Abstract: A system and method for determining location of a fluid leak at a drape of a reduced pressure delivery system being used on a tissue site of a patient may include applying a reduced pressure to the tissue site of the patient. The drape may be imaged to generate image data, and a determination of a location of a fluid leak of the drape may be made from the image data. As a result of the determination of the location of the fluid leak, the drape may be corrected. The imaging may be made in a non-visible spectrum. The non-visible spectrum may be in an IR spectrum or UV spectrum. In one embodiment, a fluid, such as compressed air, may be applied to the dressing via the interface between the drape and tissue of the patient to improve imaging in the non-visible spectrum.

Abstract: The intracardiac pumping device has a pump (11) connected at its distal end (13) to a canula (15). At the distal end, the canula (15) has a suction head (16) for drawing blood. The suction head is extended by a non-sucking projection (20). The projection stabilizes the position of the pumping device in the heart. It extends the canula (15) mechanically without degrading the hydraulic conditions. It also serves as a spacer to prevent the suction head (16) from adhering to a wall of the heart.

Abstract: The presence or absence of a high pressure condition in an implantable blood pump is determined at least in part based on a comparison between a determined amount of differential pressure across the pump and a pressure threshold value. The amount of differential pressure parameter may be determined based at least in part on a parameter related to flow, such as a parameter related to thrust on the rotor of the pump. In response to determining the presence of a high pressure condition, an updated speed of rotation of the rotor that is less than the rotor's initial speed may be determined. The rotor's speed may be increased when the flow rate of blood is determined to be at least equal to a flow recovery threshold value.

Abstract: A transfer assembly comprising an intracorporeal transfer coil of an implant, and an extracorporeal transfer coil of an extracorporeal supply unit. The transfer coil of the implant has permanently associated therewith a transmitting element. The transfer coil of the supply unit has permanently associated therewith at least one receiving element. Further, the supply unit comprises an evaluation module connected with the receiving element and issuing a locating signal depending on an offset and/or a direction of offset of the transmitting element relative to the receiving element.

Abstract: A system and a method for starting a rotor of an implantable blood pump are described. For example, a blood pump system includes a rotary motor having a stator and a rotor. The rotor has permanent magnetic poles for magnetic levitation of the rotor, and the stator has a plurality of pole pieces arranged circumferentially at intervals. The blood pump system includes a controller configured to control a start phase of the rotor, wherein the start phase is prior to the rotor being positioned in a predefined geometric volume for pumping blood and wherein the start phase includes performing a rotation of the rotor by an angle larger than an angle corresponding to a quarter of an angular distance between two neighboring magnetic poles of the rotor.

Abstract: In a rigid hemodialysis salt container of plastic material including a venting valve formed in a container wall with a venting opening extending through the container wall, a seal member covers the venting opening at the inside of the container wall and is connected to the container wall by cementing or welding such that, with the occurrence of a predetermined pressure difference between ambient air pressure and a vacuum generated in the container, the seal member is at least locally ripped off.

Abstract: Devices, systems, and methods for obtaining one or more desired fluid components, using a back-flushable filter device comprising a filter and at least one diffusing plate, are disclosed.

Abstract: A device monitors a blood path from a blood vessel access of a human subject through an extracorporeal blood processing apparatus and back to the blood vessel access. A pumping device in the blood path is operable to pump blood through the blood path from the blood withdrawal device to the blood return device. The monitoring device obtains pressure data from a pressure sensor arranged upstream of the pumping device in the blood path, and processes the pressure data for detection of a disruption of the blood path downstream of the pumping device, e.g. caused by VND (Venous Needle Dislodgement).

Abstract: An apparatus is disclosed for storing and changing needles for connection with a medicament delivery device, comprising an inner housing, a reservoir disposed within the inner housing, and a needle holder disposed within the inner housing, for fluidly connecting a medicament container of the medicament delivery device with the reservoir. The apparatus also includes a plurality of patient needles displaceably disposed on the needle holder, and an outer housing displaceably disposed about the inner housing and providing a user interface to individually select one of the plurality of patient needles, connect the selected needle with the reservoir, expose the selected needle outside of the apparatus for injection, and store the selected needle.

Abstract: A relatively compact protective apparatus for a pressure sensor includes a diaphragm, a plate, and a sleeve that couples the sensor to the apparatus; the diaphragm, whose perimeter edge is attached to the sleeve between the plate and sleeve, forms a compressible cavity in fluid communication, via an opening in the plate, with another cavity formed between the plate and the coupled sensor. A diameter of the diaphragm is relatively small, so the diaphragm includes an undulating zone for enhanced sensitivity in response to pressure. A configuration of the cavities and the opening allows a contained volume of air to transmit a relatively low pressure, via the diaphragm, to the coupled pressure sensor, yet prevents transmission of relatively high pressures to the pressure sensor. A wall of a system fluid circuit line or a manifold connector may be configured to incorporate the protective apparatus therein.

Abstract: The present invention relates to a shoulder-mounted multifunctional hanging device having a structure for fitting onto the body of a user. The shoulder-mounted multifunctional hanging device having a body-fitting structure comprises: a first support unit having a connection portion extending in the lateral direction, and a concave portion contacting the acromion; a second support unit extending from the first support unit and mounted on supraspinatus; and a recess unit that is recessed up to the area in which the first support unit and the second unit are connected. The shoulder-mounted multifunctional hanging device of the present invention is shaped to fit to the structure of the shoulder of a user, and the user may thus be administered an infusion solution in a more comfortable manner without inconvenience to the shoulder.

Abstract: A piston pump is described for pumping a fluid, comprising at least two cylinders each having a piston which is movable inside the associated cylinder along the longitudinal axis of the cylinder by means of a drive, wherein cylinders are attached to a common pump flange. In each cylinder a chamber is formed having a volume that changes when the associated piston is moved in the cylinder. The pump flange extends along the direction of motion of the pistons, and at least one inlet port and one outlet port are attached to the pump flange, whose longitudinal axes run along the pump flange. A central valve plate is attached to the side of the pump flange facing away from the cylinders that bear on the pump flange and continuously rotates transversely to the pump flange during pumping operation of the piston pump. Respective passages are introduced to the pump flange in the region of each inlet and outlet port, and cylinder openings are introduced to the pump flange in the region of each cylinder.

Abstract: The present invention relates to a pump rotor for a peristaltic hose pump, in particular a medical peristaltic hose pump, with at least one actuating device, by which the pump rotor can be actuated hydraulically and/or pneumatically. Furthermore the present invention in particular relates to a medical peristaltic hose pump and to a method for actuating a pump rotor of a peristaltic hose pump.

Abstract: Infusion systems for pumping fluid into a body of a user, and methods for providing infusion systems, are disclosed. The infusion systems include an infusion pump, wherein the infusion pump comprises an infusion pump housing including a cavity. A fluid storage is removably inserted into the cavity of the infusion pump housing wherein, the fluid storage comprises a cartridge and an adapter connected to the cartridge such that the adapter encases the cartridge, and an infusion set is removably connected to the fluid storage.

Abstract: Pending medication orders are presented on the controller of an infusion pump to which a patient has been identified. All pending medication orders are displayed on the screen of the controller and any may be selected by the clinician. Selecting a pending order at the controller that involves an infusion to the patient also results in automatic programming of the infusion pump in accordance with that order. Selection of an oral medication at the controller results, as does selection of any other order, in notification to the healthcare facility server that the order is being administered. Such notification resolves open controlled item transactions as well as provides information that may be relevant to a patient's EMAR. Selection of a pending order may occur manually or automatically through identification of a medication.

Abstract: An apparatus, method and program product detects an occlusion in a fluid line by determining if a relationship between force measurements departs from an expected relationship.

Abstract: A system for the effective, reliable and foolproof delivery of controlled amounts of a medical fluid to a patient is provided. The system includes an integrated compressed gas unit having an inlet port to which at least one compressed gas cylinder is selectively connected and an outlet port in communication with the inlet port. The integrated compressed gas unit also includes a regulator valve assembly positioned between the outlet port and the inlet port, wherein the regulator valve assembly includes a press button actuator and regulator adjustment dial. The system also includes a flow control system delivering the fluid in precisely controlled amounts.

Abstract: Some embodiments of an infusion pump system may be configured to detect when at least one component of the pump system is exposed to an impact above a threshold level. In particular embodiments, the infusion pump system can be equipped with a drive system detection system configured to detect when one or more components of the drive system are damaged or inoperable.

Abstract: The present invention relates to a drug delivery device for dispensing of a dose of a medicinal product, comprising: a housing having at least one housing component (100; 200; 300) a cartridge comprising the medicinal product, a dose dispensing mechanism operably engaged with the cartridge for setting and/or dispensing of a predefined dose of the medicinal product, and a display element (102; 202; 302) being movably disposed relative to the at least one housing component (100; 200; 300), wherein the display element (102; 202; 302) and the housing component (100; 200; 300) are mutually moveable for selectively concealing and/or revealing information provided on the display element (102; 202; 302).

Abstract: The invention refers to an auto-injector comprising: a body, a syringe with a hollow injection needle and a stopper, wherein the syringe is slidably arranged with respect to the body, a torsion spring capable of, upon activation: pushing the needle from a covered position inside the body into an advanced position through the orifice and past the proximal end (P), operating the syringe to supply the dose of medicament (M), and activating means arranged to lock the spring means in a pressurized state prior to manual operation and capable of, upon manual operation, releasing the spring means for injection, wherein the torsion spring is grounded at one end in the body and at the other end in a first gear member rotatable about a longitudinal axis, wherein the first gear member, upon rotation, is arranged for translating a second gear member toward the proximal end (P), the second gear member prevented from rotating and arranged to be coupled to the stopper in order to push it towards the proximal end (P), wher

Abstract: A disposable injector with a cylinder/piston unit that can be filled at least temporarily with active substance, with a housing in which a pretensioned and releasable mechanical spring energy reservoir is arranged, and with at least one piston-actuating ram positioned between the spring energy reservoir and the piston of the cylinder/piston unit. The piston-actuating ram has two draw hooks that engage around the housing in some areas. In addition, the piston-actuating ram is separable from the housing by the relaxing spring energy reservoir. With the present invention, a disposable injector is developed which, with a small overall size, comprises only a small number of components and, while being easy to handle, ensures safe storage and operation.

Abstract: A medicament delivery device is presented having a housing, a safety sleeve movable between an extended position and a retracted position relative to the housing, a guide sleeve rotatably disposed in the housing, a plunger slidably disposed in the safety sleeve, and a button coupled to the housing. When the safety sleeve is in the retracted position, translation of the button relative to the housing causes the guide sleeve to rotate relative to the safety sleeve. Rotation of the guide sleeve relative to the safety sleeve allows the plunger to translate a predetermined axial distance relative to the safety sleeve.

Abstract: In an elongated casing, an active agent container connected to an injection needle can be shifted axially by a spring force. Auto-injectors which are sold or distributed filled and with the springs tensed have to be provided with a needle protecting cap to ensure the sterility of the injection needle. When such a needle protecting cap is removed as preparation for using the auto-injector, a tensile force can be exerted on the active agent container. Therefore, the active agent container comprising the injection needle must be prevented from being undesirably pulled forwards. At least one latching tongue prevents the active agent container from being prematurely shifted with respect to the casing, by abutting a flange arranged on a sliding sleeve which accommodates the active agent container. When the auto-injector is placed onto a person's skin, a needle protecting tube is shifted into the casing, forcing the latching tongue away from the flange and, thus, freeing the travel path for needle movement.

Abstract: In accordance with some embodiments of the present invention there is provided a method of preparing a compound device for use. The device may include a sealed component and an active outer surface. The outer surface may be protected by a surface cover. Preparing the device may include activating the active outer surface by removing the surface cover and exposing an internal portion of the sealed component to the exterior of the device by unsealing the sealed component and synchronizing the activating and said unsealing using a coupler attached to the surface cover and the sealed component.

Abstract: Drug delivery device, comprising a needle, which a distal end and a proximal end comprises an inner surface forming a channel, an outer surface, a first salient located on the outer surface.

Abstract: The invention relates to an auto-injector for administering a dose of a liquid medicament, comprising: an elongate housing, a syringe with needle and a stopper, a drive spring for pushing the needle from a covered position into an advanced position, for operating the syringe and for retracting the syringe, activating means for locking or releasing the spring means. A retraction sleeve is axially movable arranged in the housing. The drive spring bears with its proximal end against a thrust face of a decoupling member. At least one resilient decoupling arm is arranged at the decoupling member for bearing against a first shoulder of the plunger. At least one aperture is arranged in the retraction sleeve allowing the decoupling arms to be flexed outward thus allowing the first shoulder to slip past the decoupling arm.

Abstract: An agent injection device is provided that is capable of injecting an agent to a known predetermined tissue depth. An injection member has an elongate injection shaft with an outlet port configured to dispense an agent at a controllable time. A controllable driver is coupled to the elongate injection shaft and is configured to drive the injection member into target tissue. A velocity control system is in communication with the controllable driver and is configured to control the velocity of the elongate injection shaft.

Abstract: A medicated module containing a second medicament is configured for removable attachment to the mouthpiece of an inhaler containing a first medicament such that a single inhalation by a user will deliver both medicaments to the user.

Abstract: The present invention provides an adapter for fitting to a drug delivery device, the adapter comprising: an outlet for communication with the mouth of a patient; an air flow path through the adapter along which air is drawn to the outlet by inhalation by the patient; an inlet adapted for connection to a mouthpiece of the drug delivery device; and an air flow rate indicator operable to indicate when the air flow rate along the air flow path is at or above a predetermined minimum level suitable for delivery of the drug to the patient. The present invention also provides a drug delivery device having, in its body, an air flow rate indicator operable to indicate when the air flow rate along the air flow path is at or above a predetermined minimum level suitable for delivery of the drug to the patient.

Abstract: The invention relates to a trigger mechanism for a drug delivery device comprising at least one energy storing element, an actuation element and a series of cascaded trigger elements. The trigger elements are pre-stressed with increasing pre-stressing and coupled to the at least one energy storing element such that the trigger elements, upon exerting a sufficient actuation force (Fa, U) on the actuation element, cause a cascaded release of increasing portions of energy stored in the at least one energy storing device. At least one of the trigger elements is equipped with a latch element directly coupling at least two trigger elements such that the latch element restrains at least one of these trigger elements to its pre-stressed state before exerting the actuation force (Fa, U).

Abstract: An electronic cigarette includes a container for storing a tobacco flavored liquid, an atomizer connected to the container to atomize the tobacco flavored liquid by an electric heating, a battery tube to power the atomizer, and an actuating film movably positioned in the battery tube to control the atomizer.

Abstract: A pneumatic single-lumen medical gas conserver combines the advantages of typical single-lumen and dual-lumen conservers. In particular, a pneumatic single-lumen conserver can provide a rapid response to patient inhalations without the need for a more expensive dual-lumen cannula hose. In addition, after delivering oxygen the conserver has a specific pneumatically-implemented delay period before being able to detect the next inhalation to inhibit “double pulse” deliveries. In addition to a conserving or pulse flow mode, the conserver can provide a user-selectable gas flow at a continuous or constant flow mode.

Abstract: A multiple stage variable speed blower for Continuous Positive Airway Pressure (CPAP) ventilation of patients includes two impellers in the gas flow path that cooperatively pressurize gas to desired pressure and flow characteristics. Thus, the multiple stage blower can provide faster pressure response and desired flow characteristics over a narrower range of motor speeds, resulting in greater reliability and less acoustic noise.

Abstract: Described is a system including a sensor and a processing arrangement. The sensor measures data corresponding to a patient's breathing patterns. The processing arrangement analyzes the breathing patterns to determine whether the breathing patterns are indicative of a REM sleep state. In another embodiment, the processing arrangement analyzes the breathing patterns to determine whether the breathing patterns are indicative of one of the following states: (i) a wake state and (ii) a sleep state. In another embodiment, a neural network analyzes the data to determine whether the breathing patterns are indicative of one of the following states: (i) a REM sleep state, (ii) a wake state and (iii) a sleep state. In another embodiment, the processing arrangement analyzes the data to determine whether the breathing pattern is indicative of an arousal.

Abstract: Provided is a high frequency oscillating ventilator comprising a housing assembly, a linear actuator, a linear coil, a piston mounted on a pushrod, a diaphragm dividing a housing into a first and second side and having an opening formed on the second side that is fluidly connected to the patient's airway for delivering gas thereto. The linear actuator is fixedly mounted to the housing assembly and has a linear coil coaxially disposed therewithin. A pushrod supports the linear coil on the linear actuator to allow relative axially sliding therebetween. The piston is directly mounted to the diaphragm such that reciprocation thereof as effectuated by the linear coil cooperating with the linear actuator alternately produces positive and negative pressure waves in the gas in the patient's airway.

Abstract: A switchable adapter for a suction tube has a manifold, a switching base rotatably connected to a pivot portion of the manifold, an air-tight component mounted between the pivot portion of the manifold and the switching base, and a cover mounted on an end of the pivot portion. The switching base has two connecting tubes. When the switching base pivots relative to the pivot portion of the manifold, the connecting tubes alternatively communicate with the manifold by rotation of the switching base. Thus, the switchable adapter is switched to allow the suction tube to suck sputa out of a trachea of a patient.

Abstract: A breathing protector for a tracheostoma is provided. The breathing protector comprises an inlet and an outlet, such that an air flow in use will pass from the surroundings of the user through said inlet to said outlet, into trachea of said user. Further, it comprises a filter housing, said filter housing comprising an inner housing part, an outer housing part, and a filter body. The inner housing part, comprising the outlet, a tracheal tube fitting and a support structure extends longitudinally and distally from the tracheal tube fitting. A base plate is arranged in a proximal zone of the tracheal tube fitting, said base plate extending radially outwards from the tracheal tube fitting. The outer housing par, comprising the inlet, forms a cage enclosing the support structure. The filter body is arranged between the support structure and the outer housing part. An assembly tool and an assembly method thereof are also provided.

Abstract: Intubation devices and method of intubation are provided for a medical provider to firmly hold an intubation stylet with the middle, the ring, and the little finger of one hand, point the tips of the intubation stylet and an endotracheal tube towards the opening of the trachea, and then advance the endotracheal tube over the stylet into the trachea with the index finger and the thumb of the same hand without an assistant to hold the stylet, while the user can use another hand to hold a laryngoscope to perform laryngoscopy to visualize the vocal cords during endotracheal intubation. The intubation device comprises a handle, a stylet holder, and an arm which is connected to both the stylet holder and the handle. The intubation device further includes a tube support, and a tube holder to further support the endotracheal tube.

Abstract: A patient interface for treatment of a user having a respiratory disorder includes a nasal portion having at least one nasal portion aperture adapted to be in communication with a supply of pressurized gas for delivery to at least one nasal opening of the user, and a mouth portion having at least one mouth portion aperture also adapted to be in communication with the supply of pressurized gas to deliver the pressurized gas to an oral cavity of the user's mouth. The at least one mouth portion aperture is separate from the at least one nasal portion aperture, and the patient interface is adapted to limit a flow of the pressurized gas out of the at least one aperture of the mouth portion to be no greater than a flow of the pressurized gas out of the at least one nasal portion aperture.

Abstract: A mask system includes a cushion adapted to seal with a face of a patient. In one form an unobtrusive full-face masks system is provided which is comfortable and has a wide fit range. The cushion may include a sealing structure (127-10) and a supporting structure (127-20). The supporting structure may include gaps or spacing in a nasal bridge region (NBR) and/or a lip region CHN.

Abstract: A connecting unit for fixing components in a breathing system includes a plug adapter (2) having a sealing element (1). The sealing element (1) has a first peripheral fastening thickening (4), a second fastening thickening (5) arranged at a distance to the first fastening thickening (4), as well as an undercut (7) between the fastening thickenings (4, 5). The second fastening thickening (5) has an outer lead-in chamfer (6) for a receiving bore into which the plug adapter (2) along with the sealing ring (1) are inserted.

Abstract: A high flow therapy system for delivering pressurized, heated and humidified respiratory gas to an airway of a patient includes a respiratory gas flow pathway for delivering the pressurized respiratory gas to the airway of the patient by way of a non-sealing respiratory interface; wherein flow rate of the pressurized respiratory gas is controlled by a microprocessor, a mixing area for mixing oxygen and air in the respiratory gas flow pathway, a humidification area for humidifying respiratory gas in the respiratory gas flow pathway, a heated delivery conduit for minimizing condensation of humidified respiratory gas, a pressure pathway for monitoring pressure of the airway of the patient and communicating the monitored pressure to the microprocessor and a sensor disposed in communication with the pressure pathway, the sensor further disposed in communication with the microprocessor and configured to measure pressure in the airway of the patient.

Abstract: A method of treating a hole formed in a catheter includes providing the catheter with an opening formed in a wall of the catheter from an external surface of the catheter to an internal surface of a lumen of the catheter such that the catheter has a sharp external edge formed between the external surface and the opening and a sharp internal edge formed between the opening and the internal surface of the lumen of the catheter. The method additionally includes pushing a proximal end of a mandrel into the opening formed in the wall of the catheter and rounding the sharp external edge of the opening formed in the wall of the catheter with a distal end of the mandrel. The method further includes maintaining the sharp internal edge formed between the opening and the internal surface of the catheter.

Abstract: Catheter assemblies are described having a catheter hub with a catheter tube and a needle hub with a needle projecting through the catheter tube. The catheter hub has a valve or a septum for stopping or slowing down the flow of fluid in or out of the catheter hub when the valve or septum is closed. The valve has features formed thereon to facilitate venting, opening, closing, or combinations thereof.

Abstract: Embodiments of the present disclosure are directed to delivery devices, methods, and systems for delivering an implant to a target site. In one embodiment, a delivery device includes a core member defining a proximal end and a distal end and an outer winding defining a proximal end and a distal end, wherein the outer winding surrounds and is coupled to the core member. The outer winding extends at least partially between the proximal end of the core member and the distal end of the core member, and the outer winding is configured for displacement within a delivery catheter. The delivery device further includes a coupling member at the distal end of the core member configured to releasably attach to an implant.

Abstract: Catheters, sheaths, or other tubular devices are provided that include a proximal end, a distal end sized for introduction into a patient's body, and a steerable distal portion. The tubular device includes a primary lumen extending between the proximal and distal ends; an auxiliary lumen adjacent the primary lumen; and one or more reinforcement members including windings extending helically along at least the distal portion, at least some of the windings passing between the primary and steering element lumens and at least some of the windings surrounding both the primary and steering element lumens. In one embodiment, a steering element is slidably disposed within the auxiliary lumen. Apparatus and methods for making such tubular devices are also provided.

Abstract: One embodiment is an improved method for providing a tube for attachment to a medical device such as a catheter that provides for intermittent changes in tube path length as a result of body movement thereby reducing the stress and pain caused by pulling on the device, as well as the optional provision to provide a very low, controlled tension that provides improved stability of the medical device without damage to the surrounding body tissues. In at least one embodiment, there is a decrease in infection risk by the patient. This controlled tension can be applied or removed intermittently by a medical practitioner or the patient. Other embodiments provide for extension in tubal path length while simultaneously providing for intermittent or continuous low tension pull on the catheter. Provision is also made for a continuous smooth fluid path with no moving internal parts.

Abstract: Anchors for securing a therapy device such as a therapy catheter relative to a burr hole, and systems and methods for using the same. Anchors in accordance with embodiments of the present disclosure may include a connector for securing the therapy catheter to a delivery catheter, wherein the connector is independently and removably attachable to the anchor. The connector may secure the therapy catheter relative to the burr hole and isolate forces that may otherwise tend to disrupt the placement of the therapy catheter.

Abstract: The present invention is an implantable medical device that is used deliver materials or energy into a patient's physiology, or from one region of a patient's physiology to another. The device includes a port element with a passageway therethrough for directing and anchoring a conduit element in a desired location. The implantable port stabilizes an elongated conduit within human physiology for long-term use, and includes a support passageway formed through the port and extending between an upper surface and a lower surface of the port, wherein the support passageway is sized and shaped for receiving the elongated conduit slideably inserted therethrough. The device includes a tissue ingrowth scaffold fixedly disposed on at least a portion of at least one surface of the implantable port for positioning in contact with adjacent tissue.

Abstract: The invention relates to a needle safety device for a medical device, the needle safety device comprising: a base portion having a bore extending along a longitudinal center axis therethrough for receiving a needle; and two opposing jaws extending from the base portion generally in the axial direction and each having a head portion in the region of its free end, wherein the needle safety device includes a locking projection for securing the needle safety device to the medical device. The needle safety device according to the invention further provides at least one elastic element mounted to the jaws in a non-surrounding manner lateral to the center axis in a region between the base portion and the head portions, wherein at least one elastic element and the jaws are configured such that the jaws can be spread apart against a restoring force of at least one elastic element in order to allow the needle received in the bore to extend all the way through the needle safety device.