A nasal ventilation mask having one or more attachment ports located adjacent to and overlying an upper lip of a patient when worn.

A nasal ventilation mask having one or more attachment ports located adjacent to and overlying an upper lip of a patient when worn.

A bilateral humeral guide for intraosseous infusion includes a three-dimensional minor symmetric shell configured to fit on either shoulder of a patient, the shell being symmetric about a plane bisecting an alignment hole configured to aid positioning of the shell on the shoulder by aligning the alignment hole on acromion of the shoulder, and two insertion-site indication holes symmetrically positioned on two opposite sides of the plane, the insertion-site indication holes including a left and a right hole each configured to indicate insertion sites for intraosseous infusion through the shell to a target region of a left or right humerus of the patient when the shell is positioned on the shoulder corresponding to the respective humerus.

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.

The present invention relates to a system (100) for managing an airway. The system comprises an elongated tube (102) having a proximal end (104), and a distal end (106), and defines a first lumen (108), extending between the proximal end (104) and the distal end (106), having a passageway and a second lumen (110), positioned adjacent to the first lumen (108), extending between the proximal end (104) and the distal end (106). The system (100) further comprises a stylet (112) that is disposed at least partially into and removable from the first lumen (108), wherein the stylet (112) is used for steering and guiding the elongated tube (102) during insertion of the elongated tube (102) into an externally accessible passageway of a patient.

The present invention relates to a system (100) for managing an airway. The system comprises an elongated tube (102) having a proximal end (104), and a distal end (106), and defines a first lumen (108), extending between the proximal end (104) and the distal end (106), having a passageway and a second lumen (110), positioned adjacent to the first lumen (108), extending between the proximal end (104) and the distal end (106). The system (100) further comprises a stylet (112) that is disposed at least partially into and removable from the first lumen (108), wherein the stylet (112) is used for steering and guiding the elongated tube (102) during insertion of the elongated tube (102) into an externally accessible passageway of a patient.

The present invention relates to a medical kit and method of administration for trigeminal balloon compression used in the treatment of trigeminal neuralgia. The kit reaches the damaged area percutaneously and penetrates the balloon most effectively to the damaged spot. The present invention is a trigeminal neuralgic balloon compression kit which can overcome the aforementioned disadvantages; it is characterized by being a product kit and application method which has a simple structure and can easily and effectively convey the balloon to the damaged area.

Provided is a filtering facepiece respirator. The respirator includes a mask body having an anterior side portion, a posterior side portion, a middle portion, a first side portion, a second side portion, a top side portion, a bottom side portion and outer edge portions. The respirator further includes a primary port positioned at the anterior middle portion of the mask body and a detachable primary port adapter which is positioned over and engages the primary port. The respirator may further include an oxygen port and oxygen port adapter and a luer port and luer port adapter.

An intubation assembly, shield assembly and related systems configured to at least partially reduce the risk of contagion from airborne illnesses. The shield assembly may be operatively connected to a vacuum system to exert a negative pressure and/or may be used as a standalone component as a barrier to reduce contamination of the local environment between therapies, treatments and/or procedures. The shield assembly may comprise ports to attach a vacuum device to provide negative pressure. An intubation apparatus assembly may be disposed on the shield assembly. The shield assembly comprises a body with a plurality of side segments and/or a transparent component(s) with a shield opening disposed thereon. The shield opening may be used for insertion of the intubation apparatus. The shield assembly may also comprise another transparent component with a longitudinally disposed slot(s) for insertion of an endotracheal tube or other intubation apparatus(es).