An implantable device having a communication system, a sensor, and a monolithic substrate is described. The monolithic substrate has an integrated sensor circuit configured to process input from the sensor into a form conveyable by the communication system.

A garment includes a securing portion operable to removably secure the garment about an abdomen of a wearer; a sensor attachment portion pivotably attached to the securing portion, the sensor attachment portion including a sensor mount configured to receive and retain a sensor therein; and a sensor received in the flexible sensor mount; the securing portion and the sensor attachment portion being configured such that, when the securing portion is secured around the back of a wearer, the sensor attachment portion pivots with respect to the securing portion so as to self-position the sensor attachment portion across (a) an upper portion of the wearer's abdomen or (b) a lower portion of the wearer's abdomen; the flexible sensor mount being configured to orient a sensor received therein to be flush with skin of the wearer when the garment is worn by the wearer and to self-adjust during the course of pregnancy.

A method of determining a fused sensor measurement is disclosed including: obtaining sensor measurements from sensors detecting a same type of physiological measurement; determining a signal quality index (SQI) of each sensor including determining an extent to which a sensor measurement differs from others among the sensor measurements obtained from each sensor; determining a weightage of each sensor based on the SQI of each sensor; and determining a fused sensor measurement from the plurality of sensors based on the weightage of each sensor and filtered sensor measurements of each sensor obtained from a Kalman filter operation. A vehicle safety system includes: a vehicle electronic control unit configured to: determine the sensor measurement extent, to determine the SQI of each sensor, determine the weightage of each sensor, determine the fused sensor measurement, determine the occupant's physiological condition, and if the physiological condition is abnormal, perform at least one vehicle operation.

The blood pressure measuring device (1) is designed as a photoplethysmographic measuring system which functions according to the “vascular unloading technique”. Metrological components and a pressure generating and pressure control system are accommodated in the base part (3). The fitted cuff part (2) has an ergonomic palm support (4), two finger supports (6) divided from one another by a web (5), and also a receiving part (7) which comprises two receiving tubes (9) for fingers. The cuff part (2) projects beyond the base part (3), both towards the front and also towards the rear, and covers the base part (3) almost completely, i.e. by more than 90%. The lateral attachment of the cable (8) facing in the direction of the forearm has the advantage that the cable can be guided along the patient's arm, the wrist does not rub against the cable (8), and in particular the carpal tunnel is also protected.

Exemplary embodiments of wearable stretch sensors and applications of using the same are disclosed. In embodiments, the sensors and the applications disclosed herein can be used to capture spinal motion and posture information.

A system includes a processor circuit configured to receive a first set of data. The first set of data includes two pressure measurements and a flow measurement from the vasculature of a patient obtained while the sympathetic nervous system of the patient is not under stimulation. The processor circuit calculates a blood flow resistance value based on the first set of data. The processor circuit then receives a second set of data. The second set of data also includes two pressure measurements and a flow measurement from the vasculature of the patient obtained while the sympathetic nervous system of the patient is stimulated. The processor circuit calculates another blood resistance value based on the second set of data. The processor circuit then compares the two blood flow resistance values to determine whether a denervation procedure would be effective to mitigate the nerve system's response to stimulation. The processor circuit outputs to a screen display metrics obtained from the measurement procedure.

A wearable device is provided. The wearable device is used by being attached to a user's skin. The wearable device includes a main body unit having a housing and a substrate, the substrate being arranged inside the housing, an electrode unit including a sensing electrode connected to the main body unit, and a patch unit including one or more conductive members, the one or more conductive members being configured to electrically connect the electrode unit to the user's skin. The electrode unit includes a shielding layer that is not electrically connected to the main body unit. The shielding layer is conductive with a floating potential.

A multiple-point basket-type or crown-shaped catheter device provides simultaneously mapping over a three-dimensional (3D) region of a subject, such as, one or more chambers of a subject's heart. The catheter device may include a series of splines each having a wave-like profile formed of a periodic series of peaks and troughs, with electrodes located at the peaks and troughs for mapping purposes.

A pellet for testing distal colonic and anorectal function. In one embodiment the pellet comprises a bag comprising the exterior of the pellet wherein the bag is comprised of a polymer that is reactive with a catalyst to form a more solid-like substance. In another embodiment, the pellet may comprise one of a grapheme layer, a wavelength transducer, or a magnetically attractive element. In another embodiment the pellet may comprise a telescopic extender and further comprise a telescope bad coupled to the telescopic extender.

An implant which includes: a housing having a chamber; and a sensor unit; a first membrane covering the chamber at a first pressure side and a second membrane covering the chamber at a second pressure side; the chamber includes a pressure transfer device being in contact to the first and second membrane and to the sensor unit arranged within the chamber between the first and second membrane, wherein a sensor control unit arranged within the housing; wherein the sensor unit is configured to determine a pressure difference between a pressure at the first pressure side of the chamber and a pressure at the second pressure side chamber of the chamber.