An identifier is provided to a medical device such as a syringe to uniquely identify the medical device. For a syringe, the unique identifier may be in the form of a bar code printed onto the thumb press, stem, or both at the plunger of the syringe. The bar code may be a 2-dimensional bar code or a 1-dimensional bar code. Alternatively, an RFID tag may be attached to the plunger, for example fitted to or embedded into the thumb press. The unique identifier provides, at minimum, the manufacturing data unique to the syringe so that the history of the syringe may be readily traced and associated with the medical records of the patient the syringe is used for.

An automated external defibrillator (AED) system includes shock generating electronics configured to provide at least one electrical shock suitable for a patient experiencing a cardiac event, a battery configured for providing power to the shock generating electronics, power management circuitry configured for managing the shock generating electronics and the battery, a single microprocessor configured for controlling the power management circuitry, and an enclosure configured to house the shock generating electronics, the battery, the power management circuitry, and the single microprocessor. In an embodiment, the AED system includes at least two cardiac pads in electrical connection with the shock generating electronics and including a medication delivery mechanism configured for delivering a predetermined dose of a medication to a patient when the cardiac pads are placed on the patient for shock delivery.

Auto-injectors and associated assemblies and methods for delivery of medicament in a controlled manner are disclosed herein.

A method and device for delivering medications that includes a syringe body, a cartridge nest with an application tip, a plunger actuator, and an electronic lock subassembly adapted for preventing administration of the medication until specific conditions are met. The medicine cartridge may comprise a form of a digital security key and/or physical security to prevent the device from administering medication unless specific configurations and conditions are met. The device may further be adapted with pre-programmed information and may be used with a smartphone, tablet, or computer application. The electronic lock subassembly will only permit the administration of medicine when the patient and/or administrator is verified via facial and voice recognition, biometric identifier, or other unique information. Upon proper permission and/or use of uniquely-keyed and matched components, the device may be used to administer medicine, including injecting medicine into the nasal cavity of a patient.

An inhalation device for e.g., nicotine products which receives a user input regulating the amount of nicotine the user wants to receive. Once the selected amount has been delivered to the user, the device shuts off its atomizer to conclude operation.

Portable or ambulatory infusion devices and systems capable of remotely updating an ambulatory fluid delivery device include safety protocols that verify the status of the ambulatory fluid delivery device before and after a field update of software. Methods of accomplishing the same field update of software are also described.

A system including a user device and a drug delivery device, the user device including a processor, a memory, a display and a camera; the drug delivery device including a body, an injection mechanism and a cap; wherein the memory of the user device stores instructions which, when executed by the processor, cause the user device to: capture at least one image and/or video of the drug delivery device; identify, in the at least one captured image and/or video, at least one distinctive feature; compare the at least one distinctive feature to at least one predefined set of distinctive features stored in the memory of the user device; identify the drug delivery device based on a match of the at least one distinctive feature identified with at least one of the predefined set of distinctive features; and output the result of identification of the drug delivery device on the display.

A method includes receiving, with an apheresis system, data associated with a donor; determining, based on the data associated with a donor, an identification of the donor; receiving, with the apheresis system, data associated with a blood component collection set; receiving, with the apheresis system, data associated with a plasma collection bottle; and performing, with the apheresis system, a plasma donation process based on the identification of the donor, the data associated with the blood component set, and the data associated with the plasma collection bottle. Receiving the data associated with the donor may include scanning, with a scanner, an image. The scanner is disposed on the apheresis system and the image may include one of a one-dimensional barcode or a two-dimensional barcode. The data associated with the donor may be displayed on a user device.

A syringe use monitoring device that can attach to a syringe and detect the type of medication being loaded and measure the force applied to the plunger and thus monitor subsequent delivery of medication and delivery pressure as a substance is being injected, and at least one display and/or alarm can indicate normal and/or abnormal conditions so that feedback can be employed during the injection process is provided.

A mist inhaler device (200) for generating a mist for inhalation by a user. The device includes a mist generator device (201) and a driver device (202). The driver device (202) is configured to drive the mist generator device (201) at an optimum frequency to maximise the efficiency of mist generation by the mist generator device (201).