Abstract: Urine collection systems and associated methods and devices are disclosed herein. A representative system can include a urine collection device, a flow control assembly configured to direct a urine flow from the patient to the urine collection device, and a urine measurement device including a first sensor and a second sensor. The first sensor is configured to generate first sensor data based on a weight of the container, and the second sensor is configured to generate second sensor data based on the urine flow from the patient to the container. The system can further include non-transitory computer readable media having instructions that, when executed by one or more processors, cause the system to perform operations comprising determining a first patient urine output based on the first sensor data; and determining a second patient urine output based on the second sensor data.

Abstract: Embodiments of the present technology can manage a patient's fluid removal based on one or more of the patient's urine output, urine conductivity, urine sodium concentration, and/or urine oxygen content. For example, in some embodiments the patient's urine sodium concentration (and/or an indication thereof including, e.g., the patient's urine conductivity) can be compared to one or more urine sodium concentration thresholds (e.g., a high urine sodium concentration threshold and/or a low urine sodium concentration threshold) to determine one or more adjustments to the patient's therapy such as, e.g., a diuretic dosage rate, a hydration fluid infusion rate, a hydration fluid matching percentage, etc. Additionally or alternatively, the patient's urine oxygen content can be compared to one or more urine oxygen content thresholds (e.g., a high urine oxygen content threshold and/or a low urine oxygen content threshold) to determine one or more adjustments to the patient's therapy.

Abstract: Urine collection systems and associated methods and devices are disclosed herein. A representative system can include a urine collection device, a flow control assembly configured to direct a urine flow from the patient to the urine collection device, and a urine measurement device including a first sensor and a second sensor. The first sensor is configured to generate first sensor data based on a weight of the container, and the second sensor is configured to generate second sensor data based on the urine flow from the patient to the container. The system can further include non-transitory computer readable media having instructions that, when executed by one or more processors, cause the system to perform operations comprising determining a first patient urine output based on the first sensor data; and determining a second patient urine output based on the second sensor data.

Abstract: Urine collection systems and associated methods and devices are disclosed herein. A representative system can include a urine collection device, a flow control assembly configured to direct a urine flow from the patient to the urine collection device, and a urine measurement device including a first sensor and a second sensor. The first sensor is configured to generate first sensor data based on a weight of the container, and the second sensor is configured to generate second sensor data based on the urine flow from the patient to the container. The system can further include non-transitory computer readable media having instructions that, when executed by one or more processors, cause the system to perform operations comprising determining a first patient urine output based on the first sensor data; and determining a second patient urine output based on the second sensor data.

Abstract: Urine collection systems and associated methods and devices are disclosed herein. A representative system can include a urine collection device, a flow control assembly configured to direct a urine flow from the patient to the urine collection device, and a urine measurement device including a first sensor and a second sensor. The first sensor is configured to generate first sensor data based on a weight of the container, and the second sensor is configured to generate second sensor data based on the urine flow from the patient to the container. The system can further include non-transitory computer readable media having instructions that, when executed by one or more processors, cause the system to perform operations comprising determining a first patient urine output based on the first sensor data; and determining a second patient urine output based on the second sensor data.

Abstract: The present technology is generally directed to flow cartridges configured to measure and/or detect analytes in urine. A representative flow cartridge includes a urine inlet configured to receive urine from a patient, a flow channel fluidly coupled to the urine inlet, and sensors fluidly coupled to the flow channel that are configured to measure parameters of the urine flow. The sensors are aligned with corresponding sensing zones of the flow channel and are operable to generate sensor data based on urine flow through the sensing zones. In some embodiment, the sensor data is used to provide fluid therapy to the patient by adjusting an amount or rate of diuretic and/or hydration fluid based on the sensor data.

Abstract: Urine collection systems and associated methods and devices are disclosed herein. A representative system can include a urine collection device, a flow control assembly configured to direct a urine flow from the patient to the urine collection device, and a urine measurement device including a first sensor and a second sensor. The first sensor is configured to generate first sensor data based on a weight of the container, and the second sensor is configured to generate second sensor data based on the urine flow from the patient to the container. The system can further include non-transitory computer readable media having instructions that, when executed by one or more processors, cause the system to perform operations comprising determining a first patient urine output based on the first sensor data; and determining a second patient urine output based on the second sensor data.

Abstract: Urine collection systems and associated methods and devices are disclosed herein. A representative system can include a urine collection device, a flow control assembly configured to direct a urine flow from the patient to the urine collection device, and a urine measurement device including a first sensor and a second sensor. The first sensor is configured to generate first sensor data based on a weight of the container, and the second sensor is configured to generate second sensor data based on the urine flow from the patient to the container. The system can further include non-transitory computer readable media having instructions that, when executed by one or more processors, cause the system to perform operations comprising determining a first patient urine output based on the first sensor data; and determining a second patient urine output based on the second sensor data.

Abstract: A soft tissue mobilization device having a hand-held portion coated with a compressible material to take the strain off the hand of the user when using the device. The hand-held portion is coated with a compressible material to take a strain off the hand of the user, is custom molded to the user's hand, and the compressible material is a compound comprising a mixture of one or more low melting point polymers.

Abstract: A height adjustable combat training assembly and method of operation enables a practitioner to strike with a fist, kick, hurtle over, and reenact combat with a real person through use of a height adjustable series of shafts, target accessories, and elongated barriers that are manipulated into myriad configurations. A base portion is filled with a weighted substance to stabilize the assembly. A base shaft attached perpendicularly into the base portion. A height adjustable shaft extends from the base shaft in a sliding relationship that is measured with a height gauging instrument. Padded sleeves encapsulate both shafts for cushioning. A flexible member extends form the terminus of the height adjustable shaft. A terminal target rests on the terminus of the second sleeve. A label attaches to the sleeves. At least one target accessory detachably attaches to the shafts or sleeves, and includes linear arm, blocking arm, laser device, and fist.

Abstract: A height adjustable combat training assembly and method of operation enables a practitioner to strike with a fist, kick, hurtle over, and reenact combat with a real person through use of a height adjustable series of shafts, target accessories, and elongated barriers that are manipulated into myriad configurations. A base portion is filled with a weighted substance to stabilize the assembly. A base shaft attached perpendicularly into the base portion. A height adjustable shaft extends from the base shaft in a sliding relationship that is measured with a height gauging instrument. Padded sleeves encapsulate both shafts for cushioning. A flexible member extends form the terminus of the height adjustable shaft. A terminal target rests on the terminus of the second sleeve. A label attaches to the sleeves. At least one target accessory detachably attaches to the shafts or sleeves, and includes linear arm, blocking arm, laser device, and fist.

Abstract: A facial gesture controller for controlling an electronic device is provided. The facial gesture controller includes a body, a plurality of sensors, and at least one processor. The body is configured to fit over the face of a user. The plurality of sensors are disposed on the body. The at least one processor is in electrical communication with the sensors. The sensors generate and transmit electrical signals to the at least one processor in response to movements of one or more facial muscles of the user. The at least one processor generates and transmits control signals corresponding to the electrical signals, received from the sensors, to the electronic device.

Abstract: A medical cleaning system is used for cleaning at least a portion of a surgical instrument. The system may include a tray, a heating pack, and a non-abrasive cleaning pouch. The tray may include a basin area used as a reservoir for maintaining, e.g., antifogging fluid, and a sloped ramp to allow liquids to flow down into its basin area. The system may also include a heating pack enclosing a heating pack solution. The heating pack solution may be a solution having nucleating properties. The heating pack solution may be activated by a mechanical activator to generate heat to the antifogging fluid. The generated heat may be transferred to the antifogging fluid residing on the non-abrasive cleaning pouch. The surgical instrument may be cleaned by wiping a portion of the surgical instrument, e.g., a lens, over the non-abrasive cleaning pouch.

Abstract: An antifogging shield prevents fogging and condensation during surgery at a junction of surgical devices. The antifogging shield includes an antifogging shield body forming an interior chamber for accommodating a surgical tool therein and an insulation material disposed within the interior chamber to minimize temperature change.

Abstract: A trans-femoral implant includes an anchor assembly and a balloon assembly configured to be separately delivered to an implant site within a heart. Once delivered, the anchor assembly and balloon assembly may be coupled to form an implant within the heart. The balloon anchor may include a fluid inflatable balloon that may be selectively filled via a balloon filling valve. The balloon assembly may further include a latching mechanism that may couple with a distal end of the anchor assembly, such that the length of the implant may be adjusted within the heart.

Abstract: A trans-femoral implant includes an anchor assembly and a balloon assembly configured to be separately delivered to an implant site within a heart. Once delivered, the anchor assembly and balloon assembly may be coupled to form an implant within the heart. The balloon anchor may include a fluid inflatable balloon that may be selectively filled via a balloon filling valve. The balloon assembly may further include a latching mechanism that may couple with a distal end of the anchor assembly, such that the length of the implant may be adjusted within the heart.

Abstract: A bipolar electrosurgical scraper device is provided comprising a handle, a blade having a thickness and a beveled distal end with the beveled distal end terminating distally in a scraping edge. The beveled distal end includes a first electrode and a second electrode with the first electrode and the second electrode provided along a width of the blade and spaced apart with respect to the thickness of the blade. The device also comprises a fluid passage at least one fluid outlet in fluid communication with the fluid passage.