Abstract: A flow diversion device for the treatment of intracranial aneurysms and other medical conditions is disclosed. The flow diversion device may include a generally tubular wire stent frame formed from a plurality of zig-zag shaped wire elements that are coupled together. The device further includes a base layer of graft material coupled to the wire stent frame and surrounding at least a portion thereof, the wire stent frame maintaining the base layer in an open condition. In some embodiments, the base layer may be formed of porous graft material having a plurality of pores formed thereon to provide a passageway for a small blood flow to maintain the long term patency of important small side branches, while also reducing blood flow to the aneurysm to promote occlusion and avoid potential rupture.

Abstract: A spiral blood flow device includes a stent made up of a plurality of expansion members joined to a plurality of axial members that permit the stent to change diameter among a continuum of expanded configurations. The axial members have fixed orientation, whereas the expansion members have a variable orientation relative to the longitudinal axis throughout the continuum of expanded configurations. A spiral flow inducing structure, which may include fins attached to the axial members, define a helical flow angle that remains constant throughout the continuum of expanded configurations.

Abstract: A stent comprising a stent body and a plurality of cells is disclosed. Each cell includes two structural members extending in an undulating pattern. Each structural member includes a plurality of cell segments defining a plurality of peaks and valleys therebetween. A first segment and a second segment defining a first peak, the second segment and a third segment defining a first valley, the third segment and a fourth segment defining a second peak, the fourth segment and a fifth segment defining a second valley, the fifth segment and a sixth segment defining a third peak. The first peak, the second peak and the first valley include a first radius of curvature. The third peak and the second valley include a second radius of curvature. The first radius of curvature is larger than the second radius of curvature.

Abstract: A delivery device assembly for delivering a medical device to a target site within a patient includes a first polarizable tine and a second reactive tine that is not polarized. The first tine is connected to a first wire that has an electric coil surrounding a portion of the first wire. A current is passed through the electric wire to cause the polarizable tine to become polarized, thereby causing the reactive tine that is not coupled to the electric coil to move toward the polarized tine. The relative movement of the tines releases the medical device from its attachment to the tines.

Abstract: A stent delivery system and methods are described. The stent delivery system can include an elongate outer member defining an outer member lumen through which a self-expanding stent is deliverable. The elongate outer member can include an anisotropic portion and a rigid portion proximal to the anisotropic portion. The anisotropic portion can be radially elastic and longitudinally inelastic. The rigid portion can be radially inelastic and longitudinally inelastic.

Abstract: The invention provides methods to prepare protein conjugates from proteins having at least two cysteines. In one embodiment, a protein with a disulfide linkage is reduced to provide two free cysteines for reaction with a 1,3-dihaloacetone or similar reactant, linking the sulfur atoms of the two cysteines together. The ketone inserted between the sulfur atoms is then used to form a Schiff base to an aminated payload molecule, thus conjugating the protein to a payload. In another embodiment, two cysteine residues are tied together by reaction with a 1,3-dihaloacetone or similar reactant. The linkage between the sulfur atoms in each case holds the protein or peptide in a constrained conformation, while also providing a convenient place for attaching a payload with good specificity and efficiency.

Abstract: A compression foot garment is integrally knit of a body yarn, and adapted for wear on a foot of a user. The foot garment incorporates first and second high compression zones, and a compression release zone between the high compression zones. The first high compression zone is adapted for applying substantially circumferential compression to the foot below the plantar fascia between the calcaneus and metatarso-phalangeal joints and generally around the midfoot. The second high compression zone is adapted for applying substantially circumferential compression to the foot above the calcaneus and generally around an ankle of the user. The first and second high compression zones may comprise elastic yarns integrated with the body yarn. The compression release zone is adapted for applying reduced compression to the foot in an area between the first and second high compression zones.

Abstract: A back support system has a belt portion that is configured to provide back and abdominal support encircling a wearer's waist, a compression pants portion and a hot or cold pack providing therapy to a wearer's lumbosacral region. The belt portion has left and right portions and a rear portion that extends upwardly from a cutout of the rear portion of the compression pants and it is attached fixedly to it. The rear portion of the belt portion has a pack support structure for receiving a hot or cold pack so as to maintain hot or cold therapy on the wearer's back. A front core support structure provides abdominal support that in combination with the back support supports the entire core of the wearer's body. The garment can be changed to an immobilizing brace device by inserting optional rigid inserts.

Abstract: Apparatus for distracting the hip joint of a patient, said apparatus comprising: a perineal post for engagement with a leg of the patient, said perineal post comprising a first portion and a second portion, wherein said first portion is configured for mounting to a table, and further wherein said second portion is movable relative to said first portion so as to change the geometry of the perineal post relative to a patient supported on the table.

Abstract: The present disclosure concerns an ostomy pouch comprising a first pouch wall and a second pouch wall joined together along a peripheral seal to form a cavity for accommodating waste material; and said pouch having an upper and a lower portion; an inlet provided in the first pouch wall for receiving waste into the pouch; said inlet opening being provided in the upper portion; wherein the pouch further comprises a top view member comprising two layers of transparent flexible film is provided an upper section of said upper portion between said first and second pouch walls and sealed to either the first or the second wall by peripheral seals, wherein said top view member is provided with a lowermost edge.

Abstract: A male external incontinence device comprising a drainage tube assembly having a proximal chamber in fluid communication with a drainage tube, the proximal chamber comprising an atmospheric equilibrium valve assembly. The atmospheric equilibrium valve assembly has an airway conduit with a upper portion in fluid communication with the proximal chamber, and a lower portion having an air inlet chamber. A one-way air valve disposed in the airway conduit above the air inlet chamber, the one-way air valve comprising a first pair of opposing walls disposed at a first set of opposing angles such that the first pair of opposing walls abut each other at an apex, the apex having a self-sealing slit.

Abstract: A medical appliance for the treatment of obstructive sleep apnea in a patient, the appliance comprising: a securing device configured to be removably affixed to the patient's jaw; and a biasing member which is insertable behind the soft palate and/or the base of the patient's tongue, thereby providing for the flow of air in the nasopharyngeal airway; wherein the securing device is connected to the biasing member to allow insertion and/or removal of the biasing member from the nasopharyngeal airway.

Abstract: Slings, kits, and methods useful in the treatment of Obstructive Sleep Apnea (OSA) are described. An exemplary sling comprises a main body extending along a lengthwise axis and having first and second opposing ends, first and second opposing sides, and first and second opposing surfaces. Each end defines an end loop that defines a passageway extending through the main body. An exemplary method of treatment comprises creating two openings in the mandible of a patient; creating two longitudinal tunnels in the tongue of the patient; creating a transverse tunnel in the tongue of the patient; advancing a sling through the transverse tunnel; pulling each end of the sling through one of the longitudinal tunnels and through one of the openings in the mandible; pulling the tongue toward the front of the mouth or mandible; and securing the sling to a tissue to support the tongue in a new position.

Abstract: An intrauterine contraceptive system may include a contraceptive intrauterine device, a retrieval thread permanently attached to the intrauterine device and an insertion device for inserting the intrauterine device into a uterus. The system may also include a release thread releasably coupled with the intrauterine device. The intrauterine device may be deployable out of a distal end of the insertion device and may be configured to change from a delivery configuration when housed in the insertion device to a deployed configuration when deployed in a uterus. The retrieval thread and the optional release thread may be at least partially housed within the insertion device during insertion of the intrauterine device into the uterus. The release thread may extend from the intrauterine device through the insertion device to an attachment point at or near a proximal end of the insertion device.

Abstract: An enclosure or plenum that supports a looped pump tube is hingedly connected to a framed thin-walled heat exchange bag through which working fluid from an intravascular heat exchange catheter flows. The frame with bag can be inserted between cold plates to exchange heat with the working fluid flowing through the bag. With the framed bag between the plates, the looped pump tube from the enclosure or plenum is receivable in the raceway of a peristaltic pump, which pumps working fluid through the system.

Abstract: Device for packaging and dispensing drops of a substance for ophthalmic use, generally fluid, semi-fluid or in suspension, emulsion or oily solution, including a dispensing accessory with a first valve made of an elastomer material that allows the substance to pass through when the dispensing accessory is stressed, without allowing outside air to pass through in the opposite direction when the dispensing accessory is relaxed, characterized in that the first valve is covered by a layer of Parylene.

Abstract: An assembled blank may include a blank tip attached to a blank base, e.g., the blank tip may be welded to the blank base. The blank tip may be manufactured by modifying flat stock, e.g., tiers of blank tips may be manufactured by modifying tiers of flat stock. The blank tip may comprise a first forceps jaw, a second forceps jaw, and a blank tip aperture. The assembled blank may be disposed within a hypodermic tube and an actuation structure of a microsurgical instrument.

Abstract: Ocular fluid management systems and methods of operating the same. One ocular fluid management system includes a chamber, a diaphragm, a sensor, and a controller. The chamber includes a first portion and a second portion. The first portion is connected to an input line for receiving fluids into the first portion and an output line for discharging fluids from the first portion. The diaphragm is contained in the chamber and changes position based on a pressure difference between the first and second portions. The sensor detects a position of the diaphragm and transmits a signal based on the detected position. The controller is configured to receive the signal and control operation of at least one of a peristaltic pump and a vacuum pump based on the signal to maintain the diaphragm in a predetermined position.

Abstract: Patterned laser treatment of the retina is provided. A visible alignment pattern having at least two separated spots is projected onto the retina. By triggering a laser subsystem, doses of laser energy are automatically provided to at least two treatment locations coincident with the alignment spots. All of the doses of laser energy may be delivered in less than about 1 second, which is a typical eye fixation time. A scanner can be used to sequentially move an alignment beam from spot to spot on the retina and to move a treatment laser beam from location to location on the retina.

Abstract: Methods and systems for performing laser-assisted surgery on an eye form a layer of bubbles in the Berger's space of the eye to increase separation between the posterior portion of the lens capsule of the eye and the anterior hyaloid surface of the eye. A laser is used to form the layer of bubbles in the Berger's space. The increased separation between the posterior portion of the lens capsule and the anterior hyaloid surface can be used to facilitate subsequent incision of the posterior portion of the lens capsule with decreased risk of compromising the anterior hyaloid surface. For example, the layer of bubbles can be formed prior to performing a capsulotomy on the posterior portion of the lens capsule.

Abstract: The present invention provides methods and systems for an eye marker device that includes a handle having an interior cavity, a marking device coupled to the handle, and a rotational scale for providing a visual representation of the angle of the marking device relative to a predetermined origination point.

Abstract: A safety system includes safety glasses and an apparatus. The safety glasses include an electronic system having a sensor configured to detect when the safety glasses are worn by a user and a wireless communication device. The apparatus includes a body housing an electrical isolation device and a wireless communication device. The body includes a first end defining a female electrical socket, a second end defining a male electrical plug and a fastening device coupled to the body and configured to move from an open position to a closed position in which an electrical cord that is electrically coupled to the body at one of the first end or the second end is also physically secured to the body by the fastening device. The electrical isolation device is configured to prevent current flow in the line conductor included in the body when the safety glasses are not being worn by the user.

Abstract: Provided is a face protector provided with a transparent film sheet to protect a viewing window of any one working mask selected from a safety face shield or a welding helmet. One or more transparent film sheets are inserted into a gap between the surface of the upper part of the viewing window and the bent inner surface of an upper support brim and thus combined with the surface of the viewing window, thereby preventing contaminants, paints, slag or metal particles, which may contaminate the viewing window during a working process, from being attached to the viewing window, securing a worker's clear view to increase worker safety, and to greatly extending the working mask.

Abstract: Systems and methods can promote wound healing, including a wound dressing having a wound-facing surface and a second surface. The wound-facing surface can be configured to contact a wound of a patient. There can also be at least one conduit having an interior lumen operably connectable to the second surface of the wound dressing, a central window configured to allow air flow from the interior lumen of the conduit to the wound-facing surface of the wound dressing, and a flexible wrap operably connectable to the conduit.

Abstract: The present invention relates to a method for fabricating absorbent article having multiple layers, and deformed zones of targeted performance, and colored regions, the method comprising the steps of forming discrete features on at least one layer, printing colored regions on at least one layer, integrating multiple layers to form an absorbent assembly, and cutting the absorbent assembly into individual absorbent articles, wherein the steps are carried out continuously.

Abstract: A self-lubricating tampon applicator includes a barrel having opposed insertion and proximal end portions and having a continuous side wall that defines an interior area and a plurality of spaced apart apertures and proximate the insertion end portion. A tampon is positioned in the interior area of the barrel. A piercing member is positioned between the tampon and the plurality of apertures. A lubricant reservoir is positioned between the tampon and the plurality of piercing members. A plunger situated in the barrel engages a proximal end of the tampon and is slidable from a starter configuration extending from the proximal end portion of the barrel to a deployed configuration positioned inside the barrel. Pressure applied to the plunger pushes the tampon and the reservoir downstream and the reservoir is pierced by the piercing member, dispensing lubricant through the plurality of apertures onto an outer surface of the barrel.

Abstract: A moisture management apparatus monitors an area for moisture events and wirelessly transmits moisture-related information to one or more notification devices. An embodiment of the moisture management apparatus includes a substrate and one or more sensors supported by the substrate. The sensor(s) emit wireless signals indicative of the moisture-related information. A sensor event communication system forwards the sensor signals to another device, such as a notification device. The sensor event communication system may monitor other types of patient events. Portions of the moisture management apparatus and/or the moisture event communication system may be embodied in a patient support apparatus, such as a bed.

Abstract: Provided is a disposable urine-absorption pad with which production costs are reduced, and with which a function for inhibiting the occurrence or aggravation of bedsores is imparted by facilitating relative movement of a skin-contact sheet in a back-and-forth direction with respect to a pad main body. This urine-absorption pad includes: an outer surface sheet; an absorption body; an inner surface sheet; a left side sheet; a right side sheet; an overlap sheet; and a low friction member. The overlap sheet is provided to a gluteal region. A right side edge of the overlap sheet is joined to a left side part of the right side sheet. A left side edge of the overlap sheet is joined to a right side part of the left side sheet. The low friction member is provided between the overlap sheet and the inner surface sheet.

Abstract: An absorbent article comprising a pair of leg cuffs (32) with an raised section (34) and an absorbent core (28) comprising at least one channel (26, 26?) at least partially oriented in the longitudinal direction (80) of the article. The article has crotch width (Wd) before use as measured between the proximal edges of the leg cuffs at the level of the crotch point of from to 70 mm to 200 mm, and a Relative Crotch Width Reduction (RCWR) of at least 30 mm/kg.

Abstract: Sanitary product disposal containers include an invertible container body having first and second ends, the container body including a first container wall having a first container wall exterior surface; a second container wall carried by the first container wall, the second container wall having a second container wall exterior surface; an end container wall extending between the first container wall and the second container wall generally at the first end of the container body; a concave sanitary product cavity formed by and between the first container wall, the second container wall and the end container wall generally at the first end of the container body; a container opening formed by and between the first container wall and the second container wall generally at the second end of the container body; and a container seal carried by the first container wall exterior surface of the first container wall and the second container wall exterior surface of the second container wall generally at the second end

Abstract: A gown dispenser system has a plurality of gowns, each having a back region, the gowns folded and stacked back region facing up, such that, pulling on the back region of a gown on top of the stack removes that gown from the stack and exposes the back region of the next gown in the stack, an enclosure containing the stack of gowns, the enclosure having an opening exposing the back region of the gown at the top of the stack, enabling a user to grasp the exposed back region and pull the topmost gown from the enclosure, exposing the next gown in the stack, and an interface mechanism attached to the enclosure, enabling the enclosure to be suspended on a substantially vertical surface, with the opening facing outward from the substantially vertical surface. Gowns are drawn from the enclosure one-at-a-time, at need.

Abstract: A platform adapted to be attached to a piece of conveying equipment such as a gurney. The platform includes a base defining a cavity. The platform further includes a coupling receiver mounted on the top of the base. The coupling receiver receives a support structure of the conveying equipment and releasably secures the platform to the conveying equipment. A platform member is slideably received within the cavity and is moveable between extended and non-extended positions.

Abstract: A life assistance system includes an automatic liftable chair and an autonomous mobile robot connected to the automatic liftable chair via a network. The life assistance system assists a user in the action of standing up from the automatic liftable chair. The life assistance system is configured such that upon reception of a stand-up assist instruction by the autonomous mobile robot, the automatic liftable chair executes a first assisting action and that upon detection of a load applied to a handle of the autonomous mobile robot, the automatic liftable chair executes a second assisting action.

Abstract: Apparatus and methods for providing therapeutic treatment for symptoms associated with GERD and/or other digestive disorders and/or other medical conditions are described herein. In some embodiments, an apparatus includes a support element that has a first end portion and a second end portion and a top surface disposed at an angle relative to a bottom surface of the support element. The second end portion has a height greater than the first end portion. A riser element is configured to be coupled proximate to the second end portion of the support element. A body element is configured to be disposed on at least one of the support element or the riser element. The body element has a first arm and a second arm connected together by an arc portion.

Abstract: A bedpan system including an anatomically configured assembly, an inner liner, and at least one sensor positioned within said liner to actuate at least one device.

Abstract: A walking training system includes a walking assistance apparatus that is mounted on a leg portion of a user, and assists the user's walking, first pulling means for pulling at least one of the walking assistance apparatus and the leg portion of the user to a front side; and second pulling means for pulling at least one of the walking assistance apparatus and the leg portion of the user to a rear side. A pulling point of the walking assistance apparatus and/or the leg portion of the user, which is pulled by the first and second pulling means is provided to be movable around the leg portion of the user.

Abstract: Provided is a method and apparatus for setting a torque of a walking assistance apparatus. A rotation angle and a rotation angular velocity of the walking assistance apparatus may be measured to set the torque. An amount of torque to be set may be calculated based on the rotation angle and the rotation angular velocity of the walking assistance apparatus.

Abstract: A massaging apparatus includes a sheet attachable to skin, multiple skin condition sensors, and multiple massage elements. Each of the skin condition sensors included in the sheet detects skin condition near the skin condition sensor. Each of the massage elements which is included in the sheet and which is disposed at a position corresponding to that of a corresponding one of the skin condition sensors is operated based on the detection result obtained by the skin condition sensor.

Abstract: Embodiments of a multifunctional head massager are disclosed. The multifunctional head massages includes a helmet including a front shell and a rear shell, and a controller connected to the helmet. A blinder for massaging eyes is detachably connected to the front shell. In the present invention, the blinder is detachably connected to the front shell, so that the head massager has the eye massage function at the same time. When users do not want to massage their eyes, the blinder can be removed, and the head massage function is not affected.

Abstract: A sensory lounging chair system and method of use. The system generally includes a frame, a pump, air tubes connecting the pump to a pair of inflatable air tubes, pressure release valves, piping and hardware, a pressure sensor, and a fabric cover. In a preferred embodiment, the pump and pressure sensor are powered by a power supply connected to a terminal board, which in turn is connected to the pump and the pressure sensor. The fabric cover provides a comfortable barrier between the occupant and the air tubes, which initially are usually deflated or less than fully inflated. As the pressure in the air tubes increase, deep touch pressure is applied to the occupant's body in the places where the air tubes are in contact with the occupant. Deep touch pressure is thus applied to the occupant via contact with the tubes through the fabric cover.

Abstract: Embodiments of the present invention provide a massager device, system, and method. A massager is configured to communicate (directly or indirectly) a user feedback message to a target in response to a determination that an event has occurred. The massager may be a sexual aid. User feedback messages may be generated based on various pre-sets and/or user selections established to determine a message medium type, content for inclusion in the user feedback message, the target, the event, and other customizations. The content of the user feedback messages may be generated according to a content selection method, such as random, user-customized, pre-sets, categorical, or based on usage parameters, such as biometric, massager settings, and temporal data.

Abstract: Some adult devices are ostensibly marketed to improve female sexual experience female by offering exercises to address relaxed vaginal muscles from birth, age, surgery etc. and for reducing incontinence. However, such devices suffer from variable placement by the user both in terms of orientation and penetrative depth such that the “results” are not reproducible and captured data used to provide feedback to the user and/or providing visual/audible prompts is flawed. Accordingly, it would be beneficial to provide a device with reproducible placement and data for enhancing the usability/benefit of the exercise regimen. It would be further beneficial for the device to either provide this exercise regime as part of a wider assessment of sexual wellness or as part of a sexual stimulation activity thereby reducing the focus on “exercise” to derive the benefits of improved pelvic muscle control.

Abstract: An autonomous mechanical CPR device is disclosed having a CPR unit attached to a free-standing support assembly. In operation, a victim is placed in the support assembly such that the CPR unit can compress the victim's chest. The CPR device is preferably portable, and it provides the recommended depth of chest compression at the recommended rate.

Abstract: A chest compression device for cardiopulmonary resuscitation may include a support structure for placement about a patient's chest and for holding a chest compressor above a patient's sternum; a chest compressor mounted on the support structure; and lateral chest supports attached to the support structure at points laterally on either side of the chest when the device is in use, such that the lateral chest supports will apply lateral pressure to the sides of the chest synchronised with a chest compression by the chest compressor.

Abstract: The present invention provides a fluid injection system (11) which transitions between a maintenance mode wherein an outlet (15) is closed and no fluid is discharged through the outlet, and an operation mode, wherein the outlet is open and fluid is discharged through the outlet. The fluid injection system injects a first fluid transported in a first pipeline (21) with a second fluid, wherein there is a temperature differential between the first fluid and the second fluid. The fluid injection system comprises a holding tank (49) for storing the second fluid, a cooling means (35) to cool the second fluid, and a pump (39) for delivering the second fluid into the first pipeline.

Abstract: A container includes a dry concentrate designed such that the dry concentrate forms an acid liquid concentrate, or a part of an acid liquid concentrate, which is suitable for manufacturing a dialysis solution, on the dissolution of the dry concentrate in a liquid, preferably in water.

Abstract: A system includes a vial stabilizer base having a first body and a plurality of fingers projecting from the first body, with the plurality of fingers being annularly disposed about the first body, and a vial adapter having a second body and a plurality of arms projecting from the second body. The second body defines a passageway. The plurality of fingers of the vial stabilizer base defines a socket having a first seat configured to receive a vial and a second seat configured to receive the vial adapter.

Abstract: A container containing a concentrate for dialysis includes a pouch or cartridge containing a solid concentrate of constituents for the dialysis solution, the pouch or cartridge being closed by a connector having a filling channel extending completely through the connector, which is for filling the pouch or cartridge with the solid concentrate, means for introducing a solution-forming liquid into the pouch or cartridge and for extracting the solution obtained, these introduction and extraction means having at least one connecting portion for connecting them to a corresponding port of the dialysis machine. The filling channel is closed by a stopper which has a reservoir containing a second constituent or group of constituents for the dialysis solution, and means for producing an outlet opening in the reservoir contacting the inside of the reservoir with the side of the stopper located in the container.

Abstract: A vial access device, includes a body having a projecting annular skirt that is elastically deformable, for engaging a complementary shaped neck of a vial. A tubular spike extends coaxially within the annular skirt for introducing into the vial, and a tubular connector protrudes from the body on the side opposite to the annular skirt and in fluid communication with the tubular spike. The tubular spike and the annular skirt are arranged, respectively, within a first and a second part, distinct from each other, and of which the first part is permanently joined to the body and the second part is connectable to the first part through an irreversible coupling.

Abstract: A connection system for connecting a first medical device component to a second medical device component is disclosed. The connection system of the present disclosure provides for quick and intuitive coupling and decoupling of two opposing medical device components through the use of a connection path and a disconnection path, the connection path being distinct from the disconnection path. Furthermore, the connection system of the present disclosure provides audible and tactile connection feedback through the use of elastically deformable connection elements.