A chest drainage system securing apparatus for securing and maintaining chest drainage systems in position following placement into a human or animal patient and preventing movement or unplanned removal thereof in response to the application of significant forces in any direction thereto, be they longitudinal, torsional/rotational or bending. The securement system includes retention devices secured to a chest tube which interact with an adhesive pad releasably attached to a patient to ensure proper positioning of the chest tube. The adhesive pad includes one or more Heimlich-type valves for sealing sucking chest wounds and for sealing an incision formed in a patients skin and chest for the placement and insertion of a chest tube.

An oocytes or ovum retrieval device is disclosed. The device may include a retrieval catheter dimensioned for transvaginal insertion into a cervical canal and for advancing distally into a fallopian tube and the ampulla of a female mammal. The retrieval catheter may include one or more fluid delivery lumens having a fluid delivery port for delivering a flushing fluid into said fallopian tube, an at least one aspiration opening in fluid connection with an internal aspiration lumen of said retrieval catheter, wherein the size of the at least one aspiration opening is determined based on a size of oocytes or ovum.

Methods and devices for positioning of subdural drain within an evacuated hematoma cavity. Embodiments include a tethered subdural drain with a puck attached to a leading end of a tether and a subdural drain attached to the terminal end of the tether. The puck is placed in vivo through a first hole in a cranium. A ex vivo guide manipulates the puck and tether through an evacuated hematoma cavity to be retrieved through a second hole in the cranium. Pulling the tether through the second hole advances the subdural drain attached thereto through the first hole and into the hematoma cavity.

A medical tool includes a handle, a tubular member, and a bendable shape memory element (SME). The tubular member is attached to and extends from the handle and is configured to be inserted into an orifice of a patient. The tubular member has a distal-end section that is configured to be bent so as to perform a medical procedure in the orifice. The bendable shape memory element (SME) is coupled to the distal-end section of the tubular member, wherein the SME is configured to straighten when heated into a pre-formed shape, thereby straightening the distal-end section.

Embodiments of the present disclosure provide a method and apparatus for filtering and surgical procedures. An exemplary apparatus includes an evacuation tube having a filter, a long axis and a hollow conduit extending through the long axis, the hollow conduit fluidly connecting a tube inlet and a tube outlet, the filter located within the hollow conduit operable to remove particles from a flow passing through the hollow conduit from the tube inlet to the tube outlet.

Urinary catheter-insertion kits can include a working tray, a storage tray, a protective paperboard, and a urinary catheter assembly, including a urinary catheter and a drainage system. The working tray can be nested on top of the storage tray. The working tray includes preformed sections configured to accommodate components of the urinary catheter-insertion kit. Methods of urinary catheterization include use of the urinary catheter-insertion kits.

In some embodiments, a catheter device may include a catheter including a proximal end and a distal end. The catheter device may further include a connector coupled to the proximal end of the catheter. The connector may include a base having a recess configured to receive the distal end of the catheter and may include a hinged portion configured to couple to the base to clamp the catheter within the recess.

An illuminated suction device comprising a suction tube having a proximal end and a distal tip at a distal end thereof, an illumination assembly comprising at least one direct light source mounted on a flexible circuit and configured to emit light toward a target area external to the distal tip of the suction tube, and at least one heat sinking member extending along a portion of the suction tube, wherein the at least one light source mounted on the flexible circuit is mechanically and thermally connected to the at least one heat sinking member.

A device and method is provided for a suction tool combined with an optical probe. A suction device is provided having a tip with a hollow tubular body, a plurality of optical fibers embedded in the tip and a concentric ring attached to the tip, wherein the ring end has an inner beveled reflective surface opposing the optical fibers. A method is provided for optically measuring tissue in a medical procedure comprising suctioning a tissue using a suction device, sending optical signals along optical fibers through the suction device; directing the signals from the optical fibers onto the tissue using a beveled surface; receiving optical signals from the tissue in optical fibers via the beveled reflective surface; measuring the received optical signals in a spectrometer or detector; and releasing, resecting or ablating the tissue through the suction device.

Systems and methods for the intravascular treatment of clot material within a blood vessel of a human patient are disclosed herein. A method in accordance with embodiments of the present technology can include, for example, positioning a distal portion of a catheter proximate to the clot material within the blood vessel. The method can further include coupling a pressure source to the catheter via a tubing subsystem including a valve or other fluid control device and, while the valve is closed, activating the pressure source to charge a vacuum. The valve can then be opened to apply the vacuum to the catheter to thereby aspirate at least a portion of the clot material from the blood vessel and into the catheter.