The present invention involves a sterilizable syringe allows for reduction in needlestick injuries using conventional sterile needles. The syringe allows for direct access to and the safe removal and disposal of needles. The device consists of a sterilizable, reusable hypodermic syringe to which a disposable needle is attached, and employs carpules containing injectable medication, viewable and either manually or automatically aspirating. Some embodiments have a protective sliding mechanism consisting of an open frame bearing one or more protective collars, one at the furthermost end of the frame and an optional second one at a more proximal position. The protective mechanism may be extended to protect an exposed needle tip and retracted during an injection. With the protective mechanism extended, the needle mounting hub is exposed to allow for its exchange or removal and safe disposal. The protective mechanism is engaged until immediately prior to the delivery of medication, disengaged on delivery, and engaged after delivery.

A CPAP comfort seal. The CPAP comfort seal includes a base comprising a first loop of fabric secured to a second loop of fabric, wherein the first loop of fabric and the second loop of fabric are secured to one another along a common perimeter edge. An opening is defined by an inner perimeter edge of the first loop of fabric and the second loop of fabric. An elastic band is disposed on the inner perimeter edge of the second loop of fabric. The opening is configured to receive a CPAP mask therethrough, such that elastic band contacts an outer side of the CPAP mask. The first loop of fabric contacts the wearer's face when the CPAP mask is secured thereto, providing additional sealing properties and increased comfort for the wearer.

An air delivery system for providing a supply of air from a source of air at positive pressure to an interfacing structure located at the entrance to the airways of a patient includes a manifold adapted to connect with the supply of positive air pressure and at least one tube connected to the manifold and adapted to deliver the supply of air to the interfacing structure. Each tube is structured to allow movement between an open phase in which the tube allows the passage of air and a collapsed phase in which the tube is collapsed. Each tube is structured such that weight of a typical patient's head against bedding apparel is sufficient to collapse the tube from the open phase to the collapsed phase.

A medical tube transports gases to and/or from a patient. The medical tube has an elongate film spirally wrapped with an elongate reinforcing member, which bond to form a lumen. The elongate film has a profile such that the elongate film does not protrude into the lumen of the medical tube upon bending of the medical tube. The elongate reinforcing member can have a D-shaped cross section that can contribute to beneficial characteristics of the medical tube. The elongate reinforcing member can also have a circular cross section.

A patient interface comprises a plenum chamber and a seal-forming structure. The seal-forming structure comprises a support structure arranged to support a sealing portion that is adapted to sealing engage the patient's face in use. The seal-forming structure may also include a seal biasing portion configured to inflate under pressurization within the cavity in the cushion assembly in use to extend the reach of the sealing portion and decouple the sealing portion from external forces.

A suction catheter for fragmenting and removing obstructive material and thrombus from the body or other body cavities that comprises a tube-like body with a proximal and distal end and a pressure lumen and discharge lumen formed in the catheter body. At the distal end of the catheter is a suction opening adjacent to the opening of the nozzle injector formation. At the proximal end of the catheter the lumens are connected to an inlet port and a discharge outlet. A hub structure is coupled to the proximal end of the catheter tubular body and includes a pressure lumen for connecting a fluid source to the pressure inlet. At the proximal end of the tubular catheter a discharge lumen is connected at the proximal hub to a discharge reservoir. The suction port at the distal end of the catheter may be formed into a separate lumen within the catheter body and may include a guidewire lumen.

Catheter systems with multiple inner lumens that converge at the catheter distal tip are preloaded with at least two guidewires. The catheters offers sequential probing with two or more guidewires, therefore improving on procedural speed and accuracy. The catheters comprise proximal and distal regions enabling angled lumens to merge into a common lumen with a diameter slightly larger to the largest of the two proximal lumens. The confluence of the two proximal lumens comprises a single lumen with a reduced profile and cross sectional area. The lumens merge with the larger lumen at an angle greater than zero degrees, and the distal tip has a diameter equal to the diameter of the smaller proximal lumen. The proximal region serves as a directed passageway for different guidewires that enter the catheter through two proximal lumens and which may be reoriented through a convergence region for sequential exiting of the catheter tip.

A button for setting and dispensing a dose of a drug from a drug delivery device is described. The button comprises a plastic component and a metal component, wherein the plastic component is at least partly received by the metal component, and wherein the metal component is configured to be manipulated by a user for setting and dispensing the dose. Furthermore, a method for assembling a button for a drug delivery device and a drug delivery device comprising the button are described.

A puncture device includes a puncture needle including an outer needle and an inner tube located in the outer needle; a housing unit accommodating the puncture needle; and a puncture mechanism within the housing unit. The puncture mechanism includes a push-in unit configured to be pushed in with respect to the housing unit, an outer needle slide unit attached to the outer needle, a stopper, an elastic member, a first end of which is fixed to the housing unit and a second end of which is fixed to the outer needle slide unit, and a fixation release unit configured to release the fixation between the push-in unit and the outer needle slide unit and the fixation between the outer needle slide unit and the inner tube.

A tracheostomy tube has an inflatable sealing cuff (11) towards its patient end (6) and a fluid-permeable cuff (31) mounted on the shaft (1) above the inflatable cuff. The fluid-permeable cuff (31) contains hydrogel granules (32) that absorb moisture in the trachea (T) and help reduces the amount of secretions leaking past the sealing cuff (11). When the tube is to be withdrawn from the trachea (T) the lower, inflatable cuff (11) is deflated allowing the upper, fluid-permeable cuff (31) to be flattened against the outside of the lower cuff.