Abstract: An interface apparatus provides a sterile barrier between a sterile field and non-sterile portions of an associated surgical lighthead. The interface apparatus is a sterile disposable cover including a lower grippable portion, an intermediate cone-shaped portion, and an upper window area. The lower grippable portion is adapted to connect onto the handle portion of an associated surgical lighthead. An intermediate cone-shaped portion connects the lower grippable portion with an upper window area. The upper window area overlays control input means of the associated surgical lighthead such as, for example, light intensity controls. At least a portion of the upper window area is transparent to enable visualization of the control inputs beneath the sterile disposable cover. The interface apparatus is of a unitary or composite construction.

Abstract: A medical accessory clamping system includes a table and an accessory clamp. The table has an upper surface and a lower surface, a first ridge positioned on the upper surface and a second ridge positioned on the lower surface of the table. The accessory clamp has a first clamping member and a second clamping member coupled to but separate from the first clamping member wherein the clamping members define a cavity for receiving a portion of the table. The first and second clamping members have recesses for receiving said first and second ridges of the table, respectively. A uniquely styled clamp and a table are also disclosed.

Abstract: A decontamination device (10) includes a washing chamber (12) defined by a series of sidewalls. Upper and lower shelves (30, 32) are horizontally disposed within the washing chamber. The lower shelf is a rigid non-removable structure divided into three washing sections (42, 44, 46). The upper shelf is disposed vertically above the lower shelf and is slidably mounted within the washing chamber. The upper shelf comprises first, second, and third washing sections (82a, 82b, 82c) and a channel (78) operatively connected to the three shelf sections. The channel provides cleaning solutions to the shelf sections. Each of the washing sections and the shelf sections receive a spindle header (50) having a series of spindles (58) over which glassware is placed. A sealing connector, disposed on each washing section and shelf section, registers with and seals around a manifold of the spindle header and provides cleaning solutions from the channel to the spindle header.

Abstract: An induction coil (36) generates a magnetic field which induces current in an induction vessel (28). The induction vessel is heated by the current and supplies the heat to a passage (34) within the vessel. A liquid to be vaporized, such as water or hydrogen peroxide solution, is supplied to the passage where it is converted to vapor. The vapor is supplied to a defined area, such as a chamber (14) of a steam or vapor hydrogen peroxide sterilizer (10), where items are microbially decontaminated by the vapor.

Abstract: A sterile water generator (B) generates a stream of sterile water on demand. A water heater (130) heats incoming, unsterile water to a sufficient temperature to achieve sterilization of the water. The sterile water is then passed through a heat exchanger (110) which transfers excess heat from the sterile water to the incoming water. This reduces the energy consumption of the water heater and reduces the temperature of the sterile water ready for use. The sterile water is delivered to a site (A), at which the water is to be used, through a sterile water delivery pathway (C) to avoid recontamination of the water. A first portion (162) of the pathway is pre-sterilized by flowing steam or hot water, generated by the water heater, along the pathway (C). A second portion (212) of the pathway is sterilized with a liquid antimicrobial from the site. The first and second portions of the pathway have at least one common leg (164).

Abstract: A lighting system (10) suited to use in an operating theater includes one or more lightheads, each having a housing (28) and a bezel (50) extending therefrom. A light source (38) is disposed within the housing. A handle (36) extends below the bezel and is rotatable relative thereto. A lighting control input means (60), associated with the bezel allows adjustment of the intensity of light emitted by the light source. A sterile cover (54) can be placed over both the handle and the bevel, allowing the input means to be manipulated by pressure on the cover with the thumb of the operator's hand, while simultaneously grasping the handle in the palm and fingers.

Abstract: A radiolucent surgical table is provided with a patient support member and includes a low shadow accessory interface profile formed by a plurality of interconnected curved surfaces disposed along the outer edge of the patient support member for selective attachment of a range of medical accessory devices. A clamping apparatus secures associated accessories to the outer edge, which has a top recess and an essentially planar and non-vertical side surface slanting inwardly from top to bottom and terminating in a flared lower edge extending beyond the bottom of the patient support member. The clamping apparatus includes an upper jaw member which has a downwardly projecting lip formed to conformably engage a section of the top recess. A lower jaw member is also included and has a hook region formed to surroundingly engage a section of the flared lower edge. A means is provided for joining the upper and lower jaw members.

Abstract: A cleaning composition includes a detectable substance which is relatively stable in the cleaning composition, for indicating whether the cleaning composition has been thoroughly removed from a vessel following a cleaning process. For pharmaceutical applications, the detectable substance is preferably a low-foaming surfactant that is detectable by high performance liquid chromatography at concentrations of around 10 ppm, or less. The surfactant is thus detectable in the same analytical procedure as are traces of pharmaceutical residues which have not been removed from the vessel. The analytical procedure is used to develop a cleaning protocol for future cleaning processes by determining the number of rinses needed for reducing the surfactant, and hence the cleaning product, and also the pharmaceutical residues, in the rinse water to predetermined acceptable levels.

Abstract: A cartridge holder (30) for an automated endoscope reprocessor (10) is mounted on a movable rack (14). As the rack is wheeled into the chamber, a connector (164) on the cartridge holder (164) automatically makes a fluid connection with a connection port (158) within the chamber. The cartridge holder includes a base (42) and a lid (44), which is pivotally connected to the base by a hinge (110). A cartridge (40) holding a dose of a disinfectant concentrate or reagents is positioned in a well (50) defined by the base and the lid closed. Water flows through the cartridge holder via a fluid passageway (A) defined in part by the lid and in part by the hinge. The water mixes with the concentrate or reagents and the resulting disinfectant solution passes out of a lower end (205) of the cartridge into the well. The solution flows upwardly, around the cartridge, through an annular space (232) between the cartridge and the well, disinfecting the well in the process.

Abstract: A rotary accelerator (10) accelerates electrons and discharges them through each of a plurality of discharge ports, electrons discharge from each port having a different energy. The electron beams are channeled to scan horns disposed to irradiate products (14) traveling on conveyers (12). More specifically, some of the scan horns are positioned in pairs with an upper scan horn (18) on one side of the product, and a lower scan horn (20) on an opposite side of the product. A beam splitter splits the electron beam alternately between the two scan horns. Alternately, two scan horns (18, 20) are both disposed on the same side of the product. As yet another alternative, a scan horn (60) is disposed horizontally to irradiate the product from the side. Optionally, one or more of the scan horns includes a x-ray target (26) for converting the electrons into x-rays.

Abstract: A powder of Anthrax spores or other microbial contamination in a series of conveyed envelopes or banknotes (2) are deactivated by pulses of energy. Preferably, the deactivation occurs in the normal processing and sorting of mail or paper currency. The pulsed energy is in the form of low kinetic energy (under 500 keV) e− beams (12) or x-rays which are pulsed in coordination with the movement of mail in the mail handling equipment or the movement of banknotes into or out of an automatic teller machine. The treatment of either mail or currency is done under nearly adiabatic conditions.

Abstract: An accelerator (10) generates an electron beam (22) of selected energy that is swept (16) up and down. A conveyor (32) moves items (30) through the electron beam for irradiation treatment. An array (40a) of inductive electron beam strength detectors is disposed on a down stream side of the item to detect the energy of the electron beam exiting the item at the plurality of altitudes. The electron beam strength entering and leaving the item are communicated to a processor (54) which determines the absorbed dose of radiation absorbed by the item. The dose information is archived (56) or compared by a parameter adjustment processor (58) with target doses and deviations are used to control one or more of MeV or beam current of the electron beam, the sweep rate, and the conveying speed of the items. Each of the detectors includes a vacuum chamber in which two current transformers (60, 62) disposed on either side of a metal foil layer (64).

Abstract: A hydrogen peroxide vapor generation unit (10) receives hydrogen peroxide and water solution at an interface (20) and interconnects with an air dryer (14) by way of nipples (72, 92). In one embodiment, the dryer includes a clamping assembly (42) which is latched (74, 94) with the nipples and which receives a disposable desiccant cartridge (40). In an alternate embodiment, a reusable desiccant cartridge (40′) is connected directly to the nipples (72, 92). When the desiccant cartridge (40′) is saturated, it is removed and placed in a regenerator unit (120). A regenerated cartridge is installed in its place.

Abstract: A portable, radiation-producing apparatus is provided that can produce highly energetic electron beam radiation and X-rays from a low voltage power source., e.g., a battery. The radiation-producing apparatus is comprised of a radiation generating device, a pulsed high voltage generator and a control system. The pulsed high voltage generator is comprised of a power source and a Tesla resonant transformer. The Tesla resonant transformer has at least one first capacitor, a primary coil, a secondary coil and at least one second capacitor. The at least one second capacitor is disposed axially within the secondary coil. The pulsed high voltage generator is connected to the radiation generating device for providing electrical energy to the radiation generating device. The control system is connected to the pulsed high voltage generator for selectively controlling the transfer of energy from the pulsed high voltage generator to the radiation generating device.

Abstract: An interface apparatus provides a sterile barrier between a sterile field and non-sterile portions of an associated surgical lighthead. The interface apparatus is a sterile disposable cover including a lower grippable portion, an intermediate cone-shaped portion, and an upper window area. The lower grippable portion is adapted to connect onto the handle portion of an associated surgical lighthead. An intermediate cone-shaped portion connects the lower grippable portion with an upper window area. The upper window area overlays control input means of the associated surgical lighthead such as, for example, light intensity controls. At least a portion of the upper window area is transparent to enable visualization of the control inputs beneath the sterile disposable cover. The interface apparatus is of a unitary or composite construction.

Abstract: A lighting system (10) suited to use in an operating theater includes one or more lightheads (14, 16), and an ambient lighting system (28) comprising one or more light emitting components (60). The light emitting components are mounted within a canopy assembly (49) of the lighthead and arranged around a central support hub (33) to provide even illumination throughout the room. The canopy assembly includes a canopy and a canopy extension (70, 70′), which is removably mounted to the canopy, allowing the ambient lighting system to be retrofitted to an existing lighting system.

Abstract: A joint (52) for connecting arm portions (40, 42) of a ceiling or wall mounted support system includes housing members (60,62) with an annular bearing (64) interposed between opposed surfaces (82,84) thereof. The housing members are clamped together on an axle (98) such that a braking force generated between the bearing and the housing member surfaces opposes rotation of one arm portion relative to the other. A variable braking force is generated between the bearing and surfaces (206) of the housing members which are generally perpendicular to the opposed surfaces (82,84). The variable braking force is generated by a spring (182) and is greatest when the arm supporting a piece of equipment (24, 26, 28, 56) is at its lowest point, relative to the horizontal. This overcomes the increased forces in the spring which otherwise tend to cause the arm portion (42) to drift upward.

Abstract: A suspension system is disclosed for suspending lightheads, monitors, cameras, or other medical apparatus from an overhead structure at a selectable height. A drop tube has a selected portion thereof surroundingly encompassed by a receiving element that has a variable inside diameter substantially conforming to a frustum of a cone. A mounting plate rigidly connects with the overhead structure and with the receiving element. The mounting plate has an opening through which an end of the drop tube passes. A wedge-shaped element has a variable outer diameter substantially conforming to a frustum of a cone. The wedge-shaped element compressively inserts into the receiving element and surroundingly encompasses the selected portion of the drop tube to effectuate a compressive clamping of the selected portion of the drop tube inside the receiving element.