A system for displaying blood glucose information includes a blood glucose monitoring device configured to monitor blood glucose levels of a user, and a display. The system may also include one or more processors, and a non-transitory computer-readable medium containing instructions that, when executed by the one or more processors, cause the system to perform operations. The operations may include obtaining the blood glucose levels from the blood glucose monitoring device, where the blood glucose levels include at least a current blood glucose level and a historic blood glucose level. The operations may also include presenting the current blood glucose level at a first location on the display based on a first scale, and presenting the historic blood glucose level at a second location on the display based on a second scale different from the first scale.

A method of displaying blood glucose information may include monitoring blood glucose levels of a user, where the blood glucose levels include at least a current blood glucose level and a historic blood glucose level. The method may also include presenting the current blood glucose level using a point indicator along an approximately horizontally centered axis based on a non-linear scale, and presenting the historic blood glucose level and a predicted future blood glucose level on the display as a single smoothed curve passing the point indicator.

Techniques disclosed herein relate generally to notification generation in a medical device system. In some embodiments, the techniques involve detecting a failure to receive an acknowledgement of a first notification at a mobile device within a predetermined time frame, and delivering, to a medical device, a second notification that indicates the failure to receive the acknowledgement of the first notification at the mobile device within the predetermined time frame.

The invention relates to a liquid storage and delivery system including a reusable housing (8) comprising a control and drive unit, a container (2), a pump module (4) fluidically connected to the container (2), and a coupling system (6) configured for removably coupling the pump module (4) to the control and drive unit (6). The pump module comprises a pump engine (20), a pump outlet (22), and a transmission input coupling (18) coupled to the pump engine (20). The housing comprising the control and drive unit also comprises a pump drive (34) configured to engage the transmission input coupling (18) of the pump module (4) when the pump module (4) is coupled to the housing comprising the control and drive unit. The container (2) is in the form of a flexible pouch and the pump module (4) is permanently integrated with the flexible pouch and forms therewith a disposable unit.

A delivery device for delivering a medical fluid to a patient has a housing configured for receiving a container at least partially filled with the medical fluid. The delivery device further has a drive mechanism associated with the housing configured for delivering the medical fluid from the container to the patient in a dosing procedure. The delivery device further has a module configured for detecting at least one of a property of the dosing procedure and a property of the medical fluid. The module has at least one dose detection sensor configured for detecting an initiation, progression, and completion of the dosing procedure based on a position of a stopper within the container. The module further has at least one temperature sensor configured for measuring a temperature of the medical fluid within the container based on a temperature of the container.

The invention relates to a device for treating an individual suffering from cardiac or circulatory arrest or from a stroke, comprising a blood withdrawal device (BE) that is applied to the individual (P), an analysis unit (BA) which is directly or indirectly connected to the blood withdrawal device for detecting a blood analysis result (BAE) providing at least one characteristic of the blood, directly or indirectly connected to a blood return device (BR) that is applied to the individual (P) and is designed to deliver a substance to the individual via the return device (BR).

An autonomous drug delivery system advantageously utilizes physiological monitor outputs so as to automatically give a bolus of a rescue drug or other necessary medication when certain criteria and confidence levels are met. An emergency button is provided to manually trigger administration of the rescue drug. The rescue drug may be an opioid antagonist in response to an analgesia overdose, a hypotensive drug to avert an excessive drop in blood pressure or an anti-arrhythmia drug to suppress abnormal heartbeats, to name a few.

The invention discloses a detection and therapeutic device and remote monitoring shoes. The detection and therapeutic device comprises a power supply module (a) which is connected with modules with electricity needs and used for powering the modules, a main processor module (b) which is used for collecting and processing signals from sensors and controlling working status of an automatic injection module (d), a detection sensor module (c) which comprises a plurality of sensors in connection with the main processor module (b) and is used for examining nerves, organs or secretions and sending back the results to the main processor module (b), an automatic injection module (d) which comprises a plurality of automatic injectors in connection with the main processor module (b) and is used for administrating according to signals for controlling from the main processor module automatically.

A system for automatically injecting naloxone into a patient, upon detection of physiological parameters indicative of an opioid overdose.

Disclosed are techniques related to determination of adjustments to fluid delivery settings. The techniques may involve accessing an input meal size category, where the input meal size category is selected from among a plurality of meal size categories via a user interface; accessing a plurality of groups of historical meal events for a person, where each group of the plurality of groups is associated with a respective meal size category of the plurality of meal size categories and includes respective historical meal events for the person categorized in the respective meal size category; identifying a group, in the plurality of groups of historical meal events for the person, having an associated meal size category that matches the input meal size category; identifying a person-specific carbohydrate amount representative of the historical meal events in the identified group; and determining a bolus dosage value of insulin based on the person-specific carbohydrate amount.