An injection device adapted to be worn on the body of a patient. The device includes an injector containing an agent for treating hypoglycaemia. A control assembly including a signal receiver is configured to receive signals from a glucose sensor, the control assembly being electrically coupled to an alarm and configured to activate the alarm upon a signal received in the signal receiver being indicative of hypoglycaemia, the control assembly being configured to cause the injector to administer through a needle a dose of the agent to the patient after a predetermined period of time of the signal receiver receiving the signal indicative of hypoglycaemia, the control assembly having a manually activated switch that when activated prior to the expiration of the predetermined period of time causes the control assembly to abort the injection of the agent.

A method and system are provided for verifying whether a non-medical client device is operating correctly with a medical device controlled by the non-medical client device (NMCD) and causing a notification to be generated. In accordance with the method, an application at the non-medical client device monitors for occurrence of a trigger event and when a trigger event is detected, the application can perform one or more diagnostic checks to verify whether a medical control application at the NMCD is operating correctly. When the application determines that the one or more diagnostic checks have failed, the medical control application can attempt to initiate one or more remedial correction measures to restore the medical control application so that it is operating correctly. When the one or more remedial correction measures were unsuccessful, the application causes the notification to be generated via a user interface of the non-medical client device.

A rapid chemical delivery system is presented. The system includes a portable handheld chemical storage receiving receptacle, wherein the receptacle is configured to receive and mate with an insertable chemical container and wherein the container houses a chemical. The system also includes a base affixed to the chemical storage receptacle, wherein a side of the base is configured to connect with an object and another opposing side is configured to attach to the chemical storage receptacle. The system further includes a rapid chemical deployment mechanism utilizing the portable handheld chemical storage receptacle and arranged to deploy the chemical from the chemical container when activated.

An overdose of opioids can cause the user to stop breathing, resulting in death. A physiological monitoring system monitors respiration based on oxygen saturation readings from a fingertip pulse oximeter in communication with a smart mobile device and sends opioid monitoring information from the smart mobile device to an opioid overdose monitoring service. The opioid overdose monitoring service notifies a first set of contacts when the opioid monitoring information.

An overdose of opioids can cause the user to stop breathing, resulting in death. A physiological monitoring system monitors respiration based on oxygen saturation readings from a fingertip pulse oximeter in communication with a smart mobile device and sends opioid monitoring information from the smart mobile device to an opioid overdose monitoring service. The opioid overdose monitoring service notifies a first set of contacts when the opioid monitoring information.

A universal wearable fluid delivery system includes a body panel which includes a plurality of connection points. A fluid dispenser includes a taut pocket defined by at least one taut surface and a portion of a surface of the body panel and is adapted to receive a fluid bag. A stretch pocket is disposed within the taut pocket. The stretch pocket is defined between a surface of at least one stretch panel and about a common portion of the surface of the body panel and is adapted to receive a pressure infusion bag disposed within. At least one strap is coupled to the body panel via two connection points of the plurality of connection points to secure the fluid dispenser to a body of a human or animal patient. A wearable fluid delivery system and a fluid dispenser and body panel assembly are also described.

A take-home drug delivery system includes a kit container defining an inner volume, a drug delivery container preparation assembly at least partially disposed within the inner volume of the kit container, and a sterile drape at least partially disposed within the inner volume of the kit container. The drug delivery container preparation assembly includes at least a drug delivery container, a drug vial containing a drug to be administered, a tubing set, and a drug delivery container mounting apparatus. The sterile drape includes a placement legend illustrated thereon.

Infusion systems, infusion devices, and related operating methods are provided. A method of operating an infusion device involves obtaining an input qualitative event attribute, such as a meal size, obtaining a quantitative event attribute associated with the qualitative event attribute that is representative of a subset of historical events for a patient associated with the qualitative event attribute, such as a representative carbohydrate amount for the qualitative meal size, and thereafter determine a dosage of fluid based at least in part on the quantitative event attribute and operate the infusion device to deliver the dosage of the fluid to the patient.

Medical devices and related patient management systems and methods are provided. A method of monitoring a plurality of patients involves a computing device obtaining measurement data for the plurality of patients from a database, obtaining one or more prioritization rules from the database, generating a prioritized list of the plurality of patients based on the measurement data in accordance with the one or more prioritization rules, and providing a dashboard graphical user interface (GUI) display including the prioritized list. The prioritized list on the dashboard GUI display is dynamically updated in accordance with the prioritization rule(s) in response to updated measurement data in the database.

A system for automatically injecting a substance. The system includes an injecting device, which includes an injecting cartridge, a biasing mechanism and a latch. The injecting cartridge includes a syringe having a needle and a plunger, and an injecting mechanism for moving the syringe and pushing the plunger of the syringe. The injecting cartridge includes a needle and a plunger, and an injecting mechanism for moving the syringe and pushing the plunger of the syringe. The biasing mechanism pivots the injecting cartridge from a storage position into an injecting position. The latch is moveable from a holding position for holding the biasing mechanism in the storage position to a release position for releasing the biasing mechanism. The system may further comprise sensors to measuring physical signs of a user. The system may also include controller to control the automatic injection of the substance.