CareFusion 2200, Inc. Patent applications |
Patent application number | Title | Published |
20160022343 | APPARATUS AND METHOD FOR STYLET-GUIDED VERTEBRAL AUGMENTATION - A stylet-guided balloon vertebroplasty system, as well as methods for bone augmentation using same are provided. In certain embodiments, a pre-curved stylet with an overlying delivery tube may be used to target an approximately centered target site within a bone structure, facilitating direction thereto of an expandable member useful for creating a cavity that may receive curable material to restore bone height and/or to reinforce the bone structure. | 01-28-2016 |
20150342583 | SURGICAL DEVICE AND LINKAGE SYSTEM FOR SAME - A laparoscopic surgical device is provided, including a removable tool-comprising shaft having an outer shaft and an inner actuation rod that may be removably or permanently connected together. A handle of the device includes a two-button mechanism for engaging and releasing the removable tool-comprising shaft. The two-button mechanism is configured to engage overlapping corresponding apertures of the outer shaft and the inner rod that extends through the outer shaft, and the handle may include a variety of configurations that can readily interchangeably be used with different tool bodies. | 12-03-2015 |
20150335467 | PATIENT WARMING SYSTEM CONNECTION DEVICE - A connection device for a patient warming system is provided. The device includes a first connector port and a second connector port that each includes a wall that circumferentially defines a longitudinal channel. The first and second connection ports are each configured to receive a tubing that leads to a patient warming device. A self-sealing valve is aligned in each of the longitudinal channels to engage an inlet and outlet port of a control unit of the patient warming system. A planar base member of the connection device joins the second end of the first connector port generally parallel to the second end of second connector port. The connection device also includes a flexure member with a first catch mechanism that releasably secures the connection device to the control unit of the patient warming system. | 11-26-2015 |
20150290409 | METHODS FOR CONTROLLING MECHANICAL LUNG VENTILATION - A method for controlling mechanical lung ventilation is described. The method may include supplying a breathing gas to an airway of a patient in an intermittent way such that a plurality of respiratory cycles are formed; measuring a volume received by the patient in one or more respiratory cycles of the plurality of respiratory cycles; comparing the measured volume of each of the one or more respiratory cycles with a user defined target volume; attributing a classifying score to each of the one or more respiratory cycles based at least partially on a deviation between the measured volume and the user defined target volume; summing the classifying scores and dividing the result by a sample size of the one or more respiratory cycles; attributing a pressure step value based at least partially on the division result; and adding the pressure step value to a present pressure. | 10-15-2015 |
20150290408 | METHODS FOR CONTROLLING MECHANICAL LUNG VENTILATION - A method for controlling mechanical lung ventilation is described. The method may include intermittently switching the airway pressure of the patient from a substantially constant high baseline pressure level to a substantially constant low baseline pressure and vice-versa such that the patient is able to breathe spontaneously in both high and low baseline pressure levels; detecting an inspiration effort by the patient inside a trigger time window that immediately precedes a switching event of the intermittently switching the airway pressure; maintaining a baseline pressure at the level in which the inspiration effort was detected so that the patient can complete the inspiration-exhalation cycle; and switching the baseline pressure level after a delay time. | 10-15-2015 |
20150290407 | LUNG VENTILATION APPARATUS - A lung ventilation apparatus and system are described. The lung ventilation apparatus may include a control panel; and a graphical user interface associated with the control panel, the graphical user interface comprising a central strip content item covering at least 50% of a total area of the graphical user interface, the central strip content item representing at least one of a patient monitoring screen or surveillance screen, the central strip content item comprising a first portion and a second portion, wherein the first portion comprises numerical elements indicating ventilation parameters of a patient, and the second portion comprises a graphical element indicating pressure at a patient airway. | 10-15-2015 |
20150257809 | METHOD FOR BALLOON-ASSISTED AUGMENTATION AND FUSION OF ADJACENT VERTEBRAL BODIES - A vertebral augmentation system and methods for vertebral augmentation and/or fusion using same are provided. In certain embodiments, a pre-curved stylet or needle with an overlying delivery tube may be used to target a site within a bone structure, facilitating direction thereto of an expandable member useful for creating a cavity that may receive curable material to restore bone height, to reinforce the bone structure, and/or to fuse two, three, or more adjacent vertebrae. An expandable member such as, for example, a balloon can be used to create a plurality of voids by displacing bone material, where the voids can be filled with curable material to augment the vertebrae and intervening space can be filled to fuse those adjacent vertebrae. | 09-17-2015 |
20150190536 | SYSTEMS, METHODS, AND DEVICES FOR STERILIZING ANTISEPTIC SOLUTIONS - A method for sterilizing an antiseptic solution includes providing a container containing the antiseptic solution, the antiseptic solution having an initial purity, selecting a sterilization temperature from about 85° C. to about 135° C. and an sterilization time from about 1 minute to about 19 hours, heating the antiseptic solution to the selected sterilization temperature, maintaining the temperature for the selected sterilization time, and terminating the heating of the antiseptic solution when the sterilization time expires. After terminating the heating, the antiseptic solution has a post-sterilization purity. The sterilization temperature and the sterilization time are selected such that after terminating the heating, the antiseptic solution is sterile and has a post-sterilization purity of at least about 92% and the percentage point change in purity from the initial purity to the post-sterilization purity is at most about 5%. | 07-09-2015 |
20150174375 | PLEURODESIS DEVICE AND METHOD - System and components for inducing pleurodesis or other sclerosis or desired adhesion conditions to treat a patient, while minimizing likelihood of tissue damage from direct application of sclerosis-enhancing materials. A tube device is provided that is configured to elute sclerosis-enhancing material and/or other medicaments via a fenestrated drainage tube. The assembly of tube device with outer (typically drainage) tube may include one or more features configured to enhance delivery of medicament and/or drainage through the same assembly. | 06-25-2015 |
20140303632 | DEVICE AND METHOD FOR DELIVERING A CURABLE MATERIAL INTO BONE - A curable material delivery cannula device and method are disclosed. The device includes a cannula and a hub. The cannula includes an open proximal end and a deflectable distal segment, and a distal orifice(s) fluidly connected to the lumen. When distally extended from the guide cannula, the deflectable segment assumes a curved shape, which may be used to create a void in the bone for receiving curable material. During use, curable material, such as bone cement, is delivered from the distal orifice(s). | 10-09-2014 |
20140276254 | PATIENT WARMING AND DVT PREVENTION SYSTEM - A patient warming and deep vein thrombosis system are provided. The system includes a first and a second compliant layer sealed together around an outer border to contain a warm liquid between the two layers and to form a wrap to surround and conform to a body portion of a patient. The wrap includes a plurality of flaps extends from opposite sides of a generally longitudinal central portion, such that one or more flaps from the opposite sides fasten to each other to surround the body portion. The flaps are openable during functional use to provide access to an underlying patient body surface. The system also includes a fluid control pump that directs the liquid through a continuous fluid flow path that extends between the two layers so as simultaneously to fill the wrap and apply pressure and heat to the body portion surrounded by the wrap. | 09-18-2014 |
20140275820 | RESUSCITATION DEVICE WITH ONBOARD PROCESSOR - A resuscitator has a patient airway interface device, a bag, a flow passage coupled between the bag and patient airway interface device, and a sensor assembly. The patient airway interface device may be a mask or an endotracheal tube. The sensor assembly has a display, at least one sensor coupled to the flow passage and configured to provide a measurement of at least one parameter, and a processor coupled to the display and the at least one sensor. The processor is configured to receive the measurement from the sensor and provide information on the display based on the received measurement. The information may include a current breath rate, a pressure-vs-time curve, and guidance to the user to assist in achieving a target breath rate. | 09-18-2014 |
20140261454 | TINTED ANTISEPTIC SOLUTIONS HAVING IMPROVED STABILITY - An antiseptic solution including, a cationic antiseptic agent, a film forming polymer, an anionic tinting agent, and a solvent, wherein the cationic antiseptic agent, the film forming polymer and the anionic tinting agent each remain solubilized within the solution for greater than about 1 hour at 25° C. and 60% relative humidity. The antiseptic agent is preferably octenidine dihydrochloride or chlorhexadine gluconate. The film forming polymer is preferably an acrylate polymer. The solvent is preferably ethanol, isopropanol, and n-propanol. When a drape is adhered to a dried surgical film via the antiseptic solution, the force required to peel the drape from the surgical film is at least about 105 g/25 mm. | 09-18-2014 |
20140235727 | ANTIMICROBIAL HYDROGEL POLYMERS - The present invention relates generally to antimicrobial hydrogel polymers, and dressings comprising one or more hydrogel-forming hydrophilic polymers, where the hydrogels and dressings further comprise one or more antimicrobial agents that are released from the hydrogel in a controlled manner. The hydrogels and dressings may be used for medical, veterinary, and/or cosmetic applications. The dressings may be applied, for example, as wound dressings, surgical dressings, and percutaneous site dressings. In certain aspects of the invention, the dressings may be beneficially used in methods of accelerating wound healing, preventing and/or reducing the incidence of wound infection, and reducing scarring associated with wounds. | 08-21-2014 |
20140205360 | ANTISEPTIC APPLICATOR - An applicator assembly includes a head portion having a proximal end, a distal end, and an interior portion defining a fluid chamber; a container for containing an antiseptic solution coupled to and in fluid communication with the proximal end of the head portion; and an application member in fluid communication with the fluid chamber and comprising a foam, having a first foam layer adjacent a second foam layer, wherein the first foam layer is disposed toward the distal end of the head portion and comprises a dye impregnated therein, and the second foam layer is disposed away from the distal end of the head portion and is free from the dye, and wherein, after the antiseptic solution passes from the container through the fluid chamber, the antiseptic solution passes into the first foam layer, whereupon the dye is solubilized by and tints the antiseptic solution. | 07-24-2014 |
20140186092 | ANTISEPTIC APPLICATOR - An applicator assembly includes a body having a proximal and a distal end, a container slidably coupled to the body, a valve cap coupled to the container, and an application member attached to the distal end, wherein an interior of the container is placed in fluid communication with the application member by way of a fluid conduit that is only accessible when one of the body and the container are axially translated in an opposite direction away from each other. | 07-03-2014 |
20140081222 | ANTISEPTIC APPICATOR HAVING HYDROPHILIC FOAM FOR USE WITH ANTISEPTIC SOLUTIONS - An applicator having a hydrophilic foam that is suitable for use with antiseptic solutions may be a hydrophilic polyurethane foam that does not reduce the amount of active ingredient in the solution as it passes through the foam so that it can be applied to the skin. The foam may be used to deliver antiseptics solutions such as octenidine salts, chlorhexidine salts, or any cationic molecule to the skin. The foam may be attached to an applicator containing an antiseptic solution, or it may be used in conjunction with an unattached antiseptic solution reservoir. The foam also allows the solution to wick into the foam and fully saturate the foam without dripping or channeling. | 03-20-2014 |
20140081221 | ANTISEPTIC APPICATOR HAVING HYDROPHOBIC FOAM FOR USE WITH ANTISEPTIC SOLUTIONS - An applicator having a hydrophobic foam that is suitable for use with antiseptic solutions may be a hydrophobic polyurethane foam that does not reduce the amount of active ingredient in the solution as it passes through the foam so that it can be applied to the skin. The foam may be used to deliver antiseptics solutions such as octenidine salts, chlorhexidine salts, or any cationic molecule to the skin. The solution may include alcohol solution. The foam may be attached to an applicator containing an antiseptic solution, or it may be used in conjunction with an unattached antiseptic solution reservoir. The foam also allows the solution to wick into the foam and fully saturate the foam without dripping or channeling. | 03-20-2014 |
20140005570 | FINE NEEDLE ASPIRATION BIOPSY DEVICE | 01-02-2014 |
20130331733 | VACUUM ASSISTED BIOPSY DEVICE - Methods and devices for providing a biopsy device with a modified handle and stylet that provides a vacuum to be delivered to the targeted tissue for removal. The vacuum may draw the tissue into the notch where the tissue may then be severed via the cannula. Alternatively, the tissue may be drawn into to the notch after being severed via the stylet and/or cannula. The vacuum may be used to bring a larger amount of tissue into the notch than would otherwise be brought in the notch if no vacuum was used, providing a larger sample through the same size access point. | 12-12-2013 |
20130327334 | NASAL CONTINUOUS POSITIVE AIRWAY PRESSURE DEVICE - A nasal continuous positive airway pressure (nCPAP) device having a hollow body with a proximal wall, a distal wall, and an exhaust port extending through the distal wall. A proximal tubular member extends through the proximal wall of the body and is arranged such that a stream of gas entering the body through the proximal tubular member will exit the proximal tubular member in a first direction and then enter the exhaust port. A nozzle extends through the body and is arranged such that a stream of gas entering the body through the nozzle will exit the nozzle and then enter the proximal tubular member in a second direction that is opposite the first direction. | 12-12-2013 |
20130281971 | CATHETER ALLOWING VARIABLE DOSING OF AN ACTIVE AGENT - A drug eluting catheter includes an active agent, such as a drug or chemical substance, which is integrated with the catheter and allows variable dosing of the agent for elution to the patient's body. The catheter includes a dosing region and graduated markings or is associated with a measurement device that includes graduated markings that correspond to a range of dose of the active agent associated with the catheter. By removing or masking an undesired dosing region prior to administration, a user may vary the dosage to suit a patient's needs. | 10-24-2013 |
20130261598 | IMPROVED METHOD OF TREATING PLEURAL EFFUSION - The present invention provides methods of treating pleural effusion in a subject, comprising removing fluid from the pleural space at an increased frequency, as compared to previous methods. | 10-03-2013 |
20130251439 | ANTISEPTIC APPLICATOR - An applicator assembly includes a head portion having a proximal end, a distal end, and an interior portion defining a fluid chamber, a container slidably coupled to the head portion, a plug sealing an end of the container, an application member attached to the distal end, and one or more orifices formed through a surface of the plug, wherein the plug is mounted in the interior portion of the head portion and an interior of the container is placed in fluid communication with the application member by way of a fluid conduit that is formed through the plug from the container to the fluid chamber when the container is axially translated toward the head portion to bring the one or more orifices into fluid communication with the container | 09-26-2013 |
20130237795 | PERFORMANCE CONCENTRIC ELECTROMYOGRAPHY NEEDLE - An electromyography needle electrode having an inner core and an outer elongated cannula surrounding the inner core, wherein the inner core includes tungsten. The inner core may comprise at least 99.95 percent tungsten. The outer elongated cannula forms an outer conductive electrode and the inner core forms an inner conductive electrode. At least one insulating layer may be formed between the outer elongated cannula and the inner core. The impedance of the anode and cathode may be matched more closely. | 09-12-2013 |
20130236564 | COPPER SALTS OF ION EXCHANGE MATERIALS FOR USE IN THE TREATMENT AND PREVENTION OF INFECTIONS - Copper salts of ion exchange materials provide copper ions at levels suitable for use as an anti-infective agent. The copper salts of ion exchange materials may be formed using ether and ester derivatives of cellulose, such as carboxymethyl cellulose (CMC), ethylcellulose (EC), methylcellulose (MC), hydroxypropyl cellulose (HPC), hydroxypropyl methyl cellulose (HPMC), hydroxyethyl methyl cellulose (HEMC), cellulose acetate, and cellulose triacetate. Wound dressings having copper salts of ion exchange materials incorporated therein are also provided, and may be used to reduce the incidence of infection in wounds. The wound dressings may also be used to prevent infections in long-term wounds, such as those formed at wound drain, catheter, and ostomy entry sites. Copper salts of ion exchange materials may be used to kill microorganisms, and may optionally be used with additional anti-infective agents. | 09-12-2013 |
20130204279 | CATHETER DESIGN FOR USE IN TREATING PLEURAL DISEASES - A catheter for use in treating pleura diseases, such as pleural effusions and pneumothorax, includes a tip portion that is configured to irritate the pleura when the catheter is inserted in the pleural cavity, thereby initiating mechanical pleurodesis. The tip portion has a substantially rough configuration and may include one or more protrusions that contact the pleura when the catheter is in use, thereby irritating the layers. This irritation causes the creation of fibrous adhesions between the parietal and visceral layers that close off the pleural cavity and prevent further fluid and/or air accumulations that occur as a result of pleural diseases. | 08-08-2013 |
20130195996 | METHOD OF PRODUCING PLEURODESIS - The present invention provides methods of producing pleurodesis in a mammalian subject, comprising administration of a low dosage of a sclerosing agent such as silver or a salt of silver. | 08-01-2013 |
20130190667 | METHODS AND APPARATUS FOR ADJUSTING BLOOD CIRCULATION - Embodiments of the invention include methods and devices for increasing blood flow and controlling the temperature of a mammal. The device generally includes collapsible and pliant body elements, capable of expanding from a first volume into an expanded second volume so which can then be reduced from the expanded second volume into a pressurized third volume. One or more thermal exchange units can be positioned in the one or more collapsible and pliant body elements. Accordingly, the temperature of the extremity of a mammal can be regulated by providing heating or cooling to the one or more thermal exchange units. | 07-25-2013 |
20130184690 | SYSTEMS, APPARATUSES AND METHODS OF TOOL EXCHANGE - A system for exchanging at least one end tool includes at least one tool exchange device for retaining each of the at least one end tool and at least one operating instrument engageable with each of the at least one end tool. The tool exchange device includes a tool retaining mechanism having an opening and a plurality of engagement features to enable mutually exclusive engagement and disengagement of the tool retaining mechanism with each of the at least one tool. Each of the at least one tool is receivable in the opening and has a biasing member engageable with the plurality of engagement features for at least one of biasing to an engaged position and a disengaged position. | 07-18-2013 |
20130172858 | REDUCED BACKFLASH JOINT AND METHOD OF MAKING SAME - A joint and a corresponding method of creating a precision-fit joint, including creating a mating surface on a first joint component so that the mating surface includes one or more interfering features, connecting a second joint component with the mating surface such that the interfering feature is compressed, and heating the mating surface above a glass transition temperature or melting temperature of the mating surface, or otherwise treating the surface, so as to induce flow of material from the interfering feature to a area of relatively low pressure between the first joint component and the second joint component. | 07-04-2013 |
20130156486 | ANTISEPTIC APPLICATOR - An applicator assembly includes a head portion having a proximal, a distal end, and an interior portion defining a fluid chamber, a container slidably coupled to the body, a breakable membrane sealing an end of the container, and a hollow puncture mechanism, wherein the hollow puncture mechanism is mounted in the interior portion of the head portion and an interior of the container is placed in fluid communication with the application member by way of a fluid conduit that is formed through the hollow puncture mechanism from the container to the fluid chamber when the container is axially translated toward the head portion and the puncture mechanism pierces the breakable membrane. | 06-20-2013 |
20130156485 | ANTISEPTIC APPLICATOR - An applicator assembly includes a head portion having a proximal, a distal end, and an interior portion defining a fluid chamber, a container slidably coupled to the body, a sealing member sealing an end of the container, and a lifting member, wherein the lifting member is mounted in the interior portion of the head portion and an interior of the container is placed in fluid communication with the application member by way of a fluid conduit that is formed around the sealing member from the container to the fluid chamber when the container is axially translated toward the head portion and the lifting member lifts the sealing member. | 06-20-2013 |
20130138118 | POWERED SIGNAL CONTROLLED HAND ACTUATED ARTICULATING DEVICE - An articulating device for aiding a user, such as, a surgeon or other medical practitioner, in manipulating a hand-actuated articulating device by providing a powered force used for moving the device, thus reducing or eliminating the need for the user to provide all the force required to move the device. The articulating device includes an input device, which receives one or more user inputs to direct a slave portion to perform work. The articulating device further includes a control portion that assists in transferring user input to the slave portion, and that further provides power assistance to at least partially drive the slave portion, in combination with the user input received by the input device. | 05-30-2013 |
20130090668 | HYDRAULIC DEVICE INCLUDING A SPOOL VALVE AND METHOD OF USE THEREOF - A spool valve for controlling fluid communication among hydraulic cylinders operating control and slave portions of a surgical device. The spool valve may be used to disconnect the control and the slave portions from one another such that there is no fluid communication between the control and slave portions. The spool valve may be used to engage or allow fluid communication between the control and slave. The spool valve may also be used to allow fluid communication between the slave and control portion and a fluid reservoir, thus allowing the hydraulic system to replenish fluid lost to evaporation, leakage, or other escape. The spool valve includes a body portion having at least two ports and a spool having at least one passageway moveable to a position so as to communicate with the at least two ports. | 04-11-2013 |
20130090570 | REDUCED PROFILE BIOPSY DEVICE - A biopsy device is disclosed that includes a housing maintaining a stylet and a cannula, a control device operable to actuate the stylet and the cannula with respect to the housing and a removable handle coupleable to the control device to load the stylet and the cannula, wherein the handle is configured to modify the device from to a loading configuration a delivery configuration such that the device has a reduced profile for obtaining a tissue sample. | 04-11-2013 |
20130053833 | OVERFORCE MECHANISM - An overforce mechanism comprising a driving assembly, a driven assembly, and a variably engageable coupling, shunts or dampens a motion of a control cylinder for a hydraulic device when that motion exceeds a predefined, unsafe threshold. The overforce mechanism avoids or reduces damage either to the device itself, to ancillary devices and/or to the patient. In an aspect, the variably engageable coupling may include a biasing mechanism and a coupling member, wherein the biasing mechanism automatically resets or releases upon reaching a force or tension threshold. Further, the overforce driven assembly may include an overforce rod that allows the force or motion to be channeled away from the source. The variably engageable coupling may comprise a dowel and spring mechanism that automatically resets with tension. | 02-28-2013 |
20120328682 | PARTICLES INCORPORATING ANTIMICROBIAL AGENTS - The present invention relates generally to particles that include one or more antimicrobial agents therein and/or thereon. The particles may be provided with one or more coatings that contain one or more antimicrobial agents, or the one or more antimicrobial agents may be embedded in the particles. The present invention also relates to goods such as medical devices, personal care products, and household devices that incorporate one or more antimicrobial particles. The goods may be provided with one or more coatings that contain the antimicrobial particles, or the antimicrobial particles may be physically embedded in the medical devices. The present invention is further directed towards methods of making such medical devices. The goods incorporating the antimicrobial particles may be used in accordance with methods of killing microorganisms and preventing infections. | 12-27-2012 |
20120302950 | ACTIVE PLEURODESIS CATHETER - System and components for inducing pleurodesis. A tube device is provided that is generally inert in a first state. The device includes a second state that is configured to provide one or both of mechanical and chemical stimulation to induce pleurodesis. Different sheath and tube configurations are provided for the actuatable features of the device. | 11-29-2012 |
20120298114 | WOUND DRESSING SYSTEM - System, method, and components for hygienic maintenance of a surgical wound configured for drainage of ascites from a body cavity. Different aspects of the system may include one or more of a wound dressing, a pocket for low-profile, hygienic, and aesthetic storage of a drainage catheter configured for attachment to a patient and/or wound dressing, and an apron device configured for installation and/or exchange of a wound dressing. | 11-29-2012 |
20120271283 | ARTICULATED SURGICAL TOOL - An articulated surgical tool and method of use are provided. The articulated surgical tool may hold an instrument and a surgical tool and may provide both macro and micro motions in the instrument and/or surgical tool, including by hydraulic operation. The articulated surgical tool may be coupled to a control system, such that manipulation of the control system results in movement of instrument and/or surgical tool, thereby eliminating the need to manually hold and position the instrument and/or surgical tool. | 10-25-2012 |
20120190997 | MAIN STREAM GAS ANALYZING DEVICE - A main stream gas analyzing device for measuring a concentration of a trace gas present in a gas stream and a method of measuring the concentration of the trace gas is disclosed. The main stream gas analyzing device includes a measuring chamber for receiving a gas flow, an infrared reflective material provided on an inner surface of the measuring chamber, an infrared radiation source directed toward the infrared reflective material of the measuring chamber and obliquely angled relative to a longitudinal axis of the measuring chamber such that infrared radiation being emitted from the infrared radiation source is reflected off of the infrared reflective material at least once, and an infrared radiation detector obliquely angled relative to the longitudinal axis of the measuring chamber to receive the reflected infrared radiation. | 07-26-2012 |
20120182134 | MECHANISMS FOR POSITIONING AND/OR HOLDING SURGICAL INSTRUMENTS AND PERFORMING OTHER FUNCTIONS, AND METHODS OF MANUFACTURE AND USE THEREOF - A positioning system is provided for use in remotely-controlled surgical procedures. Also provided are methods of manufacture and use of such a positioning system. The positioning system may hold an instrument, and may provide multiple degrees of freedom of movement to the instrument. The positioning system may be coupled to a control unit, such that manipulation of the control unit results in movement of the positioning mechanism, thereby eliminating the need to manually hold and position the instrument. According to some aspects, the positioning system may be hydraulically actuated. | 07-19-2012 |
20120141186 | ANTISEPTIC APPLICATOR - An applicator assembly may include body having a proximal end portion and a distal end portion, a container having a closed proximal end, an interior, and an open distal end, wherein the container is coupled to the proximal end portion, a material bonded to the open distal end and sealing the interior of the container, and an application member attached to the distal end portion, wherein the interior of the container is placed in fluid communication with the application member by way of a compressive force applied along circumferential areas toward the distal end of the container. A method of manufacturing an applicator for applying a solution to a surface is provided. | 06-07-2012 |
20120125334 | HUMIDIFICATION SYSTEM - The present invention provides a method and apparatus for reducing condensed humidifying agent in a humidification system by pulsing a delivery of humidifying agent into a respiratory circuit. During a non-pulsed interval, gas flowing through the respiratory circuit will evaporate the condensed humidifying agent present in the respiratory circuit. The present invention also provides a method and apparatus for delivering humidified gas to a patient, wherein the delivery avoids the problems associated with a stationary water humidifier. In the method, the delivery of humidifying agent is precisely controlled to deliver a flow of humidifying agent to a volume of gas. | 05-24-2012 |
20120101482 | CATHETER PATCH APPLICATOR ASSEMBLY - In accordance with aspects of the present invention, an applicator assembly suitable for application of a catheter patch with one hand comprises an upper arm with a proximal end and a distal portion, a lower arm with a proximal end and a distal portion, and a hinge member fixedly joining the proximal ends of the upper arm and the lower arm, wherein an upper surface of the upper arm distal portion abuts a lower surface of the lower arm distal portion. In accordance with another aspect of the present invention, a catheter patch assembly may be secured against a lower surface of the upper arm distal portion. The distal portion of the lower arm may include a securing mechanism for securing the catheter patch assembly to the applicator assembly. A method of applying a catheter patch is provided. | 04-26-2012 |
20120083825 | DETACHABLE SHAFT - A surgical device comprising: a mechanical manipulation mechanism configured for transmitting a first set of control signals; and at least one mechanical slave cylinder coupled with the mechanical manipulation mechanism and positioned at a distal end of the surgical device, the at least one mechanical slave cylinder configured for receiving the first set of control signals, wherein the at least one mechanical slave cylinder comprises: a piston configured for responding to the first set of control signals by moving between a proximal end and a distal end of the mechanical slave cylinder; and a detachable shaft configured for detachably coupling with a distal end of the piston and for the moving with the piston. | 04-05-2012 |
20120012112 | RESPIRATORY THERAPY DEVICE - A respiratory therapy device including a housing and an interrupter valve assembly. The housing is sized for handling by a patient and defines a patient breathing passage extending from a patient end and through which a patient inhales and exhales air. The interrupter valve assembly is carried by the housing and includes a control port, a valve body, and a drive mechanism. Expiratory airflow is released from the patient breathing passage through the control port. The valve body is sized to at least partially obstruct fluid flow through the control port. The drive mechanism moves the valve body relative to the control port in response to the expiratory airflow such that the valve body repeatedly transitions between a position of maximum obstruction and a position of minimum obstruction relative to the control port to create an oscillatory positive expiratory pressure effect. | 01-19-2012 |
20120004572 | REDUCED PROFILE BIOPSY DEVICE - A biopsy device is disclosed that includes a housing maintaining a stylet and a cannula. A control device is operably coupled to operate the stylet and the cannula. A handle operates to modify the device from a loading configuration with an expanded profile to a delivery configuration with a reduced profile. | 01-05-2012 |
20120003029 | ANTISEPTIC APPLICATOR ASSEMBLY - An applicator assembly includes a body defining a pocket, a closed ampoule received in the pocket, an integrated protective device attached to the body and enclosing the pocket, a lever projecting from the body, at least one tappet that bears against an external surface of the pocket and fractures the ampoule when the lever is pivoted, and an application member secured to the body, wherein an interior of the pocket is placed in fluid communication with the application member by way of through-holes provided in the integrated protective device. A method for manufacturing the applicator assembly includes rotating the protective device from an open position into a closed position to enclose the ampoule in the pocket before the application member is attached to the body so that the fluid to be dispensed will flow through the protective device and contact the application member when the ampoule is fractured. | 01-05-2012 |
20110319842 | ANTISEPTIC APPLICATOR - An applicator assembly includes a body having a proximal and a distal end, a container slidably coupled to the body, a valve cap coupled to the container, and an application member attached to the distal end, wherein an interior of the container is placed in fluid communication with the application member by way of a fluid conduit that is only accessible when one of the body and the container are axially translated in an opposite direction away from each other. | 12-29-2011 |
20110306952 | SURGICAL DEVICE WITH REUSABLE HANDLE - A laparoscopic surgical device is provided, including a removable tool-comprising shaft having an outer shaft and an inner actuation rod that may be removably or permanently connected together. A handle of the device includes a two-button mechanism for engaging and releasing the removable tool-comprising shaft. The two-button mechanism is configured to engage overlapping corresponding apertures of the outer shaft and the inner rod that extends through the outer shaft. | 12-15-2011 |
20110303219 | GAS BLENDER WITH AUXILIARY MIXED GAS OUTLET - A gas blender with auxiliary mixed gas outlet for mixing a primary gas, generally air, and a secondary gas, generally oxygen, to obtain a mixed gas having several controlled characteristics. The gas blender may be incorporated into a Continuous Positive Airway Pressure (CPAP) device. The gas blender controls the mixing to produce the mixed gas having a predetermined mixture setpoint, generally an oxygen percentage, and a predetermined control setpoint, generally a pressure setpoint or flow rate setpoint. The gas blender provides an auxiliary mixed gas source for use by an auxiliary piece of equipment such as a nebulizer or resuscitation bag. The gas blender includes a primary gas inlet passageway, a secondary gas inlet passageway, a gas mixing apparatus, a mixed gas distribution passageway with an auxiliary mixed gas outlet, a gas sensor, a delivery sensor, a mixed gas delivery control valve, a mixed gas controlled passageway, and a controller. | 12-15-2011 |
20110108031 | HEATED CONDUIT FOR RESPIRATORY HUMIDIFICATION - A conduit for carrying humidified gases includes a tube extending between a first end and a second end and a helical wire positioned in the tube. The helical wire is formed of a conductive core defining a shape of the helical wire. An electrical receptacle is positioned at the first end of the tube and electrically coupled to the communication ends of the helical wire. | 05-12-2011 |
20110108028 | FLOAT VALVE SYSTEM FOR A RESPIRATORY HUMIDIFICATION SYSTEM - A float valve system for controlling an amount of liquid in a chamber is disclosed that includes a first valve seat and a second valve seat. Liquid enters the chamber in a first direction to the first valve seat and is transferred in a second direction to the second valve seat. First and second actuating members are provided to selectively open and close the first valve seat and the second valve seat, respectively. A first float is coupled to the first actuating member so as to close the first valve seat upon fluid in the chamber reaching a first predetermined level and a second float is coupled to the second actuating member so as to close the second valve seat upon fluid in the chamber reaching a second predetermined level that is different from the first predetermined level. | 05-12-2011 |
20100307487 | RESPIRATORY THERAPY DEVICE AND METHOD - A respiratory therapy device including a housing and an interrupter valve assembly. The housing includes a patient inlet, an exhaust outlet, a chamber, and a supply inlet. The interrupter valve assembly is associated with the housing and includes a control port fluidly connecting the patient inlet and the first chamber, and a valve body adapted to selectively obstruct fluid flow through the control port. In a passive mode, positive fluid flow to the supply inlet does not occur, and the interrupter valve assembly interacts with exhaled air create an oscillatory PEP effect. In an active mode, fluid flow to the supply inlet occurs and the interrupter valve assembly operates to create a CHFO effect. The respiratory device can serve as a passive oscillatory PEP device, and when connected to a positive pressure source, as an active device. | 12-09-2010 |
20100258128 | INFANT NASAL INTERFACE MASK - An infant nasal interface mask for use with a nasal continuous positive airway pressure (nCPAP) system including a mask body and a base. The mask body forms a cavity and is defined by a leading portion, an intermediate shell portion, and a trailing portion. The leading portion terminates in a leading edge forming an aperture open to the cavity and having a generally triangular shape for placement over a patient's nose. The trailing portion includes a bellows segment characterized by an increased flexibility as compared to a flexibility of the intermediate shell portion. The base extends from the trailing portion opposite the leading portion and forms at least one longitudinal passage extending through a thickness of the base and fluidly connected to the cavity. The intermediate shell portion is laterally pivotable relative to the base via the bellows segment. | 10-14-2010 |
20100221193 | COLOR CHANGE SURGICAL PREP SOLUTION - This invention discloses a surgical prep solution formulation, either film forming or non-film forming, that changes color upon a change in pH to indicate that the solvent has sufficiently evaporated. The major components of this surgical prep solution include: antimicrobial agents, solvents, pH adjusters, color changing pH indicators, and optionally: film forming polymers, dyes and viscosity regulators. The pH of the solution may rise or fall depending on the pH of the original solution as compared with the normal pH range of the acid mantle of the human skin or the normal pH range of a sterilizing solution. As the pH changes, the pH indicator may cause the surgical prep solution to change color. Concurrently, as the fluids evaporate, the pH indicators interact with atmospheric CO | 09-02-2010 |
20100108073 | NASAL INTERFACE PRONG DEVICE - An infant nasal interface prong device for use with an nCPAP system. The device includes first and second nasal prongs and a base. Each prong includes a bellows segment, a tip, and a lumen. The tip extends from the bellows segment to a tip end and is adapted for insertion with an infant's naris. The lumen extends through the tip and the bellows segment. In an undeflected state, a central axis of the lumen along the bellows segment is transversely offset from the lumen axis at the tip end. The base is connected to each of the nasal prongs and is adapted for coupling to a CPAP generator. The bellows segment renders the corresponding prong highly flexible relative to the base. The offset positioning of the tip end promotes desired positioning of the base/CPAP generator, relative to the patient and more closely conforms to the expected nasal anatomy. | 05-06-2010 |