Patent classifications
A61M1/00
Catheter Device Including a Connector
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.
ILLUMINATED SUCTION DEVICE
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.
CANISTER STATUS DETERMINATION
A method and apparatus are disclosed for determining status of a canister of a topical negative pressure (TNP) system. The method includes the steps of monitoring pressure provided by a pump element of the TNP system, determining at least one characteristic associated with the monitored pressure and determining status of at least one parameter associated with a canister of the TNP system responsive to the determined characteristics.
Vacuum assisted wound dressing
Apparatus for the application of topical negative pressure therapy to a wound site is described, the apparatus comprising: a wound contacting element for retaining wound exudate fluid therein; a wound covering element that provides a substantially airtight seal over the wound contacting element and wound site; a vacuum connection tube connecting a wound cavity to a vacuum source; and a vacuum source connected to a distal end of the vacuum connection tube.
Needle arrangement
A medical needle arrangement (100, 1000, 1400) is disclosed. The needle arrangement (100, 1000, 1400) comprises: a needle sheath (104, 002, 1402), and a needle (202, 1102, 1406) comprising: an elongated portion and a sealing member (204, 1003, 1403) being arranged to a front end of the elongated portion. The needle arrangement is adapted to bet set in: a closed position, in which the sealing member (204, 1003, 1403) is arranged to abut at least a portion of a front end surface of the needle sheath (104, 1002, 1402) thereby restricting intrusion of foreign matter in an area between the needle sheath and the needle, and an open position, in which a gap (1204, 1506) is formed between the sealing member (204, 1003, 1403) and the front end surface of the needle sheath (104, 1002, 1402). Embodiments include needle arrangement for injection, for aspiration, and for biopsy purposes.
Method of robotic hub communication, detection, and control
Various surgical systems are disclosed. A surgical system can include a surgical robot and a surgical hub. The surgical robot can include a control unit in signal communication with a control console and a robotic tool. The surgical hub can include a display. The surgical hub can be in signal communication with the control unit. A facility can include a plurality of surgical hubs that communicate data from the surgical robots to a primary server. To alleviate bandwidth competition among the surgical hubs, the surgical hubs can include prioritization protocols for collecting, storing, and/or communicating data to the primary server.
Negative pressure wound treatment apparatuses and methods with integrated electronics
Disclosed embodiments relate to apparatuses and methods for wound treatment. A wound dressing apparatus can comprises a wound contact layer, at least one absorbent layer, an electronics unit comprising a negative pressure source unit, and a cover layer. The electronics unit can comprise a plurality of sensors positioned on a printed circuit board and an inlet protection mechanism of the negative pressure source unit comprises a first recess in fluid communication with a first sensor and the outlet or exhaust mechanism negative pressure source unit comprises a second recess in fluid communication with a second sensor.
FECAL MANAGEMENT SYSTEMS AND METHODS
Fecal management methods and apparatuses (e.g., devices, systems, etc.) are described herein. The fecal management apparatuses may apply one or more fecal removal cycles of suction and irrigation (and in some examples air) to actively remove fecal material. The apparatus may control the timing of delivery of the fecal removal cycles as well as the parameters of the applied suction, irrigation and/or air within and between fecal removal cycles.
Wound therapy system with wound volume estimation using geometric approximation
A wound therapy system includes an instillation fluid canister configured to contain an instillation fluid, a pump fluidly coupled to the instillation fluid canister and operable to deliver the instillation fluid from the instillation fluid canister to a wound, a user interface configured to receive user input indicating one or more geometric attributes of the wound, and a controller electronically coupled to the pump and the user interface. The controller is configured to determine a volume of the wound based on the user input, determine a volume of the instillation fluid to deliver to the wound based on the volume of the wound, and operate the pump to deliver the determined volume of the instillation fluid to the wound.
ANALYTICAL METHOD FOR CONTROLLED AND MEASURED COLLECTED INTERNAL FLUID AFTER SURGERY
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”.