Abstract: A wound therapy device is disclosed. The wound therapy device may include a housing for covering at least a portion of a wound and for sealing to a body surface of a patient. The housing may also include a liquid collector for retaining liquid therein and a vacuum connection for coupling to a vacuum source. The vacuum connection may be in gaseous communication with the liquid collector. The vacuum connection may be separated from the liquid collector by a liquid barrier.

Abstract: In one general aspect, a cuff for attachment to a heart includes an attachment component configured to engage a blood pump to attach the cuff to the blood pump and a sewing ring for attachment to the heart. The sewing ring is coupled to the attachment component, and the attachment component and the sewing ring each define a central opening configured to admit an inflow cannula of a blood pump. The sewing ring comprises a member that provides rigidity to flatten a portion of a myocardium of the heart when the cuff is attached to the heart.

Abstract: A blood pump comprising a cartridge, the cartridge comprising a first recess therein, said first recess having a surface, and a flexible diaphragm closing said first recess, the first recess and the flexible diaphragm defining a first pump chamber, said first pump chamber having an inlet and an outlet wherein the flexible diaphragm of the first pump chamber is movable between a first position, separated in use from the surface of the first recess, in which said first pump chamber has a maximum volume, and a second position, substantially adjacent to the surface of the first recess, in which said first pump chamber has a minimum volume a pump driver arranged to interface with the cartridge, said pump driver operable to move the flexible diaphragm of the first pump chamber in a first direction into said first recess to, in use, pump blood from the chamber and to move the flexible diaphragm of the first pump chamber in a second direction away from the first recess to, in use, draw blood into said first pump cham

Abstract: A system is provided for pumping fluid, with the system including a fluid pump and a cassette. The pump includes a motor and a piston that is movable toward and away from a flexible diaphragm of the cassette. A linkage connects the motor and the piston to move the piston toward and away from the diaphragm. At least a portion of the piston or the diaphragm is magnetized, with the other having at least a portion that is magnetized or formed of a ferromagnetic material, thereby magnetically coupling the piston and the diaphragm such that movement of the piston moves the diaphragm into and out of a cassette cavity aligned with the diaphragm and piston. Movement of the diaphragm into and out of the cavity changes the effective volume of the cavity, which has the effect of drawing fluid into or forcing fluid out of the cavity.

Abstract: Apparatus and methods are described including identifying a subject as suffering from a condition selected from the group consisting of: cardiac dysfunction, congestive heart failure, reduced renal blood flow, increased renal vascular resistance, arterial hypertension, and kidney dysfunction. In response thereto, blood pressure within a renal vein of the subject is reduced, by placing a blood pump inside the subject's renal vein and activating the impeller to pump blood from the renal vein into the subject's vena cava. Other applications are also described.

Abstract: A system for acquiring or measuring information relating to a state of dialysance, identifying a dialyzer apparatus, or identifying a membrane filter device during the operation of the dialyzer apparatus in a dialysis treatment of a patient. The dialyzer apparatus includes a housing having an internal volume portion and a membrane filter device arranged within the internal volume portion. The housing allows transmission of radiation. A sensor device connected to the housing of the dialyzer apparatus includes a signal receiving device designed to receive a radiation signal from the housing, the signal characteristic of the state or the identification of the dialyzer apparatus or of the membrane filter unit of the dialyzer apparatus.

Abstract: The present invention provides a hemodialysis machine comprising a removably mountable cartridge having at least one inlet and at least one outlet, the cartridge defining a fluid pathway between said at least one inlet and said at least one outlet, a sanitisation device having an inlet and an outlet, a conduit connected between an outlet of the cartridge and the inlet of the sanitisation device and, a conduit connected between the outlet of the sanitisation device and an inlet of the cartridge.

Abstract: A kit for blood component processing comprising a fluid circuit into which blood is drawn, wherein the fluid circuit comprises a plurality of pathways; wherein the first pathway is configured to receive blood drawn from a blood source and leads to a separation device, wherein the separation device is configured to separate the blood into components; wherein the second pathway is configured to receive a first component from the separation device and transport at least a portion of the first component to a first processing device, wherein the first processing device may alter the first component to produce a first output; and wherein the third pathway is configured to receive a second component from the separation device and transport at least a portion of the second component to a second processing device, wherein the second processing device may alter the second component to produce a second output.

Abstract: A catheter for vascular insertion, including a catheter body defining a first lumen and a second lumen, and including a distal region. The distal region includes an atraumatic nose portion defining a first distal opening in fluid communication with the first lumen, and a second distal opening in fluid communication with the second lumen. The distal region also includes a first lateral opening defined by the catheter body and in fluid communication with the first lumen, and a second lateral opening defined by the catheter body and in fluid communication with the second lumen. One or both of the first and second lateral openings may be defined by an angle cross-cut through an outer perimeter of the catheter body.

Abstract: A system of authenticating a medical solution used in a blood processing procedure, comprising a blood processing system having a user interface and access to a database of medical solutions identifiable by identifiers, wherein the blood processing system guides a user through steps of the procedure and the user interface prompts the user to execute an action as part of a step; a fluid circuit having an inlet for a medical solution, wherein the fluid circuit is coupled to the fluid processing system; wherein a step of the blood processing procedure comprises drawing a solution into the circuit, wherein the interface receives a user input of an identifier of the solution prior to the fluid processing system executing the step; wherein the fluid processing system is configured to compare the received identifier to medical solution identifiers within the database and, based on a result of the comparison, executing the step.

Abstract: The present disclosure relates to systems and methods for the separation of blood into blood products and, more particularly, to systems and methods that permit automated recovery of white blood cells after producing a leukocyte-reduced blood product.

Abstract: An apparatus is disclosed for storing and dispensing a pen needle for an injection device, including a packaging assembly including a pliable outer cover, the outer cover having a hub portion, a needle portion disposed at a distal end of the hub portion, and a flange disposed at a proximal end of the hub portion, the hub portion having internally protruding splines or other structures for engaging a hub of a pen needle. The hub portion is sufficiently pliable for a user to press gripping portions of the hub portion so that corresponding internal portions of the hub portion between the splines contacts the pen needle hub to increase a surface area contact between the outer cover and a pen needle therein.

Abstract: A medical therapy system for delivering at least two therapies based on a geographic location of the medical therapy system is disclosed. The medical therapy system includes an infusion pump having a case that contains a processor, memory, a drive mechanism, a reservoir, a radio, and a sensor suite. The sensor suite includes a global positioning system (GPS) receiver to determine a location of the infusion pump. The processor receives the location of the infusion pump and executes first instructions stored in the memory. The processor executes second instructions stored in the memory only when the location of the infusion pump is within a safe zone defined around specified GPS coordinates.

Abstract: A medication infusion device comprises a memory means at a medication reservoir storing data identifying medication in the reservoir, a memory reading means at an infusion pump unit reads data from said memory means, and control means controls an infusion, based on data read by said memory reading means, to start the infusion when the medication is correct. A fluid connection detection means detects fluid connection of the medication reservoir to the infusion pump unit and transmits to control means whether the medication reservoir is connected. The control means controls an infusion in accordance with the transmission from the fluid connection detection means so that when there is no connection between the medication reservoir and infusion pump unit, the infusion pump unit will not be started or, if already started, stopped.

Abstract: A medication management system (MMS) includes a medication management unit (MMU) associated with a medical device. The MMU downloads a medication order to the medical device only if information from a first input matches information from a second input. The medical device receives delivery information only from the MMU. The medication order is performed only after delivery data validation. The MMU also determines drug-drug incompatibility. The MMU can modulate (start, stop, and dynamically adjust) medication order performance. The medical device wirelessly receives a patient ID to automatically associate with the patient. During delivery, the medical device caches an updated drug library to replace an existing one. The medical device displays a patient picture for validation. The MMU evaluates the performance of medical devices and caregivers based medical device feedback. The MMU adjusts the output of medical device information conveyed to a caregiver.

Abstract: An applicator for dispensing a fluid for use during a medical procedure includes a dispensing body for containing the fluid. The dispensing body includes a conduit, and a mixing tip operatively connected to the conduit for receiving the fluid from the dispensing body. The mixing tip includes a tip body having an interior passage. The interior passage includes an inlet at a first end fluidly connected to the conduit for receiving the fluid from the conduit and an outlet in a distal wall at a second end opposite to the first end. An insert body is positioned within the interior passage. A first passage is positioned between the insert body and the tip body and fluidly couples the interior passage with the outlet in the distal wall. A mixing chamber is positioned between the insert body and the distal wall. The mixing chamber includes a static mixing element.

Abstract: A pump is disclosed that comprises a primary control unit comprising a first processor and one or more modular pumping units removably docked to the primary control unit. Each modular pumping unit comprises a pumping mechanism and a second processor configured to control the pumping mechanism and communicate with the first processor. The modular pumping unit is configured to manipulate a portion of a fluid delivery set to pump a fluid. The first processor and the second processor are configured to exchange one or more operating parameters when the modular pumping unit is docked to the primary control unit. The modular pumping unit is configured to pump the fluid after being undocked.

Abstract: A manually actuated pump, such as a bolus delivery circuit of an insulin pump, combines a direct drive piston system with a lost motion valve system, to deliver reliably a full bolus dose, while precluding partial dosing or inadvertent overdosing conditions. The pump may also include a signaling device to indicate when a full bolus dose is delivered.

Abstract: Embodiments of the invention described herein include low cost infusion devices having basal and/or bolus fluid delivery options. Embodiments of the device include a housing, a reservoir to contain the fluid, a source of pressure to exert a force to expel the fluid contained in the reservoir, a bolus port adapted to receive an optional extra dose of fluid, and a cannula in fluid communication with the reservoir and the bolus port. The cannula is adapted for insertion into the user's skin for delivery of the fluid to the user's body. The device can provide a continuous delivery of the fluid along a first fluid flow path from the reservoir to the cannula and the optional extra dose of fluid along a second fluid flow path from the bolus port to the cannula.

Abstract: An apparatus (110) includes an activation mechanism (20) and a safety latch (122). The activation mechanism is operative to deploy a needle (116) to protrude out of a housing (112), the needle (116) having a longitudinal axis. The safety latch (122) is movably mounted on the housing (112) and formed with a needle opening (129) to allow the needle (116) to pass therethrough. The safety latch (122) has a first position wherein the needle (116) is aligned to pass through the needle opening (129) and a second position wherein the safety latch (122) is moved with respect to the housing (112) such that the needle (116) is blocked from movement in a direction parallel to the longitudinal axis thereof by a portion of the safety latch (122) distanced from the needle opening (129).

Abstract: A medical device for delivery of a fluid to a patient from a line terminating in a tubing needle. The medical device includes a cannula assembly for coupling the fluid into a cannula that is inserted into the patient. The cannula assembly has a first locking element disposed in a fixed position with respect to the cannula. Coupling the line to the cannula assembly is an infusion flap. The infusion flap includes a second locking element for engaging the first locking element of the cannula assembly and a lift tab for disconnecting the infusion flap from the cannula assembly. Coupling of the first and second locking elements requires initial mating of the infusion flap and cannula assembly followed by locking through rotation of the infusion flap with respect to the cannula assembly.

Abstract: Occlusions in a delivery line of an infusion pump can be detected by measuring pressure differentials in the pump over short periods of time in order to minimize the effects of long term systematic sensor changes. In a delivery mode such as basal insulin delivery where a small portion of a volume of fluid is delivered, pressure readings can be obtained before and after the motor move to deliver each portion and compared. The differentials after one or more motor moves can be compared to determine whether an occlusion is present. In a delivery mode such as bolus insulin delivery in which an entire volume of fluid is delivered, pressure differentials can be obtained for consecutive deliveries at a common point in the delivery cycle of each delivery. Comparison of these pressure values can be used to determine whether an occlusion is present.

Abstract: A jet injector that includes a prefilled syringe. The syringe includes a fluid chamber that contains a medicament. The syringe also has an injection-assisting needle, and a plunger is movable within the fluid chamber. A housing is configured for allowing insertion of the needle to a penetration depth. An energy source is configured for biasing the plunger to produce an injecting pressure in the medicament in the fluid chamber of between about 80 and 1000 p.s.i. to jet inject the medicament from the fluid chamber through the needle to an injection site.

Abstract: A system comprising a sensor assembly adapted to measure a magnetic field, and a mechanical assembly comprising an indicator element with a magnet moving together therewith, the magnet being configured to generate a spatial magnetic field which relative to the sensor assembly varies corresponding to the spatial position and orientation of the magnet, wherein the indicator element is adapted to both rotate and move axially during operation of the assembly. Processor means is configured to determine on the basis of measured values both a rotational position and an axial position of the indicator element.

Abstract: A syringe system and components thereof are disclosed. The system may include a syringe body having a hollow lumen, a proximal open end, and a distal end. The syringe body may be configured to house a fluid therein. The syringe system may further include a plunger positioned in the hollow lumen of the syringe body, forming a seal with an inner wall of the syringe body. The plunger may include a removable piston having a shaft extending from the distal end towards the proximal open end, a stopper removably connected to a distal portion of the shaft, and at least one coupler attached to the distal portion of the shaft. The stopper may be configured to slidably move within the hollow lumen to facilitate movement of the fluid within the syringe body. The coupler may be configured to facilitate removal and attachment of the stopper from the piston.

Abstract: The present invention relates to a supplementary device for a manually operable injection device. The device has a body and a mating unit configured to releasably mount the body to the injection device in a specific position relative to an outside surface of the injection device.

Abstract: A method of amplifying an injection force of a drug delivery device, comprising the steps of storing energy in an additive force device, connecting the additive force device to the drug delivery device, setting a dose of medicament to be administered, and selectively releasing the stored energy of the additive force device to amplify an injection force of the drug delivery device.

Abstract: Drug delivery system comprising a housing and expelling means with a first rotational member adapted to rotate relative to the housing corresponding to a set and/or expelled dose and comprising a first force transmitting surface, a second rotational member adapted to rotate relative to the housing corresponding to a set and/or expelled dose and comprising a second force transmit ting surface. At least portions of the first and second force transmitting surfaces are adapted to engage each other during setting and/or expelling of a dose, and the first rotational member including the force transmitting surface is formed from a polymeric material containing magnetic particles, wherein the polymeric material having been magnetized to provide a magnet producing a magnetic spatial field. Hereby a spatial magnetic field is generated which varies corresponding to the rotational movement of the first rotation al member.

Abstract: The present invention relates to a handheld injection device comprising a housing (10), a piston rod (130) located within the housing (10), a drive member (100) and a power reservoir (110) for driving the drive member (100). The drive member (100) is permanently coupled to the piston rod (130), with the drive member (100) being axially movable between a dose setting position, in which the drive member (100) is rotationally constrained to the housing (10), and a dose dispensing position, in which the drive member (100) is rotationally decoupled from the housing (10). The power reservoir (110) comprises a reverse wound flat spiral spring having a first end attached to a first spool (120) and a second end attached to a second spool, which is axially and rotationally constrained to drive member (100).

Abstract: The invention refers to a handheld injection device comprising a housing (10; 410), a dose indicator (90; 480) positioned within and axially constrained to the housing (10; 410) and rotatable with respect to the housing (10; 410) during dose setting and during dose dispensing, a gauge element (80; 490), which is at least partly interposed between the housing (10; 410) and the dose indicator (90; 480), wherein the gauge element (80; 490) is axially guided within the housing (10; 410) and in threaded engagement with the dose indicator (90; 480) such that rotation of the dose indicator (90; 480) causes an axial displacement of the gauge element (80; 490). A contrast element having a first marking is provided and at least a region of the gauge element (80; 490) is provided with a second marking, with the first marking and/or the second marking being visible through a first window (12a) or aperture in the housing (10; 410) depending on the axial position of the gauge element (80; 490) within the housing (10; 410).

Abstract: The invention refers to an injection device comprising a housing (10), containing a cartridge (170) with an amount of liquid to be dispensed, a drive sleeve (41), which is rotationally constrained to the housing (10) during dose setting and spring driven rotatable relative to the housing (10) during dose dispensing, a dose dial member (60) for setting a dose to be dispensed, which is rotatable relative to the housing (10) during dose setting and during dose dispensing, and which is rotationally coupled to the drive sleeve (41) during dose dispensing. The device further comprises a last dose protection mechanism (41, 50, 60) for preventing the setting of a dose, which exceeds the amount of liquid left in the cartridge (170), with a limiter (50), which is interposed between the drive sleeve (41) and the dose dial member (60). Further, the device comprises two different display members (110, 120), each indicating the set dose.

Abstract: The invention refers to an injection device comprising a housing (10; 340; 410), a dose setting member (60, 80; 350; 420, 440) being operable in a first direction to set a desired dose to be dispensed, and a piston rod (30; 530) being adapted to cooperate with a piston so as to cause a set dose to be injected from a cartridge (170). Further, a first part (123; 300; 480) and a second part (114; 310; 490) of the injection device are provided, which are adapted to perform a relative rotational movement with respect to each other during dispensing of a dose, and which are adapted to provide a non-visual feedback signal to a user only at the end of dispensing of a set dose. The dose setting member (60, 80; 350; 420, 440) is further operable in a second direction which is opposite to the first direction to cancel a set dose.

Abstract: The invention refers to an injection device comprising a housing (10; 410), a resilient member (90; 510) adapted to provide a force necessary for ejecting a dose from the injection device, and a dose setting member (80, 60; 420, 440) operatively connected to a dose indicator (120; 480) which is positioned within the housing (10; 410). The dose setting member (80, 60; 420, 440) and the dose indicator (120; 480) cooperate to set the dose to be ejected from the injection device. The dose indicator (120; 480), during dose setting, is adapted to undergo a rotational movement within the housing (10; 410) and relative to the housing (10; 410). Further, a gauge element (110; 490) is provided which is rotationally constrained to the housing (10; 410) and axially displaceable relative to the housing (10; 410). The gauge element (110; 490) and the dose indicator (120; 480) form a limiter mechanism defining a maximum settable dose and/or a minimum settable dose.

Abstract: The invention refers to an injection device comprising a housing (10; 410), a resilient member (90; 510) adapted to provide a force necessary for ejecting a dose from the injection device, and a dose setting member (80, 60) operatively connected to a dose indicator (120; 480) which is positioned within the housing (10; 410). The dose setting member (80, 60; 420, 440) and the dose indicator (120; 480) cooperate to set the dose to be ejected from the injection device. The dose indicator (120; 480), during dose setting, is adapted to undergo a mere rotational movement within the housing (10; 410) and relative to the housing (10; 410).

Abstract: An apparatus is disclosed for storing and dispensing a pen needle for an injection device, including a packaging assembly including a pliable outer cover, the outer cover having a hub portion, a needle portion disposed at a distal end of the hub portion, and a flange disposed at a proximal end of the hub portion, the hub portion having internally protruding splines or other structures for engaging a hub of a pen needle. The hub portion is sufficiently pliable for a user to press gripping portions of the hub portion so that corresponding internal portions of the hub portion between the splines contacts the pen needle hub to increase a surface area contact between the outer cover and a pen needle therein.

Abstract: An apparatus is disclosed for storing and dispensing a pen needle for an injection device, including a packaging assembly including a pliable outer cover, the outer cover having a hub portion, a needle portion disposed at a distal end of the hub portion, and a flange disposed at a proximal end of the hub portion, the hub portion having internally protruding splines or other structures for engaging a hub of a pen needle. The hub portion is sufficiently pliable for a user to press gripping portions of the hub portion so that corresponding internal portions of the hub portion between the splines contacts the pen needle hub to increase a surface area contact between the outer cover and a pen needle therein.

Abstract: The present invention relates to a safety cap for a disposable syringe. In particular, the safety cap for covering a needle of the syringe has a cutout insertion portion formed at one side thereof and a ball provided at the inner upper end of the cutout insertion portion, so that it is possible to couple the needle of the syringe to the safety cap by inserting the needle into the ball and then rotating the needle about the ball. Further, the safety cap has a fitting groove formed at the lower end portion thereof, so that the safety cap can be coupled to and covered on the upper portion of the used syringe through the cutout insertion portion from the lateral side of the syringe, and be then forcibly coupled to the upper portion of the syringe through the fitting groove. Therefore, the safety cap can prevent a user, after using the syringe, from having a wound by being pierced by the needle or from being infected by germs through the wound.

Abstract: A method of producing a needle-mounted outer cylinder involves a melt-bond process of melting and bonding a proximal portion of a needle tube to an outer cylinder in a state in which the needle tube is in a needle insertion hole of the outer cylinder and in a state in which the outer cylinder is erect. The melt-bond process is performed by imparting energy to a portion of the needle tube distal from a proximal end of the needle insertion hole and from a proximal end of the needle tube causing the needle tube to generate heat so that resin forming an inner surface of the needle insertion hole melts and thereafter by causing the melted resin to flow downward inside the needle insertion hole to thereby fill a gap between an outer surface of the proximal portion of the needle tube and the needle insertion hole.

Abstract: The traditions, studies and international practice, prove that the inhalation of hot steams with or without the impurity of a medicine, helps the prevention and treatment of respiratory system diseases in hospitalization or home treatment. The device of application of the therapy is simple, easy to use, safe and affordable cost. This invention concerns a system with: 1) A inventive pipe—conductor of air, with an embodied safe system of electric points and power connections—cables for the supply of the nebulizer device with air and power simultaneously. 2) A nebulizer device that permits the simultaneous heating of the solution and nebula at 35-40° C. via a temperature regulator. In addition it posses system which via the electromagnets or the mechanism opens and closes impellers or a silicone leaf and settles the provision of nebula towards the inhalation mask. 3) A mask of inhalations with conical channels that routes the expired air to the sensor and the inhaled nebula to the mouth and nasal cavity.

Abstract: The present disclosure pertains to a system and method for monitoring usage of a respiratory medicament delivery device. Regular use of a respiratory medicament delivery device at intervals prescribed by a doctor may be critical to a subject's health. The system described herein is configured to monitor usage of a respiratory medicament delivery device such that manual tracking of a patient's adherence to a dosage plan by a doctor, for example, is not required. Monitoring usage of the medicament device delivery device may allow the doctor to judge the adherence of the subject to the dosage plan and encourage increased adherence. Improved adherence by the subject may result in improvement in the condition of the subject and economic benefits including reducing costs associated with re-hospitalization after discharge. In some embodiments, the system comprises a medicament delivery device and a usage event monitoring device.

Abstract: A metering element for an inhalation device is provided. The metering element comprises a plurality of openings being configured to receive a substance, wherein at least one of the openings has a different size than at least one other opening. Furthermore, an assembly for an inhalation device is provided. The assembly comprises a metering element with a plurality of openings and a powder channel which comprises an opening, wherein an arrangement of the openings is adapted to the shape of the powder channel such that each opening extends into the opening of the powder channel for a different amount.

Abstract: A nasal delivery device for and method of delivering particulate substance to the nasal airway of a subject, the delivery device comprising: a body assembly including a mouthpiece unit which includes a mouthpiece through which the subject in use exhales, and a substance-supply unit which is fluidly connected to the mouthpiece unit and actuatable to provide particulate substance for delivery to the nasal airway of the subject; wherein the body assembly is configured to receive a replaceable nosepiece unit which includes a nosepiece and contains a container containing particulate substance.

Abstract: The function of a respiration system, with a patient port (1) with connected inspiration branch (3) and expiration branch, is checked. A rebreathing line (9) connects the inspiration branch to the expiration branch. A reservoir (25) is connected to a reservoir port (27) in the rebreathing line. An actuatable control valve (29) is provided in the rebreathing line between the expiration branch and the reservoir port. A pressure sensor (33) is connected to the rebreathing line. A control unit (39) is connected to the control valve and to pressure sensor. The process includes closing the control valve for a preset inspiration time and opening it for a preset expiration time. The value sent by the pressure sensor is detected with the control valve opened during the expiration time and compared with a preset first threshold valve. An error message is generated when the value sent exceeds the first threshold value.

Abstract: Ventilator enables operator to enter into the microprocessor estimate of a patient's individual characteristic, such as weight, which the microprocessor uses to control delivered tidal volume and other parameters to match the patient. The operator can select one of several ventilator operational modes (intube, mask, CPR). Sensors input data to the microprocessor to maintain parameter optimizations and accuracy. Visual/audible alarms and tools activate when one or more parameters exceed or fail to exceed predetermined values for patient's weight. Manual over-ride is available. The ventilator has a quick start capability in which the operator turns on power, selects the automatic operating mode, enters patient's characteristic, selects control option starting automatic ventilation of proper volumes inhalation/exhalation periods, pressure, and oxy-air mixture.

Abstract: An intubation device for intubating a patient includes a handle for holding the intubation device by a user, a single-use intubation blade that includes a retainer clip and a mounting lug held fixedly to the intubation blade by the retainer clip, a ratchet collar that is rotatably connected to the handle. The ratchet collar is rotatable with respect to the intubation blade in a first travel direction to mount the intubation blade to the handle and in a second travel direction to dismount the intubation blade from the handle. The intubation device also includes a disabling mechanism for preventing re-use of the intubation. The disabling mechanism includes a break-away section of the retainer clip, and gear teeth that have a first gear tooth surface. When the ratchet collar is rotated the first gear tooth surface breaks the break-away section dislocating the mounting lug.

Abstract: The endotracheal tube bite block comprises two equivalent semi-circular elongated bodies partially connected to one another via linking tabs which enable the two semi-circular elongated bodies to move towards one another forming a circular elongated body to encapsulate the endotracheal tube. The endotracheal tube bite block has slope shaped design which will be placed inside the patient's mouth and rest between the teeth. The endotracheal tube bite block further comprises pressure tabs which prevent complete collapse of the device under extreme biting pressures.

Abstract: A faceplate (22) for use with a cushion (24) in a patient interface device includes a generally triangular shaped body portion (26) having a first side adapted to engage the cushion, a second side (30) disposed opposite the first side, and an aperture (32) formed therein passing between the first side and the second side. The body portion has a height (h) between a bottom edge and an apex edge and a width (a). The ratio of the width to the height is within the range of about 0.85% to 1.15% of the golden ratio (a+b/a=a/b).

Abstract: A nasal prong (26) for a cushion member adapted for use with a patient interface device that includes a casing (134,136), a flap (132) extending from the casing and being adapted to be inserted into a nostril of a patient, and a bottom cap (138). The casing and the bottom cap define a space. A fill material (140) is disposed in the space defined by the casing and the bottom cap, wherein the casing is structured to deform and conform to a shape of a portion of the nostril when the nostril applies pressure to the casing.

Abstract: A mask is disclosed that has a gas outlet which is quiet and provides for a diffused outlet flow of gases. The outlet is preferably a slot formed between a hollow body and cover over said hollow body. The mask also preferably extends and seals under a user's chin in use.

Abstract: A mask with cushion that has an outer film is disclosed. The film may be self-skinning or a film formed about or glued to the cushion body. In another form the cushion may be formed with at least a portion having a plurality of adjacent voids having honeycomb-like structure.