Abstract: A waist belt used for supporting a disposable absorbent assembly is disclosed. The belt includes a central segment positioned along the longitudinal centerline of the belt, at least two intermediate segments transversely outwardly extending from the central segment, and at least two distal segments transversely outwardly extending from an intermediate segment. Each intermediate segment covers a side hip of the wearer when the belt is worn. The longitudinal length of each intermediate segment is greater than that of the central segment, and greater than that of each distal segment. The belt further includes a fastener element positioned on at least one of the distal segments for releasably securing the belt around the waist of the wearer, and an attachment surface formed at least on each intermediate segment for releasably attaching the disposable assembly to the belt. An absorbent article comprising such a belt is also disclosed.

Abstract: Methods and devices for selectively removing an agent from a physiological efferent fluid collection site are provided. A feature of the invention is that a non-occlusive aspiration device is employed to selectively remove the target agent from the site only when the target agent is present in the site. Also provided are systems and kits for performing the subject methods. The subject invention finds use in a variety of different applications, including the selective removal of both therapeutic and diagnostic agents from a variety of different physiological sites.

Abstract: A catheter apparatus is provided that includes a tubular body having a distal end. The body defines first and second lumens. The first lumen has a first adapter that includes a first valve biased to seal the proximal end. The first lumen defines a first lateral port and the second lumen defines a second lateral port. A push rod is connected to the first valve for corresponding movement therewith and extends to a tip. The tip includes a first member extending into the first lumen and a second member extending into the second lumen such that the first member seals the first lateral port and the second member seals the second lateral port in a closed position of the tip. The first valve is engageable such that fluid communication is established between the proximal end of the first lumen and the first lumen, and the first and second members move to an open position whereby fluid communication is established.

Abstract: A device for delivering a drug includes a body having a proximal end and a distal end and an opening in the distal end thereof. An orifice mechanism at the distal end of the body communicates with the opening. The orifice mechanism includes an inner member having a proximal end and a distal end; a winding helically wound around the inner member; and wherein the winding and the inner member define a first channel for carrying a drug therethrough. An inlet is at the proximal end of the winding and an outlet is at the distal end of the inner member.

Abstract: Methods for removing certain of the cells of the epithelium prior to performing corneal ablation, comprising, ablating certain of the cells of the epithelium in an area above the cornea to form an initial, substantially circular refractive curve in the epithelium, wherein the initial refractive curve is formed above an area of the cornea that will be ablated during the corrective eye surgery, and ablating certain additional cells of the epithelium to translate the initial refractive curve downward to define a bed in the epithelium, wherein the certain additional cells of the epithelium are ablated until the Bowman's membrane is at least partially exposed.

Abstract: A method for measuring at least one of an energy and a position of a pulsed laser beam, notably in an ophthalmologic excimer laser. The pulsed laser beam is intermittently directed at a sensor, which measures its energy and/or position. In addition, a device for measuring at least one of an energy and a position of a pulsed laser beam. The device includes a sensor configured to measure at least one of the energy and the position of the pulsed laser beam, and a beam deflection device, which is configured to guide the pulsed laser beam and to intermittently direct the pulsed laser beam at the sensor.

Abstract: A surgical instrument comprises two oppositely-positioned working numbers each having proximal and distal ends and each having a working surface. The instrument also comprises at least one ring member affixed to a least one of the working members to encompass one or more of a user's fingers. In one embodiment at least one working surface has a heating element to cut or seal and cut tissue.

Abstract: An instrument and method are provided for sealing and joining or hemostatically dividing tissue, which is particularly suitable for laparoscopic and endoscopic surgery. The instrument makes use of the controlled application of a combination of heat and pressure to seal adjacent tissues, to join adjacent tissues, or to anastomose tissues, whereby tissue is heated for an optimal time and at an optimal temperature under optimal pressure to maximize tissue seal strength while minimizing collateral tissue damage. The instrument of the present invention is lightweight and therefore portable, and is particularly useful in field conditions where a source of external power may not be readily available.

Abstract: An electrosurgical generator for supplying RF power to an electrosurgical instrument for cutting or vaporising tissue has an RF output stage (42) with an RF power bridge (Q1, Q2, Q3, Q4), a pair of output lines (74) and a series-resonant output network (48). The output impedance of the output stage (42) at the output lines (74) is less than 200/?P ohms, where P is the maximum continuous RF output power of the generator. The generator offers improved cutting and vaporising performance, especially in relation to the reliability with which an arc can be struck when presented with an initial low impedance load. Overloading of the output stage is prevented by rapidly operating protection circuitry responsive to a predetermined electrical condition such as a substantial short-circuit across the output lines. In the preferred embodiment, the output stage is capable of maintaining output pulses at least 1kW peak by supplying the power bridge from a large reservoir capacitor (60).

Abstract: A magnetically navigable catheter includes a sheath having a proximal end and a distal end, and an extension member having a proximal end and a distal end, slidably mounted in the sheath so that the distal end portion of the extension member telescopes from the distal end of the sheath. The distal end portion of the extension member being relatively more flexible than the distal end of the sheath. There may be one or more electrodes on the distal end of the extension member. There is also at least one magnet, and preferably more than one magnet, on the distal end portion of the extension member to allow the distal end of extension member to be oriented by the application of an externally applied magnetic field.

Abstract: The present invention provides apparatus and method for removal of body hair using electroporation. The apparatus has a pulse generator capable of generator electrical pulses of the desired amplitude and duration to kill hair follicles and an applicator having a first electrode placed in contact with a hair follicle and a second electrode interacting with the first electrode to provide an electroporating field in the tissue volume surrounding a hair to be removed. The apparatus may include a TENS system to provide patient relief from discomfort experienced by application of the electroporation pulses.

Abstract: An electrosurgical cutting blade (1) comprises a first electrode (2), a second electrode (3), and an electrical insulator (4) separating the first and second electrodes. The first and second electrodes have dissimilar characteristics (cross-sectional area, thermal conductivity etc.) such that the first electrode (2) is encouraged to become an active electrode and the second electrode (3) is encouraged to become a return electrode. The spacing between the first and second electrodes (between 0.25 mm and 3.0 mm) and the peak voltage supplied to the electrodes (2 and 3) are both selected such that arcing does not occur directly between the electrodes, but between the first electrode and the tissue at the target site. The arrangement is such that, in use, a thermal differential of at least 50° C. is established between the first and second electrodes (2 and 3), such that the second electrode is maintained below a temperature of 70° C.

Abstract: A lordotic guard and method for guiding a bone removal device to form an implantation space in the human spine and, if desired, for inserting a spinal implant into the implantation space. The guard has a body having a first portion and a second portion in pivotal relationship to one another proximate the leading end between an open position and a closed position. The first and second portions define an opening for providing a protected pathway to the disc space and the adjacent vertebral bodies. At least one disc space penetrating extension extends from the leading end of the body adapted for insertion at least in part into the disc space. First and second portions of the extension are in pivotal relationship to one another about an axis that passes through at least a portion of the pathway.

Abstract: A locking device is provided for securing a rod in a receiving part, in particular a polyaxial bone screw. The locking device has a sleeve-type element with a cylindrical outer face and is dimensioned such that the element is displaceable between the legs of the receiving part. The element has an inner thread for receiving an inner screw. An outer nut can be screwed on to an outer thread of the legs to fix the element. The element acts on a pressure element provided in the receiving part to fix the position of the head of the polyaxial bone screw and the inner screw acts on the rod to fix it. The element is preferably provided with slits. During screwing in of the inner screw, the element splays out against the outer nut and thus effectively prevents loosening or detaching.

Abstract: A connection assembly between a spinal implant rod and a vertebral anchor. The assembly has a split ring, a clamp, a collet and optionally a nut. The split ring is located inside the clamp and the collet is inserted through each of the clamp's arms. In use, the spinal implant rod is placed inside the split ring and the shaft or shank of the vertebral anchor is placed inside the collet. Drawing the arms of the clamp together then tightens the connection assembly, which closes the collet around the vertebral anchor and closes the split ring around the implant rod. Threading a nut on one end of the collet or directly threading the collet into one of the arms of the clamp tightens the assembly.

Abstract: A bioabsorbable, cannulated tissue tack having an oblong head is used in sutureless soft tissue fixation to bone, particularly in arthroscopic shoulder surgery. A plurality of ribs are formed along the shaft of the tack. Repair of the glenohumeral joint is performed by installing the tack through a hole formed through the soft tissue of the labrum and into the cancellous bone of the glenoid rim. Aligning the oblong head of the tack lengthwise along the glenoid rim provides a low profile that avoids articular impingement on the tack head.

Abstract: A medical retrieval device has a multi-prong retrieval assembly. The multi-prong retrieval assembly has a first position, in which the retrieval assembly extends from the distal end of the sheath to form an open ended grasping device, and a second position, in which the retrieval assembly extends from the distal end of the sheath to form a substantially close ended basket-type retrieval device. When the retrieval assembly is used as a basket-type retrieval device, the distal ends of the prongs of the retrieval assembly that form the basket are not connected to each other. Thus, captured objects may be released by the operator, or by applying sufficient force to separate one or more of the prongs.

Abstract: The invention is directed to an appliance for the epilation of the human skin, having a housing to accommodate a motor and a drive mechanism for driving at least one clamping device (43) by which the user's hairs can be extracted. Moreover, a stimulation mechanism is provided to reduce the sense of pain during epilation. This mechanism includes at least one element (55) that is movable toward and away from the skin when the appliance is placed in epilating position on the user's skin. According to certain embodiments of the present invention, the at least one element (55) has a free end (56) and is arranged adjacent to the side of the rotary clamping device (43). In consequence, the user perceives at least subjectively a reduced sense of pain during epilation. Still further, a method for epilation and a method for the use of the appliance of the present invention are described.

Abstract: A fingertip-actuated surgical clip applier includes a first body and a second body substantially structurally identical to the first body. The first body includes a main section and a first jaw extending in a distal direction from the main section. The main section includes a hinge region and a first longitudinal wall extending between the first jaw and the hinge region. The first longitudinal wall includes a first outside surface adapted for contacting a first fingertip. The second body includes a second jaw and a second longitudinal wall. The second longitudinal wall includes a second outside surface adapted for contacting a second fingertip. The second body is inverted in relation to the first body and is pivotably connected to the hinge region. The first and second jaws are pivotable toward each other to a closed position and away from each other to an open position.

Abstract: A surgical clip applying apparatus comprises an actuator device, a ratchet mechanism, a locking mechanism, and a clip driving device. The actuator device comprises an interior and a cam mechanism disposed therein. The cam mechanism comprises an axial cam surface. The locking mechanism is movable by the actuator device within the interior in a distal direction and in a proximal direction. While moving in the distal direction, the locking mechanism contacts the axial cam surface, thereby causing the locking mechanism to engage the ratchet mechanism to limit movement of the locking mechanism in the proximal direction. Continued movement of the locking mechanism in the distal direction causes the locking mechanism to move off the axial cam surface, thereby enabling the locking mechanism to bypass the ratchet mechanism during a return stroke.

Abstract: An instrument and method for suturing wound closures is provided having a handle, shaft and suture engagement mechanism. The instrument provides for multiple placements or “bites” of suture in tissues to enable a wide variety of suturing techniques, including the ability to “run” a suture. The instrument further facilitates suture knot tying. The method of this instrument provides for rapid and effective remote suture placement and knot tying.

Abstract: Magnetic anchoring devices are disclosed herein. Expandable devices that are inserted into the stomach of a patient are attached to its interior wall by magnetically coupling. Such expandable devices, like inflatable balloons, comprise at least one magnetic device, which may be a magnet, a magnetizable material, or a magnetic metal. The magnetic device may be positioned on the external or interior surface of the expandable device or may be integral thereto. The magnetic device is magnetically coupled to a magnetic anchor positioned on a surface of the stomach wall. In this way, the expandable devices are anchored to the stomach walls, preventing migration of the device to other areas of the body where they may become obstructions and pose health risks.

Abstract: A body tissue graft for use in a patient includes a frame structure made of a first elastic material, a covering of a second elastic material on the frame structure, the covering substantially filling openings in the frame structure, and a connector connected to the frame structure. Projections are secured to the connector structure. The projections facilitate attachment of the tubular graft in a patient by securing the graft to the body tissue with which the graft is employed. The connector selectively circumferentially expands and the projections selectively circumferentially expand. This may be done using an inflatable balloon to circumferentially expand the projections. A restraining member may be provided to restrain the projections in a cone shape so that an end of the graft may be used to open an aperture through a side wall of existing body organ tubing and a portion of the projections may enter the aperture.

Abstract: A system suitable for collecting a body fluid, in particular blood from a body region of a person to be examined which comprises a lancing device which is suitable for holding a lancet, a lancet magazine for storing two or several lancets which has a transport device for the lancets and has an opening into which the lancing device can be inserted to remove a lancet from the lancet magazine, and two or several lancets, and which comprises a method for removing a lancet from a lancet magazine in which a lancet located in the lancet magazine is manually or automatically transported into a removal position in the interior of the lancet magazine, a lancing device is partially inserted into the opening provided in the lancet magazine in the process of which the lancing device automatically grips the lancet located in the removal position when it is partially inserted and the lancing device with the gripped lancet is removed from the lancet magazine.

Abstract: Sanitary coupling for needle and mechanized punch for micropigmentation and tattooing, having a threaded bolt that can perform shuttle micromovements of the protruding sheaf of the casing of the mechanized punch to which the base of a needle is coupled. The bolt passes through the casing of the mechanized punch through an orifice located in a prolongation and/or sleeve thereof. The base of the needle consists of a disc-like body which on one of its faces presents a threaded orifice for coupling to the thread of the bolt, and its edge is extended to form a complementary overlapping skirt around the form of the prolongation of the sleeve of the casing. On the other face of the disc-like body a protruding portion is centered where the non-dismountable body of the needle is attached. The edges of the disc-like body extend to form a housing for fluid collection.

Abstract: A tool for dilating tunnels in bone, in order to compact the cancellous bone around the tunnel and providing better holding for interference screws and the like, comprises a plurality of elongated segments mounted for radial motion with respect to an axis of elongation. When actuated, the segments move radially outwardly, parallel to the axis of elongation, compacting the bone.

Abstract: The invention relates to a medical instrument, comprising a shaft, the proximal end of which has a handle, with at least two grip pieces and the distal end of which has a tool, with at least two jaw pieces, whereby at least one jaw piece of the tool may be adjusted relative to the at least one other jaw piece for opening and closing, by means a grip piece on the handle, embodied so as to pivot. Each adjustable jaw piece and the corresponding grip piece in the handle, for adjusting the jaw piece, are connected to each other, by means of a pull-/push-rod and each adjustable jaw piece is connected to the pull-/push-rod, by means of a compensation lever. According to the invention, the best possible force transfer with a good cutting feel for the operator may be achieved, whereby the compensation lever is pivotably fixed on one end to the pull-/push-rod and displaceably mounted at the other end in a guide groove, formed in the adjustable jaw piece.

Abstract: A surgical instrument suitable for use in an implant procedure is disclosed. A surgical instrument of the invention can be particularly advantageous for use in grasping, holding and placement of implants in an intervertebral disc space. In a typical embodiment, the surgical instrument has a grasping region to hold the implant, and an impact head for receiving a force in order to insert the implant.

Abstract: The present invention relates to a method of making clips which can be used to engage body tissue for the purpose of closing wounds. Such clips are generally annular in shape and have radially inwardly extending tines. It is often desirable for such clips to have a small lateral dimension, but manufacturing difficulty has been encountered in making small clips because of the difficulty in cutting materials accurately when attempting to produce a clip with closely packed elements. The present invention avoids these difficulties by first forming a precursor which, in one embodiment, has the tines extending radially outwardly from the annular body and then forms the clip by inverting the precursor such that the tines extend radially inwardly. In an alternate embodiment, the precursor is formed with an over-sized lateral dimension and then compressed inwardly to bring the tines closer together and to reduce the lateral dimension of the precursor.

Abstract: A teething device is provided which includes a fluid-filled membrane sized to be at least partially received in the mouth of a child, a housing attached to the fluid-filled membrane, a handle sized to be grasped by a child, a vibrator configured to impart vibration to the fluid-filled membrane and a pressure switch selectively connecting the vibrator to a power source when a threshold pressure is applied to an outer surface of the membrane.

Abstract: The invention is directed to a method of bonding a hermetically sealed electronics package to an electrode or a flexible circuit and the resulting electronics package, that is suitable for implantation in living tissue, such as for a retinal or cortical electrode array to enable restoration of sight to certain non-sighted individuals. The hermetically sealed electronics package is directly bonded to the flex circuit or electrode by one of several methods, including attachment by an electrically conductive adhesive, such as epoxy or polyimide, containing platinum metal flake in biocompatible glue; diffusion bonding of platinum bumps covered by an insulating layer; thermal welding of wire staples; or an integrated interconnect fabrication. The resulting electronic device is biocompatible and is suitable for long-term implantation in living tissue.

Abstract: A contrast therapy system. According to one aspect of the invention, the contrast therapy system includes a hot reservoir for holding a relatively hot fluid and a cold reservoir for holding a relatively cold fluid. The system also includes a mixing valve for receiving a selected ratio of the hot and cold fluids from the hot and cold reservoirs. The mixing valve is operable to deliver a therapy fluid with a therapy temperature determined by the selected ratio. The system also includes a therapy pad for receiving the therapy fluid from the mixing valve and returning the therapy fluid to at least one of the hot reservoir and the cold reservoir.

Abstract: A method and apparatus is provided for determining an effective thermal mass of a patient. The effective thermal mass is employed to determine a gain factor used in a feedback control system controlling patient temperature. The method begins by inducing hypothermia or hyperthermia in at least a selected portion of the patient with a device having a heat transfer surface. Next, power is transferred between the device and the patient. A change in temperature over time, which arises in the selected portion of the patient, is measured while performing the step of inducing hypothermia or hyperthermia. Finally, an effective thermal mass is calculated based on the measured power and the measured temperature change over time.

Abstract: An endovascular heat transfer device which can have a smooth exterior surface, or a surface with ridges and grooves. The device can have a plurality of elongated, articulated segments, with each having such a surface. A flexible joint connects adjacent elongated, articulated segments. The flexible joints can be bellows or flexible tubes. An inner lumen is disposed within the heat transfer segments. The inner lumen is capable of transporting a pressurized working fluid to a distal end of the heat transfer element.

Abstract: An intravascular platform for supporting an intravascular device includes two loops of wire each configured to assume a shape lying generally on a virtual cylinder of given diameter. The two loops are interconnected by at least one connecting wire which maintains the loops axially spaced from each other. Also disclosed are axially-extended loop forms, and associated intravascular devices.

Abstract: One aspect of the invention relates to a graft, a surface of which is coated with an amphiphilic block copolymer that includes both hydrophobic and hydrophilic polymer chains. An amphiphilic block copolymer coating according to the invention can serve as a carrier for a very broad range of drugs, possibly including every drug presently used, being considered for use, or likely to be used in the future to inhibit stenosis. The release rates of the drugs can be controlled, for example, through the length of the polymer chains, through their ratio, or through the degree of cross-linking.

Abstract: A prosthesis for transluminal implantation consists of a flexible tubular interbraided structure of metal or polymeric monofilaments, and polymeric multifilament yarns. The prosthesis can be elastically deformed to reduce its diameter through axial elongation. The monofilaments and multifilament yarns are arranged in axially spaced apart helices, concentric on a common central axis of the prosthesis. The monofilaments are selectively shaped before their interbraiding with the multifilament yarns, either by an age-hardening or other heat-setting stage, or a cold-working stage that controllably plastically deforms the strands. The shaped structural strands cooperate to impart to the prosthesis its nominal shape and resilience. The textile strands cooperate to provide a sheeting that occupies interstices between adjacent structural strands, to reduce permeability and thereby enhance the utility of the prosthesis as a vascular graft.

Abstract: A diagnostic device for determining the amount of change required in a coronary sinus to reduce valve regurgitation. The device includes a distal tube having a distal anchor at a distal end portion of the distal tube, a proximal tube having a proximal anchor at a distal end portion of the proximal tube, and an adjustor to move the distal tube relative to the proximal tube. The proximal tube and the distal tube together form a telescoping elongate body adapted to fit within the coronary sinus, and the device includes a scale to measure the movement of the distal anchor relative to the proximal anchor.

Abstract: An apparatus and method for fixation of a soft tissue graft. The apparatus may include a member having a first surface and a second surface. Each of the surfaces extend a distance relative to one another. A member is operable to resist movement of the apparatus relative to an anatomical portion. An interference member may be provided to fixedly associate the apparatus with the anatomical structure.

Abstract: A spinal fusion device for implantation between adjacent vertebrae is formed in the approximate shape of a hollow cube. The device has an upper section and a lower section relatively movable with regard to each other. The sidewalls of the upper section and the lower section terminate in complementary inclined planes so that as the sections move away from each other the height of the device lessens and as the sections move toward each other the height of the device increases. A distractor is placed within the hollow body and contacts the upper and lower sections by a link which is used to adjust the height of the device.

Abstract: An endoprosthesis utilizes a biomechanical structure based on the lever model of first degree. Contrary to the widespread practice, the inventive structure has a stem placed inside the femur bone, which is not rigidly attached to this bone. Accordingly, the bone, following its known tendency to slightly pivot away from the medial plane of the body in response to the loads, does not directly contact the stem. The neck portion experiences even greater loads then the stem. The supporting anchor has a region extending laterally from the stem and pressing against a supporting surface of the housing, which also extends laterally from the body of the housing. Since the stem, supporting anchor and neck are typically constitute a one-piece component, the lateral surfaces of the supporting anchor and housing are in continuous frictional contact during displacement of the stem and housing relative to one another.

Abstract: An endoscopic device separates ingested food from gastric fluids or gastric fluids and digestive enzymes, to treat obesity. In a particular embodiment a gastric bypass stent comprises a tubular member and two or more stent members defining a lumen. The tubular member has a substantially liquid impervious coating or covering and one or more lateral openings to permit one-way liquid flow.

Abstract: A prosthetic foot (70) incorporates a foot keel (71) and a calf shank (72) connected to the foot keel to form an ankle joint area of the prosthetic foot. The foot keel has forefoot and hindfoot portions and an upwardly arched midfoot portion extending between the forefoot and midfoot portions. The calf shank includes a downward convexly curved lower end which is secured to the foot keel by way of a coupling element (73). The lower end of the calf shank extends upwardly, and initially anteriorly therefrom into a reversely curved portion (75) of the calf shank leading to an upstanding upper end thereof.

Abstract: Provided are a hair bleach composition, hair dye composition and a hair treatment additive having excellent bleaching power, capable of dyeing the hair with a bright and good color, and less damaging to the hair and less irritating to the scalp. Described specifically, they are a two-part hair bleach composition, which contains (a) a nitrogenous compound represented by the following formula (1) or (2): or salt thereof, or (A) a nitrogenous compound having a solubility parameter log P in octanol/water ranging from ?1 to 4 and a hydrogen peroxide remaining ratio of from 5 to 90%, or salt thereof, (b) an oxidizing agent, and optionally (c) an alkali agent and, after mixing, has a pH of from 7.5 to 12; a two-part hair dye composition comprising (a) or (A), (b) and (c) and further (d) an oxidation dye or direct dye; and an additive used therefor.

Abstract: A composition for dyeing keratin fibers, for example, human keratin fibers, such as hair, comprising at least one dye chosen from heteroyldiarylmethane type direct dyes, for example, monoheteroyidiarylmethane direct dyes, and the leuco precursors thereof; and also to methods for dyeing keratin fibers, for example, human keratin fibers, such as hair, using the composition, and multi-compartment devices.

Abstract: A composition for dyeing keratin fibers, such as human keratin fibers, and further such as the hair, comprising at least one dye chosen from heteroylmethane type direct dyes, such as triheteroylmethane direct dyes and leuco precursors of such dyes, as defined herein. A method that uses the composition for dyeing keratin fibers, such as human keratin fibers, and further such as the hair, and a kit or device containing same.

Abstract: Keratin fibers are colored by an agent comprising a coupler which is a m-phenylenediamine derivative of the formula (I) wherein R1 is a C1–C4 alkyl group or a C1–C4 monohydroxyalkyl group; R2 is a methyl or an ethyl group; each of R3 and R4 is independently a branched or unbranched C2–C6 hydroxyalkyl group; and a cosmetically acceptable carrier. These couplers exhibit improved toxicological and dermatological properties and permit hair colorations in a broad color spectrum with good fastness properties.

Abstract: A method for forming a pattern of an organic semiconductor film comprises applying at least a bicyclo compound onto a base material, the bicyclo compound being converted to an organic semiconductor on the base material through retro-Diels-Alder reaction which removes a part of the bicyclo skeleton to allow extension of pi electron system.

Abstract: The present invention relates to a polishing composition more suitable for use in polishing synthetic resin products or metal products. The polishing composition includes a reaction product produced by a reaction between a polyalkylene oxide and a compound having a functional group having reactivity with a hydroxyl group, aluminum oxide, a polishing accelerator including at least one salt selected from the group consisting of a metal salt of an inorganic acid or organic acid and an ammonium salt of an inorganic acid or organic acid, and water.

Abstract: A polishing composition for reducing the haze level of the surface of silicon wafers contains hydroxyethyl cellulose, polyethylene oxide, an alkaline compound, water, and silicon dioxide.