Abstract: In one example, fleet devices are monitored. The fleet devices include engines. A controller, such as an engine controller or centralized controller, receives sensor data indicative of a load on the engine from one or more of the fleet devices. The controller analyzes the load from the sensor data to identify a management function. The controller generates a message including the management function.

Abstract: In one example, fleet devices are monitored. The fleet devices include engines. A controller, such as an engine controller or centralized controller, receives sensor data indicative of a load on the engine from one or more of the fleet devices. The controller analyzes the load from the sensor data to identify a management function. The controller generates a message including the management function.

Abstract: In one example, fleet devices are monitored. The fleet devices include engines. A controller, such as an engine controller or centralized controller, receives sensor data indicative of a load on the engine from one or more of the fleet devices. The controller analyzes the load from the sensor data to identify a management function. The controller generates a message including the management function.

Abstract: In one example, fleet devices are monitored. The fleet devices include engines. A controller, such as an engine controller or centralized controller, receives sensor data indicative of a load on the engine from one or more of the fleet devices. The controller analyzes the load from the sensor data to identify a management function. The controller generates a message including the management function.

Abstract: A bandage can be used to secure a needle to an access site so as to prevent unintended movement or withdrawal of the needle from the access site during administration of a treatment to a patient. After treatment, the needle can be removed by manipulating a portion of the bandage. Another portion of the bandage can be maintained in position over the access site during needle removal and can be used to promote clotting of the site after needle removal. The bandage may include a clotting agent, a hemostasis pad, and/or a clot-promoting structure. Additionally or alternatively, finger pressure can be applied to the access site through the bandage. For example, the bandage may include a viewing window without any adhesive to allow visual monitoring of the access site during treatment. Finger pressure may be applied to the viewing window and thereby to the access site during and after needle removal to encourage hemostasis.

Abstract: A bandage can be used to secure a needle to an access site so as to prevent unintended movement or withdrawal of the needle from the access site during administration of a treatment to a patient. After treatment, the needle can be removed by manipulating a portion of the bandage. Another portion of the bandage can be maintained in position over the access site during needle removal and can be used to promote clotting of the site after needle removal. The bandage may include a clotting agent, a hemostasis pad, and/or a clot-promoting structure. Additionally or alternatively, finger pressure can be applied to the access site through the bandage. For example, the bandage may include a viewing window without any adhesive to allow visual monitoring of the access site during treatment. Finger pressure may be applied to the viewing window and thereby to the access site during and after needle removal to encourage hemostasis.

Abstract: A bandage can be used to secure a needle to an access site so as to prevent unintended movement or withdrawal of the needle from the access site during administration of a treatment to a patient. After treatment, the needle can be removed by manipulating a portion of the bandage. Another portion of the bandage can be maintained in position over the access site during needle removal and can be used to promote clotting of the site after needle removal. The bandage may include a clotting agent, a hemostasis pad, and/or a clot-promoting structure. Additionally or alternatively, finger pressure can be applied to the access site through the bandage. For example, the bandage may include a viewing window without any adhesive to allow visual monitoring of the access site during treatment. Finger pressure may be applied to the viewing window and thereby to the access site during and after needle removal to encourage hemostasis.

Abstract: A bandage can be used to secure a needle to an access site so as to prevent unintended movement or withdrawal of the needle from the access site during administration of a treatment to a patient. After treatment, the needle can be removed by manipulating a portion of the bandage. Another portion of the bandage can be maintained in position over the access site during needle removal and can be used to promote clotting of the site after needle removal. The bandage may include a clotting agent, a hemostasis pad, and/or a clot-promoting structure. Additionally or alternatively, finger pressure can be applied to the access site through the bandage. For example, the bandage may include a viewing window without any adhesive to allow visual monitoring of the access site during treatment. Finger pressure may be applied to the viewing window and thereby to the access site during and after needle removal to encourage hemostasis.

Abstract: A securement device for an intravenous, winged needle set, which comprises: an inverted U-shaped, self-supporting strap, the strap having vertical legs attached to a central portion of a base. The base has a bottom to rest on the skin of the patient. A portion of the base forward of the strap has an upper surface that slopes downwardly to a forward end at an angle to the skin and the bottom of the base. Improved retention and ease of application is provided with such a device.

Abstract: A mounting bracket is provided for holding a medical device adjacent a medical apparatus. The mounting bracket includes spring arms that allow the bracket to be spring loaded and inserted between a medical apparatus and a pole. The bracket includes fingers for flexibly receiving a medical device thereon, so that the device may be securely mounted adjacent the medical apparatus. The bracket includes a base having the first spring arm and second spring arm extending therefrom.

Abstract: A winged needle comprises a hollow medical needle which typically is no smaller than 18 gauge carried by a hub. The hub has wings projecting laterally outwardly, the wings having outer tips that are spaced from each other by essentially 20 to 30 mm. A guard for a winged needle tube set is also disclosed, in which the guard comprises a needle guard tube free of wing-receiving slots and defining a forward, open end to receive a winged needle having outwardly extending, substantially unbent wings as positioned within the guard. In some embodiments, the guard comprises a substantially fixed, open mouth having a width of at least 20 mm and a height of at least 5 mm. A novel anchor strip having two flex lines is also provided to the guard.

Abstract: A tubular medical fluid flow set comprises a pressure sensing chamber connected in flow-through relation to fluid flow tubing of the set. The pressure sensing chamber defines a movable, flexible, impermeable diaphragm dividing the chamber into two separate compartments. The fluid flow tubing communicates with one of the compartments and is isolated from the other of the compartments. A port is carried on the chamber, the port having a seal therein, and communicating with the other of the compartments. Thus, the other of the compartments is hermetically sealed until the port is opened for connection with a pressure measuring device, to keep the flexible diaphragm in a desired, initial position prior to opening of the seal.

Abstract: A flexible valve for a blood treatment set. A flexible fitting including a first chamber, a second chamber, and a slit barrier connecting the first chamber and second chamber and positioned therebetween. An actuating member is positioned in rotating engagement with the slit barrier that is moveable from a first rotational position, in which the slit is closed, to a second position, in which the slit is open. The flexible valve is attachable to a port of a blood treatment chamber. A user opens the valve by rotating the actuating member from a first position to a second position and closes the valve by rotating the valve from the second position to a first position.

Abstract: A closure for a tubular access port in a medical fluid flow line or other container comprises a removable cap for enclosing and sealing the tubular access port. The cap has a closed end wall. The end wall carries an extending poker to facilitate the pushing of an antiseptic-carrying material into a lumen of the access port. The poker has an outer diameter that is less than the inner diameter of the access port. A method of using the poker is also described.

Abstract: A rotary valve for a fluid flow line comprises a valve tube having at least one lumen for unobstructed fluid flow of the fluid flow line therethrough. The valve tube has at least one side aperture communicating with the lumen. A housing is provided which is sealingly and rotatably mounted on the exterior of the valve tube. The housing defines at least one lateral port which registers with the side aperture in a first rotational position of the housing, while the lateral port is sealingly and rotationally spaced from the side aperture in a second rotational position of the housing. Preferably, the lumen is unobstructed and open in every rotational position of the housing.

Abstract: A pad of elastomeric material having a softness of typically no more than about durometer 50 Shore 00. The pad may carry adhesive and/or a housing for adhering the pad to a surface, either manually, or by adhesive tape, or another strap. Such a pad exhibits hemostatic and leak prevention properties against needle puncture holes in the skin or the wall of a hollow medical device. Particularly, hemostasis may be prevented with low pressure application of the pad to the skin. The pad may be previously applied to the skin of the patient or a wall of a medical device such as tubing or a solution bag, and the needle may then penetrate both the pad and the skin or medical device wall, to make a resealable puncture with leakage reduction and hemostasis when the needle is withdrawn.

Abstract: A method for monitoring for leaks or disconnections in an extracorporeal blood circuit, comprising the steps of operating a blood pump to circulate blood through an extracorporeal blood circuit; opening a shunt connection between the arterial and venous blood flow portions; sensing the presence of air from any leaks or disconnections within the venous blood flow portion, and taking corrective action if the presence of air is noted. The shunt connection is typically periodically but only briefly opened, to check for leaks in the typically positive pressure portion of the venous set.

Abstract: A one-piece elastomeric cap is proportioned to fit over an outer end of a female luer-lock connector. The cap comprises an outer cap member defining a generally cylindrical, bore-defining portion and an end wall to close off the bore. A generally cylindrical projection extends inwardly into the bore from the end wall. The projection is proportioned to sealingly fill at least an outer portion of the lumen of the female luer or luer-lock connector occupying said bore; the outer cap member preferably further defines at least one radially outwardly extending space adjacent to the end wall and extending radially outwardly from the bore, to receive outwardly-extending threads or lugs of the female luer-lock connector inserted within said cap.

Abstract: A combined arterial and venous blood tubing set is provided for transport of blood between a patient and a blood processing unit. The set comprises an arterial set component comprising arterial tubing having an arterial patient connector at one end and an arterial unit connector at the other. A venous set component has venous tubing with a venous patient connector at one end and a venous unit connector at the other end. The arterial and venous patient connectors, and the arterial and venous unit connectors, are respectively, substantially, and releasably directly connected to each other. As a result of this, the arterial, and venous set components cooperate to form a loop. Other features of improved sets are also disclosed.

Abstract: A pad of elastomeric material having a softness of no more than about durometer 50 Shore 00. The pad may carry adhesive and/or a housing for adhering the pad to a surface, either directly or indirectly through an envelope which surrounds the pad and carries the adhesive. Such a pad exhibits hemostatic and leak prevention properties against needle puncture holes in the skin or the wall of a hollow medical device. Particularly, hemostasis may be prevented with low pressure application of the pad to the skin. The pad may be previously applied to the skin of the patient or a wall of a medical device such as tubing or a solution bag, and the needle may then penetrate both the pad and the skin or medical device wall, to make a resealable puncture with leakage reduction and hemostasis when the needle is withdrawn.