Abstract: A system including a steam generation system and a chamber. The steam generation system includes a complex and the steam generation system is configured to receive water, concentrate electromagnetic (EM) radiation received from an EM radiation source, apply the EM radiation to the complex, where the complex absorbs the EM radiation to generate heat, and transform, using the heat generated by the complex, the water to steam. The chamber is configured to receive the steam and an object, wherein the object is of medical waste, medical equipment, fabric, and fecal matter.

Abstract: A system for use in an orthopedic surgical procedure including a container for orthopedic surgical instruments. The container includes a first shell, and a second shell configured to be coupled to the first shell to define a chamber therein. The second shell is configured to be coupled to the first shell in a plurality of orientations including a first orientation in which fluid is permitted to advance into and out of the chamber, and a second orientation in fluid is prevented from advancing into and out of the chamber.

Abstract: A process for imparting scent to air comprising the steps of: providing a plurality of particles in a reservoir; heating the reservoir to melt the particles to form a melt; and contacting the melt with air; wherein the particles include polyethylene glycol, perfume, and starch granules and each particle has a mass between about 0.95 mg and about 5 grams.

Abstract: The present disclosure provides antimicrobial peptides, and compositions comprising same. The present disclosure further provides methods of inhibiting microbial growth.

Abstract: A system includes a chest tube drainage system comprising a first chamber in fluid communication with a port connectable to a chest tube, a second chamber in fluid communication with a port connectable to a suction device, and a fluid seal connected to and disposed between the first chamber and the second chamber. The system also includes one or more gas sensors attached to the chest tube drainage system, the one or more gas sensors configured to detect at least one of gaseous carbon dioxide and gaseous oxygen, a controller connected to the one or more gas sensors, and at least one indicator coupled to the controller. The controller is configured to determine if a threshold level of carbon dioxide is exceeded, and to activate the at least one indicator if the threshold level of carbon dioxide is not exceeded.

Abstract: An apparatus and method for aspirating, irrigating and/or cleansing wounds is provided. The apparatus and method include one or more of the following: simultaneous aspiration and irrigation of the wound, supplying of thermal energy to fluid circulated through the wound; supplying physiologically active agents to the wound; a biodegradable scaffold in contact with the wound bed; and application of stress or flow stress to the wound bed.

Abstract: A syringe for medical applications includes a syringe body having an inner wall, a first stop, located along the inner wall, to leave at least one first blank surface on the inner wall; and a plunger sliding along the inner wall of along a longitudinal axis of the syringe, the plunger including a plunger head and an operating rod, connected to the plunger head, including, on its outer surface, at least one first rack arranged longitudinally along the operating rod, the first rack including protruding teeth. The first stop and the protruding teeth are also shaped and constituted so as to prevent the plunger from lowering again due to pressure on the operating rod, unless the first rack is disengaged by rotating the plunger within the syringe body around the longitudinal axis so that the first rack faces the first blank surface of the inner wall of the syringe body.

Abstract: Some embodiments disclosed herein are directed to a pump assembly comprising a voice coil, a magnet and a diaphragm, wherein the voice coil is configured to move the diaphragm to pump a fluid through the pump assembly in response to a drive signal applied to the voice coil. Some embodiments disclosed herein are directed to an apparatus for applying negative pressure to a wound comprising a source of negative pressure configured to be coupled to a dressing, the source of negative comprising a voice coil actuator and a diaphragm, and a controller configured to produce a drive signal for the voice coil actuator.

Abstract: A reduced pressure treatment system includes a control unit having a control system and a reduced pressure source. The reduced pressure treatment system further includes a manifold unit in fluid communication with the reduced pressure source and a component module to augment treatment. The component module is configured to communicate with the control system of the control unit, and the component module includes a first mounting region configured to be coupled to a complimentary mounting region of the control unit. The component module further includes a second mounting region identical to the complimentary mounting region of the control unit to allow a second component module to be coupled to the first component module.

Abstract: Various “contactless” bearing mechanisms including hydrodynamic and magnetic bearings are provided for a rotary pump as alternatives to mechanical contact bearings. In one embodiment, a pump apparatus includes a pump housing defining a pumping chamber. The housing has a spindle extending into the pumping chamber. A spindle magnet assembly includes first and second magnets disposed within the spindle. The first and second magnets are arranged proximate each other with their respective magnetic vectors opposing each other. The lack of mechanical contact bearings enables longer life pump operation and less damage to working fluids such as blood.

Abstract: A cannula is provided with one or more pressure transducers for measuring fluid pressure interiorly or exteriorly of the cannula. The pressure transducers may be mounted integrally with the tubular wall defining the main lumen of the cannula, or they may comprise differential pressure transducers mounted in dedicated lumens in communication with the main lumen. The pressure measurements from the transducers is used to determine fluid flow rate.

Abstract: Systems and methods are disclosed for performing hemodialysis that include fluid handling systems that provide accurate control over the type and level of hemodialysis being performed. The system includes a first pump for pumping dialysate into a dialyzer and a second pump for pumping dialysate out of the dialyzer. The system also includes a third pump that provides improved control of a level of ultrafiltration, hemodiafiltration, or both.

Abstract: A dialysis disposable sterilization apparatus includes a connector and a protective cap fitted to the connector. The apparatus also includes a sealing ring provided by one of the protective cap or the connector, the sealing ring forming a seal between the cap and the connector, the seal capable of holding pressure. The apparatus further includes a stabilization rib provided by the connector, the stabilization rib positioned and arranged to (i) tend to prevent the protective cap from vibrating about the sealing ring and (ii) enable a sterilizing gas to flow past the stabilization rib to contact the sealing ring.

Abstract: A device can be used to retain circulating tumor cells (CTCs). The device can include a cross-flow module with a retentate channel and a permeate channel. A filter in the cross-flow module can separate the retentate channel from the permeate channel. The filter can be constructed such that CTCs are retained in the retentate channel while other cells can pass through the filter into the permeate channel. A recirculation channel can direct a flow from an outlet of the retentate channel back to an inlet of the retentate channel to thereby concentrate CTCs in the retentate flow.

Abstract: An extracorporeal reservoir device including a housing, a venous inlet sub-assembly, and a venous filter. The venous sub-assembly is mounted to the housing and includes a downtube and a luer port connector body. The connector body extends from the downtube and forms a passageway open to a lumen of the downtube. The connector body is arranged such that fluid flow from the passageway merges with a flow path of fluid along the primary lumen at an angle of less than 90°. Secondary blood flow through the port connector body is less likely to induce turbulent flow into venous blood flow within the downtube, and is thus less likely to break up any bubbles carried by the venous blood. For example, at port flow rates of less than 500 mL/minute, fluid flow from the port connector body does not induce turbulent flow into fluid flowing through the primary lumen.

Abstract: Described herein are pharmaceutical packaging systems which prevent oxidative degradation of oxygen-sensitive drugs, such systems including a primary packaging container with an oxygen permeable component, a secondary packaging with very low permeability to oxygen and an oxygen absorber.

Abstract: A delivery system for delivering fluidic media to a user having a second housing portion configured to be selectively operatively engaged with and disengaged from a first housing portion, the first housing portion and the second housing portion configured to be slidable relative to each other to operatively engage each other; and a fluid connector supported by one the housing portions in a position to engage a reservoir supported by an other of the housing portions in a case where the first housing portion and the second housing portion are slid relative to each other to operatively engage each other.

Abstract: A patient care system includes a control unit capable of coupling with multiple modular medical devices. A modular medical device can be coupled with the control unit, wherein the behavior of the modular medical device automatically adjusts based on the status of being coupled or un-coupled with the control unit.

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 an impact detection system that can sense when an impact above the threshold level has occurred to the pump device, which thereby enables the infusion pump system to initiate appropriate patient safety countermeasures.

Abstract: An on-body injector and method of use including an on-body injector for use with an injection device. The on-body injector includes a bolus reservoir; a bolus injection needle in fluid communication with the bolus reservoir, the bolus injection needle having a bolus injection needle tip aligned with the injection port, the bolus injection needle being slideably biased away from the injection port to define a gap between the bolus injection needle tip and the injection port; and a button operably connected to the bolus injection needle to slide the bolus injection needle along the injection axis. The button is operable to advance the bolus injection needle tip to close the gap and advance the bolus injection needle tip into the injection port. The button is further operable to advance a plunger through the bolus reservoir to deliver a predetermined bolus volume to the patient through the injection flow path.

Abstract: An intravenous infusion tubing fitment comprises a body, a rotatable knob coupled with the body, and a pressure dome seated within the knob. The body defines; a first inlet configured for coupling with a first segment of tubing; a first outlet into a pressure dome; a second inlet from the pressure dome; and a second outlet configured for coupling with a second segment of tubing. The knob defines an expansion opening within a surface of the knob. The pressure dome is formed of a flexible elastomeric material and defines a fluid flow path between the first outlet and the second inlet. The pressure dome includes a vane configured to variably regulate flow through the fluid flow path in response to rotation of the knob. The pressure dome is configured to expand through the expansion opening in response to fluid pressure in the fluid flow path.

Abstract: A finger grip extension for a syringe is configured to increase the leverage the hand of an operator on the plunger of a syringe during injection of medical fluid into, or withdrawal of medical fluid from a body site. The finger grip extension for a syringe is used with a syringe having a barrel portion having an open proximal end and a distal end for mounting a medical fluid conduit thereon. The open proximal end of the syringe barrel terminates in a rim or flange. The syringe also includes a plunger having a proximal end and a distal end for insertion into the open proximal end of a syringe. The extension grip includes an upwardly extending portion located inside or outside of a syringe barrel. The upwardly extending portion includes a finger support at the uppermost portion thereof.

Abstract: A method for assembling a syringe includes supporting a syringe barrel having a stopper being movably disposed therein. A distal end of a plunger rod is inserted into the compartment of the syringe barrel. An initial digital image is taken of the stopper within the syringe barrel. The distal end of the plunger rod is coupled to the stopper located within the syringe barrel so that the plunger rod is secured to the stopper. A plurality of further digital images of the stopper within the syringe barrel are taken during or after coupling the distal end of the plunger rod to the stopper. Information determined from each of the further digital images is compared to information determined from the initial digital image using a computer processor to determine if the stopper in each of the further digital images has moved relative to the syringe barrel.

Abstract: Methods and devices for metering and delivering a desired dose of medication from a syringe are described. The devices may include a dosage limiting sleeve adjustably disposed around a syringe body, wherein the alignment of the dosage limiting sleeve relative to the syringe body indicates the dose to be administered by depressing a plunger until the dosage limiting sleeve is engaged.

Abstract: The present invention relates to a field of drug injection, and discloses a drug information detection device and a drug information detection type injection device. The drug information detection device is configured to detect an injected dose of an injection pen containing drug. The drug information detection device includes a housing, a rotary encoder configured to convert rotational information of the adjusting knob into drug injected dose information, and a control assembly. The rotary encoder includes an encoder body and a rotary block rotatably connected to the encoder body. The encoder body and the control assembly are electrically connected to each other. The housing is configured to cover the encoder body and the control assembly.

Abstract: A drive assembly comprises a housing, a drive member moveable for setting a dose and for delivering the dose. A piston rod adapted to be driven by the drive member in the distal direction during movement of the drive member in the distal direction for dose delivery and a restriction member for restricting proximal movement of the piston rod during proximal movement of the drive member by mechanical interaction of the restriction member with a stop feature. The restriction member and stop feature arranged for the piston rod to be moved proximally a first distance during a first movement of the drive member before the restriction member and stop feature interact mechanically. The first distance the piston rod moves proximally during the first movement of the drive member is different than a subsequent distance the piston rod moves during a subsequent proximal movement of the drive member.

Abstract: A needle shield arrangement for a syringe (10), having a generally cylindrical body with a needle (16) at its forward end, includes a shield portion (20) adapted for shielding the needle (16); a syringe engaging portion (22) for engagement with the syringe body, and a frangible connecting portion (24) connecting the shield portion and the syringe engagement portion.

Abstract: An elastic cap detachably mountable to a barrel tip portion of a barrel so as to seal a tip of a needle hole includes a cylindrical receiving hole configured to receive at least part of a barrel tip portion and a puncture needle of a barrel. The receiving hole includes a first inner diameter portion having a smaller diameter than an outer diameter of the annular head; a stopper portion provided at an end of the first inner diameter portion; and a second inner diameter portion that is formed from the stopper portion to a bottom wall provided at an end of the second inner diameter portion, the second inner diameter portion having a smaller diameter than the first inner diameter portion.

Abstract: A syringe (1B) comprises: a syringe body (1C) including a plunger (32) to be operated for injection of a drug solution; a cylindrical needle cover (11B) housing an injection needle (100A); and a spring (18) held in a compressed state by the needle cover (11B). The needle cover (11B) has seats (153A) and (155B) in a pair that abut on corresponding opposite ends of the spring (18) to restrict the position of the spring (18). Pushing in the plunger (32) further after injection deforms the seat (155A) to release restriction on the spring (18). The spring (18) free from the restriction abuts on the syringe body (1C). This biases the needle cover (11B) to move the needle cover (11B) to a position where the injection needle (100A) is housed.

Abstract: Disclosed is a nebulizer having attached housing, which is attached in a way that permits removal, which housing holds containers of liquid medication for dispensing via nebulization, which nebulizer is constructed to allow containers holding the medication to be used and held within the housing provided that such containers match or conform to the certain mechanical requirements of the nebulizer and housing.

Abstract: An aerosolization system includes a container that is configured to deliver a unit dosage of a liquid when squeezed a single time. The system also includes an aerosolizer that is constructed of a housing defining a mouthpiece, and an aerosol generator disposed in the housing. The aerosol generator includes a vibratable membrane having a front face and a rear face, and a vibratable element used to vibrate the membrane. Further, the housing includes an opening that is adapted to receive a unit dosage of the liquid from the container. The opening provides a liquid path to the rear face of the vibratable membrane.

Abstract: A device for dispensing a medium is disclosed. The device comprises an elongated body including a chamber for containing a medium and an outlet through which the medium exits the device into an oral or nasal opening. A dispensing system selectively places the chamber and the outlet in communication, causing medium to flow out of the device.

Abstract: The claimed subject matter relates to a device for dosing and aerosolization of aerosolizable material. The device includes a body with an aerosolization channel with a distal attachment for connecting a source of carrier gas. The carrier gas provides pressure pulses to the aerosolization channel. A proximal attachment allows the aerosolized material to move to a reservoir for receiving the aerosolizable material. The reservoir is connected to the body via the the aerosolization channel. At least part of the walls of the device are self-exciting membranes that can be put into oscillation by the pressure pulses.

Abstract: The invention concerns a gel covering of a patient interface. This gel covering has a mask connection area by which its side that faces away from the patient is joined with a mask body. The patient interface can be designed, for example, as a respiratory mask. On its side that faces the patient's face, the respiratory mask has thin, inwardly formed, peripheral contact lips. The respiratory mask has accessories that allow it to be fastened on the patient's head as well as a hose connection for supplying air. At least one region formed from a filler is placed in or on the walls of the gel covering. The method is used to produce the gel covering of the invention.

Abstract: A pressure support device includes a humidification system (10) to control the humidity of a pressurized flow of breathable gas generated by the pressure support device. The humidification system includes a liquid storage chamber (32) and a humidification chamber (34). When in an operational orientation, liquid travels from the liquid storage chamber to the humidification chamber through a serpentine feed path (38) due to gravity. The serpentine shape of feed path halts the flow of liquid responsive to the device being tilted out of an operational orientation.

Abstract: A positive pressure gas supply system configured to supply positive pressure gas to a patient includes a CPAP unit configured to generate a flow of positive pressure gas. A humidifier base is positioned to receive the flow of positive pressure gas from the CPAP unit. A receiving portion of the humidifier base is configured to removably receive a refilling module. The refilling module is configured to hold a volume of water, complete a gas flow path partially defined by the humidifier base, and humidify the positive pressure gas. In addition, a respiration tube connecting portion is positioned to remain in communication with a gas discharge passage of the humidifier base when the refilling module is removed from the humidifier base. The respiration tube connecting portion is configured to be connected to a respiration tube and deliver the humidified positive pressure gas to the respiration tube.

Abstract: A humidifier assembly for a CPAP includes a base housing with a gas inlet configured to receive respiratory gas from the CPAP unit. The base housing includes a first connecting device located at a sidewall of the base housing and configured to directly, removably connect the base housing to the CPAP unit. The base housing also includes a second connecting device configured to be coupled to an air delivery hose. The humidifier assembly further includes a liquid storage container that is removably received in the base housing. The liquid storage container includes a liquid storage space configured to store liquid and a humidifying region configured to receive the respiratory gas from the gas feed opening and receive a partial amount of the liquid stored in the liquid storage space to enrich the respiratory gas with moisture.

Abstract: A catheter assembly includes a catheter hub defining an interior cavity and a catheter tube extending distally thereof. A rigid actuator extends proximally in the interior cavity and supports a seal member thereon. The seal member includes a central membrane, a distal portion, and a proximal portion. An hourglass shaped actuator cavity is formed in the distal portion and receives a barbed end of the actuator. The outer surface of the seal member is in partial circumferential engagement with the catheter hub to define an air path that allows fluid communication between areas of the interior cavity distal and proximal of the seal member. A punch tool is provided to form a tri-slit in the membrane of the seal member.

Abstract: A catheter includes an inner layer, and a braid provided on an outer periphery of the inner layer. The braid includes a first wire and a second wire that are woven together. The catheter further includes a tip provided on a distal end of the inner layer and a distal end of the braid. A residual portion having a sharp shape formed at a distal end of the first wire when the first wire is cut is not left untreated, but is formed into a bulging portion.

Abstract: A catheter procedure system including a bedside system and a remote workstation is provided. The bedside system includes a catheter including an expandable percutaneous intervention device, a robotic catheter system configured to move the catheter, and an inflation device configured to cause expansion of the expandable percutaneous intervention device. The remote workstation includes a user interface configured to receive a at least first user input and a second user input and a control system operatively coupled to the user interface for remotely controlling both the robotic catheter system and the inflation device. The remote workstation includes a monitor configured to display information related to the expandable percutaneous intervention device.

Abstract: A magnetically-guided catheter includes a tip positioning magnet in the distal electrode assembly configured to interact with externally applied magnetic fields for magnetically-guided movement. A magnetically-guided mapping catheter includes an electrically-conductive capsule in the form of a casing that includes a distal ablation surface and isolates the positioning magnet from bio-fluids to prevent corrosion. An open irrigation ablation catheter includes an isolated manifold that isolates the positioning magnet from contact with irrigation fluid to prevent corrosion.

Abstract: A catheter includes a tip electrode with a shell and a support member to provide a plenum chamber. The plug is formed with a U-shaped passage for a safety line to wrap around and secure the support member (with the shell affixed thereto) to the catheter. Additional passages are formed in the plug to accommodate components such as irrigation tubing, lead wire and thermocouple wire pair. A method of manufacture provides distal installation and/or anchoring of the safety line, lead wire and thermocouple wire pair in the support member prior to sealing the support member and mounting the shell.

Abstract: A catheter having an internal advancing mechanism that can advance stiffening wires or other devices, has a catheter with a catheter body, a tip section distal the catheter body, a device extending through at least the catheter body, and a control handle proximal the catheter body, where the control handle has an advancing mechanism with a threaded member, an adjustment member, and a guided member to which the device is connected, and the advancing mechanism is configured to advance and retract the device along the catheter body as controlled by a user. Each of the threaded member and the adjustment member has a generally cylindrical configuration. The threaded member has an outer surface configured with a helical guide channel. The adjustment member is configured to guide the guided member to move within the helical guide channel to advance and retract the device. The adjustment member can be rotatable over the threaded member by the user to control advancement and retraction of the device.

Abstract: The invention relates to a low profile lumen free balloon catheter and a system for advancing the lumen free balloon from a build wire to a wire guide. The low profile balloon lacks an internal wire guide cannula between the catheter shaft and the soft tip. A releasable engagement is provided to connect/disconnect the build wire to/from the wire guide. A soft tip seals around the wire guide following advancement of the balloon catheter over the wire guide.

Abstract: A device for stabilizing a patient catheter includes a docking pod with a body, an inlet, an outlet, an internal fluid path between the inlet and the outlet, and a securement surface located on an underside of the docking pod. A docking pod adhesive layer located at least partially on the securement surface of the docking pod may secure the docking pod to the patient such that the securement surface and the docking pod adhesive layer form a generally planar or concave surface when secured to the patient. A valve mechanism located within the internal fluid path of the docking pod may control fluid flow through the docking pod. The device may also have a luer connector that is fluidly connected to the outlet of the docking pod and configured to be connected to the catheter.

Abstract: Some embodiments of a medical device anchor system include an anchor sleeve that receives a catheter (or other medical instrument) though a working channel of the anchor sleeve. The anchor sleeve may include a first actuator that controls the extension of one or more subcutaneous tines into the subcutaneous region under the skin. The anchor sleeve can also include a second actuator that can cause the anchor sleeve to lock onto an outer portion of the catheter (or other medical instrument) arrange in the working channel.

Abstract: A guidewire insertion aid is is configured to feed out a guidewire inserted in a housing in order to insert said guidewire into the lumen of a piece of medical equipment. In some examples, the insertion aid comprises: a main body, a housing support part and a guidewire support part. A sliding contact part is disposed between the housing support part and the guidewire support part. The sliding contact part extends in the lengthwise direction of the main body and has a sliding contact surface for the guidewire. A feed-out member is provided on the main body and has a water-retentive water-retention member. The feed-out member is disposed with the water-retention member side thereof facing towards the sliding contact surface. The feed-out member can be displaced while the guidewire is held between said feed-out member and the sliding contact part.

Abstract: Methods for treating hydrocephalus using a shunt, the shunt having one or more CSF intake openings in a distal portion, a valve disposed in a proximal portion of the shunt, and a lumen extending between the one or more CSF intake openings and the valve, the method comprises deploying the shunt in a body of a patient so that the distal portion of the shunt is at least partially disposed within a CP angle cistern, a body of the shunt is at least partially disposed within an IPS of the patient, and the proximal portion of the shunt is at least partially disposed within or proximate to a JV of the patient, wherein, after deployment of the shunt, CSF flows from the CP angle cistern to the JV via the shunt lumen at a flow rate in a range of 5 ml per hour to 15 ml per hour.

Abstract: Systems and methods for treating a lung of a patient. One embodiment of a method comprises positioning a leadless marker in the lung of the patient relative to the target, and collecting position data of the marker. This method further comprises determining the location of the marker in an external reference frame outside of the patient based on the collected position data, and providing an objective output in the external reference frame that is responsive to movement of the marker. The objective output is provided at a frequency (i.e., periodicity) that results in a clinically acceptable tracking error. In addition, the objective output can also be provided at least substantially contemporaneously with collecting the position data used to determine the location of the marker.

Abstract: Disclosed are injection molded devices including microneedles on a substrate base. The microneedles may include a plurality of nano-sized structures fabricated thereon. The molds used to form the microneedles are assembled from a plurality of mold segments, each defining portions of the microneedles. Upon assembly of the multiple mold segments, microneedle negative cavities are formed. The molds may be used in an injection molding process to form microneedle arrays. Devices may be utilized for interacting with a component of the dermal connective tissue.