Abstract: Methods and apparatuses are disclosed for the diagnosis and removal of the devitalized and/or dead cell material formed in the lid margin to attempt to restore a normal lid margin. In this manner, the devitalized and/or dead cell material are removed or the amount present is reduced or no longer present to prevent, reduce, or affect the transport of lipid secreted by the meibomian glands to the tear film to reduce evaporative dry eye and improve dry eye conditions in patients. The diagnosis and removal of devitalized and/or dead cell material may be performed at desired intervals. Patients that suffer from conditions that block meibomian gland orifices, partial, infrequent, or inhibited blinking resulting in reduced lipid secretions from meibomian glands, and/or blockages in meibomian gland channels reducing secretion of lipids through the meibomian gland orifices may require more frequent diagnosis and treatment to remove devitalized and/or dead cell material.

Abstract: Glaucoma can be treated by implanting an intraocular shunt into the eye. Such procedures can employ various deployment devices, shunts, and implantation techniques. A method for treating glaucoma can include positioning an intraocular shunt in eye tissue such that the shunt conducts fluid from the anterior chamber to the suprachoroidal space and delivers a pharmaceutical or biological agent to the eye.

Abstract: Surgical assemblies for ocular surgery are provided. Such assemblies include direct measuring devices of intraocular pressure, surgical accessories utilisable in conjunction with a surgical instrument suitable for performing eye surgery, such surgical accessories being insertable in an ocular cavity through an accessory ocular incision. Direct measuring devices of intraocular pressure may be coupled to the surgical accessories so as to be insertable in the ocular cavity along with said surgical accessories through said accessory ocular incision.

Abstract: A method of laser eye surgery including linking retinal vessel architecture to corneal topography. This enables registration of the steep axis of the cornea in order to orient a toric intraocular lens, and/or to place astigmatic keratotomy incisions. First, a detailed pre-operative retinal image of the vasculature of the retina is obtained. In addition, a pre-operative image of the topography of the eye is obtained. The retinal image is then correlated or superimposed on the topography image to provide a reference. After the patient lies down under the laser eye surgery system, and during the surgery, the retinal vasculature is monitored which provides a reference to the surgery system about the topography of the eye. This process enables registration of the steep axis of the cornea in order to orient a toric intraocular lens and/or to place astigmatic keratotomy incisions.

Abstract: An ophthalmic surgical laser system and method for forming a lenticule in a subject's eye using “fast-scan-slow-sweep” scanning scheme. A high frequency scanner forms a fast scan line, which is placed by the XY and Z scanners at a location tangential to a parallel of latitude of the surface of the lenticule. The XY and Z scanners then move the scan line in a slow sweep trajectory along a meridian of longitude of the surface of the lenticule in one sweep. Multiple sweeps are performed along different meridians to form the entire lenticule surface, and a prism is used to change the orientation of the scan line of the high frequency scanner between successive sweeps. In each sweep, the sweeping speed along the meridian is variable, being the slowest at the edge of the lenticule and the fastest near the apex.

Abstract: A system and method for increasing the amplitude of accommodation and/or changing the refractive power and/or enabling the removal of the clear or cataractous lens material of a natural crystalline lens is provided. Generally, the system comprises a laser, optics for delivering the laser beam and a control system for delivering the laser beam to the lens in a particular pattern. There is further provided a device for determining the shape and position of the lens with respect to the laser. There is yet further provided a method and system for delivering a laser beam in the lens of the eye in a predetermined shot pattern that utilize as series of shots that form a shell cut, a partial shell cut, a laser suture cut and/or a volumetric shaped removal, which essentially following the shape of a suture layer of the lens.

Abstract: An apparatus includes a rigid body, a flexible sealing element, a nozzle assembly, and an electrode. The rigid body defines a channel, a reservoir, and a vent path. The reservoir is in fluid communication with the channel. The vent path is in fluid communication with the reservoir. The reservoir is configured to provide spacing between the channel and the vent path. The sealing element is positioned distal to the rigid body. The nozzle assembly includes a nozzle head and a post. The post extends distally through the channel of the rigid body. The nozzle head projects distally from a distal end of the post. The electrode is disposed within the channel of the rigid body. The reservoir extends laterally from a longitudinal axis defined by the electrode.

Abstract: A sound or thermal baffling device comprising an enclosure containing a variable density fluid and a force generating means for preserving and creating the structure and form of the enclosure, the shape and composition of the enclosure crafted to vary the baffling characteristics of the enclosure, and a further embodiment showing how a cellular material containing a variable density fluid may be created and used, and a still further embodiment showing improvements to ear protectors and head phone sets, including latching means for attaching these and other devices to the ears and head. Various applications involving previous as well as new uses are set out, including a description of how dynamic sound baffling may be implemented.

Abstract: An apparatus for cleansing wounds in which irrigant fluid from a reservoir connected to a conformable wound dressing and wound exudate from the dressing are recirculated by a device for moving fluid through a flow path which passes through the dressing and a means for fluid cleansing and back to the dressing. The cleansing means (which may be a single-phase, e.g. microfiltration, system or a two-phase, e.g. dialytic system) removes materials deleterious to wound healing, and the cleansed fluid, still containing materials that are beneficial in promoting wound healing, is returned to the wound bed. The dressing and a method of treatment using the apparatus.

Abstract: An apparatus comprising a support wrap. The support wrap including at least an upper portion, the upper portion of said the support wrap having a first side extending along a first direction by a first length, the upper portion of said the support wrap having a second side extending along a second direction by a second length, the upper portion of said the support wrap having a third side extending along a third direction by a third length, the first direction is in a different direction than the second direction, the first direction is in a different direction than the third direction, the first length being greater than the second length, the first length being greater than the third length, the upper portion including a first upper fastening member, and said first upper fastening member capable of fastening said first side to said second side.

Abstract: The present disclosure includes methods and systems to generate compression garment fit information from 3D images taken of one or more body parts of a patient indicated for application of compression therapy. The body parts can include legs or arms or other areas. Three-dimensional (“3D”) imaging information can be used to derive compression garment fit information, where the shape description information includes for each body part: tissue compressibility information, outer circumference information, and length information. Comparisons between corresponding body parts on a person can also be conducted.

Abstract: A closable compression garment comprises a first end, a second end, and a main body. The first end contains an opening sized and shaped to receive a lower extremity such as a foot, ankle, or leg within an interior portion. The main body contains a closure system which allows for the compression garment to traverse between a first insertion/removal position and a second closed position.

Abstract: A nonwoven fabric layered body, including: an elastic nonwoven fabric; and an extensible spunbond nonwoven fabric that is disposed on at least one surface side of the elastic nonwoven fabric and that has a degree of maximum load elongation of 50% or more in at least one direction, the nonwoven fabric layered body satisfying the following (1) and (2). (1) The elastic nonwoven fabric includes a resin composition containing a specific low-crystalline polypropylene, and an ?-olefin copolymer A containing an ethylene-derived constitutional unit and a propylene-derived constitutional unit, and having a melting point of 100° C. or more and a crystallization degree of 15% or less. (2) The resin composition contains from 5 parts by mass to 50 parts by mass of the ?-olefin copolymer A with respect to 100 parts by mass of the resin composition.

Abstract: Biodegradable facial pads for exfoliation purposes are disclosed. The facial pad includes a top layer and a bottom layer made of a hydro-entangled, non-woven fibrous material. A coarse fabric material that may have undulations to provide exfoliating effect is sandwiched between the top layer and the bottom layer. The coarse fabric layer is configured to provide stiffness to the pads so as to aid and facilitate exfoliation. The top layer, bottom layer and the coarse material layer are pinched together along the edges to form an exfoliating pad of specified weight. The top layer is configured to overlay the coarse fabric layer to incorporate the undulations in the coarse fabric layer. This may form exfoliating peaks and absorbent cotton valleys that are suitable for removal of dead cells from the skin when used for exfoliating purposes.

Abstract: A reusable shield and liner for use by a woman during menstruation is disclosed. The liner has a predetermined shape and comprises two or more layers. The predetermined shape can be an octagon, a circle, or an oral. The shield contains one water-resistant layer.

Abstract: A method of manufacturing an absorbent web includes moving a foraminous member in a machine direction. The foraminous member has at least one masking plate with a partitioned area including at least one partition defining a plurality of segments. The method further includes drawing air through the foraminous member and depositing fibrous material onto the foraminous member to form an absorbent web. The absorbent web has a bridged area with a reduced basis weight corresponding to the partitioned area of the masking plate. The bridged area has vertical interfaces separating web segments and fibrous material at least partly bridging the vertical interfaces.

Abstract: The unit for feeding lateral flaps of a hygiene absorbent article having: an input conveyor of a first continuous strip; a cutting assembly provided with a receiving drum, of the first suction-pick up heads that hold the lateral flaps and which are mounted to as to be radially movable on the receiving drum, and at least one blade which cyclically cuts the first strip crosswise; a spacer assembly having a pair of spacer drums provided with second suction-pick up heads that receive the lateral flaps of the receiving drum; and an actuator system, which cyclically moves each first suction-pick up head radially between a radial pick-up position and a radial release position, in the area of an output station.

Abstract: A disposable absorbent pant having a front belt portion and a rear belt portion is disclosed. The front and rear belt portions are joined at side seams and the rear belt portion has a greater length than the front belt portion. A lower edge of the rear belt portion forms at least in part edges of left and right leg openings to the rear of the side seams. The rear belt portion includes first and second layers of nonwoven web material sandwiching a plurality of laterally extending and laterally pre-strained elastic strands, disposed below the side seams. A first of the plurality of elastic strands differs from a second of the plurality of elastic strands by one or more of amount of pre-strain, tensile modulus, decitex, and combinations thereof.

Abstract: An absorbent article includes two planar liquid permeable topsheet layers with a first topsheet layer suspended from the longitudinal ends of the second topsheet layer. The first topsheet layer is of shorter length than the second topsheet layer such that the relaxed absorbent article includes a curvature along its length. The first topsheet layer defines a central opening and two end openings which allow for air circulation through the article and also for the second topsheet layer to be seen through the openings in the first topsheet layer. While the first topsheet layer is at least extensible, it is desirably elastic.

Abstract: A stretchable structure of an absorbent article includes a stretchable region and a non-stretchable region. A laminate of a first sheet layer, second sheet layer, and elastic film between the first and second sheet layers extends over the stretchable and non-stretchable regions. The first and second sheet layers are bonded to each other at a large number of dot-like joints via through holes formed in the elastic film stretched along the surfaces of the first and second sheet layers in a stretchable direction. The dot-like joints are arrayed at intervals in the stretchable direction and a direction perpendicular to the stretchable direction. An end of the stretchable region adjacent to the non-stretchable region is a buffer stretchable section. The area rate of dot-like joints in the buffer stretchable section is larger than the area rate of dot-like joints in the main section not including the buffer stretchable section.

Abstract: An absorbent core for absorbent articles such as diapers comprising a core wrap comprising a top side and a bottom side, an absorbent material between the top side and the bottom side of the core wrap, a first and second longitudinally-extending channel-forming areas disposed on opposite sides of the longitudinal axis and substantially free of absorbent material preferably through which the top side of the core wrap is preferably attached to the bottom side of the core wrap. The core has a central absorbent zone between the first and the second channel-forming areas and a first and second lateral absorbent zones disposed laterally outwardly. The basis weight of the absorbent material in the central absorbent zone is higher than the basis weight of the absorbent material in each of the lateral absorbent zones for at least a first transversal section (S1). This relation is inverted along a second transversal section (S2) of the core.

Abstract: An evaluation method of a wearing state of a disposable diaper including an elastic region in a waist portion or leg-surrounding portions, the evaluation method including: an evaluation image acquiring process in which a terminal including a photographing function acquires an image including at least a part of the elastic region as an evaluation image in the wearing state of the disposable diaper; and an evaluation process of evaluating the wearing state of the disposable diaper based on a degree of deformation of the evaluation image.

Abstract: A wheelchair includes a lower assembly including a lower frame having wheels rotatably mounted thereto, an upper assembly including an upper frame supporting a seat, a backrest and at least one movable armrest, and a lift mechanism configured to move the upper assembly relative to the lower assembly between a lowered position and a raised position, wherein a user can move sideways out of the seat in the raised position with the movable armrest lowered.

Abstract: The present disclosure illustrates a motorized mount with a plurality of degrees of freedom coupled to a seating system. The motorized mount assembly can include an attachment assembly configured to attach to a seating assembly. A vertical control assembly can be connected to the attachment assembly with an arm having a first end attached to vertical control assembly by a first hinge. A mounting assembly can be attached to a second end of the arm. The mounting assembly can configured to receive a personal computing device. A linear actuator may be attached to the vertical control assembly to raise and lower the arm and mounting assembly. A first motor can be configured to attach to the arm. A second motor can be configured to attach between the arm and the mounting assembly.

Abstract: There is provided a patient support that may be adjustable in height, width, length or a combination thereof. The patient support may be useable with normal sized patients or with bariatric patients. The patient support has a variety of features to enhance operability and/or functionality, including a width adjustable caster frame, width adjustable deck portions, a width adjustable headboard and an extendible foot board to provide extra length. An enhanced lift mechanism can accommodate bariatric patients and alternative functionality in achieving deck positions improves patient comfort. Various parts of the patient support including deck panels and the footboard may be removed and replaced with ease without complicated connectors.

Abstract: A user module for a patient support is provided. The user module is coupled to a patient support barrier, such as a siderail or a footboard.

Abstract: Embodiments disclosed include devices for increasing bed mobility. A mobility strap apparatus includes a bed-strap; a fastening end coupled to the bed-strap; and a hand-grip coupled to the top surface of the bed-strap. Rigid affixing of the bed-strap to a bed provides stable support to users when moving or stabilizing oneself on a bed. A mobility strap grid provides a bed-strap configured to be longitudinally aligned with a bed; a bed-strap configured to be laterally aligned with the bed, intersecting and substantially perpendicular to the longitudinally aligned bed-strap; a fastening end coupled to a bed-strap; and a hand-grip coupled to the top surface of a bed-strap.

Abstract: A low cost, disposable bio-secure environment to temporarily hold, and where required to transport, patients who are suspected of having an infectious or contagious disease requiring contact, droplet and/or respiratory isolation precautions. The described Environmental Unit's unique design provides a unit that is disposable and relatively inexpensive. The frame is designed to integrate and adapt to various hospital stretchers and beds. The unit is large enough for a patient to sit up and allows movement of arms and legs and the ability to eat and drink while isolated on a bed.

Abstract: An expandable plate configured to expand and to hold, move and maintain a body part in a specific position as needed in orthopedic surgery. The expandable plate has a bed with a guide assembly formed in a top surface configured to fit to cavity assembly of a track so as to slide in relation thereto. A carriage unit can be positioned on the track to hold a body part in a specific position, whereby when an additional linear dimension is required for a surgical procedure, the track can be expanded to extend the body part to the predetermined position using the same positioner device.

Abstract: The present solution is generally directed to a patient positioning system used to position body parts, such as a knee, during a medical or surgical procedure. Further, the present solution is generally directed to a system and method for establishing and tracking virtual boundaries, and controlling a patient positioning system to adjust those virtual boundaries to facilitate an automated surgery procedure. Further, the present solution is generally directed to the synergistic combination of an autonomous patient positioning sub-system with a robotic surgical manipulator sub-system.

Abstract: A surgical boot mount for mounting a surgical boot to a support rod of a limb holder, the surgical boot mount comprising: a projection having a first section and a second section, wherein the first section is attached to the sole of the surgical boot, wherein the first section comprises a first diameter and the second section comprises a second diameter, and further wherein the second diameter is larger than the first diameter; and a releasable locking mechanism mounted to the support rod of the limb holder, wherein the releasable locking mechanism comprises a first key comprising a first keyway and a second key comprising a second keyway, wherein the second key is slidably connected to the first key, wherein the first key is biased away from the second key, wherein the first keyway and the second keyway overlap to form an opening at least as large as the second diameter when an inwardly-directed force is applied to the first key so as to overcome the bias, and further wherein the opening is reduced to a size

Abstract: A patient support apparatus includes a base, a seat supported by the base and a backrest pivotable between an upright position and a reclined position. In one embodiment, a backrest support member is coupled to the backrest and is adapted to move between a stowed position in which the backrest support member does not support the backrest and a deployed position in which the backrest support member does support the backrest. Movement to the deployed position occurs in response to activation of an emergency control. In other embodiments, the base includes a portion that moves into an extended position underneath the backrest when the backrest is in the reclined position. Movement of the base portion to the extended position also occurs in response to activation of an emergency control.

Abstract: A novel technique for the fabrication of a casket dome lid from, for example, Smooth-One-Side (“S1S”) hardboard is disclosed. The invention is also directed to the fabrication of a casket lid which has a domed configuration both in the lateral and longitudinal directions of the lid. The method comprises the steps of providing a lid blank having a first end, second end, and a central region; providing a pair of diagonal voids oriented at corners of the first end of said blank and extending inward toward the central region; placing the lid blank in a vacuum fixture; and flexing the lid blank into a domed configuration via the vacuum fixture, such that the blank is domed in both a longitudinal and a transverse direction.

Abstract: Disclosed is a reciprocating-hit treatment instrument including a body having a reciprocating mechanism, wherein the body includes a main handle portion at the lower portion, a sub-handle portion at the upper portion, a base portion extruding from one side of the connection portion between the main handle portion and the sub-handle portion on the body, a reciprocating rod with the front end extending out from the base portion while the rear end fixedly connected with the reciprocating mechanism and able to perform a reciprocating motion in the direction of its own length under the driven by the reciprocating mechanism, and a treatment ball connected with the front end of the reciprocating rod; the main handle portion, the sub-handle portion, and the base portion are integrally connected, and the main handle portion and the sub-handle portion are connected with each other in the shape of a bar.

Abstract: A Sleep Board Solution. The sleep system assembly has five key benefits: First: providing a solid foundation which aligns the hips, shoulders, back and neck naturally while sleeping. Second: providing a completely unique engineered and manufactured multi-layered foam support system that applies a mild constant traction to the spine and back during the sleep cycle stretching the discs and vertebra to enhance blood flow and promote natural healing during the sleep cycle. The third benefit is that it provides maximum sleeping comfort while totally eliminating any discomfort from the “bottoming out” of hips, shoulders, elbows or knees through the multilayered foam against the solid foundation. In adapting the system, an individual's specific needs/issues are first analyzed in order to optimize the system features for that individual.

Abstract: The described knee rehabilitation device can include any suitable component. In some implementations, however, it includes a sitting surface that is configured to support a user; a knee arm that comprises a leg coupling mechanism, that is pivotally coupled to the rehabilitation device, and that is configured to pivot through a range of motion; and a drive mechanism that is configured to force the knee arm through the range of motion. In some cases, the drive mechanism includes a first hard stop that prevents the knee arm from extending past a first set point, and the drive mechanism further includes a second hard stop that prevents the knee arm from being retracted past a second set point. In some cases, the device is further configured to be programmed to electronically limit the knee arm's range of motion. Other implementations are discussed.

Abstract: An elevating walker chair that allows both riding and walking. The chair elevates by a parallelogram power unit. The seat transforms between a saddle and seat upon changes in saddle/seat elevation. Also a lifting parallelogram power unit structure. Disclosed is an elevating walker chair for people with limited mobility resulting from compromised musculature, coordination or balance, or for able bodied individuals that must perform tasks for which assistance is desired.

Abstract: A medical drape for use with a reduced pressure system for providing reduced pressure to a tissue site is described. In some embodiments, the drape may include a flexible film, and an adhesive layer coupled to the flexible film. The adhesive layer may include a first adhesive disposed on a first portion of the flexible film in a first pattern. The first adhesive can be configured to secure the flexible film proximate to the tissue site. The adhesive layer generally includes a second adhesive disposed on a second portion of the flexible film in a second pattern. The second adhesive can be configured to seal the flexible film proximate to the tissue site. The first pattern and the second pattern are preferably registered so that the first portion and the second portion are offset to cover substantially different portions of the flexible film.

Abstract: A legs and feet massage apparatus for providing massaging effects to the legs and feet of a user includes a leg and feet frame and a legs and feet massage roller assembly. In one embodiment of an aspect of the invention, the legs and feet frame may include guide rails. Each guide rail includes an upper end, a lower end, an upper section, a lower section, a connecting section, and a guide channel. The roller assembly includes sets of massage roller devices that are spaced apart and that are rotated by a motor. The massage roller devices are moved along the guide channels by the motor whereby the massage roller devices move along the guide channels while also are adapted to provide massaging effects to the feet and legs of the user. In another aspect of the invention, a massage chair includes a legs and feet massage apparatus.

Abstract: A self-massage roller having a bottle, a covering, and, optionally, a removable cap. The bottle provides a vessel for holding liquids. The covering includes a base layer and a plurality of nubs. The base layer overlays the outer surface of the bottle. Each nub in the plurality of nubs protrudes from the base layer in a direction radially away from the outer surface of the bottle. Each nub is a massage element, and the plurality of nubs forms a textured surface for myofascial release of certain muscles of the user. In another version, each nub is attached directly to the outer surface of the bottle without an intervening base layer. In versions with a cap, the cap may include a flip-up spout, or it may have a plunger valve that opens upon pulling the plunger outward and closes upon pushing in the plunger.

Abstract: Methods and devices are described which allow sound waves to be safely be applied to the eyelid of an eye of a patient or through the eyelid to other structures in the eye or to or through structures in the facial region to effect changes to one or more structures in and around the eye or directly through the cornea or sclera to regions of the eye to treat one or more diseases of the eye.

Abstract: A system for use during administration of cardiopulmonary resuscitation (CPR) chest compressions on a victim is described. The system includes a chest compression monitor that includes a motion sensor configured to generate signals indicative of the victim's chest motion and a control system communicatively coupled to the chest compression monitor and configured to receive the generated signals, detect compression waveform features representative of the chest compressions based on the received signals, compare the features to a pre-determined criterion that distinguishes between a manual source of the chest compressions and a piston-based chest compression device source, determine whether the source of the chest compressions is the manual or the piston-based chest compression device source based on the comparison, and generate an output based on whether the source of the chest compressions is determined to be the manual or the piston-based chest compression device source.

Abstract: A portfolio for organizing and managing the storage, access and administration of prescription and/or over-the-counter medications. The portfolio that includes various storage mechanism, holders and tools that can be used for managing a patient's medications. The portfolio includes sensors to detect when medication containers are being accessed and display devices to present status information pertaining to the medication containers installed within the portfolio.

Abstract: A lockable container for securing items or objects, the container including a first element, which may include a cylindrical member and a retainer for capturing two or more rotatable rings on the cylindrical member, and a second element, which is mateable with the first element, cooperating with the rings to close an open end of the cylindrical member of the first element.

Abstract: The invention provides, in some aspects, a container system for medical solutions such as peritoneal dialysis (PD) solutions. The invention particularly features a system which includes a first compartment that contains a first medical solution, e.g., a PD osmotic agent, and a second compartment that contains a second medical solution, e.g., a PD buffer agent. The compartments maintain their respective contents separately from one another for purposes of transport, storage and/or sterilization. However, the compartments are fluidly couplable, so that their respective contents can be combined with one another, e.g., following sterilization of the agents and prior to their introduction into the patient's abdomen. To that end, a container system can include a diffuser that is disposed in a fluid pathway between the first and second compartments, e.g., to facilitate homogeneous mixing of the first and second PD agents.

Abstract: Disclosed is an infusion accessory capable of detecting infusion liquid parameters, which is a lid body, comprising a first portion provided with one or more detecting members and a second portion having one or more liquid channels. Relative position changes may occur between the first portion and the second portion, the liquid channels and the detecting members may be switched between an open position and a closed position as position changes occur between the first portion and the second portion, the open position enables communication between the liquid channels and the detecting members so that liquid in the liquid channels may flow into the detecting members, the close position enables sealing between the liquid channels and the detecting members so that the liquid in the liquid channels cannot flow into the detecting members and the liquid that already flows into the detecting members cannot return to the liquid channels.

Abstract: A carousel configured to house a plurality of pump cartridges for a compounder system is provided. The carousel may include a plurality of cartridge pockets each having an extended portion that covers a portion of a cartridge and a bottom surface having an extension with a recess. The bottom surface recess of each cartridge pocket may be shaped and sized to receive a needle housing of a pump cartridge in the cartridge pocket. A recess may be provided in the extended portion of each pocket that receives a protrusion that extends from a top surface of a backpack coupled to the pump cartridge to secure the pump cartridge in the cartridge pocket. The bottom surface recess may have an additional bottom surface that prevents actuation of the needle housing of the pump cartridge.

Abstract: The current disclosure is directed to a container with a dispensing schedule and, in various described implementations, to a container and a complementary cap that includes a dispensing schedule. During each dispensing cycle, which includes removing the cap from the container to allow access to the contents of the container and re-securing the cap to the container, the display schedule is automatically advanced to a next indication. In one implementation, the container is a bottle with a threaded neck and the cap is complementarily threaded and has a cylindrical rim and a schedule display. An indication on or within the schedule display is displayed through an aperture in the cap rim. Features included in the cap and the schedule display interoperate to ensure that the displayed indication is advanced to a next indication when the cap is unscrewed from, and subsequently threaded onto, the bottle.

Abstract: The present invention relates to a feeding system (1) for infants comprising a bottle (2) for storing and releasing a fluid, at least one sensor (10, 20, 30) arranged in or at the bottle (2) for measuring one or more bottle parameters, a data processing unit (12, 22, 32) for processing the measured bottle parameters to generate an advice related to at least one bottle parameter, and an indicator (13, 23, 33) for issuing said advice to a user of the feeding system (1).

Abstract: The liquid-dispensing pacifier comprises a nipple, a fluid dispenser, and a guard. The guard prevents the liquid-dispensing pacifier from being swallowed by the baby. The nipple is shaped to resemble a female human teat and provides one or more apertures through which a fluid may exit the nipple from a chamber within the nipple. As non-limiting examples, the fluid may be breast milk or formula. The fluid is introduced into the nipple from the fluid dispenser. The fluid dispenser may be a reservoir or syringe that is coupled to the nipple. Fluid may travel from the reservoir to the chamber in the nipple via a valve or feeding tube. The valve may be opened by sucking action of the baby. The syringe may inject fluid into the chamber through one or more apertures, values, or tubes.