909results about How to "Simple and inexpensive to manufacture" patented technology

A medical cauterization snare includes a tubular member such as a catheter, a rod or wire disposed at least partially inside the tubular member, and a resilient loop of a first size attached to a distal end of the rod or wire. The loop includes a nose on a side of the loop opposite the wire. The loop further includes two loop sections each extending between the wire and the nose. The loop sections are each formed with a respective notch or dent for enabling a use of the loop in a second size smaller than the first size. Positioning the loop relative to the tubular member so that the notches or dents are disposed at a mouth opening of the tubular member generates this secondary deployment configuration.

A universal mechanical dilator combined with massaging action comprises a probe (12) consisting of a two rods (22 and 24), a drive unit (14) and an adapter (16) that connects the probe (12) to the drive unit. The instrument is intended for dilation of the urethra or other ducts of a human body and can operate in three different modes: pure dilation, pure vibration, and dilations combined with vibrations. This is achieved by using the adapter (16) as an adjustable coupling. The probe (12) together with the adapter (16) can be disconnected from the drive unit (14) and used separately as a mechanical manual dilator. At its distal end, the probe (12) has means for connecting replaceable tips (28a, 32a) used for various applications, i.e., urethral, anal, vaginal, etc. The invention also relates to a method of treatment of voiding or an orectal diseases by combining dilations with vibrations. The instrument can also be used for training sphincteric muscles.

A transdermal drug delivery system for the topical application of one or more active agents contained in one or more polymeric and / or adhesive carrier layers, proximate to a non-drug containing polymeric backing layer which can control the delivery rate and profile of the transdermal drug delivery system by adjusting the moisture vapor transmission rate of the polymeric backing layer.

A medical implant (20) includes first and second ring members (22,24), each including a resilient framework (26) having a generally cylindrical form. A tubular sleeve (28) is fixed to the first and second ring members so as to hold the ring members in mutual longitudinal alignment, thereby defining a lumen (32) passing through the ring members. A constricting element (30) is fit around the sleeve at a location intermediate the first and second ring members so as to reduce a diameter of the lumen at the location.

An attachment structure for a load-bearing fabric including an expandable carrier secured to an un-stretched load-bearing fabric. To attach the carrier to a support frame, the carrier and fabric are stretched together to desired shape and secured to the frame. An indexing system registers the carrier and frame and optionally stretches the fabric a predetermined amount. The carrier and frame can include a lip that flexes in one direction and maintains the fabric in a stretched condition in another. A tool that joins the carrier and frame generally includes a drive roller and a primary roller adapted to move toward one another and join a carrier and the support frame disposed therebetween. The tool may include alignment rollers near the primary and drive rollers to track along and align the carrier and frame.

A safety needle device includes a housing including a passageway with a needle cannula extending therefrom. A shielding member is movable between a first position in which a puncture tip of the needle cannula is exposed therefrom and a second position in which the puncture tip of the needle cannula is encompassed therein. The shielding member is maintained in the first position against a biasing force which biases the shielding member toward the second position. A fluid and / or temperature activation material, such as a hydrogel or a compressed sponge, is associated with the shielding member and is adapted to deform upon contact with a fluid medium and / or a certain temperature or temperature range. Fluid flowing through the needle cannula, such as blood flow during a blood collection procedure, causes the activation material to deform, such as through expansion, thereby releasing the shielding member from the first position and allowing the drive member to bias the shielding member toward the second position.

A medical cauterization snare includes a tubular member such as a catheter, a rod or wire disposed at least partially inside the tubular member, and a resilient loop of a first size attached to a distal end of the rod or wire. The loop includes a nose on a side of the loop opposite the wire. The loop further includes two loop sections each extending between the wire and the nose. The loop sections are each formed with a respective notch or dent for enabling a use of the loop in a second size smaller than the first size. Positioning the loop relative to the tubular member so that the notches or dents are disposed at a mouth opening of the tubular member generates this secondary deployment configuration.

The present invention relates to RJ45 modular inserts that are connected to a printed circuit board used to transfer high speed signals for telecommunication interface media connections. The printed circuit board is configured to reduce near-end cross-talk (“NEXT”) without compromising impedance. NEXT is substantially reduced by utilizing a low reactance dielectric insert with a two-stage combination positive and negative compensation removal technique. By utilizing this method, the pair-to-pair NEXT is substantially reduced and differential pair impedance are controlled in a simple and cost effective manner.

A stand-up bag of a heat-sealable plastic film comprising two opposing side walls (1, 2) sealed together along the lateral edges thereof by means of side seams (5, 6), an inwardly folded bottom wall (4) provided between the lower portions of the side walls (1, 2) and sealed to the respective side walls (1, 2) along transverse bottom seams (7) and along bottom side seams, and an inwardly folded top wall (3) extending between the side walls and connected to the respective side walls (1, 2) along transverse top connections (11, 12) and sealed to the respective side walls (1, 2) along top side seams. One of the side walls (1) comprises a first side wall section (1a) and a second side wall section (1b) which overlaps the first side wall section (1a) in an overlapping area (15). In the overlapping area (15) the two side wall sections (1a, 1b) are connected by means of longitudinal peelable connections (19, 20) along the side seams (5, 6) and by means of a transverse peelable connection (18). The second side wall section (1b) extends a distance past the transverse peelable connection (18) to form a gripping member (21).

A planar wound dressing for the heel of the foot, having an adhesive layer with a backing layer, and three slits which can be reversibly closed and joined to form a non-planar wound dressing that conforms to and adheres to the heel of the foot. The wound dressing is constructed so that one slit is placed over the Achilles tendon, the second slit is placed over the inner ankle, and the third slit is placed over the outer ankle. With this orientation after closure of the slits the wound dressing covers the heel uniformly without wrinkles, gaps, leakage, contamination, or infection. The wound dressing is particularly useful in protecting and preventing blisters on the heel that occur in sports such as soccer, track, and the like.

A patch panel assembly having a bracket with a base extending between first and second side walls. The bracket defines a cable receiving passageway. First and second patch panels are coupled to the first and second side walls for pivotal movement about first and second vertical pivot axes between open and closed positions. The patch panels are selectively engageable with one another in their closed positions for limiting access across the cable receiving passageway.

A portable baby bottle blender includes a baby bottle having a top collar with external threads and a bottom collar with external threads. A top cap has a central aperture. The top cap is internally threaded to be removable threaded onto the top collar of the baby bottle and holds a feeding nipple extending through the central aperture of the top cap onto the top collar. A sealing O-ring fits onto the bottom collar of the baby bottle. A bottom cap has a rim internally threaded. An agitating unit is centrally retained within the bottom cap. When the rim of the bottom cap is removably threaded onto the bottom collar of the baby bottle and against the sealing O-ring, the agitating unit extends into the bottom collar of the baby bottle. A base member has a top recess to receive the bottom cap on the baby bottle therein. A spur-crown gear coupling is for operating the agitating unit, so that the mixing blade assembly mixes formula within water placed through the top collar of the baby bottle.

The present invention is dental prosthetics manufactured from polymers rather than ceramics. Various plastics are disclosed for use in making said prosthetics, as are techniques for improving plastic performance in the prosthetics. The prosthetics are first injection molded into pre-set blocks for use in milling machines that dentists use or custom fit prosthetics with less wait time and less cost. Alternatively, an electronic model may be produced using image scanners. The electronic model may then be downloaded into rapid prototyping machine and a prosthetic therein built. Use of these methods may create various monolithic prosthetics, including multi-tooth prosthetics and whole bridges.

A fluid dispenser device a body (1), a fluid reservoir (3), a dispensing member, such as a pump or a metering valve having a piston or a valve member that is mounted to move axially, which dispensing member is fitted to the reservoir (3), and an actuating element (5) mounted to move between a rest position and an actuating position, for actuating the dispensing member and thus for selectively dispensing the fluid contained in the reservoir (3), fluid dispenser device being characterized in that the direction in which actuating element (5) moves is different from, and in particular perpendicular to, the axial direction in which the piston or the valve member of the dispensing member moves, the actuating element (5) having an end portion provided with the cam surface (6) which co-operates with the reservoir (3) or a fixing ring (8) adapted to fix the dispensing member to the reservoir (3) so that the actuating member (5) being moved substantially radially into its actuating position causes the reservoir (3) to be moved axially relative to the piston or to the valve member of the dispensing member so as to dispense a dose of fluid.

Various electrically controlled devices of a bicycle are electrically coupled together by multi-conductor electrical cords. The ends of the electrical cords have an electrical connector that mates with a corresponding electrical connector provided in one of the electrically controlled devices. Each electrical connector of the electrical cords has an electrical contact housing with electrical contacts, an outer casing molded about the electrical contact housing, and an annular sealing member formed of a resilient and compressible material. The outer casing has an attachment portion fixed to one end of the electrical contact housing and a tubular portion radially spaced from the other end of the electrical contact housing. The annular sealing member is located in an annular space formed between the tubular portion and the electrical contact housing.

A thermoacoustic refrigerator having a relatively small size which utilizes one or more piezoelectric drivers to generate high frequency sound within a resonator at a frequency of between about 4000 Hz and ultrasonic frequencies. The interaction of the high frequency sound with one or more stacks create a temperature gradient across the stack which is conducted through a pair of heat exchangers located on opposite sides of each stack. The stack is comprised of an open-celled material that allows axial, radial, and azimuthal resonance modes of the resonator within the stack resulting in enhanced cooling power of the thermoacoustic refrigerator.

A progressing cavity stator and a method for fabricating such a stator are disclosed. Exemplary embodiments of the progressing cavity stator include a plurality of rigid longitudinal stator sections concatenated end-to-end in a stator tube. The stator sections are rotationally aligned so that each of the internal lobes extends in a substantially continuous helix from one end of the stator to the other. The stator further includes an elastomer liner deployed on an inner surface of the concatenated stator sections. Exemplary embodiments of this invention include a comparatively rigid stator having high torque output and are relatively simple and inexpensive to manufacture as compared to prior art rigid stators.

A stent-graft fabricated from a thin-walled, high strength material provides for a more durable and lower profile endoprosthesis. The stent-graft comprises one or more stent segments covered with a fabric formed by the weaving, knitting or braiding of a biocompatible, high tensile strength, abrasion resistant, highly durable yarn such as ultra high molecular weight polyethylene. The one or more stent segments may be balloon expandable or self-expanding. The fabric may be attached to the stent segments utilizing any number of known materials and techniques. The fabric may be attached to the stent segments utilizing an attachment device that secures the fabric to a strut of the stent segment by sandwiching the fabric between itself and the stent strut.

A biocompatible metallic material may be configured into any number of implantable medical devices including intraluminal stents. The intraluminal stents may be specifically configured to optimize the number of discrete equiaxed grains that comprise the wall dimension so as to provide the intended user with a high strength, controlled recoil device as a function of expanded inside diameter. One biocompatible metallic material may comprise a Cobalt-Chromium alloy having substantially reduced Iron and / or Silicon content.

A device for heating, cooling and emitting fragrance into bedding on a mattress of a bed which comprises a vented bladder placed upon the mattress under the bedding of the bed. A mechanism is for producing forced air being hot / cool and scented. A flexible air hose extends between the vented bladder and the forced air producing mechanism, to carry the hot / cool and scented air from the forced air producing mechanism to the vented bladder and into the bedding.

A biocompatible material may be configured into any number of implantable medical devices including intraluminal stents. The biocompatible material may comprise metallic and non-metallic materials. These materials may be designed with a microstructure that facilitates or enables the design of devices with a wide range of geometries adaptable to various loading conditions. Both the load bearing elements and the substantially non-load bearing elements may utilize these materials. Additionally, therapeutic agents may be incorporated into the microstructure or the bulk material.

A progressing cavity stator and a method for fabricating such a stator are disclosed. Exemplary embodiments of the progressing cavity stator include a plurality of rigid longitudinal stator sections concatenated end-to-end in a stator tube. The stator sections are rotationally aligned so that each of the internal lobes extends in a substantially continuous helix from one end of the stator to the other. The stator further includes an elastomer liner deployed on an inner surface of the concatenated stator sections. Exemplary embodiments of this invention include a comparatively rigid stator having high torque output and are relatively simple and inexpensive to manufacture as compared to prior art rigid stators.

An exercise device for a person, comprising at least two substantially rigid rails, each rail having an outer surface, and inner surface, and at least one peripheral edge connecting the outer surface to the inner surface. The at least one peripheral edge includes at least one axle slot formed therein. At least one substantially cylindrical axle has two ends and is adapted for rotatably and removably receiving at least one substantially cylindrical roller thereon. Each end of each axle is adapted to be captured within one of the axle slots of one of the rails. Each roller has a peripheral surface and a maximum diameter. Each axle is spaced a distance from an adjacent axle of at least the maximum diameter of the rollers, whereby each roller may rotate freely on the at least one axle. The exercise device is able to support a person lying on his back on the rollers on a flat surface.

In one or more embodiments, a vibration system comprises a vibratable plate, a support member surrounding the vibratable plate, and a vibration-inducing member surrounding the support member, wherein the vibration-inducing member is configured to radially expand and contract against the support member so as to produce axial vibration of the vibratable plate. In one embodiment, the vibratable plate has an outer circumference; a tubular member is concentrically disposed about the outer circumference of the plate, and an annular vibration-inducing member is concentrically disposed about the outer circumference of the tubular member. The vibration-inducing member is preferably a piezoelectric ring that is radially expandable and contractable against the wall of the tubular member to cause the plate to vibrate in the axial direction. In another embodiment, an aerosol generating system comprises an piezoelectric ring that is radially expandable and contractable upon actuation thereof; a tubular member disposed within the center hole of the piezoelectric ring, and a circular vibratable aperture plate disposed across the internal lumen of the tubular member. The piezoelectric ring is radially expandable and contractable against the tubular member to cause the aperture plate to vibrate in the axial direction, and a reservoir of liquid is coupled to the tubular member so as to supply the liquid to the vibratable aperture plate and produce an aerosol upon vibration thereof.

There is disclosed an improved stand-off for large vacuum compression storage bags made from a thermoplastic material such as polyethylene or other thermoplastic material and preferably made by extrusion. The stand-off includes a base having an aperture therein for alignment with the valve of the bag. The base further includes a plurality of ribs. The stand-off may include a variety of geometries provided that it is of sufficient length and width to cover the valve area. It may extend from one side of the bag to the other side of the bag or include variations thereof in size.