Abstract: A preferred embodiment of the present invention provides a method and system for high availability remote centralized data management. In a preferred embodiment, the system includes a primary remote centralized data storage storing medical data, and a redundant remote centralized data storage storing a redundant copy of the medical data. In a preferred embodiment, the system also includes a primary data server for storing the medical data in the primary remote centralized data storage. In a preferred embodiment, the primary data server also stores the medical data in the redundant remote centralized data storage. Preferably, the system also includes a redundant data server for storing the medical data in the redundant remote centralized data storage and also the primary remote centralized data storage. Additionally, in a preferred embodiment, the system includes an interface allowing access to the system.

Abstract: A patient's heart condition is monitored by a patient-location based unit. The patient-location based unit includes a receptacle for receiving a cartridge that includes heart condition monitoring information. The patient-location based unit receives information from the patient, monitors the patient's heart condition, and communicates with the patient regarding the patient's heart condition. The patient-location based unit also communicates with a central server. Both the patient-location based unit and central server communicate with a health care professional computer by transferring, to the health care professional computer, information related to the monitored patient's heart condition.

Abstract: A method and system suitable for automated surveillance of intensive care unit patients for information denoting likelihood of in-hospital survival or mortality, represented in the timeseries of scoring systems such as APACHE III. Techniques from digital signal processing and Lyapunov stability analysis are combined in a method that allows for optimization of statistical hypothesis testing that is robust against short time series of as few as five time points. Once optimized, the method and system can achieve high-sensitivity high-specificity classification of survivorship, while avoiding false-positive prediction of mortality.

Abstract: An ultrasonic probe for microscopic operations in accordance with the present invention consists mainly of an ultrasonic probe body, an elongated tubular member, and a bent handle member. The ultrasonic probe body has a transducer assembly attached to the distal end of a soft elongated tube that is extended from a connector to be coupled to an ultrasonic observation apparatus, and has a coupler mounted on the tube thereof. The transducer assembly and tube are passed through the elongated tubular member. The handle member is attached to the proximal end of the tubular member and includes a coupling mechanism for use in coupling the coupler to the handle member so that the coupler can be uncoupled freely.

Abstract: An embryo-transfer catheter has an extruded shaft with a gas-filled lumen that extends helically along the catheter to provide an ultrasound marker. The catheter has a side opening close to a closed rounded patient end. The catheter could be completely transparent to x-rays or the plastics from which it is formed could incorporate an x-ray opaque filler, such as barium sulphate.

Abstract: A system for diagnosing and monitoring respiratory insufficiency for automated remote patient care is presented. A database stores monitoring sets containing recorded measures relating to patient information recorded on a substantially continuous basis. A server retrieving and processing the monitoring sets includes a comparison module determining a patient status change by comparing at least one recorded measure from each of the monitoring sets to at least one other recorded measure with both recorded measures relating to a same type of patient information; and an analysis module testing each patient status change against an indicator threshold corresponding to the same type of patient information as the recorded measures which were compared, the indicator threshold corresponding to a quantifiable physiological measure of a pathophysiology indicative of respiratory insufficiency.

Abstract: A system for conducting multiple diagnostic hearing tests is disclosed. The system comprises a yoke wearable around the neck of a patient, for providing a housing for conduits and wiring to conduct the hearing tests. The yoke may also coupled to one or more ear probes for engaging the ear of the patient, and to at least one microphone for measuring ambient noise during at least a portion of a hearing test.

Abstract: A method and a system for automatic taking of specimen from a static or living test object, comprising the steps and functional elements of guiding a specimen collector (10) by means of a guiding device (20) to a specimen terminal (22) attached to the test object (1); extracting a fluid specimen from the test object (1) to the specimen collector (10); guiding the specimen collector (10) by means of the guiding device (20) to a specimen container (50); and delivering or outputting the specimen from the specimen collector (10) to the specimen container (50).

Abstract: An interstitial fluid (ISF) extraction device includes a penetration member configured for penetrating a target site of a user's skin layer and, subsequently, residing in the user's skin layer and extracting an ISF sample therefrom and at least three concentrically-arranged pressure rings, each adapted for applying pressure to the user's skin layer in the vicinity of the target site while the penetration member is residing in the user's skin layer. In addition, the ISF extraction device is configured such that (i) the pressure rings apply pressure in an oscillating manner with asymmetric deployment and retraction cycles and (ii) only one of the at least three concentrically-arranged pressure rings is deployed at a time, thereby mitigating an ISF glucose lag of the ISF sample extracted by the penetration member.

Abstract: A system for the destruction of adipose tissue utilizing high intensity focused ultrasound (HIFU) within a patient's body. The system comprises a controller for data storage and the operation and control of a plurality of elements. One elements is a means for mapping a human body to establish three dimensional coordinate position data for existing adipose tissue. The controller is able to identify the plurality of adipose tissue locations on said human body and establish a protocol for the destruction of the adipose tissue. A HIFU transducer assembly having one or more piezoelectric element(s) is used along with at least one sensor wherein the sensor provides feed back information to the controller for the safe operation of the piezoelectric element(s). The sensor is electronically coupled to the controller, and the controller provides essential treatment command information to one or more piezoelectric element(s) based on positioning information obtained from the three dimensional coordinate position data.

Abstract: An Improved Facial Rejuvenation Device and Method. The device is small and portable. The device further has an ergonomic nozzle shape defined by a housing having a suction bore defined by a throttle positioned within it. The throttle may perform its throttling action by adjusting the diameter of the suction bore formed within the housing. The method employs the unique device to create a localized suction force to the skin in the vicinity of a previously-applied medicinal formulation. The device further may have a housing defined by a conical outer shape terminating in a sealing ring at its tip.

Abstract: The present invention relates generally to compression devices and, more particularly to a method using air flow to close the exhaust valve in each sleeve, allows air to fill the sleeve to a pretuned pressure, and finally deflating the sleeve by letting the air flow through the outlet valve. This creates a pressure gradient and a pneumatic cycle means that facilitates the massaging movement on the limb towards direction of the heart. The magnetic force in valves is uniquely adapted for controlling low-pressure compression. A magnetically adjustable valve is adapted for use in a compression device to control and regulate low to very low pressures and comprising of a movable magnetic part and a metal part, defining an air gap there between.

Abstract: A cervical immobilizing device includes a pair of arms that can be folded to an upright position to engage and support a patient's head, an actuating device for folding the arms to the supporting position, and a locking device for locking the position of the arms in the folded supporting position. The actuating device is coupled to the outer ends of the arms for folding the arms to an upright position symmetrically and uniformly. In one embodiment, the actuator device is a flexible member that passes around a guide to a position and gripped by the user. The locking device can be a clinching, ratcheting or clamping device, or a combination thereof, on the actuator device. In one embodiment, the folding arms include a coupling device for coupling the arms to a base in a sliding arrangement to enable the arms to slide along the base to a folded position.

Abstract: A retractable safety needle apparatus is provided. The apparatus includes a needle holder with opposite proximal and distal ends. A needle assembly is mounted in the needle holder for movement from a first position where a distal cannula projects distally beyond the needle holder and a second position where the distal cannula is entirely within the needle holder. A spring is provided for propelling the needle assembly proximally and into the second position. The needle assembly includes a deflectable actuator for releasably holding the needle assembly in the first position and against the biasing forces of the spring. Portions of the needle holder adjacent the distal end are tapered to facilitate alignment of the needle assembly and to provide visual cues for proper orientation and gripping locations.

Abstract: An inflow conduit of a ventricular assist device configured to prevent formation of recirculation and stagnation zones as well as collapse due to external forces or pump induced suction can be rigid and have a funnel like shape with an elbow to accommodate a patient anatomy. Stiffening elements and pressure sensing devices can also be provided associated with the inflow conduit.

Abstract: A device for subcutaneous administration of a medicament to a patient is disclosed, including a cannula housing with an interior chamber, a cannula connected to the housing and being in flow communication with the chamber, a flexible tubing having a first end and a second end, the first end being coupled to the housing such that the tubing is in flow communication with the chamber, and wherein, the second end carries a source coupling for coupling the tubing to the medicament. The tubing between the first and the second end is folded for forming a configuration with at least two essentially parallel courses of tubing, the tubing is secured in the configuration by a first holder device arranged between the first and second end of the tubing; and that the tubing can be displaced in relation to the first holder device for varying the length of the courses of tubing.

Abstract: An automated fluid control system for controlling fluid flow between a catheter, a saline supply, a contrast supply and an injector is disclosed. Pinch valves are provided in the saline input and output lines and contrast input and output lines. A controller is linked to the pinch valves to sequentially open and close the pinch valves during functions which include contrast injection and saline injection.

Abstract: Method for producing a syringe with a glued cannula, in which a syringe body is provided with a lubricant internally at high temperature, and either the lubricant is prevented from penetrating into a cannula receptacle of the syringe body, or the lubricant is cleared from the cannula receptacle of the syringe body afterward, and a cannula is glued into the cannula receptacle; and a syringe with a body comprising a cylinder portion and a narrowed cannula receptacle portion, whereby the cylinder portion is provided internally with a lubricant—this being deposited at high temperature—a cannula receptacle of the receptacle portion is cleared of lubricant, and a cannula is glued into the cannula receptacle.

Abstract: Absorbent article, such as a sanitary towel, a panty liner, an incontinence pad or the like, which article has two transverse end edges, two longitudinal side edges, a liquid-permeable surface layer, an essentially liquidtight backing layer, and an absorbent core located between the liquid-permeable surface layer and the essentially liquidtight backing layer and also side flaps at the longitudinal side edges on both sides of the absorbent core, the side flaps being folded and detachably tacked to the surface layer, said tacking being mechanical.

Abstract: The present invention discloses and claims a system and method for disguising a personal care product. The personal care product includes a pattern that matches a design on an undergarment so that the personal care product blends into the background of the undergarment. The method for disguising the personal care product includes creating a pattern to match the design on the undergarment and placing the pattern on the personal care product.

Abstract: A catheter assembly includes catheter having proximal and distal ends and at least one lumen extending between the ends. At least one end of the catheter is formed from a material that can be trimmed to achieve a selected length for the catheter. A tubular connector is telescoped over the catheter and a hub is joined to the tubular connector. Proximal portions of the hub are configured for connection to a medical apparatus. A cuff is mounted around the tubular connector or the catheter. The cuff is formed from a material that will permit or promote the growth of scar tissue for anchoring the catheter device at least on a semi-permanent basis in a patient.

Abstract: A corneal surgery apparatus capable of irradiating a laser beam at a desired position on a cornea more accurately. The apparatus has an optical system for irradiating a laser beam onto a cornea, a unit which moves an irradiation position of the beam relative to an eye, a unit having an element for picking up an image of an anterior-segment, which processes an image signal from the element to detect a characteristic point in the image, a unit which stores positional information on the characteristic point when the eye is in a predetermined reference state, a unit which detects duction condition of the eye based on positional information on the characteristic point when the eye is in a surgery state and that being stored, and a unit which controls the moving unit based on a detection result of the duction detection unit.

Abstract: Ultrashort laser pulses are used to induce photodisruptive breakdown in vasculature in an animal to controllably produce hemorrhage, thrombosis or breach of the blood-brain barrier in individual, specifically-targeted blood vessels. Damage is limited to the targeted vessels such that neighboring vessels exhibit no signs of vascular damage, including vessels directly above and directly below the targeted vessel. Ultrashort laser pulses of lower energy are also used to observe and quantify the baseline and altered states of blood flow. Observation and measurement may be performed by TPLSM, OCT or other known techniques, providing a real-time, in vivo model for the dynamics and effects of vascular injury.

Abstract: The invention relates to a medical probe signal generator. More particularly, it relates to a medical probe signal generator architecture. The present invention further relates to a medical probe signal generator having an automatic probe type detector, a user interface and operational parameter settings automatically configured according to a type of medical probe connected to the generator.

Abstract: Alloys for medical, surgical and microsurgical instruments are proposed which comprise 0.01% to 20% by weight of germanium, from 0-25% of shallow hydrogenic and/or non-hydrogenic acceptor dopants in terms of weight ratio in relation to germanium, from 0% up to 20% by weight of one or more of the following compounds such as platinum, gold, palladium, iridium, ruthenium, osmium, rhodium, niobium, tantalum, tungsten, aluminium, silicon, hafnium, yttrium, lanthanum, zirconium with the remainder, up to 100% by weight, constituted by silver and inevitable impurities, wherein instruments from these alloys possess properties such as no capacitive impedance in relation to the electrode-tissue interface; a Far Infrared Radiation (FIR) emitting capacity when energized by any form of energy; sulfurization, corrosion and oxidation resistant and have suitable hardness for their intended use; emit anions and may possess fractal surfaces.

Abstract: This invention relates to an electrosurgical device having a hollow shaft, an electrically conductive distal tip that is also adapted for penetrating bone, and an intermediate electrically insulating spacer.

Abstract: A working instrument for use in a resectoscope with a pushing force-transmitting elongated support, whose proximal end area includes an attachment section for attachment in a resectoscope, and whose distal end area carries a working device. The working instrument includes, in its distal end area, a handle element. The handle element projects in a distal direction beyond the support and the working device and is connected to the working instrument so as to transmit pushing forces and can be removed.

Abstract: An improved method and apparatus for reducing a hip fracture utilizing a minimally invasive procedure which does not require incision of the quadriceps. A femoral implant in accordance with the present invention achieves intramedullary fixation as well as fixation into the femoral head to allow for the compression needed for a femoral fracture to heal. To position the femoral implant of the present invention, an incision is made along the greater trochanter. Because the greater trochanter is not circumferentially covered with muscles, the incision can be made and the wound developed through the skin and fascia to expose the greater trochanter, without incising muscle, including, e.g., the quadriceps. After exposing the greater trochanter, novel instruments of the present invention are utilized to prepare a cavity in the femur extending from the greater trochanter into the femoral head and further extending from the greater trochanter into the intramedullary canal of the femur.

Abstract: A method of penetrating tissue is provided. The method comprises using a lancet driver to advance a lancet into the tissue; advancing the lancet at a first desired velocity in a first layer of tissue; advancing the lancet at a second desired velocity in a second layer of tissue; and advancing the lancet at a third desired velocity in a third layer of tissue. In one embodiment, the method may including using a processor having logic for controlling velocity of the lancet in each layer of tissue.

Abstract: A medical punch includes a longitudinally dividable anvil with a reduced cross-sectional dimension facilitating insertion of the anvil into the vessel wall to achieve a clean aperture in the vessel wall by cooperative shearing action of a cutting edge and an anvil edge. In another embodiment, the instrument incorporates a measuring device for determining the thickness of a vessel wall between an anvil and a distal end of a cylindrical structure which together form a caliper, and the measuring device can also constitute a medical punch by cooperative shearing action of a cutting edge and an anvil to achieve a clean aperture in the vessel wall.

Abstract: The present invention provides for a hair restoration device and methods of manufacturing and using the same. In one embodiment, the hair restoration device is comprised of (i) a hairbrush body housing a plurality of wide-pattern laser LEDs configured to cooperate to project a precision laser light pattern at a focal plane proximate a skin area to be irradiated; and (ii) bristles extending from the hairbrush body and terminating substantially at the focal plane.

Abstract: Apparatus for delivering and deploying a stent formed of a shape memory alloy to a desired position in a tubular area of the body, and/or for repositioning and/or retrieving a stent formed of a two-way shape memory alloy. An arrangement is provided by which the temperature of the stent is locally adjusted during delivery, repositioning and/or retrieval in a safe and controlled manner by engagement with an expandable and collapsible thermal transfer member situated on a catheter assembly.

Abstract: A stent for implantation in a body lumen for protecting from rupture a fibrous cap in order to treat vulnerable plaque. One embodiment of the stent achieves staged expansion through stronger and weaker circumferential regions, and includes optional anchors positioned at the circumferential transition between the stronger and weaker regions. During the first stage expansion, the weaker region expands moving the anchors laterally apart. The anchors straddle the fibrous cap and embed into the vessel wall. The second stage expansion of the stent exerts gentler stresses by the weaker region against the fibrous cap while the stronger region exerts greater stresses on the remainder of the vessel wall to open the vessel.

Abstract: A flexible sizer body for evaluating a valve annulus to determine a size of a prosthetic heart valve to be sewn to the valve annulus during heart valve replacement surgery. The prosthetic heart valve includes an annular extension having a first flexibility and a sewing ring having a second flexibility. The flexible sizer body includes an outer ring and an annular wall coupled to and extending from the outer ring. The annular wall has a flexibility substantially similar to the first flexibility of the annular extension of the prosthetic heart valve.

Abstract: An artificial disc having a pair of opposing baseplates, for seating against opposing vertebral bone surfaces, separated by a ball and socket joint that includes a solid ball mounted to protrude from one of the baseplates. The ball is captured within a curvate socket formed in a peak of a convex structure integral with the other of the baseplates. The socket is formed by opposing curvate pockets, one on the convex structure and one on a retaining cap that is secured to the other of the baseplates. The ball rotates and angulates in the socket. The ball and socket joint therefore permits the baseplates to rotate and angulate relative to one another.

Abstract: Systems for minimally invasive disc augmentation include an anulus augmentation component and a nucleus augmentation component. Both are suited for minimally invasive deployment. The nucleus augmentation component restores disc height and/or replaces missing nucleus pulposus. The anulus augmentation component shields weakened regions of the anulus fibrosis and/or resists escape of natural nucleus pulposus and/or the nucleus augmentation component. Methods and deployment devices are also disclosed.

Abstract: A knee replacement system provides a knee implant that may be used to more accurately replicate the diameter of a natural knee. In one embodiment, a patellofemoral component is connected to the posterior portion of a condylar component by screws that pass through the femur allowing the patellofemoral component and the condylar component to be torqued against opposing sides of the femur. Two additional screws are used to connect the patellofemoral component to an anterior portion of the condylar component. A gap may be left between the patellofemoral component and the anterior portion of the condylar component if needed to provide precise replication of the diameter of the natural knee from the patellofemoral component to the condylar component.

Abstract: The present invention relates to novel cationic yellow dyes of formula (1) wherein R1 and R2 are each independently of the other a C1-C8alkyl radical or an unsubstituted or substituted benzyl radical, R3 is hydrogen, C1-C8alkyl, C1-C8alkoxy, cyanide or halide, preferably hydrogen and X is an anion, with the proviso that at least one of the substitutents R1 is a benzyl radical and R2 is a methyl radical, R2 is not hydrogen, also to compositions therof, especially comprising other dyes, to processes for the preparation therof and to the use therof in the dyeing of organic material, such as keratin, wool, leather, silk, cellulose or polyamides, especially keratin-containging fibres, cotton or nylon, and preferably human hair.

Abstract: An apparatus and method are provided for aligning a plurality of semiconductor devices placed on a carrier. Alignment guides are located adjacent to each device in use, and arranged such that they correspond to a desired alignment of each semiconductor device. For alignment, the semiconductor devices are held by a positioning device comprising a plurality of holders, each holder being configured to generate a force to hold a semiconductor device. Actuators are also provided that are operative to move the positioning device and holders to bias the semiconductor devices against the alignment guides to orientate the semiconductor devices until they are aligned with said alignment guides.

Abstract: A hydrogen generator of the present invention is provided with: a reformer for generating a reformed gas containing hydrogen from a feed material containing an organic compound at least containing carbon and hydrogen and water; a heater for heating the reformer to a temperature required for generating the reformed gas; a carbon monoxide reducing unit having a carbon monoxide reducing catalyst for reducing carbon monoxide contained in the reformed gas generated in the reformer; and a temperature detector for detecting at least one of a temperature of the reformed gas in the carbon monoxide reducing unit and a temperature of the carbon monoxide reducing catalyst, wherein an amount of the feed material to be supplied to the reformer is controlled based on a comparison between a detected temperature detected by the temperature detector and a reference temperature set in accordance with the amount of the feed material.

Abstract: A porous abrasive article that allows air and dust particles to pass through. The abrasive article has a screen abrasive and a polymer netting with hooks. The screen abrasive has an abrasive layer comprising a plurality of abrasive particles and at least one binder. The polymer netting cooperates with the screen abrasive to allow the flow of particles through the abrasive article.

Abstract: Polishing compositions are described that are appropriate for fine polishing to very low tolerances. The polishing compositions include particles with small diameters with very narrow distributions in size and effectively no particles with diameters several times larger than the average diameter. Furthermore, the particles generally have very high uniformity with respect to having a single crystalline phase. Preferred particles have an average diameter less than about 200 nm. Laser pyrolysis processes are described for the production of the appropriate particles including metal oxides, metal carbides, metal sulfides, SiO2 and SiC.

Abstract: Al2O3—La2O3—Y2O3—MgO ceramics (including glasses, crystalline ceramics, and glass-ceramics) and methods of making the same. Ceramics according to the present invention can be made, formed as, or converted into glass beads, articles (e.g., plates), fibers, particles, and thin coatings. The particles and fibers are useful, for example, as thermal insulation, filler, or reinforcing material in composites (e.g., ceramic, metal, or polymeric matrix composites). The thin coatings can be useful, for example, as protective coatings in applications involving wear, as well as for thermal management. Some embodiments of ceramic particles according to the present invention can be are particularly useful as abrasive particles.

Abstract: CMP pad dressers and their methods of manufacture are disclosed. One aspect of the present invention provides a CMP pad dresser having improved superabrasive grit retention in a resin layer. The CMP pad includes a resin layer, superabrasive grit held in the resin layer such that an exposed portion of each superabrasive grit protrudes from the resin layer, and a metal coating layer disposed between each superabrasive grit and the resin layer, where the exposed portions are substantially free of the metal coating layer. The metal coating layer acts to increase the retention of the superabrasive grit in the resin layer as compared to superabrasive grit absent the metal coating layer.

Abstract: An improved bag docking assembly for aligning a vacuum bag for engagement with a dirty air outlet nozzle on a vacuum cleaner, and for retaining the vacuum bag in the position of engagement. The assembly incorporates an anchor member and a mounting member. The anchor member serves to attach the bag docking assembly to the vacuum cleaner. The anchor member can be a substantially flat piece of plastic having a central opening for closely receiving the dirty air outlet nozzle on the vacuum cleaner. The central opening can have a shoulder for engaging a rim or similar protrusion formed about the perimeter of the dirty air outlet nozzle. Additionally, protrusions are located on the anchor member that align with voids in the vacuum bag collar to ensure that correct alignment of the vacuum bag has been achieved.

Abstract: An Advanced Maritime Emissions Control System (AMECS) includes several Exhaust Intake Bonnets (EIBs) of different size and/or shape, an Emissions Capture System (ECS), and an Advanced Maritime Emissions Control Unit (AMECU) mounted on an Unpowered Seagoing Barge (USB). The EIB includes a cage formed by downward curved ribs, a shroud which is lowerable to cover the ribs, a belt near a lower edge of the EIB for retaining and sealing the EIB to a stack, and a mechanism for tightening the lower edge of the EIB (and thus the belt) around the stack. The ECS lifts one of the several EIBs onto the stack of an Ocean Going Vessel (OGV). Exhaust from the stack is drawn through a large diameter duct to the AMECU. The AMECU processes the exhaust through multiple treatment stages. The stages include pre conditioning the exhaust, oxidizing, reducing, polishing, and precipitating.

Abstract: A system for collecting and disposing of liquid medical waste includes a fluid collection cart and a draining and cleaning station. The fluid collection cart includes a pair of containers, each of which includes a draining port and a cap. Each cap includes an outer portion having a flushing port and a bore formed therein and an inner portion having vacuum and patient ports formed therein. The inner cap portion is disposable and removably positioned within the bore of the outer cap portion. Liquid level detectors also communicate with each container. The cart also includes a regulator so a low vacuum level may be pulled on one of the containers while a full vacuum level is pulled on the other container. Fluids are collected in the containers via suction tubes connected to the patient ports. The flushing and drain ports of the containers are connected to corresponding flushing and drain connectors on the station when the containers are full so that they may be drained and flushed.

Abstract: A smoke evacuating system for use during surgical procedures, particularly minimally invasive procedures involving the use of a laser or cautery at a surgical site having an associated higher than ambient pressure, wherein the system includes a filter with a site side and an outlet side and a fluid conduit extending between the surgical site and the filter. The filter includes a filter media and a housing substantially surrounding the filter media with a space between the filter media and the housing to collect condensed vapor. The filter exhibits low resistance or a low pressure drop and resists fluid flow, whereby the higher than ambient pressure is not substantially diminished and generates a fluid flow in the fluid flow path tending to carry smoke to and through the filter.

Abstract: A centrifugal particle separator includes a first vane assembly and a second vane assembly. The first vane assembly includes a centrally positioned hub, a collar encircling the hub and a plurality of first vanes. Each first vane can have an inner end connected to the hub and an outer end connected to the collar, wherein a trailing edge of at least one of the plurality of first vanes can extend past an edge of the collar. The second vane assembly includes a centrally positioned hub, a collar encircling the hub and a plurality of second vanes circumferentially disposed about the hub. Each second vane can have an inner end connected to the hub and an outer end connected to the collar, wherein a leading edge of at least one of the plurality of second vanes can extend past an edge of the collar. When the first and second vane assemblies are secured together, at least one of the plurality of first vanes protrudes into the second vane assembly.

Abstract: A filter housing includes an inlet for receiving airflow, a cavity for receiving a filter and an airflow passage between the inlet and the filter. At least one vane is positioned in the airflow passage for partitioning the airflow passage into a plurality of ducts. Each vane has a non-linear shape in the direction of flow through the airflow passage. This helps to reduce acoustic emissions from the machine since sound waves emitted by the fan and/or motor are caused to bounce off the vanes, which allows the vanes to absorb some of the sound energy. The filter housing can form part of a vacuum cleaner.