A vaporization device includes biometric recognition systems. A vaporizer device is provided. The vaporizer device includes a vaporizer body comprising a cartridge receptacle, a heating element, a power source, and a sensor. The vaporizer device further includes a vaporizer cartridge that is selectively coupled to the vaporizer body, the vaporizer cartridge comprising one or more translucent surfaces and a passageway between the sensor and the one or more translucent surfaces. The vaporizer device further includes a controller configured to determine, based on data from the sensor, whether a user is authorized to use the vaporizer device. The controller further configured to provide power to the heating element to generate an aerosol responsive to determining the authorization of the user. Related methods and articles of manufacture are also described.

Method of operating a non-invasive blood pressure, NIBP, monitor to measure the blood pressure of a subject, the NIBP monitor comprising a cuff, a pressure sensor for measuring the pressure in the cuff and for outputting a pressure signal representing the pressure in the cuff and a physiological parameter sensor, the method comprising obtaining a first measurement of pulse rate or heart rate for the subject during inflation of the cuff, the first measurement being obtained from the pressure signal; obtaining a second measurement of the pulse rate or heart rate for the subject during inflation of the cuff, the second measurement being obtained from the physiological parameter sensor; comparing the first measurement and the second measurement; and estimating the reliability of a blood pressure measurement obtained by the NIBP monitor during inflation of the cuff based on the result of the step of comparing.

Systems, devices, and methods are operable to track usage of a surgical instrument and modify the performance of the surgical instrument based on the prior usage of the surgical instrument. Some surgical instruments are designed to have a limited service life beginning at their first use, or a limit to their overall usage in order to ensure safe use of the sensitive instruments. However, a lack of ability to track usage characteristics when the instrument is separated from an external power supply allows for user abuse and avoidance of such safety mechanisms. Adding a battery or capacitor to the instrument may allow for an ability to track usage when the instrument is separated from an external power supply. Implementing special user prompts, device use ratios, and device use half-life upon powering down of an instrument may additionally be used to prevent circumvention of safety features.

A monitoring device for physiological signal monitoring includes a first light receiving and transmitting device and a control device. The first light receiving and transmitting device generates a first light signal to an object and receives a second light signal to generate a first electrical signal. The control device controls the first light receiving and transmitting device to generate the first light signal in a first period, and controls the first light receiving and transmitting device to receive the second light signal to generate the first electrical signal in a second period. The invention further includes an operating method for physiological signal monitoring.

A system (100) is provided for processing status information of a medical device (020-023). The medical device performs a medical function at a bedside of a patient and is arranged for generating an alarm signal (030) to alert a caregiver of the patient to an occurrence of an event which is associated with the performing of the medical function. A status interface (120) acquires a device signal (024) of the medical device, the device signal comprising status information which is indicative of a current status of the performing of the medical function. Moreover, an analysis subsystem (140) analyzes the status information to estimate an imminent occurrence of the event based on said current status, and a notification subsystem notifies the caregiver of the imminent occurrence away from the bedside of the patient of the event by a generating a notification signal (162) for a notification device (060-064). The priority of notifying the caregiver is based on an estimate of whether the patient is asleep. The system enables the caregiver to be notified about the event ahead of time, i.e., before the event occurs and thus before the medical device generates an alarm signal. Advantageously, the patient is less disturbed by alarm signals during sleep.

A vision protection method is provided to ensure a viewer to rest his/her eyes after viewing on an electronic device for a certain period, wherein the eyesight protection method includes the steps of detecting at least one of eye activities of the viewer and working parameter of the electronic device in a working mode of the electronic device during the viewer is working on a current work displaying by the electronic device; switching the working mode of the electronic device to a resting mode when an abnormal eye activity of the viewer is detected; and switching the electronic device from the resting mode back to the working mode to resume the display of the current work of the electronic device. Therefore, the viewer is enforced to rest his/her eyes after every certain period.

An ophthalmic surgical system includes an imaging device configured to acquire a first image of a fundus of an eye and a hemorrhage detecting unit. The hemorrhage detecting unit includes a processor configured to receive the first fundus image from the imaging device, analyze the first fundus image to detect a hemorrhage in the eye, and in response to detecting the hemorrhage, send a signal to an intraocular pressure controller. The ophthalmic surgical system further includes the intraocular pressure controller, which includes a processor configured to receive the signal from the hemorrhage detecting unit, in response to the received signal, determine if a current intraoperative pressure of the eye is below a predetermined threshold, and in response to determining the current intraoperative pressure of the eye is below the predetermined threshold, generate a signal to increase the intraoperative pressure of the eye.

An example accessory for an inhaler includes: a housing to couple to the inhaler; an accelerometer disposed in the housing, the accelerometer to obtain (i) motion data representing motion of the inhaler and (ii) orientation data representing an orientation of the inhaler; a microphone disposed in the housing, the microphone to obtain audio data for determining an inhalation rate of a user of the inhaler; a force sensor disposed in the housing, the force sensor to obtain force data representing force applied to the accessory; a communications interface disposed in the housing; a memory disposed in the housing; and a processor disposed in the housing, the processor interconnected with the communications interface and the memory the processor to: detect actuation of the inhaler based on the force data applied to the accessory; and generate dosage administration data based on the motion data, the orientation data and the audio data.

A system for analyzing the energy delivered to ECG device from the defibrillator is disclosed. The system includes an energy analyzing unit configured to measure the energy delivered to the ECG device from the defibrillator, wherein the energy gets diverted to the ECG device during operation of the defibrillator; and a presentation unit capable of presenting the measured energy in the ECG device.

Embodiments described herein include sensors and sensor systems having probe-off detection features. For example, sensors and physiological monitors described herein include hardware and/or software capable of providing an indication of the integrity of the connection between the sensor and the patient. In various embodiments, the physiological monitor is configured to output an indication of a probe-off condition for an acoustic sensor (or other type of sensor). For example, in an embodiment, a signal from an acoustic sensor is compared with a signal from a second sensor to determine a probe-off condition.