A blood component collection system, which is one form of a biological component collection system, is equipped with a centrifugal separation device and a biological component collection device. The biological component collection device comprises a pressed soft portion pressed by a load detecting unit. The centrifugal separation device includes a collection and returning pump, and a control unit having an internal pressure computation unit which calculates a circuit internal pressure of the biological component collection device on the basis of a detection value of the load detecting unit. The internal pressure computation unit performs a zero reset process of setting a pressure value corresponding to the detection value of the load detecting unit, so as to become zero at each instance of a predetermined timing at which the collection and returning pump is stopped.

An endoscopic bite block comprises a base, an elongated guide, and an oxygen inflow tube. The base includes a body and a central passageway extending through the body. The central passageway is configured to receive an endoscope. The elongated guide includes a longitudinal curvature corresponding in shape to an oral-pharyngeal cavity of a patient. The elongated guide extends from the base and toward a retropharyngeal space of the patient. The elongated guide includes a lateral curvature for guiding the endoscope along the longitudinal curvature of the elongated guide. The oxygen inflow tube is configured to receive oxygen gas from an oxygen source. The oxygen inflow tube extends from the base along the elongated guide such that the oxygen inflow tube is configured to deliver the received oxygen gas to the retropharyngeal space of the patient.

An endoscopic bite block comprises a base, an elongated guide, and an oxygen inflow tube. The base includes a body and a central passageway extending through the body. The central passageway is configured to receive an endoscope. The elongated guide includes a longitudinal curvature corresponding in shape to an oral-pharyngeal cavity of a patient. The elongated guide extends from the base and toward a retropharyngeal space of the patient. The elongated guide includes a lateral curvature for guiding the endoscope along the longitudinal curvature of the elongated guide. The oxygen inflow tube is configured to receive oxygen gas from an oxygen source. The oxygen inflow tube extends from the base along the elongated guide such that the oxygen inflow tube is configured to deliver the received oxygen gas to the retropharyngeal space of the patient.

A patient interface may include a plenum chamber pressurisable to a therapeutic pressure, a seal-forming structure constructed and arranged to form a seal with a region of the patient's face surrounding an entrance to the patient's airways, a positioning and stabilising structure to provide a force to hold the seal-forming structure in a therapeutically effective position on the patient's head, and a vent structure to allow a continuous flow of gases exhaled by the patient from an interior of the plenum chamber to ambient, wherein the patient interface is configured to leave the patient's mouth uncovered during therapy, wherein the seal-forming structure comprises two lateral support regions, each located at a lateralmost side of the seal-forming structure, and a medial region positioned between the lateral support regions, the hole passing through the medial region, and wherein the lateral support regions are thicker than the medial region.

A patient interface may include a plenum chamber pressurisable to a therapeutic pressure, a seal-forming structure constructed and arranged to form a seal with a region of the patient's face surrounding an entrance to the patient's airways, a positioning and stabilising structure to provide a force to hold the seal-forming structure in a therapeutically effective position on the patient's head, and a vent structure to allow a continuous flow of gases exhaled by the patient from an interior of the plenum chamber to ambient, wherein the patient interface is configured to leave the patient's mouth uncovered during therapy, wherein the seal-forming structure comprises two lateral support regions, each located at a lateralmost side of the seal-forming structure, and a medial region positioned between the lateral support regions, the hole passing through the medial region, and wherein the lateral support regions are thicker than the medial region.

The present invention provides an oral device that is inserted into the mouth of a patient during sedation to minimize the risk of airway obstruction and method of use. The oral device comprises a mouthpiece. A gas inlet conduit, a gas outlet conduit, and a fluid outlet conduit are adjacent to the vestibular portion of the mouthpiece. The gas inlet conduit may be used to provide oxygen to the mouth of a patient. The gas outlet conduit may be used to remove end-tidal carbon dioxide from the mouth of a patient. The fluid outlet conduit may be used to remove fluid from the mouth of a patient. The oral device may also include a tongue stabilizer to minimize movement of the tongue. The mouthpiece may include fluid outlet ports to remove fluid from the mouth of a patient and an instrument passage to allow medical instruments to pass through the oral device.

The present invention provides an oral device that is inserted into the mouth of a patient during sedation to minimize the risk of airway obstruction and method of use. The oral device comprises a mouthpiece. A gas inlet conduit, a gas outlet conduit, and a fluid outlet conduit are adjacent to the vestibular portion of the mouthpiece. The gas inlet conduit may be used to provide oxygen to the mouth of a patient. The gas outlet conduit may be used to remove end-tidal carbon dioxide from the mouth of a patient. The fluid outlet conduit may be used to remove fluid from the mouth of a patient. The oral device may also include a tongue stabilizer to minimize movement of the tongue. The mouthpiece may include fluid outlet ports to remove fluid from the mouth of a patient and an instrument passage to allow medical instruments to pass through the oral device.

Kits, devices, systems and related methods for obtaining a nasopharyngeal sample utilize a rinsing fluid supply component and a collecting component, which may be used as separate modules or integrated with a housing to form a handheld unit that may be operated with a single hand. The dispensing component may include a flexible reservoir pump containing a supply of rinsing fluid, and a first nostril interface adapted to engage a first nostril of a patient and guide a stream of rinsing fluid into the patient's nasal cavity. The collecting component may include a collection container and a second nostril interface adapted to engage a second nostril of a patient and collect effluent. An absorbent shield may be arranged on the integrated unit to absorb stray fluid.

A ventilator system includes a ventilator and a host. The ventilator comprises a ventilation drive configured to drive ventilation gas from a gas source to a patient and a patient interface section configured to guide inspiratory gas along an inspiratory path from the ventilation drive to a patient connection, and guide expiratory gas along an expiratory path from the patient connection out of the ventilator. The patient interface section is configured to releasably connect to the ventilation drive. The ventilator is configured to removably connect to the host such that at least one of the inspiratory path and the expiratory path are diverted through the host when the ventilator is removably connected to the host.

A ventilator system includes a ventilator and a host. The ventilator comprises a ventilation drive configured to drive ventilation gas from a gas source to a patient and a patient interface section configured to guide inspiratory gas along an inspiratory path from the ventilation drive to a patient connection, and guide expiratory gas along an expiratory path from the patient connection out of the ventilator. The patient interface section is configured to releasably connect to the ventilation drive. The ventilator is configured to removably connect to the host such that at least one of the inspiratory path and the expiratory path are diverted through the host when the ventilator is removably connected to the host.