Abstract: An apparatus for delivering therapeutic agent to an eye comprises a body, a cannula, a hollow needle, a cannula actuation assembly, and a needle actuation assembly. The cannula extends distally from the body and is sized and configured to be insertable between a choroid and a sclera of a patient's eye. The cannula actuation assembly is operable to actuate the cannula relative to the body. The needle actuation assembly is operable to actuate the needle relative to the cannula. The cannula may be inserted through a sclerotomy to position a distal end of the cannula at a posterior region of the eye, between the choroid and sclera. The needle may be advanced through the choroid to deliver the therapeutic agent adjacent to the potential space between the neurosensory retina and the retinal pigment epithelium layer, adjacent to the area of geographic atrophy.

Abstract: A system and method of treating hyperactivity of an eyelid closing muscle in a subject includes providing a stimulation system in the subject with the hyperactivity of the eyelid closing muscle, sensing an activity of the eyelid closing muscle, and selectively stimulating eyelid opening muscle(s) or innervating nerves, eyelid opening reflexes, or eyelid opening reflexes in non-muscular tissue, using the stimulation system, without substantially activating the eyelid closing muscle. The system and method evokes eyelid movement in the subject.

Abstract: Eliminating leaks of molded fluid channels by providing a front housing, rear housing, and a gasket, wherein the front housing has one or more molded fluid channels and one or more seal channels, and wherein at least a portion of the gasket is located between the front and rear housing; molding the gasket onto the rear housing to create a single unit, wherein the gasket has one or more seal lips configured and dimensioned to couple with the one or more seal channels; and assembling the front housing to the rear housing having the gasket, wherein the one or more seal lips couple with the seal channels. A surgical cassette manifold having a front and rear housing, and a gasket therebetween. The front housing having molded fluid channels that mate with the gasket and the gasket having multiple valves and a sensor/diaphragm accessible through the rear housing.

Abstract: A surgical ophthalmic intra ocular access tool comprising a platform having a walled structure with central space(s), that is placed on the surface of the eye; a set or more of track(s) with entry and exit port(s) travelling within the wall(s) at a certain angle and length; a needle hub receiver(s) that allows universal attachment of any injecting device(s) with an opening to the bottom of the surgical ophthalmic intra ocular access tool; a projecting marker(s) on one or more sides; a set of repeated projections from the underside of the surgical ophthalmic intra ocular access tool to facilitate gripping to the eye tissue underneath; a rail like system outlining the inner as well as the outer walls, allowing multiple accessory(s) to be attached to either rail to facilitate surgical intervention(s) and predesigned holes at lower edge of said surgical ophthalmic intra ocular access tool in contact with eye wall(s) allowing for suturing in order to obtain secure attachment(s) or augmented wall(s) support.

Abstract: Methods and systems for automatically pulsing different aspiration levels to an ocular probe are disclosed. The probe may be a phacoemulsification probe. A first aspiration level, supplied by a first pump, may be applied to the probe simultaneously with ultrasonic energy. A second aspiration level, supplied by a second pump, may be automatically switched from the first aspiration level, and applied to the probe in a pulsed manner.

Abstract: A system for conducting a vitrectomy includes: a gas source; a vitrector including a cutting mechanism that opens and closes according to a pressure at the vitrector; and a pulse-generating system receiving gas from the gas source and generating pulses at the vitrector. The pulses cause the pressure at the vitrector to vary according to a cycle, and the varying pressure at the vitrector causes the cutting mechanism of the vitrector to open and close. At a first time in the cycle, the pulse-generating system, raises the pressure at the vitrector to a maximum pressure. At a second time in the cycle, the pulse-generating system reduces the pressure at the vitrector to a minimum pressure that is greater than ambient, the pressure at the vitrector being maintained at least at the minimum pressure. The difference between the maximum pressure and minimum pressure is minimized to reduce gas consumption.

Abstract: The present invention provides for a deformable, insertable device for relieving intraocular pressure comprising a body portion composed of a biocompatible porous material with pores throughout to permit drainage of fluid from the anterior chamber to the scleral tissue without collapse of the anterior chamber. The invention also includes a method for inserting the device into the eye and for using ultrasound intraoperatively to determine the position of surgical tools and devices within the sclera. The invention also includes a device excising sclera in an eye to create a chamber for insertion of the insertable device into the eye.

Abstract: A method for treating glaucoma with an implantable glaucoma device includes inserting a hollow elongated needle into the eye between the cornea and iris and into the anterior chamber of the eye to form a needle tract in the eye, introducing a distal end of a guidewire through the needle and into the anterior chamber, introducing a snare through a corneal incision into the anterior chamber. The snare has a sheath and a hook or loop inside the sheath and extendible therefrom. The method includes capturing a segment of the guidewire proximate the distal end of the guidewire with the snare within the anterior chamber, removing the needle from over the guidewire outside of the eye, coupling a glaucoma drainage device to a proximal end of the guidewire that extends outside of the eye, and pulling on the captured guidewire segment with the snare to pull the glaucoma drainage device into the needle tract and into the anterior chamber of the eye until the glaucoma device is located in an implanted position in the eye.

Abstract: An ophthalmic phototherapy device and associated treatment methods to expose an eye to selected multi-wavelengths of light to promote the healing of damaged or diseased eye tissue. The device includes a housing having an interior; an eyepiece disposed on the housing and configured and arranged for placement of an eye of the patient adjacent the eyepiece; a first light source producing a first light beam having a first therapeutic wavelength and disposed within the housing; a second light source producing a second light beam having a second therapeutic wavelength and disposed within the housing, where the second therapeutic wavelength differs from the first therapeutic wavelength by at least 25 nm.

Abstract: A fiducial is generated on an internal anatomical structure of the eye of a patient with a surgical laser. A tonic artificial intraocular lens (IOL) is positioned so that a marker of the tonic IOL is in a predetermined positional relationship relative to the fiducial. This positioning aligns the tonic IOL with the astigmatic or other axis of the eye. The toric IOL is then implanted in the eye of the patient with high accuracy.

Abstract: A method and a system for detecting a movement of a surface on an irradiated sample involves a light source for irradiating the surface with a coherent light beam, a detector for detecting variations caused by the movement in a speckle pattern produced by reflections of the light beam at the surface, selecting a single speckle from the speckle pattern, and detecting the variations at the selected speckle.

Abstract: A system and process for treating retinal diseases includes passing a plurality of radiant beams, i.e., laser light beams, through an optical lens or mask to optically shape the beams. The shaped beams are applied to at least a portion of the retina. Due to the selected parameters of the beams—pulse length, power and duty cycle—the beams can be applied to substantially the entire retina, including the fovea, without damaging retinal or foveal tissue, while still attaining the benefits of retinal phototherapy or photostimulation.

Abstract: An ophthalmic laser treatment system and method providing for a liquid optical interface (LOI) with a patient eye surface (PES) using an elliptical ocular suction ring (OSR) is disclosed. A disposable ocular patient interface (OPI) provides for simultaneous differential vacuum mating of the PES, OSR, OPI, and an optical window retainer (OWR). The PES, OSR, OPI, and OWR form an enclosed volume in which liquid may be interjected to cover the PES during laser treatment. A vacuum suction pump (VSP) provides controlled vacuum to the OPI ensuring proper differential vacuum mating (DVM) between the PES, OSR, OPI, and OWR during laser treatment. The OWR connects to a laser objective bracket (LOB) via an ocular force sensor (OFS) and an optical separator bracket (OSB). The OFS senses applied pressure to the PES and provides data to a computerized control device (CCD) that limits applied pressure to the PES during laser treatment.

Abstract: A tympanostomy tube delivery device comprises a shaft assembly, a pressure equalization tube, and a sensor. The shaft assembly comprises a cannula and a pusher operable to translate relative to the cannula. The pressure equalization tube is positioned within the shaft assembly. The pusher is operable to drive the pressure equalization tube out of the shaft assembly. The sensor is operable to detect a physical parameter associated with engagement between the distal end of the shaft assembly and a tympanic membrane. A controller may activate a feedback device to inform an operator that the distal end of the shaft assembly has achieved suitable apposition with the tympanic membrane, based on information from the sensor.

Abstract: An ear cleaning device is provided for removing debris from an ear. In one form, the ear cleaning device includes a shaft, a head connected to the shaft, and a contiguous pocket structure of the head. The contiguous pocket structure includes a plurality of pockets that may be configured to receive debris. In another form, the ear cleaning device has a handle, a bulbous cleaner connected to the handle, and a solid inner core of the bulbous cleaner. The bulbous cleaner has two or more spaced, longitudinal walls disposed outward of the inner core that are configured to remove debris with turning of the ear cleaning device about a longitudinal axis of the device.

Abstract: In one example embodiment, a dressing connector is described that provides a first fluid path between a first connector and a second connector, and a second fluid path between a third connector and a fourth connector. A liquid barrier may be disposed in the first fluid path. The first fluid path and the second fluid path are generally exposed to an exterior surface of the dressing connector. In some embodiments, a tube may also be bonded to the third connector to provide a third fluid path between the dressing connector and another component. In more particular embodiments, the liquid barrier may be a filter, such as a hydrophobic bacterial filter, a sintered polymer filter, and/or a charcoal filter.

Abstract: A binder layer for a laminated wound dressing is brought into contact with a sheet coated with a pattern-coated adhesive sheet. As the binder layer is in contact with the pattern-coated adhesive sheet, a series of closed-loop cuts are made in the binder layer. The closed-loop cuts are made in such a way that the material enclosed by each closed loop is substantially physically separated from the remainder of the binder layer. Then the binder layer is moved away from the pattern-coated adhesive sheet, so that the binder layer and the pattern-coated adhesive sheet are no longer in contact. When the binder layer and the pattern-coated adhesive sheet are moved apart, the material enclosed in the closed-loop cuts—i.e., the cut waste fragments—are retained on the pattern-coated adhesive sheet, ensuring that the binder layer includes a series of cleared perforations.

Abstract: A medical compression garment is provided including a midline opening cut in a medial segment of the elastic garment, dividing its front fabric portion into first and second sections. Fasteners, such as hook-and-loop fasteners, are attached to the first and second sections which connect together to close the opening. Pulls may be included. To don the garment, a wearer places their legs into the garment and pulls the garment along the legs until its top is aligned with the groin. The wearer then inverts and pulls the first and second sections of the garment together and fastens them to close the opening. Afterwards, the wearer pulls up the garment until it reaches the waist. When the wearer subsequently wants to take off the garment, the wearer unfastens the first and second sections and pull the garment down from the waist. The garment thus facilitates the donning and removal process.

Abstract: Methods and apparatuses for manufacturing multiple different articles are provided. One apparatus embodiment includes a first intravaginal article assembly module; a second intravaginal article assembly module; and an applicator module capable of receiving and handling applicators suitable for both first intravaginal articles from the first intravaginal article assembly module and second intravaginal articles from the second intravaginal article assembly module. The apparatus only operates with one of the first intravaginal article assembly module and the second intravaginal article assembly module at one time. The first intravaginal articles are absorbent articles and the second intravaginal articles are non-absorbent articles.

Abstract: An absorbent article including features facilitating toilet training of a wearer is provided. The article includes at least a first appearing graphic that changes from an initial, less visible state to a subsequent, more visible state in the absence of wetness, thereby to provide positive encouragement to a child during toilet training. The appearing graphic becomes less visible if subjected to liquid. A wetness sensation member may also be provided to give tactile, negative sensation to the child, thereby giving feedback received by at least two different senses. Additionally or alternatively, a second appearing graphic, different from the first appearing graphic, may be provided to increase a child's interest in the toilet training process. The first and second appearing graphics may become visible at different times, thereby providing a sequential or spaced reveal of the image.

Abstract: The present invention relates to a method and system for aseptically filling of flexible packages containing dry cloth. Such a method may include a first stage that is performed in a non-sterile environment. The first stage may include cutting a first substantially dry cloth to a predetermined size; inserting the first cloth into a flexible package; sealing a first end of the flexible package; and sterilizing the flexible package. The method may also include a second stage performed in a sterile environment. The second stage may include filling the flexible package with a medical solution such that the substantially dry cloth absorbs at least a portion of the medical solution; and sealing the an open end of the flexible package.

Abstract: A bed is provided. The bed may include a lift system which raises and lowers a support deck of the bed. The lift system may include multiple individually actuatable lift systems. The bed may include a powered bed mover system.

Abstract: A movable sanitary station for use with a hospital bed includes a cabinet with a front side, a back side, a right side, a left side, a bottom and a top. The back side of the cabinet has a concave shape forming a semi-cylindrical cavity having an axis extending laterally along the back side of the cabinet, permitting a mattress of the bed to protrude forward into the semi-cylindrical cavity. The top extends over the mattress of the bed to cover a gap between a foot of the mattress and the back side of the cabinet. The movable sanitary station also includes a set of wheels for supporting and moving the cabinet and a toilet seat integrated in a central portion of the top of the cabinet and surrounding a first aperture formed through the top of the cabinet.

Abstract: A body weight support system includes a trolley, a powered conductor operatively coupled to a power supply, and a patient attachment mechanism. The trolley can include a drive system, a control system, and a patient support system. The drive system is movably coupled to a support rail. At least a portion of the control system is physically and electrically coupled to the powered conductor. The patient support mechanism is at least temporarily coupled to the patient attachment mechanism. The control system can control at least a portion of the patient support mechanism based at least in part on a force applied to the patient attachment mechanism.

Abstract: A mobile chamber apparatus includes a support structure of inflatable support members, and a chamber assembly. The inflatable support members may include transverse and upright sections. The chamber assembly may include a top wall, a bottom wall, and one or more side walls. Connectors may detachably couple the support structure and the chamber assembly. Installed, the support structure supports the chamber assembly to enclose an interior space. Inlets may deliver a supply airflow to the interior space, and outlets may deliver a return airflow from the interior space. An environmental control unit may deliver the supply airflow and receive the return airflow. At least one mechanism may be provided for introducing an allergen into the interior space. Human patients may be exposed to the allergen in the interior space, and therefore the mobile chamber apparatus may be used for clinical trials to study allergy response.

Abstract: The present invention provides an incubator hood having a hydrophilized portion on at least a part of its inner surface, the hydrophilized portion containing a hydrophilic polymer and an antibacterial agent, and a surface of the hydrophilized portion having a water contact angle of up to 30°, and also provides an incubator having the incubator hood as well as a hydrophilic sheet and a hydrophilic antibacterial film for use in forming the hydrophilized portion on the incubator hood. Thus the present invention provides an incubator hood, an incubator, a hydrophilic sheet and a hydrophilic antibacterial film that have excellent antifogging properties and antibacterial properties and can suppress the growth of bacteria.

Abstract: An arrangement for the neuropostural and sensorial suspension of the premature newborn in incubators, comprising a support for receiving the newborn and connected to an actuator, such that the support is suspended inside the incubator compartment, surrounding the premature newborn so that the newborn is kept in a position similar to that in which it was in the uterus thus allowing its harmonious intrauterine development.

Abstract: A transport and storage system, for servicing of a number of treatment and care areas in a hospital, is provided. The system connects each treatment and care area to a first transport route reserved for transport of clean goods to or from the treatment and care area, and a second transport route reserved for transport of non-clean goods to or from the treatment and care area, the first and second transport routes being separated. In the system, a partition is provided between the transport routes and the treatment and care areas, with a lock gate being included in the partition. The transport routes include a conveyor to containers, with the conveyor being connected to the lock gate and the containers having a container brim enclosable by an opening in the lock gate.

Abstract: A patient support apparatus for spinal conditions comprising a knee support 10,12, a patient torso support 32,60 for supporting a patient in the kneeling position, means 32 for supporting a patient's torso in a range of inclinations below horizontal in order to cause a mass of the patient's torso to tension the spine. The torso support 32,60 is supported by a radius arm 50 that is pivoted below the torso support 32,60, is free to swivel about a fixed joint 52 located forward of, and below the level of, the knee support 10,12, and is inclined upwardly forwardly towards a ring pad support 60 for a patient's head.

Abstract: A headrest adjustment system includes a tension block having a threaded aperture extending entirely through the tension block. The tension block is configured to be coupled to a chair. The headrest adjustment system also includes a screw configured to be moved through the threaded aperture along an axis, and a clamp lever pivotally coupled to the tension block. The clamp lever has an inclined surface. The axis intersects the inclined surface at an oblique angle. The headrest adjustment system also includes a headrest tension bracket configured to be coupled to the chair. The headrest tension bracket has a first end and a second end and the second end includes a flange. The clamp lever is configured to contact and press against the flange upon movement of the screw.

Abstract: The present invention relates to a method for treating inflammatory symptoms associated with plantar fasciitis in a foot. The method involves stretching gastrocnemius and soleus muscles associated with the foot by placing the sole of the foot on an inclined ramp surface and cooling at least one portion of the sole of the foot. The method may further involve providing localized pressure to at least one portion of the plantar fascia, and to a portion of the foot below the toes, to cause dorsiflexion thereof.

Abstract: According to an aspect of the present invention, it is possible to implement a joint assembly operating similar to a user's actual ankle joint. An ankle joint included in a walking assistant robot is pivotable around a rotation axis located outside the ankle joint.

Abstract: An electric walking aid and control method thereof are disclosed. A location of the electric walking aid, and a distance between the electric walking aid and the user, are dynamically controlled and adjusted to provide the user with static and dynamic support function, so as to support the user under static and dynamic situation of interaction between walk and stand, during the walking training process.

Abstract: A treatment device for medical and/or cosmetic therapy includes a negative-pressure chamber receiving a lower half of a person's body. The negative-pressure chamber is designed as a tube and has an admission opening sealed off from the person's body by a closure element. A first part of a table is arranged in the interior of the negative-pressure chamber. A second part of the table is arranged outside the negative-pressure chamber. The first part and the second part are each guided longitudinally on a linear guide. The first part can be moved at least partially out of the negative-pressure chamber and the second part can be moved away from the admission opening. A synchronization between the first part and the second part allows the first and second parts to be moved at the same speed in the same direction.

Abstract: A compression device controller for use with a compression garment includes a pressurized fluid source (e.g., a pump), a manifold in fluid communication with the pressurized fluid source, a pressure sensor in communication with the manifold, at least two bladder ports, and at least two two-way valves. The pressure sensor is arranged to measure a signal representative of pressure in the manifold. Each bladder port is connectable in fluid communication to a respective inflatable bladder of the compression garment. Each two-way valve is in fluid communication with the manifold and with a respective bladder port. Each two-way valve is actuatable to control fluid communication between the manifold and the respective bladder port.

Abstract: A portable system for preventing Deep Vein Thrombosis (DVT) in hospitalized patients through a pair of successively pressurized leggings designed to assist in the return of venous blood from the legs to the heart.

Abstract: A system and apparatus for promoting perfusion at a tissue site containing a sprain by applying a vacuum to intact skin extending over or surrounding the tissue site. The system and apparatus comprise a manifold formed from a porous material and configured to be disposed proximate the intact skin for distributing vacuum to the intact skin, and a sleeve adapted to cover the manifold and form a chamber containing the manifold to seal the manifold within the chamber between the sleeve and the intact skin. The system and apparatus further comprise a fluid coupling member adapted to deliver vacuum to the manifold for distribution to the intact skin. A method for applying vacuum to the intact skin of a tissue site is also disclosed and described herein.

Abstract: A massage device includes a device housing, with an electromechanical arrangement arranged in the housing for generating mechanical vibrations, along with an electronic controller arranged in the housing for activating the arrangement for generating mechanical vibrations, and with a power source, connected to the arrangement for generating mechanical vibrations and the electronic controller. The arrangement for generating mechanical vibrations includes at least one coil element and at least one ferromagnetic core arranged parallel or coaxial with the coil element and movably guided parallel to a cylinder axis, characterized in that the at least one ferromagnetic core has a mass m1, the mass ratio m1:m2 of which to the total mass m2 of the massage device is in the range from 1:100 to 1:3.

Abstract: Systems and methods for providing network connectivity and remote monitoring, optimization, and control of pool/spa equipment are provided. “Internet-of-Things” (IoT) functionality is provided for pool and spa equipment in a flexible and cost-effective manner. Network connectivity and remote monitoring/control of pool and spa equipment is provided by various components such as a network communication and local control subsystem installed in pool/spa equipment, and other components. Also disclosed are various control processes (“pool logic”) which can be embodied as software code installed in any of the various embodiments of the present disclosure.

Abstract: A soaking basin is provided having a magnetic jet assembly positioned to provide a therapeutic liquid circulation within the basin. The magnetic jet includes an impeller assembly and a drive assembly. The impeller assembly operatively coupled to the magnetic drive assembly only via magnetic attraction, such that a basin wall and a disposable liner are disposed between the impeller assembly and the magnetic drive assembly.

Abstract: A spa is provided that includes: a basin; a motor having a shaft defining a rotation axis; a hub mounted to the shaft, the hub having North and South pole domains spaced apart from each other and arranged to encircle the rotation axis in alternating relation; and an impeller which is disposed in the basin in axially spaced relation to the hub and is at least substantially constrained against movement but for rotation about the axis, the impeller including a rotor body of a non-magnetic, electrically-conductive material having relatively low magnetic permeability. The improvement in which is that there are lights and coils coupled to the impeller for rotation therewith, the lights and coils being coupled and adapted such that, in use, the rotating magnetic fields associated with the drive hub created induced currents in the coils which actuate the lights and create a net force that rotates the impeller.

Abstract: An acupuncture device can include a frame, an enclosure disposed on the frame to protect the frame, multiple stimulators mounted on the frame. The stimulators can be electrically coupled with a controller that transmits electric pulses to the stimulators for electro-acupuncture purpose. The size of the frame is adjustable to fit different body sizes of the users. The stimulators can be carried by the adjustment of the frame. The acupuncture device can also include one or more position references and the stimulators are positioned at relative distances from the position references. When the size of the frame is adjusted, the stimulators are carried by the frame to new positions that are at relative distances from the position references in proportionality with the extent of adjustment of the frame. Hence, the relative distance between a stimulator and a position reference in light of the size of the frame is maintained.

Abstract: An acupressure apparatus includes a tub configured to receive the user's feet for acupressure treatment, an acupressure station having a pair of designated foot placing areas for facilitating accurate positioning of the feet on the acupressure station, a plurality of upward projections formed on an upper surface of the acupressure station, and a plurality of watering holes formed around the projections, and a water supply conduit connected to the bottom wall of the tub for supplying compressed water by operation of a water pump. The watering holes formed in the acupressure station are directed to acupressure points of the feet such that the compressed water delivered through the watering holes provides acupressure stimulations to the acupressure points of the feet.

Abstract: A wearable medical container is provided. The wearable medicinal container has a plurality of spaced apart medicament cavities, each separately securable through its own snap-lock configured cavity lid. The plurality of spaced apart medicament cavities may be housed in an enclosure of a container base, which itself may be closed off by a container lid movable between the closed position and an open position for accessing the plurality of spaced apart medicament cavities. Each medicament cavity contains a single medicament dosage, preventing it from being damaged, while making it accessible. Being wearable through an association with a strap, the wearable medical container is useful for urgent critical medicinal administration.

Abstract: Fluid containers having a volume marking(s) and conductive element(s) disposed at the volume marking(s) and a common conductive element are provided. For example, the fluid container has a wall forming the volume. The conductive element(s) and the common conductive element have a portion disposed within the volume and a portion external to the volume. The container further has a RFID tag, where the conductive element(s) and the common conductive element are connected thereto via respective conductive wires. A fluid detection system having the fluid containers is also provided. The system comprises one or more containers and a patient site monitor having a RF reader that interrogates the RFID tag at a preset interval. Responsive to the signal, the tag supplies a predetermined current to the conductive element and the common conductive element and detects a voltage and generates an alert based on the same.

Abstract: A system includes a vial access device including a vial access housing having a wall defining an elongate opening between an opening proximal end and an opening distal end, the vial access housing including a spike and a vial connection element attachable to a first vial defining a first vial size to secure the vial access device to the first vial, and an adapter movable within the elongate opening of the vial access housing. The adapter is transitionable between a first position where the adapter is adjacent the opening distal end of the vial access housing and the adapter is attachable to a second vial defining a second vial size and a second position where the adapter is adjacent the opening proximal end of the vial access housing and the vial connection element of the vial access device is attachable to the first vial.

Abstract: A cap system for sealing injectable drugs within a vial is disclosed. The system includes an elastomeric stopper, a retainer member, a locking member, a cap assembly and a piercing member. The retainer member is arranged to snap onto the vial and the locking member slid with respect to the retainer member to permanently seal the vial. The cap assembly includes a cap and a band and is coupled to the locking member. The cap releasably holds the piercing member. The band is arranged to be removed to enable the cap to move the piercing member to penetrate the stopper, whereupon the cap can be removed. The piercing member is arranged to be connected to a syringe or other instrument to withdraw the vial's contents.

Abstract: A system for storing and dispensing discrete doses of pharmaceuticals includes: a housing with an internal cavity having a front wall with first and second windows; multiple storage locations positioned within the housing; and a carrier assembly positioned and movable within the housing. The carrier assembly is configured to receive a pharmaceutical dose package loaded into either the first or second window and convey the pharmaceutical dose package to one of the storage locations for storage therein, and is further configured to retrieve a pharmaceutical dose package from one of the storage locations and return the pharmaceutical dose package to the first or second window for dispensing therefrom.

Abstract: A flow control apparatus adapted for a feeding set includes a housing capable of receiving at least a portion of the feeding set, a pumping device for acting on the feeding set to produce fluid flow in the feeding set for delivery of fluid. The apparatus has a sensor arranged with respect to the pumping device to produce a signal indicative of a rotational position of a rotor, and a control circuit in communication with the sensor and in communication with the pumping device. The control circuit controls operation of the motor at a first output to rotate the rotor to produce fluid flow in the feeding set and at a second output effectively less than the first output, the control circuit monitoring the sensor signal during operation of the motor at the second output to determine occlusion in the feeding set.

Abstract: A method of forming a stabilized calcium phosphate moiety for use in dental or biomedical applications includes providing a solution or dispersion including a calcium salt and reacting an organic phosphate having a polymerizable methacrylate or vinyl group with the solution or dispersion in order to form the calcium phosphate moiety having at least one pendant polymerizable group and at least one organic functional group, which may be the same group. A polymerizable composite system having a stabilized calcium phosphate formed according to the method is also provided.