Abstract: A vented transfer lid includes an inner collar projecting from a top panel of the transfer lid and having an outer circumferential surface having a texturized electrical discharge machining (EDM) surface finish. In some example forms, an interior surface of the top panel includes a texturized EDM surface finish. In example forms, the transfer lid includes a transfer port wherein at least a portion of an interior surface of the transfer port includes a texturized EDM surface finish. In other embodiments, at least a portion of the vented transfer lid comprises a nonpolar boundary such that fluids exposed to the nonpolar boundary bead and form droplets having a dimension rendering them incapable of passing through one or more vent paths.

Abstract: Systems and methods for testing a pump assembly for a cooled radiofrequency treatment procedure. In some embodiments, the pump assembly and at least one pump head are driven by at least one respective motor, where the at least one pump head is coupled to tubing for delivering a cooling fluid to a medical probe assembly. The at least one pump head is configured to pump the cooling fluid through the tubing for the cooled radiofrequency treatment procedure. The system can also include a programmable controller operatively connective to the pump assembly and configured to control the pump assembly, and one or more pump function sensors for sensing operation parameters associated with the pump assembly and communicating the pump operation parameters to the controller. The controller can determine that the pump assembly is operating properly based on the operation parameters and can adjust the operation of the motor or output an alert.

Abstract: A configurable pathway deviation indication system for medical device placement includes one or more user-adjustable pathway boundaries and an indication activated upon reaching or breaching of any of the pathway boundaries. The system may include a medical device configured to be inserted into a patient; a location transmitter configured to transmit a signal related to a position of the medical device; and a detector device configured to receive information related to the patient's body and the location transmitter. The system may be operatively coupled to the location transmitter and the at least one detector device. The system may further include a display and a computing system comprising one or more processors and or more non-transitory computer-readable media. The system can display the position of the location transmitter; determine if the position of the location transmitter reaches any pathway boundaries; and provide the indication when the pathway boundary is breached and/or approached.

Abstract: An enteral dosing control coupling comprising a cylindrical collar defining a hollow internal chamber and a lumen extension tip projecting axially into the internal chamber, the lumen extension tip defining an internal lumen extending therethrough. In example forms, the lumen extension tip is integrally formed with the cylindrical collar. In other example forms, the lumen extension tip is a separate piece and is removably engageable within the cylindrical collar. In some example forms, the present invention relates to syringes, connectors, couplings, etc. having ISO 80369-3 formatted couplings. In other example forms, the present invention relates to connectors, couplings, etc. for adapting coupling formats other than the ISO 80369-3 coupling format to the ISO 80369-3 coupling format.

Abstract: A non-electrically driven enteral feeding pump including an expandable elastomeric bladder is provided. The enteral feeding pump includes a fluid delivery tube. The fluid delivery tube controls flow rate of fluid from the pump. The present invention further describes an enteral feeding pump assembly including the portable enteral feeding pump and a peristaltic pump. The peristaltic pump can be configured to be operatively coupled to the elastomeric bladder of the enteral feeding pump for transferring fluid from a reservoir external to the elastomeric bladder into a chamber of the elastomeric bladder.

Abstract: A therapy wrap for treatment of at least a portion of an animate body having improved kink resistance. The therapy wrap may be selectively reinforced for improved kink resistance in only a portion of the wrap. The reinforcement may decrease the kink radius. The wrap may include a kink reducer in all or only a selected kink-prone region. The kink reducer may be selectively configured attachment points or spot welds. The therapy wrap may include a reinforcement layer of one or more discrete reinforcement members. The wrap may be formed by pre-tensioning the material layers while forming the fluid bladder and/or gas pressure bladder. The therapy wrap may be adapted to compensate for conditions that normally cause kinking of the wrap or buckling of the fluidic channels. Also disclosed are methods of manufacturing the wrap and methods of administering a temperature-controlled treatment to an anatomical body part.

Abstract: Tube tip detection systems, enteral tubes, and methods for detecting tube misplacement in a patient's airway are provided. For example, a tube tip detection system comprises an enteral tube having a tip, a first sensing component disposed at the tip, and a feedback display. Feedback from the first sensing component is displayed on the feedback display to indicate to a user of the tube tip detection system whether the tip is misplaced in a patient's airway. Similarly, an enteral tube comprises a tip, a length, and a sensing component. The sensing component is a micro-electro-mechanical system (MEMS) infrared carbon dioxide sensor. Further, a detection method comprises embedding a carbon dioxide sensing component into an enteral tube, inserting the enteral tube into the patient through the patient's nose or mouth, and monitoring feedback from the carbon dioxide sensing component to determine if the enteral tube is traveling into the patient's airway.

Abstract: A bolus delivery device is provided that comprises a housing and a reservoir defined by an activation dome and a reservoir seat and disposed within the housing for receipt of a volume of a fluid. The bolus delivery device further comprises a bladder disposed in the housing that is in fluid communication with the reservoir for receipt of the fluid from the reservoir; an actuator; an inlet conduit in fluid communication with the reservoir for providing the fluid to the reservoir; and an outlet conduit in fluid communication with the bladder for providing the fluid to a patient. The actuator is in operative communication with the reservoir to initiate a flow of the fluid from the reservoir to the bladder. The bladder expands as the bladder receives the fluid and contracts as the bladder dispenses the fluid. An infusion assembly including a bolus delivery device also is provided.

Abstract: A fluid transfer connector or adapter for coupling a container or pharmacy bottle for facilitating the transfer of fluid or medicine from the bottle to a syringe, or from the syringe to the bottle. Optionally, an additional connector can be provided for coupling the fluid transfer connector to the syringe.

Abstract: An apparatus, system and method for detecting the distance between a plurality of position detectors using ultrasound includes a processor and a memory device. The system further includes first and second position detector devices each configured to detect the position of a medical device within a patient, the first position detector device including a first transceiver and being operatively coupled to the processor. The second position detector device includes a second transceiver and is operatively coupled to the processor. The first position detector device transmits a signal through the first transceiver and receives a signal from the second position detector device relating to the distance between the first and the second position detector devices. The processor calculates the distance between the first position detector device and the second position detector device. Each transceiver is configured to transmit and receive one or more sound signals in the audio or ultrasonic range.

Abstract: A medical device position notification system including a medical device and at least one sensor associated with the medical device, a processor, and a display device. The medical device is configured to be inserted into an orifice of the patient. The sensor measures information related to the position of the medical device in the patient's body, and communicates the information with the processor in real-time. The display device is coupled to the processor and is configured to display a tracing path of the position of the medical device in real-time. The display device is further configured to display a notification of the position of the medical device within the patient's body, such as a notification alert that the medical device has deviated from a predetermined path.

Abstract: Priming systems and infusion assemblies are provided. For example, a priming system comprises a priming conduit having a priming portion and a pressure portion. The priming portion is in fluid communication with a first fluid source, with an inlet and an outlet for ingress and egress of a first fluid from the first fluid source. The pressure portion is in fluid communication with a second fluid source connected by a connector. Disposed within the priming conduit are a biasing member and a valve having an open position and a closed position. The biasing member is in operable communication with the valve to urge the valve into the closed position such that the valve defaults to the closed position. The open position allows the first fluid to flow from the inlet to the outlet and the closed position prevents the first fluid from flowing from the inlet to the outlet.

Abstract: A securement device for a system for securing a nasal tube is provided. The securement device includes a bridle having a body extending between a first end and a second end. The body has a lobed or star shape. The securement device further includes a magnetic connection portion disposed at the first end of the bridle. A system for securing a nasal tube can include a securement device as described above, and a retrieval probe. The retrieval probe can include a catheter extending between a proximal end and a distal end; and a magnetic tip disposed at the proximal end. The magnetic connection portion of the bridle and the magnetic tip of the retrieval probe can be configured to magnetically couple during a procedure for inserting the bridle in a nasal passageway of a patient.

Abstract: The present disclosure is directed to a system and method for selectively and reversibly modulating targeted neural and non-neural tissue of a nervous system for the treatment of pain. An electrical stimulation is delivered to the treatment site that selectively and reversibly modulates the targeted neural- and non-neural tissue of the nervous structure, inhibiting pain while preserving other sensory and motor function, and proprioception.

Abstract: A patient compliance system is provided that includes a patient monitoring material for determining movement activity associated with a joint of the patient. The patient monitoring material includes at least one sensor for sensing the movement activity and a transmitter. The system also includes a device having a receiver and a processor. The transmitter transmits the movement activity to the receiver, and the processor determines parameters associated with compliance with a rehabilitation/physical therapy program based on the movement activity. A method for monitoring movement activity of a patient is also provided. The method includes sensing movement activity associated with a joint of the patient via at least one sensor embedded within or attached to a patient monitoring material that surrounds the joint; transmitting the movement activity to a device; and determining parameters associated with compliance with a rehabilitation/physical therapy program based on the movement activity via a processor.

Abstract: A tubing assembly for use in conjunction with electronic catheter guidance systems is provided and includes a catheter and a sensor. The catheter extends in a longitudinal direction and has a proximal end and a distal end that define a lumen therebetween. Further, the catheter is configured for placement within a digestive tract of a patient. The sensor includes a temperature sensor, relative humidity sensor, or both, and can be located within the lumen of the catheter or in an air sampling chamber connected to the catheter. The sensor can communicate with a processor to deliver temperature and/or relative humidity readings to a display device. A constant temperature or relative humidity profile, or both after a pre-determined amount of time can indicate placement of the catheter in the digestive tract. A catheter guidance system and a method for accurately placing a catheter in the digestive tract are also provided.

Abstract: A system and method for locating a target nerve associated with a facet joint via nerve stimulation and monitoring of electrical muscle activity in a multifidus muscle adjacent the target nerve are described. The system includes a probe housed within a cannula and comprising a probe electrode; a recording electrode for monitoring electrical muscle activity in a medial fascicle of the multifidus muscle; a signal generator; and a controller coupled to the probe electrode and recording electrode. The controller delivers a nerve stimulation from the signal generator to the nerve via the probe electrode and monitors electrical muscle activity in the medial fascicle via the recording electrode. The probe's proximity to the nerve is determined by the electrical muscle activity in the medial fascicle elicited as a result of the nerve stimulation, where the controller provides feedback to a user to guide placement of the probe adjacent the nerve.

Abstract: Systems, methods, and apparatus for cleaning and sealing threaded connector ports are disclosed. An exemplary cleaning system includes a basin and cleaning apparatus including a sealing connector, an alignment peg, and an outer foam sleeve having a tubular portion. The sealing connector includes a body portion having a gripping portion, an internal thread cleaning portion, and a longitudinal axis. Another cleaning apparatus also includes a cap cleaning end having a cap cavity and an inner foam pad. Another system includes a threaded connector port and a cleaning apparatus including an alignment peg, a disposable foam platform, and a handle body, which includes a grip portion and a pair of cleaning arms. The cleaning arms and foam pads are adapted to engage the female threads of a threaded connector port. A sealing apparatus includes a disposable liner having locator flaps and a placement tool having a handle and locator fingers.