The present invention provides a technology relating to a bio-signal measurement band which may prevent intrusion of foreign matter from the outside and reduce interference from external electromagnetic waves. Since intrusion of foreign matter from the outside is prevented, there is an advantage in that damage and deformation occurring within the bio-signal measurement band is prevented and thus the accuracy of measured bio-signals may be improved. In addition, since the bio-signal measurement band has a structure in which the bio-signal measurement band is shielded except the electrode thereof, there is an advantage in that the problem of a reduction of accuracy due to external electromagnetic waves is solved and thus bio-signals may be measured with improved accuracy.

A radiofrequency (RF) shielding conduits that can be embedded within a doorframe and/or a door of a magnetic resonance imaging (MRI) room are disclosed. The RF shielding conduits can form, upon closing of door onto the doorframe, an RF shielding channel to enclose and/or allow passage of tubing of medical equipment extending from an interior of the MRI room to an environment that is external to the MRI room, while providing a RF shielding of the MRI room.

Disclosed are devices and methods for estimating blood pressure, which implement a pulse-transit-time-based blood pressure model that can be calibrated. Some implementations provide reliable and user friendly means for calibrating the blood pressure model using blood pressure perturbation methods and multiple sensors.

A radiofrequency (RF) shielding conduits that can be embedded within a doorframe and/or a door of a magnetic resonance imaging (MRI) room are disclosed. The RF shielding conduits can form, upon closing of door onto the doorframe, an RF shielding channel to enclose and/or allow passage of tubing of medical equipment extending from an interior of the MRI room to an environment that is external to the MRI room, while providing a RF shielding of the MRI room.

Disclosed are devices and methods for non-invasively measuring arterial stiffness using pulse wave analysis of photoplethysmogram data. In some implementations, wearable biometric monitoring devices provided herein for measuring arterial stiffness have the ability to automatically and intelligently obtain PPG data under suitable conditions while the user is engaged in activities or exercises. In some implementations, wearable biometric monitoring devices are provided herein with the ability to remove PPG data variance caused by factors unrelated to arterial stiffness. In some implementations, wearable biometric monitoring devices have the ability to perform PWA while accounting for the user’s activities, conditions, or status.

A biological data measurement device has patches. A patch to be mounted on the human body basically includes first and second heat insulators, first and second temperature measurement circuits, and a belt-shaped wiring film (bus wire). Therefore, the configuration is simple. For example, a thickness can be approximately several mm, and a weight can be approximately several grams. The patch is easily mounted on the human body, and is inexpensive. The patch is equipped with a selection circuit, and selectively outputs a temperature signal of a first thermometer and a temperature signal of a second thermometer at a predetermined timing. Accordingly, even in a case where the patches are mounted on a plurality of locations of the human body, the number of wires is settled by the number required for one patch. The number of wires can be significantly reduced, compared to the number of wires in the related art.

A device for functional electrical stimulation (FES), neuromuscular electrical stimulation (NMES), and/or in receiving electromyography (EMG) signals includes a sleeve and electrodes. The sleeve is sized and shaped to be worn on a human arm, and comprises a stretchable fabric The electrodes are secured with the sleeve and positioned to contact skin of the human arm when the sleeve is worn on the human arm. An electronic circuit is configured to operate the electrodes. The electronic circuit includes relays connecting the electrodes with a stimulator for performing FES or NMES, and EMG readout circuitry connecting the electrodes with an EMG amplifier. The relays are closed during FES or NMES to connect the stimulator with the electrodes. The relays are open during EMG readout to isolate the stimulator from the EMG amplifier.

An input device includes two conductors that are sewn onto a fiber sheet and an output unit configured to determine an impedance variation in a predetermined area on the basis of a voltage value between the two conductors to which a high-frequency current is applied.

Apparatus for imaging during surgical procedures includes an operating room for the surgical procedure and an MRI for obtaining images periodically through the surgical procedure by moving the magnet up to the table. The magnet wire is formed of a superconducting material such as magnesium di-boride or Niobium-Titanium which is cooled by a vacuum cryocooling system to superconductivity without use of liquid helium. The magnet weighs less than 1 to 2 tonne and has a floor area in the range 15 to 35 sq feet so that it can be carried on the floor by a support system having an air cushion covering the base area of the magnet having side skirts so as to spread the weight over the entire base area. The magnet remains in the room during surgery and is powered off to turn off the magnetic field when in the second position remote from the table.

An ultrasound endoscope includes an insertion part including a distal end part having an ultrasound transducer array, a cable inserted into the insertion part, and a substrate, including electrode pads connected to the ultrasound transducers, respectively, that electrically connects the ultrasound transducers and the cable, and is disposed in the distal end part. The cable has a non-coaxial cable including a first cable bundle consisting of signal wires and ground wires, a first shield layer coating the first cable bundle, and an outer coat coating a second cable bundle consisting of the non-coaxial cables. Each first cable bundle is individually led out from the cable, and each signal wire is electrically connected to the corresponding electrode pad. The ultrasound transducers are configured in drive units and driven simultaneously. A signal wire group includes at least two kinds of signal wires different in length from a distal end of the first cable bundle.