A method of managing a medical suction device through a network may be embodied by the management server through the steps of: storing operation information of at least one medical suction device in a storage unit provided in the management server, generating an operation start determination reference value of the medical suction device based on the operation information, receiving information on conditions of a patient from a medical suction device installed at an outside, and determining whether to start an operation of the medical suction device that has transmitted the information on conditions of the patient based on the operation start determination reference value and the information on conditions of the patient.

A fat suction and graft syringe includes a negative pressure adjustment mechanism. The negative pressure state in a barrel can be maintained during a procedure only by pulling and releasing a plunger, and only by slightly rotating the plunger. The plunger can be pushed inside the barrel without being constrained by a multi-level holding plate and a single-surface rotation clip, whereby the syringe has enhanced convenience in the use and production thereof so that many practitioners accustomed to using a normal syringe can easily use the syringe without separately learning how to manipulate the syringe.

A method for operating a breastpump unit for expression of human breastmilk and a breastpump unit. The breastpump unit having a pump assembly for generating vacuum pressure, a reservoir for receiving breastmilk, and a breast shield for sealing application to a breast to be pumped. The breast shield has a flexible inner chamber for receiving a nipple of the breast and a second chamber, in particular an outer chamber extending about the outside of the inner chamber and which at least partially surrounds a nipple that is inserted into the inner chamber. The method includes a cycle including evacuating the inner chamber and the reservoir by the pump assembly to a first vacuum pressure, connecting the second chamber to the pump assembly and to the reservoir 24 and evacuating the second chamber to a second vacuum pressure, in which the second vacuum pressure is higher or greater than the first vacuum pressure, and at least partly releasing the vacuum from the second chamber to a lower vacuum pressure, in particular lower than the first vacuum pressure.

In one embodiment, an irrigated medical system includes a medical tool, an irrigation line configured to fluidically connect an irrigation reservoir storing irrigation fluid to the medical tool, and provide at least some of the irrigation fluid to the medical tool, a force sensor configured to be coupled with the irrigation reservoir, and provide a signal responsively to a force exerted by the irrigation reservoir on the force sensor over time as irrigation fluid in the irrigation reservoir is depleted, and a controller configured to find an irrigation rate of the irrigation fluid flowing in the irrigation line responsively to the signal.

An evacuation system and method for removing and/or treating gaseous and/or particulate byproducts of surgical procedures includes an end effector such as a side vent trocar, an operating room tower or the equivalent, a disposal vessel, a vacuum source and optionally a filter. The end effector may be coupled to the tower by a conduit, the tower may be coupled to the collection tank by a conduit, and the collection tank may be coupled to the vacuum source. Gaseous and/or particulate byproducts may flow from the surgical site through the trocar, conduits, tower tank and filter, and the flow may be regulated at least in part by the components of the system.

A reduced-pressure treatment system for debriding a treatment area of a tissue site and applying reduced pressure is disclosed. The reduced-pressure treatment system includes a hydrogel having a blocked acid debriding agent. The hydrogel is adapted to cover the treatment area and enhance autolytic debridement at the treatment area. The reduced-pressure treatment system includes a manifold that is adapted to cover the hydrogel and distribute reduced pressure to the tissue site. The reduce-pressure treatment system also includes a sealing drape for forming a fluid seal over the tissue site and manifold. Other systems, methods, and dressings are presented.

Surgical systems can include evacuation systems for evacuating smoke, fluid, and/or particulates from a surgical site. A surgical evacuation system can be intelligent and may include one or more sensors for detecting one or more properties of the surgical system, evacuation system, surgical procedure, surgical site, and/or patient tissue, for example.

One implementation of the present disclosure is a method for dynamically controlling an alarm of a negative pressure wound therapy (NPWT) device, according to some embodiments. In some embodiments, the method includes initiating NPWT, comparing an initial pump duty to a threshold value to determine a dressing application quality, monitoring a leakage rate of the NPWT, setting a leak threshold value based on the dressing application quality, determining leakage event occurrences in response to the leakage rate exceeding the leak threshold value at multiple times, adjusting the leak threshold value based on at least one of a number of the leakage events over the time period, a time duration between sequentially occurring leakage events of the leakage events, and the dressing application quality, and causing a user interface device to display a leak alert in response to the leakage rate exceeding the adjusted leak threshold value.

A method of priming a surgical instrument, wherein the surgical instrument includes a shaft assembly including a lumen, and a valve assembly. The valve assembly includes a first inlet configured to receive the fluid from a fluid source, a second inlet configured to receive a suction from a vacuum source, an outlet in fluid communication with the lumen, a valve chamber, and at least one valve plug. The method includes activating the fluid source to provide the fluid to the first inlet, activating the vacuum source to provide the suction to the second inlet, transitioning the at least one valve plug from a first position to a second position, and transferring a first portion of the fluid from the first inlet toward the vacuum source through the second inlet thereby priming the surgical instrument.

Described herein is a safety system that works collectively with an automated fluid drain control apparatus and systems and clinical experts to establish protocols and methods for given patient populations to ensure that the drainage of fluid from patients is both safe and effective. It further enables the transportation of drain orders from systems external to the drain system and returns to them the drainage data on a periodic basis for inclusion into the patient chart.