Provided is a negative-pressure wound therapy apparatus capable of causing negative pressure in a closed space defined by a wound dressing and a wound region with a sufficient suction flow rate as needed even with a miniaturized pump device. In atypical use that needs a high suction flow rate, because a pump device (30) with a high suction flow rate is attached to a wound dressing (10) and sucks gas from a closed space (904) defined by a wound region (903) and the wound dressing (10), even when a pump device (20) for typical use is miniaturized and the suction flow rate of the pump device (20) is reduced, a therapy apparatus (100) can achieve a suction flow rate sufficient for atypical use. Thus, the pressure value in the closed space (904) can decrease to a desired value more quickly.

A wound dressing includes a superabsorbent layer, a backing layer, and a charcoal layer. The superabsorbent layer is configured to absorb wound fluid and has a first side and a second, wound-facing side. The backing layer also has a first side and a second, wound-facing side. The backing layer is substantially impermeable to liquid and substantially permeable to vapor. The charcoal layer is positioned between the first side of the superabsorbent layer and the second, wound-facing side of the backing layer. The charcoal layer is configured to increase a moisture vapor transmission rate of the wound dressing.

A wound dressing includes a perforated film layer, a hydrophilic foam layer, a drape layer, and superabsorbent projections. The perforated film layer is configured to engage a wound bed and has a first side and a second side, the second side configured to face the wound bed. The hydrophilic foam layer also has a first side and a second side, the second side configured to face the first side of the perforated film layer. The drape layer also has a first side and a second side, the second side configured to face the first side of the hydrophilic foam layer. The hydrophilic foam layer also has a plurality of superabsorbent projections fixed to and extending from the first side of the hydrophilic foam layer towards the second side of the drape layer. The drape layer further has a first drape and a second drape, the first drape comprising an adhesive-coated ring configured to peripherally surround and overlap the second drape.

A method for manufacturing a wound dressing having a substrate, and a wound dressing manufactured by such a method are described. The method has a step of providing a sacrificial layer of material to be perforated by means of a hot pin perforator, in order to remove any molten residues on the heated pins of the hot pin perforator, before the same pins are used to make holes in the substrate. The presented method is cost effective, robust and reduces the risk of contaminating substances being embedded in the substrate during the hole making process.

In one aspect, the present disclosure provides a system A system, including a light source, a detector, and a controller in electrical communication with the light source and the detector. The controller is configured to execute a program stored in the controller to trigger the light source to emit a first pulse of light having a first pulse duration for illumination of a target, actuate the detector after a first delay time following emission of the first pulse of light to begin detecting a first signal from the target for a first detection time, and repeat the steps of triggering the light source and actuating the detector at least once, varying for each repetition at least one of the first pulse duration, the first delay time, and the first detection time.

A medical wetness sensing device includes a base adapted to be disposed on a wearer of the medical wetness sensing device. The base includes a first electrical conductor and a second electrical conductor electrically insulated from the first electrical conductor. The first electrical conductor includes a hinge portion enabling a first portion of the first electrical conductor to deflect, at the hinge portion, relative to a second portion of the first electrical conductor. The medical wetness sensing device includes a controller electrically connected to the first electrical conductor and the second electrical conductor. The controller is configured to detect a presence or an absence of a medical fluid electrically connecting the first and second electrical conductors.

The present invention discloses a tubeless energy drainage device for trauma, pertaining to the field of tubeless drainage technology, especially relating to a tubeless energy drainage device for trauma. The device includes energy transmission carriers, lead wires, and a frequency electrical energy generator. The frequency energy resonance generator transmits electrical energy to the energy transmission carriers, activates metal potassium ions on the energy transmission carriers, and creates resonance through conduction of metal ions in a wound covering layer and changing frequency of a wound, thereby achieving retrograde drainage of the wound's own sinus in a drainage area. The device disclosed by the present invention is of great significance for the rapid and full drainage of intractable wounds and battlefield wounds, and the drainage, healing, and pain relief of minute wound fistulas that cannot be tubed.

A wound debridement system includes a wound dressing having an active layer and a wound interface layer. The active layer is formed from one or more transmission layers that are arranged about a central post. Activation of the transmission layers is configured to cause the movement of the wound interface layer relative to a tissue site to which the wound dressing is applied. A drive unit is operably attached to the central post. The drive unit is configured to generate and transfer a vibrational energy and/or a rotational movement to the transmission layer(s) via the central post. The resultant vibration and/or rotation of the transmission layer(s) is imparted onto the wound interface layer, thereby effectuating the desired movement of the wound interface layer relative to the tissue site, which allows for the debridement of debris that may be located at the tissue site.

An improved syndesmosis reduction device has a wrap of elastic material extending a length L from a first end to a second end with an open window or slot positioned in an intermediate portion of the wrap spaced from the ends. The wrap is configured to achieve a reduction of an injured ankle and is facilitated by the elastic nature of the ankle wrap. The reduction is facilitated by circumferentially wrapping the wrap from a leg to a foot or vice versa in a compressive fashion by securing the first end by wrapping and stretching the wrap to the second end. The window or slot is to permit an incision at the ankle for hardware placement without the need to remove the wrap and without loss of the reduction achieved.

Non-adhesive articles include an elastomeric layer, where the elastomeric layer has a plurality of cuts arrayed in a pattern. The cuts are gaps, but the gaps are not visible to the naked eye when the article is in an unstressed state, and in a stressed state, at least some of the cuts become gaps that are visible to the naked eye. The gaps are perforations in the elastomeric layer and are apertures through which one can view through the elastomeric layer. The perforations indicate the presence of stress in the article, and the elastomeric layer has a lower effective modulus of elasticity in at least one axis than an identical elastomeric layer without the plurality of cuts.