An electronic apparatus according to various embodiments of the present disclosure may comprise: a sensor unit for sensing the movement of the electronic apparatus; a communication unit for communicating with an external apparatus; an input unit for receiving a user input; an output unit for providing information to a user; and a control unit for outputting a message inducing a particular action to the user through the output unit on the basis of medical information of the user and the movement of the electronic apparatus, or controlling the communication unit to transmit information related to the electronic apparatus to an external apparatus.

A wearable device for reflecting a fatigue level of a human body is disclosed. The device comprises a physiological signal acquisition module, a signal conditioning module, a parameter extraction module and a decision module. The physiological signal acquisition module is configured to acquire physiological signals of a testee. An output end of the physiological signal acquisition module is connected to an input end of the signal conditioning module. The signal conditioning module is configured to perform signal conditioning on the physiological signals. An output end of the signal conditioning module is connected to an input end of the parameter extraction module. The parameter extraction module is configured to extract time-domain and frequency-domain parameters in a specific time window. An output end of the parameter extraction module is connected to an input end of the decision module. The decision module is configured to decide a fatigue level of the testee.

A wearable device for reflecting a fatigue level of a human body is disclosed. The device comprises a physiological signal acquisition module, a signal conditioning module, a parameter extraction module and a decision module. The physiological signal acquisition module is configured to acquire physiological signals of a testee. An output end of the physiological signal acquisition module is connected to an input end of the signal conditioning module. The signal conditioning module is configured to perform signal conditioning on the physiological signals. An output end of the signal conditioning module is connected to an input end of the parameter extraction module. The parameter extraction module is configured to extract time-domain and frequency-domain parameters in a specific time window. An output end of the parameter extraction module is connected to an input end of the decision module. The decision module is configured to decide a fatigue level of the testee.

Apparatus and methods for monitoring pregnancy or labour are disclosed. In one embodiment the apparatus includes an electromyography (EMG) sensor having two or more EMG electrodes to monitor fetal or maternal activity during pregnancy or labour and one or more position sensors to monitor the relative positioning of the two or more EMG electrodes during the fetal or maternal activity. In one embodiment, the apparatus includes a monitoring device to be placed on a body and having a plurality of sensors integrated into the monitoring device, the plurality of sensors including at least: a first sensor configured to detect a first type of signal from the body indicative of a first type of fetal or maternal activity during pregnancy or labour; and a second sensor configured to detect a second type of signal from the body, different from the first type of signal, also indicative of the first type of fetal or maternal activity during pregnancy or labour.

A diagnosis device, and more particularly, a compartment syndrome diagnostic device is described herein. The diagnostic device may include a display that renders information associated with stimulation of a motor unit suspected of suffering from compartment syndrome. The diagnostic device may generate a stimulation signal for stimulating the motor unit through an electrode. The device may determine whether the motor unit is at risk for compartment syndrome based on the response of the motor unit to the stimulation. The diagnostic device may also measure pressure of a compartment. The device may determine whether the motor unit is at risk for compartment syndrome based on the measured pressure and the response of the motor unit to the stimulation.

A diagnosis device, and more particularly, a compartment syndrome diagnostic device is described herein. The diagnostic device may include a display that renders information associated with stimulation of a motor unit suspected of suffering from compartment syndrome. The diagnostic device may generate a stimulation signal for stimulating the motor unit through an electrode. The device may determine whether the motor unit is at risk for compartment syndrome based on the response of the motor unit to the stimulation. The diagnostic device may also measure pressure of a compartment. The device may determine whether the motor unit is at risk for compartment syndrome based on the measured pressure and the response of the motor unit to the stimulation.

This invention presents an intraoral device for generation of contact perception between teeth, the device being configured for application to the upper or lower dental arch of a user and comprising a contact means (20, 20′) configured to be associated with at least a portion of one to four posterior teeth (D1) of the upper or lower dental arch, the device (10) being configured to generate a perception of contact to the user upon the contact between the contact means (20, 20′) and at least a portion of the opposing arch to at least a portion of one to four posterior teeth (D1), offering the option of an accessible intraoral device for practical use to the user, and that does not impair the mouth functions of the user during its use in the waking period. This invention further comprises a method of applying the device which allows the user to apply the device without assistance of a skilled professional, and a method for determining the thickness of the aforesaid device.

This invention presents an intraoral device for generation of contact perception between teeth, the device being configured for application to the upper or lower dental arch of a user and comprising a contact means (20, 20′) configured to be associated with at least a portion of one to four posterior teeth (D1) of the upper or lower dental arch, the device (10) being configured to generate a perception of contact to the user upon the contact between the contact means (20, 20′) and at least a portion of the opposing arch to at least a portion of one to four posterior teeth (D1), offering the option of an accessible intraoral device for practical use to the user, and that does not impair the mouth functions of the user during its use in the waking period. This invention further comprises a method of applying the device which allows the user to apply the device without assistance of a skilled professional, and a method for determining the thickness of the aforesaid device.

A fault detection device includes at least one electricity generating unit, to impress a signal on a first useful signal path; at least one first comparison unit, to determine if the signal of the first useful signal path lies within a measuring range; and at least one first interference signal path, designed as a current measurement path, for current-detecting measurement of a first interference signal. A signal path defect analysis unit, is included to detect a signal path defect, upon the impressed signal not being measured on the at least one first interference signal path and upon the checked signal of the comparison unit being determined to lie within the measuring range. Furthermore, corresponding methods are for the detection of signal path defects in a voltage measuring system for measuring bioelectric signals are defined.

A fault detection device includes at least one electricity generating unit, to impress a signal on a first useful signal path; at least one first comparison unit, to determine if the signal of the first useful signal path lies within a measuring range; and at least one first interference signal path, designed as a current measurement path, for current-detecting measurement of a first interference signal. A signal path defect analysis unit, is included to detect a signal path defect, upon the impressed signal not being measured on the at least one first interference signal path and upon the checked signal of the comparison unit being determined to lie within the measuring range. Furthermore, corresponding methods are for the detection of signal path defects in a voltage measuring system for measuring bioelectric signals are defined.