Abstract: To provide a simple embodiment of a rotor (2) for a fluid pump which is nevertheless very flexible in handling and compressible, in accordance with the invention a conveying blade is provided having at least two arms (12, 13, 14) and a membrane spanned between them hi the expanded state, wherein the struts each have at least one joint, in particular more than one joint, which enables an angling in a first direction in a first movement and bounds an overelongation beyond an elongation angle of in particular 180 in the opposite second direction. In particular when a plurality of joints (15, 16, 17) are provided at the struts, they, and with them the conveying blades, are particularly flexible for simple compressibility.

Abstract: A blood pump control system includes a local processing terminal and a remote processing terminal. The local processing terminal is configured to transmit to the remote processing terminal, collected current state parameters of the blood pump and heart activity indexes, and to drive and control the blood pump according to blood pump adjusting parameters received from the remote processing terminal. The remote processing terminal is configured to obtain current blood pump adjusting parameters according to the current state parameters, and the heart activity indexes received from the local processing terminal, and set adjusting conditions; and to transmit the blood pump adjusting parameters back to the local processing terminal.

Abstract: A method may be provided for the operation of a pump device, which comprises at least one pump as well as a suction element which is connected to the at least one pump and which has a suction opening positioned in a cavity of a body of a patient that sucks a fluid by way of producing a reduced pressure in the suction element, wherein an acceleration is measured and monitored during the operation of the pump device, wherein the reduced pressure in the suction element is reduced at least for a limited reaction time period, given the occurrence of an acceleration variable which lies above a fixed threshold valve. A correspondingly configured pump device may be provided.

Abstract: Systems, methods, and devices for treating pulmonary arterial hypertension are provided. The system comprises an implantable actuator that compresses the pulmonary artery.

Abstract: A cannula assembly for applying a flow cannula for the introduction, circulation or diversion of flow media, in particular blood, in the human or animal body. The flow cannula has a main portion and a tip portion. The tip portion is elastic and, in a functional position, is configured to protrude in an arc shape at an angle from the main portion, and in an application position, is held in the direction of the longitudinal extent of the main portion by a guide device. The flow cannula may be fitted for the indication of pulmonary hypertension and pulmonary insufficiency. The one of more flow cannulas so connected to the heart, for example, through an incision of the jugular vein or subclavian vein may be connected, on the outside, to a membrane ventilator, such as a Novalung®, with oxygen supply and/or additional pump support.

Abstract: A needle system and methods for using the needle system are described. The needle system is generally intended for medical use and can be used when performing a dialysis on a patient, for example, hemodialysis. In general, the needle system can address problems that commonly arise when using conventional single or double needle systems during hemodialysis.

Abstract: The invention relates to a process for monitoring the supply of substitution fluid upstream or downstream of a dialyser or filter arranged in an extracorporeal blood stream. One embodiment provides, for the detection of predilution or postdilution, for measuring the pressure in the blood stream downstream of the dialyser or filter, predilution or postdilution being recognized on the basis of the change in pressure following the shutting off and/or starting up of the substituate pump provided for conveying the substitution fluid. Another embodiment provides for recognizing predilution or postdilution on the basis of the comparison of the oscillating pressure signal attributable to the substituate pump to a characteristic reference signal. The characteristic reference signal to which the pressure signal of the substituate pump is compared is preferably the oscillating pressure signal of a blood pump arranged in the blood stream for conveying the blood upstream of the dialyser or filter.

Abstract: A fluid filtration system comprising a cross-flow filter is arranged to permit a first pump to recirculate part of the retentate of the filter to the inlet of the cross-flow filter and a second pump to return part of the permeate to the inlet of the cross-flow filter. A third pump is configured supply source fluid to the inlet of the filter. The flow path between the second pump and the cross-flow filter inlet may include an adsorption filter that may selectively remove contaminants, toxins, or pathogens in the permeate. A controller may control the first, second and third pumps to provide predetermined flow ratios among the fluid flow paths of the system in order to achieve a desired filtration level. This system may be applicable to the removal of harmful substances from blood, by first separating the plasma from the blood and then removing harmful substances from the plasma.

Abstract: A method for priming a hemodialysis treatment includes: providing a disposable cassette including at least a portion of a dialysate circuit and at least a portion of a blood circuit; placing a dialyzer in fluid communication with the dialysate circuit via a to-dialyzer dialysate line and a from-dialyzer dialysate line; placing the dialyzer in fluid communication with the blood circuit via an arterial blood line and a venous blood line; placing a source of dialysis fluid in fluid communication with the dialyzer; priming the dialysate circuit with dialysis fluid from the source while both the to-dialyzer dialysate line and the from-dialyzer dialysate line are connected at their dialyzer ends to the dialyzer; and priming the blood circuit with dialysis fluid from the source by actuating at least one valve provided by the disposable cassette.

Abstract: A nasal douche having a valve, container part and cap part, wherein the container part serves to receive irrigation liquid and carries cap part. The cap part has a nose attachment with an outlet opening for irrigation liquid connected fluidically to interior of container part via discharge channel, wherein nose attachment is intended to be attached to a nostril of the user. The container part or cap part is assigned a mouthpiece for controlling the valve, wherein the valve is closed in a rest position and flow of irrigation liquid out through the nose attachment is thus suppressed, and wherein the valve can be brought to an open position, under the action of respiratory air when the user blows into the mouthpiece, and irrigation liquid thus flows out through the nose attachment, wherein respiratory air or ambient air flows into the container part to allow the outward flow.

Abstract: Systems and methods are provided for syringe organization including a backing, a plurality of pockets coupled to the backing and a coordination scheme indicating the contents of individual pockets.

Abstract: A system includes a parameter generation system to determine parameters of at least one phase of an injection procedure based at least in part upon a type of the injection procedure. The parameter generator system determines the amount of a pharmaceutical that is to be delivered to a patient at least in part on the basis of the concentration of an agent in the pharmaceutical and at least on part on the basis of a function that depends upon and varies with a patient parameter. The patient parameter can, for example, be weight, body mass index, body surface area or cardiac output. The pharmaceutical can, for example, include a contrast enhancing agent for use in an imaging procedure.

Abstract: A tube feeding syringe holder having a continuously flexible, shape-holding arm supporting a drop-in syringe receiver at its terminal end. The syringe receiver is a generally circular, non-expanding collar with a bore sized to permit a syringe to be dropped into place axially, in a one-handed operation. The apparatus allows the feeding operation to be hands-free once started. In a preferred form the flexible arm is mounted on a tripod base with a vertically adjustable support post.

Abstract: A carrier for carrying medication to be delivered intravenously to a patient includes a carrying frame, a support base, and a container holder for holding a container of medication attached to the carrying frame. The support base and carrying frame are sized, shaped, and mutually positioned such that the carrying frame extends from the support base so as to be supported above the floor from the support base. The carrying frame has at least one location configured for attaching the medication delivery device and at least one ledge, positioned adjacent to the at least one location for resting the medication delivery device, the ledge is positioned between the container holder and the support base, while attaching the medication delivery device to the carrying frame.

Abstract: The invention relates to a miniature portable pump with mechanical actuation, preferably without a motor, provided with a bowed piston for injecting fluid by manual dosing and/or continuously. The pump consists of a small number of parts with very low production cost, for injecting medication, preferably subcutaneously.

Abstract: A safety needle device comprising a body piece including a rear end connected to a cannula and a front end having a needle for connecting to a patient, a sliding gap at the front end of the body piece, a lock button at a rear end of the body piece, a sliding piece adopting a locked position wherein the sliding piece is folded and locked onto the body piece and a sliding position wherein the sliding piece is unfolded and unlocked from the body piece; retaining flaps at a bottom of the sliding piece for receiving the fingers of a hand of a user when the needle device must be disconnected from the patient, and locking parts in the sliding piece to lock the sliding piece and the body piece in a position wherein the needle is removed from the patient and protected by walls of the sliding piece.

Abstract: A sealed delivery system for dispensing metered volumes of a pure or sterile flowable substance is presented. In exemplary embodiments of the present invention, a hand-held sealed delivery system comprises a continuously sealing one-way valve assembly at a distal end, and a volume reducing reservoir at a proximal end. The pure or sterile flowable substance can be stored in the volume reducing reservoir. In operation, a user pushes down upon a push button driven actuator assembly, acting upon a metering pumping chamber, which is in fluid communication with the pure or sterile flowable substance stored in the volume reducing reservoir via a check valve. Depression of the push button driven actuator causes a dispensing pump to push a metered volume of flowable substance through the continuously sealing one way dispensing valve assembly.

Abstract: Infusion systems, infusion devices, and related operating methods are provided. An exemplary method of operating an infusion device to deliver fluid to a user in accordance with an operating mode involves identifying a fluid type associated with the fluid currently onboard the infusion device from among a plurality of possible fluid types that is different from a previous type of fluid previously onboard the infusion device. The identified fluid type has pharmacokinetics characteristics that are different from pharmacokinetics characteristics associated with the previous fluid type. The method continues by updating one or more parameters referenced by a control module of the infusion device implementing the operating mode to reflect the pharmacokinetics characteristics associated with the identified fluid type and autonomously operating the infusion device to deliver the fluid of the identified fluid type to the user in accordance with the operating mode and the one or more updated control parameters.

Abstract: A system, a device and a method associated with an insulin administering device is provided to control administering and recording of information associated with the administering. The insulin administering device is configured to connect with a computing device, such as a mobile phone, a tablet PC, a wearable device, a laptop computer or other suitable device, communicating commands and status updates. The control of such administering system may be useful for medical assessment and care of a subject suffering from a medical condition requiring administering of injected medicines such as a diabetic patient with need to inject insulin or glucagon regularly. The current invention may use various administering devices such as an insulin pen, a syringe, an insulin pump and more. The communication channel between the computing device and the insulin administering device may use audio communication channel, visual communication channel or capacitive communication channel.

Abstract: A portable unit comprises a sampling mechanism used by a patient to take a sample of a bodily fluid or tissue that can be tested for any property indicative of a medical condition of the patient, a microprocessor for determining a treatment for the condition based on a test of the sample, and an administration mechanism for administering the treatment based on the determination by the microprocessor. Operationally, the unit samples a bodily function, evaluates the sample, determines from stored protocols and criteria if treatment is required, and administers treatment.

Abstract: Disclosed are methods and medical device systems for automated delivery of therapies for pain and determination of need for and safety of treatment. In one embodiment, such a medical device system may comprise a sensor configured to sense at least one body signal from a patient; and a medical device configured to receive a first sensed body signal from the sensor; determine a patient pain index based at least in part on said first sensed body signal; determine whether said patient pain index is above at least a first pain index threshold; determine a safety index based at least in part on a second sensed body signal; select a pain treatment regimen based on at least one of said safety index and or a determination that said pain index is above said first pain index threshold; and deliver said pain treatment regimen.

Abstract: There is provided a device for automatic synchronized injection and aspiration of fluids comprising: a first linear actuator; a second linear actuator; a first coupling mechanism attached at a distal end portion of the first linear actuator, the first coupling mechanism arranged for detachable coupling to a first plunger of a first syringe; a second coupling mechanism attached at a distal end portion of the second linear actuator, the second coupling mechanism arranged for detachable coupling to a second plunger of a second syringe; and a synchronization mechanism mechanically coupled to the first and second linear actuators, the mechanism arranged so that insertion of the first plunger further into a first barrel of the first syringe is synchronized with extraction of the second plunger from a second barrel of the second syringe, thereby injection from the first syringe is synchronized with aspiration into the second syringe.

Abstract: A portable auto-injector configured to store a dry medication separately from a liquid component, wherein removal of a cap operates a first actuation mechanism which opens a valve and thus allows for the initiation of a mixing step prior to injection. An extendable needle guard is provided over the delivery assembly which prevents premature injection as well as inadvertent sticks or other cross contamination of a needle. The needle guard can also form part of a secondary trigger mechanism which injects the mixed components after the mixing stage is complete.

Abstract: A syringe includes a first syringe barrel and a second syringe barrel. Each barrel includes a delivery end to which an end piece with a channel is secured, a piston which is arranged movable in the syringe barrel and can be moved towards the delivery end in order to deliver a fluid located between the delivery end and the piston via the channel. The two syringe barrels are mechanically connected to each other such that the distance between them cannot be changed. At least one of the two end pieces can be secured to the allocated delivery end in different positions for adjustment of the distance between the two channels.

Abstract: An injection device comprises a housing (5), an axially moveable dose delivery mechanism (10), an actuation button (20) for imparting movement to said delivery mechanism (10), and a dose setting arrangement (30) to select a dose volume. The dose setting arrangement (30) comprises a threaded member (31) arranged to engage a formation (9) on, or fixed relative to, the housing (5) such that axial movement relative to the housing (5) results in relative angular movement of the threaded member (31). The dose setting arrangement also includes a stop (9a); fixed relative to the housing, and arranged to cooperate with the threaded member (31) limiting axial movement thereof. Complementary engagement features (16, 36) are provided which are moveable between an engaged position in which relative axial movement of the delivery mechanism (10) and threaded member (31) is prevented; and a disengaged position in which the threaded member (31) may be moved relative to the delivery mechanism (10) to adjust the dose.

Abstract: A sub-assembly for a medicament delivery device including a housing, a propellant source contained in and axially moveable relative to said housing, and a button axially moveable relative to said housing. At least part of said button is disposed axially rearwardly of part of said propellant source. The button includes one or more radially flexible blocking members, and the button is moveable between a first axial position in which the one or more radially flexible blocking members are radially restrained by the housing in a radially inward position that limits rearward axial movement of the propellant source, and a second axial position in which the one or more radially flexible blocking members are able to flex to a radially outward position and permit rearward axial movement of the propellant source relative to the button and the housing.

Abstract: A medicine dispensing device can include a recess configured to receive a medicine cartridge having a plunger assembly and a medicine chamber, and a gear assembly configured to cause displacement of the plunger assembly to dispense medicine or draw medicine into the chamber. The gear assembly can be activated by both a motorized and manual activation mechanism.

Abstract: Described is a medicament delivery device (1) comprising a body (2), a container carrier (7) slidably disposed in the body (2), and a sleeve (6) slidably coupled to the container carrier (7).

Abstract: An exemplary embodiment of injector includes a trigger mechanism, an energy source, and a user-operable firing-initiation member. The trigger member can include a trigger member having a retainer portion, and a ram assembly having a ram configured to pressurize a medicament container for expelling a medicament therefrom and a trigger engagement member configured to engage the retainer portion of the trigger member in a pre-firing condition. The energy source can be associated with the ram for powering the ram to expel the medicament, and the user-operable firing-initiation member can be operable for causing an axial rotation between the trigger engagement member and the retainer portion from the pre-firing condition to a firing condition in which the trigger engagement member is released from the retainer portion to allow the energy source to fire the ram.

Abstract: A drug delivery device is provided comprising a housing having an exterior surface, a drug-filled reservoir with an outlet, drug expelling means, and a flexible sheet. On the flexible sheet is formed or mounted input means adapted to be actuated corresponding to an event indicative of drug being expelled, a display adapted to display a time parameter, a processor, and an energy source. The processor is adapted to, based on input from the detection means, control the display to display a time parameter related to the time the event was detected, and the flexible sheet is attached at least in part to the outer surface of the housing.

Abstract: A flexible self-adhesive label (10), for a syringe (200) comprising a barrel (210) with a front end and a rear end and having a tip (220) at the front end of the barrel. The label comprises a main body (20), for labelling the barrel of the syringe, the main body having a front end and a rear end. The label further comprises a tongue (30) at the front end of the main body. The tongue includes an aperture (32) for engaging with the tip of the syringe, for locating the main body (20) of the label in a longitudinal direction with respect to the barrel. Also provided is a method of labelling and filling a syringe, using the label.

Abstract: A dose control mechanism for a syringe includes an engaging screw thread arrangement between an exterior surface of a plunger and a longitudinally extending channel of a housing. The engaging screw thread arrangement includes at least one thread segment and a pitch guide including a variable pitch thread. At least a portion of the longitudinally extending channel of the housing including one of the pitch guide and the at least one thread segment, and the plunger includes the other of the pitch guide and the at least one thread segment. The plunger resides at least partially within the housing with the at least one thread segment engaged with the pitch guide. An accurate dose drug delivery syringe includes such a dose control mechanism, a barrel, a plunger seal, and a barrel adapter assembly having a barrel tip and a needle.

Abstract: A drug delivery device is provided having a housing, a lead screw that is rotatably fixed with respect to the housing during dose setting and during dose delivery and that is axially moveable in a delivery direction relative to the housing for dose delivery, a number sleeve threadedly engaged with the housing to be screwable relative to the housing, and a dial link which is axially moveable and rotatable with respect to the housing for dose setting and which is prevented from rotation with respect to the housing for dose delivery. The dial link is rotatably fixed with the number sleeve when the dial link and the number sleeve are in a first arrangement, and the number sleeve and the dial link are rotatable with respect to one another when the dial link and the number sleeve are in a second arrangement.

Abstract: The invention relates to an apparatus, in particular for ejecting a fluid, having an electric motor (500), the motor comprising at least one motor winding (506a-d), having a control unit (656) for controlling the motor (500), wherein the apparatus further comprises an electronic detection circuitry (620) configured to determine an electrical quantity, the electrical quantity being a function of the electric resistance (Rw) of the motor winding (506a-d), and wherein the control unit (656) is configured to control the motor (500) as a function of the electrical quantity. The invention further relates to a method for controlling such an apparatus, comprising the steps of: determining an electrical quantity, the electrical quantity being a function of the electric resistance (Rw) of the motor winding (506a-d); and controlling the motor (500) as a function of the electrical quantity.

Abstract: A drug injection device is disclosed.

Abstract: The system allows optimizing the dispensing of aerosol medicaments. In particular the system allows the administration of an exogenous pulmonary surfactant to very young patients (e.g. preterm neonates). A catheter (101) conveys atomized surfactant directly to the retropharyngeal region in order to increase efficiency of the medicament administration without being invasive: this is particularly important for very young patients, such as pre-term born neonates suffering from neonatal Respiratory Distress Syndrome (nRDS). The catheter is made of biocompatible flexible material (e.g. plastic material). It is possible to couple the catheter with a rigid scaffolding (e.g. metallic) to increase stiffness of the device and to improve easiness of positioning operations. The delivery of the atomized medicament is done by means of an air blasting technique.

Abstract: A delivery device for and method of delivering substance, the delivery device comprising: an outlet member through which substance is in use delivered in an entraining gas flow; and a substance supply unit for supplying substance to be entrained by an entraining gas flow as one or both of a vapor or a fine aerosol mist, wherein the substance supply unit comprises a flow channel which is fluidly connected to the outlet member, and a substance supporting element for supporting substance, at least a surface of which is in use disposed in the flow channel.

Abstract: Various embodiments of a tracheostomy tube having neck flanges with filleted ends are provided. In certain embodiments, the neck flange may include a fillet extending from a bottom surface of the neck flange to a tip of the neck flange. In addition, the filleted end may also be tapered from a top surface of the neck flange to the tip of the neck flange. The neck flange may also include several curved edges, such as curved edges from the tip of the neck flange to side surfaces of the neck flange, and a curved bottom surface from side surface to side surface of the neck flange.

Abstract: A laryngeal mask anchoring device serves to seat an airway tube in an operational position against edentulous gums and the roof of the mouth to securely hold the airway tube in a desired position. The device also guides the airway tube towards the lungs, and braces the mouth open for manipulations to the airway tube. The device collapses into a substantially flat configuration for storage and portability. An upper and lower brace directly engage the edentulous gums. The braces are substantially smooth and pliable, and are configured to mate with substantially smooth, bald gums. A supportive platform with a slightly curved surface forms a supportive brace to hold the airway tube into place against the roof of the mouth. The slightly curved configuration of the platform nestles the airway tube, and the large surface area presses the airway tube against the roof of the mouth.

Abstract: An improved-seal mask for the respiratory therapy of the type comprising a shaped shell (12) at least covering mouth, nose and eyes of a patient (11), and provided, along a perimeter (13) which is suitable for being placed in contact against the patient's face, with a sealing gasket (14), said shaped shell (12) being provided with at least one inlet fitting (15) for the mixture of air and oxygen, said mask also comprising a neckpiece (20) provided with a plurality of prongs (21), each joined in a fixed or removable manner to a corresponding fastening point (17), distributed over the perimeter of the shaped shell (12), is provided with five fastening points (17) for the neckpiece (20), wherein two upper fastening points (17?) are arranged at the height of the eyes, symmetrically with respect to a sagittal plane, two lower fastening points (17?) are arranged at the height of the chin, symmetrically with respect to a sagittal plane, and a fifth fastening point (17??) is arranged centrally along an upper edge (18

Abstract: A mask for the respiratory therapy with dedicated access for a nasogastric tube comprising a shaped shell (12) at least covering mouth, nose and eyes of a patient (11), and provided, along a perimeter (13) which is suitable for being placed in contact against the patient's face, with a sealing gasket (14), said shaped shell (12) being provided with at least one inlet fitting (15) for the mixture of air and oxygen, said mask also comprising a neckpiece (20) provided with a plurality of prongs (21), each joined in a fixed or removable manner to a corresponding fastening point (17), distributed over the perimeter (13) of the shaped shell (12), is provided with a pneumatic-sealed dedicated access (30) for a nasogastric tube (31), wherein the shaped shell (12) bears a hole (32) having sufficient dimensions for the passage of the end of the nasogastric tube.

Abstract: A patient interface device includes a fluid coupling member structured to be coupled to a source of breathing gas, and a patient sealing assembly structured to be coupled to the fluid coupling member. The patient sealing assembly includes a central cushion portion, a first side portion and a second side portion, wherein the central cushion portion is structured to enable a size of the central cushion portion to be adjusted in a direction that is generally perpendicular to a longitudinal axis of the patient sealing assembly from a first size configured to provide a nasal/oral mask configured to cover a nose and mouth of a patient to a second size configured to provide a nasal mask configured to cover only the nose of the patient.

Abstract: An oxygen delivery mask for transoral medical procedures that provides an efficient means for safely delivering oxygen to patients at higher flow rates. The oxygen delivery mask comprises a mask body defining a wearable face covering that includes a nasal compartment, a mouth opening, two fastening apertures, four mask inlets and a mask outlet with an integral delivery tube that includes four inlet ports and a sealed hole and an exhaust port. The oxygen delivery mask is shaped to contour to the face of a wearer, and when in use, enables input gas to be directed from the delivery tube into the inside of the mask and output exhaust gas to be expelled from the inside of the mask. The oxygen delivery mask thereby allows for treatments with oxygen flow rates greater than three liters/minute to be delivered to patients without concern of causing trauma to the patient's nostrils.

Abstract: A gas generator for health is provided. The gas generator for health includes an electrolysis device, a gas mixing chamber and a gas output device. The electrolysis device is for electrolyzing water to produce a combination gas including hydrogen and oxygen. The gas mixing chamber includes a shell and a cover. The shell has an anti-explosion hole. The cover is separatably disposed on the anti-explosion hole, and the diameter of the anti-explosion hole is larger than 0.5 cm. The gas mixing chamber is connected to the electrolysis device for receiving the combination gas. A vaporized gas is generated by the gas mixing chamber and mixed with the combination gas to produce a healthy gas. The gas output device is connected to the gas mixing chamber for outputting the healthy gas to a user to breath.

Abstract: Some embodiments of the invention include a tracheal humidification device. The tracheal humidification device may include a first body portion and a second body portion. The first body portion may include a tracheostomy connection port formed to couple with a tracheostomy connection tube; and a heat moisture exchanger port formed to couple with a heat moisture exchanger. The second body portion may be coupled with the first body portion, for example, rotatably coupled. The second body portion may include a nebulizer port formed to couple with a nebulizer and having a closable seal that is closable when the nebulizer is not coupled with the nebulizer port; and a suction port having a closable cap.

Abstract: A float tent can include: a frame having a pool frame portion with a tent frame portion thereof over the pool frame portion; a tent having the tent frame portion, the tent having a closable opening; and a pool having the pool frame portion, the pool having pool sides dimensioned to hold at least 8 inches of water and having a pool base dimension sufficient for a person to lay in the pool without touching pool sides. The tent can include tent walls having an angle that inhibits condensation drip, the angle being with respect to the pool base, such as at least 4.5 degrees. The tent can include a material that is opaque. The float tent can include a heater configured to heat the water to skin temperature of the person. The float tent can include a water circulation pump and filter.

Abstract: Methods and devices are provided for fluid dispensers with rotational activation mechanisms. The device may include a reservoir that is sealed to prevent an escape of fluid. The sealed reservoir includes an internal barrier. The device includes a wicking assembly that includes a wick and a rotational element. Rotation of the rotational element breaks the internal barrier of the sealed reservoir and allows the fluid in the reservoir to contact the wick.

Abstract: Methods, systems and devices that provide a therapeutic solution to alleviate the pain and discomfort of phantom limb syndrome are disclosed. The methods and systems of the present invention generally comprise capturing data from recording devices operably coupled to a processor and/or computing device, the recording devices configured to capture data associated with intact portions of a missing limb, one or more intact limbs and/or portions of the environment surrounding the missing limb, identifying the data captured, generating a three-dimensional virtual image of the missing limb and the surrounding environment from the data captured, and displaying the three-dimensional virtual image and the portions of the surrounding environment to the amputee such that the missing limb appears intact. The present invention advantageously provides a therapeutic and more immediate solution to alleviate the pain and discomfort from phantom limb syndrome.

Abstract: A device for well-being and body care includes a unit adapted to drip a fluid onto the body of a person to be treated and a unit collecting the fluid dripping from the body of the person, wherein such unit adapted to drip the fluid onto the body of the person to be treated, includes a tank connected, through a first duct, to a pump, the pump being then connected, through a second duct, to a percolator adapted to delicately flow the fluid onto the body of the person to be treated.

Abstract: Arrangements and methods for delivering bioactive agents and/or cells into an extended volume of tissue are disclosed. In one embodiment, a cell-delivering needle arrangement has a tube positioned within a tube and fixedly attached to a wall thereof. In one exemplary method, a cell-delivering needle is advanced into tissue, a suspension of cells is passed through a first lumen and out of side ports, and a suspension of cells is passed through a second lumen and out of a distal opening. Other embodiments are disclosed.