Patent classifications
A61M2210/083
WEARABLE FLUID DELIVERY SYSTEM
A universal wearable fluid delivery system includes a body panel which includes a plurality of connection points. A fluid dispenser includes a taut pocket defined by at least one taut surface and a portion of a surface of the body panel and is adapted to receive a fluid bag. A stretch pocket is disposed within the taut pocket. The stretch pocket is defined between a surface of at least one stretch panel and about a common portion of the surface of the body panel and is adapted to receive a pressure infusion bag disposed within. At least one strap is coupled to the body panel via two connection points of the plurality of connection points to secure the fluid dispenser to a body of a human or animal patient. A wearable fluid delivery system and a fluid dispenser and body panel assembly are also described.
Transilluminating Immobilizer for Intravenous and Intra-arterial procedures
A transilluminating immobilizer and methods for the same for intravenous procedures (IV), intra-arterial procedures (IA) and vessel access. The device features a component for restraining an extremity and a transilluminating component for location of vessels during IV and IA placement.
Device And Method To Locate Site Of Intramuscular Injection
Devices, kits and methods for determining the site of intramuscular injection in adult and child patients are disclosed. The device includes a top element and two legs that are configured to be fastened in a first position and a second position. When placed in the first position and second position, the device forms a substantially triangular region having a center that corresponds to the site of injection.
CONTOURED FOAM DRESSING SHAPED FOR PROVIDING NEGATIVE PRESSURE TO INCISIONS IN THE SHOULDER
A negative pressure wound treatment (NPWT) dressing system for treating shoulder incisions. The NPWT dressing system includes a wound dressing, an immobilization device configured to immobilize a shoulder of a patient, and a negative pressure source coupled to the immobilization device. The wound dressing includes a drape layer, a manifold layer, and a reduced-pressure interface integrated with the drape layer and the negative pressure source. The drape layer has a first surface and a second, wound-facing, surface. The drape layer is substantially impermeable to liquid and substantially permeable to vapor. The manifold layer has a first surface and a second, wound-facing surface. The manifold layer has a first lobe, a second lobe substantially aligned with the first lobe, and a third lobe extending substantially perpendicular to the first lobe and the second lobe.
SKIN THERAPY SYSTEMS
A convenient and hygienic skin therapy system comprising an encaser, one or more therapeutic compositions, a sealing means and optional accessories is disclosed. A method of using such a skin therapy system is also provided. The skin therapy system and the use thereof provides an effective, efficient and safe therapeutic approach.
IRRIGATION FLUID CONTAINMENT SYSTEMS
Various irrigation fluid containment systems and components are disclosed. In some embodiments, the irrigation fluid containment system comprises a medical kit and/or an irrigation kit. In some embodiments, the irrigation fluid containment system comprises a medical basin and/or an irrigation basin. In some embodiments, the irrigation fluid containment system comprises an irrigation shield. In some embodiments, the irrigation fluid containment system comprises a suction hose.
SYSTEMS AND METHODS FOR REDUCING CONTAMINANTS IN A PORTION OF A PATIENT
Systems and methods for reducing pathogens near an implant are discussed. In some cases, the methods include reducing contaminants in a portion of a patient that has an implant and that is disposed interior to a closed surface of skin of the patient. The method can further include placing a conduit in the closed surface of skin and flowing an antimicrobial fluid into that portion of the patient to contact the antimicrobial fluid with a surface of the implant and tissue adjacent to the implant. In some cases, the antimicrobial fluid is then removed from the portion of the patient having the implant. As part of this method, biofilm near the implant can be mechanically, ultrasonically, electrically, chemically, enzymatically, or otherwise disrupted. Other implementations are described.
SENSORIAL ELECTRONIC DEVICE FOR THE REHABILITATION OF PATIENTS WITH PARKINSON'S DISEASE
This invention refers to a device that reduces and counteracts human motor symptoms (tremor in the upper limbs, muscular stiffness, bradykinesia or slowness in movements, postural disruptions, Parkinsonian walking and freezing in the walking) caused by Parkinson's disease. The device produces vibration by means of a micro-motor that can be modulated in time, speed and power. A laser diode generates a light that is projected in the ground in the form of a horizontal line, a Bluetooth module communicates this device with different intelligent electronic devices and with applications. These components are powered by a rechargeable handheld power source. The components are powered by a rechargeable handheld electric energy source.
WEARABLE FIDGET SPINNERS
Wearable devices that provide tactile, visual stimulation, and movement/manipulation for a user are described. The devices can include a spinner that rotates with respect to a base. The spinner can be spun by the user to produce visual stimulation that the user may find pleasing and soothing, and which may provide therapeutic effects. The spinner may also include tactile features, such as a series of protrusions and recesses, that the user can touch or rub to create a tactile sensation, which may also help the user to relieve and/or regulate stress. The spinner also allows the user to manipulate the spinner with fingers in small repetitive movements that may reduce restlessness. The devices may be sized and shaped such that the user may uninterruptedly perform everyday tasks and discretely wear and use the devices in certain social environments such as the classroom.
Sleep Monitoring and Sleep Aid Usage
A method or apparatus to improve sleep aid efficacy is described. The method comprises monitoring the sleeping patterns of a user utilizing a non-intrusive sleep monitoring device. The method further correlates the user's sleep quality and sleep quantity with use of the sleep aid. In one embodiment, the method adjusts the sleep aid based on the sleep statistics.