According to an example aspect of the present invention, there is provided a biopsy needle device comprising a biopsy needle attachment mechanism arranged to mechanically couple a biopsy needle to the biopsy needle device, an actuator mechanism comprising a transducer configured to interconnect electrical signals at one port to mechanical motion at another port, the actuator mechanism configured to transmit flexural vibration to the biopsy needle when the biopsy needle is coupled to the biopsy needle device, a sensor device configured to measure a power of the flexural vibration transmitted to the biopsy needle via the transducer and a reflected power of flexural vibration received by the biopsy needle device from the biopsy needle, and circuitry configured to determine a difference between the power of the flexural vibration transmitted to the biopsy needle and the reflected power of flexural vibration received by the biopsy needle device from the biopsy needle.

An intraoral moisture measuring device includes: a swing member that swings with respect to a main body about a predetermined swing center; a moisture amount detection unit provided at a tip of the swing member, for detecting a moisture amount by being directly or indirectly abutted against a measurement site in a mouth; and a biasing member for biasing the swing member in one of swing directions. Consequently, the intraoral moisture measuring device is capable of measuring intraoral moisture in a simple and highly-accurate manner.

While power consumption is suppressed, biological information is measured without fail when a condition of a subject changes. An aspect of the present invention is configured to acquire a biological signal related to a beat of a heart of the subject from a biometric sensor, detect a feature of the biological signal from the biological signal acquired, determine an abnormal change in the feature based on the feature detected and first threshold information set in advance, set an operation mode of the biometric sensor to a continuous operation mode when the abnormal change in the feature is determined, and set the operation mode of the biometric sensor to an intermittent operation mode in a period without the abnormal change.

A sensor, system, and method for detecting and correcting for changes to an analyte indicator of an analyte sensor. The analyte indicator may be configured to exhibit a first detectable property that varies in accordance with an analyte concentration and an extent to which the analyte indicator has degraded. The analyte sensor may also include a degradation indicator configured to exhibit a second detectable property that varies in accordance with an extent to which the degradation indicator has degraded. The analyte sensor may generate (i) an analyte measurement based on the first detectable property exhibited by the analyte indicator and (ii) a degradation measurement based on the second detectable property exhibited by the degradation indicator. The analyte sensor may be part of a system that also includes a transceiver. The transceiver may use the analyte and degradation measurements to calculate an analyte level.

A system and method are provided for detecting air embolisms in lines for hemodynamic monitoring. In use, using a first sensor, one or more gas bubbles are detected within a first line for hemodynamic monitoring. In response to the detecting, a first clamp attached to the first line for hemodynamic monitoring is contracted.

A device for measuring oxygen saturation includes circuitry configured to determine a measured difference of forward voltage based on a first forward voltage at a first light emitting diode and a second forward voltage a second light emitting diode and determine that the first and second light emitting diodes are valid based on a calibrated difference of forward voltage and the measured difference of forward voltage. In response to the determination that the first and second light emitting diodes are valid, the circuitry is configured to determine an oxygen saturation level.

A device for measuring oxygen saturation includes circuitry configured to determine a series resistance for a light emitting diode based on a first diode voltage at the light emitting diode for a first current, a second diode voltage at the light emitting diode for a second current, and a third diode voltage at the light emitting diode for a third current. The circuitry is further configured to determine an intensity of a received photonic signal corresponding to an output photonic signal output using the light emitting diode. The circuitry is further configured to determine an oxygen saturation level based on the intensity of the received photonic signal and the series resistance.

A pain estimation apparatus includes: an information acquisition unit configured to perform a process for acquiring, in an endoscopic examination, examination state information for estimation including insertion state information for estimation including at least one of insertion shape information for estimation about an insertion shape of an insertion section of an endoscope inserted inside a body of a subject or operation force amount information for estimation about an amount of force applied to the insertion section, and information different from either of the insertion shape information for estimation and the operation force amount information for estimation; and a pain estimation processing means configured to generate pain information about pain of the subject based on the examination state information for estimation including the information different from either of the insertion shape information for estimation and the operation force amount information for estimation, and the insertion state information for estimation.

A system includes a console assembly, a trocar assembly operably coupled to the console assembly, a camera assembly operably coupled to the console assembly having a stereoscopic camera assembly, and at least one rotational positional sensor configured to detect rotation of the stereoscopic camera assembly about at least one of a pitch axis or a yaw axis. The console assembly includes a first actuator and a first actuator pulley operable coupled to the first actuator. The trocar assembly includes a trocar having an inner and outer diameter, and a seal sub-assembly comprising at least one seal and the seal sub-assembly operably coupled to the trocar. The camera assembly includes a camera support tube having a distal and a proximal end, the stereoscopic camera operably coupled to the distal end of the support tube and a first and second camera module having a first and second optical axis.

An apparatus (100) comprises at least one electronic processor (101, 113) programmed to: control an associated medical imaging device (120) to acquire an image (130); compute values of textural features (132) for the acquired image; generate a signature (140) from the computed values of the textural features; and at least one of: display the signature on a display device (105); and apply an artificial intelligence (AI) component (150) to the generated signature to output image artifact metrics (152) for a set of image artifacts and display an image quality assessment based on the image artifact metrics on the display device.