Abstract: Embodiments of an implantable device for delivering a therapeutic agent to a patient include a reservoir configured to contain a liquid comprising the therapeutic agent, and a cannula in fluid communication with the reservoir. The cannula is shaped to facilitate insertion thereof into a patient's eyeball.

Abstract: An ophthalmic shunt includes a seal or septum through which multiple injections of the therapeutic agent can be made as needed, thereby avoiding repeated injury to the sclera. The therapeutic agent is temporarily carried in a tube connected to the septum. The therapeutic agent release may be rapid or sustained over a period of time.

Abstract: A method for energy setting of pulsed, focused laser radiation is provided. In the method, a relationship between a threshold pulse energy required for causing irreversible damage in a material and a pulse duration is established. The relationship allows for obtaining a threshold pulse energy for each of a plurality of pulse durations, including one or more pulse durations in a range between 200 fs and smaller. The relationship defines a decreasing threshold pulse energy for a decreasing pulse duration in the range between 200 fs and smaller. For a given pulse duration in the range between 200 fs and smaller, an associated threshold pulse energy is determined based on the established relationship. The pulse energy of the laser radiation is set based on the determined associated threshold pulse energy.

Abstract: The present invention relates generally to providing pressurized infusion of liquids and, more particularly, is directed to providing a stable and pressurized flow of irrigation fluid to the eye during surgery.

Abstract: An intraocular shunt can be manufactured using a system that includes a liquid bath and a wire, which is moved through the bath. When moved through the bath, the wire is coated with a material, such as gelatin. For example, the liquid bath can have a top layer, including water, and a bottom layer, including gelatin. The coated wire passes through an aperture formed in a plate component of the system. The gelatin can be dried on the wire in a humidity-controlled space, thereby forming the shunt.

Abstract: An eye protective mask designed for the practice of outdoor sports, for example, includes an eye protective screen, a frame supporting the screen, and a comfort element affixed to the frame. The comfort element includes a nasal portion configured to come into contact with a portion of the user's nose, and a frontal portion configured to come into contact with a portion of the user's forehead. The material used for the nasal portion has different mechanical compression properties from the material used for the frontal portion, such that the maximum compression, or stroke, of the material of the nasal portion caused by a predetermined compressive force is greater than the compression of the material of the frontal portion caused by the same predetermined compressive force.

Abstract: A toroidal compression bandage includes: a soft fibrous material, defined by an absorbency of a predetermined amount; a compression bandage form comprised of soft fibrous absorbent material in a rolled, wrapped form and of a shape defined by a circle revolved in three-dimensional space about a circular axis coplanar with the circle, wherein the axis of revolution does not touch the rotated circle, to define a torus ring compression bandage; an aperture defined within a center area of the torus ring compression bandage as it is formed, the aperture having a predetermined diameter and configured for placement directly over a trauma wound to avoid contact with the trauma wound; and a compression surface defined on an underside of the torus ring compression bandage, the compression surface configured for circumferential placement around the trauma wound to avoid direct contact of the trauma wound, and for absorption placement around the trauma wound.

Abstract: A negative pressure wound dressing is provided. The negative pressure wound dressing sequentially includes a backing layer, a water blocking layer, an absorbent layer and a wound contacting layer. Wherein, the backing layer includes a connecting aperture for fluidly communicating to a negative pressure source. The wound contacting layer includes a surface layer for wound contacting and a plurality of chambers containing a medication, wherein openings of the chambers are disposed on the surface layer for releasing the medication contained in the chamber. The medication can be prevented from being suctioned to the absorbent layer and can be released toward the wound to enhance the wound healing by using the negative pressure wound dressing.

Abstract: A reduced-pressure, wound closure system is presented that generates a closing force on a surface wound and optionally provides reduced pressure to a body cavity or tissue site. The sealed contracting member, when placed under reduced pressure, generates the closing force. One illustrative system includes a first attachment member and a second attachment member, a sealed contracting member coupled to the first attachment member and the second attachment member, and wherein the closing force is generated between the first attachment member and the second attachment member when reduced pressure is supplied to the sealed contracting member. Other systems and methods are presented.

Abstract: Wound dressings and wound inserts comprising a porous film layer and at least a channel, wound inserts of forming wound inserts comprising a porous film layer and at least a channel, and wound-treatment wound inserts.

Abstract: Aspects of the methods and apparatuses relate to making elastic laminates, and more particularly, methods and apparatuses for applying elastic material in a curved path onto an advancing substrate. The elastic material may be in various forms, such as for example, elastic strands and/or ribbons. Apparatuses and methods disclosed herein may also provide for the application of viscous fluids, such as adhesives, in pre-determined patterns to the elastic material while being positioned on an advancing substrate.

Abstract: A method for in vitro testing of an absorbent article includes the steps of inserting the absorbent article into a radiolucent simulated body cavity, placing the radiolucent simulated body cavity into a radiolucent pressure chamber, placing the radiolucent pressure chamber into a radiological device, pressurizing the radiolucent pressure chamber to a predetermined pressure, providing test liquid through the test liquid port and to the absorbent article, acquiring data relating to the absorbent article and the test liquid via the radiological device and an associated computing device, and analyzing the acquired data. The radiological pressure chamber includes a simulated body cavity arranged and configured to accommodate the absorbent article, a test liquid port, and a pressure control system. The radiolucent test device has at least one radio scanning element rotatable about radiolucent test device support having the pressure chamber disposed thereon.

Abstract: The present invention relates to sensor signal analysis. It relates particularly, but not exclusively, to methods, systems and devices for monitoring and processing the sensor signals to determine automatically characteristics of events represented by the sensor signals. The present invention is particularly, but not exclusively, related to methods, systems and devices for monitoring moisture in absorbent articles such as diapers, incontinence garments, dressings and pads resulting from wetness events caused by, for example, urinary and/or faecal incontinence. In an embodiment, the invention includes a method for processing sensor signals representing an event in an absorbent article. The method comprises: receiving sensor signals from a sensor representing one or more events in an absorbent article; and processing the sensor signals to determine a characteristic of at least one event in the absorbent article.

Abstract: A disposable absorbent article comprising a first waist region, a second waist region, a crotch region disposed between the first waist region and second waist region; a first waist edge and a second waist edge; and a first longitudinal edge and a second longitudinal edge; the disposable absorbent article comprising a waistband and a leg gasketing system, wherein the waistband has a first gather count and the leg gasketing system has a second gather count such that the ratio of the first gather count to the second gather count is from about 0.75 to about 1.25.

Abstract: A disposable absorbent pant that includes a central chassis and a belt structure is disclosed herein.

Abstract: In an absorbent article a three-dimensional opening hole mesh sheet, having a face which faces skin of a wearer of the absorbent article and a reverse or opposite side face within the absorbent article, is combined with an absorber which includes an air-laid pulp non-woven fabric. The mesh sheet has an array of mechanically embossed concave portions forming protrusions on the skin-facing face of the mesh sheet and recesses on the reverse or opposite face, i.e., the unexposed face inside the absorbent article.

Abstract: An absorbent core assembly for use in a product for absorbing a liquid is disclosed. The core assembly has a first section and a second section. The first section is a quilted porous material that contains a slow acting but high absorption capacity SAP therein. The, second section is a quilted porous material that contains a fast acting but lower absorption capacity SAP therein. The first and second sections are in fluid communication with each other, whereupon a liquid which is exposed to the core assembly flows through the first section to the fast acting SAP in the second section to be absorbed quickly and rapidly by the fast acting SAP therein, while the slow acting SAP desorbs or takes liquid away from the fast acting SAP as well as absorbing the liquid itself to thereby trap the liquid in the core assembly.

Abstract: A rescue device includes at least two parallel columns defining a core section. The columns are located in a substantially flat plane with each column lying adjacent at least one other column. Each column includes rods, a connection device, and at least one sleeve. Each rod is located within a sleeve and the rods are connectable in series by the connection devices to form a column. The rescue device further includes at least one linking element. Each sleeve is connected to at least one linking element.

Abstract: Emergency vehicle patient transport systems are disclosed. In one embodiment, an emergency vehicle patient transport system includes: a loading passage providing access to an interior of an emergency vehicle; one or more tracks coupled to a floor of the emergency vehicle, a ceiling of the emergency vehicle, a wall of the emergency vehicle or combinations thereof wherein, a travel path is delineated by the one or more tracks; and a chair slidingly engaged with the one or more tracks, and vertically positioned between the floor and the ceiling. The chair locks in one or more set positions. And, the one or more set positions are selected from a group consisting of an airway care position, an extended airway care position, a procedural care position, a responder position, a patient care position, and a patient load position.

Abstract: A two-wheeled self-balancing wheelchair is provided, including: a housing having support brackets which are mounted directly below rotary shafts of the motors located at both sides of the bottom side of the housing, rotary shafts of the motors which are drawn out from the housing, and wheels which are mounted to the rotary shafts and rotate in a way as to read an inclination angle of a rider's body; a saddle frame which is mounted on the upper part of the housing; and multipoint supports mounted at the front and rear of the support brackets, each of the multipoint supports having a first hinge part and a second hinge part which are formed at the front ends of the multipoint support to be able to rotate by bolts and are connected with each other through a connection bar and a third hinge part.

Abstract: Electric locomotion means comprising a dynamically stabilised vehicle (10) comprising two wheels (11), said vehicle (10) having a transverse axis defined by an axis of rotation of said wheels (11) and a longitudinal axis that is perpendicular to said transverse axis and defines a direction of advancement of said vehicle (10), said vehicle comprising a pivot (24) arranged along said longitudinal axis and rotatable about said longitudinal axis, said pivot (24) being configured to transfer a steering control to said wheels (11); a seat (44) positioned on said vehicle; characterised in that said seat (44) is configured to accommodate a user affected by motor disability of the lower limbs, said seat (44) being tillable sideways by a lateral shift of the user's weight; said locomotion means further comprising transmission means (25) arranged between said seat (44) and said pivot (24), said transmission means (25) being configured to transfer a tilting movement of the seat (44) to said pivot (24).

Abstract: The present invention is provided with a support mechanism for an armrest part that includes a gas spring. The support mechanism supports the armrest part in a state of being able to change a posture between an ordinary posture and a forward-tilt posture when the gas spring is locked, and the support mechanism supports the armrest part so as to make the armrest part move with forming an arc from a sitting corresponding position to a standing corresponding position that is located at a forward upper position when the gas spring is unlocked. A gas spring switch part that does not obstruct the locked state of the gas spring when the armrest part is in the ordinary posture and that releases the locked state of the gas spring at a time when the armrest part is in the forward-tilt posture is arranged between the gas spring and the armrest part.

Abstract: Adjustable article of furniture comprising at least one adjustable element and furnished with an actuator system comprising at least one electrically driven linear actuator with an electrical motor and an electrical controller with an operation device, wherein the system in equipped with a battery pack for operating the system during mobile situations, where a mains supply is not readily available. The battery pack is equipped with a frontend, which allows for the battery pack to be retrofitted on existing actuator systems, without compromising the functionality of the actuator system in connection with charging of the battery. Moreover, the frontend is adapted to facilitate continued viewing of remaining power on the battery pack even though the technology of the battery pack is replaced, e.g. from lead battery to lithium ion battery.

Abstract: A mattress system is provided that is optimized for the hospital setting and includes a guiderail system that accepts a variety of accessories for attachment thereto. The guiderail system may have integrated data lines, power lines, gas lines, and/or fluid lines. Also provided are radioabsorbant shields, trays and other components designed for optimal use with the mattress system.

Abstract: A patient support including a base; a patient support surface supported by the base; an electrically powered device; a rechargeable power storage device for powering the electrically powered device; and a receiving coil electrically coupled to the rechargeable power supply for inductive coupling with a transmitting coil. The receiving coil is for recharging the rechargeable power supply when the receiving coil is inductively coupled to the transmitting coil.

Abstract: The present invention provides a topical oxygen therapy system for treating chronic non-healing wounds. The system is configured to be extremely portable, allowing patients to be completely ambulatory during treatment. The topical oxygen therapy system includes an oxygen source and a wound dressing capsule. The oxygen source includes a miniature compressed oxygen cylinder and a miniature pressure regulator that delivers oxygen through an outlet tube to the interior of the wound dressing capsule. The oxygen source may be attached directly to or integrated into the wound dressing capsule. Alternatively, the oxygen source and wound dressing capsule may be separate modules connected by a flexible tube.

Abstract: An incubator is provided that prevents damage to the arm of an operator when an arm abuts against the upper end segment of a baby guard relatively hard while inserting the arm into an infant accommodation space. The walls of the baby guards around the infant accommodation space have bent segments that are sufficiently strong to serve as a guard structure on the periphery of the infant accommodation space. Each of the bent segments in the upper end segments of the walls includes an inclined segment and a substantially horizontal segment integrally connected to a distal end of the inclined segment. At least some of the walls can pivot between upward and downward positions, thereby closing or revealing cassette trays.

Abstract: The present invention relates to devices and methods for exercising the lower limbs, in particular for exercising lower limbs. The devices are suitable for training the lower limbs of persons suffering from paraplegia or hemiplegia or musculoskeletal disorders in general. In some aspects, the present invention relates to powered articulated systems (ASs) and to the rehabilitation by aid of said ASs. The parallel or hybrid ASs of the invention are based on a parallel or hybrid, lambda-type framework and are controlled by a data processing unit. The ASs are preferably controlled by a closed-loop, real time control system.

Abstract: A portable human exoskeleton system (1) includes a pelvis module (10), a leg module (20) and a foot module (30). The pelvis module (10) includes a bendable member (11) and a pelvis module connector (12). The foot module (30) includes a foot module connector (33). The leg module (20) includes: a femur module (21) detachably coupled to the pelvis module connector (12); a tibia module (22) detachably coupled to the foot module connector (33); and a knee joint component (23) having at least two linkages with different lengths wherein each linkage is pivotally coupled to the femur module (21) and the tibia module (22). Weight above the hip of the user is exerted on the pelvis module (10), and transferred to the leg module (20) and the foot module (30). The exoskeleton system is easily disassembled and carried, and can be worn inside attire without affecting appearance of the user.

Abstract: A walking assistance device configured to permit the independent movement of an individual via simulated weight reduction is described. The device is configured to partially suspend a portion of a user's weight via a suspension system, facilitating the movement of a user with experiencing difficulty walking without assistance. The suspension system of the device preferably employs at least one cable in communication with a pulley system, an electric lifting actuator, and a harness. The harness of the device is configured to affix to the legs and torso of the user, and connects to at least one cable of the pulley system via at least one hook. The lifting actuator engages the pulley system, enabling the user to control the percentage of weight lifted. A frame houses the suspension system of the device, and is configured to move laterally via wheels on the bottom of the frame of the device.

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: A sensory upright chair system to provide deep touch pressure to a person and method of use. The system includes a frame, a pump, a pair of inflatable air tubes, a pressure release valve, hoses and hardware, a pressure sensor, and a fabric cover. The pump and pressure sensor are connected to a power supply, and connected to the air tubes and pressure release valve via hoses and hardware. Switching on the power supply provides controlled inflation to the air tubes. A user sits in the chair between deflated air tubes. As the pressure in the air tubes increase, deep touch pressure is applied to the occupant's body where the air tubes contact the occupant. The fabric cover provides a comfortable barrier between the occupant and the air tubes. Deep touch pressure is thus applied to the occupant via contact with the tubes through the fabric cover.

Abstract: The disclosure relates to a system including a processor configured to generate stimulation control signals in response to a detection of a respiratory disorder. The system further includes at least one kinesthetic effector with a vibrating electromechanical transducer applied to a site on a patient's skin for delivering a kinesthetic stimulation energy determined by the control signals. The processor is further configured to determine the effectiveness of a stimulation by detecting a disappearance of the respiratory disorder. The processor is further configured to determine a therapy by selecting a stimulation strategy among several stimulation strategies according to a type of expected or detected disorder.

Abstract: The disclosure relates to a system including a processor configured to generate stimulation control signals in response to a detection of a respiratory disorder. The system further includes at least one kinesthetic effector with a vibrating electromechanical transducer applied to a site on a patient's skin for delivering a kinesthetic stimulation energy determined by the control signals. The processor is further configured to determine the effectiveness of a stimulation by detecting a cessation of the respiratory disorder. The processor is further configured to extend the stimulation control signals for a determined duration following the cessation of the respiratory disorder.

Abstract: The disclosure relates to a device including a processor configured to detect a respiratory disorder episode and generate kinesthetic stimulation control signals in response to the detection of a respiratory disorder episode. The device further includes at least one kinesthetic effector adapted to be applied to a patient's outer skin site and includes a vibrating electromechanical transducer capable of receiving stimulation control signals and outputting a kinesthetic stimulation energy determined by the stimulation control signals. The processor is further configured to determine the effectiveness of stimulation by detecting a cessation of the respiratory disorder episode. The processor is further configured to determine a stimulation energy by selecting an initial energy value and varying the energy value as a function of the effectiveness of previous stimulation.

Abstract: A heating and cooling mat assembly includes a mat having a bottom wall, a top wall and a perimeter wall. A conduit is positioned in the man and has fluid therein. A pump is in fluid communication with the conduit to pump the fluid through the conduit. A heat emitter is thermal communication with the liquid in the conduit. The heat emitter warms the liquid when the heat emitter is turned on. A cartridge is removably couplable to the mat. The cartridge includes a pair of first ports. The conduit is in fluid communication with a pair of second ports. Each of the first ports is removably coupled to one of the second ports to fluidly couple the conduit to the cartridge. The cartridge is fillable with a cold fluid so that the conduit is cooled when the pump is turned on and the cartridge is coupled to the conduit.

Abstract: A sound treatment system includes an audio system for transmitting tones of predetermined frequencies through a plurality of outputs. A sound transmitting device is electrically connectable to one or more of the outputs, and includes a speaker for transmitting the tones received. The speaker is adjacent to crystal which is vibrationally responsive to the tones. A method of using the system includes generating tonal segments of predetermined duration, modulating the frequencies, and compiling these into an audio program. One or more sound transmitting devices are placed on desired locations of the body, and their inputs connected to corresponding outputs of the audio system. The generating step includes compiling selected predetermined frequencies into an audio program to generate the tonal segments, as well as modulating tones of one or more desired frequencies to generate the tonal segments.

Abstract: A vibratory massage roller is provided for therapeutic massage, intimate massage, physical therapy, yoga, physical conditioning, and general well-being. The massage roller and method for balancing the massage roller, increasing the overall utility and therapeutic value so as to more efficiently massage a subject through resort to a vibrational roller having a tubular casing containing a motor housed in the center of the tubular casing, a central axle projecting from the motor, a plurality of eccentric propellers, positioned at different points along the central axle, the tubular casing vibrationally linked to the axle by the plurality of eccentric propellers via a plurality of housing supports and an optional surface casing extending over a length of the vibratory roller.

Abstract: A device, system and method for increasing air intake by a subject is described. The device includes a vibration motor and a control unit for controlling vibrational motion output by the vibration motor. The methods include positioning the vibration motor on one or more limbs of a subject, and stimulating nerves in the limbs via the generated vibrational motion, whereby the stimulated nerve signals the brain to increase breathing rate or air intake by the subject. Accordingly, the device of the present invention activates nerve fibers that carry kinesthetic cues from the limbs in a pattern that simulates normal limb motion, and thus triggers inherent reflexes that increase ventilation in response to such motion.

Abstract: A system for improving cardiac output of a patient suffering from pulseless electrical activity or shock and yet displays myocardial wall motion including: a sensor to detect myocardial activity to determine the presence of residual left ventricular pump function having a contraction or ejection phase and a filling or relaxation phase, a device to prompt the application of or apply a compressive force repeatedly applied to the chest based on the sensed myocardial activity such that the compressive force is applied during at least some of the ejection phases and is ceased during at least some of the relaxation phases to permit residual cardiac filling, thereby enhancing cardiac output and organ perfusion.

Abstract: Apparatus for applying pressure, heat, cold or accu-pressure to a limb, comprises band members, at least a portion of which are elastic. A tab element, at least a portion of which is stiff and plastic, forms a catch for receiving and holding various treatment modalities. A shield, at least a portion of which is thin, flexible and smooth, prevents the user from becoming uncomfortable during treatment. A safety tab, at least a portion of which is stiff and plastic prevents the apparatus from coming undone, and thereby facilitates securement of the armband around the affected area. A pocket element receives various treatment modalities. A rectangular frame, at least a portion of which is stiff and plastic, connects band members and forms a cuff-like apparatus.

Abstract: A device is provided for storing, organizing, and accessing prescription pills that comprises a pill tray and tray lid engaged in a slidable configuration. The pill tray possesses upward protrusions on opposing ends of its flat base, while the tray lid possesses linear channels on opposing ends of its flat body. With the tray lid placed over the pill tray, the channels of the lid meet the protrusions of the tray to engage in a male/female sliding configuration. The pill tray contains an array of pill chambers that is covered and uncovered by sliding the tray lid along this channel configuration. The pills are placed within the pill chambers of the pill tray, and viewable through holes found on the tray lid once it has covered the pill tray. Each viewing hole corresponds to a pill chamber.

Abstract: Methods and apparatuses are disclosed with regard to syringe-transfer of a solution or other fluid within a carpule. One embodiment includes an apparatus that is a non-standard carpule barrel having a top portion, a bottom portion, and a barrel portion therebetween. The top portion includes an opening for receiving a syringe plunger and at least a first portion of a connection mechanism for connecting to an upper portion of the syringe. The bottom portion includes another opening capable of holding a bottom end of the carpule, wherein the carpule may be a standard carpule or a non-standard carpule. The barrel portion is located between the top portion and bottom portion, wherein the barrel portion includes a cradle, and wherein the cradle has a length capable of holding a standard carpule or a non-standard carpule and a width greater than the standard carpule.

Abstract: A pouch for mixing and dispensing a composition including a pouch body and a port body. The pouch body includes opposing, first and second major flexible walls sealed to one another along respective peripheries thereof to define an internal chamber and a pouch perimeter. The pouch body has a C-like shape. The port body projects from the first wall and is fluidly open to the internal chamber. With this configuration, various components, such as a powder component and a liquid component, can be mixed by a user's hand(s) in pressing the walls in a kneading fashion, with the resultant composition being dispensed through the port body. In some embodiments, the pouch is provided to a user with a powder component pre-loaded in the internal chamber.

Abstract: There is provided a method for handling a medicinal agent container that allows reduction of the time and effort of an operator handling the medicinal agent container. The method for handling a medicinal agent container includes the steps of: setting a container in a container holding body capable of holding a plurality of containers, the container being capable of being filled with a medicinal agent; filling the medicinal agent of interest into the container held by the container holding body; sealing the container; and wrapping the container held by the container holding body and the container holding body into one package.

Abstract: A transfer device for filing a fluid reservoir of a fluid infusion device with a fluid is provided. The transfer device comprises a first end to couple to a source of the fluid, and a second end to couple to a pressurizing device. The transfer device also comprises a body interconnecting the first end and the second end, and having an end to couple to the fluid reservoir.

Abstract: Devices, systems and methods for automatically positioning a syringe in a target orientation suitable for withdrawing medication from a container, and for filling the syringe with the medication. The device comprises a syringe conveyor, which is configured to receive the syringe in an initial orientation, and to bring the syringe to a target orientation by being translated and rotated while holding the syringe in a steady orientation relative to the syringe conveyor. The device further comprises a supporting module, configured to support the syringe conveyor while allowing a translation and a rotation thereof. The device comprises a syringe holder configured to hold the syringe, and a gripper coupled to the syringe holder.

Abstract: A device is provided for storing, organizing, and dispensing prescription pills that comprises a clamshell container configured to house a sealable pill tray and sliding card. The pill tray contains an array of pill chambers that are covered by an adhesive seal composed of foil or paper. The clamshell container comprises a top portion and a bottom portion, the top portion having an array of pill holes that correspond with the chambers of the pill tray. The top of the sliding card has markings corresponding to the pill chambers beneath it and slides over the pill tray and beneath the top portion of the clam shell. Pills are placed within the pill holes on top of the sliding card. When the sliding card is removed, the pills fall through the pill holes and into the pill chambers of the pill tray.

Abstract: A prescription drug monitoring/dispensing device ensures prescription medication housed within is taken only as directed, and not abused or sold on the streets. The device serves as an intricately guarded casing that may only dispense the preprogrammed dosage amounts at preset times, as directed by a prescribing physician. The device may include a housing having a biometric finger scanner and a display screen in communication therewith, a loading tube capable of holding a pill therein, a rotating hub in communication with the loading tube, a rotating disc in communication with the loading tube, and an exit port capable of dispensing the pill out from the housing.

Abstract: Automated medication dispensing devices, kits, systems, methods, and related applications thereof, such as using computer readable (e.g., NFC [near field communication], or QR) standards for monitoring and verifying patient and caregiver activities and health related data-information. The medication dispensing device includes: a housing having a sliding mechanism configured to receive, hold, and release a removably slidable medication holder containing a plurality of individual medication holding compartments. The medication holder for dispensing medication includes: a receptacle (as either a disposable blister pack, or a reusable medication tray) containing a plurality of individual medication holding compartments, and having one side configured with one or more outward facing holes or an outward facing external handle to facilitate removably sliding the medication holder into and out of a medication dispensing device.