A surgical stapler apparatus or assembly comprises a surgical stapler device having an internal channel extending from a stapler actuating handle to a stapler head of the device and a gas insufflation device having a pressurized gas supply connected to the internal channel of the stapler device via an inlet port at a handle portion intersecting with the channel in order to supply pressurized gas to the channel as the stapler shaft is inserted into the lumen of a colon, rectum or the like. Pressurized gas travels along the channel and out of the stapler head at the distal end of the stapler device in order to inflate the lumen ahead of the advancing stapler head, easing insertion.

Methods and devices related to the fields of skin care, hair restoration and lip care wherein the systems may be used by an individual for infusing treatment media into skin or lips for cosmetic and rejuvenation purposes, hair restoration purposes or other therapeutic purposes.

A method of determining a pressure of a body cavity with a controller of a fluid management system includes determining a pressure and a volume of a cuff disposed about a collapsible bag, determining a volume of the collapsible bag based on the pressure and the volume of the cuff, and determining a pressure of the collapsible bag based on the volume of the collapsible bag. The method also includes calculating a fluid flow from the collapsible bag into a body cavity from the collapsible bag and determining a pressure of the body cavity based on the fluid flow.

Disclosed are various embodiments for an anti-reflux nasal aspirator that includes a nozzle comprising a nozzle outlet, a bulb configured to provide suction at the nozzle outlet in response to a squeezing force applied to the bulb, an anti-reflux coupler positioned between the bulb and the nozzle through which air passes from the bulb to the nozzle, and a one-way air valve positioned in an aperture located at a base of the bulb. The anti-reflux coupler may include a check valve configured to prevent reflux of debris into the bulb. The check valve may include one of an umbrella valve; a duckbill valve; a slit-cutting valve; and a flapper valve.

There is described a dry powder medicament delivery device comprising: a medicament container containing a unit dose of dry powder medicament; a medicament dispensing assembly; and optionally an air source.

The present disclosure relates generally to the field of medical treatment and therapy of mammalian tissue. More specifically, it relates to coverings and/or dressings that provide negative pressure at mammalian tissue sites, such as at one or more sites of surgical, non-surgical, and/or traumatic wounds, to promote closure and healing of the wounds. A key embodiment of the disclosed invention entails the use of a dressing that comprises a sponge that is shaped so as to create a vector force inward bringing wound edges together to promote healing, especially upon application of negative pressure. Other key features of the disclosed invention are its simplicity, its low cost, and that it is completely mechanical and lacks the need for any electronic components. The disclosure also relates to devices, systems, kits and methods for providing said negative pressure at said mammalian tissue sites and promote healing.

A nasal bulb aspirator that can be sized to fit the needs of infants through adults and is designed to ensure that the tip remains hygienically intact by a one-way valve and a counterbalance system that prevents the tip from touching surrounding surfaces, thereby limiting cross contamination from possibly resistant pathogens.

A wound treatment appliance is provided for treating all or a portion of a wound. In some embodiments, the appliance comprises an impermeable flexible overlay that covers all or a portion of the wound for purposes of applying a reduced pressure to the covered portion of the wound. In other embodiments, the impermeable flexible overlay comprises suction assistance means, such as channels, which assist in the application of reduced pressure to the area of the wound and removal of exudate from the wound. In other embodiments, the wound treatment appliance also includes a vacuum system to supply reduced pressure to the wound in the area under the flexible overlay. In yet other embodiments, the wound treatment appliance also includes wound packing means to prevent overgrowth of the wound or to encourage growth of the wound tissue into an absorbable matrix comprising the wound packing means. In still other embodiments, the appliance may include a suction drain. In other embodiments, the appliance may include a collection chamber to collect and store exudate from the wound. In yet other embodiments, a suction bulb may be used to provide a source of reduced pressure to an impermeable overlay that covers all or a portion of the wound. Finally, methods are provided for using various embodiments of the wound treatment appliance.

A pressure regulating or pressure relief device comprises an inlet and an outlet chamber with an outlet. The inlet is in fluid communication with the outlet chamber. A valve seat is located between the inlet and the outlet. A valve member is biased to seal against the valve seat, and displaces from the valve seat by an inlet pressure at the inlet increasing above a pressure threshold to allow a flow of gases from the inlet to the outlet via the outlet chamber. The flow of gases through the outlet causes an outlet pressure in the outlet chamber to act on the valve member together with the inlet pressure to displace the valve member from the valve seat.

Methods and devices for delivering a dose, such as a medicament, for inhalation. A dose may be stored by a delivery device and dispersed and delivered in a metered fashion to a subject, such as by the subject inhaling via a mouthpiece of the delivery device. One or more chambers of the device may have a toroidal shape and may be arranged to be selectively opened for fluid communication with a flow path of the delivery device, such as by sliding the chamber relative to a portion of the flow path. The flow path may include a restriction that permits air to bypass the chamber, and/or the chamber may be arranged so that fluid entering the chamber interacts with fluid exiting the chamber so as to enhance dispersion of the dose.