Abstract: An intravenous catheter introducer assembly having a safety feature to prevent accidental needle sticks. The introducer assembly includes a needle assembly having a groove disposed on its outer surface. The introducer includes a protector made of a hollow member having an open distal end and an inwardly disposed resilient flange or a clip disposed thereon. The protector is coaxially slidably disposed around the needle with the flange abutting the outer surface of the needle and adapted to engage the groove when a catheter assembly is removed from the needle.

Abstract: A valve (10) comprises a housing (12) with a valve element (14) which normally fluidicly couples a low pressure operating device, such as a transducer (30) and tubing (34) to be coupled to a patient (36) along a first flow path (42) including a flexible control wall (58) which normally interrupts a second flow path (72) between a high pressure generating source such as an injector syringe (32) and the tubing (34), but which flexes, in response to high pressure excursions from the syringe (32) to allow the second flow path (72) to open as it flexes into the first flow path (42) to thereby restrict same thus providing protection to the transducer (30) during the high pressure excursion from the syringe (32).

Abstract: A needle tip protector (80) includes a needle gripping U-shaped clip (81).

Abstract: A disposable warmer cartridge is used to heat fluids to be infused to the patient to prevent hypothermia in the patient. The cartridge has in its chamber a pair of spaced in parallel electrodes that have substantially the same dimension. When RF power is fed to the electrodes, an alternating electric field is generated between the electrodes to directly heat the fluid that is in the chamber. The heating of the fluid is achieved in a substantially instantaneous manner by controlling the energization of the electrodes through the distributed impedance of the electric field between the electrodes. Heat is readily controlled by modulating the RF power fed to the electrodes. Feedback to control the temperature of the fluid in the cartridge may be provided by non-contact and direct contact sensor(s).

Abstract: A fixed needle syringe has a syringe barrel with its distal portion modified to accept a needle protective housing. In particular, the distal portion is formed with the a groove dimensioned to accept a collar that is attached to the housing. The inside surface of the collar is provided with a number of flanges that fit within the groove formed at the distal portion of the syringe barrel of the fixed needle syringe. Protrusions are provided at the inside surface of the collar to frictionally act against the syringe barrel, so that the needle protective housing does not freely rotate, but is rotatable relative to the syringe barrel by the application of a predetermined torque to either the collar or the housing attached thereto. An internal hook is provided in the housing to grasp the needle of the syringe, when the housing is pivoted to cover the needle extending from the needle hub of the syringe.

Abstract: A catheter and introducer needle assembly having a needle with a proximal and distal end attached to a needle hub and a bent area therebetween. The device further includes a tubular catheter having proximal and distal ends in which the introducer needle can be coaxially received within the catheter. The device has a hollow catheter hub having a distal end attached to the proximal end of the catheter and is in fluid communication therewith. The assembly includes a needle tip protector having a proximal end and a distal end disposed within the catheter hub. The distal end of the protector covers the needle tip when the needle is removed from the catheter. The protector has a proximal opening at its proximal end wherein the bent area is angled away from the proximal opening such that when the needle is removed from the catheter the protector remains attached to the needle.

Abstract: A bodily fluid space entry detection method includes entry of the distal, sharp tip of a needle cannula into a bodily fluid space such as a blood vessel or epidural space to allow bodily fluid such as blood or spinal fluid to establish electrical conduction along the cannula and energizing an alert source, LED, and/or a buzzer, in response.

Abstract: An inflatable convective thermal blanket is designed to have at least one section on its top surface that has securely mounted thereon at least one fluid absorbent mechanism for absorbing fluids from a subject that is placed onto the blanket, or from fluids fallen onto the blanket from other sources. The one section is configured onto the blanket in such a way that it forms a well for collecting the fluids. The fluid absorbent mechanism, which may be in the form of a pad, would absorb the collected fluid to thereby minimize evaporative and cooling effects on the subject. Instead of mounting it on top of the blanket, the fluid absorbent pad may be mounted to the underside of the blanket, with appropriate holes and/or openings provided at the fluid collecting section, so that the collected fluids are drained onto the fluid absorbent pad.

Abstract: An inflatable convective thermal blanket is designed to have at least one section on its top surface that has securely mounted thereon at least one fluid absorbent mechanism for absorbing fluids from a subject that is placed onto the blanket, or from fluids fallen onto the blanket from other sources. The one section is configured onto the blanket in such a way that it forms a well for collecting the fluids. The fluid absorbent mechanism, which may be in the form of a pad, would absorb the collected fluid to thereby minimize evaporative and cooling effects on the subject. Instead of mounting it on top of the blanket, the fluid absorbent pad may be mounted to the underside of the blanket, with appropriate holes and/or openings provided at the fluid collecting section, so that the collected fluids are drained onto the fluid absorbent pad.

Abstract: To enable a user to readily determine the gauge of the needle of a needle assembly that has a base and a needle protective housing pivotably attached thereto, the needle assembly is injection molded from a color coded molding material which color was preassigned to correspond to the gauge of the needle. As a result, both the base and the protective housing of the needle assembly are the same specific color, and reflect or provide an indication of the given gauge of the needle. The needle sheath that covers the needle prior to use may be made of a plastics material that may be clear, or have the same or a different color than that of the needle assembly.

Abstract: To enable a user to readily determine the gauge of the needle of a needle assembly that has a base and a needle protective housing pivotably attached thereto, the needle assembly is injection molded from a color coded molding material which color was preassigned to correspond to the gauge of the needle. As a result, both the base and the protective housing of the needle assembly have the same specific color, and reflect or provide an indication of the given gauge of the needle. The needle sheath that covers the needle prior to use may be made of a plastics material that may be clear, or have the same or a different color than that of the needle assembly. The gauge of the needle of a fixed needle syringe could also be ascertained by its color coded needle protective housing. Color coded markings that correspond to the gauge of the needle may also be printed onto the syringe barrel of the fixed needle syringe.

Abstract: To ensure that there is no misconnection between a needle, such as for example a spinal or epidural needle, and the appropriate medication, the needle hub the needle is formed, by molding or extrusion, to have a given configuration. An adapter is placed between the needle and a conventional fluid store, or medical line. The end of the adapter that connects to the needle assembly is formed to have a configuration that is complementary to that of the hub of the needle assembly, so that the adapter and the needle hub may be readily mated to each other. The other end of the adapter is formed to have another configuration, for example a conventional luer, that is readily connectable to a conventional fluid store, such as a syringe that has a conventional luer. The adapter is formed by inter-fitting two elements to effect an integral locking mechanism to prevent the uncoupling of the fluid store and the adapter, once they are securely coupled.

Abstract: A fixed needle syringe has a syringe barrel with its distal portion modified to accept a needle protective housing. In particular, the distal portion is formed with the a groove dimensioned to accept a collar that is attached to the housing. The inside surface of the collar is provided with a number of flanges that fit within the groove formed at the distal portion of the syringe barrel of the fixed needle syringe. Protrusions are provided at the inside surface of the collar to frictionally act against the syringe barrel, so that the needle protective housing does not freely rotate, but is rotatable relative to the syringe barrel by the application of a predetermined torque to either the collar or the housing attached thereto. An internal hook is provided in the housing to grasp the needle of the syringe, when the housing is pivoted to cover the needle extending from the needle hub of the syringe.

Abstract: A product inventory management system including a cabinet configured to contain an inventory of product units having RFID tags and further configured to monitor the inventory by wirelessly detecting the RFID tags, and a server system configured to communicate over a network with the cabinet, the server system capable of managing the inventory of the cabinet. There is also a method for product inventory management, including receiving, in a server system and via a network, inventory data from a cabinet, the inventory data corresponding to an inventory of product units stored in the cabinet, and generating an order to have additional product units added to the cabinet according to the cabinet inventory.

Abstract: A needle tip protector (10, 10?) including a pair of apertured members (28, 30 or 28?, 30?) with spring arms (22, 24) urging the apertured members (28, 30 or 28?, 30?) out of alignment to create a barrier to a needle tip (16). A needle gripping U-shaped clip (81) may also provide a needle tip protector (80).

Abstract: A product inventory management cabinet including a cabinet chassis configured to contain an inventory of product units having RFID tags, a reader configured to wirelessly detect the RFID tags, and a data processing system connected to communicate with the reader and to maintain a product inventory list and a consumed product list according to the detected RFID tags. There is also a method for product inventory management, including detecting a plurality of RFID tags in a cabinet, each RFID tag associated with a product unit and creating a current inventory list comprising identifiers corresponding to the detected plurality of RFID tags.

Abstract: A collar to which a needle protection housing is attached has a proximal end and a distal end. The proximal end of the collar has a number of internal protrusions that are fitted within the space defined by the two sets of flanges extending from the proximal portion of a needle hub. The distal end of the collar has a number of fingers or retainers that are used to grasp and removably couple a needle sheath. The needle sheath covers the needle that extends from the distal end of the needle hub before use. A needle protection housing is pivotally connected to the collar, and is pivoted to cover the needle after use. A channel or opening in the protective housing through which the needle passes is formed by a pair of progressively angled lips that extend longitudinally along the length of the housing.

Abstract: An improved nebulizer breathing system wherein a supplemental gas may be introduced into the nebulizer head at a position after the liquefied medication has been fractured or nebulized, so that the introduction of the supplemental gas does not effect the rate at which the nebulized liquefied medication is applied to the user, and the mixture of gases to be administered to a patient is added to the breathing system at a position removed from the point at which the gas mixture is administered to the patient.

Abstract: To retrofit a conventional needle hub assembly with a needle protection housing, a sleeve having a collar rotatably fitted thereabout is fitted to the needle hub. The sleeve has a proximal portion and a distal portion. The proximal portion has a diameter that is dimensioned to fit over the needle hub while the distal portion has a diameter that allows the needle cap of the needle hub assembly to be inserted thereinto so as to be frictionally coupled to the needle hub. There are a plurality of flanges or ears extending at the proximal end of the proximal portion. These flanges are configured to overlie the flanges formed at the base of the needle hub used to mate with the luer of a syringe. When the needle hub assembly is threadingly mated to the luer of the syringe, the sleeve, along with the collar mounted thereabout and to which the needle protection housing is attached, is also mated to the luer.