A wearable device includes a blood pressure sensor configured to continuously measure blood pressure of a measurement subject; a check section configured to, in response to an instruction for commencing a continuous measurement of the blood pressure, check whether a treatment device to be used during the continuous measurement of the blood pressure is attached to the measurement subject; a measurement controller configured to, when the check section confirms that the treatment device is attached, execute a continuous measurement of the blood pressure with the blood pressure sensor; and a display section configured to, when the check section does not confirm that the treatment device is attached, display a form of guidance to prompt attachment of the treatment device.

A non-transitory computer readable medium storing data and computer implementable instructions that, when executed by at least one processor, cause the at least one processor to perform operations for generating cross section views of a wound, the operations including receiving 3D information of a wound based on information captured using an image sensor associated with an image plane substantially parallel to the wound; generating a cross section view of the wound by analyzing the 3D information; and providing data configured to cause a presentation of the generated cross section view of the wound.

A surgical robotic system including at least one movable cart including a robotic arm having a surgical instrument is disclosed. The system further includes a control tower having at least one component and a power supply system coupled to the at least one movable cart via a cable. The power supply system includes: a tower power supply chassis configured to supply first direct current to the at least one movable cart; a power distribution unit configured to supply second direct current to the at least one component; a first uninterruptable power supply coupled to the tower power supply chassis; and a second uninterruptable power supply coupled to the power distribution unit. The control tower further includes a startup controller configured to control the power supply system to transition between a plurality of power stages.

The invention relates to medical devices for carrying out internal examination, such as laryngoscopes. The laryngoscope is provided with a camera element within a channel inside the blade.

Because reprocessing or refurbishing of physiological sensors reuses large portions of an existing sensor, the material costs for refurbishing sensors is significantly lower than the material costs for making an entirely new sensor. Typically, existing reprocessors replace only the adhesive portion of an adhesive physiological sensor and reuse the sensing components. However, re-using the sensing components can reduce the reliability of the refurbished sensor and/or reduce the number of sensors eligible for refurbishing due to out-of-specification sensor components. It is therefore desirable to provide a process for refurbishing physiological sensors that replaces the sensing components of the sensor. While sensing components are replaced, generally, sensor cable and/or patient monitor attachments are retained, resulting in cost savings over producing new sensors.

A congenital heart disease monitor utilizes a sensor capable of emitting multiple wavelengths of optical radiation into a tissue site and detecting the optical radiation after attenuation by pulsatile blood flowing within the tissue site. A patient monitor is capable of receiving a sensor signal corresponding to the detected optical radiation and calculating at least one physiological parameter in response. The physiological parameter is measured at a baseline site and a comparison site and a difference in these measurements is calculated. A potential congenital heart disease condition in indicated according to the measured physiological parameter at each of the sites or the calculated difference in the measured physiological parameter between the sites or both.

A radiation imaging apparatus includes a pixel array including, in an imaging region where a plurality of pixels is arranged in a matrix, a detection pixel group in which a plurality of detection pixels is arranged in a row direction, and a control unit configured to control imaging. A grid having a stripe structure in which a radiation transmissive layer and a radiation absorption layer that are strip-shaped and extend in a first direction are alternately arranged in a second direction is disposed and can be used in the radiation imaging apparatus. The radiation imaging apparatus further includes a determination unit configured to determine whether a mode in which the imaging using signals from the detection pixel group is controlled is executable by the control unit, based on information about an angle between the row direction and the first direction.

Various smart medical connection embodiments of the present disclosure encompass a magnetic connectivity manager energizing ferromagnet(s) in response to a powering on the magnetic connectivity manager and a sensing of a connection strain on a medical base (21) and/or a patient base (31) of the device, whereby a magnetic connectivity interface (22, 32) activates a magnetic connectivity between metallic module(s) and the ferromagnet(s) for interfacing the conduit channels of the bases. The various smart medical connection embodiments of the present disclosure further encompass the magnetic connectivity manager deenergizing the ferromagnet(s) in response to a powering down of the magnetic connectivity manager and/or a sensing of a disconnection strain on the base(s), whereby the magnetic connectivity interface (22, 32) deactivates the magnetic connectivity between the metallic module(s) and the ferromagnet(s) for interfacing the conduit channels of the bases.

Method for ascertaining and setting a filling volume of a balloon of a catheter, which is placed in the esophagus of a living being, wherein the balloon is filled and/or emptied using a fluid. According to the invention, the balloon is filled and/or emptied step-by-step using at least two volume steps, a pressure difference between a pressure at the end of an expiration (Pmin) and a pressure at the end of an inspiration (Pmax) is determined for at least two volume steps, a relative pressure difference between Pmin and Pmax is determined, a border range is defined on the basis of the relative pressure difference, and an optimum filling volume is ascertained in consideration of the border range.

Methods of performing diagnostic tests on electroencephalography (EEG) recording devices comprising at least one stimulator coupled with a plurality of EEG electrode recording channels and corresponding recording channel connectors are performed by a test fixture comprising a plurality of resistors coupled with one or more of the EEG electrode recording channels and corresponding recording channel connectors. The methods include performing an impedance test for determining if each EEG recording channel of the EEG recording device has a predefined impedance, performing a channel uniqueness test for each EEG recording channel, performing a test for verifying the state of a switch of the stimulator of the EEG recording device, and performing a test for verifying connector IDs of the recording channel connectors connecting the EEG electrodes to respective EEG recording channels.