A method for managing sleep of a user comprises obtaining, by a computing system, sleep data and environmental data for the user; determining, by the computing system, a sleep state of the user based on the sleep data; determining, by the computing system, one or more awakening actions based on the sleep state of the user and the environmental data; and causing one or more devices in an environment of the user to perform the one or more awakening actions to awaken the user.

Environmental characteristics of habitable environments (e.g., hotel or motel rooms, spas, resorts, cruise boat cabins, offices, hospitals and/or homes, apartments or residences) are controlled to eliminate, reduce or ameliorate adverse or harmful aspects and introduce, increase or enhance beneficial aspects in order to improve a “wellness” or sense of “wellbeing” provided via the environments. Control of intensity and wavelength distribution of passive and active Illumination addresses various issues, symptoms or syndromes, for instance to maintain a circadian rhythm or cycle, adjust for “jet lag” or season affective disorder, etc. Air quality and attributes are controlled. Scent(s) may be dispersed. Hypoallergenic items (e.g., bedding, linens) may be used. Water quality is controlled. Noise is reduced and sounds (e.g., masking, music, natural) may be provided. Passive and active pathogen controls are employed. Controls are provided for the occupant and/or facility personnel, as is instruction, and surveys, including assessing wellness.

A filling aid. The filling aid includes a locking portion including a groove feature; and a locking feature having a locked and an unlocked position; and a filling syringe holder slidably attached to the locking portion, the filling syringe holder including a filling needle cradle portion having a tongue feature; and a needle housing portion comprising at least one tab having a starting position and a filling position, wherein the groove feature configured to accommodate the tongue feature, and wherein the locking feature interact with the filling syringe holder wherein when the locking feature moves from the locked position to the unlocked position the needle housing portion moves from the starting position to the filling position.

A medical device includes a first housing portion (FHP) and a second housing portion (SHP) configured to be to be movable relative to each other from a first position to operatively engage at a second position to couple at least one of a drive device and a needle-inserting device supported by one of the FHP and the SHP to a reservoir supported by the other of the FHP and the SHP. Electronic circuitry configured to detect at least one of a first magnetic interaction between a magnet and at least one of a first magnetically attractive material and a first magnet-responsive device and a second magnetic interaction between the magnet and at least one of a second magnetically attractive material and a second magnet-responsive device, and to provide a signal or a change in state in response to detecting at least one of the interactions.

Devices and methods for managing chest or wound drainage are disclosed where in one embodiment, the system generally comprises a chest tube configured for insertion at least partially within a body of a subject, a drainage tube fluidly coupled with the chest tube, a reservoir fluidly coupled with the drainage tube, a pump in communication with the reservoir, and a controller in fluid communication with the drainage tube. The controller may be configured to determine a readiness for removal of the chest tube from the body based upon one or more removal parameters which are obtained over a period of time via the controller.

An optical connector includes a first sub-assembly that is factory-installed to a first end of an optical fiber and a second sub-assembly that is field-installed to the first end of the optical fiber. The optical fiber and first sub-assembly can be routed through a structure (e.g., a building) prior to installation of the second sub-assembly. The second sub-assembly interlocks with the first sub-assembly to inhibit relative axial movement therebetween. Example first sub-assemblies include a ferrule, a hub, and a strain-relief sleeve that mount to an optical fiber. Example second sub-assemblies include a mounting block; and an outer connector housing forming a plug portion.

A portable modular assistive device for storing, measuring, drawing and administering liquid injectable medication or other fluids from a vial and syringe, specifically to insulin for consumers and medical professionals in homes, while traveling and in medical facilities, having means to allow users to quickly, securely, easily and accurately measure and draw the desired amount of insulin and then administer the medication. The device is a portable syringe guide and vial holder comprising a horizontal elongated stabilizer made of rigid light-weight material with high tolerance and low friction, a rigid liquid medication vial protector at one end; a rigid movable syringe carriage with an opening on the top side to firmly hold the assembled syringe and needle to perfectly align the needle to the center section of the rubber top of the vial; a flexible expandable color-coded security strap; a flexible expandable color-coded resistance spacer ring, a removeable adjustable magnifier and calibrator bar, a rigid end cap at the other end of the horizontal stabilizer, with said holder having means to allow users to transport said holder in a pocket or pouch without risk of spillage from the vial, dislodging the components or damage to the vial, needle or syringe. Thus, a considerably more versatile, cost-effective, durable and efficient syringe guide and vial holder is provided that can accommodate a plurality of syringe and needle sizes as well as various liquid medications and other fluids in vials in the first embodiment as well as in other embodiments with ease of tracking quantities, contents, sizes and locations of a variety of vials, syringes and needles.

A method for functional testing of aerosol provision devices may include performing a functional state transition test of a power unit. The functional state transition test of the power unit may include extracting a unique identifier from the power unit of an aerosol provision device responsive to operable coupling of the power unit to a test fixture, determining a transition code based on the unique identifier, providing the transition code to the power unit via the test fixture to transition the power unit from an initial state to a transitioned state, and transitioning the power unit to the initial state.

An arrangement for an inhaler comprises at least one electric evaporator for evaporating liquid supplied from the evaporator, and for adding the evaporated liquid to an air flow flowing through the inhaler to form an aerosol, and a flow rate measuring arrangement for measuring the volume and/or mass flow of the air flow flowing through the inhaler. The flow rate measuring arrangement comprises a heating device, a downstream temperature sensor arranged downstream of the heating device for measuring an air outlet temperature and an electronic control device, wherein the electronic control device is adapted to determine the volume and/or mass flow of the air flow flowing through the inhaler on the basis of a temperature difference between the air outlet temperature and an air inlet temperature of the air flow upstream of the heating device.

A medical fluid delivery system and apparatus for remote machine updating and control are disclosed. An example medical fluid delivery apparatus includes a processor and a dialysis fluid circuit including at least one dialysis fluid pump. The processor is configured to receive a disinfection input to begin a disinfection procedure and cause the at least one dialysis fluid pump to perform a disinfection procedure on the dialysis fluid circuit using a disinfection fluid. The processor is also configured to, after the disinfection procedure is complete, start a disinfection timer. When a dialysis input is received before the disinfection timer reaches zero, the processor enables a dialysis treatment to be performed. When the disinfection timer reaches zero before the dialysis input is received, the processor prevents the dialysis treatment from being performed until the disinfection procedure is performed again.