Electrodes for use in electroencephalographic recording, including consciousness and seizure monitoring applications, have novel features that speed, facilitate or enforce proper placement of the electrodes, including any of alignment indicators, tabs and juts, color coding, and an insulating bridge between reference and ground electrodes which ensures a safe application distance between the conductive regions of the two electrodes in the event of cardiac defibrillation. A method of using a set of at least four such electrodes is also disclosed.

A mobile device for measuring at least one electrical biosignal. The device comprises a first input and a second input, a measuring circuit part for providing an output signal indicating the electrical biosignal to be measured, the measuring circuit part comprising a first input and a second input, and a charging circuit part for charging a rechargeable battery inserted in the device, the charging circuit part comprising a first input and a second input. The first input of the measuring circuit part and the first input of the charging circuit part are connected to the first input of the mobile device and the second input of the measuring circuit part and the second input of the charging circuit part are connected to the second input of the mobile device.

In the present invention, a medical device authorization system is employed to associate software contained on a medical computing system/computer, such as an EP mapping and recording system, that pertains to a specific medical device, e.g., a transducer, connected to the computer such that the software is only utilized by the computer in conjunction with a catheter that is authorized for use with the computer. The authorization system utilizes an analog authorization waveform/signal that is mixed with the analog device/catheter measured signals transmitted to the computer. The authorization waveform distorts the measured signals in a manner that renders the signals able to be displayed by the system but unusable, unless the computer includes a signal filter operably connected to the device/transducer interface that is configured to remove the interfering authorization waveform from the measured signal.

An electrode structure of a bio-signal measurement comprises electrodes adapted to be adhered on skin with an adhesive and separated from each other. A connector arrangement for an electric contact with an external electric device is on an opposite side of the electrode structure. Electric conductors are electrically connected with the electrodes and the connector arrangement. The electrode structure comprises attachable sections directly adjacent to one of the at least two electrodes, the attachable sections being adapted to be adhered on the skin. The electrode structure comprises a flexible and elastic loose section, which is free from an adherence to the skin, each of the attachable sections being located between an electrode and a loose section.

A diagnostic imaging catheter includes: a drive shaft including a signal transmitter and receiver at a distal end portion and configured to rotate and move forward and backward; a support tube on an outer periphery of the drive shaft along an axial direction and configured to move forward and backward i with the drive shaft; a sheath in which the drive shaft is positioned; a relay connector connected to a proximal end of the sheath; and a sealing member providing a seal between the relay connector and the support tube at a position proximal of the sheath proximal end. The relay connector includes a main lumen extending from the sealing member to the sheath proximal end and an injection lumen communicating with the main lumen at a communication port. A distal end of the support tube is movable to a position proximal of the front edge of the communication port.

An assembly for enabling a caregiver to secure a physiological monitoring device to an arm of a user can include the physiological monitoring device a cradle configured to removably secure to the physiological monitoring device and to the user’s arm. The physiological monitoring device can include a first connector port configured to electrically connect to a first cable and a first locking tab movable between an extended position and a retracted position. The cradle can include a base, first and second sidewalls, a back wall connected to the base and the first and second sidewalls. The cradle can further include a first opening in the back wall configured to receive the first connector port and a second opening in the first sidewall configured to receive the first locking tab when the physiological monitoring device is secured to the cradle and the first locking tab is in the extended position.

A connector is provided with a holding component, a support component, a terminal electrically connected to a contact of a guide wire held by the holding component, and a guide component rotatable around an axial line of the guide wire with respect to the support component. The holding component is provided with a body having an insertion hole for the guide wire and a holding piece extending along an axial line of the insertion hole from the body and capable of being elastically deformed inward in a radial direction with respect to the axial line. The guide component has a guide surface guiding the holding piece inward in the radial direction. The holding component is slid along the axis line of the insertion hole with respect to the guide component, whereby the holding piece abuts on the guide surface to be elastically deformed inward in the radial direction.

A blood pressure monitor configured to removably mount to a cuff in a substantially symmetrical position with respect to a width of the cuff can include a housing defining an interior, a first port, and a second port. The first port can: secure to a first prong of the cuff when the cuff is mounted in a first orientation; receive and secure to a second prong of the cuff when the cuff is mounted in a second orientation; and enable fluid communication between the interior and at least one of a first fluid passage within the first prong and a second fluid passage within the second prong. The second port can: secure to the second prong of the cuff when the cuff is mounted in the first orientation; and receive and secure to the first prong of the cuff when the cuff is mounted in the second orientation.

A regional oximetry sensor can have a sensor head configured to secure to skin of a user and a stem extending from the sensor head. The sensor head can include an emitter configured to transmit optical radiation into the skin and at least one detector configured to receive the optical radiation after attenuation by blood flow within the skin. The stem can be configured to transmit electrical signals from the sensor head to a cable. A plurality of notches can extend from a perimeter of the sensor head towards an interior thereof. The plurality of notches can form a plurality of independently flexible cutouts in the sensor head configured to allow for movement of at least a portion of the skin of the user underlying the sensor head when the regional oximetry sensor is in use.

A high-reliability analyte detection device, includes: a bottom shell ; a sensor, with the sensor being assembled on the bottom shell, the sensor including a signal output end and a detection end, wherein the signal output end is provided with at least two mutually insulated first electrical connection areas, and the signal output end is curved or bent toward the bottom surface of the bottom shell; a transmitter, with the transmitter and the bottom shell being engaged with each other, and the transmitter being provided with at least two mutually insulated second electrical connection areas which correspond to the first electrical connection areas, wherein the first electrical connection areas are electrically connected to the corresponding second electrical connection areas; and an elastic member, with the signal output end being in contact with the elastic member.