A medical electrode array system comprising a thin-film substrate, a plurality of electrode contacts disposed on the thin-film substrate, and a plurality of traces. The plurality of electrode contacts is configured to provide electrical contact points. The plurality of traces is electrically connected to the plurality of electrode contacts. A electrode contact of the plurality of electrode contacts has a dedicated trace of the plurality of traces that provides electrical connectivity to the electrode contact. The thin-film substrate is configured to flex to maintain continuous contact with contours of patient anatomy. The plurality of traces includes flexible spring-like portions to add flexibility to the thin-film substrate.

A system and method for performing an electrocardiogram is described herein. The system may include one or more of an electrode strip, a data recorder, a connector, one or more computing platforms, and/or other components. The electrode strip may include multiple electrodes configured to provide signals conveying information associated with electrocardiograms. The multiple electrodes may be integrated into the electrode strip. The data recorder may be configured to receive and record information associated with electrocardiograms. Information associated with electrocardiograms may be communicated from the electrode strip to the data recorder via a connector. The connector may include a cableless connector. In some implementations, the information associated with electrocardiograms may be transmitted to one or more computing platforms.

A charging station for providing power to a physiological monitoring device can include a charging bay and a tray. The charging bay can include a charging port configured to receive power from a power source. The tray can be positioned within and movably mounted relative to the charging bay. The tray can be further configured to secure the physiological monitoring device and move between a first position and a second position. In the first position, the tray can be spaced away from the charging port, and, in the second position, the tray can be positioned proximate the charging port, thereby allowing the physiological monitoring device to electrically connect to the charging port.

A method and system are devised for quickly detecting an abnormal concentration of potassium ions in blood from an electrocardiogram. The system includes at least one vector-converting device that includes a processor, a transmitter, at least one memory and at least one storage unit. The at least one storage includes a model data module and a predicting and converting module. The model data module includes data of a model of the concentration of potassium in the blood. The model of the concentration of potassium in the blood includes at least one reference electrocardiogram and corresponding reference data of the concentration of potassium in the blood. The predicting and converting module converts an electrocardiogram into a corresponding predicted concentration of potassium in the blood according to the reference concentration of potassium in blood. The vector conversions device is connected to at least one electrocardiogram generator and at least one monitor. Thus, the electrocardiogram obtained by the electrocardiogram generator is converted to the corresponding predicted concentration of potassium in the blood. The corresponding predicted concentration of potassium in the blood is shown on a monitor to facilitate the medical personnel to take proper actions to reduce the risks of sudden cardiac death.

Embodiments of the present disclosure relate to implantable biosensors configured to be implanted into tissue of a subject at an implantation site. In an exemplary embodiment, the implantable biosensor comprising: an electronic module and a compliant sensing tether extending from the electronic module. The compliant sensing tether comprising a proximal portion coupled to the electronic module, a distal portion spaced apart from the electronics module, and an intermediate portion joining the proximal portion to the distal portion. The proximal portion has a first flexibility and the distal portion having a second flexibility. The second flexibility of the distal portion being greater than the first flexibility of the proximal portion. The distal portion comprises a sensor configured to sense a signal corresponding to an analyte of the subject, wherein the signal corresponding to the analyte is transferred to the electronics module via the compliant sensing tether.

Disclosed is a stent-mesh and microelectrode assembly that is deployable using a catheter or cannula to form a neural interface for recording and/or stimulation of neural tissue. In some embodiments, the assembly may include a thin-film microelectrode array attached to a spring-like stent-mesh component. The thin-film microelectrode array may include an electrode body having two lateral wing-like appendages located distal to a thin-film flexible cable that terminates at the proximal end in a thin-film connector region. The stent-mesh may be attached to the thin-film microelectrode array and configured to be advanced to a target area in a collapsed state and then expanded after reaching the target area to transition the thin-film microelectrode array to a deployed configuration. Accordingly, the assembly may deliver the thin-film microelectrode array to a target area in a minimally invasive manner.

An exemplary apparatus for operating with an electroencephalograms apparatus can be provided, which can include, for example a flexible conductor disposed in a shape of a coil, an electrode disposed on a first end of the flexible conductor, and a coupling configuration disposed on a second end of the flexible conductor, where the coupling configuration can be designed to couple the flexible conductor to the electroencephalograms apparatus. The flexible conductor can be stretchable.

A conductive human interface has a fabric layer with an interior surface and an exterior surface. A soft coating overlies the interior surface of the fabric layer. An electrode or sensor is included to connect with a residual limb. A conductive path connects the electrode or sensor with an electrical connector which, in turn connects with a prosthetic or other assistive device. The conductive path includes a conductor having a section overlying the fabric layer. The overlying section of the conductor can be cord of conductive thread. A nonconductive support thread can extend through the fabric layer from the exterior surface to the interior surface, and further around the conductor to secure the overlying section of the conductor to the fabric layer.

A wearable device (100) includes a body (1) and a detection electrode (21). The body (1) includes an electrocardiosignal collection circuit (11), and an inner electrode (12) and an outer electrode (13) that are electrically connected to the electrocardiosignal collection circuit (11). The inner electrode (12) is configured to collect an electric potential signal of a first wearing position (200), and the outer electrode (13) is configured to collect an electric potential signal of a non-wearing position (300). The detection electrode (21) can move relative to the body (1), and the detection electrode (21) is configured to electrically connect to the electrocardiosignal collection circuit (11) and collect an electric potential signal of a second wearing position (400). The non-wearing position (300) and the second wearing position (400) are different from the first wearing position (200). The wearable device (100) can measure electrocardiosignal data in time.

A connector may include a first housing configured to detachably secure a first input cable of a first sensor configured to generate a first signal, and a second housing configured to detachably secure a second input cable of a second sensor configured to generate a second signal. The second housing may be configured to transmit the second signal from the second input cable to the first housing. The first housing may be configured to transmit at least one of the first signal and the second signal to an output cable. A coupling of the first housing may be configured to mate with a coupling of the second housing such that the first housing and the second housing are configured to be detachably secured to each other. The coupling may be mechanical, electro-mechanical, or magnetic. Either sensor may be an electrocardiogram sensor or a pulse oximetry sensor.