The present invention relates to a flexible pressure sensor using a multi-material 3D-printed microchannel mold, and a method for manufacturing the same, and more particularly, to a flexible pressure sensor having improved flexibility, sensitivity, and stability for use in a wearable device, and a method for manufacturing the same. Further, the present invention relates to a physical sensor for measuring a force applied from the outside, and more particularly, to a multi-directional physical sensor using a multi-layer microchannel array, which may sense all forces applied from the outside in three-dimensional directions such as a perpendicular direction and a parallel direction by applying the multi-layer microchannel array to a body having a three-dimensionally protruding shape.

A modular stethoscope system has multiple ear pieces and chest pieces. The modular stethoscope system allows multiple peoples’ heartbeat and breathing sounds to be shared. The apparatus can have multiple heart modules that are placed on users’ chests that can each receive circulatory and/or respiratory audio signals from the users. The heart modules can be coupled to each other and/or coupled to multiple audio output devices so that some or all of the users can hear the combined heartbeats. The heart modules’ inputs and outputs can be shared through direct physical links and/or converted into electrical or wireless signals that can be received by other electrical audio output devices so that multiple users can listen to multiple heartbeat outputs.

Disclosed is an implant and method of making an implant. The implant having a housing that defines a cavity. The housing includes a sensor comprising a base attached to a diaphragm wherein said base may be positioned within said cavity. The sensor may be a capacitive pressure sensor. The diaphragm may be connected to the housing to hermetically seal said housing. The sensor may include electrical contacts positioned on the diaphragm. The attachment between the base and the diaphragm may define a capacitive gap and at least one discontinuity configured to enhance at least one performance parameter of said implant.

A finger insert for use with a nailfold imaging device includes a housing to receive the user's finger and an immersion substance (e.g., immersion oil), and a deformable pad that holds the user's finger in place during imaging, as well as prevent bubble formation in the substance. The housing includes a transparent wall to facilitate imaging of the finger. The transparent wall includes multiple angled portions that prevent or reduce contact between the nailfold and the wall, to ensure sufficient blood flow through the nailfold region for imaging.

An implantable extravascular pressure sensing system including a cuff having a first brace portion, a second brace portion, and a plurality of biasing members movably coupling the first brace portion and the second brace portion to each other, the first brace portion defining a fluid chamber, the fluid chamber defining a recessed aperture, a flexible diaphragm coupled to the fluid chamber and sealing the recessed aperture, a fluid disposed within the fluid chamber for exhibiting a hydraulic pressure in communication with the flexible diaphragm, and a pressure sensor coupled to the first brace portion, the pressure sensor being configured to measure a change in the hydraulic pressure when a force is imparted on the flexible diaphragm.

The present invention discloses a holder carrying thereon a sensor to measure a physiological signal of an analyte in a biological fluid, wherein the sensor has a signal detection end and a signal output end, and the holder includes an implantation hole being a channel for implanting the sensor and containing a part of the sensor, a containing indentation containing the signal output end, a fixing indentation fixing thereto the sensor and communicating with the containing indentation, a waterproof seal disposed above the implantation hole, an elastic divider disposed in the implantation hole to separate the implantation hole and covering all over a cross-sectional area of the implantation hole, and a blocking element disposed between the implantation hole and the fixing indentation to hold the sensor.

An apparatus (1) for performing manometric measurements by way of medical devices of the pneumatic type, comprises a processing unit (10), and a pressure transducer (4), which is connected to the unit (10) and adapted to be fluid-dynamically connected to the pneumatic device (3). The processing unit (10) comprises: a setting module (11) configured for setting a reference parameter, which is a function of conformational and/or dimensional features of the device (3); and a measurement module (12) configured for processing the measurements made by the transducer (4), according to the reference parameters (a, b, c) which were set for calculating respective objective pressure values. The medical device (3) of the pneumatic type is fluid-dynamically connectable to a measurement apparatus (1), which is provided with an hollow and compressible active portion (30) and provided with an internal fluid-dynamic path adapted to put into communication the apparatus (1) with the cavity of the active portion (30).

A connector to connect to a liquid metal wire includes a hollow conduit configured to connect to a tubular wire casing, and further includes a reservoir including a solid metal conductor. The reservoir is to receive liquid metal to substantially fill a volume of the reservoir such that the liquid metal extends into the tubular wire casing. The tubular wire casing, filled with the liquid metal, becomes the liquid metal wire.

A sensor system is adapted for use with an article of footwear and includes an insert member including a first layer and a second layer, a port connected to the insert and configured for communication with an electronic module, a plurality of force and/or pressure sensors on the insert member, and a plurality of leads connecting the sensors to the port.

An electrode includes a body and a breakable container of contact-enhancing fluid on or in the body. The container is impermeable to the fluid, and is breakable in response to physical manipulation of the electrode to disperse the fluid into the body.