A61M1/87

Unisex Urine Collection Assembly
20230052238 · 2023-02-16 ·

A unisex urine collection assembly for use by either sex in a non-ambulatory setting includes a tube, which has a cutout positioned in a top face thereof and extending from proximate to a midpoint toward a first end thereof. A second end of the tube is closed. A connector engaged to the first end of the tube can engage a conduit extending from a suctioning unit. Each of a pair of pads is engaged to the tube and extends from a respective opposed edge of the cutout thereinto so that the pads defines a slot. The pads are resiliently flexible and can sealably engage skin of the user. The pads can be positioned between labia of a female user or to bracket a penis inserted into the slot by a male user. Urine expelled by the user is suctioned from the tube into a reservoir.

Aspiration catheter systems and methods of use
11576691 · 2023-02-14 · ·

Described are methods, systems, devices for facilitation of intraluminal medical procedures within the neurovasculature. A catheter advancement device includes a flexible elongate body having a proximal end, a distal end, and a single lumen extending therebetween. The flexible elongate body has a proximal segment, an intermediate segment, and a tip segment. The proximal segment includes a hypotube coated with a polymer. The intermediate segment includes an unreinforced polymer having a durometer of no more than 72D. The tip segment is formed of a polymer different from the intermediate segment and has a durometer of no more than about 35D and a length of at least 5 cm. The tip segment has a tapered portion that tapers distally from a first outer diameter to a second outer diameter over a length of between 1 and 3 cm.

Analytical method for controlled and measured internal fluid after surgery

A system and apparatus for the collection of serous or serosanguinous fluid from a percutaneous site after surgery. A pump unit with one or more pumps or powered sources provide continuous negative pressure suction to draw fluid from the percutaneous site and pumps the fluid into disposable reservoirs with one-way valves that are easy to handle while maintaining sterility and a seal to prevent the loss of vacuum. Air is continuously removed from the reservoirs. Measurement and analysis of the output is performed automatically. Additionally, through such a peristaltic pump device, controlled collection of measured surgical and/or bodily fluid from a subject patient may be undertaken allowing for more effective and closer analysis, as well.

Chest Drainage System Securing Apparatus

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.

DOME CATHETER SYSTEM FOR TRANSCUTANEOUS VACUUM ASSISTED CLOSURE OF PERIANAL OR ENTEROCUTANEOUS ABCESSES AND FISTULA TRACTS AND METHOD THEREOF
20230226267 · 2023-07-20 ·

A catheter for transcutaneous and transluminal vacuum closure of perianal or entero-cutaneous fistulas and abscesses containing a body ending in a dome having a low-friction surface and equipped with a series of openings on the surface that connect inside the catheter body into a catheter chamber, which is then connected to a tube connected to a vacuum generating system characterized in that the catheter body on the outside has edges arranged in the shape of many helicoid coils, and in the grooves between these coils the series of openings are made into the chamber inside the catheter.

ANALYTICAL METHOD FOR CONTROLLED AND MEASURED COLLECTED INTERNAL FLUID AFTER SURGERY
20230226269 · 2023-07-20 ·

A method of analyzing fluid collected from a wound site, the method comprising the steps of: (a) providing a pump unit comprising: one or more pumps, one or more fluid collectors, and one or more drainage structures each in communication with an exit site of the wound site to draw the fluid through the one or more drainage structures into the pump unit and create a negative pressure at the exit site to remove and transport the fluid from the exit site and into the one or more fluid collectors, wherein the pump unit is configured to create a negative pressure, wherein the fluid removal from the exit site is provided at a controlled and measured rate; b) collecting the fluid within the one or more fluid collectors; c) removing the one or more fluid collectors; e) capping the one or more fluid collectors with a cap; and d) analyzing the collected fluid of step “b” once the fluid connectors are removed in step “c”.

SURGICAL SUCTION DEVICE
20230009147 · 2023-01-12 ·

A surgical suction device (10) comprising:

a connector (12),

a surgical cavity insertion tube (14), and

a suction tip (16),

wherein the surgical cavity insertion tube (14) is connected at a proximal end thereof to the connector (12) and at a distal end thereof to the suction tip (16). The suction tip (16) comprises an inner hollow shaft (18) and an outer hollow shaft (20) coaxial to each other, the inner hollow shaft (18) having a first central opening (22) at a distal end thereof, and the outer hollow shaft (20) having an end wall (24) at a distal end thereof, wherein the end wall (24) has a second central opening (26) in axial alignment with the first central opening (22) of the inner hollow shaft (18). The outer hollow shaft (20) has one or more openings (28) on a lateral wall (30) thereof.

SELF-CLEANING ELECTRIC NASAL ASPIRATOR
20220395625 · 2022-12-15 ·

Provided is a self-cleaning electric nasal aspirator. The self-cleaning electric nasal aspirator includes a suction assembly. The suction assembly includes a suction nozzle and a storage compartment. The suction nozzle is in communication with the storage compartment. The storage compartment is configured to temporarily store nasal mucus sucked out through the suction nozzle. The suction assembly further includes a suction compartment and a storage compartment cover. The storage compartment cover is disposed at an upper end of the storage compartment. A liquid storage space is formed by being enclosed by the storage compartment cover and the storage compartment. The suction compartment is sleeved outside the storage compartment and the storage compartment cover. The self-cleaning electric nasal aspirator can prevent nasal mucus from overflowing to the surface of the self-cleaning electric nasal aspirator and has a self-cleaning function.

TARGETED SUCTION CATHETER
20220379089 · 2022-12-01 ·

A suction catheter assembly structured to be movably positioned within a lumen of the body including an elongated base having a channel extending interiorly along the length thereof and further structured to connect the channel to a source of negative pressure. A tip is fixedly or removably connected to a distal end of said base and includes an inlet port and a flow path disposed in fluid communication with the channel. A viewing structure is connected to and movable with the base and is oriented relative thereto to define a line of sight providing observation of a path of travel of said base within the body lumen or medical tubing and is disposed laterally outward from at least a majority of a length of said flow path and the inlet port in substantially aligned, parallel relation to a central axis of said channel.

Stimulation of cartilage formation using reduced pressure treatment

System and methods for stimulating cartilage formation at a first tissue site through a second tissue site is presented. The system includes a fluid source for supplying a therapeutic solution, a reduced pressure source for supplying reduced pressure, a fluid delivery manifold for deploying adjacent the first tissue site, and a vacuum manifold for deploying within the second tissue site. The fluid delivery manifold extends between a proximal end fluidly coupled to the fluid supply and a distal end having at least one aperture for delivering the therapeutic solution to the defect adjacent the articulating surface of the first tissue site. The vacuum manifold extends between a proximal end fluidly coupled to the reduced pressure source and a distal end having at least one aperture for delivering the reduced pressure to the first tissue site adjacent the opposing surface of the first tissue site.