Abstract: A ventilation system is provided, the ventilation system comprising at least one air flow generating device, the at least one air flow generating device having a calibrated speed to produce a downward air flow capable of forcing a cloud of infectious bacterial, viral or pathogen particles or droplets out of an ingestion zone of a mouth, a nose and eyes of an individual, at least one ultraviolet C light lamp positioned proximate at least one wall of an area in a pathway of an infected air flow, the infected air flow containing the cloud of infectious bacterial, viral or pathogen particles or droplets, an ultraviolet C radiation field created by the at least one ultraviolet C light lamp, the ultraviolet C radiation field extending throughout the area from the at least one wall near a ceiling of the area and the infected air flow containing the cloud of infectious bacterial, viral or pathogen particles or droplets passing through the ultraviolet C radiation field, wherein the at least one air flow generating dev

Abstract: There is provided an infusion pump system for delivering a predetermined medical solution at a preset reference infusion speed. The system comprises a medical solution container; an infusion line through which the medical solution is drawn out of the medical solution container; an infusion pump configured to discharge the medical solution via the infusion line. The infusion pump is controlled so that the discharge speed of the infusion pump is computed on the basis of a current discharge speed of the infusion pump and the infusion speed of the medical solution, the resulting discharge speed is corrected by a predefined correction coefficient, and the medical solution is discharged at the corrected discharge speed.

Abstract: There is provided an infusion pump system for delivering a predetermined medical solution at a preset reference infusion speed. The system comprises a medical solution container; an infusion line through which the medical solution is drawn out of the medical solution container; an infusion pump configured to discharge the medical solution via the infusion line. The infusion pump is controlled so that the discharge speed of the infusion pump is computed on the basis of a current discharge speed of the infusion pump and the infusion speed of the medical solution, the resulting discharge speed is corrected by a predefined correction coefficient, and the medical solution is discharged at the corrected discharge speed.

Abstract: Methods and apparatus for managing safety information are disclosed. In an embodiment, a computing device, or any other suitable device or system, receives employee identification information and associated job site location information (e.g., employee ID and job site location ID). The computing device then receives job site evaluation information including a selection from a user of a job site safety attribute that is associated with the job site (e.g., flammable materials present). The computing device also receives safety inspection information associated with the job site safety attribute (e.g., fire extinguishers in place). The computing device displays job site safety briefing information associated with the employee identification information and the job site safety attribute (e.g., employee warned about fire hazard). The computing device receives incident information associated with the employee identification information and the job site safety attribute (e.g., employee burned).

Abstract: Infusion pumps according to the present invention maximize fluid throughput while minimizing vaporization of gas by employing specific flow path architecture, flow path dimensional ranges, and voltage and frequency ranges for activation of piezoelectric bodies.

Abstract: Infusion pumps according to the present invention maximize fluid throughput while minimizing vaporization of gas by employing specific flow path architecture, flow path dimensional ranges, and voltage and frequency ranges for activation of piezoelectric bodies.

Abstract: The combination of an optical sight and an attachable/detachable adjustable range sighting device accessory, in which the optical sight comprises a support and an array of fixedly positioned fiber optics sighting devices carried by the support; and the accessory comprising a displaceable fiber optics sighting device and a mechanism for shifting the position of the displaceable fiber optics device relative to the array of fixedly positioned sighting devices.

Abstract: The present invention relates to an electrochemical sensor for the detection of biological molecules and a process for the production thereof. In the sensor, an electrode system comprising at least one working electrode (1), one counter electrode (3) and a reference electrode (4) operate inside of a reaction camber (18). The reaction chamber (18) is intended to contain a system of reagents in solution, comprising at: least one electrochemical mediator Said working electrode is made of series of nanoelectrodes (11, 12) of a noble metal, inserted in an isolating layer (10) consisting of a resin suitable for lithography and nano-lithography, functionalised or functionalisable for the binding to biological molecules to be detected. The invention further refers to a kit comprising said sensor and a process for the production thereof.

Abstract: A menu driven reprogrammable drug pump is provided with a memory, such as flash memory, a display, a keyboard, and a communications port to allow a generic pump to be programmed with a desired pump application (therapy) program and patient specific settings. Programming and data transfer with another pump or a computer to and from the patient pump is by the communications port that allows local and/or remote communications with the pump. Flash memory stores the pump application program during use. Patient safety is provided by a cassette identification system, an occlusion detection system, and a latch/lock detection system. Automated testing of the pump is by a closed loop testing system.

Abstract: A menu driven reprogrammable drug pump is provided with a memory, such as flash memory, a display, a keyboard, and a communications port to allow a generic pump to be programmed with a desired pump application (therapy) program and patient specific settings. Programming and data transfer with another pump or a computer to and from the patient pump is by the communications port that allows local and/or remote communications with the pump. Flash memory stores the pump application program during use. Patient safety is provided by a cassette identification system, an occlusion detection system, and a latch/lock detection system. Automated testing of the pump is by a closed loop testing system.

Abstract: A menu driven reprogrammable drug pump is provided with a memory, such as flash memory, a display, a keyboard, and a communications port to allow a generic pump to be programmed with a desired pump application (therapy) program and patient specific settings. Programming and data transfer with another pump or a computer to and from the patient pump is by the communications port that allows local and/or remote communications with the pump. Flash memory stores the pump application program during use. Patient safety is provided by a cassette identification system, an occlusion detection system, and a latch/lock detection system. Automated testing of the pump is by a closed loop testing system.

Abstract: A cassette is described including a housing, an inner reservoir located within the housing, a valve coupled to the inner reservoir and coupled to the housing, and a delivery conduit coupled to the inner reservoir and emerging from the delivery opening of the cassette. The cassette also includes a dispensing apparatus that defines a passage and has a first activating device that opens the valve of the cassette. The dispensing apparatus also has a second activating member capable of establishing fluid communication with a medicant container. A method of mixing a powdered drug and a liquid includes establishing fluid communication between the reservoir and the medicant container, dispensing at least a portion of the liquid into the medicant container, and transferring the mixed drug into the reservoir.

Abstract: A bag arrangement for containing fluid for use with an infusion pump. The bag arrangement includes a first end and a second end, and includes a panel defining a interior chamber. The arrangement further includes a fluid outlet port in the panel, the outlet port in fluid communication with the interior chamber. An elongated hollow member is in fluid communication with the port, and extends from the first end toward the second end of the bag arrangement tangentially along the panel.

Abstract: A menu driven reprogrammable drug pump is provided with a memory, such as flash memory, a display, a keyboard, and a communications port to allow a generic pump to be programmed with a desired pump application (therapy) program and patient specific settings. Programming and data transfer with another pump or a computer to and from the patient pump is by the communications port that allows local and/or remote communications with the pump. Flash memory stores the pump application program during use.

Abstract: A hydrophobic electrostatic breathing filter is fabricated by applying a thin layer of adhesive to the pinch ring of a patient side filter housing portion. A hydrophobic membrane is positioned over the adhesively coated pinch ring to effect a hermetic seal between the pinch ring and membrane using the adhesive interface. Electrostatic filter media and scrim are positioned adjacent the pinch ring of a machine side filter housing portion, and the patient and machine side portions of the housing are then welded together to hold the electrostatic filter media/scrim in place adjacent the hermetically sealed hydrophobic membrane by a mechanical clamping force exerted by the pinch rings. The resultant filter includes a hydrophobic membrane which is hermetically sealed across the patient side of the filter housing, and an electrostatic filter media/scrim element which is independent of the hydrophobic membrane and which is mechanically held in place adjacent the hydrophobic membrane.

Abstract: A cassette is described including a housing, an inner reservoir located within the housing, a valve coupled to the inner reservoir and coupled to the housing, and a delivery conduit coupled to the inner reservoir and emerging from the delivery opening of the cassette. The cassette also includes a dispensing apparatus that defines a passage and has a first activating device that opens the valve of the cassette. The dispensing apparatus also has a second activating member capable of establishing fluid communication with a medicant container. A method of mixing a powdered drug and a liquid includes establishing fluid communication between the reservoir and the medicant container, dispensing at least a portion of the liquid into the medicant container, and transferring the mixed drug into the reservoir.

Abstract: The present invention concerns a pump provided with a control module and an attachable fluid reservoir cassette. The control module includes a pumping mechanism for pumping fluid from the fluid reservoir to the patient. The cassette is provided with appropriate indicia to identify differences between a plurality of cassettes. The control module further includes cassette indicia identification structure for identifying indicia on the cassette. One type of cassette identification system includes a projection extending from the cassette and structure associated with the control module which engages the projection. Another type of cassette identification system includes a light reflecting system which utilizes light from the control module and reflected off the cassette. Still other types of cassette identification systems utilize other non-contact switches or sensors to sense indicia on the cassette to identify the cassette from a plurality of cassettes.

Abstract: The present invention relates to a method and apparatus used to place a catheter having a distal end and a proximal end where the proximal end cannot be trimmed within a patient. The method and apparatus utilize a device operative in locating the tip of a catheter, which includes a detector assembly having a detector and a locator. The detector of the detector assembly is locked into positioned remote from the distal end of the catheter prior to inserting the catheter in the patient. The distal end of the catheter is trimmed, as to define a trimmed distal end, the detector is then unlocked and placed proximate the trimmed end. In the preferred embodiment the detector is locked into place proximate the trimmed distal end and the catheter is placed within the patient.

Abstract: A sensing device for a pump control module is described that is designed for use with a cassette having a pump surface with a projection. The sensing device is positioned on an interface surface of a pump control module, and includes an occlusion sensor and a cassette identification sensor. A pump control module, a cassette and a method of use are also described for administering a drug to a patient through a delivery conduit, utilizing the sensing device.