Abstract: To reduce the noise level of air convective warmer, the air filter of the warmer is fitted with an air intercept mechanism to disrupt the flow of air that traverses inside the interior cavity of the air filter. By thus disrupting the air flow, the noise that otherwise would have been generated due to a non-interrupted air stream flow is lowered. The air intercept mechanism may be in the form of at least one partition positioned inside the interior cavity of the air filter. Alternatively, double-ended open tubes may be used, so long as the interior cavity of the filter is sealed, with only the tubes providing the passages for air to output from the air filter. Yet a third embodiment of the air reduction filter has an air impermeable material covering at least one portion of the surface area of the filtering material to prevent the inflow air from directly entering into the interior cavity of the air filter through the covered surface area.

Abstract: Methods and apparatus are provided for electrically isolating an ambulatory medical device for infusing treatment materials into a patient when the medical device is connected to a peripheral device via an active communication cable. In one embodiment, the ambulatory medical device includes first circuitry controlling infusion of a medicament to the patient by a fluid conduit connectable to the patient and second circuitry controlling communications when an active communication cable is connected to the medical device. The first and second circuitry are electrically isolated using a pair of first and second isolation transceivers, where the first pair of isolation transceivers communicate a control signal and the second pair of isolation transceivers are giant magneto-resistive (GMR) transceivers that communicate at least one data signal.

Abstract: A pump for delivering insulin to a user. The pump comprises a pump mechanism and a meal-bolus program module. The meal-bolus program module is programmed to control the pump mechanism to deliver a meal bolus. An alarm program module is in data communication with the alarm, the timer, and the meal-bolus program module. The alarm module is programmed to generate an alarm signal when the meal-bolus program module does not control the pump mechanism to deliver a meal bolus within a predetermined period of time.

Abstract: Various software features useable in a medical infusion pump are disclosed. In certain aspects, localized alarm and message handling systems are disclosed. In other aspects, variable intensity alarms are disclosed. In further aspects, cost tracking systems and methods for medical infusion pumps are disclosed. In still further aspects, methods and systems implementing a variable delay of pressure decay in a medical infusion pump are disclosed. In other aspects, methods and systems implementing a timed intermittent bolus by pressure are disclosed.

Abstract: An apparatus for maintaining a library of program data for medical pumps, the apparatus comprising: memory loaded with a database, the database including a plurality of program data records and a plurality of data key records, each program data record containing a set of program data items, at least some of the program data items included in the database for controlling operation of a medical pump, each data key record containing a data key and each data key identifying one of the data program records; a database management system programmed to link a data key to a set of program data; and a scanner in data communication with the database management system, the database management system being further programmed to receive a code scanned by the scanner, save the code in a data key record, and link the code to a set of program data, the code being a data key.

Abstract: A one piece molded vacuum tube holder is fitted with a one piece molded needle hub assembly. A needle protection device is further rotatably mounted to the neck of the one piece vacuum tube holder. One portion of a locking mechanism is provided at the neck of the one piece vacuum tube holder and a second portion of the locking mechanism is provided at the needle hub of the needle hub assembly, so that when the needle hub assembly is press fit to the vacuum tube holder, the two portions of the locking mechanism will coact to fixedly retain the needle hub assembly within the vacuum tube holder. The one piece vacuum tube holder is configured to have an elongate needle cover integrally extending from its neck. A finger grasp mechanism may be coupled to the needle cover.

Abstract: An apparatus and method for detecting an occlusion in a downstream fluid line of a medical pump in relation to increased pressure in the downstream fluid line between the beginning and the end of each interval of a series of intervals of operation of the pump even if one or more intervals between the first and last intervals does not reflect such an increase in pressure in the downstream fluid line.

Abstract: The present invention safety device is a one-piece needle assembly that has a base and a housing pivotally connected to the base. The base has a distal portion to which a needle is fitted. At the base there is formed longitudinally along its distal portion a catch mechanism that may be in the form of an anchor projection. At the back wall of the housing there is extended another catch mechanism that may be configured in the form of two clasping fingers. Also providing in the housing is an integral hook. As the housing and the base are pivoted relative to each other, and as the needle makes contact with the hook, the respective catch mechanisms at the base and the housing also make contact with each other, resulting in the coupling of the catch mechanisms and the coupling of the needle to the hook. As a result, the catch mechanisms are interlocked and the needle is fixedly retained by the hook within the housing.

Abstract: A catheter assembly includes a catheter hub defining an interior cavity and a catheter tube extending distally thereof. A rigid actuator extends proximally in the interior cavity and supports a seal member thereon. The seal member includes a central membrane, a distal portion, and a proximal portion. An hourglass shaped actuator cavity is formed in the distal portion and receives a barbed end of the actuator. The outer surface of the seal member is in partial circumferential engagement with the catheter hub to define an air path that allows fluid communication between areas of the interior cavity distal and proximal of the seal member. A punch tool is provided to form a tri-slit in the membrane of the seal member. The seal member may be configured for multi-use and include a biasing member that moves the seal member to force the membrane back over the actuator to close the membrane.

Abstract: A catheter assembly includes a catheter hub defining an interior cavity and a catheter tube extending distally thereof. A rigid actuator extends proximally in the interior cavity and supports a seal member thereon. The seal member includes a central membrane, a distal portion, and a proximal portion. An hourglass shaped actuator cavity is formed in the distal portion and receives a barbed end of the actuator. The outer surface of the seal member is in partial circumferential engagement with the catheter hub to define an air path that allows fluid communication between areas of the interior cavity distal and proximal of the seal member. A punch tool is provided to form a tri-slit in the membrane of the seal member.

Abstract: A safety catheter device includes a catheter hub, a housing removably coupled to the catheter hub; a needle, and a member, the housing including a radially outwardly directed projection operable to engage the interior aspect of the catheter hub and radially moveable inwardly sufficiently to disengage therefrom, the projection being held against moving radially inwardly sufficiently to disengage when the needle is in a first position with the needle distal tip exposed and being free to move radially inwardly sufficiently to disengage coincident with the needle being moved into a second position with the needle distal tip disposed in the housing.

Abstract: A needle assembly has a needle hub that has a body to which are formed two plates at opposite sides thereof in a parallel relationship. The plates have respective upper edges and lower edges that lie substantially along respective planes, so that the needle hub may be stably placed onto a surface by means of the respective edges. A partition is formed orthogonally proximate to the front ends of the parallel plates. The partition and the parallel plates together provide upper and lower three point stable supports for the needle hub. A notch at the partition provides a guided line of sight to the tip of the needle for the user. The connector at the proximal portion of the needle hub has a non-conventional configuration that allows it to mate only with a counterpart special connector of a fluid conveying device that has a complementary non-conventional configuration.

Abstract: The present invention safety device is a one-piece needle assembly that has a base and a housing pivotally connected to the base. The base has a distal portion to which a needle is fitted. At the base there is formed longitudinally along its distal portion a catch mechanism that may be in the form of an anchor projection. At the back wall of the housing there is extended another catch mechanism that may be configured in the form of two clasping fingers. Also providing in the housing is an integral hook. As the housing and the base are pivoted relative to each other, and as the needle makes contact with the hook, the respective catch mechanisms at the base and the housing also make contact with each other, resulting in the coupling of the catch mechanisms and the coupling of the needle to the hook. As a result, the catch mechanisms are interlocked and the needle is fixedly retained by the hook within the housing.

Abstract: A one piece molded vacuum tube holder is fitted with a one piece molded needle hub assembly. One portion of a locking mechanism is provided at the neck of the one piece vacuum tube holder and a second portion of the locking mechanism is provided at the needle hub of the needle hub assembly. The needle hub assembly is press fit to the vacuum tube holder. The one piece vacuum tube holder is configured to have an elongate needle cover integrally extending from its neck. A tamper evident notched joint is provided at the junction where the needle cover is connected to the neck. The opening of the vacuum tube holder through which a conventional vacuum tube is inserted may be sealed for sterilization and transport of the device. A wingnut finger grasp mechanism may be coupled to the needle cover.

Abstract: A medical device has a base having an internally tapered wall mounted to a neck of a tube holder that has a reverse taper, so that rotation of the base relative to the neck may be effected with a controlled drag to provide a smooth and secure relative rotation. The base may be rotated relative to the holder by rotationally moving a needle protection housing hingedly attached to the base. The housing may be rotated to any orientation relative to the tube holder so long as a torsional force greater than the predetermined friction between the tapered surfaces is applied thereto. The base is designed to have a ring at its base that biases against the base of the neck in a self-adjustable manner. Other devices may also be fitted with reverse tapered complementary connection fittings to securely couple to each other.

Abstract: A heat exchanger has a multi-lumen tubing having one end connected to a supply fitting and another end connected to a return fitting. The tubing has a central lumen, a middle lumen that surrounds the central lumen and an outer lumen that surrounds the middle lumen. When infusate traverses along the heat exchanger, it is heated by the heating fluid that flows along the central lumen, and also by the rerouted heating fluid that flows along the outer lumen of the tubing. The heat exchanger is fluidly coupled to a heater by its inlet and outlet so that the temperature of the heating fluid for warming the infusate is maintained at a predetermined temperature.

Abstract: An implantable portal includes a septum that has embedded therein an indicia adapted to identify at least one characteristic of the portal. The indicia may be formed as an impression at a base layer of the septum, and is filled with a radiopaque material. The septum base layer is covered by liquid silicone, which bonds with the septum base layer when solidified, so that an integral one-piece septum, with the identifier indicia embedded therein, is effected. The indicia embedded septum is fitted to the reservoir housing of the portal for providing identification information for that portal. The septum embedded indicia is viewable visually and also by x-ray or computer tomography imaging.

Abstract: A convective underbody blanket has a head portion and a body portion. Provided at the head portion is a non-inflatable head area surrounded by a channel that has arranged thereat at least one row of air apertures that are oriented toward the non-inflatable head area when the channel is inflated. At the body portion there is provided a non-inflatable body area. Along each longitudinal side of the body area there is at least one longitudinal channel. Each of the longitudinal channels is in fluid communication with the channel that surrounds the non-inflatable head area. The longitudinal channels that sandwich the non-inflatable body area extend substantially along the length of the non-inflatable body area and are in fluid communication with each other by way of a cross channel formed at the foot end of the blanket.

Abstract: A safety needle assembly has a collar or ring that is rotatably mounted to a needle hub. The needle assembly may be connected to a syringe by the user grasping the needle hub in first and second embodiments, or turning of the needle sheath in other embodiments. The collar of the needle assembly may be rotated by turning the needle sheath. The needle hub may also interact with the collar by rotating the needle sheath. Mechanisms are provided at both the collar and the housing so that once the contaminated needle is covered, the needle assembly may be removed from the syringe for disposal by rotating the needle housing.