled with pH indicator means sensitive to changes in the ion exchange resin effected by the alkylene oxide employed in the sterilization and subsequently by the air employed in the desorption step.