A wiping tip (1) includes a hollow cylindrical member (10), and a cotton-like wiping member (20) arranged on the cylindrical member (10). The cotton-like wiping member (20) constitutes a thin film portion (21) covering an opening at an end of the cylindrical member (10), and an outer circumferential portion (23) extending from the thin film portion (21) and covering an outer circumferential face of the cylindrical member (10) over a predetermined length from the end.

Disclosed herein are medical systems and methods for ultrasonic decomposition of intraluminal clots. A medical system can include a stylet configured to insert into a lumen of a catheter. The stylet can include one or more electrical impedance sensors, as well as one or more ultrasound transducers or a resonant section of the stylet. The one-or-more impedance sensors can be configured to detect changes in impedance for identifying intraluminal clots in the catheter. The one-or-more ultrasound transducers can be configured for decomposing the intraluminal clots to reestablish patency in the catheter, while the resonant section of the stylet can be configured to resonate with an externally applied ultrasonic frequency for decomposing the intraluminal clots to reestablish patency in the catheter. The medical system can further include a console to which the stylet is connected in an operable state of the medical system.

A cleaning catheter (200) insertable into a tracheal ventilation tube (160) and an input module (156) are provided for use with a suction source (601), the input module (156) coupled to the cleaning catheter (200) and including (i) an inflation module (330), including an inflation chamber (335) separate from the suction source (601); (ii) a flow regulator (700), configured to assume first and second fluid-control states; and (iii) a mechanical user control element (320), which is configured (a) to mechanically and non-electrically set the fluid-control states, (b) to assume first and second configurations, and (c) to mechanically and non-electrically increase pressure in an interior of an inflation chamber (335) during a transition of the mechanical user control element (320) from the first configuration to the second configuration. The flow regulator (700), when in the first fluid-control state connects the suction source (601) and an interior of an inflatable element (588) of the cleaning catheter (200) in fluid communication to deflate the inflatable element (588).

A combination flush catheter and selective catheter as one convertible catheter and methods of using the same. The selective catheter may be a reverse curve or guide catheter. The additional steps of removal of the flush catheter and re-insertion of the selective catheter may be eliminated, reducing the possibility of errors and making the procedure smoother and shorter.

Systems and methods for cleaning and disinfecting contaminated tube lumens are described herein. One system includes an ultraviolet light source and a sterile fluid reservoir fluidly coupled to a liquid light guide. The system is configured to allow simultaneous access and propagation of ultraviolet light and fluid in a tube having a lumen to be cleaned and disinfected. The light guide can be moved inside the tube and simultaneously emit ultraviolet light through its walls and at its distal end into the interior of the contaminated tube. A flush of sterile fluid from an open end of the liquid light guide removes debris and micro-organism detached from the inner surface during light exposure. The sterile fluid can be a high refractive index ionic solution promoting light propagation.

Methods and devices for actuating a clearance device to clear obstructive debris from medical tubes are disclosed. More particularly, a shuttle that includes a first primary magnetic element that is adapted to magnetically engage and translate a magnetic guide within a tube is disclosed. The first primary magnetic element is aligned so that a first primary magnetic field emanating therefrom is aligned substantially perpendicular to a longitudinal axis of the tube when viewed from a side of the shuttle.

A device has a drainage conduit for draining fluids from a patient. The drainage conduit may be flexible. One or more flexible delivery conduits deliver medication to the patient. The one or more flexible delivery conduits are attached to the flexible drainage conduit. The one or more flexible delivery conduits are detachable from the flexible drainage conduits at at-least one end of the drainage conduit so that the delivery conduits can be peeled off the drainage conduit at the proximal and deployed with the proximal ends of the delivery conduits separated from the proximal end of the drainage conduit.

A system and/or method are disclosed to inhibit sorption to a surface in a biological medium and/or biofouling by means of an alternating electric field. For example, one or more insulated electrodes may be positioned near the surface. For example, insulation may limit electric current flow between the biological medium and the electrode and/or between the surface and the electrode and/or between the electrodes. In some embodiments, the alternating charge in the vicinity of the surface may inhibit the buildup of biological films and/or sorption to the surface. For example, the system may be used to inhibit fouling of an implanted medical device (e.g. a catheter).

Systems and methods are provided for removing air from a medical device, such as a stent-graft and/or its delivery device. In an exemplary embodiment, the stent-graft or its delivery system or both are exposed to perfluorocarbon, by immersing the stent-graft or flushing the delivery device to remove air from the stent-graft. Optionally, the stent-graft and/or delivery system may be flushed multiple times, e.g., with perfluorocarbon before or after flushing with carbon dioxide, saline, a bio-inert gas, and the like. Thereafter, the stent-graft may be introduced into a patient's body and deployed at a target location, such as the site of an abdominal aortic aneurysm.

A device to couple a vascular access device to a medical device may include a body, a spring, and a housing. The body may include a distal end, a proximal end, and a lumen extending through the distal end and the proximal end. The proximal end of the body may include a connector. The housing may be coupled to a proximal end of the spring and may enclose the connector. A distal end of the spring may be coupled to the body. The housing may include a flap, which may include an antimicrobial compound. When the housing is disposed in a proximal position, the flap may cover the connector, the antimicrobial compound may contact the connector, and the spring may be uncompressed. In response to movement of the housing from the proximal position to a distal position, the spring may be compressed and the flap may open.