An antenna assembly includes: a wearable antenna including a conductive signal layer having a radiating surface; a feed conductive layer; and an insulating layer in between the conductive signal layer and the feed conductive layer, and wherein the conductive signal layer, the feed conductive layer, and the insulating layer are fabric-based, wherein the wearable antenna is shaped and sized to be embedded in a subject's clothing with sufficient flexibility to be stretched and bent as the subject implanted with a passive implantable stimulator device maintains routine daily activities, and wherein the wearable antenna is electrically tuned and configured to have the radiating surface of the conductive signal layer facing the subject's skin and a feed point of the feed conductive layer connecting to a controller such that the wearable antenna is non-inductively coupled to the implanted passive stimulator device to supply power the passive implantable stimulator device wirelessly and non-inductively.

A bleeding control device for mitigating bleeding includes an outer storage container housing, a compressed gas canister, wound blocking contents and a control element. The bleeding control device may be used to deliver variable contents to a wound at the site of injury to control the bleeding of a victim as temporary solution for mitigating the bleeding until more advanced medical care can be provided. A bleeding control device includes a canister housing, a compressed gas canister arranged within the canister housing, a tube connected to the canister housing, an inflatable balloon disposed on the tube, the inflatable balloon being fluidly connected to the compressed gas canister, and a control element configured to activate the compressed gas canister to inflate the inflatable balloon.

Multi-layer contact patches, as well as related apparatus, kits, systems, and methods, enable improved allergen testing and diagnosis. Multi-layer contact patches include a shield layer releasably coupled to an adhesive layer. The adhesive layer at least partially defines and is fixably coupled to an allergen complex layer. The allergen complex layer defines a plurality of allergen complex cavities. At least a subset of the allergen complex cavities include an allergen complex positioned therein, each allergen complex comprising an absorbent matrix and an allergen.

Disclosed herein is a device which is intended to deliver and maintain reduced pressure to body surfaces for application of reduced pressure wound therapy (RPWT) also known as negative pressure wound therapy (NPWT). During application of this type of therapy, a substantially airtight seal is formed around a section of tissue to be treated. This seal is formed by a dressing which provides fluid communication from a section of tissue to a reduced pressure source. Disclosed herein is a dressing system which is configured to enhance usability and functionality of this dressing. First, the system may be configured to allow full rotation of the fluid communication conduit to the reduced pressure source along the axis substantially normal to the dressing. Second, the system may be configured to include a one-way valve to prevent backflow of any drainage fluids. Third, the system may be configured with transparent windows covered by opaque flaps to allow inspection through the dressing. Fourth, the system may be configured to include an indicator which visually makes clear whether reduced pressure is being applied or not. Fifth, the system is configured to minimize the profile of the dressing system.

Percutaneous access devices (PAD), bandages, or other implantable medical devices are provided that are equipped with filters, environmental controls, and sensors that promote the formation of a natural biologic seal between the skin and the device to form a barrier to microbial invasion into the body. Levels of humidity and pressure are monitored and dynamically controlled to optimize wound closure about an implanted device or when a PAD is not present a wound itself. Methods and systems for actively assessing wound closure are incorporated into the design of percutaneous skin access devices (PAD), bone anchors, or a wound dressing or bandage alone without at PAD. Pressure and humidity sensors provide active feedback for making changes to the ecology of the wound site or PAD insertion site. A filter is used to aerate the wound while also preventing pathogens in the ambient air from reaching the wound.

The present disclosure generally relates to smart bandages comprising a dressing and pressure sensor. The pressure sensor measures at least one pressure reading at a wound area while the dressing bandages the wound area. The pressure sensor includes a force sensitive film configured to generate a pressure signal based on pressure applied thereto and is operably coupled to the dressing such that pressure applied to the wound area is coupled to the force sensitive film via the dressing. A near field communication device of the pressure sensor is operably coupled to the force sensitive film for reporting the pressure signal. The smart bandage may include a user interface that is configured to display reported signals to a user for comparing the pressure at the wound area with a threshold pressure. The disclosure further provides a method of treating the wound area by applying the smart bandage to the wound area.

The present invention provides a dermal patch for selectively retaining one or more analyte(s) from a body of a subject comprising: a membrane layer (101) for retaining one or more analyte(s) from a body of a subject, with a first and a second side, wherein the first side is adapted to be in fluid communication with the skin of the subject; optionally holding means for securing the membrane layer in place; an adhesive layer (104); and a backing layer; wherein between the backing layer and the membrane layer (101) there is an expandable layer (103) for applying pressure to the membrane layer.

A pressure monitoring system and method for warning a patient or caregiver that soft tissue pressure has exceeded some predetermined level that over time would necessitate moving the patient to prevent or at least reduce a risk of soft tissue damage. The pressure monitoring system and method utilize a dressing assembly adapted to be applied to or near a surface of the patient's body and generate electrical outputs corresponding to soft tissue pressure sensed at the surface. The dressing assembly includes a pocket formed therein for removable, secured and protected insertion of one or more sensors.

Medical device kits for use in placing, maintaining, altering, and/or removing medical devices in, on, and/or from the body of a patient are disclosed. Such medical device kits can include one or more wrap assemblies for use in the placement/maintenance procedure. In accordance with present embodiments, the one or more wrap assemblies of the medical device kit can include various features to assist the clinician performing the particular procedure. In one embodiment, a medical wrap assembly is disclosed, comprising a foldable wrap body that includes a front surface, wherein the front surface is configured to define a sterile field. A plurality of pockets is included on the front surface of the wrap body. The pockets are configured to contain therein a plurality of medical components. The medical components are arranged in the pockets in a predetermined order of use for the medical procedure.

Aspects of the invention generally relate to medical devices and associated methods of manufacture and use, and more particularly to scar modulation dressings. Aspects of the invention relate to improving wound healing and improving scar maturation. In a first aspect, there is a system including: a sheet configured to be applied to the skin of a patient over a wound or scar bed; a device that is separate from the sheet and that is configured to be used to massage the sheet to cause: (1) static charging of the sheet, and (2) physical massaging of the wound covered by the sheet.