Abstract: A load balancing arm for a medical device support system. The load balancing arm includes a proximal hub, an adjustable bearing element, a support arm, a spring and a link. A distal end of the support arm is configured to support a medical device load and a proximal end is pivotably mounted to a main bearing element for pivotable movement about a main pivot axis. The spring extends within a cavity of the support arm and is mounted to exert a biasing force between the main pivot axis and a distal end of the spring. The link has a proximal end pivotably mounted to the adjustable bearing element for pivotable movement about an adjustable pivot axis, and a distal end pivotably mounted to the distal end of the spring such that the biasing force exerted by the spring is transmitted through the link to the adjustable bearing element.

Abstract: A medical device suspension system includes a spindle extending along a longitudinal axis and a cable management cover surrounding the spindle. A gap is formed between the cable management cover and the spindle. A hub is rotatably mounted to the spindle and includes a housing. A top hub cover is disposed along the longitudinal axis between the hub and the cable management cover and defines an end of the gap, the top hub cover including a passage in fluid communication with an internal volume of the housing. The top hub cover is rotatable with respect to the spindle about the longitudinal axis. A cable is provided within the gap, the cable entering the gap at a fixed location about the longitudinal axis and passing into the housing through the passage. Rotation of the top hub cover about the longitudinal axis causes the passage to rotate about the longitudinal axis.

Abstract: A device and method for operating a lighting system varies a characteristic of visible light emitted by a first lighthead according to a predefined profile, and fixes a characteristic of visible light emitted by a second lighthead. A light sensor configured to view a focal area of the second lighthead detects a characteristic of visible light on a target surface over a period of time, and the characteristic of the light detected by the light sensor over the period of time is compared to the characteristic of light defined in the predetermined profile. A mode of operation of the first and second lighthead is determined based on the comparison.

Abstract: A liquid sporulation method is described. A liquid culture is prepared by adding bacterial cells to a sporulation broth. The liquid culture is incubated. Spores are harvested from the incubated liquid culture by separating the spores from a culture supernatant. In some embodiments, the harvested spores are suspended in an aqueous medium to form a spore suspension. At least a portion of the culture supernatant is combined with the spore suspension.

Abstract: A sterilization challenge device for verifying the efficacy of a gas sterilization process includes an outer container, an inner container, a chemical indicator, and a cap. The outer container includes an open end, a closed end, a chamber configured to contain the inner container containing the chemical indicator, and at least one hole arranged proximate the open end. The cap is configured to engage with the outer container to close the open end, and the at least one hole is configured to provide a flow path for the gaseous sterilant into the chamber.

Abstract: A light system monitors an area of interest for exposure to radiant energy provided by an operating room light head. At least one operating parameter of the light head is obtained, and based on the at least one operating parameter it is determined if the area of interest has been or will be exposed to radiant energy exceeding a prescribed threshold over a prescribed time period. Based on the determination, the system at least one of automatically adjusts an operating setting of the at least one light head or generates a warning of possible overexposure to radiant energy in the area of interest.

Abstract: Knuckle joint assembly for a medical device support system. The knuckle joint assembly includes a cartridge assembly that includes a cartridge housing and a rotary bearing. The cartridge housing includes a bore having a central axis and a bearing mount in the bore. The rotary bearing is press fitted in the bearing mount and configured to receive axially therethrough a spindle to rotatably support the spindle about the central axis. The knuckle joint assembly includes a retaining clip and a retaining pin. The retaining clip is selectively movable to disengage and engage a groove in a spindle to respectively support or release the spindle along a central axis. The retaining pin is movable between a first position to allow movement of the retaining clip between positions but prevent removal of the retaining clip, and a second position to block movement of the retaining clip from the engaged position.

Abstract: A method of sterilizing material includes receiving the material in a sterilizing chamber, vaporizing sterilant supplied to vaporizer from a sterilant source, exposing the material to the vaporized sterilant by conducting a sterilization cycle in the sterilizing chamber, heating ambient filtered air supplied to the vaporizer from an ambient filtered air source, and removing residuals of the vaporized sterilant absorbed or adsorbed by the material during the sterilization cycle by conducting an aeration cycle in the sterilizing chamber. The removing of the residuals includes conducting a plurality of aeration pulses to provide the sterilizing chamber with an aeration atmosphere comprising the heated filtered air to vaporize the absorbed or adsorbed residuals, and conducting a plurality of aeration vacuum pulses to evacuate the aeration atmosphere and vaporized residuals from the sterilizing chamber.

Abstract: A sterilizable pouch includes at least one sheet, wherein outer peripheral edges of the at least one sheet are sealed together to define a pouch having an interior space for receiving an article therein. A first releasable seam spans between a first peripheral edge of the at least one sheet to a second, opposite, peripheral edge of the at least one sheet, the first releasable seam dividing the at least one sheet into a first sheet part and a second sheet part. A second releasable seam and a third releasable seam each substantially span from a third peripheral edge of the at least one sheet to a fourth, opposite, peripheral edge of the at least one sheet and along the first peripheral edge and the second peripheral edge, respectively.

Abstract: A system for identification of abnormalities related to illumination of a target and automatic compensation therefor includes a lighthead and a controller. The lighthead is configured to illuminate the target. The lighthead includes a plurality of lighting modules configured to emit light therefrom. Each of the lighting modules includes a distance sensor configured to measure a distance from the lighting module to a surface toward which the lighting module is pointed. The controller is configured to identify one or more abnormalities of the measured distances, determine a true distance from the lighthead to the target based on the measured distances, predict an amount of illumination based on the true distance that would be supplied to the target without the identified abnormalities, and compensate for the identified abnormalities by respectively adjusting an amount of light emitted from the lighting modules to illuminate the target according to the predicted amount of illumination.

Abstract: A light head for a medical device support system. The light head includes first and second zones of light sources, an optical system, and a control system. The first and second zones of light sources emit respective first and second beams of light that form an illumination pattern having a pattern size at a region of interest. The optical system adjusts a beam spread of the second beam of light to change the pattern size of the illumination pattern from a first pattern size to a second pattern size. The control system varies power to the first and second zones of light sources in response to adjustment of the beam spread of the second beam of light to maintain a substantially constant magnitude of illuminance at the region of interest as the pattern size is changed from the first pattern size to the second pattern size.

Abstract: A test instrument and a method for producing a test instrument used to evaluate a cleaning, disinfection and/or drying processes of internal flexible channels includes obtaining a medical instrument having a flexible probe section configured for insertion into a body, the flexible probe section including at least one internal flexible channel and at least one external device port, and attaching an access device between the at least one external device port and the at least one internal flexible channel to enable selective access into the internal flexible channel.

Abstract: A steam sterilizer having a door movable relative to an opening between a first open position and a second closed position. A plurality of spaced-apart roller assemblies are aligned along edges of the door to align the door relative to the opening as the door moves between the open and closed position. Each of the roller assemblies are comprised of a cylindrical roller having an outer annual recess extending along the periphery thereof. The recess is dimensioned to receive a lateral edge of the door. The roller is mounted on a shaft and is movable against a biasing force axially along the axis of the shaft.

Abstract: A light system monitors an area of interest for exposure to radiant energy provided by an operating room light head. At least one operating parameter of the light head is obtained, and based on the at least one operating parameter it is determined if the area of interest has been or will be exposed to radiant energy exceeding a prescribed threshold over a prescribed time period. Based on the determination, the system at least one of automatically adjusts an operating setting of the at least one light head or generates a warning of possible overexposure to radiant energy in the area of interest.

Abstract: A steam sterilizer having a door movable relative to an opening between a first open position and a second closed position. A plurality of spaced-apart roller assemblies are aligned along edges of the door to align the door relative to the opening as the door moves between the open and closed position. Each of the roller assemblies are comprised of a cylindrical roller having an outer annual recess extending along the periphery thereof. The recess is dimensioned to receive a lateral edge of the door. The roller is mounted on a shaft and is movable against a biasing force axially along the axis of the shaft.

Abstract: A method and apparatus for improving the optical properties of an LED using a retroreflector element. A light emitting apparatus includes a substrate, at least one light emitting device attached to the substrate and including an outer primary light emitting surface through which substantially all light is emitted, and a retroreflector assembly attached to the substrate. The retroreflector assembly includes a proximal surface adjacent to the substrate, a distal surface spaced away from the substrate, and a retroreflective portion arranged between proximal surface and the distal surface. A distance from the distal surface to the substrate is less than or equal to a distance from the outer primary light emitting surface to the substrate.

Abstract: A device and method for testing for the presence of liquid in a cannula of a medical instrument is described. The device includes a flexible guide member having a first end, a second end and a length extending from the first end to the second end, an elongated member arranged within the flexible guide member, and an absorbent material attached to one of the elongated member. The flexible guide member is inserted into the cannula, the flexible guide member is manipulated to cause the absorbent material to move through the cannula. The absorbent material is analyzed for the presence of liquid.

Abstract: A biological sterilization indicator for evaluating the effectiveness of a sterilization process includes a cap containing a culture medium, a container containing a concentration of microorganism, and a breakable barrier attached to the cap to encapsulate the culture medium therein. The breakable barrier is formed from a multilayer structure including an aluminum layer and a sealing layer. The biological indicator is configured such that the breakable barrier may be broken at a selected time by engaging the cap and the container at an activated position to introduce the culture medium into the container.

Abstract: A support arm for supporting a surgical device in an operating room. The support arm is comprised of an elongated, tubular extrusion having an inverted, generally tear-drop shaped outer surface that has an airfoil shape. The airfoil shape is symmetrical about an axis extending from a leading end of the airfoil to a trailing end of the airfoil shape.