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).

A medical tube holder comprising a face frame assembly, a strap assembly, a holding assembly and an adapter clip. The face frame assembly has a central member with a base with a first end and a second end, and an attachment rail extending therefrom between the ends. The strap assembly is attachable to the face frame assembly and is configured to extend about the head of a patient so as to secure the face frame assembly. The holding assembly includes a base plate, with an arm extending from a proximal end of the base plate and terminating at a transverse channel. The transverse channel is slidably movable along the attachment rail to attach the holding assembly to the face frame. The adapter clip includes a block member attachable to a medical tube, and, is attached to the holding assembly so as to define a maximum spacing therebetween.

A medical tube holder comprising a face frame assembly, a strap assembly, a holding assembly and an adapter clip. The face frame assembly has a central member with a base with a first end and a second end, and an attachment rail extending therefrom between the ends. The strap assembly is attachable to the face frame assembly and is configured to extend about the head of a patient so as to secure the face frame assembly. The holding assembly includes a base plate, with an arm extending from a proximal end of the base plate and terminating at a transverse channel. The transverse channel is slidably movable along the attachment rail to attach the holding assembly to the face frame. The adapter clip includes a block member attachable to a medical tube, and, is attached to the holding assembly so as to define a maximum spacing therebetween.

The present invention relates to an adapter for non-invasive mechanical ventilation probes with an inhalation port and orifice occluder. Specifically, the invention comprises a probe adapter with an inhalation port and orifice occluder, coupled to the oronasal mask disposed on a user or patient. According to the present invention, the probe adapter also receives a metered dose inhaler that further receives an anesthetic circuit with two enteral probes, a left enteral probe and a right enteral probe. The technical field of the invention belongs to the field of medical devices for respiratory therapy, for use in patients with assisted non-invasive mechanical ventilation and concomitant use of enteral probes with the requirement of metered dosage inhaled medicinal products.

The present invention relates to an adapter for non-invasive mechanical ventilation probes with an inhalation port and orifice occluder. Specifically, the invention comprises a probe adapter with an inhalation port and orifice occluder, coupled to the oronasal mask disposed on a user or patient. According to the present invention, the probe adapter also receives a metered dose inhaler that further receives an anesthetic circuit with two enteral probes, a left enteral probe and a right enteral probe. The technical field of the invention belongs to the field of medical devices for respiratory therapy, for use in patients with assisted non-invasive mechanical ventilation and concomitant use of enteral probes with the requirement of metered dosage inhaled medicinal products.

An intubation apparatus and, method of use, for intubating a patient. The apparatus includes an airway ventilation device having tubing located between an inlet end and an outlet end, the outlet end being configured to be locatable in the airway of a patient, intermediary tubing having a first end releasably connectable to the inlet end of the airway ventilation device and a second end having a fitting configured to connect to a gas supply, and an introducer having a first end that is alternatively releasably connectable to the first end of the intermediary tubing and a second end having a blunt tip.

An intubation apparatus and, method of use, for intubating a patient. The apparatus includes an airway ventilation device having tubing located between an inlet end and an outlet end, the outlet end being configured to be locatable in the airway of a patient, intermediary tubing having a first end releasably connectable to the inlet end of the airway ventilation device and a second end having a fitting configured to connect to a gas supply, and an introducer having a first end that is alternatively releasably connectable to the first end of the intermediary tubing and a second end having a blunt tip.

A mask bead for a patient interface, having at least one lip, wherein the at least one lip extends from a transition region toward a central opening and borders the central opening. At least one lip comprises at least one portion which is capable of guiding a tube between the mask bead and the facial skin of a user.

A mask bead for a patient interface, having at least one lip, wherein the at least one lip extends from a transition region toward a central opening and borders the central opening. At least one lip comprises at least one portion which is capable of guiding a tube between the mask bead and the facial skin of a user.

A delivery device for a compound including: a housing, vial holding a compound; and a source of propellant, wherein the housing provides an inlet and an outlet for the vial, wherein the inlet is in fluid communication with the source of propellant and is directed against the in-line nasal delivery device compound and the outlet allows for delivery of the compound.