Abstract: 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.

Abstract: A non-stick medical tubing is provided. The non-stick tubing comprises a plastic resin mixture including a first plastic resin component and a second plastic resin component, the second plastic resin comprising a medical grade amide compound, the plastic resin mixture extruded by an extruding apparatus as a mono-layered tube such that the medical grade amide compound is present on an inner surface of the medical tube after extrusion to promote release of contacting surfaces of the inner surface of the medical tubing after contact.

Abstract: A flexible wrist-type element and methods of operation thereof, including variations having an angularly moveable hub housing a rotatable and operable end effector driven via a drive train having one or more universal-type joints and/or other flexible couplings moveable via an input mechanism within a housing.

Abstract: The present invention includes an apparatus and a method for testing exhaled breath condensate for at least one biometric marker, including a substrate for collecting exhaled breath condensate, the substrate capable of being brought to a temperature below a dew point of vapor in exhaled breath, a collector for retaining the substrate and for receiving a biometric marker reagent. The invention may further include receiving exhaled breath in a collector, the collector comprising a substrate, the substrate being at a temperature below a dew point of vapor in exhaled breath, collecting the exhaled breath condensate on the substrate, and bringing a biometric marker reagent in contact with the substrate.

Abstract: A container is described. The container includes a receptacle, lid, and fastener. The receptacle includes a latch. The lid is coupled to the receptacle and moves between an open and a closed position. The fastener is coupled to the lid and fastens the lid to the receptacle. The fastener includes first, second, third, and fourth portions. The first portion is coupled to the lid and extends along a first axis that is perpendicular to a plane of the lid when the lid is in the closed position. The second portion is coupled to the first portion and extends along a second axis that is perpendicular to the first axis. The third portion is coupled to the second portion and extends along an axis that is parallel to the first axis. The fourth portion is coupled to the third portion and includes a contact member that couples to the latch.

Abstract: A continuous positive airway pressure system features a housing forming an airway chamber, and an air pressure inlet and an air pressure outlet. The housing further defines internally a pair of tapered air jets, and a pair of tapered air receivers. The air receivers are located downstream of the air supply jets and disposed coaxially with respective ones of the air supply jets. Each receiver has a taper in an opposite direction to the direction of the taper of the air supply jets. A pair of nasal prongs is located downstream of the air receiving jets. Each receiver comprises a hemispherical section that is oriented at an angle off the center line of the supply.

Abstract: A phase-controlled power supply is disclosed. The power supply includes a power conditioner with an input configured to connect to an external source of electrical power, the power conditioner being configured to provide conditioned power on its output. The power supply also includes a transformer having a primary winding and a secondary winding, and a switching module coupled between the output of the power conditioner and to the primary winding of the transformer. The switching module has two modes of operation and a control signal input configured to accept a first control signal. The switching module includes a switching element configured to connect the power conditioner output to the primary winding of the transformer. The switching module operates in the first mode when the first control signal is in a first state, switching the first switching element at a first frequency and first duty cycle.

Abstract: A respiratory therapy system includes a driver unit and a patient interface device. The driver unit is adapted to deliver pressurized gas flow from a source to the patient interface device. At least one electronic valve can be used to deliver a desired flow to the patient interface device.

Abstract: An apparatus and method for introducing material into an injection site of a patient is disclosed. The device includes a cannula and a carrier. The cannula is inserted into an injection site of a patient. The carrier is connected to an injector containing a volume of material. Material may be pre-loaded into the carrier so that the material is delivered to a distal end of the carrier from the injector and the carrier is thus pre-loaded with material. A portion of the distal end of the pre-loaded carrier is inserted into the cannula and material is delivered to an injection site. The supply section can be rotatable with respect to the longitudinal axis of the inner section.

Abstract: A medical device including an operation determiner for determining operations to be performed by the medical device in response to a gesture of the device with respect to the medical device, and an operation data accessor for accessing operation data for the operation performed by the medical device.

Abstract: A system and method for creating, managing and loading selected configuration datasets used to program a patient care device to have a selected behavior is provided. A common configuration database includes medical treatment guidelines and device operating characteristics for a plurality of patient care device types. A processor operatively connected to the configuration database is programmed to construct at least one device-specific configuration dataset for a selected device behavior from the common configuration database and load the device-specific dataset into the memory of a patient care device. Further, the device-specific configuration datasets may contain device communication information, including communication protocols and data structures, for a plurality of patient care devices types and behaviors to enable communication between patient care devices.

Abstract: Storing of medical supplies is performed according to rules promoting safety and ergonomics. The physical arrangement of medical supplies within a storage unit is analyzed. An inventory of medical supplies to be stored in the storage unit is established. A new physical arrangement of medical supplies within the storage unit is determined based on the rules for storing medical supplies and the inventory. The storage unit is configured according to the new physical arrangement. The physical locations within the storage unit where each of the medical supplies is to be stored are indicated. The medical supplies are stored in the indicated locations.

Abstract: A tool kit for interchanging tools within an at least partially closed area is provided. The tool kit includes at least one tool, each tool being preferably provided within a tubular housing, and adapted to pivot out from the tool kit so that they can be attached to a receiving tool. The tool is designed to be returned to the tool kit after use, and if desired, switched with a different tool. In one embodiment, a surgical system permitting surgical tools to be interchanged within a patient's body is provided. A method of interchanging surgical tools within a patient's body is also provided.

Abstract: 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.

Abstract: 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.

Abstract: A system and method of managing therapy provided to patients in an institution. The system monitors all aspects of the medication delivery to a patient, as well as other information related to the patient, such as values of vital signs, laboratory results and patient factors such as history, diagnosis, allergies and the like. The system includes one or more databases of information, including institutionally developed rules, guidelines and protocol representing the best medical practices of the institution. The system provides alerts and/or recommendations based on the application of the rules to the information being monitored, and alerts care givers accordingly, providing for dynamic adjustment of the patient's therapy. The system also monitors the status of the alerts, and if no action is taken in a selected period of time, may escalate the priority of the alert and/or halt the delivery of medication to the patient until the alert is resolved.

Abstract: A method for manufacturing a non stick medical tube is provided. The method includes providing a first plastic resin to a tubing extrusion device and providing a second plastic resin to a tubing extrusion device, the second plastic resin comprising a medical grade amide compound. The method further includes mixing the first plastic resin with the second plastic resin and extruding the resin mixture such that said medical grade amide compound is present on an inner surface of said medical tube after extrusion to promote release of contacting surfaces of said inner surface of the medical tubing after contact.

Abstract: A supply cabinet is fitted with an outer sensor and an inner sensor. The outer and inner sensor wirelessly sense inventory items tagged with radio frequency tags and in proximity of the sensors. A method of tracking inventory items stored in a supply cabinet includes determining, based on time sequencing of sensing by the outer and the inner sensor, if an inventory item was removed from the cabinet or stored into the cabinet, and updating an inventory database accordingly. An alarm is optionally triggered if an inventory item is removed by an unauthorized user.

Abstract: A cartridge for use in a dispensing system is disclosed. The cartridge includes a body having an exterior and a plurality of bins. A plurality of lids are movably attached to the body and are configured to cover a bin. A release mechanism is movable along an axis. A plurality of latches are movably attached to the body. Each latch is configured to secure the respective lid when in a first position and to release the respective lid when in a second position. The release mechanism will not cause a latch to move to the second position when the release mechanism is moving along the axis in a first direction. The release mechanism will cause a single latch to move to the second position while leaving the remaining latches in the first position when the release mechanism is moving along the axis in a second direction.