Abstract: Various control methods can indirectly determine incorrect connections between components in a respiratory therapy system. For example, incorrect connections can occur between a patient interface, a humidifier and/or a gases source. The methods can indirectly detect if reverse flow conditions or other error conditions exist. A reverse flow condition can occur when gases flows in a direction different from an intended direction of flow. The methods can be implemented at the humidifier side, at the gases source side, or both.

Abstract: The present invention provides an inhaler comprising a housing which contains a blister strip having a plurality of blisters which contain powdered medicament for inhalation, a mouthpiece mounted to the housing through which the medicament is inhaled by a user, an indexing and opening mechanism for indexing the blister strip and for opening the blisters which is operated by an actuator, wherein the blister strip is indexed by forward motion of the actuator from a first position to a second position, such as by opening a cover, and is also indexed in the same direction by reverse motion of the actuator from the second positon to the first position, such as by closing the cover.

Abstract: The present invention provides an inhaler comprising a housing which contains a blister strip having a plurality of blisters which contain powdered medicament for inhalation; a mouthpiece through which the medicament is inhaled by a user; an indexing wheel for indexing the blister strip; an opening mechanism for opening the blisters; an actuator which is movable between a first position and a second position in order to operate the indexing wheel and the opening mechanism; and a coupling mechanism for coupling the actuator to the indexing wheel so that the indexing wheel rotates together with the actuator during part of the motion of the actuator; characterized in that the coupling mechanism comprises a shuttle that rotates on the same axis as, and translates axially relative to, the indexing wheel.

Abstract: A strength assist device includes: a multi-link part including one or more links; a profile controller that is connected to one end portion of the multi-link part, and rotates around a central rotational axis; and an elastic force providing part that is connected to the other end portion of the multi-link part, and provides an elastic force to the multi-link part. When the profile controller rotates and one end portion of the multi-link part revolves around the central rotational axis, the elastic force applied to the multi-link part varies.

Abstract: An adjustable chest compression device that can adjust to accommodate a variety of patient sizes. The chest compression device can include adjustable support legs structured to support the chest compression mechanism at a distance from the base member and adjust to accommodate a patient size. Another adjustable chest compression device can include adjustable legs that can adjust to accommodate different patient sizes, as well as perform the chest compressions using the adjustable legs. An extension, such as a back plate and/or leg extension can be added to a chest compression device to make the chest compression device taller and/or wider to accommodate larger patients.

Abstract: A rope-driven soft hand function rehabilitation device includes four finger exoskeleton mechanisms, a thumb exoskeleton mechanism, and a soft rubber glove. An index-finger exoskeleton mechanism includes an index-finger distal phalanx loop, an index-finger middle phalanx loop, and an index-finger proximal phalanx loop which are mutually connected via a hinge structure. The thumb exoskeleton mechanism includes a thumb proximal phalanx loop and a thumb distal phalanx loop which are connected via a hinge structure. The rope is fastened to the hand function rehabilitation device via an aluminum sleeve which prevents the rope from slipping off during finger flexion/extension and abduction/adduction when the fingers are pulled by the rope at the palm and the hand back.

Abstract: A vacuum shield assembly intended for attachment to an existing medical mask for air suction, nebulization, BIPAP, and/or CPAP. The vacuum shield assembly generally comprises a shield body and a retaining assembly. The retaining assembly may attach the vacuum shield assembly to a vacuum tube of the existing mask, which may be connected to a negative pressure vacuum. The retaining assembly may also be attached to a nebulizer unit or component thereof, or to an oxygen supply tube of a BIPAP or CPAP mask. The shield body may comprise a lower segment, which may comprise a connecting component configured and dimensioned for attachment to, and for a fluid communication, with the retaining assembly. The shield body may be configured and dimensioned to correspond to the geometry of the existing mask. As an example, the shield body may comprise a substantially concave configuration with a substantially semi-ovoidal edge.

Abstract: A facemask is disclosed. The facemask comprising an outer facemask layer and an inner facemask layer, which are fixed to each other to define a facemask interior. The outer facemask layer has an opening. A disk is rotatably fixed within the facemask interior such that a first portion of the disk is viewable through the opening in the outer facemask layer and such that the disk may be rotated so that a second portion of the disk may be viewable through the opening in the outer facemask layer. A fastener rotatably fixes the disk within the facemask interior.