An apparatus for estimating bio-information according to an embodiment includes: a sensor that measures a pulse wave signal from an object and contact pressure of the object; and a processor that obtains an oscillometric envelope based on an amplitude of the pulse wave signal and the contact pressure, and estimates bio-information based on a center of mass of a phase of contact pressure of the obtained oscillometric envelope.

The invention comprises a method and apparatus for noninvasively determining state of a person, comprising the steps of: providing an analyzer comprising a first and second spectrometer unit and a main controller subsystem; replaceably attaching the first spectrometer unit to the person at a first illumination zone; the first spectrometer unit delivering first photons, from first illumination optics, along a first mean z-axis optical path normal to a first x/y-plane tangentially contacting the first illumination zone of the person; replaceably attaching a second spectrometer unit to the person at a second illumination zone; the second spectrometer delivering second photons, from second illumination optics, along a second mean z-axis optical path perpendicular to a second x/y-plane tangentially contacting the second illumination zone of the skin, the first x/y-plane noncoplanar with the second x/y-plane; and the main controller processing detected signals to generate at least one measure of state of the person.

A condition classifying device includes: an input interface configured to receive first data corresponding to a blood refilling state after ischemia of a subject, and second data corresponding to a physiological parameter that exhibits changes caused by vasodilation of the subject; a processor configured to perform a classification of a condition of the subject related to sepsis based on the first data and the second data; and an output interface configured to output a result of the classification.

A method includes determining that a portion of a force applied to a sensor system was applied to a non-inclusive region of the sensor system. An activation area of the non-inclusive region may be determined. A force distribution of the non-inclusive region may be determined. A corresponding force measurement of the non-inclusive region based on the activation area and the force distribution may be calculated.

The invention relates to a method for determining the occurrence of a vascular collapse of a blood vessel in or on the eye. According to the invention, it is proposed that the vascular collapse be determined from a measured temporal change of blood flow in the blood vessel.

The present invention is directed generally to a method and apparatus for human brain neuroprotection during surgery. The invention includes use of a heart-lung machine to generate periodic rectangular pulsation of blood flow. The invention uses a non-invasive CA monitor to continuously record transient functions such as dynamic autoregulation functions of a human brain cerebrovascular autoregulation system and process the data to generate an alarm to indicate CA impairment and take steps to minimize the CA impairment event.

A device for measuring hair properties has a first part (I) and a second part (II) between which hair (H) is guided. The first part includes a measuring probe (MP), and the second part is arranged for deforming the hair against the measuring probe. While the device moves along the hair, the measuring probe experiences both a friction force resulting from the hair being guided along the measuring probe, and a deformation force resulting from hair deformation by the second part against the measuring probe. The second part includes a pressure element (PB, S) for pressing the hair against the measuring probe. In alternative embodiments, the second part comprises alignment elements (AE) at opposite sides of the measuring probe, and guidance elements (G) for mitigating an influence of an angle at which the device is applied to the hair to the friction force and/or the deformation force.

An object of the present invention is to provide a durometer enabling a contact portion in contact with an object to perform smooth piston motion. The durometer includes a main body unit including a movable unit pressed continuously against an object to be measured, a first sensor outputting acceleration information corresponding to an acceleration of movement of a contact part of the object to be measured in contact with the movable unit in a pressing direction, a second sensor outputting reactive force information corresponding to a reactive force at the contact part of the object to be measured in contact with the movable unit, a motor, a crank mechanism driven by the motor and causing the main body unit and the movable unit to perform piston motion, and at least one buffering member disposed on a periphery of the main body unit.

A foot pedal device configured to provide force feedback to an operator during ophthalmic surgery is described. The foot pedal device includes a processor and a memory containing instructions which, when executed by the processor, cause the processor to transmit, in response to a movement of a moveable member, a control signal to a surgical console for initiating an action of an ophthalmic surgery tool coupled with the surgical console. The foot pedal device includes a force feedback mechanism configured to selectively apply a resistance force in opposition to the movement of the movable member. The memory contains instructions which, when executed by the processor, cause the processor to receive, from the surgical console, a trigger signal, and send a force feedback signal to the force feedback mechanism. The force feedback mechanism is configured to apply the resistance force to the movable member upon receiving the force feedback signal.

A method that simulates a response of a target person to one or more simulation inputs comprises: contacting a body of a first test subject with a force-sensing probe; measuring a first force applied by the probe to the body of the first test subject; obtaining a first relative movement comprising a first movement of the probe relative to the body of the first test subject; determining one or more model parameters associated with the body of the first test subject based on the measured first force and the first relative movement; incorporating the one or more model parameters into a target model of at least a portion of a body of a target person; obtaining a simulation input for application to the target model; and simulating a response of the target person in response to the simulation input using the target model.