A surgical stapling instrument includes a shaft assembly, an end effector at a distal end of the shaft assembly and having a first jaw with an anvil and a second jaw operable to cooperate with the first jaw to clamp tissue, and a cartridge inserted into the second jaw. The cartridge includes staples, a movable member translatable distally during a firing stroke to discharge the staples into tissue, a first sensor assembly configured to monitor a first condition of the cartridge, and a second sensor assembly configured to monitor a second condition of the cartridge. A first processor is coupled with the first and second sensor assemblies and is configured to receive first and second signals from the sensor assemblies, respectively, where each signal is indicative of the respective condition of the cartridge. The first processor is configured to selectively permit or restrict the firing stroke based upon the signals.

A medical device is configured to detect an atrial tachyarrhythmia episode. The device senses a cardiac signal, identifies R-waves in the cardiac signal attendant ventricular depolarizations and determines classification factors from the R-waves identified over a predetermined time period. The device classifies the predetermined time period as one of unclassified, atrial tachyarrhythmia and non-atrial tachyarrhythmia by comparing the determined classification factors to classification criteria. A classification criterion is adjusted from a first classification criterion to a second classification criterion after at least one time period being classified as atrial tachyarrhythmia. An atrial tachyarrhythmia episode is detected by the device in response to at least one subsequent time period being classified as atrial tachyarrhythmia based on the adjusted classification criterion.

A vaporization device includes a first portion and a second portion. The first portion includes a first body defining a first interior volume, a first half of a split-pod, a second half of a split-pod, an opening, a first heating apparatus, and a second heating apparatus. The first half of the split-pod is configured to hold a nicotine-containing liquid. The second half of the split-pod is configured to hold a non-nicotine-containing liquid. The opening separates the first half from the second half of the split-pod. The first heating apparatus is dedicated to the first half. The second heating apparatus is dedicated to the second half. The second portion includes a second body defining a second interior volume and a computing system. The computing system is disposed within the second interior volume. The computing system is configured to vary an amount of current supplied to the first and second heating apparatuses.

A medical instrument display includes an image storage that stores a plurality of image data of a medical instrument, a data analyzer that searches a plurality of image data stored in the image storage on a certain condition, and a display controller that causes a display to display a first medical instrument image that has been selected from thumbnail images, the thumbnail images being based on a plurality of the image data obtained by the search, and a second medical instrument image in good order, the second medical instrument image being different from the first medical instrument image.

A capnography system includes a CO.sub.2 sensing system having a CO.sub.2 sensor configured to measure a CO.sub.2 concentration in exhaled breath of a subject, a processor configured to derive one or more breath related parameters based on the measured CO.sub.2 concentration, and a communication unit. The capnography system includes a tubing system configured to allow flow of respiratory gasses therethrough. The tubing system includes a connector configured to connect the tubing system to the CO.sub.2 sensing system and a communication component configured to provide an indication of a type of the tubing system to the communication unit. The communication unit is configured to transfer data to the processor based on the indication obtained from the communication component, and the processor is configured to change or suggest a change of an operation mode of the CO.sub.2 sensing system based on the data.

A wearable article comprising: a first biosensor; an erasable and programmable memory configured to store information relating to the wearable article and/or the first biosensor; and an interface for connection to an electronic module. The interface is configured to permit the transfer of information between the memory and an electronic module connected to the interface. The electronic module is able to read information from the memory and write information to the memory via the interface. The memory may have a single-wire input-output interface. The information may comprise wearable article size information. The wearable article size information may be used to determine a compensation that should be performed to sensor data received from the wearable article to compensate for electrical properties of the wearable article.

An ophthalmic portable laser slit lamp for ophthalmic examination and a method of eye inspection. The device comprises a portable housing containing an electronic timer circuit, a rechargeable battery, a laser module containing a laser emitting diode, a fixed focusing lens that sets the appropriate focal distance for the examination method and a line generator lens acting as a slit aperture. The laser beam aimed to the eye of the patient illuminates the eye with a very thin straight laser line at a fixed focal distance. The device also comprises a safety timer circuit that protects the patients eye against irradiation overload. The method of the invention allows the surgeon to detect surgical eye disorders at the operating room and helps to carry out a correct diagnosis in a much more precise and effective way than any light or laser spot device.

The switchover between an expiring on-body medicament delivery device and a replacement on-body medicament is made to eliminate or significantly decrease the time where an on-body medicament delivery device is operational to deliver medicament to a user. The replacement on-body medicament device is attached to the user and prepped for operation while the expiring on-body medicament delivery device is still operational. The switchover between on-body sensors also may be improved. Methods for calibrating a replacement on-body sensor while the expiring on-body sensor is still operative are provided. The calibrating may be performed quickly so that there is no gap in operation between expiration of the expiring on-body sensor and full operation of the replacement on-body sensor.

The present disclosure relates to a notification method of a continuous glucose monitoring system. A notification method of a continuous glucose monitoring system, according to one embodiment of the present invention, may comprise the steps of: performing a communication connection between a body attachment unit and a communication terminal for the communication terminal to receive blood glucose data measured from the body attachment unit which is attached to a human body and continuously measures blood glucose; transmitting information on the body attachment unit from the body attachment unit to the communication terminal and calculating a remaining use period of the body attachment unit; and generating, in the communication terminal, a notification on the remaining use period of the body attachment unit. According to the present disclosure, as the notification for the remaining period of the body attachment unit is generated in the communication terminal, there is an effect wherein a user can prepare in advance a body attachment unit to be replaced before the use period of the body attachment unit ends.

Data-stream bridging for sensor transitions is described. A first data stream of glucose measurements is received from a first glucose sensor worn by a user. A termination event for the first glucose sensor is detected when production and/or communication of the first glucose measurements via the first data stream ceases. Next, a second data stream of glucose measurements is received from a second glucose sensor worn by the user that replaces the first glucose sensor. During a warmup period for the second glucose sensor, estimated glucose values are output for the user based on both the first data stream of glucose measurements received from the first glucose sensor prior to the termination event and the second data stream of glucose measurements received from the second glucose sensor.