A catheter enclosure device for locking an intravenous catheter therein with tamper-evident features to deter unauthorized use. The catheter enclosure device may be particularly useful for peripherally inserted central catheters (PICC). The enclosure device comprises an open-top box and a removable lid for covering the box. The open-top box has a compartment for holding the proximal end of an intravenous catheter. The lid comprises a panel for covering the open portion of the open-top box and a folding wing that overhangs the forward end of the box when covering the box. The folding wing further comprises a retaining anchor. When the folding wing is folded down, the retaining anchor inserts into a locking slot on the forward end of the box, thereby preventing the lid from being removed off the box. Also disclosed are methods for using the catheter enclosure device.

Apparatus and methods are described for manufacturing a housing for an impeller of a blood pump. A mandrel is placed inside an inner lining, with a central cylindrical portion of a frame disposed around the inner lining, the mandrel being shorter than a length of the inner lining. A portion of an elongate tube is placed around at least a portion of the frame. The inner lining, the frame and the portion of the elongate tube are heated, via the mandrel, and, while heating the inner lining, the frame, and the portion of the elongate tube, pressure is applied from outside the portion of the elongate tube, such as to cause the portion of the elongate tube to become coupled to the frame. Other applications are also described.

Various systems and methods are provided for creating a wicking structure. In one example, a method for creating a wicking structure can include creating, using a 3D printing technique, a macro wicking element including a lattice structure formed by a grid of a first material, the lattice structure including pores formed between the grid of first material. The method can also include creating, using the 3D printing technique, a first micro wicking element including powder particles distributed within the pores of the lattice structure, and creating, using the 3D printing technique, a second micro wicking element by removing at least a portion of the lattice structure.

A patient interface includes a cushion configured to sealingly engage the patient's face, a support structure configured to support the cushion, the support structure being more rigid than the cushion, a plenum chamber formed at least in part by the cushion, and a connector configured to convey the pressurized respiratory gas to the plenum chamber. The connector includes a first portion formed from a first material and adapted to removably connect to the support structure. A plurality of vent holes are formed on the first portion. The connector also includes a continuous flexible portion that is formed from a second material, is more flexible than the first portion, and is configured to flex to permit engagement and disengagement of the first portion. The continuous flexible portion comprises a pair of opposing release buttons that are configured to be inwardly flexed to allow release of the connector from the support structure.

A bougie is disclosed with a body, and a first depth indicator and a second depth indicator on the body. The body has a first end, a second end, and at least one surface extending between the first and second ends. The first depth indicator is spaced a first distance from the first end and indicates a first predetermined depth range such that the first end is positioned a first predetermined insertion range past the mouth of the patient when the body is positioned into the mouth of the patient. The second depth indicator is spaced a second distance from the second end and indicates a second predetermined depth range such that the second end is positioned a second predetermined insertion range past the mouth when the body is positioned into the mouth of the patient.

A method of dispensing a therapeutic fluid from a line includes providing an inlet line connectable to an upstream fluid source. The inlet line is in downstream fluid communication with a pumping chamber. The pumping chamber has a pump outlet. The method also includes actuating a force application assembly so as to restrict retrograde flow of fluid through the inlet while pressurizing the pumping chamber to urge flow through the pump outlet. A corresponding system employs the method.

A sub-assembly of a medicament delivery device is presented, where the sub-assembly includes a plunger rod that is biased, a main body arranged on the plunger rod, and a coupling member movable relative to the main body, where the main body includes a first locking element, the coupling member includes a second locking element, and where the first locking element and the second locking element are configured to be releasably engaged with each other such that the coupling member is prevented from moving relative to the main body.

The disclosure relates to a subcutaneously implanted port device for establishing access to the vascular system of a patient requiring multiple blood treatments over an extended period of time. The systems, devices and methods disclosed herein may reduce miscannulation, promote intra-session hemostasis, and decrease the incidence of bacteremia and sepsis among other improvements and advantages. The devices include a port with a tapered seat for receiving an access tube, the first tapered seat having a proximal portion, a distal portion, and a conical section extending between the proximal portion and the distal portion; and an interface surface configured to engage a blood vessel or a vascular access catheter. The proximal portion of the tapered seat is configured to receive the access tube therethrough, and the tapered seat creates a mismatch fit with a diameter of the access tube when in use for an increase in flow during treatment.

A method of manufacturing a patient interface for sealed delivery of a flow of air at a continuously positive pressure with respect to ambient air pressure to an entrance to the patient's airways includes collecting anthropometric data of a patient's face. Anticipated considerations are identified from the collected anthropometric data during use of the patient interface. The collected anthropometric data is processed to provide a transformed data set based on the anticipated considerations, the transformed data set corresponding to at least one customised patient interface component. At least one patient interface component is modeled based on the transformed data set.

A urinary catheter may include a catheter shaft and a connector coupled with the proximal end of the catheter shaft. The connector may have a first arm ending in a fluid outlet configured to allow urine to flow out of the urinary catheter and a second arm with an aperture and ending in an inflation inlet used for introducing inflation fluid into the urinary catheter. The catheter may further include a primary lumen, an inflation lumen, a retention balloon mounted to the catheter shaft proximal to a fluid inlet and over a distal filling hole, and a pilot balloon mounted on the second arm of the connector over the aperture. The pilot balloon inflates at an inflation pressure that is higher than the inflation pressure of the retention balloon and lower than a predetermined pressure threshold.